A growing number of reports have documented associations between COVID-19 vaccination and autoimmunity, suggesting, for example, a causal link between vaccination and new-onset and/or relapsing autoimmune disorders such as type 1 diabetes mellitus, rheumatoid arthritis, multiple sclerosis, systemic lupus erythematosus, -Medrxiv 04/09/2023.
Work in healthcare. Got vaccine March 2021 in Vancouver BC. 4 days later got severely sick during zoom staff mtg. Dizziness, aphasia, felt like whole body malfunction, blurred vision, ER dx Vestibular Migraine, PPPD, SOB walking even slight incline. The week before, I did my usual 10 K run! How does this happen? Advised to keep getting vaccine despite having to go on sick leave. Vaccine mandatory. I was gaslit by ER docs, GP and neurologist, ENT all confirmed PPPD. But this dx didn’t explain daily crashes with severe tremors and tinnitus and a boat load of other multi system symptoms I couldn’t describe. My symptoms have morphed into leg weakness arm weakness, falling for no reason, waking up with stif arms and hands. Then this goes away and now I’m itchy on my legs, intermittent rash on face arms and legs, flushing. Dx a year ago with MECFS, now dx with MCAS. Now I have limb pain, esp. elbows and arms and legs. Arms the worst. I ended up getting 3 vaccines and got worse with each one. I applied to be excemot from having to get the vaccine but was denied. I’m so angry I’ve lost my career and my quality of life. I have moderate positive ANA and I finally found a rheumatologist who is doing more testing. I may have Lupus. I’m suffering everyday. Tho I try not to get depressed. After 23 years in healthcare I’m so disappointed in how I’ve been treated. There is no such thing as an interdisciplinary approach to the Canadian healthcare system. The specialist are not interested in helping you. Only focusing on their narrow lense. I spent my career advocating for patients and I’m exhausted trying to do the same for myself. The fatigue I endure is like nothing I have ever experienced before the vaccine. Acknowledging the vaccine can harm 6 in 10,000. People would be helpful. I can’t stand that I have to listen to doctors discuss long covid and I mentally, change the long covid into long vax as it’s the exact same syndrome yet most doctors CONTINUE to be cowards about verbalizing the many of us who never got COVID but suffer as much and likely more than long covid sufferers as we have been silenced.
@@Katie_purry02 I had a full blood panel done 2 weeks before I caught Covid. My TPO antibodies were at 65, which is the lowest they have been for me since diagnosed. After 2 years 3 months of Long Covid, my antibody levels are now at 74. (One month after having Covid my TPO was 248.)
Yes it does! After a mild covid case in April 2020, I have had Long Covid ever since. I tested positive in the mid range for Autoimmune disease. But the Pulmonary doc ruled out all known autoimmune diseases. So they don’t know what’s going on or how to fix me. 😣
Me too. It is like they don't care and have no clue how to fix anyone with long covid. Are you hanging in there? Cause the pain is horrible. People think we are all drama... but the pain... the pain is real.
@@someartlife01 I’m hanging in there there, thanks. My only symptom is shortness of breath. Feels like my chest is being constricted. It’s worse now when allergy season is here. You hang in there too!! 🙏🏻
Hi, I got covid for the 2nd time this year 24 Feb and got long covid - couldn't get out of bed (think I had a milder version of long covid after the first time, in retrospect). Crippling fatigue. Went on antihistamines - you need an H1 and H2 blocker, for me that is Loratadine and Famotadine, taking one AM and one PM. I am also taking nattokinase, serrapeptase, NAC and quercetin complex. Plus probiotics - have also recently added Kefir (apparently it has a greater range of probiotics than yoghurt) and have a little sauerkraut on a sandwich every day. Also taking a pile of vitamins! If you get a magnesium supplement, make it magnesium glycinate as this is the one the body absorbs well. For vitamin D - get vitamin D3 & K2. Go hard on B vitamins. I'm also doing a niacin flush (B3). Brand is Solgar (not all B3 will make you flush. I seemed to get better fairly rapidly after taking these supplements (still on everything) - don't know if it was any one thing, or the combination. Hope you can find the way out.
@@karenhensley3069 Hi, try antihistamines, H1 and H2 blocker, for me this is Loratadine and Famotidine. Also NAC will help enormously. Best wishes to you.
I'm forwarding the following msg to you that I put on a group I'm in My anxiety amped up just thinking about sharing on here...😳😰...exhale and breathe.... Hi I'm Angel I'm 61. I live in Gold Beach, Oregon USA. Itz a small coastal town on the Pacific Ocean. We moved here 2yrs ago. We, is my Furbaby dog, Brenna & me. She z my 💓 and the reason I'm still here. I've been down in bed ill since October of last year. I got extremely stressed out and angry about a situation. And a migraine started. It was getting bad, I started getting nauseous. So I took my meds for migraine and nausea and went to bed. Ive been dealing with these since I was a kid. I know the drill well. Take the meds, get a Pepsi, go to bed, go to sleep and when I wake up the migraine and nausea will be gone. I woke up the next day and I still had the migraine and nausea. And then All of my other health issues, activated flared up. IBS, Fibromyalgia, COPD, Lower Back Pain, The Bipolar and The Anxiety. January 2 this cough started and it was annoying, it got worse, I got cough drops and cough syrup.I started coughing really bad, the cough sounded really bad and I started having shortness of breath. And I'm like I think I have COVID. I went on line ordered COVID testing kits. They came did one of the tests...it was positive. It was terrible. I would cough so hard that I couldn't breathe. I was scared that I would die and it would be days before anyone would know. This is taking too long. I apologize. What I have is Long Vaxx Syndrome and Long COVID. I AM DEPRESSED DISTRESSED!!!
