• The Shedding Disease
    What's going on and what to do about it

    Dr. Syed Haider

    Back in the 1300s during the Black Death plague outbreak in Europe, people were dropping like flies from this mystery illness. No one knew how it spread or how to protect themselves.

    Imagine their shock when some folks started getting sick without ever coming into direct contact with a plague victim!

    Turns out, the plague was spreading through fleas hitching a ride on rats. Even if you never touched a sick person, a plague-carrying flea could jump off a rat and bite you, infecting you with the deadly disease.

    Image
    Huge rat > truly gigantic flea > normal or tiny (?) peasant
    Crazy, right?

    Fast forward to today, and as most of you already know we might be facing a somewhat similar situation with the clot shots.

    For the FOBs (Fresh off the Boat from normie land), hear me out…

    So there's been a ton of stories popping up lately about unvaxxed people, mostly women, having all sorts of weird health issues after being around recently vaccinated folks.

    We're talking things like wacky periods, miscarriages, crazy autoimmune flares, cancers, strokes, etc, all in people who never got the jab themselves.

    At first it seemed like coincidence, but the reports kept piling up.

    It got many doctors scratching their heads (others like me didn’t scratch, we just knew) and wondering, could there be something to this?

    Image
    Man scratches head, Not me.
    Could vaccinated people be "shedding" something that's making unvaccinated people sick?

    There's a few theories flying around.

    One is that the spike proteins made by the vaccines are hitching a ride in tiny bubbles called exosomes that are released in breath, sweat, and other bodily fluids. So an unvaxxed person breathes in these exosomes and boom(!), the toxic spike proteins get into their body and start wreaking havoc. Some people seem super sensitive and react to even tiny amounts.

    Image
    Exosomes are just little bits of our cells membranes that bud off, and can carry anything inside them. In a way viruses are just a class of exosomes, but carrying genetic material that originated outside us (and then multiplied inside us).
    Another idea is that the vaccines are turning people into stealthy virus super-spreaders without them even knowing it. They might feel fine, but they could be carrying and shedding high amounts of virus to everyone around them. So it's not really something in the shot that's being shed, its that they catch COVID, have no symptoms and then just go around spreading COVID everywhere and it’s the COVID that causes the problem (sounds like Big Pharma cope to me, kind of like: it's all in their heads! So yeah, I’m not buying it either).

    Thank you for reading Dr. Syed Haider. This post is public so feel free to share it.

    Share

    There's even studies showing the vaccines contain DNA junk from the manufacturing process that might be messing with our microbiome and turning vaxxed people into walking bio-hazards (this is more like it).

    Some theories are farther out there, like it’s some kind of energetic imbalance, or it’s graphene oxide, or even some kind of nanotech (all your cells are belong to us! not very convincing imo).

    Image
    This is not real! My take on the "flashing lights" in the nanotech videos: spinning particulate crystals dispersing incident light from the microscope? The apparently self-assembling structures: chemical gardens? The broadcasted MAC addresses? Put that sample in a Faraday cage and check it again.
    Anyway, regardless of the mechanism there’s something strange going on.

    The science is still new (there's not much of a career in studying this stuff), but evidence is beginning to stack up suggesting that this "vaccine shedding" stuff might be legit.

    Researchers are finding vaccine cooties like mRNA, spike proteins, and weird DNA bits in saliva, vaginal secretions, sperm, breast milk, even the air around vaxxed people.

    Image
    For the love of God don’t vax the kiddos.
    So what to do?

    Figure out your personal risk level. Some folks seem to be more sensitive than others, especially if you already have health issues (or had spike toxicity before). Might be smart to take extra precautions.

    Rain check: avoid swapping saliva or other Fun Time Activities with vaxxed people if you can, at least for a few weeks to months after they get the shot.

    Feed your body the good stuff to beef up your natural defenses. We're talking clean eats, plenty of Zzz's, and immune-boosting supps like the sunshine vitamin (I mean actual sunshine), as well as actual supplements like C, D, zinc, and quercetin.

    Consider adding some anti-shedding supplements to your arsenal, like

    DETOX [spike buster] to bust up clots or ivermectin to nuke those spike proteins. Work with a dialed in doc (i.e. me) to find the right combo for you.

    If you got mega-dosed with someone's shed, you might need to pull out the big detox guns like plasma donation (which is better tho the paid, or more expensive, less available therapeutic plasmapheresis), ozone therapy, ultraviolet blood irradiation, low-dose naltrexone, microbiome restoration (i.e. stool transplants, probably somewhere in South America or maybe Australia), or IV exosomes. We can help with a custom detox plan at mygotodoc.com (that's me).

    Don't forget to clean your space! Some have reported you can detoxify a room where shedding occurred using hypochlorous acid (Danolyte) or Chlorine Dioxide. UV light systems may also be able to zap any shed cooties floating around (plus they kills normal COVID too, bonus!)

    Share

    Bottom line, we need way more research on this shedding stuff ASAP. But until we know for sure it's not a thing, better safe than shedding or shed upon.

    We all have the right to choose what goes in our bodies, and that includes not getting stealth dosed with someone else's vaccine gunk.

    The health bigwigs need to step up and take this seriously stat (yea right - someone needs to take them to the woodshed, or just shed on them).


    Until then (forever?), keep your eyes open, trust your gut, and do what you gotta do to stay safe out there!

    And if you think you got shed upon, speak up and find a doc who will actually listen (again: moi).

    Shedding is no joke, but together we'll get through this and come out stronger on the other side.

    Drop a comment below and let me know if you’ve been shed upon, what you know works and what else we should do (Nuremberg 2.0, anyone?).

    https://blog.mygotodoc.com/p/the-shedding-disease

    https://telegra.ph/The-Shedding-Disease-03-20
    The Shedding Disease What's going on and what to do about it Dr. Syed Haider Back in the 1300s during the Black Death plague outbreak in Europe, people were dropping like flies from this mystery illness. No one knew how it spread or how to protect themselves. Imagine their shock when some folks started getting sick without ever coming into direct contact with a plague victim! Turns out, the plague was spreading through fleas hitching a ride on rats. Even if you never touched a sick person, a plague-carrying flea could jump off a rat and bite you, infecting you with the deadly disease. Image Huge rat > truly gigantic flea > normal or tiny (?) peasant Crazy, right? Fast forward to today, and as most of you already know we might be facing a somewhat similar situation with the clot shots. For the FOBs (Fresh off the Boat from normie land), hear me out… So there's been a ton of stories popping up lately about unvaxxed people, mostly women, having all sorts of weird health issues after being around recently vaccinated folks. We're talking things like wacky periods, miscarriages, crazy autoimmune flares, cancers, strokes, etc, all in people who never got the jab themselves. At first it seemed like coincidence, but the reports kept piling up. It got many doctors scratching their heads (others like me didn’t scratch, we just knew) and wondering, could there be something to this? Image Man scratches head, Not me. Could vaccinated people be "shedding" something that's making unvaccinated people sick? There's a few theories flying around. One is that the spike proteins made by the vaccines are hitching a ride in tiny bubbles called exosomes that are released in breath, sweat, and other bodily fluids. So an unvaxxed person breathes in these exosomes and boom(!), the toxic spike proteins get into their body and start wreaking havoc. Some people seem super sensitive and react to even tiny amounts. Image Exosomes are just little bits of our cells membranes that bud off, and can carry anything inside them. In a way viruses are just a class of exosomes, but carrying genetic material that originated outside us (and then multiplied inside us). Another idea is that the vaccines are turning people into stealthy virus super-spreaders without them even knowing it. They might feel fine, but they could be carrying and shedding high amounts of virus to everyone around them. So it's not really something in the shot that's being shed, its that they catch COVID, have no symptoms and then just go around spreading COVID everywhere and it’s the COVID that causes the problem (sounds like Big Pharma cope to me, kind of like: it's all in their heads! So yeah, I’m not buying it either). Thank you for reading Dr. Syed Haider. This post is public so feel free to share it. Share There's even studies showing the vaccines contain DNA junk from the manufacturing process that might be messing with our microbiome and turning vaxxed people into walking bio-hazards (this is more like it). Some theories are farther out there, like it’s some kind of energetic imbalance, or it’s graphene oxide, or even some kind of nanotech (all your cells are belong to us! not very convincing imo). Image This is not real! My take on the "flashing lights" in the nanotech videos: spinning particulate crystals dispersing incident light from the microscope? The apparently self-assembling structures: chemical gardens? The broadcasted MAC addresses? Put that sample in a Faraday cage and check it again. Anyway, regardless of the mechanism there’s something strange going on. The science is still new (there's not much of a career in studying this stuff), but evidence is beginning to stack up suggesting that this "vaccine shedding" stuff might be legit. Researchers are finding vaccine cooties like mRNA, spike proteins, and weird DNA bits in saliva, vaginal secretions, sperm, breast milk, even the air around vaxxed people. Image For the love of God don’t vax the kiddos. So what to do? Figure out your personal risk level. Some folks seem to be more sensitive than others, especially if you already have health issues (or had spike toxicity before). Might be smart to take extra precautions. Rain check: avoid swapping saliva or other Fun Time Activities with vaxxed people if you can, at least for a few weeks to months after they get the shot. Feed your body the good stuff to beef up your natural defenses. We're talking clean eats, plenty of Zzz's, and immune-boosting supps like the sunshine vitamin (I mean actual sunshine), as well as actual supplements like C, D, zinc, and quercetin. Consider adding some anti-shedding supplements to your arsenal, like DETOX [spike buster] to bust up clots or ivermectin to nuke those spike proteins. Work with a dialed in doc (i.e. me) to find the right combo for you. If you got mega-dosed with someone's shed, you might need to pull out the big detox guns like plasma donation (which is better tho the paid, or more expensive, less available therapeutic plasmapheresis), ozone therapy, ultraviolet blood irradiation, low-dose naltrexone, microbiome restoration (i.e. stool transplants, probably somewhere in South America or maybe Australia), or IV exosomes. We can help with a custom detox plan at mygotodoc.com (that's me). Don't forget to clean your space! Some have reported you can detoxify a room where shedding occurred using hypochlorous acid (Danolyte) or Chlorine Dioxide. UV light systems may also be able to zap any shed cooties floating around (plus they kills normal COVID too, bonus!) Share Bottom line, we need way more research on this shedding stuff ASAP. But until we know for sure it's not a thing, better safe than shedding or shed upon. We all have the right to choose what goes in our bodies, and that includes not getting stealth dosed with someone else's vaccine gunk. The health bigwigs need to step up and take this seriously stat (yea right - someone needs to take them to the woodshed, or just shed on them). Until then (forever?), keep your eyes open, trust your gut, and do what you gotta do to stay safe out there! And if you think you got shed upon, speak up and find a doc who will actually listen (again: moi). Shedding is no joke, but together we'll get through this and come out stronger on the other side. Drop a comment below and let me know if you’ve been shed upon, what you know works and what else we should do (Nuremberg 2.0, anyone?). https://blog.mygotodoc.com/p/the-shedding-disease https://telegra.ph/The-Shedding-Disease-03-20
    BLOG.MYGOTODOC.COM
    The Shedding Disease
    What's going on and what to do about it
    Angry
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    0 Kommentare 1 Anteile 2006 Ansichten
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    Master Peace Master Peace is a 100% natural nano-zeolite supplement for heavy metal chelation. This product is volcanic ash harvested from the sea flour bed and infused with marine plasma. The zeolite is structured and reduced in a stabilised nanoparticle form with zero chemicals. These are natural nano-minerals. Note: Master Peace nano-zeolite does not contain nanotechnology. ORDER HERE Sign up and order here: https://masterpeacebyhcs.com/?ref=11225
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  • Karen McNulty Walsh, Peter Genzer, Brookhaven National Laboratory - Super strong magnetic fields leave imprint on nuclear matter:

    https://phys.org/news/2024-02-super-strong-magnetic-fields-imprint.html

    #HeavyIonCollision #ElectromagneticField #MagneticField #QuarkGluonPlasma #QGP #AtomicPhysics #Physics
    Karen McNulty Walsh, Peter Genzer, Brookhaven National Laboratory - Super strong magnetic fields leave imprint on nuclear matter: https://phys.org/news/2024-02-super-strong-magnetic-fields-imprint.html #HeavyIonCollision #ElectromagneticField #MagneticField #QuarkGluonPlasma #QGP #AtomicPhysics #Physics
    PHYS.ORG
    Super strong magnetic fields leave imprint on nuclear matter
    A new analysis by the STAR collaboration at the Relativistic Heavy Ion Collider (RHIC), a particle collider at the U.S. Department of Energy's (DOE) Brookhaven National Laboratory, provides the first direct evidence of the imprint left by what may be the universe's most powerful magnetic fields on "deconfined" nuclear matter. The evidence comes from measuring the way differently charged particles separate when emerging from collisions of atomic nuclei at this DOE Office of Science user facility.
    0 Kommentare 0 Anteile 960 Ansichten
  • The Ultimate mRNA/Spike Detox?
    Whole Blood/Plasma Donation or Chinese Bloodletting

    Dr. Syed Haider
    Hijama Cupping Therapy Kiya hai aur is k Faiyday? Roman Urdu main Parhain
    The mRNA shots deliver toxic lipid nano particles (LNPs), whole spike mRNA, fragments of mRNA and trigger the production of spike protein and antibodies to the same, and possibly fragments of spike protein (see this substack).

    Furthermore both LNPs and spike protein trigger the creation of microclots in blood vessels.

    There are methods for detoxing from spike protein - for example you can take enzymes like bromelain to digest the spike protein, it can be bound up and more easily removed by taking ivermectin, you can induce autophagy to destroy it by fasting, cold and heat therapies and with supplements like resveratrol and spermidine.

    For microclots you can break them down with blood thinners like aspirin and enzymes like nattokinase and serrapeptase.

    But what about the mRNA and LNPs? How can those be removed?

    Thank you for reading Dr. Syed Haider. This post is public so feel free to share it.

    Share

    The mRNA shot components are taken up by cells throughout our bodies, but also found free floating in our blood, where they join other toxins, including horrific forever chemicals like dioxins, but also many other normal blood components including antibodies, proteins like albumin, red blood cells, white cells, platelets, fats, vitamins and minerals.

    Most of these blood components, except for red blood cells, can passively or actively diffuse out of the blood into our organs and tissues.

    Active diffusion means energy is involved in the process as when infection fighting white cells actively migrate out of the blood into tissues where they have been attracted by inflammatory messaging molecules.

    With active diffusion particles can be moved from an area of lower concentration to an area of higher concentration - something that cannot happen without adding energy to the transport process.

    Passive diffusion means no energy is involved, and the substance in question simply diffuses down a concentration gradient from an area of higher concentration to an area of lower concentration, until the concentrations equalize in all areas - think of smoke or cooking smells diffusing out of the kitchen to fill the whole house.


    So when substances like LNPs carrying mRNA enter the blood they will passively diffuse out into other tissues until the concentrations in the blood and those other tissues equalize.

    If a substance is removed from the blood, what is still in tissues will then diffuse back into the blood until the concentration in blood and tissues equalizes again - at a lower level than before, because there is less total left in the body.

    Repeatedly removing a substance from the blood would eventually deplete the whole body stores of that substance down to zero, unless it were being replaced from the outside (like the natural components of blood from diet and supplements).

    1000s of patients around the world have flocked to specialized centers that perform a procedure called H.E.L.P. apheresis in the hopes of filtering out microclots, free circulating spike protein and mRNA from their bloodstreams.

    I spoke with Dr Beate Jaeger for the free online Long COVID Reset Summit about her work with over 1500 long COVID and Vax injured patients, using both H.E.L.P. as well as prescription anticoagulants like plavix and heparin.

    She reported that with H.E.L.P. apheresis 95-99% of patients showed some degree of benefit and over 80% had very significant improvements or even complete reversal of symptoms.


    In one of the most remarkable and fast turnarounds she saw someone who had been confined to a wheelchair get up for the first time after a session.

    H.E.L.P. apheresis is a specialized version of the more general apheresis procedure which is a simple technology for separating blood components.

    Specifically H.E.L.P. stands for: “heparin-mediated extracorporeal low-density lipoprotein (LDL) fibrinogen precipitation”.

    Essentially a heparin infused filter aids in removal of LDL cholesterol, lipoprotein (a) (levels are far more predictive for heart disease than traditional cholesterol tests) and the clotting protein fibrinogen from the blood of patients.

    Historically this was used for patients with high cholesterol that couldn’t be adequately managed with statins and other traditional lipid lowering therapies.

    Now it has been repurposed to help remove microclots and spike protein, which binds to the heparin.

    Unfortunately there are only 1 or 2 centers that perform this in the US for long COVID and Vax injuries, and just a handful around the world.

    The procedure is also expensive - usually at least $1500 per treatment and often many treatments are required.

    Now, the heparin filter may be particularly helpful for binding spike protein, but there is a far more accessible technology called plasmapheresis (AKA plasma donation) which may work similarly.

    Plasmapheresis uses a centrifuge to separate our whole blood by weight from heaviest to lightest component into: red cells, white blood cells, platelets and a mix of everything else - termed plasma.

    Blood components, including plasma, white blood cells, platelets and red blood cells
    The plasma is removed while the blood cells and platelets are remixed with sterile salt water (at the same concentration as normal blood salt levels and added to the cells because the plasma component takes all the liquid and salt with it) and infused back into the person.

    Plasmapheresis (again the exact same procedure as plasma donation) is used therapeutically in a wide range of medical conditions wherein a toxic component (eg an autoimune antibody) is present in the blood.

    These conditions include Guillaine Barre Syndrome, Myesthenia Gravis, idiopathic dilated cardiomyopathy, hashimotos encephalopathy, multiple sclerosis, myeloma, severe systemic lupus erythematosis (SLE), ap[lastic anemia, acute liver failure, burn shock, complex regional pain syndrome, severe pemphigus vulgaris, stiff-person syndrome, thyroid storm, systemic amyloidosis and many more.

    Of most interest here is the usefulness of plasmapheresis for treating systemic amyloidosis, a disease caused by the buildup of amyloid protein throughout the body, because spike protein toxicity also includes the creation of amyloid inside microclots as well as outside the vasculature.

    There are few contraindications to plasmapheresis including allergies to the common blood thinner heparin (since the tubing is heparinized to avoid blood clotting), low blood calcium levels and ACE inhibitor use within 24 hours.

    Possible side effects are minimal and can include low electrolytes levels including low blood calcium and magnesium (which may require replacement), hypothermia since blood is hot and that heat is removed from the body, and an increased tendency to bleed due to removal of clotting proteins.

    But in general it is a very safe procedure that is conducted on both healthy and ill people daily throughout the world.

    So if everything but the blood cells and platelets are removed we would expect that any toxins would be removed from the blood whether they be circulating forever chemicals, LNPs, mRNA, unwanted antibodies (eg autoantibodies), heavy metals, etc.

    At the same time we would be removing some vitamins and minerals, so if this procedure was done frequently you would want to be sure you focused on a highly nutrient dense diet as well as appropriate supplementation.

    Plasma donation is either free or at some private centers reimbursed at $20-$50 per procedure, because it is sold and used to create medical products.

    Depending on the center donations can be given as often as twice weekly or as little as 6 times a year, and each donation can remove as much as 800ml of plasma.

    Alternatively whole blood donations are only possible every 56 days. In a whole blood donation, nothing is separated or reinfused, you just remove about 500ml of whole blood.

    You'll Decide: Reality-Based Fiscal Policy Or Bloodletting - Colorado Pols
    Bloodletting has actually been used as a therapeutic procedure for millennia throughout the world (perhaps most notoriously it’s been suspected by medical historians that physicians may have killed George Washington by overdoing it during his final deathbed illness).

    There are many different ways it has been done including by leeches and wet cupping (tiny nicks made in the skin covered by suction cups that draw blood out).

    Dean Mouscher is an advanced clinical acupuncturist in Illinois who performs and teaches traditional techniques of blood letting for ameliorating the toughest to treat medical conditions.

    His methods are described in his popular manual, The Complete Guide to Chinese Medicine Bloodletting.

    He explained in a comment on the last post about removing forever chemicals like dioxins that the location of bloodletting may actually be more important than the amount of blood removed:

    “…as an acupuncturist I use many modalities in my practice, but none comes close to the magical efficacy of bloodletting. Chinese Medicine Bloodletting is different from the old Western bloodletting as it is based on taking small amounts of blood from exactly the right point, rather than pints from the cubital fossa. As it happens, Chinese medicine has bloodletting points specifically for detox, right on the scapula.”

    Wet (HIJAMA) Cupping - Holistic Buddha
    This is very interesting, because you would expect that in a structure as complex as the human body, toxins would concentrate in certain areas, so removing blood from those areas might be far more effective (and less draining) than removing large amounts from elsewhere.

    Unsurprisingly there have been no studies that I could find of bloodletting, plasma donation, or even H.E.L.P. apheresis for either mRNA shot detoxification or Long COVID.

    The best we have to go on for now are Dr Beate Jaegers reports and although she is very interested in conducting formal research she doesn’t have the funding to do so.

    The one study I could find that supported the use of whole blood and plasma donation for toxin removal was described in the last Substack on the Ohio train wreck toxic explosion, in this quote taken from a May 2022 Guardian article:

    “A new study published in JAMA Network Open tracked PFAS levels in 285 Australian firefighters, who are regularly exposed to PFAS in firefighting foam and accrue high levels of the chemicals in their bodies. Over a year, one group of firefighters donated plasma every six weeks, another donated blood every 12 weeks, and a third group acted as a control.

    “This randomized clinical trial showed that regular blood or plasma donations result in a significant reduction in serum PFAS levels for participants,” the study’s authors wrote. Blood donors reduced their PFAS levels by 10%, and plasma donors reduced theirs by 30%. Both groups maintained their reduction for at least three months post-trial. The study did not explore whether a reduction in PFAS in the blood necessarily leads to better health.”

    Despite the lack of published evidence some long haulers and vax injured have tried plasmapheresis on themselves and reported impressive results, which are often immediate.

    If you have done this yourself, know someone who has or have more data please drop me a line here on Substack, at my clinic site mygotodoc.com, or on Twitter: @drsyedhaider.

    https://blog.mygotodoc.com/p/the-ultimate-mrnaspike-detox


    https://telegra.ph/The-Ultimate-mRNASpike-Detox-09-17

    https://donshafi911.blogspot.com/2023/09/the-ultimate-mrnaspike-detox-whole.html
    The Ultimate mRNA/Spike Detox? Whole Blood/Plasma Donation or Chinese Bloodletting Dr. Syed Haider Hijama Cupping Therapy Kiya hai aur is k Faiyday? Roman Urdu main Parhain The mRNA shots deliver toxic lipid nano particles (LNPs), whole spike mRNA, fragments of mRNA and trigger the production of spike protein and antibodies to the same, and possibly fragments of spike protein (see this substack). Furthermore both LNPs and spike protein trigger the creation of microclots in blood vessels. There are methods for detoxing from spike protein - for example you can take enzymes like bromelain to digest the spike protein, it can be bound up and more easily removed by taking ivermectin, you can induce autophagy to destroy it by fasting, cold and heat therapies and with supplements like resveratrol and spermidine. For microclots you can break them down with blood thinners like aspirin and enzymes like nattokinase and serrapeptase. But what about the mRNA and LNPs? How can those be removed? Thank you for reading Dr. Syed Haider. This post is public so feel free to share it. Share The mRNA shot components are taken up by cells throughout our bodies, but also found free floating in our blood, where they join other toxins, including horrific forever chemicals like dioxins, but also many other normal blood components including antibodies, proteins like albumin, red blood cells, white cells, platelets, fats, vitamins and minerals. Most of these blood components, except for red blood cells, can passively or actively diffuse out of the blood into our organs and tissues. Active diffusion means energy is involved in the process as when infection fighting white cells actively migrate out of the blood into tissues where they have been attracted by inflammatory messaging molecules. With active diffusion particles can be moved from an area of lower concentration to an area of higher concentration - something that cannot happen without adding energy to the transport process. Passive diffusion means no energy is involved, and the substance in question simply diffuses down a concentration gradient from an area of higher concentration to an area of lower concentration, until the concentrations equalize in all areas - think of smoke or cooking smells diffusing out of the kitchen to fill the whole house. So when substances like LNPs carrying mRNA enter the blood they will passively diffuse out into other tissues until the concentrations in the blood and those other tissues equalize. If a substance is removed from the blood, what is still in tissues will then diffuse back into the blood until the concentration in blood and tissues equalizes again - at a lower level than before, because there is less total left in the body. Repeatedly removing a substance from the blood would eventually deplete the whole body stores of that substance down to zero, unless it were being replaced from the outside (like the natural components of blood from diet and supplements). 1000s of patients around the world have flocked to specialized centers that perform a procedure called H.E.L.P. apheresis in the hopes of filtering out microclots, free circulating spike protein and mRNA from their bloodstreams. I spoke with Dr Beate Jaeger for the free online Long COVID Reset Summit about her work with over 1500 long COVID and Vax injured patients, using both H.E.L.P. as well as prescription anticoagulants like plavix and heparin. She reported that with H.E.L.P. apheresis 95-99% of patients showed some degree of benefit and over 80% had very significant improvements or even complete reversal of symptoms. In one of the most remarkable and fast turnarounds she saw someone who had been confined to a wheelchair get up for the first time after a session. H.E.L.P. apheresis is a specialized version of the more general apheresis procedure which is a simple technology for separating blood components. Specifically H.E.L.P. stands for: “heparin-mediated extracorporeal low-density lipoprotein (LDL) fibrinogen precipitation”. Essentially a heparin infused filter aids in removal of LDL cholesterol, lipoprotein (a) (levels are far more predictive for heart disease than traditional cholesterol tests) and the clotting protein fibrinogen from the blood of patients. Historically this was used for patients with high cholesterol that couldn’t be adequately managed with statins and other traditional lipid lowering therapies. Now it has been repurposed to help remove microclots and spike protein, which binds to the heparin. Unfortunately there are only 1 or 2 centers that perform this in the US for long COVID and Vax injuries, and just a handful around the world. The procedure is also expensive - usually at least $1500 per treatment and often many treatments are required. Now, the heparin filter may be particularly helpful for binding spike protein, but there is a far more accessible technology called plasmapheresis (AKA plasma donation) which may work similarly. Plasmapheresis uses a centrifuge to separate our whole blood by weight from heaviest to lightest component into: red cells, white blood cells, platelets and a mix of everything else - termed plasma. Blood components, including plasma, white blood cells, platelets and red blood cells The plasma is removed while the blood cells and platelets are remixed with sterile salt water (at the same concentration as normal blood salt levels and added to the cells because the plasma component takes all the liquid and salt with it) and infused back into the person. Plasmapheresis (again the exact same procedure as plasma donation) is used therapeutically in a wide range of medical conditions wherein a toxic component (eg an autoimune antibody) is present in the blood. These conditions include Guillaine Barre Syndrome, Myesthenia Gravis, idiopathic dilated cardiomyopathy, hashimotos encephalopathy, multiple sclerosis, myeloma, severe systemic lupus erythematosis (SLE), ap[lastic anemia, acute liver failure, burn shock, complex regional pain syndrome, severe pemphigus vulgaris, stiff-person syndrome, thyroid storm, systemic amyloidosis and many more. Of most interest here is the usefulness of plasmapheresis for treating systemic amyloidosis, a disease caused by the buildup of amyloid protein throughout the body, because spike protein toxicity also includes the creation of amyloid inside microclots as well as outside the vasculature. There are few contraindications to plasmapheresis including allergies to the common blood thinner heparin (since the tubing is heparinized to avoid blood clotting), low blood calcium levels and ACE inhibitor use within 24 hours. Possible side effects are minimal and can include low electrolytes levels including low blood calcium and magnesium (which may require replacement), hypothermia since blood is hot and that heat is removed from the body, and an increased tendency to bleed due to removal of clotting proteins. But in general it is a very safe procedure that is conducted on both healthy and ill people daily throughout the world. So if everything but the blood cells and platelets are removed we would expect that any toxins would be removed from the blood whether they be circulating forever chemicals, LNPs, mRNA, unwanted antibodies (eg autoantibodies), heavy metals, etc. At the same time we would be removing some vitamins and minerals, so if this procedure was done frequently you would want to be sure you focused on a highly nutrient dense diet as well as appropriate supplementation. Plasma donation is either free or at some private centers reimbursed at $20-$50 per procedure, because it is sold and used to create medical products. Depending on the center donations can be given as often as twice weekly or as little as 6 times a year, and each donation can remove as much as 800ml of plasma. Alternatively whole blood donations are only possible every 56 days. In a whole blood donation, nothing is separated or reinfused, you just remove about 500ml of whole blood. You'll Decide: Reality-Based Fiscal Policy Or Bloodletting - Colorado Pols Bloodletting has actually been used as a therapeutic procedure for millennia throughout the world (perhaps most notoriously it’s been suspected by medical historians that physicians may have killed George Washington by overdoing it during his final deathbed illness). There are many different ways it has been done including by leeches and wet cupping (tiny nicks made in the skin covered by suction cups that draw blood out). Dean Mouscher is an advanced clinical acupuncturist in Illinois who performs and teaches traditional techniques of blood letting for ameliorating the toughest to treat medical conditions. His methods are described in his popular manual, The Complete Guide to Chinese Medicine Bloodletting. He explained in a comment on the last post about removing forever chemicals like dioxins that the location of bloodletting may actually be more important than the amount of blood removed: “…as an acupuncturist I use many modalities in my practice, but none comes close to the magical efficacy of bloodletting. Chinese Medicine Bloodletting is different from the old Western bloodletting as it is based on taking small amounts of blood from exactly the right point, rather than pints from the cubital fossa. As it happens, Chinese medicine has bloodletting points specifically for detox, right on the scapula.” Wet (HIJAMA) Cupping - Holistic Buddha This is very interesting, because you would expect that in a structure as complex as the human body, toxins would concentrate in certain areas, so removing blood from those areas might be far more effective (and less draining) than removing large amounts from elsewhere. Unsurprisingly there have been no studies that I could find of bloodletting, plasma donation, or even H.E.L.P. apheresis for either mRNA shot detoxification or Long COVID. The best we have to go on for now are Dr Beate Jaegers reports and although she is very interested in conducting formal research she doesn’t have the funding to do so. The one study I could find that supported the use of whole blood and plasma donation for toxin removal was described in the last Substack on the Ohio train wreck toxic explosion, in this quote taken from a May 2022 Guardian article: “A new study published in JAMA Network Open tracked PFAS levels in 285 Australian firefighters, who are regularly exposed to PFAS in firefighting foam and accrue high levels of the chemicals in their bodies. Over a year, one group of firefighters donated plasma every six weeks, another donated blood every 12 weeks, and a third group acted as a control. “This randomized clinical trial showed that regular blood or plasma donations result in a significant reduction in serum PFAS levels for participants,” the study’s authors wrote. Blood donors reduced their PFAS levels by 10%, and plasma donors reduced theirs by 30%. Both groups maintained their reduction for at least three months post-trial. The study did not explore whether a reduction in PFAS in the blood necessarily leads to better health.” Despite the lack of published evidence some long haulers and vax injured have tried plasmapheresis on themselves and reported impressive results, which are often immediate. If you have done this yourself, know someone who has or have more data please drop me a line here on Substack, at my clinic site mygotodoc.com, or on Twitter: @drsyedhaider. https://blog.mygotodoc.com/p/the-ultimate-mrnaspike-detox https://telegra.ph/The-Ultimate-mRNASpike-Detox-09-17 https://donshafi911.blogspot.com/2023/09/the-ultimate-mrnaspike-detox-whole.html
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  • The COVID-19 Vaccine Antigen Is ANTHRAX
    Dr. Ariyana Love
    By Dr. Ariyana Love

    Covid-19 vaccines use self-replicating, programmable nanotechnology and synthetic, modified RNA (modRNA) otherwise known as Spike Protein.

