Before the shot even came out, I already knew I wasn’t interested in getting it because I have Mast cell disorder/idiopathic anaphylaxis, I’ve reacted to a vaccine before, and I’m also on immunosuppressive medication. I know most people would say that’s more reason to get it but I feel the opposite, I don’t like adding anything that coul…
Before the shot even came out, I already knew I wasn’t interested in getting it because I have Mast cell disorder/idiopathic anaphylaxis, I’ve reacted to a vaccine before, and I’m also on immunosuppressive medication. I know most people would say that’s more reason to get it but I feel the opposite, I don’t like adding anything that could interact or contribute to my immunocompromised state unless absolutely necessary. So, then I read this article written by an ME/CFS specialist, not a fun disorder to have that is already associated with immunological, neurological issues. She calls the shots “highly hyper-reactive vaccines that will cause her patients to relapse/flare”. I also have neurological issues, Dysautonomia/POTS, and obviously posited the same type of reaction to my disorders and I was like, forget that too! Again, this is *before* they were distributed to the public so, clearly I think doctors were already being told something about that spike protein. So, fast forward to after shots rolled out, I started seeing all my fellow Mast cell, Crohn’s, and POTS friends start to complain about bad side effects and severe flares of their disorders but, because they were so brainwashed at this point, most tried to explain them away or justify that it was “worth it”. Then of course you see in the news the increased incidents of neurological and immune side effects. I don’t believe it’s a coincidence that one of the diagnoses you’re seeing alongside all this Long Covid hype now happens to be ME/CFS. A huge percentage of these people that are being told that they have LC are vaccinated, when they truly are likely vaccine injured. This whole thing is just a human rights catastrophe and train wreck.
You're exactly right. My son is a PhD in pharmacology and is the national director for immunoglobulin and other specialty therapies for a pharma company. He tells me that he sees cases of neurological vaxx damage come across his desk every week. These people are so severely damaged that they are completely disabled and come to him as a last resort when everything else has failed. One injured doctor, a radiologist, was so damaged he was contemplating suicide. Since these therapies are considered experimental, they are not covered by insurance and cost more than $20,000. And no guarantees.
Yes, a lot of people think IVIG would be a good treatment for all forms of POTS and Dysautonomias but they are only doing trials I believe for immune mediated forms and those who have POTS along with Sjogren’s. I will say, I just watched many of the lectures from this years Dysautonomia International Conference and shocker…a doctor was actually willing to mention/admit that cases of vaccine induced autoimmune autonomic neuropathy exist, including a case that was dismissed as psychosomatic until another doctor on staff luckily caught clinical signs of it being a vaccine injury and insisted on taking over the case. However, it was really only mentioned very briefly during one talk and almost all the emphasis in the lectures this year was placed on Long COVID. Basically according to all these neurologists and specialists, everyone in society who is walking around suffering adverse effects, especially all these increased neurological disorders, new onset POTS, new onset ME/CFS, etc….it’s just all Long COVID and that’s the end of it. How an entire generation of medical professionals can ignore the fact that most of these people who have had COVID and are now complaining about long term issues, well they have also had multiple doses of a brand new “vaccine”. Hmm…nope, nothing to see here though. No willingness to think about anything other than Long COVID. But what if you’ve never had COVID pray tell? Well, then your symptoms are clearly fake…psychosomatic…duh.
Sorry, yes Long COVID. I had spelled it out in the previous sentence and then right after just used it’s abbreviation. ME/CFS is ‘Myalgic encephalomyelitis/chronic fatigue syndrome’. Sorry did not spell that one out but from my experience literally no one knows it by it’s proper name and everyone just calls it ME/CFS…you can see why, it’s quite a mouthful! Lol.
Before the shot even came out, I already knew I wasn’t interested in getting it because I have Mast cell disorder/idiopathic anaphylaxis, I’ve reacted to a vaccine before, and I’m also on immunosuppressive medication. I know most people would say that’s more reason to get it but I feel the opposite, I don’t like adding anything that could interact or contribute to my immunocompromised state unless absolutely necessary. So, then I read this article written by an ME/CFS specialist, not a fun disorder to have that is already associated with immunological, neurological issues. She calls the shots “highly hyper-reactive vaccines that will cause her patients to relapse/flare”. I also have neurological issues, Dysautonomia/POTS, and obviously posited the same type of reaction to my disorders and I was like, forget that too! Again, this is *before* they were distributed to the public so, clearly I think doctors were already being told something about that spike protein. So, fast forward to after shots rolled out, I started seeing all my fellow Mast cell, Crohn’s, and POTS friends start to complain about bad side effects and severe flares of their disorders but, because they were so brainwashed at this point, most tried to explain them away or justify that it was “worth it”. Then of course you see in the news the increased incidents of neurological and immune side effects. I don’t believe it’s a coincidence that one of the diagnoses you’re seeing alongside all this Long Covid hype now happens to be ME/CFS. A huge percentage of these people that are being told that they have LC are vaccinated, when they truly are likely vaccine injured. This whole thing is just a human rights catastrophe and train wreck.
You're exactly right. My son is a PhD in pharmacology and is the national director for immunoglobulin and other specialty therapies for a pharma company. He tells me that he sees cases of neurological vaxx damage come across his desk every week. These people are so severely damaged that they are completely disabled and come to him as a last resort when everything else has failed. One injured doctor, a radiologist, was so damaged he was contemplating suicide. Since these therapies are considered experimental, they are not covered by insurance and cost more than $20,000. And no guarantees.
Yes, a lot of people think IVIG would be a good treatment for all forms of POTS and Dysautonomias but they are only doing trials I believe for immune mediated forms and those who have POTS along with Sjogren’s. I will say, I just watched many of the lectures from this years Dysautonomia International Conference and shocker…a doctor was actually willing to mention/admit that cases of vaccine induced autoimmune autonomic neuropathy exist, including a case that was dismissed as psychosomatic until another doctor on staff luckily caught clinical signs of it being a vaccine injury and insisted on taking over the case. However, it was really only mentioned very briefly during one talk and almost all the emphasis in the lectures this year was placed on Long COVID. Basically according to all these neurologists and specialists, everyone in society who is walking around suffering adverse effects, especially all these increased neurological disorders, new onset POTS, new onset ME/CFS, etc….it’s just all Long COVID and that’s the end of it. How an entire generation of medical professionals can ignore the fact that most of these people who have had COVID and are now complaining about long term issues, well they have also had multiple doses of a brand new “vaccine”. Hmm…nope, nothing to see here though. No willingness to think about anything other than Long COVID. But what if you’ve never had COVID pray tell? Well, then your symptoms are clearly fake…psychosomatic…duh.
LC? I get frustrated with initials because I don't know them. I prefer naming the disease the first time it appesrd in print.
Sorry, yes Long COVID. I had spelled it out in the previous sentence and then right after just used it’s abbreviation. ME/CFS is ‘Myalgic encephalomyelitis/chronic fatigue syndrome’. Sorry did not spell that one out but from my experience literally no one knows it by it’s proper name and everyone just calls it ME/CFS…you can see why, it’s quite a mouthful! Lol.
Long covid, I believe
Thanks. Makes sense. My brain just wouldn't go there. I had just struggled with ME/CFS.