If you haven't figured out by now that it's the jabs causing the autoimmune disease, then you haven't been paying attention. Catching cvd after a jab can also potentially trigger it due to immune priming, in the same way the the subsequent jabs tend to trigger these conditions after initial priming by the first jab (more so than from the first jab itself).
Sure - it seems the more you keep irritating the immune system with repetitive stimuli, the more its tolerance breaks down.. But immune priming can occur through past infections aswel - are you, therefore, suggesting the immune priming from a vaccination route is essentially different from a past infection which sets people up for more complications?
@@drjamie_drjudith These aren't traditional vaccines. far from it - they're derived from gene therapy techniques, adapted to function vaguely 'like' a vaccine. The glaring difference with these fauxines is that the antigen (spike protein) is being produced within, and expressed by YOUR OWN CELLS ( it's been shown that the lipid nano particle encapsulated mRNA does indeed disperse throughout the body, and that the spike protein continues to be expressed for at least 9 months). When the immune system subsequently encounters, and activates a response to spike protein (via vaccine or virus), your own cells expressing spike protein become a target, which in a nutshell, IS an autoimmune disease.
This was first shown by the Japanese biodistribution study performed on the pfi zer fauxxine prior to it being unleashed on humanity (study was leaked to the public around the time the fauxxine was rolled out.). It's also worth noting the the original design purpose of nano-lipid encapsulation was for the delivery of drugs across the blood-brain barrier, so besides evading the immune system, biodistribution is what this encapsulation technique does. I also meant to mention in the previous comments, that the fauxxine only instructs the production of spike protein, without the nucleocapsid viral body, which contributes to later immune system misidentification (autoimmunity). I can't post links in YT comments, as YT will just make the comment disappear.
@@boydw1 Thank you for sharing Boyd! The correlation of autoimmunity post-vax has been documented you're right, and we acknowledge that, but I do not think it is accurate to say that it is causing all the autoimmunity associated with long COVID. Cause is a strong word and we need way more research to confirm anything like that before broadcasting statements of that kind (out of self preservation). Plenty of unvaccinated have developed this aswel from infection. If, as you say, the vax trains the body to attack itself and thus induce autoimmunity, surely this is the same as the virus itself in that the bodies immune system learns to identify and attack our own cells which contain the virus? Hence through this mechanism, EBV and HSV-6 are well documented to trigger the onset of autoimmune conditions, without vaccines. Furthermore, the vax doesn’t primarily train our immune system to attack self antigens, it trains it to attack SARS-COV-2 spike antigen. The translation of this, to then a phenomenon of molecular mimicry and loss of tolerance of our immune system to start attacking our own cells, is a big step and one that is more complex.. But, it does happen, and we are equally interested to find out how, so again thank you for sharing!
@@drjamie_drjudith No, the immune identification is not the same for the fauxxine, as normal immune identification is not limited to spike proteins, but also includes recognition of the nucleocapsid viral body. With the fauxxine no nucleocapsid is produced. I'd be highly skeptical of whether "long covid" exists AT ALL. It appears to be little more than a smokescreen for the deleterious immune impacts of the fauxxine (Note also the plethora of poor excuses that have been given for the rise in heart attacks & strokes). While some degree of longer term impacts are not entirely uncommon from any flu, we need to bear in mind that for the vast majority, covid was not a serious illness, with typical symptoms ranging between "asymptomatic" & "ordinary flu". The problems with mRNA technology were already obvious prior to covid, from the failure of previous animal trials, in which there was a preponderance of illness & death due to ADE (an autoimmune condition). Pfizer's own postmarketing data for the covid fauxxine lists 1291 side effects. We also need to consider the impacts of Remdesivir - a drug twice previously rejected due to causing multiple organ failure in 20% of recipients.
Thank you for explaining this so well. I got lots of weird symptoms post covid a few months ago and at first didnt know why, i was worried about stomach diseases & early cancers until burning sensations moved beyond the GI to other areas of my body and I recalled how after the first covid vaccine, i developed a temporary small fibre neuropathy with burning numbness and pins and needles in my feet that lasted a few months. This made me wonder if i was dealing with Long Covid, and an issue with the nervous system. I had to change to a smaller womens dr practice to get heard and get more than just complete blood test which was fine...my new clinic recently ran thyroid panel including thyroid antibodies and it was the thyroid antibodies that came up elevated, 116 or so and i was told they think its Hashimotos. But i have also had kidney issues with dull pain on & off, sometimes trace blood found in the samples and white blood cells and i saw protein one day a few times but the kidney function tests come up ok...but i am suspecting the possibility of more than one autoimmune disease now effecting me. I think my immune system was activated so many times in quick succession, our family had like 3 or 4 back to back infections from kindergarten/and husbands work, I am 6 months postpartum so theres hormones there and stress, my diet probably wasnt amazing and now i can see all these things combined could have, with my reaction to the first vaccine, been the combination of triggering factors. I am however only 33, slim & healthy bmi, no pre existing condition, non smoker, barely drink etc so the long covid/autoimmune disorder was a surprise but hopefully i am able to make big improvements. I am looking into dietry adjustments and i continiously research.