    We are told that a vaccine antigen is used in the Covid-19 technology to “evoke an immune response” but what if the Covid-19 vaccine antigen is ANTHRAX?

    “…hardly any natural pathogens are really well suited to being biowarfare agents from a military point of view. Such a bioweapon must fulfill a variety of demands: it needs to be produced in large amounts, it must act fast, it must be environmentally robust, and the disease must be treatable… only a minority of natural pathogens are suitable for military purposes. “Anthrax is of course the first choice because the causative agent, B. anthracis, fulfills nearly all of these specifications.”

    Anthrax was developed by Russia in 1950. According to the NIH, the USSR’s ‘invisible anthrax’ was created by introducing an “alien gene” into the highly deadly Bacillus Anthracis bacteria. This means that Cross-Species-Genomics capability was acquired by governments before 1950. A lethal bacterium and an alien gene were genetically altered and blended together to produce the deadly bioweapon known as Anthrax. Russia’s Anthrax could be treated with antibiotics even several days after exposure, and thus it met the requirements under the Biological Weapons Convention.

    A bioweapon of choice, Anthony Fauci decided to increase Anthrax lethality and the NIH began genetic attenuation before 2006. Through GAIN-and-LOSS-of-Function the NIH produced a more drastic and deadly Anthrax that’s resistant to antibiotics and more.

    According to a University of Minnesota publication, the United States D.O.D smuggled shipments of live B anthracis spores from the Army’s Dugway Proving Ground in Utah, to other labs in the United States and abroad (Source: USA Today). The U.S. Army sent shipments of live samples of Anthrax to 86 labs outside the U.S. over a period of 10 years (Source: The Daily Beast).

    Transfers of samples of live B anthracis and the H5N1 influenza bioweapon were sent from CDC labs to other labs. CDC correspondence released under the Freedom of Information Act shows that labs studying bioterror pathogens “have failed over and over to comply with important safety and security regulations.”

    The D.O.D. tried to cover for the CDC, claiming “system failure” was to blame for the lab leaks, but we already know that the D.O.D spearheaded this “Covid-19 vaccine” roll-out.


    Please see: Aerosolized inoculation of Anthrax – Aerosolized Intratracheal Inoculation of Recombinant Protective Antigen (rPA) Vaccine Provides


    In 2007, Anthony Fauci created the H7N9 bioweapon, otherwise known as the “influenza vaccine.” The NIH, CCP and the Israeli state collaborated through GAIN-and-LOSS-of-Function to produce the H7N9 “flu vaccine” and the new and improved “Aerosolized Anthrax Vaccine”.

    Ofir Israeli from the Israel Institute of Biological Research, sequenced the Bacillus anthracis V770-NP1-R Strain in 2014, creating a synthetic chemical bioweapon. The Israeli state oversaw the animal trials for the Anthrax “vaccine” and told us it was safe and effective. Meanwhile, the Israeli company called Sanofi Pasteur developed the first H7N9 “vaccine” and trialed it for the NIH in 2014. Also in 2014, the NIH developed the H7N9 “influenza vaccine” to be droplet transmissible.

    Simultaneously, in 2014 China achieved a 99% transmissibility of the H7N9 “flu vaccine”. China also trialed the first aerosolized intratracheal Anthrax “vaccine” on mice. The study revealed severe side effects.


    PLEASE SEE: NIH Using DEAD CORPSES To Make “Virus”; Gain Of Function Weaponized Dead Corpses


    The Israeli state, NIH and China turned their new and improved Anthrax bioweapon into an attenuated antigen to be used in vaccines under the guise of “evoking an immune response” and “vaccine immunity.” The nations have been intentionally poisoned with biowarfare.

    In March 2022, the Russian military discovered that the Covid-19 bioweapons are being developed in U.S. biolabs in Ukraine. This includes the plague, Ebola, Filoviruses’, Anthrax and more. Anthrax causes hemorrhaging. So does Ebola and Marburg.

    Ebola is used in the J&J and Sinovax jabs, while Filovirus is used in Moderna. Ebola and Marburg are both Anthrax. H7N9 is used in all “flu vaccines” while Anthrax is being used as a “vaccine adjuvant” in all Covid-19 jabs and swabs.

    Through Loss-Of-Function, genetic deletions were performed inside the B. anthracis bacteria to improve replication of the bacteria in vivo. This ensured hospital protocols would not work to stop the Anthrax from replicating inside the human body after inoculation due to it being antibiotic resistant.

    The B. anthracis bacteria was also genetically modified to survive in insect hosts so as not to sporulate before it’s injected into the human host by a Bill Gates GMO mosquito which is part of DARPA’s weaponized insect project called The Sentinels.

    Incidentally, the CDC owns the Anthrax isolate patent that was funded by the U.S. Government. This is treason. The CDC also says that a bioterrorist attack would most likely be Anthrax.

    Please see: Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero

    SPIKE PROTEIN IS AEROSOLIZED ANTHRAX

    There are 232 B. anthracis genomes that are currently available in the GenBank database. There’s an Anthrax “vaccine” for cattle and two strains are licensed for use in humans. There exist two patents for an “Aerosolized Anthrax Vaccine.”

    The first Anthrax “vaccine” patent for humans is partly owned by the U.S. Government. The second is a “Recombinant Anthrax Vaccine”.

    “The spores of the toxigenic, nonencapsulated B. anthracis STI-1 strain and the cell-free PA-based “vaccines” consisting of aluminum hydroxide-adsorbed supernatant material from cultures of the toxigenic, nonencapsulated B. anthracis strain V770-NPI-R or alum-precipitated culture filtrate from the Sterne strain. Each of these Anthrax toxins are being used for “cellular entry in humans“. The LF is a metalloprotease recently shown to cleave the amino termini of the mitogen-activated protein kinase kinases 1 and 2, which results in their inactivation.”

    The above quote from the Recombinant Anthrax Vaccine patent reveals that the poisonous Anthrax “antigen” is being used to genetically modify the genome of humans (cellular entry into humans). By cleaving to the amino termini, protein kinases 1 and 2 are inactivated. This is accomplished by genetic deletions.

    The molecular basis of Anthrax “vaccines” includes “spores and DNA plasmids” that are entering human cells.

    The following quote about the Anthrax “protective antigen” is particularly revealing:

    “PA (protective antigen) is the common receptor binding domain of the toxins and can interact with the two different effector domains, EF and LF, to mediate their entry into target cells (14).”

    Anthrax is being used to “regulate gene expression by binding to DNA sequences and modulating transcriptional activity through their effector domains”.

    Pharma has essentially found a way to encode any synthetic proteins into the human genome from any species they want, including bacteria. The “Aerosolized Anthrax Antigen” is being encoded into target cells to make those cells produce the chemical drug called Anthrax. This is how the Anthrax “vaccine” is aerosolized. Once a person is inoculated with the Covid-19 bioweapon through subcutaneous injection or nasopharyngeal delivery with contaminated PCR swabs, the weapon system will begin genetic deletions and encoding the genome of target cells with the Anthrax spike protein. A person begins producing the toxic spike protein and shedding Anthrax into the air, exposing everyone to Inhalation Anthrax. It’s a weapon system that is intentionally aerosolized.

    This study admits that the Anthrax spores from B. anthracis STI-1 strain and B. anthracis strain V770-NPI-R used in the “aerosolized Anthrax vaccines” are toxigenic. The Sterne strain which is used to inoculate our food supply (animals) is also genotoxic.

    This NIH study explains how a “replicon” of the Bacillus anthracis bacteria was cloned into an Escherichia coli (E. coli) “vector” using cross-species-genomics. These two bacteria were synthetically fused together to enhance lethality.

    ALHYDROGEL

    According to the “aerosolized Anthrax vaccine” patents, the so-called “vaccine adjuvant” used is a DARPA weapon system called Alhydrogel.

    Hydrogel technology was developed over many years during a collaboration between DARPA and Profusa, a private biotech company specializing in the development of tissue-integrated biosensors. In 2018, DARPA published a video revealing their intention to use this biosensing technology for both military and public health.

    In the Alhydrogel invention, Anthrax was fused together into a nanogel called Alhydrogel, consisting of fibrous nanoparticles (Nanofibers) that are “antigen specific to CD4+ T cells”.

    In layman’s terms, the nanorobots are intentionally programmed to target and alter the genome of CD4-T cells, inducing cell death. This essential part of our immune system (T-cells) stop foreign invaders from entering our cells. Destroying our T-cells enables the government’s operating system to take root in the body and quicken death.

    Alhydrogel is infused with 750 μg of aluminum, making it magnetic. Nanofibers are used for self-assembly and electrospinning, for tissue engineering and delivery of drugs and chemicals into the brain. Being magnetic and nanotech based, the Alhydrogel can replicate everywhere in the body and wire a new neural network.

    Astonishingly, Alhydrogel is already the most widely used vaccine adjuvant! There are many Alhydrogel patents that contain toxic cocktails that will overwhelm anyone’s immune system.

    This Alhydrogel patent demonstrates it’s use of the B anthracis bacteria, E. coli, N. gonorrhoeae, Chlamydia, Staphylococcus, TB and more. It also contains the H5N1 influenza bioweapon, RNA, DNA synthesis and Polysorbate 80 for Blood Brain Barrier (BBB) permeability. This begs the question, where do venereal diseases come from?

    This Nature article reveals that 2% Alhydrogel is used in all Covid-19 “vaccines”. Previously, aluminum salts were the only adjuvants licensed for vaccine use in humans in the U.S. In recent decades, nanoparticle adjuvants in hydrated gels were introduced. The article continues by saying that the “influenza vaccine” was the first to use Alhydrogel.

    “Aluminum salt-based adjuvants such as alhydrogel have been a mainstay of vaccines for decades” boasts Christopher B. Fox and colleagues at the Infectious Disease Research Institute in Seattle, USA.

    Both nanoparticles and Anthrax have been used in vaccines for decades already, without the Informed Consent of the public.

    Alhydrogel was improved and transformed into the Nanoalum adjuvant.

    Here, we introduce a top-down manufacturing process—high-pressure microfluidization—to generate aluminum oxyhydroxide nanoparticles, hereupon referred to as nanoalum, using the clinically approved Alhydrogel adjuvant as the precursor.

    Alhydrogel is also carried in the lipid coating of nanoparticles.

    The “Aerosolized Anthrax Vaccines” also contain SEQ ID NO: 1 which is owned by the Pirbright Institute (Bill & Melinda Gates). SEQ ID NO: 1 contains the world’s most deadly genetically modified parasites.


    Please see: MEGA BOMBS! GMO Parasites Are The mRNA Vector!


    ANTHRAX SYMPTOMS AND TREATMENT

    Anthrax has been deployed on the population by three methods; injection, inhalation and skin penetration. The mortality rate for Anthrax varies depending on the method of exposure. It’s approximately 20% fatality for cutaneous Anthrax and 25–75% for Gastrointestinal Anthrax. Inhalation Anthrax is by far the worst with a fatality rate that is 80% or higher. Inhalation Anthrax is what we’re all being exposed to from the Covid-19 jabs and contaminated PCR swabs.

    Antibiotics constitute the mainstay of treatment against Anthrax, despite the fact that they won’t work to stop its replication due to the NIH, China and Israel’s GAIN-and-LOSS-of-Function enhancements (antibiotic resistance).

    Pharmaceutical experimental genotoxic drugs such as Oblitoxaximab and Raxibacumab are being touted as Anthrax treatments but these are monoclonal antibodies. We know from the monoclonal antibody patents that they’re also the “mRNA vaccine” weapon system. Anytime you inject recombinant proteins or modRNA into humans, it’s extremely toxic and will be rejected by our immune system 100% of the time.


    Please read: Monoclonal Antibodies Is mRNA Gene Knockdown Tech, Encoding HIV – Patent Review


    Pharma wants us to believe that the only known effective “prevention” against Anthrax is the Anthrax “vaccine”. However, the Anthrax “vaccine” inoculation given to U.S. military troops was a horrific disaster. U.S. Army statistics that were never published, show the Anthrax “vaccine” induces turbo cancers.

    The toxicological harms of Anthrax are many. It causes severe heart issues. Could this be a contributing factor to Myocarditis and Pericarditis?

    Anthrax also coagulates the blood.

    “Pathophysiological changes associated with anthrax lethal toxin included loss of plasma proteins, decreased platelet count, slower clotting times, fibrin deposits in tissue sections, and gross and histopathological evidence of hemorrhage. These findings suggest that blood vessel leakage and hemorrhage lead to disseminating intravascular coagulation and/or circulatory shock as an underlying pathophysiological mechanism.”

    Read more here and here.

    Anthrax induces hemorrhaging. So this explains all the excessive bleeding people have experienced over the last 4 years, following Covid-19 inoculation and from aerosolized exposure, otherwise known as the “shedding” phenomenon. This is a result of Inhalation Anthrax.

    It becomes clear that the newly dubbed “White Lung Syndrome” and the Chinese ‘pneumonia’ outbreak is none other than Inhalation Anthrax. Mycoplasma pneumonia is on the rise, and it’s listed on Pfizer’s internal documentation as a known Adverse Effect of the Covid-19 inoculation.


    This study reveals that Mycoplasma Pneumonia is aerosolized. WHO also confirms this phenomenon is Mycoplasma Pneumonia.

    All naturally occurring bacterium have cell walls. Mycoplasmas are spherical to filamentous cells with no cell walls. It’s genetically manipulated in a laboratory by GAIN-of-Function for the purpose of enhancing replication inside the human body, making it more lethal.

    Mice “treated” with anthrax lethal toxin (LT) exhibit hemorrhage and liver damage. Monocyte procoagulant responses to anthrax peptidoglycan are reinforced by proinflammatory cytokine signaling and histological lesions in the spleen.

    Anthrax has already been tested on the public. According to the NIH, Anthrax spores were intentionally released into “some environments” in NYC during 9/11. According to the NIH, the FBI launched an investigation called “Amerithrax”. It was “one of the largest and most complex (investigation) in the history of law enforcement”, according to the FBI.

    Heroine users in Europe have been tested with Injection Anthrax.

    Our skies are sprayed with smart dust and chemicals daily. Our governments have launched an all-out war against their constituents. We are being poisoned in a myriad of ways, so please keep this in mind:

    “Anthrax is easy to produce in large quantities, highly lethal, relatively easy to develop as a weapon, easily spread over a large area, easily stored and dangerous for a long time. Given appropriate weather and wind conditions, 50 kilograms of aerosolised anthrax spores released from an aircraft along a 2 kilometer line could create a lethal cloud of anthrax spores that would extend beyond 20 kilometers downwind. The aerosol cloud would be colorless, odorless and invisible following its release. Given the small size of the spores, people indoors would receive the same amount of exposure as on the street. There are currently no atmospheric warning systems to detect an aerosol cloud of anthrax spores. The first sign of a bioterrorist attack would most likely be patients presenting with symptoms of inhalation anthrax. A 1970 analysis by World Health Organization concluded that the release of aerosolized anthrax upwind to a population of 5,000,000 could lead to an estimated 250,000 casualties, of whom as many as 100,000 could be expected to die. A later analysis, by the Office of Technology Assessment of the U.S. Congress estimated that 130,000 to 3 million deaths could occur following the release of 100 kilograms of aerosolized anthrax over Washington D.C., making such an attack as lethal as a hydrogen bomb.”

    TREATMENT

    If you have been inoculated with Covid-19 or PCR swabbed, and you are suffering from heart pain, unusual bleeding, skin rashes and abrasions, it could be Injection Anthrax. If you are “unvaccinated” and hemorrhaging from being around “vaccinated”, then you may have been exposed to Inhalation Anthrax.

    Many doctors, including myself, have documented persistent bleeding rectally, violent bleeding vaginally, nasally and in the eyes. Since October 4th, I have received many reports of a red eye syndrome where the entire eye is blood-red. This makes sense because eye tissue is more sensitive. If you have been exposed to Inhalation Anthrax, you may feel hot and severely flushed, and you may break out in big, red splotches on your skin, followed by a completely red eye in the morning.

    Although they don’t get much attention, “anti-toxins have long been considered an essential ‘adjunctive’ therapy, and remain so”, according to the NIH. Anti-toxins are the natural medicines that detox poisons. In other words, you need an effective natural medicine detox protocol.

    I have been successfully detoxing people from the Covid-19 bioweapons for three years. Since I began treating people presenting with Anthrax poisoning with strong antibacterials, my clients are experiencing quicker detox results. If you would like to schedule a consultation with me, please do so through my online booking system.

    Please follow me on Telegram @drloveariyana and X @drloveariyana.

    If you would like to donate to my research, please do so here.


    UPDATE: My Anthrax article is now fully edited and published on Substack. Please review and SHARE.

    The Covid-19 Vaccine Antigen Is ANTHRAX

    Read more:
    https://open.substack.com/pub/drloveariyana/p/the-covid-19-vaccine-antigen-is-anthrax?r=2juwfo&utm_campaign=post&utm_medium=web&showWelcomeOnShare=true


    https://donshafi911.blogspot.com/2024/02/the-covid-19-vaccine-antigen-is-anthrax.html
    The COVID-19 Vaccine Antigen Is ANTHRAX Dr. Ariyana Love By Dr. Ariyana Love Covid-19 vaccines use self-replicating, programmable nanotechnology and synthetic, modified RNA (modRNA) otherwise known as Spike Protein. We are told that a vaccine antigen is used in the Covid-19 technology to “evoke an immune response” but what if the Covid-19 vaccine antigen is ANTHRAX? “…hardly any natural pathogens are really well suited to being biowarfare agents from a military point of view. Such a bioweapon must fulfill a variety of demands: it needs to be produced in large amounts, it must act fast, it must be environmentally robust, and the disease must be treatable… only a minority of natural pathogens are suitable for military purposes. “Anthrax is of course the first choice because the causative agent, B. anthracis, fulfills nearly all of these specifications.” Anthrax was developed by Russia in 1950. According to the NIH, the USSR’s ‘invisible anthrax’ was created by introducing an “alien gene” into the highly deadly Bacillus Anthracis bacteria. This means that Cross-Species-Genomics capability was acquired by governments before 1950. A lethal bacterium and an alien gene were genetically altered and blended together to produce the deadly bioweapon known as Anthrax. Russia’s Anthrax could be treated with antibiotics even several days after exposure, and thus it met the requirements under the Biological Weapons Convention. A bioweapon of choice, Anthony Fauci decided to increase Anthrax lethality and the NIH began genetic attenuation before 2006. Through GAIN-and-LOSS-of-Function the NIH produced a more drastic and deadly Anthrax that’s resistant to antibiotics and more. According to a University of Minnesota publication, the United States D.O.D smuggled shipments of live B anthracis spores from the Army’s Dugway Proving Ground in Utah, to other labs in the United States and abroad (Source: USA Today). The U.S. Army sent shipments of live samples of Anthrax to 86 labs outside the U.S. over a period of 10 years (Source: The Daily Beast). Transfers of samples of live B anthracis and the H5N1 influenza bioweapon were sent from CDC labs to other labs. CDC correspondence released under the Freedom of Information Act shows that labs studying bioterror pathogens “have failed over and over to comply with important safety and security regulations.” The D.O.D. tried to cover for the CDC, claiming “system failure” was to blame for the lab leaks, but we already know that the D.O.D spearheaded this “Covid-19 vaccine” roll-out. Please see: Aerosolized inoculation of Anthrax – Aerosolized Intratracheal Inoculation of Recombinant Protective Antigen (rPA) Vaccine Provides In 2007, Anthony Fauci created the H7N9 bioweapon, otherwise known as the “influenza vaccine.” The NIH, CCP and the Israeli state collaborated through GAIN-and-LOSS-of-Function to produce the H7N9 “flu vaccine” and the new and improved “Aerosolized Anthrax Vaccine”. Ofir Israeli from the Israel Institute of Biological Research, sequenced the Bacillus anthracis V770-NP1-R Strain in 2014, creating a synthetic chemical bioweapon. The Israeli state oversaw the animal trials for the Anthrax “vaccine” and told us it was safe and effective. Meanwhile, the Israeli company called Sanofi Pasteur developed the first H7N9 “vaccine” and trialed it for the NIH in 2014. Also in 2014, the NIH developed the H7N9 “influenza vaccine” to be droplet transmissible. Simultaneously, in 2014 China achieved a 99% transmissibility of the H7N9 “flu vaccine”. China also trialed the first aerosolized intratracheal Anthrax “vaccine” on mice. The study revealed severe side effects. PLEASE SEE: NIH Using DEAD CORPSES To Make “Virus”; Gain Of Function Weaponized Dead Corpses The Israeli state, NIH and China turned their new and improved Anthrax bioweapon into an attenuated antigen to be used in vaccines under the guise of “evoking an immune response” and “vaccine immunity.” The nations have been intentionally poisoned with biowarfare. In March 2022, the Russian military discovered that the Covid-19 bioweapons are being developed in U.S. biolabs in Ukraine. This includes the plague, Ebola, Filoviruses’, Anthrax and more. Anthrax causes hemorrhaging. So does Ebola and Marburg. Ebola is used in the J&J and Sinovax jabs, while Filovirus is used in Moderna. Ebola and Marburg are both Anthrax. H7N9 is used in all “flu vaccines” while Anthrax is being used as a “vaccine adjuvant” in all Covid-19 jabs and swabs. Through Loss-Of-Function, genetic deletions were performed inside the B. anthracis bacteria to improve replication of the bacteria in vivo. This ensured hospital protocols would not work to stop the Anthrax from replicating inside the human body after inoculation due to it being antibiotic resistant. The B. anthracis bacteria was also genetically modified to survive in insect hosts so as not to sporulate before it’s injected into the human host by a Bill Gates GMO mosquito which is part of DARPA’s weaponized insect project called The Sentinels. Incidentally, the CDC owns the Anthrax isolate patent that was funded by the U.S. Government. This is treason. The CDC also says that a bioterrorist attack would most likely be Anthrax. Please see: Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero SPIKE PROTEIN IS AEROSOLIZED ANTHRAX There are 232 B. anthracis genomes that are currently available in the GenBank database. There’s an Anthrax “vaccine” for cattle and two strains are licensed for use in humans. There exist two patents for an “Aerosolized Anthrax Vaccine.” The first Anthrax “vaccine” patent for humans is partly owned by the U.S. Government. The second is a “Recombinant Anthrax Vaccine”. “The spores of the toxigenic, nonencapsulated B. anthracis STI-1 strain and the cell-free PA-based “vaccines” consisting of aluminum hydroxide-adsorbed supernatant material from cultures of the toxigenic, nonencapsulated B. anthracis strain V770-NPI-R or alum-precipitated culture filtrate from the Sterne strain. Each of these Anthrax toxins are being used for “cellular entry in humans“. The LF is a metalloprotease recently shown to cleave the amino termini of the mitogen-activated protein kinase kinases 1 and 2, which results in their inactivation.” The above quote from the Recombinant Anthrax Vaccine patent reveals that the poisonous Anthrax “antigen” is being used to genetically modify the genome of humans (cellular entry into humans). By cleaving to the amino termini, protein kinases 1 and 2 are inactivated. This is accomplished by genetic deletions. The molecular basis of Anthrax “vaccines” includes “spores and DNA plasmids” that are entering human cells. The following quote about the Anthrax “protective antigen” is particularly revealing: “PA (protective antigen) is the common receptor binding domain of the toxins and can interact with the two different effector domains, EF and LF, to mediate their entry into target cells (14).” Anthrax is being used to “regulate gene expression by binding to DNA sequences and modulating transcriptional activity through their effector domains”. Pharma has essentially found a way to encode any synthetic proteins into the human genome from any species they want, including bacteria. The “Aerosolized Anthrax Antigen” is being encoded into target cells to make those cells produce the chemical drug called Anthrax. This is how the Anthrax “vaccine” is aerosolized. Once a person is inoculated with the Covid-19 bioweapon through subcutaneous injection or nasopharyngeal delivery with contaminated PCR swabs, the weapon system will begin genetic deletions and encoding the genome of target cells with the Anthrax spike protein. A person begins producing the toxic spike protein and shedding Anthrax into the air, exposing everyone to Inhalation Anthrax. It’s a weapon system that is intentionally aerosolized. This study admits that the Anthrax spores from B. anthracis STI-1 strain and B. anthracis strain V770-NPI-R used in the “aerosolized Anthrax vaccines” are toxigenic. The Sterne strain which is used to inoculate our food supply (animals) is also genotoxic. This NIH study explains how a “replicon” of the Bacillus anthracis bacteria was cloned into an Escherichia coli (E. coli) “vector” using cross-species-genomics. These two bacteria were synthetically fused together to enhance lethality. ALHYDROGEL According to the “aerosolized Anthrax vaccine” patents, the so-called “vaccine adjuvant” used is a DARPA weapon system called Alhydrogel. Hydrogel technology was developed over many years during a collaboration between DARPA and Profusa, a private biotech company specializing in the development of tissue-integrated biosensors. In 2018, DARPA published a video revealing their intention to use this biosensing technology for both military and public health. In the Alhydrogel invention, Anthrax was fused together into a nanogel called Alhydrogel, consisting of fibrous nanoparticles (Nanofibers) that are “antigen specific to CD4+ T cells”. In layman’s terms, the nanorobots are intentionally programmed to target and alter the genome of CD4-T cells, inducing cell death. This essential part of our immune system (T-cells) stop foreign invaders from entering our cells. Destroying our T-cells enables the government’s operating system to take root in the body and quicken death. Alhydrogel is infused with 750 μg of aluminum, making it magnetic. Nanofibers are used for self-assembly and electrospinning, for tissue engineering and delivery of drugs and chemicals into the brain. Being magnetic and nanotech based, the Alhydrogel can replicate everywhere in the body and wire a new neural network. Astonishingly, Alhydrogel is already the most widely used vaccine adjuvant! There are many Alhydrogel patents that contain toxic cocktails that will overwhelm anyone’s immune system. This Alhydrogel patent demonstrates it’s use of the B anthracis bacteria, E. coli, N. gonorrhoeae, Chlamydia, Staphylococcus, TB and more. It also contains the H5N1 influenza bioweapon, RNA, DNA synthesis and Polysorbate 80 for Blood Brain Barrier (BBB) permeability. This begs the question, where do venereal diseases come from? This Nature article reveals that 2% Alhydrogel is used in all Covid-19 “vaccines”. Previously, aluminum salts were the only adjuvants licensed for vaccine use in humans in the U.S. In recent decades, nanoparticle adjuvants in hydrated gels were introduced. The article continues by saying that the “influenza vaccine” was the first to use Alhydrogel. “Aluminum salt-based adjuvants such as alhydrogel have been a mainstay of vaccines for decades” boasts Christopher B. Fox and colleagues at the Infectious Disease Research Institute in Seattle, USA. Both nanoparticles and Anthrax have been used in vaccines for decades already, without the Informed Consent of the public. Alhydrogel was improved and transformed into the Nanoalum adjuvant. Here, we introduce a top-down manufacturing process—high-pressure microfluidization—to generate aluminum oxyhydroxide nanoparticles, hereupon referred to as nanoalum, using the clinically approved Alhydrogel adjuvant as the precursor. Alhydrogel is also carried in the lipid coating of nanoparticles. The “Aerosolized Anthrax Vaccines” also contain SEQ ID NO: 1 which is owned by the Pirbright Institute (Bill & Melinda Gates). SEQ ID NO: 1 contains the world’s most deadly genetically modified parasites. Please see: MEGA BOMBS! GMO Parasites Are The mRNA Vector! ANTHRAX SYMPTOMS AND TREATMENT Anthrax has been deployed on the population by three methods; injection, inhalation and skin penetration. The mortality rate for Anthrax varies depending on the method of exposure. It’s approximately 20% fatality for cutaneous Anthrax and 25–75% for Gastrointestinal Anthrax. Inhalation Anthrax is by far the worst with a fatality rate that is 80% or higher. Inhalation Anthrax is what we’re all being exposed to from the Covid-19 jabs and contaminated PCR swabs. Antibiotics constitute the mainstay of treatment against Anthrax, despite the fact that they won’t work to stop its replication due to the NIH, China and Israel’s GAIN-and-LOSS-of-Function enhancements (antibiotic resistance). Pharmaceutical experimental genotoxic drugs such as Oblitoxaximab and Raxibacumab are being touted as Anthrax treatments but these are monoclonal antibodies. We know from the monoclonal antibody patents that they’re also the “mRNA vaccine” weapon system. Anytime you inject recombinant proteins or modRNA into humans, it’s extremely toxic and will be rejected by our immune system 100% of the time. Please read: Monoclonal Antibodies Is mRNA Gene Knockdown Tech, Encoding HIV – Patent Review Pharma wants us to believe that the only known effective “prevention” against Anthrax is the Anthrax “vaccine”. However, the Anthrax “vaccine” inoculation given to U.S. military troops was a horrific disaster. U.S. Army statistics that were never published, show the Anthrax “vaccine” induces turbo cancers. The toxicological harms of Anthrax are many. It causes severe heart issues. Could this be a contributing factor to Myocarditis and Pericarditis? Anthrax also coagulates the blood. “Pathophysiological changes associated with anthrax lethal toxin included loss of plasma proteins, decreased platelet count, slower clotting times, fibrin deposits in tissue sections, and gross and histopathological evidence of hemorrhage. These findings suggest that blood vessel leakage and hemorrhage lead to disseminating intravascular coagulation and/or circulatory shock as an underlying pathophysiological mechanism.” Read more here and here. Anthrax induces hemorrhaging. So this explains all the excessive bleeding people have experienced over the last 4 years, following Covid-19 inoculation and from aerosolized exposure, otherwise known as the “shedding” phenomenon. This is a result of Inhalation Anthrax. It becomes clear that the newly dubbed “White Lung Syndrome” and the Chinese ‘pneumonia’ outbreak is none other than Inhalation Anthrax. Mycoplasma pneumonia is on the rise, and it’s listed on Pfizer’s internal documentation as a known Adverse Effect of the Covid-19 inoculation. This study reveals that Mycoplasma Pneumonia is aerosolized. WHO also confirms this phenomenon is Mycoplasma Pneumonia. All naturally occurring bacterium have cell walls. Mycoplasmas are spherical to filamentous cells with no cell walls. It’s genetically manipulated in a laboratory by GAIN-of-Function for the purpose of enhancing replication inside the human body, making it more lethal. Mice “treated” with anthrax lethal toxin (LT) exhibit hemorrhage and liver damage. Monocyte procoagulant responses to anthrax peptidoglycan are reinforced by proinflammatory cytokine signaling and histological lesions in the spleen. Anthrax has already been tested on the public. According to the NIH, Anthrax spores were intentionally released into “some environments” in NYC during 9/11. According to the NIH, the FBI launched an investigation called “Amerithrax”. It was “one of the largest and most complex (investigation) in the history of law enforcement”, according to the FBI. Heroine users in Europe have been tested with Injection Anthrax. Our skies are sprayed with smart dust and chemicals daily. Our governments have launched an all-out war against their constituents. We are being poisoned in a myriad of ways, so please keep this in mind: “Anthrax is easy to produce in large quantities, highly lethal, relatively easy to develop as a weapon, easily spread over a large area, easily stored and dangerous for a long time. Given appropriate weather and wind conditions, 50 kilograms of aerosolised anthrax spores released from an aircraft along a 2 kilometer line could create a lethal cloud of anthrax spores that would extend beyond 20 kilometers downwind. The aerosol cloud would be colorless, odorless and invisible following its release. Given the small size of the spores, people indoors would receive the same amount of exposure as on the street. There are currently no atmospheric warning systems to detect an aerosol cloud of anthrax spores. The first sign of a bioterrorist attack would most likely be patients presenting with symptoms of inhalation anthrax. A 1970 analysis by World Health Organization concluded that the release of aerosolized anthrax upwind to a population of 5,000,000 could lead to an estimated 250,000 casualties, of whom as many as 100,000 could be expected to die. A later analysis, by the Office of Technology Assessment of the U.S. Congress estimated that 130,000 to 3 million deaths could occur following the release of 100 kilograms of aerosolized anthrax over Washington D.C., making such an attack as lethal as a hydrogen bomb.” TREATMENT If you have been inoculated with Covid-19 or PCR swabbed, and you are suffering from heart pain, unusual bleeding, skin rashes and abrasions, it could be Injection Anthrax. If you are “unvaccinated” and hemorrhaging from being around “vaccinated”, then you may have been exposed to Inhalation Anthrax. Many doctors, including myself, have documented persistent bleeding rectally, violent bleeding vaginally, nasally and in the eyes. Since October 4th, I have received many reports of a red eye syndrome where the entire eye is blood-red. This makes sense because eye tissue is more sensitive. If you have been exposed to Inhalation Anthrax, you may feel hot and severely flushed, and you may break out in big, red splotches on your skin, followed by a completely red eye in the morning. Although they don’t get much attention, “anti-toxins have long been considered an essential ‘adjunctive’ therapy, and remain so”, according to the NIH. Anti-toxins are the natural medicines that detox poisons. In other words, you need an effective natural medicine detox protocol. I have been successfully detoxing people from the Covid-19 bioweapons for three years. Since I began treating people presenting with Anthrax poisoning with strong antibacterials, my clients are experiencing quicker detox results. If you would like to schedule a consultation with me, please do so through my online booking system. Please follow me on Telegram @drloveariyana and X @drloveariyana. If you would like to donate to my research, please do so here. UPDATE: My Anthrax article is now fully edited and published on Substack. Please review and SHARE. The Covid-19 Vaccine Antigen Is ANTHRAX Read more: https://open.substack.com/pub/drloveariyana/p/the-covid-19-vaccine-antigen-is-anthrax?r=2juwfo&utm_campaign=post&utm_medium=web&showWelcomeOnShare=true https://donshafi911.blogspot.com/2024/02/the-covid-19-vaccine-antigen-is-anthrax.html
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  • Luciferase Microarray Patches Contain DARPA Hydrogel & Autonomous Insect Cyborg Sentinels
    June 21, 2023 by Dr. Ariyana Love
    By Dr. Ariyana Love

    Queensland’s first needle-free “vaccine” facility just opened in Australia, yesterday. The microarray patch for intradermal delivery technology is also being called a Nanopatch and it’s aimed at our children.