sorry this might be a long read but your comment intrigued me because i’m dealing with something kinda similar. wow watching all these videos about long covid and getting into reading comments from people dealing with symptoms they’ve never had before covid. i’m a 29yr old female who’s never had any health issues previously just the common ADHD since being younger. super active playing volleyball basketball softball my whole life and to this very day not unhealthy by any means. 1st time having covid i was in bed for two weeks straight couldn’t eat drink or get out of bed literally. my body hurt so bad and i sounded terrible with the cough i had. i caught it a few weeks after getting the vac (had to bc i worked in a nursing home) i’ve never experienced a feeling like that in my life, i thought i was gonna die. but anyways a couple months go by and all of a sudden i would have to drive an hour to my job (it was winter time during this time) and my hands and my feet would go completely numb a few minutes in, would tingle feel like needles, when i would get to my job it would take an hour just to get feeling back in my hands and feet even using a heater. just holding a cold drink my hands would tingle / go numb. this started happening every day, especially my feet. my toes can go numb just by walking on a semi cold floor. it’s absolutely annoying. then i started losing circulation quick mainly my legs but my arms also. i’ll wake up with numb limbs. i’ll squat down for a few seconds and lose feeling in my legs. oh sometimes there’s just a constant vibration in my one foot when i’m just laying there doing nothing. so the whole numbness tingling in hands and feet happen.. oh yeah another add on to this.. after getting it, a few months down the line i started getting sick literally every month with a horrible awful cough, atleast once a month for almost a year i was hacking, i ended up cracking a few ribs during this time and man they hurt like a bitch😩 couldn’t make sudden moves, reach my arms above my head, stretch or anything without immense pain. but anyways so randomly a few months after that i started having pain in my feet probably every other night or so. it feels like someone’s lighting my feet on fire from the inside. it’s not like burning on the outside on my skin it’s all inside. so burning and tingling while i try to sleep, sometimes super unbearable. lower back pain, (where i assume my kidneys are) it switches sides most times my right but it can switch to my left, random stabs of pain in the back of my thighs, feeling weak.. so remember all these symptoms. a couple months ago i was in bed and was not feeling right at all. (i decide to take myself to the hospital at 3 in the morning bc i started freaking out) all of those symptoms above were going on, the lower back pain was the worst i had, i would stand up to change clothes and felt like my legs were giving out on me, my vision couldn’t quite focus idk how to explain it, right below the knuckles, on all of my fingers were completely white like my circulation cut off, i kept feeling like i couldn’t catch my breathe and was feeling faint like i was going to pass out. so im at the ER, they give me meds to help calm me down, take my blood etc, they tell me i’m constipated…. with a side of raynaud’s disease LMAO. imagine hearing that all these months of dealing with pain and they tell you ohhh you’re constipated. i was livid. i had a feeling about having raynauds but that only explains my hands and feet. i ended up in the hospital again i think 3 days later and they told me im dealing with autoimmune diseases and need to follow up with a bunch of different doctors to test for autoimmune diseases, my blood vessels and something else. its been months and they are still trying to figure out what’s going on with me. its frustrating especially dealing with the pain in the bottom of my feet almost every night. the only thing that subsides the pain for a few is i’ve been wearing these gel socks and i throw them in the freezer and put them on at night.. but that only helps a quarter of the pain for so long. have you gotten answers from doctors yet? i feel we kinda have similar symptoms going on
@bshawmeows sorry to hear you dealt with all that, yes so much of what you say sounds very familiar and I was initially passed around various Dr's who had no clue or my primary Dr who I never saw because she was busy with others but she'd update my test result file and replied to my email to say what i was saying was a "story" because the full blood count and general blood work was ok. I change drs practice and my new Dr ran the thyroid panel including TPO for thyroid auto antibodies which found the Hashimotos so it took a while but finally it was some validation that no it wasn't a "story" and something wa s going on. But hey even if I hasnt had that result finally, a Dr should never dismiss and should listen re symptoms as in Long Covid many sufferers never find anything observable in their bloods and tests and I see their comments and frustrations of how they have all this pain and suffering but nothing shows up as being wrong in their tests so they feel invisible. A good Dr would be educated on the huge spectrum that is Long Covid. You asked what Dr has done for me at this stage. After finding the autoimmune issue, they've testing my thyroid every 3 months I believe it is and monitoring. Not much else so I've taken control of my own health by researching and looking heavily into diet. I'm trying to follow a type of autoimmune protocol diet, more so a paelo diet and it looks like cutting out gluten is huge so I'm trying to holistically heal my body as best I can, and doing things like sauna and jogging. My vitamin d was very low so I was given 3 monthly tabs to take. I was after covid getting random BP spikes too which is unusual as my BP was always low side normal. I started taking methylation supplements after listening to a Joe Rogan podcast where the topic of BP was addressed. My BP began to settle back down to normal range. Sounds like you've also had some coming and going type kidney pain at the back as well. This seems to have settled down for me but it does feel like symptoms flare up and flare down which makes me worry about Long Covid being autoimmune. If Dr's at the hospital suggested multiple autoimmune, are they putting you onto specialists? I'm yet to be referred to a specialist, I think ideally it would be a referral to maybe an immuniologist or something. All the best with recovery!
@@bshawmeowsand yes the burning and pins and needles sensations you describe I deal with too on and off. It's not as bad as it was initially but I worry this too is autoimmune and will have flare ups and false sense of security when it has settled cos some type of factor might make it flare up again like in my case this specific small fibre neuropathy happened right after my first covid inoculation. Burning feet, pins and needles and numbness which was chronic but after a few months it settled down and it eventually went away and for a few years things were fine on the surface until the most recent infection last year and all the burning pins and needles sensations came back which has again begun to settle down but I still get tingling up and down my back and the other week I randomly got lots of new pins and needles and numbness in my hands and fingers and it was actually quite painful making it hard to sleep. I'm not sure now if it's nerves or more or more a circulation issue. I'm noticing I get very easy piting and indentations on legs and feet. I was watching some videos last night about Long covid with Dr's talking about how it's got something to do with mast cell activation and spike protein not leaving the system and the mast cells releasing all these cytokines and causing an over reaction. They were saying the goal needs to be to get spike out of the system but I'm not sure for myself what that involves and what I need to take supplement wise so I'll keep researching. I did see an acupuncturist who randomly asked me if I had MS (another autoimmune) 😢I was like not that I know of but now I'm thinking is that the tingling pins and needles stuff. I know that lots if people online talk about these burning/pins and needles/numb type issues either post vaccine or post infection.