    3D printed microarray patches (MAP’s) are comprised of a series of micrometer-sized projections that can painlessly puncture the skin and access the epidermal/dermal layer, delivering drugs and chemicals into the interstitial fluids of the human body. It also allows for external control of delayed release of drugs and repeated dosage over time. This technology was already being developed back in the 1970’s.

    In May of 2023, Micron Biomedical announced Phase 1/2 data from the first-ever clinical trial of a “vaccine” patch in children – including infants as young as nine months old. This study was tested on Gambian children.

    In October of 2022, the first official Luciferase patch trial on children using a placebo, began in Brisbane, Australia. The trial was led by Vaxxas. A number of phase-one clinical trials in adults were already conducted by Vaxxas according to Project Manager, Ben Baker.

    Vaxxas, founded by UQ commercialization company UniQuest in 2011, received $A30 million (US$22 million) through the Biomedical Advanced Research and Development Authority (BARDA) to support “pandemic” deployment of their high-density micro-array patch (HD-MAP). Vaxxas is partnered with the U.S. Government and funded by Bill and Melinda Gates. The microarray patch is supposedly intended to inoculate children from middle to low income countries with measles, rubella, and polio.

    This microarray patch technology is scheduled to be mandated for children worldwide and it’s on the national immunization schedule for children in Australia. UNICEF is driving the research, development and scale of microarray patches for children. They’re keen on “identifying barriers for scaling and investigating the need for market pull incentives to spark interest and endorsement by vaccine manufacturers.” And of course the World Harm Organization (WHO) is involved with pushing the measles-rubella microarray patch on children.

    DNA from human origin

    The antibody used in the microarray (MA) patches comes from human origin, according to scientific literature (See paragraph #4 and 2.2. Antibody Stability Study). The patches use “nonspecific human Ig” and the “human hlg” which is a human leukocyte antigen, as well as other “nonspecific” amounts of human DNA plasma, including human lgG1 and human lgG2. It is well known that injecting human DNA into humans induces inflammation, autoimmunity and rapid cancer growth.

    The core–shell MA patch has two delayed burst releases at days 10 and 21. Included in the patches is the use of “nondegradable poly(ethylene-co-vinyl acetate) (EVA, for the sustained release of human DNA), hyaluronic acid scaffolds, glycol chitosan, and oxidized alginate hydrogels.” (See paragraph two).

    Glycol chitosan is insect DNA which is highly toxic to humans. It has never been approved by the FDA for use in humans. Hyaluronic acid based scaffolds is used for tissue engineering and so is synthetic mRNA.

    Johnson and Johnson developed the Luciferase microarray patch (See paragraph entitled, 2.3. Vector) containing the Adenovirus 5 vector for targeted deletion of the E1 and E3 genes, located on the X-chromosome.

    PLEASE READ: EPIGENETICS: Vaccines Are Deleting Human Genes & Transfecting Cells With Ebola/Marburg

    This scientific paper reveals that Luciferase hydrogel is chimeric DNA from cross species genomic splicing. The Luciferase patches are being marketed (See bottom of page) as something that will “reduce the rate of HIV infections”. Incidentally, governments are coercing schools to mandate HIV testing of children.

    DARPA hydrogel

    The Defense Advanced Research Projects Agency (DARPA) is a research and development agency of the United States Department of Defense responsible for the development of emerging technologies for use by the military.

    DARPA’s hydrogel replicates into rectangular crystal structures within minutes after coming into contact with body fluids. It grows a crystalline sheath above your muscle and beneath your skin which is magnetic. It acts as an antennae inside the human body that can transmit your internal data through the Internet and receive commands from towers as it replicates and expands throughout the entire body.

    Whole parasite “vaccines”

    Also contained within some embodiment’s of the DARPA hydrogel patches are Sentinels. Under a highly classified program DARPA has been weaponizing insects for decades such as GMO mosquitos that carry GMO parasite eggs coded with synthetic mRNA. These parasite eggs are otherwise known as “whole parasite vaccines“.

    PLEASE READ: Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero

    This peer-reviewed paper discusses “Cyropreserved Whole-Parasite Vaccines” using the deadly P. falciparum Malaria parasite to target in particular, the CD4+ T cells and destroy them by inducing cell death. Please also read here, here and here.

    The Sentinels

    Sentinels are also found within the DARPA hydrogel Luciferase microarray patches.

    DARPA has a full Hybrid Insect MEMS program called “Sentinel”. The D.O.D. is also in on this. Much of the funding for this project comes from DARPA’s Microsystems Technology Office (MTO), which has devoted more than US$2 million to the Hybrid Insect MEMS (HI-MEMS) program.

    Micro-Electro-Mechanical Systems (MEMS), otherwise known as micromachined devices uses organic insects that have been morphed into externally controllable electromechanical devices and ‘living’ biosensors, using genetically modified microorganisms. Micro-mechanical systems are placed inside the insects during the early stages of metamorphosis, allowing for tissue-machine interface and control over insect locomotion. Insect cyborgs have most of the machine component inside the insect body providing stealthy robots that use muscle actuators. Motion trajectories are obtained either from GPS coordinates, or using RF, optical, ultrasonic signals based remote control. The Sentinels work as microsensors and they also can modulate light beams. Through heterogeneous integration, they have merged the Sentinels into a circuitry nanotech system.

    While this is a highly classified and secretive project, there’s a paper trail. In 2018, the U.S. Government awarded DARPA a research and development contract funding DARPA’s SENTINEL # HR001118S0005 project to the tune of 10 million dollars. The first Sentinel patent was registered by GeneNews, in 2010. The second Sentinel patent # 7,662,558, entitled “Method of profiling gene expression in a human subject” was registered in 2018.

    But who could anticipate that Sentinels would be used inside the human body? Since 2009, Sentinels have been used internally for a breast cancer excision. They can slice right through tumors which explains why my clients are being internally lacerated by these Sentinels, inflicting terrible pain and causing red skin lesions to appear. Also according to client testimonials and peer-reviewed literature, Sentinels shoot out electromagnetic beams and attempt to influence your nervous system using electricity. They borrow into the nervous system and can “read thoughts,” anticipate your movements and attempt to control their host.

    The hydrogel-based encapsulation (nanotech) system for genetically modified organisms (GMMs) incorporates a biocompatible multilayer tough shell and an alginate-based core. Sentinels are the core controller of the Operating System. They regulate cell to cell communication between the AI parasites, organoids, hydras, worms and poisonous anaerobic bacteria in vivo, as the linked document shows.

    “Microelectronic integrated circuits can be thought of as the “brains” of a system and MEMS augments this decision-making capability with “eyes” and “arms”, to allow microsystems to sense and control the environment. Sensors gather information from the environment through measuring mechanical, thermal, biological, chemical, optical, and magnetic phenomena. The electronics then process the information derived from the sensors and through some decision making capability direct the actuators to respond by moving, positioning, regulating, pumping, and filtering, thereby controlling the environment for some desired outcome or purpose. Furthermore, because MEMS devices are manufactured using batch fabrication techniques, similar to ICs, unprecedented levels of functionality, reliability, and sophistication can be placed on a small silicon chip at a relatively low cost.”

    DARPA openly admits to using AI for brain computer interface with humans through it’s Explainable Artificial Intelligence (XAI) program. Sentinels are contained within a small silicon chip that looks very similar to the chips Dr. Pablo Campra found in the Covid-19 vials.

    In 2017, Finland developed nanocellulose-alginate hydrogel suitable for 3D printing.

    Implantable hydrogel biosensors are scheduled to be used in Covid-19 inoculations and microarray patches. Hillman Laboratories partnered with John Hopkins University, admit that they want to “take the microarray patches door to door“.

    One of my clients was a victim of a U.S. government pilot project in Seattle Washington. GMO mosquitos are being unleashed in Florida and other states as well. My client, her daughter and best friend were congregated at a church function outdoors when they were “beaten by mosquito’s,” as she put it. These mosquito’s were smaller than the typical mosquitos they have in Washington state and they had unusual markings. They could not feel the bites but saw the mosquito’s biting. Later, people from the congregation broke out in welts where they were bitten and had terrible pains all over their bodies. Now my client and her daughter are riddled with Sentinels which crawl everywhere in their bodies and torture them. These Sentinels belong to DARPA’s weaponized insects project. My clients best friend could not endure and she died before they discovered my protocols. I have several other clients whom are being tortured by Sentinels and my protocols are helping them. Other clients have already detoxed the Sentinel and DARPA hydrogel out of their bodies.

    ALSO READ: “YIKES! Hydrogel Nano-biotechnology in Vaccines and Nasal Swab Tests Capable of Electronically Linking Human Brains to Cloud Wirelessly” by State of The Nation.

    Please consider donating to Dr. Ariyana Love’s investigative research and ministry, here.

    If you require a health consultation please schedule with Dr. Love, here.

    Contact Dr. Love at metanutrients@mailfence.com or call her cell at +1 928-892-8736.

    Follow Dr. Love on Telegram @DrAriyanaLove and on Twitter @drloveariyana.

    https://ambassadorlove.blog/2023/06/21/luciferase-microarray-patches-contain-darpa-hydrogel-autonomous-insect-cyborg-sentinels/
    Luciferase Microarray Patches Contain DARPA Hydrogel & Autonomous Insect Cyborg Sentinels June 21, 2023 by Dr. Ariyana Love By Dr. Ariyana Love Queensland’s first needle-free “vaccine” facility just opened in Australia, yesterday. The microarray patch for intradermal delivery technology is also being called a Nanopatch and it’s aimed at our children. 3D printed microarray patches (MAP’s) are comprised of a series of micrometer-sized projections that can painlessly puncture the skin and access the epidermal/dermal layer, delivering drugs and chemicals into the interstitial fluids of the human body. It also allows for external control of delayed release of drugs and repeated dosage over time. This technology was already being developed back in the 1970’s. In May of 2023, Micron Biomedical announced Phase 1/2 data from the first-ever clinical trial of a “vaccine” patch in children – including infants as young as nine months old. This study was tested on Gambian children. In October of 2022, the first official Luciferase patch trial on children using a placebo, began in Brisbane, Australia. The trial was led by Vaxxas. A number of phase-one clinical trials in adults were already conducted by Vaxxas according to Project Manager, Ben Baker. Vaxxas, founded by UQ commercialization company UniQuest in 2011, received $A30 million (US$22 million) through the Biomedical Advanced Research and Development Authority (BARDA) to support “pandemic” deployment of their high-density micro-array patch (HD-MAP). Vaxxas is partnered with the U.S. Government and funded by Bill and Melinda Gates. The microarray patch is supposedly intended to inoculate children from middle to low income countries with measles, rubella, and polio. This microarray patch technology is scheduled to be mandated for children worldwide and it’s on the national immunization schedule for children in Australia. UNICEF is driving the research, development and scale of microarray patches for children. They’re keen on “identifying barriers for scaling and investigating the need for market pull incentives to spark interest and endorsement by vaccine manufacturers.” And of course the World Harm Organization (WHO) is involved with pushing the measles-rubella microarray patch on children. DNA from human origin The antibody used in the microarray (MA) patches comes from human origin, according to scientific literature (See paragraph #4 and 2.2. Antibody Stability Study). The patches use “nonspecific human Ig” and the “human hlg” which is a human leukocyte antigen, as well as other “nonspecific” amounts of human DNA plasma, including human lgG1 and human lgG2. It is well known that injecting human DNA into humans induces inflammation, autoimmunity and rapid cancer growth. The core–shell MA patch has two delayed burst releases at days 10 and 21. Included in the patches is the use of “nondegradable poly(ethylene-co-vinyl acetate) (EVA, for the sustained release of human DNA), hyaluronic acid scaffolds, glycol chitosan, and oxidized alginate hydrogels.” (See paragraph two). Glycol chitosan is insect DNA which is highly toxic to humans. It has never been approved by the FDA for use in humans. Hyaluronic acid based scaffolds is used for tissue engineering and so is synthetic mRNA. Johnson and Johnson developed the Luciferase microarray patch (See paragraph entitled, 2.3. Vector) containing the Adenovirus 5 vector for targeted deletion of the E1 and E3 genes, located on the X-chromosome. PLEASE READ: EPIGENETICS: Vaccines Are Deleting Human Genes & Transfecting Cells With Ebola/Marburg This scientific paper reveals that Luciferase hydrogel is chimeric DNA from cross species genomic splicing. The Luciferase patches are being marketed (See bottom of page) as something that will “reduce the rate of HIV infections”. Incidentally, governments are coercing schools to mandate HIV testing of children. DARPA hydrogel The Defense Advanced Research Projects Agency (DARPA) is a research and development agency of the United States Department of Defense responsible for the development of emerging technologies for use by the military. DARPA’s hydrogel replicates into rectangular crystal structures within minutes after coming into contact with body fluids. It grows a crystalline sheath above your muscle and beneath your skin which is magnetic. It acts as an antennae inside the human body that can transmit your internal data through the Internet and receive commands from towers as it replicates and expands throughout the entire body. Whole parasite “vaccines” Also contained within some embodiment’s of the DARPA hydrogel patches are Sentinels. Under a highly classified program DARPA has been weaponizing insects for decades such as GMO mosquitos that carry GMO parasite eggs coded with synthetic mRNA. These parasite eggs are otherwise known as “whole parasite vaccines“. PLEASE READ: Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero This peer-reviewed paper discusses “Cyropreserved Whole-Parasite Vaccines” using the deadly P. falciparum Malaria parasite to target in particular, the CD4+ T cells and destroy them by inducing cell death. Please also read here, here and here. The Sentinels Sentinels are also found within the DARPA hydrogel Luciferase microarray patches. DARPA has a full Hybrid Insect MEMS program called “Sentinel”. The D.O.D. is also in on this. Much of the funding for this project comes from DARPA’s Microsystems Technology Office (MTO), which has devoted more than US$2 million to the Hybrid Insect MEMS (HI-MEMS) program. Micro-Electro-Mechanical Systems (MEMS), otherwise known as micromachined devices uses organic insects that have been morphed into externally controllable electromechanical devices and ‘living’ biosensors, using genetically modified microorganisms. Micro-mechanical systems are placed inside the insects during the early stages of metamorphosis, allowing for tissue-machine interface and control over insect locomotion. Insect cyborgs have most of the machine component inside the insect body providing stealthy robots that use muscle actuators. Motion trajectories are obtained either from GPS coordinates, or using RF, optical, ultrasonic signals based remote control. The Sentinels work as microsensors and they also can modulate light beams. Through heterogeneous integration, they have merged the Sentinels into a circuitry nanotech system. While this is a highly classified and secretive project, there’s a paper trail. In 2018, the U.S. Government awarded DARPA a research and development contract funding DARPA’s SENTINEL # HR001118S0005 project to the tune of 10 million dollars. The first Sentinel patent was registered by GeneNews, in 2010. The second Sentinel patent # 7,662,558, entitled “Method of profiling gene expression in a human subject” was registered in 2018. But who could anticipate that Sentinels would be used inside the human body? Since 2009, Sentinels have been used internally for a breast cancer excision. They can slice right through tumors which explains why my clients are being internally lacerated by these Sentinels, inflicting terrible pain and causing red skin lesions to appear. Also according to client testimonials and peer-reviewed literature, Sentinels shoot out electromagnetic beams and attempt to influence your nervous system using electricity. They borrow into the nervous system and can “read thoughts,” anticipate your movements and attempt to control their host. The hydrogel-based encapsulation (nanotech) system for genetically modified organisms (GMMs) incorporates a biocompatible multilayer tough shell and an alginate-based core. Sentinels are the core controller of the Operating System. They regulate cell to cell communication between the AI parasites, organoids, hydras, worms and poisonous anaerobic bacteria in vivo, as the linked document shows. “Microelectronic integrated circuits can be thought of as the “brains” of a system and MEMS augments this decision-making capability with “eyes” and “arms”, to allow microsystems to sense and control the environment. Sensors gather information from the environment through measuring mechanical, thermal, biological, chemical, optical, and magnetic phenomena. The electronics then process the information derived from the sensors and through some decision making capability direct the actuators to respond by moving, positioning, regulating, pumping, and filtering, thereby controlling the environment for some desired outcome or purpose. Furthermore, because MEMS devices are manufactured using batch fabrication techniques, similar to ICs, unprecedented levels of functionality, reliability, and sophistication can be placed on a small silicon chip at a relatively low cost.” DARPA openly admits to using AI for brain computer interface with humans through it’s Explainable Artificial Intelligence (XAI) program. Sentinels are contained within a small silicon chip that looks very similar to the chips Dr. Pablo Campra found in the Covid-19 vials. In 2017, Finland developed nanocellulose-alginate hydrogel suitable for 3D printing. Implantable hydrogel biosensors are scheduled to be used in Covid-19 inoculations and microarray patches. Hillman Laboratories partnered with John Hopkins University, admit that they want to “take the microarray patches door to door“. One of my clients was a victim of a U.S. government pilot project in Seattle Washington. GMO mosquitos are being unleashed in Florida and other states as well. My client, her daughter and best friend were congregated at a church function outdoors when they were “beaten by mosquito’s,” as she put it. These mosquito’s were smaller than the typical mosquitos they have in Washington state and they had unusual markings. They could not feel the bites but saw the mosquito’s biting. Later, people from the congregation broke out in welts where they were bitten and had terrible pains all over their bodies. Now my client and her daughter are riddled with Sentinels which crawl everywhere in their bodies and torture them. These Sentinels belong to DARPA’s weaponized insects project. My clients best friend could not endure and she died before they discovered my protocols. I have several other clients whom are being tortured by Sentinels and my protocols are helping them. Other clients have already detoxed the Sentinel and DARPA hydrogel out of their bodies. ALSO READ: “YIKES! Hydrogel Nano-biotechnology in Vaccines and Nasal Swab Tests Capable of Electronically Linking Human Brains to Cloud Wirelessly” by State of The Nation. Please consider donating to Dr. Ariyana Love’s investigative research and ministry, here. If you require a health consultation please schedule with Dr. Love, here. Contact Dr. Love at metanutrients@mailfence.com or call her cell at +1 928-892-8736. Follow Dr. Love on Telegram @DrAriyanaLove and on Twitter @drloveariyana. https://ambassadorlove.blog/2023/06/21/luciferase-microarray-patches-contain-darpa-hydrogel-autonomous-insect-cyborg-sentinels/
    AMBASSADORLOVE.BLOG
    Luciferase Microarray Patches Contain DARPA Hydrogel & Autonomous Insect Cyborg Sentinels
    By Dr. Ariyana Love Queensland’s first needle-free “vaccine” facility just opened in Australia, yesterday. The microarray patch for intradermal delivery technology is also being c…
    0 Kommentare 0 Anteile 16299 Ansichten
  • Screening for Silent Spike Toxicity
    Spike levels build up over time with repeated exposures and eventually the dam breaks. Here's how to detect toxicity before it causes symptoms.

    Dr. Syed Haider
    Pet Toxin Safety - Mill Creek Animal Hospital
    This post will provide a deep dive on tests for spike toxicity, including the best screening tests for those who have no symptoms, but have been exposed. These tests detect specific spike-induced inflammation, clotting, AIDS, turbo cancer, etc, and can help get ahead of disease developing underneath the surface. In a future post I plan to cover the best tests for fine tuning a healing protocol.

    There are now hundreds if not thousands of physicians treating spike toxicity with varying protocols and degrees of success.

    In my experience most hesitate to escalate ivermectin enough. At high enough doses it almost always helps (at mygotodoc.com I usually start where others end, at 0.2mg/kg/day and then may gradually escalate as high as 10 times more than that ie 2mg/kg/day in some patients over the course of 5-10 weeks).

    Most physicians treating spike toxicity also refrain from much or any testing.

    This makes sense on a budget, and I often come across patients who can’t afford testing and we skip it as well, but if it can be afforded then it can be helpful in fine tuning the protocol and sometimes uncovering key missing ingredients, like nutritional deficiencies, or particularly stubborn micro clotting requiring escalated dosing and varied types of anticoagulants.

    The other place for testing is in screening of the general population without symptoms, both vaxxed and unvaxxed (though when you really press you often do find new symptoms have sprouted up since the beginning of the pandemic).

    But even in those who truly have no new symptoms and feel perfectly fine, it seems that it may simply be a matter of time before spike toxicity catches up with them, especially if, like so many people, they can’t detox quickly enough, can’t break up the atypical microclots fast enough, and then are reexposed to a new variant, or a big shedding bolus, and that tips the scales and sends them into outright long haul.

    People find it hard to believe that they could feel fantastic and yet there could be something brewing inside that is just 1 straw away from breaking their backs.

    Yet almost everyone was in this very situation even before the pandemic.

    We all have a health span and a lifespan, and for most in the modern world the overlap between them has been dramatically shrinking for generations, and it has only gained speed with each passing year, and especially the last 3 years since the pandemic hit.

    Health is wealthqbak - http://asianpin.com/health-is-wealthqbak/ | Funny cartoons jokes, Funny cartoon pictures, Funny cartoons
    source
    In plain English, we often gradually become chronically ill and then debilitated starting decades before we finally die. In the worst cases spending the last years of our lives in nursing homes, oblivious to our surroundings and infrequently visiting loved ones.

    The reason for this is a chronic mismatch between our bodies and our environments - not just lack of exercise and poor diets, but also the chemical soup we find ourselves in, the toxins in the air, water and soil, the lack of fresh air and sunlight throughout the day, the lack of grounding, and too much toxic blue light at night that is soaked up by our eyes and very skin while we lounge in front of our screens, greatly stressing ourselves, while thinking we’re relaxing, followed by restless, unfulfilling sleep.

    Most of us are drawing down on our health savings accounts - not the tax free HSA - but a metaphorical account that represents our life force.

    Thank you for reading Dr. Syed Haider. This post is public so feel free to share it.

    Share

    Just like a regular bank account, if it isn’t managed properly and wealth is overused, it will eventually get close to zero, by which time we will be liable to illness at the drop of a hat - anything that is too taxing can overdraw the account since what’s flowing into it can’t overcome what’s flowing out.

    And then some of us become chronically overdrawn, living on credit, and in the toxic embrace of chronic illness because of it, dragging us into the depths, while we struggle vainly to get back above the surface.

    This is why when you finally realize you have to change your ways to get better, it makes no sense to give up those changes as soon as you break free of illness.

    You are just above zero, still liable to dipping below the surface again. You need to build up your reserves of health over time and not overdraw your account again. You have to become a good steward of your body and resources. And over time you can get to the point where you’re on solid ground again and can put up with small and large stressors without backsliding. But you should always keep in mind how bad it can get to motivate you to stay on the straight and narrow going forward.





    To get back to the topic, the spike protein builds up in our bodies over time and causes detectable changes to our immune and vascular systems. There is an immune fingerprint of various cytokine markers, there are the microclots, there are alterations to the red blood cell zeta potential, there are predictable decreases of various micronutrients. There may be early warning signs of AIDS, or cancer or organ dysfunction.

    Nowadays almost all new patients with Long COVID or Vax injury made it through a few shots, or a few rounds of COVID without getting long haul, but the final infection or shot put them over the edge.

    If they had come before they got that last shot or infection I could have detected their susceptibility in the lab and we could have worked to correct it.

    This is the epidemic of Silent Spike Toxicity.

    And these are the tests we have available to screen for it:

    The Microclot Test: only available from 1 lab in the US (mail order). Detects abnormal clotting not seen on any other test. The single most specific spike toxicity test.

    The Comprehensive Spike Screening Panel: includes imaging tests: EKG, CXR, Echo. Blood tests that detect damage to the heart, lungs, liver, kidneys. Checks zeta potential. Can show the immune fingerprint of spike. Detection of AIDS. Typical gut microbiome changes. Advanced cancer screening (blood & whole body MRI), and more.

    The Masterjohn-Schilling Spike Healing Panel: detects neuroinflammation, free radicals, mitochondrial dysfunction, autoantibodies, reactivated viruses and bacteria, MCAS, specific micronutrients that are depleted by spike toxicity, and more.

    Masterjohn’s Deep Dive Nutrition Panel goes beyond nutrients depleted by spike toxicity to provide a complete snapshot of functional nutrition and is indispensable for deep healing when half measures don’t work.


    source
    A quick note on tests in general: There is no perfect test. Tests are evaluated by their sensitivity and specificities, but we don’t have research on any of these for spike toxicity diseases. Sensitivity is how good a test is at ruling out a diagnosis and specificity is how good it is at ruling in a diagnosis.

    The best screening tests would be 100% specific - meaning if you have the diagnosis it will be detected 100% of the time, but in order to gain that level of specificity they often have to cast a wide net and give up some sensitivity. What this means practically is that if the diagnosis is present you will test positive, but there will also be some people who don’t have the diagnosis who also test positive.

    Highly specific tests are usually paired with confirmatory tests that are hopefully highly sensitive. Meaning they can weed out the people who were including in the first round of screening, but don’t actually have the diagnosis in question.

    In the absence of research into spike toxicity diseases and optimal screening regimens we have to fall back on expert opinion.

    It seems that the microclot test is likely the best screening test, because those treating spike toxicity have never come across someone with the clinical symptoms of the disease who doesn’t have elevated microclots. Unfortunately microclots can be elevated by other conditions. So a confirmatory test like the incelldx Incellkyne panel might be ordered from the Comprehensive Spike Screening panel, along with other tests we’ll discuss below.

    If the diagnosis of spike toxicity is made then the Masterjohn-Schilling panel is the best next step for fine tuning the protocol, ensuring that the right micronutrients are topped up and the right treatments are prescribed.

    If not improving after targeted and sustained treatment, then the Deep Dive Nutrition panel is indicated to uncover rare and unusual nutritional deficits that could be holding you back.

    Here I’ll cover the primary screening tests: The Microclot Test and the Comprehensive Spike Screening Panel. In a future article I may cover the more expansive and complicated panels that are used primarily in treatment.

    Share

    The Microclot Test

    figure 3
    source
    Typical microclots are usually found in the elderly and those with chronic illnesses like diabetes.

    Spike induced atypical amyloid fibrin microclots are found in those with spike induced blood toxicity.

    The difference between typical and atypical are that spike induced microclots are very difficult to break down, so difficult that they often do not break down at all.

    This explains why the D-dimer isn’t helpful for detecting spike toxicity.