Please can someone tell me what blood tests do I need to ask the doctors for in order to prove that I have this. I have been told I have long covid. I am / was very fit and healthy. I have eaten a vegetarian-vegan diet for 20+ years. Pre covid I was hardly ever ill. Since it I am ill so much. I feel there is no help out there for me. Where do I look for support? I will do anything to not feel like this any more. I run my own business and am struggling to keep going due to dipping into illness so much.
Hi Charles - sorry to hear about how much you have been affected by this! There are investigations your doctor can do to screen for autoimmunity, however, in my experience many of those come back inconclusive for people - narrowing down and diagnosing autoimmune disease can be tricky due to the principles discussed in this video. There are private labs that can offer comprehensive panels which I discussed in a video specifically on testing which you can find on our channel. I would advise you to work with someone who can direct your on testing options and solutions rather than doing it yourself though as you could spend alot of money on tests which are not actually appropriate... A functional medicine practitioner is a good option - you may also reach out to us for support via the link in our channel bio if you would like to. Kind regards.
I always had skin psoriasis. I've got the jabs and was ok. But then, I've got covid. Skin psoriasis turned into psoriatic arthritis, spondility ankylosis, brain fog...
Technically Rachael Maddow lied about it being what we used to call a "V". Check the patent holders on the "T's" Did they exist before the wet market "B's" ? Gain of function is proven, so was Ivermectin, so is and was censorship of the "Science."
Yes, autoimmunity can be triggered post vaccination.. Spike protein from vaccine or infection - they both trigger the immune system and in the right situation (as described in this video) can lead to an autoimmune phenomenon.. What we may/may not find out with time is whether there is a difference in the immune activity in reaction to either source of the spike protein - both post vax and post infection long haulers have very similar symptoms so it's not clear at the moment..
@@drjamie_drjudith However, aberrant or excessive production of pro-inflammatory cytokines is associated with uncontrolled local and systemic inflammation, resulting in cell death and often irreversible tissue damage. infection has shown to cause cytokines, vaccines do not prevent infeciton or replication cycle and would not prevent cytokines, covid 19 is known to cause multi organ damage, known to cause cytokines, known to provoke a immune response and even asymptomatic infection still lands individuals with long term symptoms, so even asymptomatic disease with no symptoms provokes enough cytokines to cause significant damage.
@@drjamie_drjudith wouldn't it make sense for a controlled group then? The un V who have had COVID-19 compared to the V. We know so many people that are very sick all the time and also know people personally that have developed aggressive cancers and they are V. The medical community is not looking at both groups here and that raises serious questions.
I already fought Multiple Sclerosis. Nobody knew what COVID-19 would do to someone with MS. A very long bout of fatigue was to be expected according to my doctors. But then I got the vaccine and it was a repeat of the original infection but more intense and 2 years later I’m fighting all sorts of stuff. Fibromyalgia, possible POTS, blood pressure yo-yo, palpitations. My MS doctor said that those aren’t MS. I agree. But all of my other doctors want to blame MS.
Hey hi thank you for your message I am having such a struggle oh my God I can't I can't even believe this oh goodness yes I have been seeing my doctor and I saw her I think it was a month ago went in and when she had listened to my heart that time before she detected that there was my heart was like skipping beats so she had me where a heart monitor that was on my body that I wore for a week and it was like it's some little computer light situation and then when the week was up put it in the envelope and mail it to the lab and and they do the analysis of it and it showed that I have an arrhythmia. I I don't completely know all the information about that I haven't checked in about all of that and then my blood pressure absolutely was crazy as could be it's all over the place low extremely high and so she wanted to put me on a medication and and the migraine has been constant since October. it's just weird!!! she put me on another inhaler thinking that it was just my asthma acting up everything was just you know being absolutely crazy so in a way as it on one side it's good to know what is happening what's going on and there's also like I I don't want to be like this I want to be up I have things to do that I want to do! I can get from my bed to the bathroom and I'm absolutely exhausted and gasping for breath it's just absolutely insane absolutely insane I can't believe I absolutely was ADAMANT and I WAS NOT TAKING THE SHOT AT ALL!!! I got pressured to get the shot by a person in my life... I caved in and I got the shot and I got horribly horribly ill I was so ill from that shot so sick it was horrible absolutely horrible and I was like oh my God !!! I thought it's done over and then it came up that they were saying you had to get a booster shot and I was like there's no way I am not getting the booster!!! NO WAY IN HELL!!!…. once again I caved into pressure from someone and got the shot and again I was horrible absolutely horrible so ill.
Can somebody recomend any cleanses they can do for toxins ect. Ive been on aip for a while but every now and again i will eat out and have a flare up because they cook everything in fucking rapeseed oil. I still have pain in my lungs every now and again, especially when ive been stressed with work. Love the way this guy delivers my nervous system feels super safe.
The spike protein is also in the virus but at least you aren't getting shots over and over and getting the whole spike injected into you multiple times. Or have side effects from the shot.
The spike protein is the entire problem. Covid virus was just the transport vessel. The vaccine was the transport vessel, the damage and all the problems are caused by the spike proteins, why? Because it's man made it's not of this world. The body doesn't know how what to do. Plus they are so small they are damaging the mitochondria etc.. Detox and block the spike that is the key.
I have pericarditis. And I had pots. My pots has mostly resolved. Both are concerning to me since it involves my heart. Ecg echo and crp levels are all ok. Also my d dimer is high 612. And I feel very breathless. 😭 unvaxxed 34 years old.