    D-dimer is always trapped inside of clots. Typical clots are always being broken down on the margins - at the edge of a typical clot there will be breakdown. Sometimes the breakdown happens slower than the growth of the clot, but there is always a battle going on between clot growth and clot destruction which will release D-dimer into the blood stream.

    Since it is virtually always elevated in the presence of clotting it is a very specific test, and is used as a screening test when a physician suspects a clotting disorder, but isn’t sure. For example if someone shows up with chest pain and it could be a pulled muscle or a pulmonary embolism (clot in the pulmonary veins), a D-dimer is a simple ad very cheap test that can be done to determine if further confirmatory, but more expensive more risky testing should be considered, like a CT Angiogram of the chest.

    For this reason every doctor going through residency comes to consider a positive D-dimer as indicative of clotting and a negative D-dimer as indicative of no clotting.

    figure 4
    source
    The D-dimer is often elevated during severe acute COVID-19 infection, and during a severe acute injection reaction, but it is not usually elevated in chronic spike toxicity, including chronic long haul and vaccine injured patients.

    The reason it isn’t elevated is that most people cannot break down the atypical microclots caused by spike protein without some additional help from medications and supplements.

    Once medications like aspirin (and sometimes prescriptions ones like plavix and eliquis), supplements like nattokinase, serrapeptase, lumbrokinase, bromelain and NAC are started the atypical microclots start to be broken down and D-dimer goes up, which in this case is usually reason for celebration.

    So the microclot test is the only test in America today that can detect elevated atypical microclots. It’s only available from one lab in the country via mail order (request it from mygotodoc.com), and it helps detect spike toxicity as well as helping track treatment.


    If initial treatment for microclots with aspirin and supplements doesn’t bring the levels down then we escalate to using higher doses, or add plavix and then later eliquis. And we can also consider plasma donation, or even therapeutic plasmapheresis, if available.



    DETOX [spike buster] PRE-ORDER NOW: initial stock is limited! Shipping late November 2023.

    The Comprehensive Spike Screening Panel

    This set of tests includes an EKG, CXR, Echo. It includes blood tests to screen for daamage to the major organs including the heart, lungs, liver, and kidneys. It checks for zeta potential in the blood, which is affected by spike toxicity. It detects an immune fingerprint of spike. It can detect AIDS. It covers stool testing for the gut microbiome as well as advanced cancer screening (via blood & whole body MRI), and more.

    Tests Included in the Panel:

    Spike antibody test: Measures your B cell’s response to the spike protein. In the absence of a direct test for spike protein this helps indirectly detect and track the spike protein levels in your body. Your body produces antibodies in response to the spike protein, and this test measures those antibodies. Generally speaking the more spike protein in your body, the higher the antibody levels. However, what's considered a problematic level varies by individual. The goal is to lower this level as much as possible. The test can also help detect those individuals who might be transmitting the spike protein to others. This is by no means a perfect test, but in the right setting it is helpful as a red flag for further workup, or as a way of monitoring response to therapies over time.

    Incellkyne Panel from Incelldx - provides an immune fingerprint of spike protein, a combination of elevated cytokine markers that are typically seen in spike protein disease. There are other immune fingerprints they have identified on this same test that indicate non spike Chronic Fatigue Syndrome and Lyme disease. If CCL-5/RANTES and/or VEGF are elevated (VEGF is almost always elevated) then the medication Maraviroc can be helpful. VEGF indicates vascular inflammation and omega-3s, infrared light exposure, and a number of other approaches can be particularly helpful to deal with that. Other inflammatory markers tested are TNF-alpha, IL-2, IL-4, IL-6, IL-8, IL-10, IL-13, GM-CSF, SCD40L, CCL3, CCL-4, and IFN-Gamma. Ivermectin is known to decrease IL-6, which is commonly elevated in Long Haul and Vax injury.

    Lymphocyte Subset Panel or Cyrex Lymphocyte MAP:



    The subset panel is the standard test for AIDS and tests for these immune subsets: CD3, CD19,CD20, CD4, CD8, CD56+. The primary pathognomic feature of AIDS would be a CD4 T cell count lower than 200, though there are other red flags such as NK cell activity <10%, or a deficit of T helper cells (CD4+), as well as these others that would only be found on the Cyrex Lymphocyte MAP test: TH1 insufficiency, Increased T-Reg (CD4+ CD25+), deficits of cytotoxic cells (CD8+, CD56+), increased TGF-beta, etc. The Lymphocyte subset panel is cheaper and available at any standard lab and may be covered by insurance, the Cyrex test is more expensive and is a mail order blood test only that has to be paid in cash up front. The Cyrex test can detect 14 different immunotypes and reveal immune under or overactivity, infections, inflammation, autoimmunity, allergies, asthma, hypersentivities and some cancers. It also helps determine what further immune tests can be done to fine tune a healing protocol.

    Galleri Cancer Screening is an advanced test for 50+ types of common cancers based on a genetic marker found in the blood. It is a good screening test because it is 99.5% specific. This might be a good option for someone with a family or personal history of cancer as it can detect occurance at a the earliest microscopic stage, far before any visual test like an MRI or CT scan would show a mass. If cancer is found ivermectin, fenbendazole, vitamin C, baking soda and many other of label easily available substances are very promising for treatment.

    Can 2 Cheap Meds, 1 Vitamin & Baking Soda Kill Any Cancer?

    Can 2 Cheap Meds, 1 Vitamin & Baking Soda Kill Any Cancer?
    Cancer rates have skyrocketed in the past century for a number of reasons not least of which is the incredibly large number of toxins spewed into the environment and incorporated into our food supplies. And now with most of humanity exposed to the cancerous spike protein there is likely to be even further acceleration. Those exposed to the fallout from …

    Read full story

    Complete Blood Count (CBC)


    Measures various components and features of the blood, including red blood cells, white blood cells, and platelets. Amongst the white blood cells we can see various abnormalities - they can be high or low, and subsets like basophils, neutrophils and eosinophils might be off. For example a patient started aspirin which is a cornerstone of most treatments of spike toxicity, but in this case raised the eosinophil level and caused some histaminergic symptoms. The symptoms were the same as her usual disease symptoms so initially were written off as a normal fluctuation in symptomatology over time, but in light of the elevated eosinophil level we finally determined that the aspirin was triggering a problem, since that is possible side effect of aspirin. Once off aspirin the symptoms and the eosinophils normalized.

    Comprehensive Metabolic Panel (CMP)


    Measures 14 different substances in the blood. It provides information about kidney and liver function, electrolyte levels, and blood sugar. Blood sugar can be high or low in spike toxicity, and that would indicate a pancreatic issue requiring further workup. Liver function often needs to be tracked in those on ivermectin and many other medications. Potassium balances sodium and usually needs to be supplemented in long haul, since most people don’t get enough, especially if blood pressure is rising.

    Cystatin C is a more specific marker of kidney dysfunction than the creatinine level that is included on the CMP.

    D-dimer: as mentioned earlier this is a product of the breakdown of clots, it’s often elevated in the acute phase of spike injury or disease, but over time the microclots being inherently difficult to break down stop releasing D-dimer unless the patient is taking a combination of supplements and/or medications to trigger this.

    Erythrocyte Sedimentation Rate (ESR)

    Decoding ESR Test: What Your Results Could Reveal About Your Health | Pathkind Labs Blog
    Measures the rate at which red blood cells settle in a standardized tube over one hour. It is a nonspecific marker of inflammation in the body. It is also an indication of the zeta potential, which is a measure of the normal negative charge on red cells that prevents them from clumping together. Spike protein lowers the normal zeta potential which usually causes ESR to rise. Potassium citrate can help reverse this trend, as can sunlight and grounding.

    hs-CRP Test (C-Reactive Protein High-Sensitivity) is another non specific marker of inflammation in the body and if found require further workup. It can be elevated in myo-pericarditis.

    Troponin T is a protein relatively specific to heart muscle cells, leaked into the blood. This is a cardiac biomarker that indicates myocardial injury and along with an EKG is. one of the primary screening tests for a heart attack as well as for myocarditis/pericarditis.

    Pro BNP (N-terminal pro-brain natriuretic peptide) is produced by the heart in response to strain, particularly heart failure.

    Electrocardiogram (EKG)

    EKG: What is it and what does it mean? – JP Stroke Foundation
    Non-invasive medical test that records the heart's electrical activity. Can be used to diagnose myocarditis/pericarditis, heart attack, and various rhythm abnormalities like atrial fibrillation, SVTs and more that can raise the risk of sudden cardiac arrest, such as that seen in some athletes who have been vaxxed.

    Echocardiogram (ECHO)


    Provides valuable information about the heart's structure, function, and blood flow and is an important test for helping visualize the inflammatory changes of myocarditis-pericarditis, such as fluid leaking into the sack around the heart.

    Chest X-ray


    source
    Non-invasive imaging test that uses X-rays to visualize the structures and organs within the chest, including the lungs, heart, ribs, diaphragm, and large arteries. Anyone with shortness of breath should have a Chest Xray as a first screening test looking for pneumonia, inflammation, scarring, nodules/cancer, etc.

    Whole Body MRI

    The Latest Quantified Self Trend: Whole-Body MRI
    Another imaging modality that can turn up hidden cancers and a whole host of other abnormalities and might be ordered for someone where the Galleri test was negative but there was still some suspicion present (here is always the risk of over diagnosis with imaging tests like this, which can lead to otherwise unnecessary stress and procedures that can themselves cause harm).

    Microbiome testing: Microbiomix Metagenomic Sequencing of Stool by Genova or Sabine Hazan’s Whole Genome Deep Sequencing by Progenabiome. Spike toxicity leads to depletion of beneficial gut bacterials species such as Bifidobacterium pseudocatenulatum, Faecalibacterium prausnitzii, Roseburia inulinivorans, and Roseburia hominis all of which are associated with long COVID complications. Presence of 'unfriendly' bacterial species is linked to poor performance on the 6-minute walk test among long COVID patients. Microbiomix is cheaper because it uses a less thorough sequencing technique, but can show some changes found due to spike toxicity. Sabine Hazan’s test is better if budgeting allows, both because it does a whole genome sequencing, but also because it benefits from her proprietary and private knowledge base (essentially studies and findings that have not yet been published). There are some supplements that can help correct deficits, and in stubborn cases a stool transplant can be transformative, though this is somewhat difficult to get done as it usually requires travel.





    And that’s a wrap!

    Next time We’ll look at the Masterjohn-Schilling panel which is our go to for optimizing treatment of long haul/vax injury and perhaps the Comprehensive Nutrition panel, which is important for anyone who has a chronic illness resistant to treatment, including long haul syndromes.

    https://blog.mygotodoc.com/p/screening-for-silent-spike-toxicity

    https://telegra.ph/Screening-for-Silent-Spike-Toxicity-01-07
    Screening for Silent Spike Toxicity Spike levels build up over time with repeated exposures and eventually the dam breaks. Here's how to detect toxicity before it causes symptoms. Dr. Syed Haider Pet Toxin Safety - Mill Creek Animal Hospital This post will provide a deep dive on tests for spike toxicity, including the best screening tests for those who have no symptoms, but have been exposed. These tests detect specific spike-induced inflammation, clotting, AIDS, turbo cancer, etc, and can help get ahead of disease developing underneath the surface. In a future post I plan to cover the best tests for fine tuning a healing protocol. There are now hundreds if not thousands of physicians treating spike toxicity with varying protocols and degrees of success. In my experience most hesitate to escalate ivermectin enough. At high enough doses it almost always helps (at mygotodoc.com I usually start where others end, at 0.2mg/kg/day and then may gradually escalate as high as 10 times more than that ie 2mg/kg/day in some patients over the course of 5-10 weeks). Most physicians treating spike toxicity also refrain from much or any testing. This makes sense on a budget, and I often come across patients who can’t afford testing and we skip it as well, but if it can be afforded then it can be helpful in fine tuning the protocol and sometimes uncovering key missing ingredients, like nutritional deficiencies, or particularly stubborn micro clotting requiring escalated dosing and varied types of anticoagulants. The other place for testing is in screening of the general population without symptoms, both vaxxed and unvaxxed (though when you really press you often do find new symptoms have sprouted up since the beginning of the pandemic). But even in those who truly have no new symptoms and feel perfectly fine, it seems that it may simply be a matter of time before spike toxicity catches up with them, especially if, like so many people, they can’t detox quickly enough, can’t break up the atypical microclots fast enough, and then are reexposed to a new variant, or a big shedding bolus, and that tips the scales and sends them into outright long haul. People find it hard to believe that they could feel fantastic and yet there could be something brewing inside that is just 1 straw away from breaking their backs. Yet almost everyone was in this very situation even before the pandemic. We all have a health span and a lifespan, and for most in the modern world the overlap between them has been dramatically shrinking for generations, and it has only gained speed with each passing year, and especially the last 3 years since the pandemic hit. Health is wealthqbak - http://asianpin.com/health-is-wealthqbak/ | Funny cartoons jokes, Funny cartoon pictures, Funny cartoons source In plain English, we often gradually become chronically ill and then debilitated starting decades before we finally die. In the worst cases spending the last years of our lives in nursing homes, oblivious to our surroundings and infrequently visiting loved ones. The reason for this is a chronic mismatch between our bodies and our environments - not just lack of exercise and poor diets, but also the chemical soup we find ourselves in, the toxins in the air, water and soil, the lack of fresh air and sunlight throughout the day, the lack of grounding, and too much toxic blue light at night that is soaked up by our eyes and very skin while we lounge in front of our screens, greatly stressing ourselves, while thinking we’re relaxing, followed by restless, unfulfilling sleep. Most of us are drawing down on our health savings accounts - not the tax free HSA - but a metaphorical account that represents our life force. Thank you for reading Dr. Syed Haider. This post is public so feel free to share it. Share Just like a regular bank account, if it isn’t managed properly and wealth is overused, it will eventually get close to zero, by which time we will be liable to illness at the drop of a hat - anything that is too taxing can overdraw the account since what’s flowing into it can’t overcome what’s flowing out. And then some of us become chronically overdrawn, living on credit, and in the toxic embrace of chronic illness because of it, dragging us into the depths, while we struggle vainly to get back above the surface. This is why when you finally realize you have to change your ways to get better, it makes no sense to give up those changes as soon as you break free of illness. You are just above zero, still liable to dipping below the surface again. You need to build up your reserves of health over time and not overdraw your account again. You have to become a good steward of your body and resources. And over time you can get to the point where you’re on solid ground again and can put up with small and large stressors without backsliding. But you should always keep in mind how bad it can get to motivate you to stay on the straight and narrow going forward. To get back to the topic, the spike protein builds up in our bodies over time and causes detectable changes to our immune and vascular systems. There is an immune fingerprint of various cytokine markers, there are the microclots, there are alterations to the red blood cell zeta potential, there are predictable decreases of various micronutrients. There may be early warning signs of AIDS, or cancer or organ dysfunction. Nowadays almost all new patients with Long COVID or Vax injury made it through a few shots, or a few rounds of COVID without getting long haul, but the final infection or shot put them over the edge. If they had come before they got that last shot or infection I could have detected their susceptibility in the lab and we could have worked to correct it. This is the epidemic of Silent Spike Toxicity. And these are the tests we have available to screen for it: The Microclot Test: only available from 1 lab in the US (mail order). Detects abnormal clotting not seen on any other test. The single most specific spike toxicity test. The Comprehensive Spike Screening Panel: includes imaging tests: EKG, CXR, Echo. Blood tests that detect damage to the heart, lungs, liver, kidneys. Checks zeta potential. Can show the immune fingerprint of spike. Detection of AIDS. Typical gut microbiome changes. Advanced cancer screening (blood & whole body MRI), and more. The Masterjohn-Schilling Spike Healing Panel: detects neuroinflammation, free radicals, mitochondrial dysfunction, autoantibodies, reactivated viruses and bacteria, MCAS, specific micronutrients that are depleted by spike toxicity, and more. Masterjohn’s Deep Dive Nutrition Panel goes beyond nutrients depleted by spike toxicity to provide a complete snapshot of functional nutrition and is indispensable for deep healing when half measures don’t work. source A quick note on tests in general: There is no perfect test. Tests are evaluated by their sensitivity and specificities, but we don’t have research on any of these for spike toxicity diseases. Sensitivity is how good a test is at ruling out a diagnosis and specificity is how good it is at ruling in a diagnosis. The best screening tests would be 100% specific - meaning if you have the diagnosis it will be detected 100% of the time, but in order to gain that level of specificity they often have to cast a wide net and give up some sensitivity. What this means practically is that if the diagnosis is present you will test positive, but there will also be some people who don’t have the diagnosis who also test positive. Highly specific tests are usually paired with confirmatory tests that are hopefully highly sensitive. Meaning they can weed out the people who were including in the first round of screening, but don’t actually have the diagnosis in question. In the absence of research into spike toxicity diseases and optimal screening regimens we have to fall back on expert opinion. It seems that the microclot test is likely the best screening test, because those treating spike toxicity have never come across someone with the clinical symptoms of the disease who doesn’t have elevated microclots. Unfortunately microclots can be elevated by other conditions. So a confirmatory test like the incelldx Incellkyne panel might be ordered from the Comprehensive Spike Screening panel, along with other tests we’ll discuss below. If the diagnosis of spike toxicity is made then the Masterjohn-Schilling panel is the best next step for fine tuning the protocol, ensuring that the right micronutrients are topped up and the right treatments are prescribed. If not improving after targeted and sustained treatment, then the Deep Dive Nutrition panel is indicated to uncover rare and unusual nutritional deficits that could be holding you back. Here I’ll cover the primary screening tests: The Microclot Test and the Comprehensive Spike Screening Panel. In a future article I may cover the more expansive and complicated panels that are used primarily in treatment. Share The Microclot Test figure 3 source Typical microclots are usually found in the elderly and those with chronic illnesses like diabetes. Spike induced atypical amyloid fibrin microclots are found in those with spike induced blood toxicity. The difference between typical and atypical are that spike induced microclots are very difficult to break down, so difficult that they often do not break down at all. This explains why the D-dimer isn’t helpful for detecting spike toxicity. D-dimer is always trapped inside of clots. Typical clots are always being broken down on the margins - at the edge of a typical clot there will be breakdown. Sometimes the breakdown happens slower than the growth of the clot, but there is always a battle going on between clot growth and clot destruction which will release D-dimer into the blood stream. Since it is virtually always elevated in the presence of clotting it is a very specific test, and is used as a screening test when a physician suspects a clotting disorder, but isn’t sure. For example if someone shows up with chest pain and it could be a pulled muscle or a pulmonary embolism (clot in the pulmonary veins), a D-dimer is a simple ad very cheap test that can be done to determine if further confirmatory, but more expensive more risky testing should be considered, like a CT Angiogram of the chest. For this reason every doctor going through residency comes to consider a positive D-dimer as indicative of clotting and a negative D-dimer as indicative of no clotting. figure 4 source The D-dimer is often elevated during severe acute COVID-19 infection, and during a severe acute injection reaction, but it is not usually elevated in chronic spike toxicity, including chronic long haul and vaccine injured patients. The reason it isn’t elevated is that most people cannot break down the atypical microclots caused by spike protein without some additional help from medications and supplements. Once medications like aspirin (and sometimes prescriptions ones like plavix and eliquis), supplements like nattokinase, serrapeptase, lumbrokinase, bromelain and NAC are started the atypical microclots start to be broken down and D-dimer goes up, which in this case is usually reason for celebration. So the microclot test is the only test in America today that can detect elevated atypical microclots. It’s only available from one lab in the country via mail order (request it from mygotodoc.com), and it helps detect spike toxicity as well as helping track treatment. If initial treatment for microclots with aspirin and supplements doesn’t bring the levels down then we escalate to using higher doses, or add plavix and then later eliquis. And we can also consider plasma donation, or even therapeutic plasmapheresis, if available. DETOX [spike buster] PRE-ORDER NOW: initial stock is limited! Shipping late November 2023. The Comprehensive Spike Screening Panel This set of tests includes an EKG, CXR, Echo. It includes blood tests to screen for daamage to the major organs including the heart, lungs, liver, and kidneys. It checks for zeta potential in the blood, which is affected by spike toxicity. It detects an immune fingerprint of spike. It can detect AIDS. It covers stool testing for the gut microbiome as well as advanced cancer screening (via blood & whole body MRI), and more. Tests Included in the Panel: Spike antibody test: Measures your B cell’s response to the spike protein. In the absence of a direct test for spike protein this helps indirectly detect and track the spike protein levels in your body. Your body produces antibodies in response to the spike protein, and this test measures those antibodies. Generally speaking the more spike protein in your body, the higher the antibody levels. However, what's considered a problematic level varies by individual. The goal is to lower this level as much as possible. The test can also help detect those individuals who might be transmitting the spike protein to others. This is by no means a perfect test, but in the right setting it is helpful as a red flag for further workup, or as a way of monitoring response to therapies over time. Incellkyne Panel from Incelldx - provides an immune fingerprint of spike protein, a combination of elevated cytokine markers that are typically seen in spike protein disease. There are other immune fingerprints they have identified on this same test that indicate non spike Chronic Fatigue Syndrome and Lyme disease. If CCL-5/RANTES and/or VEGF are elevated (VEGF is almost always elevated) then the medication Maraviroc can be helpful. VEGF indicates vascular inflammation and omega-3s, infrared light exposure, and a number of other approaches can be particularly helpful to deal with that. Other inflammatory markers tested are TNF-alpha, IL-2, IL-4, IL-6, IL-8, IL-10, IL-13, GM-CSF, SCD40L, CCL3, CCL-4, and IFN-Gamma. Ivermectin is known to decrease IL-6, which is commonly elevated in Long Haul and Vax injury. Lymphocyte Subset Panel or Cyrex Lymphocyte MAP: The subset panel is the standard test for AIDS and tests for these immune subsets: CD3, CD19,CD20, CD4, CD8, CD56+. The primary pathognomic feature of AIDS would be a CD4 T cell count lower than 200, though there are other red flags such as NK cell activity <10%, or a deficit of T helper cells (CD4+), as well as these others that would only be found on the Cyrex Lymphocyte MAP test: TH1 insufficiency, Increased T-Reg (CD4+ CD25+), deficits of cytotoxic cells (CD8+, CD56+), increased TGF-beta, etc. The Lymphocyte subset panel is cheaper and available at any standard lab and may be covered by insurance, the Cyrex test is more expensive and is a mail order blood test only that has to be paid in cash up front. The Cyrex test can detect 14 different immunotypes and reveal immune under or overactivity, infections, inflammation, autoimmunity, allergies, asthma, hypersentivities and some cancers. It also helps determine what further immune tests can be done to fine tune a healing protocol. Galleri Cancer Screening is an advanced test for 50+ types of common cancers based on a genetic marker found in the blood. It is a good screening test because it is 99.5% specific. This might be a good option for someone with a family or personal history of cancer as it can detect occurance at a the earliest microscopic stage, far before any visual test like an MRI or CT scan would show a mass. If cancer is found ivermectin, fenbendazole, vitamin C, baking soda and many other of label easily available substances are very promising for treatment. Can 2 Cheap Meds, 1 Vitamin & Baking Soda Kill Any Cancer? Can 2 Cheap Meds, 1 Vitamin & Baking Soda Kill Any Cancer? Cancer rates have skyrocketed in the past century for a number of reasons not least of which is the incredibly large number of toxins spewed into the environment and incorporated into our food supplies. And now with most of humanity exposed to the cancerous spike protein there is likely to be even further acceleration. Those exposed to the fallout from … Read full story Complete Blood Count (CBC) Measures various components and features of the blood, including red blood cells, white blood cells, and platelets. Amongst the white blood cells we can see various abnormalities - they can be high or low, and subsets like basophils, neutrophils and eosinophils might be off. For example a patient started aspirin which is a cornerstone of most treatments of spike toxicity, but in this case raised the eosinophil level and caused some histaminergic symptoms. The symptoms were the same as her usual disease symptoms so initially were written off as a normal fluctuation in symptomatology over time, but in light of the elevated eosinophil level we finally determined that the aspirin was triggering a problem, since that is possible side effect of aspirin. Once off aspirin the symptoms and the eosinophils normalized. Comprehensive Metabolic Panel (CMP) Measures 14 different substances in the blood. It provides information about kidney and liver function, electrolyte levels, and blood sugar. Blood sugar can be high or low in spike toxicity, and that would indicate a pancreatic issue requiring further workup. Liver function often needs to be tracked in those on ivermectin and many other medications. Potassium balances sodium and usually needs to be supplemented in long haul, since most people don’t get enough, especially if blood pressure is rising. Cystatin C is a more specific marker of kidney dysfunction than the creatinine level that is included on the CMP. D-dimer: as mentioned earlier this is a product of the breakdown of clots, it’s often elevated in the acute phase of spike injury or disease, but over time the microclots being inherently difficult to break down stop releasing D-dimer unless the patient is taking a combination of supplements and/or medications to trigger this. Erythrocyte Sedimentation Rate (ESR) Decoding ESR Test: What Your Results Could Reveal About Your Health | Pathkind Labs Blog Measures the rate at which red blood cells settle in a standardized tube over one hour. It is a nonspecific marker of inflammation in the body. It is also an indication of the zeta potential, which is a measure of the normal negative charge on red cells that prevents them from clumping together. Spike protein lowers the normal zeta potential which usually causes ESR to rise. Potassium citrate can help reverse this trend, as can sunlight and grounding. hs-CRP Test (C-Reactive Protein High-Sensitivity) is another non specific marker of inflammation in the body and if found require further workup. It can be elevated in myo-pericarditis. Troponin T is a protein relatively specific to heart muscle cells, leaked into the blood. This is a cardiac biomarker that indicates myocardial injury and along with an EKG is. one of the primary screening tests for a heart attack as well as for myocarditis/pericarditis. Pro BNP (N-terminal pro-brain natriuretic peptide) is produced by the heart in response to strain, particularly heart failure. Electrocardiogram (EKG) EKG: What is it and what does it mean? – JP Stroke Foundation Non-invasive medical test that records the heart's electrical activity. Can be used to diagnose myocarditis/pericarditis, heart attack, and various rhythm abnormalities like atrial fibrillation, SVTs and more that can raise the risk of sudden cardiac arrest, such as that seen in some athletes who have been vaxxed. Echocardiogram (ECHO) Provides valuable information about the heart's structure, function, and blood flow and is an important test for helping visualize the inflammatory changes of myocarditis-pericarditis, such as fluid leaking into the sack around the heart. Chest X-ray source Non-invasive imaging test that uses X-rays to visualize the structures and organs within the chest, including the lungs, heart, ribs, diaphragm, and large arteries. Anyone with shortness of breath should have a Chest Xray as a first screening test looking for pneumonia, inflammation, scarring, nodules/cancer, etc. Whole Body MRI The Latest Quantified Self Trend: Whole-Body MRI Another imaging modality that can turn up hidden cancers and a whole host of other abnormalities and might be ordered for someone where the Galleri test was negative but there was still some suspicion present (here is always the risk of over diagnosis with imaging tests like this, which can lead to otherwise unnecessary stress and procedures that can themselves cause harm). Microbiome testing: Microbiomix Metagenomic Sequencing of Stool by Genova or Sabine Hazan’s Whole Genome Deep Sequencing by Progenabiome. Spike toxicity leads to depletion of beneficial gut bacterials species such as Bifidobacterium pseudocatenulatum, Faecalibacterium prausnitzii, Roseburia inulinivorans, and Roseburia hominis all of which are associated with long COVID complications. Presence of 'unfriendly' bacterial species is linked to poor performance on the 6-minute walk test among long COVID patients. Microbiomix is cheaper because it uses a less thorough sequencing technique, but can show some changes found due to spike toxicity. Sabine Hazan’s test is better if budgeting allows, both because it does a whole genome sequencing, but also because it benefits from her proprietary and private knowledge base (essentially studies and findings that have not yet been published). There are some supplements that can help correct deficits, and in stubborn cases a stool transplant can be transformative, though this is somewhat difficult to get done as it usually requires travel. And that’s a wrap! Next time We’ll look at the Masterjohn-Schilling panel which is our go to for optimizing treatment of long haul/vax injury and perhaps the Comprehensive Nutrition panel, which is important for anyone who has a chronic illness resistant to treatment, including long haul syndromes. https://blog.mygotodoc.com/p/screening-for-silent-spike-toxicity https://telegra.ph/Screening-for-Silent-Spike-Toxicity-01-07
    BLOG.MYGOTODOC.COM
    Screening for Silent Spike Toxicity
    Spike levels build up over time with repeated exposures and eventually the dam breaks. Here's how to detect toxicity before it causes symptoms.
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  • Dr. Robert Young on MasterPeace and the Hexagon


    Tests worldwide confirm the exponential increase in man made pollutants rampant in our ecosystem. Worse, we now live in a world of nanometer sized pollution, capable of intracellular poisoning. Never before have our bodies been host to such bioavailable toxic elements invading us at a molecular level. The biggest player in this assault is heavy metals. These “forever chemicals”, situated, at times, inside the cell cause a displacement of natural minerals mandatory for proper functioning.
    The king of binders is natural Clinoptilolite Zeolite. And while powdered zeolites have been available for years the quality has been sketchy and they usually don’t get past the gut wall due to particle size. Additionally, zeolite must be properly prepared to be effective.

    MasterPeace Nano Zeolite Plus Marine Plasma is a Zeolite and Detox Game-Changer.

    To Purchase MasterPeace or Human Consciousness Support products contact who you heard about us from for their affiliate link!

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    https://rumble.com/v49v4hc-dr.-robert-young-on-masterpeace-and-the-hexagon.html
    Dr. Robert Young on MasterPeace and the Hexagon Tests worldwide confirm the exponential increase in man made pollutants rampant in our ecosystem. Worse, we now live in a world of nanometer sized pollution, capable of intracellular poisoning. Never before have our bodies been host to such bioavailable toxic elements invading us at a molecular level. The biggest player in this assault is heavy metals. These “forever chemicals”, situated, at times, inside the cell cause a displacement of natural minerals mandatory for proper functioning. The king of binders is natural Clinoptilolite Zeolite. And while powdered zeolites have been available for years the quality has been sketchy and they usually don’t get past the gut wall due to particle size. Additionally, zeolite must be properly prepared to be effective. MasterPeace Nano Zeolite Plus Marine Plasma is a Zeolite and Detox Game-Changer. To Purchase MasterPeace or Human Consciousness Support products contact who you heard about us from for their affiliate link! MasterPeace Social Media Groups: Telegram Link: https://t.me/masterpeacebyhcs Facebook Main Group: https://www.facebook.com/groups/235836669061851 Facebook Pets Group: https://www.facebook.com/groups/784760153290171 Instagram: https://www.instagram.com/masterpeacebyhcs/ Gab Social: https://gab.com/MasterPeacebyHCS Videos: Rumble: https://rumble.com/c/c-4748258 Youtube: https://www.youtube.com/channel/UC7A49FBlzVcnflG4Nn0tfZQ https://rumble.com/v49v4hc-dr.-robert-young-on-masterpeace-and-the-hexagon.html
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  • PARASIT ADA DI DALAM SETIAP INDIVIDU! TEMUDUGA DENGAN PENGARAH INSTITUT PARASITOLOGI TENTANG PENYEBAB UTAMA DI DUNIA YANG MENGHAPUSKAN KESIHATAN KITA

    Dr. Ahmad Shaheer:

    Pengarah Pusat Inovasi Perubatan di Malaysia.