Sorry to hear about your current situation Carmella - that must be driving alot of anxiety for you! If we can be of any assistance, please do contact us via our website.
All the way from kenya 🇰🇪 Africa am experiencing heart palpitations and stomach issues,more so bloatin,constipation.Dizzines,joint pains and excessive farting What can I do Doc
My head feels.like it is going to explode so woozy stomach pains headaches now black eyes sore eyes pressure in head sinus pain .had none of this before shots horrible 19months
Covid activated Narcolepsy in me. I have a normal sleep study that was done just 2 months prior to my first covid infection. Got covid/covid pneumonia and within 1 month could not stay awake in the daytime. 2 sleep studies later i have narcolepsy 2.
Sorry to hear about your situation!I did a video on sleep and Long COVID specifically if you search our channel - it focussed mainly on insomnia, but perhaps you can pull some useful things from it?
How do you detect autoimmune response to long covid with a test available in a typical clinical setting? All I got was an ANA blood test but I'm guessing that is not enough. I've suffered head compression and paresthesia on the LHS of my face since Sep 2021 and no doctor can tell me why or what's wrong with me. I do have elevated ctokines: IL-10, SCD40L, IFN_GAMMA, and VEGF. Maybe more, but those are the ones I have had tested that are elevated. Any of that point to autoimmunity? Is there anything in the literature that speaks to this?
Hi Brad. Yes, this is an unclear area right now in mainstream healthcare and will take some time for any specific diagnostic testing to be established in mainstream guidelines in relation to specifically Long COVID. I have seen a number of clients who have had ANA come back as negative or positive but not significant enough to be diagnostic for an autoimmune diagnosis so they are in this grey zone. It can commonly take time for that to happen as any potential autoimmune disease takes time to manifest in a clear way to then be placed in a diagnostic category.. Monitoring through a rheumatology department is part of that process, or Immunosciences Lab by Aristo Vojdani offers comprehensive autoimmune panels, but I would caution against ordering these without working with a practitioner/doctor to guide you on results etc. There are clearly things going on with your immune system and elevated cytokines indicate an inflammatory process, but this can happen independent of any autoimmune process. Whether that is related to the paraesthesia you are experiencing, it is hard to say. I would imagine you have had brain scans done for those symptoms, and so if they are clear for pathological causes, the problem usually relates to inflammation and more functional causes. Hope that helps, but please feel free to contact us via our website should you have any further questions.
However, aberrant or excessive production of pro-inflammatory cytokines is associated with uncontrolled local and systemic inflammation, resulting in cell death and often irreversible tissue damage
for Alopecia check out Chinese medicine. My friend lost all of her hair on her head... so Chinese medicine 6 months later her hair is all back. It is grown back! Try to find herbs and Chinese medicine.
The video is very nice and explains a ton of information. But honestly, people just want a cure. But no one knows a cure. I want people to understand that those who are having long covid like me I am trying different supplements to try and help reduce the pain. Let me know what you have tried also. But here is a list of things that can help with the pain. Please try it out and let me know if it helped you also. Listen to your body as your body and you are the best doctors. 1. Heat Sauna or hot water with Epsom Salt Try to do it 2 or 4 times a week. Your skin may be sensitive so you might want to be extra careful with the Hot water bath with Epsom Salt 2 to 5 cups depending on your tub size and do it for 40 minutes. For Dry Sauna for those who are sensitive to water then 20 to 40 minutes. Do drink water and take breaks. 40 minutes is a long time in a sauna. 2. Supplements 1. Magnesium 100 mg - can help with muscle pain take low amounts and increase slowly 2. vitamin B1 100 mg - can help with energy production 3. CoQ10 60 mg - helps with energy production 4. Boswellia Root powder - helps with joint pain and inflammation 5. Ginger root - Can help reduce pain in muscles If you are having trouble with Mood because of the pain such as Depression try the following. 1. CBD - you can get drops or a drink. Do not take much and test yourself on it. The CBD can reduce inflammation and help with the pain. 2. GABBA - helps with depression 3. Ashwagandha - helps with depression 3. Exercise - if you can do it good for you. If you can not. Try only 4 minutes and build up your strength. But listen to the body if you can't do it don't do it. Because if you overdo it you'll crash and can't get out of bed. DIET CHANGES: 1. No bread or grain. 2. No sweets or candy or anything like it 3. No coffee 4. No beer 5. smoking A diet that you can change to help with pain 1. KETO - veggies and meat Try fasting 1 time a week for 12 to 14 hours. I have tried so many drugs from the doctor and none of those drugs helped. Tried over 20 drugs and they made me sick. Maybe you can try drugs with Western medicine but honestly, they made me sicker. Try Chinese Medicine to get better. If you found a supplement or something that has helped you please let me know. because we need a cure for this and a way to get better. Sadly in my area, I am on my own. Doctors don't know and don't study it and most just do not care. If you have a nice doctor very good for you. Because I live in an area where they do not care if you die.
A growing number of reports have documented associations between COVID-19 vaccination and autoimmunity, suggesting, for example, a causal link between vaccination and new-onset and/or relapsing autoimmune disorders such as type 1 diabetes mellitus, rheumatoid arthritis, multiple sclerosis, systemic lupus erythematosus,
-Medrxiv 04/09/2023.