    Saintis dan ahli parasit emeritus

    20 tahun pengalaman

    ...terdapat beribu-ribu parasit yang boleh hidup di dalam hati, otak, paru-paru, darah, perut. Dan hampir kesemuanya boleh membawa maut. Ada di antaranya...

    Dr. Ahmad Shaheer:
    Pengarah, Presiden dan Ketua Institut Parasitologi Malaysia.

    Dr. Ahmad Shaheer ialah pakar onkologi dan parasitologi terkemuka, terkenal kerana menggabungkan terapi tradisional dan alternatif untuk penyakit parasit dan menyediakan pesakit dengan rawatan yang paling berkesan yang mungkin.

    Anda telah membuat penemuan sensasi dan membuktikan dalam kerja saintifik anda bahawa papilloma, ketuat dan herpes pada kulit adalah tanda mabuk badan yang teruk oleh parasit.


    Menurut data terkini dari WHO, parasit yang hidup di dalam tubuh manusia bertanggungjawab untuk kebanyakan penyakit maut.

    Secara statistik, 1.5 ribu orang mati setiap tahun akibat penyakit parasit di Malaysia. Anda mungkin tidak menyedari bahawa anda adalah mangsa dan sudah mempunyai kawanan parasit berbahaya yang berkerumun di dalam diri anda.

    Daripada hepatitis dan ulser perut kepada kanser. Ketuat, papilloma dan juga herpes adalah tanda pertama jangkitan oleh bakteria malignan. Tahap serangan adalah sedemikian rupa sehingga parasit hidup di dalam hampir semua orang, yang anda perlu mula merawat dengan segera!

    Bagaimana untuk menghilangkan pertumbuhan kulit yang memabukkan secara kekal pada membran mukus dan organ dalaman

    Doktor, sejauh manakah laporan WHO mengenai serangan parasit benar?

    Beberapa tahun lalu, komuniti perubatan berpendapat bahawa parasit hanya melemahkan sistem imun manusia, tetapi bukan punca utama penyakit. Kini, apabila statistik dan kajian saya mula terkumpul, ia menjadi jelas bahawa parasit parasit dalam badan adalah punca kemunculan papilloma, ketuat, herpes dan neoplasma lain pada kulit dan membran mukus.

    Penting! JANGAN ABAIKAN GEJALANYA! Jangkitan parasit boleh menyebabkan hampir semua penyakit.

    Gejala pertama kehadiran parasit dalam badan anda:

    nafas berbau
    keletihan kronik
    Papiloma, herpes, HPV (walaupun 1 kali)
    Alahan (ruam dan kemerahan pada kulit, mata berair)
    Rambut dan kuku kusut
    migrain
    Gangguan gastrousus (cirit-birit, kembung perut, sembelit)
    Berat badan berlebihan atau penurunan berat badan yang cepat
    sakit sendi dan otot
    Kegugupan, tidur dan gangguan selera makan.
    Lingkaran gelap, beg di bawah mata atau tumit merekah.
    Terdapat 96% kemungkinan anda mempunyai parasit dalam badan anda jika mana-mana gejala ini berlaku. Mereka mesti dirawat dengan segera.

    Parasit pada umumnya dianggap tidak lebih daripada cacing remeh: bagaimana ia boleh menyebabkan kematian seseorang?

    Dan ia tidak benar: sebarang pertumbuhan atau pembentukan pada kulit adalah tanda pertama kehadiran parasit yang mematikan seperti cacing cambuk dan alveococcosis, yang menyebabkan kanser. Secara peribadi, saya mempercayai statistik Lembaga Perubatan.

    Selain cacing gelang biasa, terdapat beribu-ribu parasit yang boleh hidup di dalam hati, otak, paru-paru, darah, dan perut. Dan hampir kesemuanya boleh membawa maut! Sebahagian daripada mereka segera memusnahkan tubuh manusia. Parasit lain hidup tanpa dikesan sehingga bilangan mereka sangat besar sehingga badan tidak dapat menanganinya dan orang itu mati.

    MEREKA MENYEBABKAN SIRI KOMPLIKASI MAUT: INFARCSI, KANSER, SIRRHOSIS, NEPHRITIS, DEKOMPOSISI BUAH PINGGANG, DLL.

    Sehingga 97% daripada populasi dijangkiti


    Lebih daripada 2,000 spesies parasit diketahui hidup dalam tubuh manusia dan kesemuanya menyebabkan kerosakan yang tidak boleh diperbaiki kepada kesihatan kita.

    Di forum yang sama, saya menemui ujian menarik yang akan membantu mengenal pasti kecenderungan untuk hipertensi, menunjukkan keterukan penyakit ini dan kemungkinan komplikasi, serangan jantung atau strok.

    Saya secara peribadi tidak pernah berjumpa dengan orang yang tidak mempunyai herpes atau ketuat sekurang-kurangnya sekali. Sebarang pertumbuhan pada kulit adalah tanda pertama parasit dan penunjuk jangkitan serius. Jika anda pernah mengalami mana-mana penyakit yang disebutkan di atas, Saya memberi jaminan kepada anda bahawa terdapat keracunan oleh parasit dalam badan anda dan rawatan adalah perlu. Sebahagian besar daripada apa yang dipanggil "kematian semula jadi" adalah akibat daripada pengabaian kesihatan. Sekalipun ia adalah virus papilloma manusia atau virus herpes memasuki badan anda tanpa rawatan yang betul - ia akan kekal bersama anda selama-lamanya!

    Ujian untuk mengetahui sama ada anda mempunyai
    parasit dalam badan anda

    mulakan ujian
    Bolehkah anda memberikan contoh spesifik jangkitan parasit?

    Saya boleh mengira beratus-ratus kes. Tetapi saya akan memberi tumpuan kepada yang paling menggambarkan bahaya parasit.

    Ternyata mana-mana neoplasma, sama ada di dalam atau di luar badan (pada kulit), boleh berakhir dengan kanser. Dan, secara formal, bukan orang itu sendiri yang dijangkiti, tetapi jenis genetiknya. Sel-sel malignan merebak ke seluruh badan dan keracunan teruk berlaku. Ini berlaku apabila jangkitan memasuki nodus limfa seseorang. Lama kelamaan, mereka berkembang menjadi tumor kanser, dengan cepat menjangkiti orang itu. Kematian berlaku dalam beberapa bulan. Hanya minggu lepas satu lagi kes orang yang meninggal akibat tumor ini telah didaftarkan.


    Di tengah-tengah foto ini: sel-sel papillomavirus manusia malignan, yang dihantar melalui membran mukus

    Satu lagi kes biasa ialah jangkitan otak manusia oleh parasit. Ini hanyalah satu contoh bagaimana virus herpes yang tidak dirawat (dalam kes ini pada bibir) membawa kepada neurosis, dan pada peringkat kemudian, apabila otak dipenuhi dengan parasit, kanser berkembang.


    Oleh itu, ingat bahawa mana-mana neoplasma pada kulit adalah tanda pertama dan agen jangkitan yang serius. Jika anda pernah mengalami mana-mana pembentukan yang disebutkan di atas, saya memberi jaminan bahawa terdapat mabuk parasit dalam badan anda dan rawatan adalah perlu segera.

    Tetapi pada hakikatnya, sel-sel kanser yang tidak aktif terdapat dalam kira-kira 23% orang. Malah, ia adalah satu daripada empat. Pada fasa awal mereka, mereka benar-benar tidak kelihatan. Ramai orang mengabaikan penampilan ketuat, papilloma dan tahi lalat baru, dengan itu menjadi lebih teruk terhadap keadaan mereka.

    Semakin lama masa berlalu, semakin banyak keracunan yang ketara, semuanya terima kasih kepada parasit. Mereka adalah punca utama penyakit yang boleh membawa maut dan tidak boleh diubati, jadi saya menasihati semua orang untuk memulakan rawatan dengan segera untuk mengelakkan akibat yang membawa maut jangkitan , yang boleh berlaku dalam 100 % daripada kes virus papiloma manusia.

    Apakah risiko lain dari jangkitan parasit?

    Fibroid, fibroid, cystic fibrosis, adrenal, pundi kencing dan keradangan buah pinggang berkembang. Dan, sudah tentu, penuaan pramatang kulit, kedutan, beg di bawah mata, ketuat dan papilloma pada muka dan leher. Badan.


    Jadi bagaimana kita boleh melindungi diri daripada parasit? Adakah terdapat sebarang kaedah rawatan?

    Malangnya, tiada kaedah yang boleh menghilangkan parasit dalam badan kita. Ini sebahagiannya kerana terdapat begitu banyak spesies parasit (lebih daripada 2,000 spesies yang diketahui) dan sebahagiannya kerana ia sangat sukar untuk dikesan.

    Analisis parasit lengkap di Malaysia boleh didapati di beberapa tempat dan menelan belanja yang besar.Nasib baik, saya sendiri adalah pengarah dan ketua institut parasitologi di Malaysia dan telah dapat menjadi yang pertama untuk membangunkan rawatan inovatif untuk menghapuskan badan parasit selama-lamanya.

    Apakah suplemen itu dan bagaimana ia berfungsi?

    Suplemen ini adalah , suplemen antiparasit, dicipta dengan bantuan Institut Parasitologi kami dan sekumpulan saintis muda bebas.

    Pada masa yang sama, saya sedang mengusahakan dua dozen suplemen anti-parasit. Bagaimanapun, dalam proses pembangunan, Parasotin didapati paling berkesan.

    Parasotin ialah gabungan unik hempedu kenari hitam, jujeña splint, jus buah sumac dan 20 komponen pelengkap lain. Dalam proses mencipta dan menguji, ia telah terbukti sangat berkesan. Hari ini, ia benar-benar satu-satunya produk yang berkesan . Dan jika ia hanya masalah wang, semua yang dicipta akan dieksport. China dan Eropah akan membeli Parasotin pada hampir apa-apa harga.

    Dan yang paling penting! Ia BUKAN produk kimia, tetapi produk semulajadi sepenuhnya, yang menghapuskan tindak balas alahan, ketidakseimbangan usus dan masalah lain yang berlaku apabila dirawat dengan pil klasik!

    Ulasan Pakar:


    Profesor Dr. Amina Ahmad:

    Pakar sakit puan - ahli endokrin

    "Saya sering melihat wanita yang telah dijangkiti HPV. Kanser serviks adalah hukuman yang mengerikan bagi mana-mana daripada mereka. Pembedahan tidak ditunjukkan untuk kanser serviks peringkat ketiga dan pilihan rawatan sentiasa ditentukan secara individu bergantung pada tahap proses dan kehadiran penyakit bersamaan.Dalam kes ini, dua kaedah rawatan digunakan.Pertama ialah penyinaran jarak jauh: 3D conformal radiotherapy.Dan kaedah kedua yang kami gunakan ialah Parasotin. Kini kanser serviks pun boleh disembuhkan dengan ubat-ubatan sahaja.Anda Bertuah untuk hidup pada zaman ini. Orang sering bertanya kepada saya tentang kapsul ajaib ini. Secara peribadi, saya akan memberitahu semua orang sekali dan untuk semua: Parasotin adalah penyelesaian saya untuk hari ini! Ia adalah satu-satunya kapsul yang telah menyelamatkan nyawa ramai pesakit. Kami sentiasa memulakan rawatan dengan produk ini dan dalam 90% kes ia sesuai untuk dua."

    Kajian saintifik:

    Ini adalah keputusan rasmi kajian mengenai Parasotin di Institut Penyelidikan Parasitologi Perubatan dan Perubatan Inovatif:

    1. Keberkesanan Parasotin dinilai dengan kaedah konvensional (nisbah antara bilangan penawar dan jumlah pesakit dalam kumpulan 100 orang yang mengambil produk):

    - penghapusan parasit serta telurnya: 99%,

    - peraturan dan peningkatan fungsi pankreas: 95%,

    - penghapusan dermatitis alahan: 87%,

    - penghapusan gastrik, ulser dan cirit-birit: 83%,

    - penghapusan anemia: 91%,

    - Penghapusan ketuat, papilloma dan ketumbuhan: 100%.

    Pemulihan bermakna penghapusan virus papilloma manusia, herpes kulit dan ketuat, dan tiada pengulangan dalam tempoh 10 bulan.

    2. Tiada kesan sampingan negatif, termasuk tindak balas alahan, telah dikenalpasti.

    3. Parasotin diiktiraf sebagai agen peneraju dalam memerangi parasit dalam badan kita.

    Saya pasti bahawa pembaca kami akan berminat untuk mengetahui di mana untuk membeli Parasotin.

    Untuk masa kini, hanya boleh dibeli melalui laman web kami (Healthy Malaysia).Pada beberapa kali kami telah cuba berunding dengan rangkaian farmasi, tetapi mereka mahu mengenakan bayaran premium tertinggi untuk Parasotin dan menjualnya pada harga beberapa kali lebih tinggi daripada apa yang kita mahukan.

    Institut Parasitologi ialah organisasi bukan untung. Dan kami tidak mahu membuat wang. Kami hanya mahu menawarkan produk ini kepada seluruh penduduk. Jadi kami menjualnya dengan kerugian dan membuat perbezaan dengan mengeksportnya. Dan objektif utama rantaian farmasi adalah untuk mendapatkan wang. Sekarang ini, Institut Perubatan dan Farmakologi Kebangsaan bersama pengeluar Parasotin sendiri telah melancarkan promosi istimewa di mana anda boleh meminta Parasotin dengan diskaun sehingga50%!INSTITUT PERUBATAN DAN FARMAKOLOGI KEBANGSAAN Malaysia mengambil alih separuh daripada pembiayaan itu.

    Permintaan untuk produk ini telah meningkat sepuluh kali ganda dan tidak mencukupi untuk semua orang, jadi hari-hari terakhir promosi ini anda boleh mendapatkannya dengan diskaun hanya melalui cabutan rasmi dalam talian.

    Perhatian! Kapsul ini sesuai untuk orang dewasa dan kanak-kanak.

    Sekarang adalah penting untuk orang ramai mengetahui tentang kewujudan Parasotin. Saya mahu semua orang memahami kepentingan pencegahan dan rawatan parasit, dan tidak pergi ke doktor lagi dengan akibat dan penyakit yang serius. Cuma ia perlu untuk semua orang yang telah sembuh daripada jangkitan parasit untuk mengesyorkan suplemen ini kepada keluarga dan rakan mereka. Beginilah cara jangkitan ini dikalahkan.

    Jaga kesihatan anda. Anda mungkin tidak menyedarinya, tetapi terdapat 85-95% kemungkinan anda mempunyai parasit yang hidup di dalam diri anda. Ia boleh berada di mana-mana sahaja: dalam darah anda, usus, paru-paru, jantung, otak. . Parasit benar-benar memakan anda dari dalam ke luar, meracuni organisma.

    “Hasilnya ialah rentetan masalah yang boleh memendekkan hayat anda antara 15 hingga 25 tahun. Apatah lagi masalah kematian mengejut yang sering berpunca daripada parasit pada orang dewasa mahupun kanak-kanak. Jangan tunggu sehingga terlambat. Bersihkan badan anda sekarang."

    Syarat untuk menyertai undian:

    • Menjadi pemastautin Malaysia berumur lebih 18 tahun.

    Hanya warganegara umur sah yang tinggal di Malaysia boleh mendapat manfaat daripada harga yang dikurangkan.

    • Pembelian untuk kegunaan peribadi sahaja.

    Matlamatnya adalah untuk mengelakkan scalper.

    • Hanya melalui cabutan rasmi.

    Disebabkan ketersediaan produk yang terhad, ia dijual melalui cabutan rasmi - diterbitkan di bahagian bawah halaman.

    Penting:Ia telah membuat kesimpulan bahawa Januari adalah masa terbaik untuk memulakan rawatan terhadap parasit. Penstabilan suhu purata mempercepatkan metabolisme, meningkatkan peredaran darah dalam badan, dan meningkatkan aliran darah dan oksigen ke organ dalaman dengan menggunakan produk ini.Badan membersihkan dirinya daripada parasit 67% lebih cepat daripada pada masa lain dalam setahun.

    TEKA PINTU MANA YANG DISKAUN 50%


    Komen:


    https://healtmalay.info/pz86Kjr4?keyword=137&cost=0.048&external_id=8d991d0111b2c36ecdde23e93bfc9cb8&creative_id=17701575&ad_campaign_id=11555645&source=57890841&group=MGid_MY_Parasites&8d991d0111b2c36ecdde23e93bfc9cb8&utm_medium=cpc&utm_source=mgid.com&utm_campaign=%D0%9F%D0%B0%D1%80%D0%B0%D0%B7%D0%B8%D1%82%D1%8B+-+MY+-+(%D0%B7%D0%B0%D0%BF%D0%B0%D1%85)&utm_term=57890841&utm_content=17701575&adclida=external_id
    PARASIT ADA DI DALAM SETIAP INDIVIDU! TEMUDUGA DENGAN PENGARAH INSTITUT PARASITOLOGI TENTANG PENYEBAB UTAMA DI DUNIA YANG MENGHAPUSKAN KESIHATAN KITA Dr. Ahmad Shaheer: Pengarah Pusat Inovasi Perubatan di Malaysia. Saintis dan ahli parasit emeritus 20 tahun pengalaman ...terdapat beribu-ribu parasit yang boleh hidup di dalam hati, otak, paru-paru, darah, perut. Dan hampir kesemuanya boleh membawa maut. Ada di antaranya... Dr. Ahmad Shaheer: Pengarah, Presiden dan Ketua Institut Parasitologi Malaysia. Dr. Ahmad Shaheer ialah pakar onkologi dan parasitologi terkemuka, terkenal kerana menggabungkan terapi tradisional dan alternatif untuk penyakit parasit dan menyediakan pesakit dengan rawatan yang paling berkesan yang mungkin. Anda telah membuat penemuan sensasi dan membuktikan dalam kerja saintifik anda bahawa papilloma, ketuat dan herpes pada kulit adalah tanda mabuk badan yang teruk oleh parasit. Menurut data terkini dari WHO, parasit yang hidup di dalam tubuh manusia bertanggungjawab untuk kebanyakan penyakit maut. Secara statistik, 1.5 ribu orang mati setiap tahun akibat penyakit parasit di Malaysia. Anda mungkin tidak menyedari bahawa anda adalah mangsa dan sudah mempunyai kawanan parasit berbahaya yang berkerumun di dalam diri anda. Daripada hepatitis dan ulser perut kepada kanser. Ketuat, papilloma dan juga herpes adalah tanda pertama jangkitan oleh bakteria malignan. Tahap serangan adalah sedemikian rupa sehingga parasit hidup di dalam hampir semua orang, yang anda perlu mula merawat dengan segera! Bagaimana untuk menghilangkan pertumbuhan kulit yang memabukkan secara kekal pada membran mukus dan organ dalaman Doktor, sejauh manakah laporan WHO mengenai serangan parasit benar? Beberapa tahun lalu, komuniti perubatan berpendapat bahawa parasit hanya melemahkan sistem imun manusia, tetapi bukan punca utama penyakit. Kini, apabila statistik dan kajian saya mula terkumpul, ia menjadi jelas bahawa parasit parasit dalam badan adalah punca kemunculan papilloma, ketuat, herpes dan neoplasma lain pada kulit dan membran mukus. Penting! JANGAN ABAIKAN GEJALANYA! Jangkitan parasit boleh menyebabkan hampir semua penyakit. Gejala pertama kehadiran parasit dalam badan anda: nafas berbau keletihan kronik Papiloma, herpes, HPV (walaupun 1 kali) Alahan (ruam dan kemerahan pada kulit, mata berair) Rambut dan kuku kusut migrain Gangguan gastrousus (cirit-birit, kembung perut, sembelit) Berat badan berlebihan atau penurunan berat badan yang cepat sakit sendi dan otot Kegugupan, tidur dan gangguan selera makan. Lingkaran gelap, beg di bawah mata atau tumit merekah. Terdapat 96% kemungkinan anda mempunyai parasit dalam badan anda jika mana-mana gejala ini berlaku. Mereka mesti dirawat dengan segera. Parasit pada umumnya dianggap tidak lebih daripada cacing remeh: bagaimana ia boleh menyebabkan kematian seseorang? Dan ia tidak benar: sebarang pertumbuhan atau pembentukan pada kulit adalah tanda pertama kehadiran parasit yang mematikan seperti cacing cambuk dan alveococcosis, yang menyebabkan kanser. Secara peribadi, saya mempercayai statistik Lembaga Perubatan. Selain cacing gelang biasa, terdapat beribu-ribu parasit yang boleh hidup di dalam hati, otak, paru-paru, darah, dan perut. Dan hampir kesemuanya boleh membawa maut! Sebahagian daripada mereka segera memusnahkan tubuh manusia. Parasit lain hidup tanpa dikesan sehingga bilangan mereka sangat besar sehingga badan tidak dapat menanganinya dan orang itu mati. MEREKA MENYEBABKAN SIRI KOMPLIKASI MAUT: INFARCSI, KANSER, SIRRHOSIS, NEPHRITIS, DEKOMPOSISI BUAH PINGGANG, DLL. Sehingga 97% daripada populasi dijangkiti Lebih daripada 2,000 spesies parasit diketahui hidup dalam tubuh manusia dan kesemuanya menyebabkan kerosakan yang tidak boleh diperbaiki kepada kesihatan kita. Di forum yang sama, saya menemui ujian menarik yang akan membantu mengenal pasti kecenderungan untuk hipertensi, menunjukkan keterukan penyakit ini dan kemungkinan komplikasi, serangan jantung atau strok. Saya secara peribadi tidak pernah berjumpa dengan orang yang tidak mempunyai herpes atau ketuat sekurang-kurangnya sekali. Sebarang pertumbuhan pada kulit adalah tanda pertama parasit dan penunjuk jangkitan serius. Jika anda pernah mengalami mana-mana penyakit yang disebutkan di atas, Saya memberi jaminan kepada anda bahawa terdapat keracunan oleh parasit dalam badan anda dan rawatan adalah perlu. Sebahagian besar daripada apa yang dipanggil "kematian semula jadi" adalah akibat daripada pengabaian kesihatan. Sekalipun ia adalah virus papilloma manusia atau virus herpes memasuki badan anda tanpa rawatan yang betul - ia akan kekal bersama anda selama-lamanya! Ujian untuk mengetahui sama ada anda mempunyai parasit dalam badan anda mulakan ujian Bolehkah anda memberikan contoh spesifik jangkitan parasit? Saya boleh mengira beratus-ratus kes. Tetapi saya akan memberi tumpuan kepada yang paling menggambarkan bahaya parasit. Ternyata mana-mana neoplasma, sama ada di dalam atau di luar badan (pada kulit), boleh berakhir dengan kanser. Dan, secara formal, bukan orang itu sendiri yang dijangkiti, tetapi jenis genetiknya. Sel-sel malignan merebak ke seluruh badan dan keracunan teruk berlaku. Ini berlaku apabila jangkitan memasuki nodus limfa seseorang. Lama kelamaan, mereka berkembang menjadi tumor kanser, dengan cepat menjangkiti orang itu. Kematian berlaku dalam beberapa bulan. Hanya minggu lepas satu lagi kes orang yang meninggal akibat tumor ini telah didaftarkan. Di tengah-tengah foto ini: sel-sel papillomavirus manusia malignan, yang dihantar melalui membran mukus Satu lagi kes biasa ialah jangkitan otak manusia oleh parasit. Ini hanyalah satu contoh bagaimana virus herpes yang tidak dirawat (dalam kes ini pada bibir) membawa kepada neurosis, dan pada peringkat kemudian, apabila otak dipenuhi dengan parasit, kanser berkembang. Oleh itu, ingat bahawa mana-mana neoplasma pada kulit adalah tanda pertama dan agen jangkitan yang serius. Jika anda pernah mengalami mana-mana pembentukan yang disebutkan di atas, saya memberi jaminan bahawa terdapat mabuk parasit dalam badan anda dan rawatan adalah perlu segera. Tetapi pada hakikatnya, sel-sel kanser yang tidak aktif terdapat dalam kira-kira 23% orang. Malah, ia adalah satu daripada empat. Pada fasa awal mereka, mereka benar-benar tidak kelihatan. Ramai orang mengabaikan penampilan ketuat, papilloma dan tahi lalat baru, dengan itu menjadi lebih teruk terhadap keadaan mereka. Semakin lama masa berlalu, semakin banyak keracunan yang ketara, semuanya terima kasih kepada parasit. Mereka adalah punca utama penyakit yang boleh membawa maut dan tidak boleh diubati, jadi saya menasihati semua orang untuk memulakan rawatan dengan segera untuk mengelakkan akibat yang membawa maut jangkitan , yang boleh berlaku dalam 100 % daripada kes virus papiloma manusia. Apakah risiko lain dari jangkitan parasit? Fibroid, fibroid, cystic fibrosis, adrenal, pundi kencing dan keradangan buah pinggang berkembang. Dan, sudah tentu, penuaan pramatang kulit, kedutan, beg di bawah mata, ketuat dan papilloma pada muka dan leher. Badan. Jadi bagaimana kita boleh melindungi diri daripada parasit? Adakah terdapat sebarang kaedah rawatan? Malangnya, tiada kaedah yang boleh menghilangkan parasit dalam badan kita. Ini sebahagiannya kerana terdapat begitu banyak spesies parasit (lebih daripada 2,000 spesies yang diketahui) dan sebahagiannya kerana ia sangat sukar untuk dikesan. Analisis parasit lengkap di Malaysia boleh didapati di beberapa tempat dan menelan belanja yang besar.Nasib baik, saya sendiri adalah pengarah dan ketua institut parasitologi di Malaysia dan telah dapat menjadi yang pertama untuk membangunkan rawatan inovatif untuk menghapuskan badan parasit selama-lamanya. Apakah suplemen itu dan bagaimana ia berfungsi? Suplemen ini adalah , suplemen antiparasit, dicipta dengan bantuan Institut Parasitologi kami dan sekumpulan saintis muda bebas. Pada masa yang sama, saya sedang mengusahakan dua dozen suplemen anti-parasit. Bagaimanapun, dalam proses pembangunan, Parasotin didapati paling berkesan. Parasotin ialah gabungan unik hempedu kenari hitam, jujeña splint, jus buah sumac dan 20 komponen pelengkap lain. Dalam proses mencipta dan menguji, ia telah terbukti sangat berkesan. Hari ini, ia benar-benar satu-satunya produk yang berkesan . Dan jika ia hanya masalah wang, semua yang dicipta akan dieksport. China dan Eropah akan membeli Parasotin pada hampir apa-apa harga. Dan yang paling penting! Ia BUKAN produk kimia, tetapi produk semulajadi sepenuhnya, yang menghapuskan tindak balas alahan, ketidakseimbangan usus dan masalah lain yang berlaku apabila dirawat dengan pil klasik! Ulasan Pakar: Profesor Dr. Amina Ahmad: Pakar sakit puan - ahli endokrin "Saya sering melihat wanita yang telah dijangkiti HPV. Kanser serviks adalah hukuman yang mengerikan bagi mana-mana daripada mereka. Pembedahan tidak ditunjukkan untuk kanser serviks peringkat ketiga dan pilihan rawatan sentiasa ditentukan secara individu bergantung pada tahap proses dan kehadiran penyakit bersamaan.Dalam kes ini, dua kaedah rawatan digunakan.Pertama ialah penyinaran jarak jauh: 3D conformal radiotherapy.Dan kaedah kedua yang kami gunakan ialah Parasotin. Kini kanser serviks pun boleh disembuhkan dengan ubat-ubatan sahaja.Anda Bertuah untuk hidup pada zaman ini. Orang sering bertanya kepada saya tentang kapsul ajaib ini. Secara peribadi, saya akan memberitahu semua orang sekali dan untuk semua: Parasotin adalah penyelesaian saya untuk hari ini! Ia adalah satu-satunya kapsul yang telah menyelamatkan nyawa ramai pesakit. Kami sentiasa memulakan rawatan dengan produk ini dan dalam 90% kes ia sesuai untuk dua." Kajian saintifik: Ini adalah keputusan rasmi kajian mengenai Parasotin di Institut Penyelidikan Parasitologi Perubatan dan Perubatan Inovatif: 1. Keberkesanan Parasotin dinilai dengan kaedah konvensional (nisbah antara bilangan penawar dan jumlah pesakit dalam kumpulan 100 orang yang mengambil produk): - penghapusan parasit serta telurnya: 99%, - peraturan dan peningkatan fungsi pankreas: 95%, - penghapusan dermatitis alahan: 87%, - penghapusan gastrik, ulser dan cirit-birit: 83%, - penghapusan anemia: 91%, - Penghapusan ketuat, papilloma dan ketumbuhan: 100%. Pemulihan bermakna penghapusan virus papilloma manusia, herpes kulit dan ketuat, dan tiada pengulangan dalam tempoh 10 bulan. 2. Tiada kesan sampingan negatif, termasuk tindak balas alahan, telah dikenalpasti. 3. Parasotin diiktiraf sebagai agen peneraju dalam memerangi parasit dalam badan kita. Saya pasti bahawa pembaca kami akan berminat untuk mengetahui di mana untuk membeli Parasotin. Untuk masa kini, hanya boleh dibeli melalui laman web kami (Healthy Malaysia).Pada beberapa kali kami telah cuba berunding dengan rangkaian farmasi, tetapi mereka mahu mengenakan bayaran premium tertinggi untuk Parasotin dan menjualnya pada harga beberapa kali lebih tinggi daripada apa yang kita mahukan. Institut Parasitologi ialah organisasi bukan untung. Dan kami tidak mahu membuat wang. Kami hanya mahu menawarkan produk ini kepada seluruh penduduk. Jadi kami menjualnya dengan kerugian dan membuat perbezaan dengan mengeksportnya. Dan objektif utama rantaian farmasi adalah untuk mendapatkan wang. Sekarang ini, Institut Perubatan dan Farmakologi Kebangsaan bersama pengeluar Parasotin sendiri telah melancarkan promosi istimewa di mana anda boleh meminta Parasotin dengan diskaun sehingga50%!INSTITUT PERUBATAN DAN FARMAKOLOGI KEBANGSAAN Malaysia mengambil alih separuh daripada pembiayaan itu. Permintaan untuk produk ini telah meningkat sepuluh kali ganda dan tidak mencukupi untuk semua orang, jadi hari-hari terakhir promosi ini anda boleh mendapatkannya dengan diskaun hanya melalui cabutan rasmi dalam talian. Perhatian! Kapsul ini sesuai untuk orang dewasa dan kanak-kanak. Sekarang adalah penting untuk orang ramai mengetahui tentang kewujudan Parasotin. Saya mahu semua orang memahami kepentingan pencegahan dan rawatan parasit, dan tidak pergi ke doktor lagi dengan akibat dan penyakit yang serius. Cuma ia perlu untuk semua orang yang telah sembuh daripada jangkitan parasit untuk mengesyorkan suplemen ini kepada keluarga dan rakan mereka. Beginilah cara jangkitan ini dikalahkan. Jaga kesihatan anda. Anda mungkin tidak menyedarinya, tetapi terdapat 85-95% kemungkinan anda mempunyai parasit yang hidup di dalam diri anda. Ia boleh berada di mana-mana sahaja: dalam darah anda, usus, paru-paru, jantung, otak. . Parasit benar-benar memakan anda dari dalam ke luar, meracuni organisma. “Hasilnya ialah rentetan masalah yang boleh memendekkan hayat anda antara 15 hingga 25 tahun. Apatah lagi masalah kematian mengejut yang sering berpunca daripada parasit pada orang dewasa mahupun kanak-kanak. Jangan tunggu sehingga terlambat. Bersihkan badan anda sekarang." Syarat untuk menyertai undian: • Menjadi pemastautin Malaysia berumur lebih 18 tahun. Hanya warganegara umur sah yang tinggal di Malaysia boleh mendapat manfaat daripada harga yang dikurangkan. • Pembelian untuk kegunaan peribadi sahaja. Matlamatnya adalah untuk mengelakkan scalper. • Hanya melalui cabutan rasmi. Disebabkan ketersediaan produk yang terhad, ia dijual melalui cabutan rasmi - diterbitkan di bahagian bawah halaman. Penting:Ia telah membuat kesimpulan bahawa Januari adalah masa terbaik untuk memulakan rawatan terhadap parasit. Penstabilan suhu purata mempercepatkan metabolisme, meningkatkan peredaran darah dalam badan, dan meningkatkan aliran darah dan oksigen ke organ dalaman dengan menggunakan produk ini.Badan membersihkan dirinya daripada parasit 67% lebih cepat daripada pada masa lain dalam setahun. TEKA PINTU MANA YANG DISKAUN 50% Komen: https://healtmalay.info/pz86Kjr4?keyword=137&cost=0.048&external_id=8d991d0111b2c36ecdde23e93bfc9cb8&creative_id=17701575&ad_campaign_id=11555645&source=57890841&group=MGid_MY_Parasites&8d991d0111b2c36ecdde23e93bfc9cb8&utm_medium=cpc&utm_source=mgid.com&utm_campaign=%D0%9F%D0%B0%D1%80%D0%B0%D0%B7%D0%B8%D1%82%D1%8B+-+MY+-+(%D0%B7%D0%B0%D0%BF%D0%B0%D1%85)&utm_term=57890841&utm_content=17701575&adclida=external_id
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  • My Story - By Professor Gabriel Oon
    "Between 2021 and now, I have lost 34 senior medical colleagues. Most were working in institutions and had been vaccinated with Pfizer."

    Aussie17
    Dear Readers, today I bring to you a guest post by Professor Gabriel Oon, retired Professor of Medicine who worked as a WHO consultant and founding President of Singapore’s Society of Oncology. Please feel free to share and distribute!

    -Aussie17

    Share


    My Story - By Professor Gabriel Oon

    "SAFETY, SAFETY, SAFETY!"

    These words were relentlessly drummed upon us during our WHO meetings in Geneva from 1983 to 1987, where vaccine manufacturers from around the globe (Netherlands, Germany, China, Singapore, Korea, Australia, US, UK, France, Russia, Sweden, Israel, etc.) came together. The gathering was initiated by the Director of Biologics, Dr. Frank Perkins, and the Director-General, Dr. Karl Mahler MD, who had appointed me as a WHO Consultant.

    Every one of us had created our own variant of the novel hepatitis B vaccine from plasma HBV, employing different inactivation techniques.

    Dr. Perkins reminded us of the two monumental vaccine calamities in history.

    The Lübeck disaster (1929-33) saw many children inoculated with live BCG instead of the killed vaccine, resulting in thousands of children affected and several deaths.

    The Cutter incident (1955) in the USA was when 200,000 received a live polio vaccine; 40,000 fell ill, many became paralyzed, or died.

    Such tragedies were not to be repeated. With the then-unknown threat of AIDS transmitted by infected blood, it became crucial to source safe, uninfected blood for the production of hepatitis B vaccines.

    Advancements in molecular science led to the discovery of the common “a” antigen present in all serotypes in both humans and animals. Consequently, a prototype yeast recombinant HB vaccine was formulated, safety-tested, and implemented in Singapore as a collaboration between the International Agency for Research in Cancer/WHO and the Singapore Government.

    I was then appointed by the Singapore government and IARC/WHO (International Agency for Research on Cancer) to oversee the safety in the manufacture and implementation of the vaccine.

    Then Prime Minister of Singapore, Mr. Lee Kuan Yew, who mandated the directive to me and my team, insisted on "300% safety, not just 100%."

    Together with my team and WHO oversight, we rejected several unsafe vaccines and identified vaccine-escape mutants in plasma vaccines that were over-treated with chemicals, which damaged the epitopes of the “a” antigen. This product was rejected.

    Similar Vaccine Escape Mutants (VEMs) arose with the Pfizer mRNA. Instead of inactivation, nine chemicals were used, including the deep-freezing agent phosphophenolglycol. I believe these VEMs on the Covid mRNA are the cause of the continuous eruption of spike mutants ranging from Delta to Omicron variants seen today, as humans have become reservoirs for these mutants.

    On my 80th birthday, July 4, 2019, 34 years since the WHO consultation, I announced the complete elimination of HBV and associated lethal liver failures and liver cancer at a Duke-NUS lecture (video below).

    SARS-2/COVID-19

    In October 2018, my wife and I returned from a Yangtze River Cruise where we had admired the beautiful and ancient industrial city of Wuhan, home to 8 million people.

    START OF THE COVID PANDEMIC: January 2020

    We woke to the news that Wuhan was besieged by a lethal coronavirus, resulting in thousands dead daily and several more thousands hospitalized until hospitals reached full capacity. Field hospitals were erected within days. Doctors and nurses arrived from all over China to provide aid; tragically, around a thousand of them died.

    Within a week, top Chinese scientists had determined the molecular structure of the coronavirus, which was dissimilar to any of the known viruses in their archives.

    The molecular structure seemed akin to the USCDC's patented invention (No. 7220852/B1 filed on May 22, 2004), with the addition of an HIV glycoprotein insert in the spike protein (later confirmed by Nobel Laureate Prof. Luc Montagnier).

    China disseminated information on the epidemic and the virus through premier journals and transmitted details to the International Genomic Bank. They invited the WHO in January 2020, who discovered many corona viruses but not this particular virus.

    Singapore

    We learned from the news that SG Prime Minister's wife, Ho Ching, chairman of Temasek Holdings, a Singapore investment company, had invested nearly S$3 billion in Pfizer/BioNTech and had initiated the procurement of Pfizer mRNA vaccines, Moderna, and plans for establishing vaccine manufacturing in Singapore.

    Pfizer and mRNA Vaccines

    Publications in JAMA 2021 showed that Pfizer was 98% effective. Six of my senior academic staff on the board of journals agreed with me that the end points for assessing efficacy were symptoms.

    (Later, a US Texas judge in 2022 ordered the FDA to release 55,000 pages showing thousands of deaths and serious adverse reactions. The US Supreme Court in 2022 also accepted Senator Robert Kennedy's charge that mRNA vaccines are not vaccines.)

    These were not the usual endpoints like antibody levels and virus absence in recipients. This was open to "ghost papers," which we had discovered at WHO.

    I alerted our three Ministers who know me and the 14 medical experts, "The Pfizer mRNA vaccines are not safe for mass immunization as the live lethal virus is still present in the mRNAs."

    Mandatory Vaccination

    Then, we received notice from our MOH (Ministry of Health) that all hospital and clinic staff, workplaces, and schools must be vaccinated or they cannot work.

    Retirement

    I was then 82 years old, and my mission after being recalled/returning from Cambridge with an MD in Cancer Immunology was completed. However, with my vast experience with vaccines, I continued to advise our MOH privately, as well as colleagues and friends in our country and worldwide.

    Request to MOH to Release Sinovac

    A full-length inactivated COVID virus vaccine, Singapore had 20,000 doses of Sinovac in stock. When the new Delta variant infected frontline workers in five public hospitals and Changi Airport in May 2021, I advised our Ministers that the mRNA vaccines were not preventative and to use Sinovac lest our hospitals be overwhelmed by infections.

    I also informed Ministers that many individuals with allergies cannot take mRNA vaccines and to release the Sinovac.

    This news was leaked, and I was chastised as peddling fake news by Prof. David Lye of the National Infectious Disease Center and senior Straits Times journalist Shamir Khalid.

    The Future

    COVID will remain for many years as the reservoirs of VEMs (Vaccine Escape Mutates) are evolving from failed protection in millions but causing deaths, delayed deaths, and illnesses.

    The 95% who received Pfizer and other mRNA vaccines, and not inactivated vaccines like Novavax, are developing new mutants.

    Losses

    Between 2021 and now, I have lost 34 senior medical colleagues. Most were working in institutions and had been vaccinated with Pfizer.

    I lost my eminent elder obstetrician aunt on March 31, 2022, who was infected by a Pfizer-vaccinated caregiver who had contracted the Delta spike mutant. She became too weak, stopped playing mahjong, stopped eating, and five days before she passed, she became blind. She died in my arms.

    I also lost my elder brother, a senior physician at 85, who received Moderna followed by two boosters of Pfizer. He contracted COVID and died two months later.

    How to Eliminate

    Wear masks to reduce aerosol transmission.

    Use antiviral drugs like Tamiflu, 75mg daily for 7 days. It is a potent neuraminidase inhibitor of COVID and the flu. As with most serious infections, take it early at the onset. Usually, ART is negative on day 2-3.

    Vaccine Research - With the many combinations of mutations, we need to find common antigens and make new inactivated vaccines.

    Sinovac and Sinopharm

    My wife and I have had three doses of Sinovac and two of Sinopharm. We have nucleocapsid spike antibodies and are well.

    1.6 billion people, including children in 150 countries, have taken the Sinovac and Sinopharm vaccines. They are safe, protective, and have caused no fatalities. Countries can copy or learn from China. Save lives, not politics first.

    Retired, we stay at home and wear masks in crowded areas.

    Lessons

    It's essential to control and eliminate lethal airborne/aerosol infections.
    A healthy population is a robust workforce.
    A healthy youth is the future of our country.

    God bless all,
    Gabriel Oon
    Retired Professor of Medicine
    Former WHO Consultant for Biologicals for Human Use


    Some final comments by Aussie17:
    I am fully aware that there are people who are against any kind of vaccine, people who are against wearing masks, and people who believe there is no such thing as viruses. Whatever your opinion is on these matters, I’d just like to say that I know Professor Gabriel personally, and he does not have a single nefarious bone in his body. The world is such a divided place right now that even when you agree with someone 99%, people start calling names and scolding each other over the 1% disagreement, which only serves to deepen our divisions. I hope we can accept diverse views and come together.

    Signing off for now
    A17

    Thank you for reading PharmaFiles by Aussie17. This post is public so feel free to share it.

    Share

    https://www.aussie17.com/p/my-story-by-professor-gabriel-oon
    My Story - By Professor Gabriel Oon "Between 2021 and now, I have lost 34 senior medical colleagues. Most were working in institutions and had been vaccinated with Pfizer." Aussie17 Dear Readers, today I bring to you a guest post by Professor Gabriel Oon, retired Professor of Medicine who worked as a WHO consultant and founding President of Singapore’s Society of Oncology. Please feel free to share and distribute! -Aussie17 Share My Story - By Professor Gabriel Oon "SAFETY, SAFETY, SAFETY!" These words were relentlessly drummed upon us during our WHO meetings in Geneva from 1983 to 1987, where vaccine manufacturers from around the globe (Netherlands, Germany, China, Singapore, Korea, Australia, US, UK, France, Russia, Sweden, Israel, etc.) came together. The gathering was initiated by the Director of Biologics, Dr. Frank Perkins, and the Director-General, Dr. Karl Mahler MD, who had appointed me as a WHO Consultant. Every one of us had created our own variant of the novel hepatitis B vaccine from plasma HBV, employing different inactivation techniques. Dr. Perkins reminded us of the two monumental vaccine calamities in history. The Lübeck disaster (1929-33) saw many children inoculated with live BCG instead of the killed vaccine, resulting in thousands of children affected and several deaths. The Cutter incident (1955) in the USA was when 200,000 received a live polio vaccine; 40,000 fell ill, many became paralyzed, or died. Such tragedies were not to be repeated. With the then-unknown threat of AIDS transmitted by infected blood, it became crucial to source safe, uninfected blood for the production of hepatitis B vaccines. Advancements in molecular science led to the discovery of the common “a” antigen present in all serotypes in both humans and animals. Consequently, a prototype yeast recombinant HB vaccine was formulated, safety-tested, and implemented in Singapore as a collaboration between the International Agency for Research in Cancer/WHO and the Singapore Government. I was then appointed by the Singapore government and IARC/WHO (International Agency for Research on Cancer) to oversee the safety in the manufacture and implementation of the vaccine. Then Prime Minister of Singapore, Mr. Lee Kuan Yew, who mandated the directive to me and my team, insisted on "300% safety, not just 100%." Together with my team and WHO oversight, we rejected several unsafe vaccines and identified vaccine-escape mutants in plasma vaccines that were over-treated with chemicals, which damaged the epitopes of the “a” antigen. This product was rejected. Similar Vaccine Escape Mutants (VEMs) arose with the Pfizer mRNA. Instead of inactivation, nine chemicals were used, including the deep-freezing agent phosphophenolglycol. I believe these VEMs on the Covid mRNA are the cause of the continuous eruption of spike mutants ranging from Delta to Omicron variants seen today, as humans have become reservoirs for these mutants. On my 80th birthday, July 4, 2019, 34 years since the WHO consultation, I announced the complete elimination of HBV and associated lethal liver failures and liver cancer at a Duke-NUS lecture (video below). SARS-2/COVID-19 In October 2018, my wife and I returned from a Yangtze River Cruise where we had admired the beautiful and ancient industrial city of Wuhan, home to 8 million people. START OF THE COVID PANDEMIC: January 2020 We woke to the news that Wuhan was besieged by a lethal coronavirus, resulting in thousands dead daily and several more thousands hospitalized until hospitals reached full capacity. Field hospitals were erected within days. Doctors and nurses arrived from all over China to provide aid; tragically, around a thousand of them died. Within a week, top Chinese scientists had determined the molecular structure of the coronavirus, which was dissimilar to any of the known viruses in their archives. The molecular structure seemed akin to the USCDC's patented invention (No. 7220852/B1 filed on May 22, 2004), with the addition of an HIV glycoprotein insert in the spike protein (later confirmed by Nobel Laureate Prof. Luc Montagnier). China disseminated information on the epidemic and the virus through premier journals and transmitted details to the International Genomic Bank. They invited the WHO in January 2020, who discovered many corona viruses but not this particular virus. Singapore We learned from the news that SG Prime Minister's wife, Ho Ching, chairman of Temasek Holdings, a Singapore investment company, had invested nearly S$3 billion in Pfizer/BioNTech and had initiated the procurement of Pfizer mRNA vaccines, Moderna, and plans for establishing vaccine manufacturing in Singapore. Pfizer and mRNA Vaccines Publications in JAMA 2021 showed that Pfizer was 98% effective. Six of my senior academic staff on the board of journals agreed with me that the end points for assessing efficacy were symptoms. (Later, a US Texas judge in 2022 ordered the FDA to release 55,000 pages showing thousands of deaths and serious adverse reactions. The US Supreme Court in 2022 also accepted Senator Robert Kennedy's charge that mRNA vaccines are not vaccines.) These were not the usual endpoints like antibody levels and virus absence in recipients. This was open to "ghost papers," which we had discovered at WHO. I alerted our three Ministers who know me and the 14 medical experts, "The Pfizer mRNA vaccines are not safe for mass immunization as the live lethal virus is still present in the mRNAs." Mandatory Vaccination Then, we received notice from our MOH (Ministry of Health) that all hospital and clinic staff, workplaces, and schools must be vaccinated or they cannot work. Retirement I was then 82 years old, and my mission after being recalled/returning from Cambridge with an MD in Cancer Immunology was completed. However, with my vast experience with vaccines, I continued to advise our MOH privately, as well as colleagues and friends in our country and worldwide. Request to MOH to Release Sinovac A full-length inactivated COVID virus vaccine, Singapore had 20,000 doses of Sinovac in stock. When the new Delta variant infected frontline workers in five public hospitals and Changi Airport in May 2021, I advised our Ministers that the mRNA vaccines were not preventative and to use Sinovac lest our hospitals be overwhelmed by infections. I also informed Ministers that many individuals with allergies cannot take mRNA vaccines and to release the Sinovac. This news was leaked, and I was chastised as peddling fake news by Prof. David Lye of the National Infectious Disease Center and senior Straits Times journalist Shamir Khalid. The Future COVID will remain for many years as the reservoirs of VEMs (Vaccine Escape Mutates) are evolving from failed protection in millions but causing deaths, delayed deaths, and illnesses. The 95% who received Pfizer and other mRNA vaccines, and not inactivated vaccines like Novavax, are developing new mutants. Losses Between 2021 and now, I have lost 34 senior medical colleagues. Most were working in institutions and had been vaccinated with Pfizer. I lost my eminent elder obstetrician aunt on March 31, 2022, who was infected by a Pfizer-vaccinated caregiver who had contracted the Delta spike mutant. She became too weak, stopped playing mahjong, stopped eating, and five days before she passed, she became blind. She died in my arms. I also lost my elder brother, a senior physician at 85, who received Moderna followed by two boosters of Pfizer. He contracted COVID and died two months later. How to Eliminate Wear masks to reduce aerosol transmission. Use antiviral drugs like Tamiflu, 75mg daily for 7 days. It is a potent neuraminidase inhibitor of COVID and the flu. As with most serious infections, take it early at the onset. Usually, ART is negative on day 2-3. Vaccine Research - With the many combinations of mutations, we need to find common antigens and make new inactivated vaccines. Sinovac and Sinopharm My wife and I have had three doses of Sinovac and two of Sinopharm. We have nucleocapsid spike antibodies and are well. 1.6 billion people, including children in 150 countries, have taken the Sinovac and Sinopharm vaccines. They are safe, protective, and have caused no fatalities. Countries can copy or learn from China. Save lives, not politics first. Retired, we stay at home and wear masks in crowded areas. Lessons It's essential to control and eliminate lethal airborne/aerosol infections. A healthy population is a robust workforce. A healthy youth is the future of our country. God bless all, Gabriel Oon Retired Professor of Medicine Former WHO Consultant for Biologicals for Human Use Some final comments by Aussie17: I am fully aware that there are people who are against any kind of vaccine, people who are against wearing masks, and people who believe there is no such thing as viruses. Whatever your opinion is on these matters, I’d just like to say that I know Professor Gabriel personally, and he does not have a single nefarious bone in his body. The world is such a divided place right now that even when you agree with someone 99%, people start calling names and scolding each other over the 1% disagreement, which only serves to deepen our divisions. I hope we can accept diverse views and come together. Signing off for now A17 Thank you for reading PharmaFiles by Aussie17. This post is public so feel free to share it. Share https://www.aussie17.com/p/my-story-by-professor-gabriel-oon
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  • Screening for Silent Spike Toxicity
    Spike levels build up over time with repeated exposures and eventually the dam breaks. Here's how to detect toxicity before it causes symptoms.
    Dr. Syed Haider
    Pet Toxin Safety - Mill Creek Animal Hospital
    This post will provide a deep dive on tests for spike toxicity, including the best screening tests for those who have no symptoms, but have been exposed. These tests detect specific spike-induced inflammation, clotting, AIDS, turbo cancer, etc, and can help get ahead of disease developing underneath the surface. In a future post I plan to cover the best tests for fine tuning a healing protocol.
    There are now hundreds if not thousands of physicians treating spike toxicity with varying protocols and degrees of success.
    In my experience most hesitate to escalate ivermectin enough. At high enough doses it almost always helps (at mygotodoc.com I usually start where others end, at 0.2mg/kg/day and then may gradually escalate as high as 10 times more than that ie 2mg/kg/day in some patients over the course of 5-10 weeks).
    Most physicians treating spike toxicity also refrain from much or any testing.
    This makes sense on a budget, and I often come across patients who can’t afford testing and we skip it as well, but if it can be afforded then it can be helpful in fine tuning the protocol and sometimes uncovering key missing ingredients, like nutritional deficiencies, or particularly stubborn micro clotting requiring escalated dosing and varied types of anticoagulants.
    The other place for testing is in screening of the general population without symptoms, both vaxxed and unvaxxed (though when you really press you often do find new symptoms have sprouted up since the beginning of the pandemic).
    But even in those who truly have no new symptoms and feel perfectly fine, it seems that it may simply be a matter of time before spike toxicity catches up with them, especially if, like so many people, they can’t detox quickly enough, can’t break up the atypical microclots fast enough, and then are reexposed to a new variant, or a big shedding bolus, and that tips the scales and sends them into outright long haul.
    People find it hard to believe that they could feel fantastic and yet there could be something brewing inside that is just 1 straw away from breaking their backs.
    Yet almost everyone was in this very situation even before the pandemic.
    We all have a health span and a lifespan, and for most in the modern world the overlap between them has been dramatically shrinking for generations, and it has only gained speed with each passing year, and especially the last 3 years since the pandemic hit.
    Health is wealthqbak - http://asianpin.com/health-is-wealthqbak/ | Funny cartoons jokes, Funny cartoon pictures, Funny cartoons
    source
    In plain English, we often gradually become chronically ill and then debilitated starting decades before we finally die. In the worst cases spending the last years of our lives in nursing homes, oblivious to our surroundings and infrequently visiting loved ones.
    The reason for this is a chronic mismatch between our bodies and our environments - not just lack of exercise and poor diets, but also the chemical soup we find ourselves in, the toxins in the air, water and soil, the lack of fresh air and sunlight throughout the day, the lack of grounding, and too much toxic blue light at night that is soaked up by our eyes and very skin while we lounge in front of our screens, greatly stressing ourselves, while thinking we’re relaxing, followed by restless, unfulfilling sleep.
    Most of us are drawing down on our health savings accounts - not the tax free HSA - but a metaphorical account that represents our life force.
    Thank you for reading Dr. Syed Haider. This post is public so feel free to share it.
    Share
    Just like a regular bank account, if it isn’t managed properly and wealth is overused, it will eventually get close to zero, by which time we will be liable to illness at the drop of a hat - anything that is too taxing can overdraw the account since what’s flowing into it can’t overcome what’s flowing out.
    And then some of us become chronically overdrawn, living on credit, and in the toxic embrace of chronic illness because of it, dragging us into the depths, while we struggle vainly to get back above the surface.
    This is why when you finally realize you have to change your ways to get better, it makes no sense to give up those changes as soon as you break free of illness.
    You are just above zero, still liable to dipping below the surface again. You need to build up your reserves of health over time and not overdraw your account again. You have to become a good steward of your body and resources. And over time you can get to the point where you’re on solid ground again and can put up with small and large stressors without backsliding. But you should always keep in mind how bad it can get to motivate you to stay on the straight and narrow going forward.
    To get back to the topic, the spike protein builds up in our bodies over time and causes detectable changes to our immune and vascular systems. There is an immune fingerprint of various cytokine markers, there are the microclots, there are alterations to the red blood cell zeta potential, there are predictable decreases of various micronutrients. There may be early warning signs of AIDS, or cancer or organ dysfunction.
    Nowadays almost all new patients with Long COVID or Vax injury made it through a few shots, or a few rounds of COVID without getting long haul, but the final infection or shot put them over the edge.
    If they had come before they got that last shot or infection I could have detected their susceptibility in the lab and we could have worked to correct it.
    This is the epidemic of Silent Spike Toxicity.
    And these are the tests we have available to screen for it:
    The Microclot Test: only available from 1 lab in the US (mail order). Detects abnormal clotting not seen on any other test. The single most specific spike toxicity test.
    The Comprehensive Spike Screening Panel: includes imaging tests: EKG, CXR, Echo. Blood tests that detect damage to the heart, lungs, liver, kidneys. Checks zeta potential. Can show the immune fingerprint of spike. Detection of AIDS. Typical gut microbiome changes. Advanced cancer screening (blood & whole body MRI), and more.
    The Masterjohn-Schilling Spike Healing Panel: detects neuroinflammation, free radicals, mitochondrial dysfunction, autoantibodies, reactivated viruses and bacteria, MCAS, specific micronutrients that are depleted by spike toxicity, and more.
    Masterjohn’s Deep Dive Nutrition Panel goes beyond nutrients depleted by spike toxicity to provide a complete snapshot of functional nutrition and is indispensable for deep healing when half measures don’t work.
    source
    A quick note on tests in general: There is no perfect test. Tests are evaluated by their sensitivity and specificities, but we don’t have research on any of these for spike toxicity diseases. Sensitivity is how good a test is at ruling out a diagnosis and specificity is how good it is at ruling in a diagnosis.
    The best screening tests would be 100% specific - meaning if you have the diagnosis it will be detected 100% of the time, but in order to gain that level of specificity they often have to cast a wide net and give up some sensitivity. What this means practically is that if the diagnosis is present you will test positive, but there will also be some people who don’t have the diagnosis who also test positive.
    Highly specific tests are usually paired with confirmatory tests that are hopefully highly sensitive. Meaning they can weed out the people who were including in the first round of screening, but don’t actually have the diagnosis in question.
    In the absence of research into spike toxicity diseases and optimal screening regimens we have to fall back on expert opinion.
    It seems that the microclot test is likely the best screening test, because those treating spike toxicity have never come across someone with the clinical symptoms of the disease who doesn’t have elevated microclots. Unfortunately microclots can be elevated by other conditions. So a confirmatory test like the incelldx Incellkyne panel might be ordered from the Comprehensive Spike Screening panel, along with other tests we’ll discuss below.
    If the diagnosis of spike toxicity is made then the Masterjohn-Schilling panel is the best next step for fine tuning the protocol, ensuring that the right micronutrients are topped up and the right treatments are prescribed.
    If not improving after targeted and sustained treatment, then the Deep Dive Nutrition panel is indicated to uncover rare and unusual nutritional deficits that could be holding you back.
    Here I’ll cover the primary screening tests: The Microclot Test and the Comprehensive Spike Screening Panel. In a future article I may cover the more expansive and complicated panels that are used primarily in treatment.
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    The Microclot Test
    figure 3
    source
    Typical microclots are usually found in the elderly and those with chronic illnesses like diabetes.
    Spike induced atypical amyloid fibrin microclots are found in those with spike induced blood toxicity.
    The difference between typical and atypical are that spike induced microclots are very difficult to break down, so difficult that they often do not break down at all.
    This explains why the D-dimer isn’t helpful for detecting spike toxicity.
    D-dimer is always trapped inside of clots. Typical clots are always being broken down on the margins - at the edge of a typical clot there will be breakdown. Sometimes the breakdown happens slower than the growth of the clot, but there is always a battle going on between clot growth and clot destruction which will release D-dimer into the blood stream.
    Since it is virtually always elevated in the presence of clotting it is a very specific test, and is used as a screening test when a physician suspects a clotting disorder, but isn’t sure. For example if someone shows up with chest pain and it could be a pulled muscle or a pulmonary embolism (clot in the pulmonary veins), a D-dimer is a simple ad very cheap test that can be done to determine if further confirmatory, but more expensive more risky testing should be considered, like a CT Angiogram of the chest.
    For this reason every doctor going through residency comes to consider a positive D-dimer as indicative of clotting and a negative D-dimer as indicative of no clotting.
    figure 4
    source
    The D-dimer is often elevated during severe acute COVID-19 infection, and during a severe acute injection reaction, but it is not usually elevated in chronic spike toxicity, including chronic long haul and vaccine injured patients.
    The reason it isn’t elevated is that most people cannot break down the atypical microclots caused by spike protein without some additional help from medications and supplements.
    Once medications like aspirin (and sometimes prescriptions ones like plavix and eliquis), supplements like nattokinase, serrapeptase, lumbrokinase, bromelain and NAC are started the atypical microclots start to be broken down and D-dimer goes up, which in this case is usually reason for celebration.
    So the microclot test is the only test in America today that can detect elevated atypical microclots. It’s only available from one lab in the country via mail order (request it from mygotodoc.com), and it helps detect spike toxicity as well as helping track treatment.
    If initial treatment for microclots with aspirin and supplements doesn’t bring the levels down then we escalate to using higher doses, or add plavix and then later eliquis. And we can also consider plasma donation, or even therapeutic plasmapheresis, if available.
    DETOX [spike buster] PRE-ORDER NOW: initial stock is limited! Shipping late November 2023.
    The Comprehensive Spike Screening Panel
    This set of tests includes an EKG, CXR, Echo. It includes blood tests to screen for daamage to the major organs including the heart, lungs, liver, and kidneys. It checks for zeta potential in the blood, which is affected by spike toxicity. It detects an immune fingerprint of spike. It can detect AIDS. It covers stool testing for the gut microbiome as well as advanced cancer screening (via blood & whole body MRI), and more.
    Tests Included in the Panel:
    Spike antibody test: Measures your B cell’s response to the spike protein. In the absence of a direct test for spike protein this helps indirectly detect and track the spike protein levels in your body. Your body produces antibodies in response to the spike protein, and this test measures those antibodies. Generally speaking the more spike protein in your body, the higher the antibody levels. However, what's considered a problematic level varies by individual. The goal is to lower this level as much as possible. The test can also help detect those individuals who might be transmitting the spike protein to others. This is by no means a perfect test, but in the right setting it is helpful as a red flag for further workup, or as a way of monitoring response to therapies over time.
    Incellkyne Panel from Incelldx - provides an immune fingerprint of spike protein, a combination of elevated cytokine markers that are typically seen in spike protein disease. There are other immune fingerprints they have identified on this same test that indicate non spike Chronic Fatigue Syndrome and Lyme disease. If CCL-5/RANTES and/or VEGF are elevated (VEGF is almost always elevated) then the medication Maraviroc can be helpful. VEGF indicates vascular inflammation and omega-3s, infrared light exposure, and a number of other approaches can be particularly helpful to deal with that. Other inflammatory markers tested are TNF-alpha, IL-2, IL-4, IL-6, IL-8, IL-10, IL-13, GM-CSF, SCD40L, CCL3, CCL-4, and IFN-Gamma. Ivermectin is known to decrease IL-6, which is commonly elevated in Long Haul and Vax injury.
    Lymphocyte Subset Panel or Cyrex Lymphocyte MAP:
    The subset panel is the standard test for AIDS and tests for these immune subsets: CD3, CD19,CD20, CD4, CD8, CD56+. The primary pathognomic feature of AIDS would be a CD4 T cell count lower than 200, though there are other red flags such as NK cell activity <10%, or a deficit of T helper cells (CD4+), as well as these others that would only be found on the Cyrex Lymphocyte MAP test: TH1 insufficiency, Increased T-Reg (CD4+ CD25+), deficits of cytotoxic cells (CD8+, CD56+), increased TGF-beta, etc. The Lymphocyte subset panel is cheaper and available at any standard lab and may be covered by insurance, the Cyrex test is more expensive and is a mail order blood test only that has to be paid in cash up front. The Cyrex test can detect 14 different immunotypes and reveal immune under or overactivity, infections, inflammation, autoimmunity, allergies, asthma, hypersentivities and some cancers. It also helps determine what further immune tests can be done to fine tune a healing protocol.
    Galleri Cancer Screening is an advanced test for 50+ types of common cancers based on a genetic marker found in the blood. It is a good screening test because it is 99.5% specific. This might be a good option for someone with a family or personal history of cancer as it can detect occurance at a the earliest microscopic stage, far before any visual test like an MRI or CT scan would show a mass. If cancer is found ivermectin, fenbendazole, vitamin C, baking soda and many other of label easily available substances are very promising for treatment.
    Can 2 Cheap Meds, 1 Vitamin & Baking Soda Kill Any Cancer?
    Can 2 Cheap Meds, 1 Vitamin & Baking Soda Kill Any Cancer?
    Cancer rates have skyrocketed in the past century for a number of reasons not least of which is the incredibly large number of toxins spewed into the environment and incorporated into our food supplies. And now with most of humanity exposed to the cancerous spike protein there is likely to be even further acceleration. Those exposed to the fallout from …
    Read full story
    Complete Blood Count (CBC)
    Measures various components and features of the blood, including red blood cells, white blood cells, and platelets. Amongst the white blood cells we can see various abnormalities - they can be high or low, and subsets like basophils, neutrophils and eosinophils might be off. For example a patient started aspirin which is a cornerstone of most treatments of spike toxicity, but in this case raised the eosinophil level and caused some histaminergic symptoms. The symptoms were the same as her usual disease symptoms so initially were written off as a normal fluctuation in symptomatology over time, but in light of the elevated eosinophil level we finally determined that the aspirin was triggering a problem, since that is possible side effect of aspirin. Once off aspirin the symptoms and the eosinophils normalized.
    Comprehensive Metabolic Panel (CMP)
    Measures 14 different substances in the blood. It provides information about kidney and liver function, electrolyte levels, and blood sugar. Blood sugar can be high or low in spike toxicity, and that would indicate a pancreatic issue requiring further workup. Liver function often needs to be tracked in those on ivermectin and many other medications. Potassium balances sodium and usually needs to be supplemented in long haul, since most people don’t get enough, especially if blood pressure is rising.
    Cystatin C is a more specific marker of kidney dysfunction than the creatinine level that is included on the CMP.
    D-dimer: as mentioned earlier this is a product of the breakdown of clots, it’s often elevated in the acute phase of spike injury or disease, but over time the microclots being inherently difficult to break down stop releasing D-dimer unless the patient is taking a combination of supplements and/or medications to trigger this.
    Erythrocyte Sedimentation Rate (ESR)
    Decoding ESR Test: What Your Results Could Reveal About Your Health | Pathkind Labs Blog
    Measures the rate at which red blood cells settle in a standardized tube over one hour. It is a nonspecific marker of inflammation in the body. It is also an indication of the zeta potential, which is a measure of the normal negative charge on red cells that prevents them from clumping together. Spike protein lowers the normal zeta potential which usually causes ESR to rise. Potassium citrate can help reverse this trend, as can sunlight and grounding.
    hs-CRP Test (C-Reactive Protein High-Sensitivity) is another non specific marker of inflammation in the body and if found require further workup. It can be elevated in myo-pericarditis.
    Troponin T is a protein relatively specific to heart muscle cells, leaked into the blood. This is a cardiac biomarker that indicates myocardial injury and along with an EKG is. one of the primary screening tests for a heart attack as well as for myocarditis/pericarditis.
    Pro BNP (N-terminal pro-brain natriuretic peptide) is produced by the heart in response to strain, particularly heart failure.
    Electrocardiogram (EKG)
    EKG: What is it and what does it mean? – JP Stroke Foundation
    Non-invasive medical test that records the heart's electrical activity. Can be used to diagnose myocarditis/pericarditis, heart attack, and various rhythm abnormalities like atrial fibrillation, SVTs and more that can raise the risk of sudden cardiac arrest, such as that seen in some athletes who have been vaxxed.
    Echocardiogram (ECHO)
    Provides valuable information about the heart's structure, function, and blood flow and is an important test for helping visualize the inflammatory changes of myocarditis-pericarditis, such as fluid leaking into the sack around the heart.
    Chest X-ray
    source
    Non-invasive imaging test that uses X-rays to visualize the structures and organs within the chest, including the lungs, heart, ribs, diaphragm, and large arteries. Anyone with shortness of breath should have a Chest Xray as a first screening test looking for pneumonia, inflammation, scarring, nodules/cancer, etc.
    Whole Body MRI
    The Latest Quantified Self Trend: Whole-Body MRI
    Another imaging modality that can turn up hidden cancers and a whole host of other abnormalities and might be ordered for someone where the Galleri test was negative but there was still some suspicion present (here is always the risk of over diagnosis with imaging tests like this, which can lead to otherwise unnecessary stress and procedures that can themselves cause harm).
    Microbiome testing: Microbiomix Metagenomic Sequencing of Stool by Genova or Sabine Hazan’s Whole Genome Deep Sequencing by Progenabiome. Spike toxicity leads to depletion of beneficial gut bacterials species such as Bifidobacterium pseudocatenulatum, Faecalibacterium prausnitzii, Roseburia inulinivorans, and Roseburia hominis all of which are associated with long COVID complications. Presence of 'unfriendly' bacterial species is linked to poor performance on the 6-minute walk test among long COVID patients. Microbiomix is cheaper because it uses a less thorough sequencing technique, but can show some changes found due to spike toxicity. Sabine Hazan’s test is better if budgeting allows, both because it does a whole genome sequencing, but also because it benefits from her proprietary and private knowledge base (essentially studies and findings that have not yet been published). There are some supplements that can help correct deficits, and in stubborn cases a stool transplant can be transformative, though this is somewhat difficult to get done as it usually requires travel.
    And that’s a wrap!
    Next time We’ll look at the Masterjohn-Schilling panel which is our go to for optimizing treatment of long haul/vax injury and perhaps the Comprehensive Nutrition panel, which is important for anyone who has a chronic illness resistant to treatment, including long haul syndromes.
    https://blog.mygotodoc.com/p/screening-for-silent-spike-toxicity?utm_campaign=post&utm_medium=web