Work in healthcare. Got vaccine March 2021 in Vancouver BC. 4 days later got severely sick during zoom staff mtg. Dizziness, aphasia, felt like whole body malfunction, blurred vision, ER dx Vestibular Migraine, PPPD, SOB walking even slight incline. The week before, I did my usual 10 K run! How does this happen? Advised to keep getting vaccine despite having to go on sick leave. Vaccine mandatory. I was gaslit by ER docs, GP and neurologist, ENT all confirmed PPPD. But this dx didn’t explain daily crashes with severe tremors and tinnitus and a boat load of other multi system symptoms I couldn’t describe. My symptoms have morphed into leg weakness arm weakness, falling for no reason, waking up with stif arms and hands. Then this goes away and now I’m itchy on my legs, intermittent rash on face arms and legs, flushing. Dx a year ago with MECFS, now dx with MCAS. Now I have limb pain, esp. elbows and arms and legs. Arms the worst. I ended up getting 3 vaccines and got worse with each one. I applied to be excemot from having to get the vaccine but was denied. I’m so angry I’ve lost my career and my quality of life. I have moderate positive ANA and I finally found a rheumatologist who is doing more testing. I may have Lupus. I’m suffering everyday. Tho I try not to get depressed. After 23 years in healthcare I’m so disappointed in how I’ve been treated. There is no such thing as an interdisciplinary approach to the Canadian healthcare system. The specialist are not interested in helping you. Only focusing on their narrow lense. I spent my career advocating for patients and I’m exhausted trying to do the same for myself. The fatigue I endure is like nothing I have ever experienced before the vaccine. Acknowledging the vaccine can harm 6 in 10,000. People would be helpful. I can’t stand that I have to listen to doctors discuss long covid and I mentally, change the long covid into long vax as it’s the exact same syndrome yet most doctors CONTINUE to be cowards about verbalizing the many of us who never got COVID but suffer as much and likely more than long covid sufferers as we have been silenced.
I got COVID and was fine. Since I took the vaccine I have not been right and now I have an autoimmune disease
It was the COVID not the vaccine
SAME!!!
Yes…. I had Hashimoto’s prior to getting along Covid, and my Hashimoto’s antibody numbers have tripled (and keep rising)
did you get treated for Covid?
Wow.
Were you declared in remission prior contracting Covid?
@@Katie_purry02 I had a full blood panel done 2 weeks before I caught Covid. My TPO antibodies were at 65, which is the lowest they have been for me since diagnosed. After 2 years 3 months of Long Covid, my antibody levels are now at 74. (One month after having Covid my TPO was 248.)
Yes it does! After a mild covid case in April 2020, I have had Long Covid ever since. I tested positive in the mid range for Autoimmune disease. But the Pulmonary doc ruled out all known autoimmune diseases. So they don’t know what’s going on or how to fix me. 😣
Me too. It is like they don't care and have no clue how to fix anyone with long covid. Are you hanging in there? Cause the pain is horrible. People think we are all drama... but the pain... the pain is real.
@@someartlife01 I’m hanging in there there, thanks. My only symptom is shortness of breath. Feels like my chest is being constricted. It’s worse now when allergy season is here. You hang in there too!! 🙏🏻
Hi, I got covid for the 2nd time this year 24 Feb and got long covid - couldn't get out of bed (think I had a milder version of long covid after the first time, in retrospect). Crippling fatigue. Went on antihistamines - you need an H1 and H2 blocker, for me that is Loratadine and Famotadine, taking one AM and one PM. I am also taking nattokinase, serrapeptase, NAC and quercetin complex. Plus probiotics - have also recently added Kefir (apparently it has a greater range of probiotics than yoghurt) and have a little sauerkraut on a sandwich every day. Also taking a pile of vitamins! If you get a magnesium supplement, make it magnesium glycinate as this is the one the body absorbs well. For vitamin D - get vitamin D3 & K2. Go hard on B vitamins. I'm also doing a niacin flush (B3). Brand is Solgar (not all B3 will make you flush. I seemed to get better fairly rapidly after taking these supplements (still on everything) - don't know if it was any one thing, or the combination. Hope you can find the way out.
@@karenhensley3069 Hi, try antihistamines, H1 and H2 blocker, for me this is Loratadine and Famotidine. Also NAC will help enormously. Best wishes to you.
@@matronofmercia5891 I’ve taken all of that. I’m glad you are getting some relief though!
I'm forwarding the following msg to you that I put on a group I'm in
My anxiety amped up just thinking about sharing on here...😳😰...exhale and breathe....
Hi I'm Angel
I'm 61. I live in Gold Beach, Oregon USA. Itz a small coastal town on the Pacific Ocean. We moved here 2yrs ago. We, is my Furbaby dog, Brenna & me. She z my 💓 and the reason I'm still here.
I've been down in bed ill since October of last year. I got extremely stressed out and angry about a situation. And a migraine started. It was getting bad, I started getting nauseous. So I took my meds for migraine and nausea and went to bed. Ive been dealing with these since I was a kid. I know the drill well. Take the meds, get a Pepsi, go to bed, go to sleep and when I wake up the migraine and nausea will be gone.
I woke up the next day and I still had the migraine and nausea. And then All of my other health issues, activated flared up. IBS, Fibromyalgia, COPD, Lower Back Pain, The Bipolar and The Anxiety. January 2 this cough started and it was annoying, it got worse, I got cough drops and cough syrup.I started coughing really bad, the cough sounded really bad and I started having shortness of breath. And I'm like I think I have COVID. I went on line ordered COVID testing kits. They came did one of the tests...it was positive.
It was terrible. I would cough so hard that I couldn't breathe. I was scared that I would die and it would be days before anyone would know.
This is taking too long. I apologize. What I have is Long Vaxx Syndrome and Long COVID.
I AM DEPRESSED DISTRESSED!!!
If you haven't figured out by now that it's the jabs causing the autoimmune disease, then you haven't been paying attention.
Catching cvd after a jab can also potentially trigger it due to immune priming, in the same way the the subsequent jabs tend to trigger these conditions after initial priming by the first jab (more so than from the first jab itself).