    https://donshafi911.blogspot.com/2024/01/screening-for-silent-spike-toxicity.html
    Screening for Silent Spike Toxicity Spike levels build up over time with repeated exposures and eventually the dam breaks. Here's how to detect toxicity before it causes symptoms. Dr. Syed Haider Pet Toxin Safety - Mill Creek Animal Hospital This post will provide a deep dive on tests for spike toxicity, including the best screening tests for those who have no symptoms, but have been exposed. These tests detect specific spike-induced inflammation, clotting, AIDS, turbo cancer, etc, and can help get ahead of disease developing underneath the surface. In a future post I plan to cover the best tests for fine tuning a healing protocol. There are now hundreds if not thousands of physicians treating spike toxicity with varying protocols and degrees of success. In my experience most hesitate to escalate ivermectin enough. At high enough doses it almost always helps (at mygotodoc.com I usually start where others end, at 0.2mg/kg/day and then may gradually escalate as high as 10 times more than that ie 2mg/kg/day in some patients over the course of 5-10 weeks). Most physicians treating spike toxicity also refrain from much or any testing. This makes sense on a budget, and I often come across patients who can’t afford testing and we skip it as well, but if it can be afforded then it can be helpful in fine tuning the protocol and sometimes uncovering key missing ingredients, like nutritional deficiencies, or particularly stubborn micro clotting requiring escalated dosing and varied types of anticoagulants. The other place for testing is in screening of the general population without symptoms, both vaxxed and unvaxxed (though when you really press you often do find new symptoms have sprouted up since the beginning of the pandemic). But even in those who truly have no new symptoms and feel perfectly fine, it seems that it may simply be a matter of time before spike toxicity catches up with them, especially if, like so many people, they can’t detox quickly enough, can’t break up the atypical microclots fast enough, and then are reexposed to a new variant, or a big shedding bolus, and that tips the scales and sends them into outright long haul. People find it hard to believe that they could feel fantastic and yet there could be something brewing inside that is just 1 straw away from breaking their backs. Yet almost everyone was in this very situation even before the pandemic. We all have a health span and a lifespan, and for most in the modern world the overlap between them has been dramatically shrinking for generations, and it has only gained speed with each passing year, and especially the last 3 years since the pandemic hit. Health is wealthqbak - http://asianpin.com/health-is-wealthqbak/ | Funny cartoons jokes, Funny cartoon pictures, Funny cartoons source In plain English, we often gradually become chronically ill and then debilitated starting decades before we finally die. In the worst cases spending the last years of our lives in nursing homes, oblivious to our surroundings and infrequently visiting loved ones. The reason for this is a chronic mismatch between our bodies and our environments - not just lack of exercise and poor diets, but also the chemical soup we find ourselves in, the toxins in the air, water and soil, the lack of fresh air and sunlight throughout the day, the lack of grounding, and too much toxic blue light at night that is soaked up by our eyes and very skin while we lounge in front of our screens, greatly stressing ourselves, while thinking we’re relaxing, followed by restless, unfulfilling sleep. Most of us are drawing down on our health savings accounts - not the tax free HSA - but a metaphorical account that represents our life force. Thank you for reading Dr. Syed Haider. This post is public so feel free to share it. Share Just like a regular bank account, if it isn’t managed properly and wealth is overused, it will eventually get close to zero, by which time we will be liable to illness at the drop of a hat - anything that is too taxing can overdraw the account since what’s flowing into it can’t overcome what’s flowing out. And then some of us become chronically overdrawn, living on credit, and in the toxic embrace of chronic illness because of it, dragging us into the depths, while we struggle vainly to get back above the surface. This is why when you finally realize you have to change your ways to get better, it makes no sense to give up those changes as soon as you break free of illness. You are just above zero, still liable to dipping below the surface again. You need to build up your reserves of health over time and not overdraw your account again. You have to become a good steward of your body and resources. And over time you can get to the point where you’re on solid ground again and can put up with small and large stressors without backsliding. But you should always keep in mind how bad it can get to motivate you to stay on the straight and narrow going forward. To get back to the topic, the spike protein builds up in our bodies over time and causes detectable changes to our immune and vascular systems. There is an immune fingerprint of various cytokine markers, there are the microclots, there are alterations to the red blood cell zeta potential, there are predictable decreases of various micronutrients. There may be early warning signs of AIDS, or cancer or organ dysfunction. Nowadays almost all new patients with Long COVID or Vax injury made it through a few shots, or a few rounds of COVID without getting long haul, but the final infection or shot put them over the edge. If they had come before they got that last shot or infection I could have detected their susceptibility in the lab and we could have worked to correct it. This is the epidemic of Silent Spike Toxicity. And these are the tests we have available to screen for it: The Microclot Test: only available from 1 lab in the US (mail order). Detects abnormal clotting not seen on any other test. The single most specific spike toxicity test. The Comprehensive Spike Screening Panel: includes imaging tests: EKG, CXR, Echo. Blood tests that detect damage to the heart, lungs, liver, kidneys. Checks zeta potential. Can show the immune fingerprint of spike. Detection of AIDS. Typical gut microbiome changes. Advanced cancer screening (blood & whole body MRI), and more. The Masterjohn-Schilling Spike Healing Panel: detects neuroinflammation, free radicals, mitochondrial dysfunction, autoantibodies, reactivated viruses and bacteria, MCAS, specific micronutrients that are depleted by spike toxicity, and more. Masterjohn’s Deep Dive Nutrition Panel goes beyond nutrients depleted by spike toxicity to provide a complete snapshot of functional nutrition and is indispensable for deep healing when half measures don’t work. source A quick note on tests in general: There is no perfect test. Tests are evaluated by their sensitivity and specificities, but we don’t have research on any of these for spike toxicity diseases. Sensitivity is how good a test is at ruling out a diagnosis and specificity is how good it is at ruling in a diagnosis. The best screening tests would be 100% specific - meaning if you have the diagnosis it will be detected 100% of the time, but in order to gain that level of specificity they often have to cast a wide net and give up some sensitivity. What this means practically is that if the diagnosis is present you will test positive, but there will also be some people who don’t have the diagnosis who also test positive. Highly specific tests are usually paired with confirmatory tests that are hopefully highly sensitive. Meaning they can weed out the people who were including in the first round of screening, but don’t actually have the diagnosis in question. In the absence of research into spike toxicity diseases and optimal screening regimens we have to fall back on expert opinion. It seems that the microclot test is likely the best screening test, because those treating spike toxicity have never come across someone with the clinical symptoms of the disease who doesn’t have elevated microclots. Unfortunately microclots can be elevated by other conditions. So a confirmatory test like the incelldx Incellkyne panel might be ordered from the Comprehensive Spike Screening panel, along with other tests we’ll discuss below. If the diagnosis of spike toxicity is made then the Masterjohn-Schilling panel is the best next step for fine tuning the protocol, ensuring that the right micronutrients are topped up and the right treatments are prescribed. If not improving after targeted and sustained treatment, then the Deep Dive Nutrition panel is indicated to uncover rare and unusual nutritional deficits that could be holding you back. Here I’ll cover the primary screening tests: The Microclot Test and the Comprehensive Spike Screening Panel. In a future article I may cover the more expansive and complicated panels that are used primarily in treatment. Share The Microclot Test figure 3 source Typical microclots are usually found in the elderly and those with chronic illnesses like diabetes. Spike induced atypical amyloid fibrin microclots are found in those with spike induced blood toxicity. The difference between typical and atypical are that spike induced microclots are very difficult to break down, so difficult that they often do not break down at all. This explains why the D-dimer isn’t helpful for detecting spike toxicity. D-dimer is always trapped inside of clots. Typical clots are always being broken down on the margins - at the edge of a typical clot there will be breakdown. Sometimes the breakdown happens slower than the growth of the clot, but there is always a battle going on between clot growth and clot destruction which will release D-dimer into the blood stream. Since it is virtually always elevated in the presence of clotting it is a very specific test, and is used as a screening test when a physician suspects a clotting disorder, but isn’t sure. For example if someone shows up with chest pain and it could be a pulled muscle or a pulmonary embolism (clot in the pulmonary veins), a D-dimer is a simple ad very cheap test that can be done to determine if further confirmatory, but more expensive more risky testing should be considered, like a CT Angiogram of the chest. For this reason every doctor going through residency comes to consider a positive D-dimer as indicative of clotting and a negative D-dimer as indicative of no clotting. figure 4 source The D-dimer is often elevated during severe acute COVID-19 infection, and during a severe acute injection reaction, but it is not usually elevated in chronic spike toxicity, including chronic long haul and vaccine injured patients. The reason it isn’t elevated is that most people cannot break down the atypical microclots caused by spike protein without some additional help from medications and supplements. Once medications like aspirin (and sometimes prescriptions ones like plavix and eliquis), supplements like nattokinase, serrapeptase, lumbrokinase, bromelain and NAC are started the atypical microclots start to be broken down and D-dimer goes up, which in this case is usually reason for celebration. So the microclot test is the only test in America today that can detect elevated atypical microclots. It’s only available from one lab in the country via mail order (request it from mygotodoc.com), and it helps detect spike toxicity as well as helping track treatment. If initial treatment for microclots with aspirin and supplements doesn’t bring the levels down then we escalate to using higher doses, or add plavix and then later eliquis. And we can also consider plasma donation, or even therapeutic plasmapheresis, if available. DETOX [spike buster] PRE-ORDER NOW: initial stock is limited! Shipping late November 2023. The Comprehensive Spike Screening Panel This set of tests includes an EKG, CXR, Echo. It includes blood tests to screen for daamage to the major organs including the heart, lungs, liver, and kidneys. It checks for zeta potential in the blood, which is affected by spike toxicity. It detects an immune fingerprint of spike. It can detect AIDS. It covers stool testing for the gut microbiome as well as advanced cancer screening (via blood & whole body MRI), and more. Tests Included in the Panel: Spike antibody test: Measures your B cell’s response to the spike protein. In the absence of a direct test for spike protein this helps indirectly detect and track the spike protein levels in your body. Your body produces antibodies in response to the spike protein, and this test measures those antibodies. Generally speaking the more spike protein in your body, the higher the antibody levels. However, what's considered a problematic level varies by individual. The goal is to lower this level as much as possible. The test can also help detect those individuals who might be transmitting the spike protein to others. This is by no means a perfect test, but in the right setting it is helpful as a red flag for further workup, or as a way of monitoring response to therapies over time. Incellkyne Panel from Incelldx - provides an immune fingerprint of spike protein, a combination of elevated cytokine markers that are typically seen in spike protein disease. There are other immune fingerprints they have identified on this same test that indicate non spike Chronic Fatigue Syndrome and Lyme disease. If CCL-5/RANTES and/or VEGF are elevated (VEGF is almost always elevated) then the medication Maraviroc can be helpful. VEGF indicates vascular inflammation and omega-3s, infrared light exposure, and a number of other approaches can be particularly helpful to deal with that. Other inflammatory markers tested are TNF-alpha, IL-2, IL-4, IL-6, IL-8, IL-10, IL-13, GM-CSF, SCD40L, CCL3, CCL-4, and IFN-Gamma. Ivermectin is known to decrease IL-6, which is commonly elevated in Long Haul and Vax injury. Lymphocyte Subset Panel or Cyrex Lymphocyte MAP: The subset panel is the standard test for AIDS and tests for these immune subsets: CD3, CD19,CD20, CD4, CD8, CD56+. The primary pathognomic feature of AIDS would be a CD4 T cell count lower than 200, though there are other red flags such as NK cell activity <10%, or a deficit of T helper cells (CD4+), as well as these others that would only be found on the Cyrex Lymphocyte MAP test: TH1 insufficiency, Increased T-Reg (CD4+ CD25+), deficits of cytotoxic cells (CD8+, CD56+), increased TGF-beta, etc. The Lymphocyte subset panel is cheaper and available at any standard lab and may be covered by insurance, the Cyrex test is more expensive and is a mail order blood test only that has to be paid in cash up front. The Cyrex test can detect 14 different immunotypes and reveal immune under or overactivity, infections, inflammation, autoimmunity, allergies, asthma, hypersentivities and some cancers. It also helps determine what further immune tests can be done to fine tune a healing protocol. Galleri Cancer Screening is an advanced test for 50+ types of common cancers based on a genetic marker found in the blood. It is a good screening test because it is 99.5% specific. This might be a good option for someone with a family or personal history of cancer as it can detect occurance at a the earliest microscopic stage, far before any visual test like an MRI or CT scan would show a mass. If cancer is found ivermectin, fenbendazole, vitamin C, baking soda and many other of label easily available substances are very promising for treatment. Can 2 Cheap Meds, 1 Vitamin & Baking Soda Kill Any Cancer? Can 2 Cheap Meds, 1 Vitamin & Baking Soda Kill Any Cancer? Cancer rates have skyrocketed in the past century for a number of reasons not least of which is the incredibly large number of toxins spewed into the environment and incorporated into our food supplies. And now with most of humanity exposed to the cancerous spike protein there is likely to be even further acceleration. Those exposed to the fallout from … Read full story Complete Blood Count (CBC) Measures various components and features of the blood, including red blood cells, white blood cells, and platelets. Amongst the white blood cells we can see various abnormalities - they can be high or low, and subsets like basophils, neutrophils and eosinophils might be off. For example a patient started aspirin which is a cornerstone of most treatments of spike toxicity, but in this case raised the eosinophil level and caused some histaminergic symptoms. The symptoms were the same as her usual disease symptoms so initially were written off as a normal fluctuation in symptomatology over time, but in light of the elevated eosinophil level we finally determined that the aspirin was triggering a problem, since that is possible side effect of aspirin. Once off aspirin the symptoms and the eosinophils normalized. Comprehensive Metabolic Panel (CMP) Measures 14 different substances in the blood. It provides information about kidney and liver function, electrolyte levels, and blood sugar. Blood sugar can be high or low in spike toxicity, and that would indicate a pancreatic issue requiring further workup. Liver function often needs to be tracked in those on ivermectin and many other medications. Potassium balances sodium and usually needs to be supplemented in long haul, since most people don’t get enough, especially if blood pressure is rising. Cystatin C is a more specific marker of kidney dysfunction than the creatinine level that is included on the CMP. D-dimer: as mentioned earlier this is a product of the breakdown of clots, it’s often elevated in the acute phase of spike injury or disease, but over time the microclots being inherently difficult to break down stop releasing D-dimer unless the patient is taking a combination of supplements and/or medications to trigger this. Erythrocyte Sedimentation Rate (ESR) Decoding ESR Test: What Your Results Could Reveal About Your Health | Pathkind Labs Blog Measures the rate at which red blood cells settle in a standardized tube over one hour. It is a nonspecific marker of inflammation in the body. It is also an indication of the zeta potential, which is a measure of the normal negative charge on red cells that prevents them from clumping together. Spike protein lowers the normal zeta potential which usually causes ESR to rise. Potassium citrate can help reverse this trend, as can sunlight and grounding. hs-CRP Test (C-Reactive Protein High-Sensitivity) is another non specific marker of inflammation in the body and if found require further workup. It can be elevated in myo-pericarditis. Troponin T is a protein relatively specific to heart muscle cells, leaked into the blood. This is a cardiac biomarker that indicates myocardial injury and along with an EKG is. one of the primary screening tests for a heart attack as well as for myocarditis/pericarditis. Pro BNP (N-terminal pro-brain natriuretic peptide) is produced by the heart in response to strain, particularly heart failure. Electrocardiogram (EKG) EKG: What is it and what does it mean? – JP Stroke Foundation Non-invasive medical test that records the heart's electrical activity. Can be used to diagnose myocarditis/pericarditis, heart attack, and various rhythm abnormalities like atrial fibrillation, SVTs and more that can raise the risk of sudden cardiac arrest, such as that seen in some athletes who have been vaxxed. Echocardiogram (ECHO) Provides valuable information about the heart's structure, function, and blood flow and is an important test for helping visualize the inflammatory changes of myocarditis-pericarditis, such as fluid leaking into the sack around the heart. Chest X-ray source Non-invasive imaging test that uses X-rays to visualize the structures and organs within the chest, including the lungs, heart, ribs, diaphragm, and large arteries. Anyone with shortness of breath should have a Chest Xray as a first screening test looking for pneumonia, inflammation, scarring, nodules/cancer, etc. Whole Body MRI The Latest Quantified Self Trend: Whole-Body MRI Another imaging modality that can turn up hidden cancers and a whole host of other abnormalities and might be ordered for someone where the Galleri test was negative but there was still some suspicion present (here is always the risk of over diagnosis with imaging tests like this, which can lead to otherwise unnecessary stress and procedures that can themselves cause harm). Microbiome testing: Microbiomix Metagenomic Sequencing of Stool by Genova or Sabine Hazan’s Whole Genome Deep Sequencing by Progenabiome. Spike toxicity leads to depletion of beneficial gut bacterials species such as Bifidobacterium pseudocatenulatum, Faecalibacterium prausnitzii, Roseburia inulinivorans, and Roseburia hominis all of which are associated with long COVID complications. Presence of 'unfriendly' bacterial species is linked to poor performance on the 6-minute walk test among long COVID patients. Microbiomix is cheaper because it uses a less thorough sequencing technique, but can show some changes found due to spike toxicity. Sabine Hazan’s test is better if budgeting allows, both because it does a whole genome sequencing, but also because it benefits from her proprietary and private knowledge base (essentially studies and findings that have not yet been published). There are some supplements that can help correct deficits, and in stubborn cases a stool transplant can be transformative, though this is somewhat difficult to get done as it usually requires travel. And that’s a wrap! Next time We’ll look at the Masterjohn-Schilling panel which is our go to for optimizing treatment of long haul/vax injury and perhaps the Comprehensive Nutrition panel, which is important for anyone who has a chronic illness resistant to treatment, including long haul syndromes. https://blog.mygotodoc.com/p/screening-for-silent-spike-toxicity?utm_campaign=post&utm_medium=web https://donshafi911.blogspot.com/2024/01/screening-for-silent-spike-toxicity.html
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    Screening for Silent Spike Toxicity
    Spike levels build up over time with repeated exposures and eventually the dam breaks. Here's how to detect toxicity before it causes symptoms.
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  • Mystery Pneumonia AKA White Lung Syndrome: What's Going On?
    More questions than answers for now, but it could be a mix of VAIDS and Vitamin A deficiency, and the unlikely edge case remains that the Middle Kingdom is giving us the middle finger yet again.

    Dr. Syed Haider

    Nothing will stop these kids from acing their exams, not even white lung disease
    China has been hit with a “mystery pneumonia”, AKA “white lung disease”, except they insist it’s not really a mystery pneumonia at all, it’s just the usual suspects like mycoplasma, Flu, RSV, rhinovirus, adenovirus, and yes, COVID-19.

    Or perhaps the word mystery refers to the mystery of why there is such a large outbreak of it this year?

    The prevalent explanations are an “immune debt” due to lockdowns overlaid on a multi-year cyclic upturn in mycoplasma infections.

    What we do know is that children are primarily affected and it has spread beyond China to many other countries, and possibly even the US now. But there does not seem to be a spike in deaths at this point.

    Beyond the immune debt and cycle theories, what else could be driving this?

    Well the elephant in the room is VAIDS, as well as Long COVID AIDS, which unfortunately is also a thing.

    But another lesser known possibility is relative vitamin A deficiency.

    Yes, Vitamin A, not Vitamin D.

    Vitamin A is important for immunity, especially from mycoplasma. It’s a fat soluble vitamin and what makes this an even more likely culprit in many cases is that so many people have been heavily supplementing with Vitamin D for the last 3 years, and Vitamin D supplementation can lead to deficiencies of Vitamins A, E and K, since all 4 of these fat soluble vitamins compete for absorption.

    So the cure of the last pandemic could have set some people up for this outbreak.

    The most common supplement regimen during and after COVID was Vitamin C, D, Zinc and Quercetin.

    The other nutritional imbalance that this regimen can trigger is a deficiency of copper due to prolonged Zinc suppelementation.

    Signs of copper deficiency also include immunodeficiency evidenced by low white blood cell count and thyroid problems, anemia, weak bones, irregular heartbeat, and loss of pigment from the skin.

    Thank you for reading Dr. Syed Haider. This post is public so feel free to share it.

    Share

    However mild deficiencies might not have any warning signs beyond increased susceptibility to illness and trouble with recovery.

    For this reason I’m working on a new supplement to balance the effects of our popular IMMUNITY [vitamins] supplement. We already included vitamin K2 in that one, to help balance the effect of D3 intake on calcium absorption, but this new one will have Vitamins A and E as well as copper and a few other ingredients like selenium, necessary for the optimal immune balance required for prevention, treatment of acute illness and recovery from long haul/vax injuries.

    Until then I would recommend most people who are supplementing with D3 on an ongoing basis to take the same dose of Vitamin A in retinol form, so if it’s 5000 IU D3, I would usually take 5000 IU of retinol as well. Vitamin E in the form of mixed tocopherols 20 IU and the K2 form of Vitamin K 100mcg per day. To balance 50 mg of zinc you probably need about 4-8 mg of copper per day. Oyster max is a powdered oyster supplement that has both zinc and copper in it.

    Optimally you would use lab testing along with a nutrient calculator to determine how. much of each micronutrient you get from your diet, and then just dial up your nutritional intake as required, or add supplemental doses based on nutritional deficiencies.





    At mygotodoc we offer comprehensive nutritional testing panels to help optimize nutrition, because the building blocks of health are at their most basic just two: nourishment and detoxification, of course those two words belie a lot of complexity.

    For example nourishment doesn’t just include food and vitamins, it also includes sunlight in the day, darkness at night, relaxation and rest, grounding, fulfilling relationships, happy thoughts, gratitude, etc.

    And detoxification doesn’t just include spike protein and heavy metals, but also plastics, industrial chemicals, chronic infections/infestations, non natural EMFs, light at night, anger and other toxic emotions, negative thoughts, harmful relationships, addictions, etc.

    Optimizing just some of these can often give your body enough strength and energy to overcome the others being suboptimal.

    Overall we need balance in life and the story of imbalanced micronutrients just serves to highlight the importance of balance in all things.


    In modern industrial societies we tend towards action over inactivity, but in truth we need both for optimal health and productivity.

    Muscles only get built during rest, not during exercise, which breaks them down to stimulate rebuilding.

    Similarly spending all our time in our heads processing the firehose of incoming information leaves us no time to chew it and digest it and make the most of it.

    Give yourself some down time to just do nothing, so that when you go back to doing something you do it better than you would have otherwise.

    This is why many cultures encourage timeouts during the day to pray or meditate instead of packing every waking moment with activity and information.

    We’re currently also undergoing an uptick in COVID infections around the world, but not an increase in severity.

    Geert Van Den Boscche’s warnings of a coming supervariant targeting the vaxed have not yet materialized

    At the same time many in the medical freedom community are hyperaware of the current happenings around the world because they expect round two of COVID or some other bioweapon along with lockdowns heading into the 2024 presidential election year.

    If this were going to happen this is when it would get started, because it takes some time to really get going.

    I hope we don’t fall for the same thing all over again, but it may just be a matter of time and the last one may have just been a dry run for the real power grab.

    No more pandemics | Bill Gates
    The next pandemic we’ve been warned is definitely coming has been termed “Disease X” by Gates and company, a placeholder name for some as yet unknown bug that could be far worse than COVID, i.e. an actual threat to human life on a scale similar to the Black Plague or the 1918 Spanish Flu.

    If something of that magnitude and severity were to be unleashed on humanity many would forget their righteous indignation over COVID lockdowns and demand stringent measures including quarantine camps and forced treatment - it sounds impossible, yet this has just become law in the state of New York.

    New Yorkers can be forcibly extracted from their homes and interred in quarantine camps.


    The Supreme Court actually ruled over a 100 years ago that compulsory vaccination was constitutional (and now the definition of vaccine extends to gene therapies).

    We’ll have to see what the future holds, but whatever it is, there is likely to be a cheap off-label treatment and if all else fails sunlight is the best disinfectant (i.e. get outside and get some sun).

    Ivermectin works for a number of viruses including RSV and Flu, and it even has activity against mycoplasma pneumonia.

    Other common meds are exceedingly helpful as well like doxycycline, which is why our Disaster-Pak prescriptions are as popular as ivermectin.

    We work with patients to prescribe an array of meds as comprehensive as possible. We have options that may work against Ebola and Marburg, as well as a whole host of other bioweapons and run of the mill infections.

    We prescribe the right doses and the right quantities, which I haven’t seen anywhere else. Usually patients who go somewhere else end up coming to us when they actually get sick, because they didn’t get anywhere near enough ivermectin or whatever else from another provider, who isn’t familiar with the latest dosing protocols.



    I’m also working on a vitamin C supplement, because in my experience high dose oral vitamin C is the single most effective treatment of any infection. A recent post on Vitamin C was one of my most popular ever:

    Is High Dose Vitamin C a PanaCea?

    Is High Dose Vitamin C a PanaCea?
    Sometimes you come across something that is so life changing you wonder how you made it through your entire life without knowing about it. Then you find out that many others already knew about it for decades and have been trying to spread the word to no avail, because there are multi billion dollar corporations that just can’t and won’t allow it.

    Read full story

    Unlike most Vitamin C supplements that come from GMO cornstarch and may have trace amounts of mold, mine will have 1000mg of non GMO tapioca sourced Vitamin C in a veggie cap (same as the C in our IMMUNITY [vitamins] supplement), which I find to be the most convenient form for rapidly consuming 30-50,000 mg of Vitamin C in a single dose (2-4 capsules at a time with a sip of water until you’re done).


    Back to our mystery pneumonia outbreak: I know why people are extra cautious given what we went through with COVID-19. Some people really did get very sick, and others ended up with debilitating long haul syndromes. China has not historically been exactly forthcoming with information on outbreaks early on.

    Social media and news reports said that 800 bed hospitals were overwhelmed with 5000-7000 patients per day, but the authorities on a call with the WHO denied that.

    This could just be a whole lot of nothing and one of the risks going forward is allowing the health authorities to turn regular or even really bad flu seasons into enough reason lock us down and take away all our rights.

    We should not want to entirely rid the world of infectious diseases even if we could, because we need to tune up our immune systems from time to time in order to prevent chronic illness.

    The same immune system that stays in shape fighting off a mild to moderate cold or flu every year, also fights off cancer cells and heart disease.

    Share

    I came cross a study once (that I can’t find - drop it in the comments if you know it) showing that 4 or more viral illnesses like chickenpox and measles as a child was associated with a 90% lower risk of heart disease as an older adult.

    So we need to keep our immune system in shape with occasional viral and bacterial infections, even though some small percentage of people will die from them.

    This sounds worse than it is though, because those people who die, would have died from something else anyway.

    COVID deaths in the elderly might have been pulled forward a year or two, which is terrible for each person who knew those who died, but fighting the natural way of things with technology can lead to far more harm than good.

    The real population “vaccines” are the infectious diseases themselves, not Big Pharma shots or government lockdowns.

    Artificially interfering with what nature demands just shuffles deaths around a bit, or God-forbid actually increases them.

    The upshot to all this is: don’t get scared, get prepared.

    https://blog.mygotodoc.com/p/mystery-pneumonia-aka-white-lung

    https://telegra.ph/Mystery-Pneumonia-AKA-White-Lung-Syndrome-Whats-Going-On-03-10
    Mystery Pneumonia AKA White Lung Syndrome: What's Going On? More questions than answers for now, but it could be a mix of VAIDS and Vitamin A deficiency, and the unlikely edge case remains that the Middle Kingdom is giving us the middle finger yet again. Dr. Syed Haider Nothing will stop these kids from acing their exams, not even white lung disease China has been hit with a “mystery pneumonia”, AKA “white lung disease”, except they insist it’s not really a mystery pneumonia at all, it’s just the usual suspects like mycoplasma, Flu, RSV, rhinovirus, adenovirus, and yes, COVID-19. Or perhaps the word mystery refers to the mystery of why there is such a large outbreak of it this year? The prevalent explanations are an “immune debt” due to lockdowns overlaid on a multi-year cyclic upturn in mycoplasma infections. What we do know is that children are primarily affected and it has spread beyond China to many other countries, and possibly even the US now. But there does not seem to be a spike in deaths at this point. Beyond the immune debt and cycle theories, what else could be driving this? Well the elephant in the room is VAIDS, as well as Long COVID AIDS, which unfortunately is also a thing. But another lesser known possibility is relative vitamin A deficiency. Yes, Vitamin A, not Vitamin D. Vitamin A is important for immunity, especially from mycoplasma. It’s a fat soluble vitamin and what makes this an even more likely culprit in many cases is that so many people have been heavily supplementing with Vitamin D for the last 3 years, and Vitamin D supplementation can lead to deficiencies of Vitamins A, E and K, since all 4 of these fat soluble vitamins compete for absorption. So the cure of the last pandemic could have set some people up for this outbreak. The most common supplement regimen during and after COVID was Vitamin C, D, Zinc and Quercetin. The other nutritional imbalance that this regimen can trigger is a deficiency of copper due to prolonged Zinc suppelementation. Signs of copper deficiency also include immunodeficiency evidenced by low white blood cell count and thyroid problems, anemia, weak bones, irregular heartbeat, and loss of pigment from the skin. Thank you for reading Dr. Syed Haider. This post is public so feel free to share it. Share However mild deficiencies might not have any warning signs beyond increased susceptibility to illness and trouble with recovery. For this reason I’m working on a new supplement to balance the effects of our popular IMMUNITY [vitamins] supplement. We already included vitamin K2 in that one, to help balance the effect of D3 intake on calcium absorption, but this new one will have Vitamins A and E as well as copper and a few other ingredients like selenium, necessary for the optimal immune balance required for prevention, treatment of acute illness and recovery from long haul/vax injuries. Until then I would recommend most people who are supplementing with D3 on an ongoing basis to take the same dose of Vitamin A in retinol form, so if it’s 5000 IU D3, I would usually take 5000 IU of retinol as well. Vitamin E in the form of mixed tocopherols 20 IU and the K2 form of Vitamin K 100mcg per day. To balance 50 mg of zinc you probably need about 4-8 mg of copper per day. Oyster max is a powdered oyster supplement that has both zinc and copper in it. Optimally you would use lab testing along with a nutrient calculator to determine how. much of each micronutrient you get from your diet, and then just dial up your nutritional intake as required, or add supplemental doses based on nutritional deficiencies. At mygotodoc we offer comprehensive nutritional testing panels to help optimize nutrition, because the building blocks of health are at their most basic just two: nourishment and detoxification, of course those two words belie a lot of complexity. For example nourishment doesn’t just include food and vitamins, it also includes sunlight in the day, darkness at night, relaxation and rest, grounding, fulfilling relationships, happy thoughts, gratitude, etc. And detoxification doesn’t just include spike protein and heavy metals, but also plastics, industrial chemicals, chronic infections/infestations, non natural EMFs, light at night, anger and other toxic emotions, negative thoughts, harmful relationships, addictions, etc. Optimizing just some of these can often give your body enough strength and energy to overcome the others being suboptimal. Overall we need balance in life and the story of imbalanced micronutrients just serves to highlight the importance of balance in all things. In modern industrial societies we tend towards action over inactivity, but in truth we need both for optimal health and productivity. Muscles only get built during rest, not during exercise, which breaks them down to stimulate rebuilding. Similarly spending all our time in our heads processing the firehose of incoming information leaves us no time to chew it and digest it and make the most of it. Give yourself some down time to just do nothing, so that when you go back to doing something you do it better than you would have otherwise. This is why many cultures encourage timeouts during the day to pray or meditate instead of packing every waking moment with activity and information. We’re currently also undergoing an uptick in COVID infections around the world, but not an increase in severity. Geert Van Den Boscche’s warnings of a coming supervariant targeting the vaxed have not yet materialized At the same time many in the medical freedom community are hyperaware of the current happenings around the world because they expect round two of COVID or some other bioweapon along with lockdowns heading into the 2024 presidential election year. If this were going to happen this is when it would get started, because it takes some time to really get going. I hope we don’t fall for the same thing all over again, but it may just be a matter of time and the last one may have just been a dry run for the real power grab. No more pandemics | Bill Gates The next pandemic we’ve been warned is definitely coming has been termed “Disease X” by Gates and company, a placeholder name for some as yet unknown bug that could be far worse than COVID, i.e. an actual threat to human life on a scale similar to the Black Plague or the 1918 Spanish Flu. If something of that magnitude and severity were to be unleashed on humanity many would forget their righteous indignation over COVID lockdowns and demand stringent measures including quarantine camps and forced treatment - it sounds impossible, yet this has just become law in the state of New York. New Yorkers can be forcibly extracted from their homes and interred in quarantine camps. The Supreme Court actually ruled over a 100 years ago that compulsory vaccination was constitutional (and now the definition of vaccine extends to gene therapies). We’ll have to see what the future holds, but whatever it is, there is likely to be a cheap off-label treatment and if all else fails sunlight is the best disinfectant (i.e. get outside and get some sun). Ivermectin works for a number of viruses including RSV and Flu, and it even has activity against mycoplasma pneumonia. Other common meds are exceedingly helpful as well like doxycycline, which is why our Disaster-Pak prescriptions are as popular as ivermectin. We work with patients to prescribe an array of meds as comprehensive as possible. We have options that may work against Ebola and Marburg, as well as a whole host of other bioweapons and run of the mill infections. We prescribe the right doses and the right quantities, which I haven’t seen anywhere else. Usually patients who go somewhere else end up coming to us when they actually get sick, because they didn’t get anywhere near enough ivermectin or whatever else from another provider, who isn’t familiar with the latest dosing protocols. I’m also working on a vitamin C supplement, because in my experience high dose oral vitamin C is the single most effective treatment of any infection. A recent post on Vitamin C was one of my most popular ever: Is High Dose Vitamin C a PanaCea? Is High Dose Vitamin C a PanaCea? Sometimes you come across something that is so life changing you wonder how you made it through your entire life without knowing about it. Then you find out that many others already knew about it for decades and have been trying to spread the word to no avail, because there are multi billion dollar corporations that just can’t and won’t allow it. Read full story Unlike most Vitamin C supplements that come from GMO cornstarch and may have trace amounts of mold, mine will have 1000mg of non GMO tapioca sourced Vitamin C in a veggie cap (same as the C in our IMMUNITY [vitamins] supplement), which I find to be the most convenient form for rapidly consuming 30-50,000 mg of Vitamin C in a single dose (2-4 capsules at a time with a sip of water until you’re done). Back to our mystery pneumonia outbreak: I know why people are extra cautious given what we went through with COVID-19. Some people really did get very sick, and others ended up with debilitating long haul syndromes. China has not historically been exactly forthcoming with information on outbreaks early on. Social media and news reports said that 800 bed hospitals were overwhelmed with 5000-7000 patients per day, but the authorities on a call with the WHO denied that. This could just be a whole lot of nothing and one of the risks going forward is allowing the health authorities to turn regular or even really bad flu seasons into enough reason lock us down and take away all our rights. We should not want to entirely rid the world of infectious diseases even if we could, because we need to tune up our immune systems from time to time in order to prevent chronic illness. The same immune system that stays in shape fighting off a mild to moderate cold or flu every year, also fights off cancer cells and heart disease. Share I came cross a study once (that I can’t find - drop it in the comments if you know it) showing that 4 or more viral illnesses like chickenpox and measles as a child was associated with a 90% lower risk of heart disease as an older adult. So we need to keep our immune system in shape with occasional viral and bacterial infections, even though some small percentage of people will die from them. This sounds worse than it is though, because those people who die, would have died from something else anyway. COVID deaths in the elderly might have been pulled forward a year or two, which is terrible for each person who knew those who died, but fighting the natural way of things with technology can lead to far more harm than good. The real population “vaccines” are the infectious diseases themselves, not Big Pharma shots or government lockdowns. Artificially interfering with what nature demands just shuffles deaths around a bit, or God-forbid actually increases them. The upshot to all this is: don’t get scared, get prepared. https://blog.mygotodoc.com/p/mystery-pneumonia-aka-white-lung https://telegra.ph/Mystery-Pneumonia-AKA-White-Lung-Syndrome-Whats-Going-On-03-10
    BLOG.MYGOTODOC.COM
    Mystery Pneumonia AKA White Lung Syndrome: What's Going On?
    More questions than answers for now, but it could be a mix of VAIDS and Vitamin A deficiency, and the unlikely edge case remains that the Middle Kingdom is giving us the middle finger yet again.
    1 Kommentare 0 Anteile 16436 Ansichten
  • My Story - By Professor Gabriel Oon
    "Between 2021 and now, I have lost 34 senior medical colleagues. Most were working in institutions and had been vaccinated with Pfizer."

    Aussie17
    Dear Readers, today I bring to you a guest post by Professor Gabriel Oon, retired Professor of Medicine who worked as a WHO consultant and founding President of Singapore’s Society of Oncology. Please feel free to share and distribute!

    -Aussie17

    Share


    My Story - By Professor Gabriel Oon

    "SAFETY, SAFETY, SAFETY!"

    These words were relentlessly drummed upon us during our WHO meetings in Geneva from 1983 to 1987, where vaccine manufacturers from around the globe (Netherlands, Germany, China, Singapore, Korea, Australia, US, UK, France, Russia, Sweden, Israel, etc.) came together. The gathering was initiated by the Director of Biologics, Dr. Frank Perkins, and the Director-General, Dr. Karl Mahler MD, who had appointed me as a WHO Consultant.

    Every one of us had created our own variant of the novel hepatitis B vaccine from plasma HBV, employing different inactivation techniques.

    Dr. Perkins reminded us of the two monumental vaccine calamities in history.

    The Lübeck disaster (1929-33) saw many children inoculated with live BCG instead of the killed vaccine, resulting in thousands of children affected and several deaths.

    The Cutter incident (1955) in the USA was when 200,000 received a live polio vaccine; 40,000 fell ill, many became paralyzed, or died.

    Such tragedies were not to be repeated. With the then-unknown threat of AIDS transmitted by infected blood, it became crucial to source safe, uninfected blood for the production of hepatitis B vaccines.

    Advancements in molecular science led to the discovery of the common “a” antigen present in all serotypes in both humans and animals. Consequently, a prototype yeast recombinant HB vaccine was formulated, safety-tested, and implemented in Singapore as a collaboration between the International Agency for Research in Cancer/WHO and the Singapore Government.

    I was then appointed by the Singapore government and IARC/WHO (International Agency for Research on Cancer) to oversee the safety in the manufacture and implementation of the vaccine.

    Then Prime Minister of Singapore, Mr. Lee Kuan Yew, who mandated the directive to me and my team, insisted on "300% safety, not just 100%."

    Together with my team and WHO oversight, we rejected several unsafe vaccines and identified vaccine-escape mutants in plasma vaccines that were over-treated with chemicals, which damaged the epitopes of the “a” antigen. This product was rejected.

    Similar Vaccine Escape Mutants (VEMs) arose with the Pfizer mRNA. Instead of inactivation, nine chemicals were used, including the deep-freezing agent phosphophenolglycol. I believe these VEMs on the Covid mRNA are the cause of the continuous eruption of spike mutants ranging from Delta to Omicron variants seen today, as humans have become reservoirs for these mutants.

    On my 80th birthday, July 4, 2019, 34 years since the WHO consultation, I announced the complete elimination of HBV and associated lethal liver failures and liver cancer at a Duke-NUS lecture (video below).

    SARS-2/COVID-19

    In October 2018, my wife and I returned from a Yangtze River Cruise where we had admired the beautiful and ancient industrial city of Wuhan, home to 8 million people.

    START OF THE COVID PANDEMIC: January 2020

    We woke to the news that Wuhan was besieged by a lethal coronavirus, resulting in thousands dead daily and several more thousands hospitalized until hospitals reached full capacity. Field hospitals were erected within days. Doctors and nurses arrived from all over China to provide aid; tragically, around a thousand of them died.

    Within a week, top Chinese scientists had determined the molecular structure of the coronavirus, which was dissimilar to any of the known viruses in their archives.

    The molecular structure seemed akin to the USCDC's patented invention (No. 7220852/B1 filed on May 22, 2004), with the addition of an HIV glycoprotein insert in the spike protein (later confirmed by Nobel Laureate Prof. Luc Montagnier).

    China disseminated information on the epidemic and the virus through premier journals and transmitted details to the International Genomic Bank. They invited the WHO in January 2020, who discovered many corona viruses but not this particular virus.

    Singapore

    We learned from the news that SG Prime Minister's wife, Ho Ching, chairman of Temasek Holdings, a Singapore investment company, had invested nearly S$3 billion in Pfizer/BioNTech and had initiated the procurement of Pfizer mRNA vaccines, Moderna, and plans for establishing vaccine manufacturing in Singapore.

    Pfizer and mRNA Vaccines

    Publications in JAMA 2021 showed that Pfizer was 98% effective. Six of my senior academic staff on the board of journals agreed with me that the end points for assessing efficacy were symptoms.

    (Later, a US Texas judge in 2022 ordered the FDA to release 55,000 pages showing thousands of deaths and serious adverse reactions. The US Supreme Court in 2022 also accepted Senator Robert Kennedy's charge that mRNA vaccines are not vaccines.)

    These were not the usual endpoints like antibody levels and virus absence in recipients. This was open to "ghost papers," which we had discovered at WHO.

    I alerted our three Ministers who know me and the 14 medical experts, "The Pfizer mRNA vaccines are not safe for mass immunization as the live lethal virus is still present in the mRNAs."

    Mandatory Vaccination

    Then, we received notice from our MOH (Ministry of Health) that all hospital and clinic staff, workplaces, and schools must be vaccinated or they cannot work.

    Retirement

    I was then 82 years old, and my mission after being recalled/returning from Cambridge with an MD in Cancer Immunology was completed. However, with my vast experience with vaccines, I continued to advise our MOH privately, as well as colleagues and friends in our country and worldwide.

    Request to MOH to Release Sinovac

    A full-length inactivated COVID virus vaccine, Singapore had 20,000 doses of Sinovac in stock. When the new Delta variant infected frontline workers in five public hospitals and Changi Airport in May 2021, I advised our Ministers that the mRNA vaccines were not preventative and to use Sinovac lest our hospitals be overwhelmed by infections.

    I also informed Ministers that many individuals with allergies cannot take mRNA vaccines and to release the Sinovac.

    This news was leaked, and I was chastised as peddling fake news by Prof. David Lye of the National Infectious Disease Center and senior Straits Times journalist Shamir Khalid.

    The Future

    COVID will remain for many years as the reservoirs of VEMs (Vaccine Escape Mutates) are evolving from failed protection in millions but causing deaths, delayed deaths, and illnesses.

    The 95% who received Pfizer and other mRNA vaccines, and not inactivated vaccines like Novavax, are developing new mutants.

    Losses

    Between 2021 and now, I have lost 34 senior medical colleagues. Most were working in institutions and had been vaccinated with Pfizer.

    I lost my eminent elder obstetrician aunt on March 31, 2022, who was infected by a Pfizer-vaccinated caregiver who had contracted the Delta spike mutant. She became too weak, stopped playing mahjong, stopped eating, and five days before she passed, she became blind. She died in my arms.

    I also lost my elder brother, a senior physician at 85, who received Moderna followed by two boosters of Pfizer. He contracted COVID and died two months later.

    How to Eliminate

    Wear masks to reduce aerosol transmission.

    Use antiviral drugs like Tamiflu, 75mg daily for 7 days. It is a potent neuraminidase inhibitor of COVID and the flu. As with most serious infections, take it early at the onset. Usually, ART is negative on day 2-3.

    Vaccine Research - With the many combinations of mutations, we need to find common antigens and make new inactivated vaccines.

    Sinovac and Sinopharm

    My wife and I have had three doses of Sinovac and two of Sinopharm. We have nucleocapsid spike antibodies and are well.

    1.6 billion people, including children in 150 countries, have taken the Sinovac and Sinopharm vaccines. They are safe, protective, and have caused no fatalities. Countries can copy or learn from China. Save lives, not politics first.

    Retired, we stay at home and wear masks in crowded areas.

    Lessons

    It's essential to control and eliminate lethal airborne/aerosol infections.
    A healthy population is a robust workforce.
    A healthy youth is the future of our country.

    God bless all,
    Gabriel Oon
    Retired Professor of Medicine
    Former WHO Consultant for Biologicals for Human Use


    Some final comments by Aussie17:
    I am fully aware that there are people who are against any kind of vaccine, people who are against wearing masks, and people who believe there is no such thing as viruses. Whatever your opinion is on these matters, I’d just like to say that I know Professor Gabriel personally, and he does not have a single nefarious bone in his body. The world is such a divided place right now that even when you agree with someone 99%, people start calling names and scolding each other over the 1% disagreement, which only serves to deepen our divisions. I hope we can accept diverse views and come together.

    Signing off for now
    A17

    Thank you for reading PharmaFiles by Aussie17. This post is public so feel free to share it.

    Share


    https://www.aussie17.com/p/my-story-by-professor-gabriel-oon
    My Story - By Professor Gabriel Oon "Between 2021 and now, I have lost 34 senior medical colleagues. Most were working in institutions and had been vaccinated with Pfizer." Aussie17 Dear Readers, today I bring to you a guest post by Professor Gabriel Oon, retired Professor of Medicine who worked as a WHO consultant and founding President of Singapore’s Society of Oncology. Please feel free to share and distribute! -Aussie17 Share My Story - By Professor Gabriel Oon "SAFETY, SAFETY, SAFETY!" These words were relentlessly drummed upon us during our WHO meetings in Geneva from 1983 to 1987, where vaccine manufacturers from around the globe (Netherlands, Germany, China, Singapore, Korea, Australia, US, UK, France, Russia, Sweden, Israel, etc.) came together. The gathering was initiated by the Director of Biologics, Dr. Frank Perkins, and the Director-General, Dr. Karl Mahler MD, who had appointed me as a WHO Consultant. Every one of us had created our own variant of the novel hepatitis B vaccine from plasma HBV, employing different inactivation techniques. Dr. Perkins reminded us of the two monumental vaccine calamities in history. The Lübeck disaster (1929-33) saw many children inoculated with live BCG instead of the killed vaccine, resulting in thousands of children affected and several deaths. The Cutter incident (1955) in the USA was when 200,000 received a live polio vaccine; 40,000 fell ill, many became paralyzed, or died. Such tragedies were not to be repeated. With the then-unknown threat of AIDS transmitted by infected blood, it became crucial to source safe, uninfected blood for the production of hepatitis B vaccines. Advancements in molecular science led to the discovery of the common “a” antigen present in all serotypes in both humans and animals. Consequently, a prototype yeast recombinant HB vaccine was formulated, safety-tested, and implemented in Singapore as a collaboration between the International Agency for Research in Cancer/WHO and the Singapore Government. I was then appointed by the Singapore government and IARC/WHO (International Agency for Research on Cancer) to oversee the safety in the manufacture and implementation of the vaccine. Then Prime Minister of Singapore, Mr. Lee Kuan Yew, who mandated the directive to me and my team, insisted on "300% safety, not just 100%." Together with my team and WHO oversight, we rejected several unsafe vaccines and identified vaccine-escape mutants in plasma vaccines that were over-treated with chemicals, which damaged the epitopes of the “a” antigen. This product was rejected. Similar Vaccine Escape Mutants (VEMs) arose with the Pfizer mRNA. Instead of inactivation, nine chemicals were used, including the deep-freezing agent phosphophenolglycol. I believe these VEMs on the Covid mRNA are the cause of the continuous eruption of spike mutants ranging from Delta to Omicron variants seen today, as humans have become reservoirs for these mutants. On my 80th birthday, July 4, 2019, 34 years since the WHO consultation, I announced the complete elimination of HBV and associated lethal liver failures and liver cancer at a Duke-NUS lecture (video below). SARS-2/COVID-19 In October 2018, my wife and I returned from a Yangtze River Cruise where we had admired the beautiful and ancient industrial city of Wuhan, home to 8 million people. START OF THE COVID PANDEMIC: January 2020 We woke to the news that Wuhan was besieged by a lethal coronavirus, resulting in thousands dead daily and several more thousands hospitalized until hospitals reached full capacity. Field hospitals were erected within days. Doctors and nurses arrived from all over China to provide aid; tragically, around a thousand of them died. Within a week, top Chinese scientists had determined the molecular structure of the coronavirus, which was dissimilar to any of the known viruses in their archives. The molecular structure seemed akin to the USCDC's patented invention (No. 7220852/B1 filed on May 22, 2004), with the addition of an HIV glycoprotein insert in the spike protein (later confirmed by Nobel Laureate Prof. Luc Montagnier). China disseminated information on the epidemic and the virus through premier journals and transmitted details to the International Genomic Bank. They invited the WHO in January 2020, who discovered many corona viruses but not this particular virus. Singapore We learned from the news that SG Prime Minister's wife, Ho Ching, chairman of Temasek Holdings, a Singapore investment company, had invested nearly S$3 billion in Pfizer/BioNTech and had initiated the procurement of Pfizer mRNA vaccines, Moderna, and plans for establishing vaccine manufacturing in Singapore. Pfizer and mRNA Vaccines Publications in JAMA 2021 showed that Pfizer was 98% effective. Six of my senior academic staff on the board of journals agreed with me that the end points for assessing efficacy were symptoms. (Later, a US Texas judge in 2022 ordered the FDA to release 55,000 pages showing thousands of deaths and serious adverse reactions. The US Supreme Court in 2022 also accepted Senator Robert Kennedy's charge that mRNA vaccines are not vaccines.) These were not the usual endpoints like antibody levels and virus absence in recipients. This was open to "ghost papers," which we had discovered at WHO. I alerted our three Ministers who know me and the 14 medical experts, "The Pfizer mRNA vaccines are not safe for mass immunization as the live lethal virus is still present in the mRNAs." Mandatory Vaccination Then, we received notice from our MOH (Ministry of Health) that all hospital and clinic staff, workplaces, and schools must be vaccinated or they cannot work. Retirement I was then 82 years old, and my mission after being recalled/returning from Cambridge with an MD in Cancer Immunology was completed. However, with my vast experience with vaccines, I continued to advise our MOH privately, as well as colleagues and friends in our country and worldwide. Request to MOH to Release Sinovac A full-length inactivated COVID virus vaccine, Singapore had 20,000 doses of Sinovac in stock. When the new Delta variant infected frontline workers in five public hospitals and Changi Airport in May 2021, I advised our Ministers that the mRNA vaccines were not preventative and to use Sinovac lest our hospitals be overwhelmed by infections. I also informed Ministers that many individuals with allergies cannot take mRNA vaccines and to release the Sinovac. This news was leaked, and I was chastised as peddling fake news by Prof. David Lye of the National Infectious Disease Center and senior Straits Times journalist Shamir Khalid. The Future COVID will remain for many years as the reservoirs of VEMs (Vaccine Escape Mutates) are evolving from failed protection in millions but causing deaths, delayed deaths, and illnesses. The 95% who received Pfizer and other mRNA vaccines, and not inactivated vaccines like Novavax, are developing new mutants. Losses Between 2021 and now, I have lost 34 senior medical colleagues. Most were working in institutions and had been vaccinated with Pfizer. I lost my eminent elder obstetrician aunt on March 31, 2022, who was infected by a Pfizer-vaccinated caregiver who had contracted the Delta spike mutant. She became too weak, stopped playing mahjong, stopped eating, and five days before she passed, she became blind. She died in my arms. I also lost my elder brother, a senior physician at 85, who received Moderna followed by two boosters of Pfizer. He contracted COVID and died two months later. How to Eliminate Wear masks to reduce aerosol transmission. Use antiviral drugs like Tamiflu, 75mg daily for 7 days. It is a potent neuraminidase inhibitor of COVID and the flu. As with most serious infections, take it early at the onset. Usually, ART is negative on day 2-3. Vaccine Research - With the many combinations of mutations, we need to find common antigens and make new inactivated vaccines. Sinovac and Sinopharm My wife and I have had three doses of Sinovac and two of Sinopharm. We have nucleocapsid spike antibodies and are well. 1.6 billion people, including children in 150 countries, have taken the Sinovac and Sinopharm vaccines. They are safe, protective, and have caused no fatalities. Countries can copy or learn from China. Save lives, not politics first. Retired, we stay at home and wear masks in crowded areas. Lessons It's essential to control and eliminate lethal airborne/aerosol infections. A healthy population is a robust workforce. A healthy youth is the future of our country. God bless all, Gabriel Oon Retired Professor of Medicine Former WHO Consultant for Biologicals for Human Use Some final comments by Aussie17: I am fully aware that there are people who are against any kind of vaccine, people who are against wearing masks, and people who believe there is no such thing as viruses. Whatever your opinion is on these matters, I’d just like to say that I know Professor Gabriel personally, and he does not have a single nefarious bone in his body. The world is such a divided place right now that even when you agree with someone 99%, people start calling names and scolding each other over the 1% disagreement, which only serves to deepen our divisions. I hope we can accept diverse views and come together. Signing off for now A17 Thank you for reading PharmaFiles by Aussie17. This post is public so feel free to share it. Share https://www.aussie17.com/p/my-story-by-professor-gabriel-oon
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    My Story - By Professor Gabriel Oon
    "Between 2021 and now, I have lost 34 senior medical colleagues. Most were working in institutions and had been vaccinated with Pfizer."
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  • Plasma Pen Treatment Near Me
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    Plasma Pen Treatment Near Me https://www.elmirastudio.com/services/plasmapen/
    Plasma Pen Fibroblast
    Elmira Studio offers Plasma Pen treatment including Skin Lifting, Skin tag removal and Advanced skin rejuvenation in Moorpark, Thousand Oaks, Westlake Village, CA
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  • Plasma Pen: The Latest Technology in Skin Rejuvenation at Elmira Studio
    https://elmiradotstudio.wordpress.com/2023/02/02/plasma-pen-the-latest-technology-in-skin-rejuvenation-at-elmira-studio/
    Plasma Pen: The Latest Technology in Skin Rejuvenation at Elmira Studio https://elmiradotstudio.wordpress.com/2023/02/02/plasma-pen-the-latest-technology-in-skin-rejuvenation-at-elmira-studio/
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    “Look years younger with Plasma Pen treatment at Elmira Studio.” Plasma Pen is a non-surgical treatment that uses a device to deliver a plasma arc to the skin. This treatment is used fo…
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