Sure - it seems the more you keep irritating the immune system with repetitive stimuli, the more its tolerance breaks down.. But immune priming can occur through past infections aswel - are you, therefore, suggesting the immune priming from a vaccination route is essentially different from a past infection which sets people up for more complications?
@@drjamie_drjudith These aren't traditional vaccines. far from it - they're derived from gene therapy techniques, adapted to function vaguely 'like' a vaccine. The glaring difference with these fauxines is that the antigen (spike protein) is being produced within, and expressed by YOUR OWN CELLS ( it's been shown that the lipid nano particle encapsulated mRNA does indeed disperse throughout the body, and that the spike protein continues to be expressed for at least 9 months).
When the immune system subsequently encounters, and activates a response to spike protein (via vaccine or virus), your own cells expressing spike protein become a target, which in a nutshell, IS an autoimmune disease.
This was first shown by the Japanese biodistribution study performed on the pfi zer fauxxine prior to it being unleashed on humanity (study was leaked to the public around the time the fauxxine was rolled out.). It's also worth noting the the original design purpose of nano-lipid encapsulation was for the delivery of drugs across the blood-brain barrier, so besides evading the immune system, biodistribution is what this encapsulation technique does.
I also meant to mention in the previous comments, that the fauxxine only instructs the production of spike protein, without the nucleocapsid viral body, which contributes to later immune system misidentification (autoimmunity).
I can't post links in YT comments, as YT will just make the comment disappear.
@@boydw1 Thank you for sharing Boyd! The correlation of autoimmunity post-vax has been documented you're right, and we acknowledge that, but I do not think it is accurate to say that it is causing all the autoimmunity associated with long COVID. Cause is a strong word and we need way more research to confirm anything like that before broadcasting statements of that kind (out of self preservation). Plenty of unvaccinated have developed this aswel from infection. If, as you say, the vax trains the body to attack itself and thus induce autoimmunity, surely this is the same as the virus itself in that the bodies immune system learns to identify and attack our own cells which contain the virus? Hence through this mechanism, EBV and HSV-6 are well documented to trigger the onset of autoimmune conditions, without vaccines. Furthermore, the vax doesn’t primarily train our immune system to attack self antigens, it trains it to attack SARS-COV-2 spike antigen. The translation of this, to then a phenomenon of molecular mimicry and loss of tolerance of our immune system to start attacking our own cells, is a big step and one that is more complex.. But, it does happen, and we are equally interested to find out how, so again thank you for sharing!
@@drjamie_drjudith No, the immune identification is not the same for the fauxxine, as normal immune identification is not limited to spike proteins, but also includes recognition of the nucleocapsid viral body. With the fauxxine no nucleocapsid is produced.
I'd be highly skeptical of whether "long covid" exists AT ALL. It appears to be little more than a smokescreen for the deleterious immune impacts of the fauxxine (Note also the plethora of poor excuses that have been given for the rise in heart attacks & strokes).
While some degree of longer term impacts are not entirely uncommon from any flu, we need to bear in mind that for the vast majority, covid was not a serious illness, with typical symptoms ranging between "asymptomatic" & "ordinary flu".
The problems with mRNA technology were already obvious prior to covid, from the failure of previous animal trials, in which there was a preponderance of illness & death due to ADE (an autoimmune condition). Pfizer's own postmarketing data for the covid fauxxine lists 1291 side effects.
We also need to consider the impacts of Remdesivir - a drug twice previously rejected due to causing multiple organ failure in 20% of recipients.
Thank you for explaining this so well.
I got lots of weird symptoms post covid a few months ago and at first didnt know why, i was worried about stomach diseases & early cancers until burning sensations moved beyond the GI to other areas of my body and I recalled how after the first covid vaccine, i developed a temporary small fibre neuropathy with burning numbness and pins and needles in my feet that lasted a few months. This made me wonder if i was dealing with Long Covid, and an issue with the nervous system. I had to change to a smaller womens dr practice to get heard and get more than just complete blood test which was fine...my new clinic recently ran thyroid panel including thyroid antibodies and it was the thyroid antibodies that came up elevated, 116 or so and i was told they think its Hashimotos. But i have also had kidney issues with dull pain on & off, sometimes trace blood found in the samples and white blood cells and i saw protein one day a few times but the kidney function tests come up ok...but i am suspecting the possibility of more than one autoimmune disease now effecting me.
I think my immune system was activated so many times in quick succession, our family had like 3 or 4 back to back infections from kindergarten/and husbands work, I am 6 months postpartum so theres hormones there and stress, my diet probably wasnt amazing and now i can see all these things combined could have, with my reaction to the first vaccine, been the combination of triggering factors. I am however only 33, slim & healthy bmi, no pre existing condition, non smoker, barely drink etc so the long covid/autoimmune disorder was a surprise but hopefully i am able to make big improvements. I am looking into dietry adjustments and i continiously research.
sorry this might be a long read but your comment intrigued me because i’m dealing with something kinda similar.
wow watching all these videos about long covid and getting into reading comments from people dealing with symptoms they’ve never had before covid. i’m a 29yr old female who’s never had any health issues previously just the common ADHD since being younger. super active playing volleyball basketball softball my whole life and to this very day not unhealthy by any means. 1st time having covid i was in bed for two weeks straight couldn’t eat drink or get out of bed literally. my body hurt so bad and i sounded terrible with the cough i had. i caught it a few weeks after getting the vac (had to bc i worked in a nursing home) i’ve never experienced a feeling like that in my life, i thought i was gonna die. but anyways a couple months go by and all of a sudden i would have to drive an hour to my job (it was winter time during this time) and my hands and my feet would go completely numb a few minutes in, would tingle feel like needles, when i would get to my job it would take an hour just to get feeling back in my hands and feet even using a heater. just holding a cold drink my hands would tingle / go numb. this started happening every day, especially my feet. my toes can go numb just by walking on a semi cold floor. it’s absolutely annoying. then i started losing circulation quick mainly my legs but my arms also. i’ll wake up with numb limbs. i’ll squat down for a few seconds and lose feeling in my legs. oh sometimes there’s just a constant vibration in my one foot when i’m just laying there doing nothing. so the whole numbness tingling in hands and feet happen.. oh yeah another add on to this.. after getting it, a few months down the line i started getting sick literally every month with a horrible awful cough, atleast once a month for almost a year i was hacking, i ended up cracking a few ribs during this time and man they hurt like a bitch😩 couldn’t make sudden moves, reach my arms above my head, stretch or anything without immense pain. but anyways so randomly a few months after that i started having pain in my feet probably every other night or so. it feels like someone’s lighting my feet on fire from the inside. it’s not like burning on the outside on my skin it’s all inside. so burning and tingling while i try to sleep, sometimes super unbearable. lower back pain, (where i assume my kidneys are) it switches sides most times my right but it can switch to my left, random stabs of pain in the back of my thighs, feeling weak.. so remember all these symptoms. a couple months ago i was in bed and was not feeling right at all. (i decide to take myself to the hospital at 3 in the morning bc i started freaking out) all of those symptoms above were going on, the lower back pain was the worst i had, i would stand up to change clothes and felt like my legs were giving out on me, my vision couldn’t quite focus idk how to explain it, right below the knuckles, on all of my fingers were completely white like my circulation cut off, i kept feeling like i couldn’t catch my breathe and was feeling faint like i was going to pass out. so im at the ER, they give me meds to help calm me down, take my blood etc, they tell me i’m constipated…. with a side of raynaud’s disease LMAO. imagine hearing that all these months of dealing with pain and they tell you ohhh you’re constipated. i was livid. i had a feeling about having raynauds but that only explains my hands and feet. i ended up in the hospital again i think 3 days later and they told me im dealing with autoimmune diseases and need to follow up with a bunch of different doctors to test for autoimmune diseases, my blood vessels and something else. its been months and they are still trying to figure out what’s going on with me. its frustrating especially dealing with the pain in the bottom of my feet almost every night. the only thing that subsides the pain for a few is i’ve been wearing these gel socks and i throw them in the freezer and put them on at night.. but that only helps a quarter of the pain for so long.
have you gotten answers from doctors yet? i feel we kinda have similar symptoms going on
@bshawmeows sorry to hear you dealt with all that, yes so much of what you say sounds very familiar and I was initially passed around various Dr's who had no clue or my primary Dr who I never saw because she was busy with others but she'd update my test result file and replied to my email to say what i was saying was a "story" because the full blood count and general blood work was ok. I change drs practice and my new Dr ran the thyroid panel including TPO for thyroid auto antibodies which found the Hashimotos so it took a while but finally it was some validation that no it wasn't a "story" and something wa s going on. But hey even if I hasnt had that result finally, a Dr should never dismiss and should listen re symptoms as in Long Covid many sufferers never find anything observable in their bloods and tests and I see their comments and frustrations of how they have all this pain and suffering but nothing shows up as being wrong in their tests so they feel invisible. A good Dr would be educated on the huge spectrum that is Long Covid. You asked what Dr has done for me at this stage. After finding the autoimmune issue, they've testing my thyroid every 3 months I believe it is and monitoring. Not much else so I've taken control of my own health by researching and looking heavily into diet. I'm trying to follow a type of autoimmune protocol diet, more so a paelo diet and it looks like cutting out gluten is huge so I'm trying to holistically heal my body as best I can, and doing things like sauna and jogging. My vitamin d was very low so I was given 3 monthly tabs to take. I was after covid getting random BP spikes too which is unusual as my BP was always low side normal. I started taking methylation supplements after listening to a Joe Rogan podcast where the topic of BP was addressed. My BP began to settle back down to normal range.
Sounds like you've also had some coming and going type kidney pain at the back as well. This seems to have settled down for me but it does feel like symptoms flare up and flare down which makes me worry about Long Covid being autoimmune.
If Dr's at the hospital suggested multiple autoimmune, are they putting you onto specialists? I'm yet to be referred to a specialist, I think ideally it would be a referral to maybe an immuniologist or something.
All the best with recovery!
@@bshawmeowsand yes the burning and pins and needles sensations you describe I deal with too on and off. It's not as bad as it was initially but I worry this too is autoimmune and will have flare ups and false sense of security when it has settled cos some type of factor might make it flare up again like in my case this specific small fibre neuropathy happened right after my first covid inoculation. Burning feet, pins and needles and numbness which was chronic but after a few months it settled down and it eventually went away and for a few years things were fine on the surface until the most recent infection last year and all the burning pins and needles sensations came back which has again begun to settle down but I still get tingling up and down my back and the other week I randomly got lots of new pins and needles and numbness in my hands and fingers and it was actually quite painful making it hard to sleep. I'm not sure now if it's nerves or more or more a circulation issue. I'm noticing I get very easy piting and indentations on legs and feet.
I was watching some videos last night about Long covid with Dr's talking about how it's got something to do with mast cell activation and spike protein not leaving the system and the mast cells releasing all these cytokines and causing an over reaction. They were saying the goal needs to be to get spike out of the system but I'm not sure for myself what that involves and what I need to take supplement wise so I'll keep researching.
I did see an acupuncturist who randomly asked me if I had MS (another autoimmune) 😢I was like not that I know of but now I'm thinking is that the tingling pins and needles stuff. I know that lots if people online talk about these burning/pins and needles/numb type issues either post vaccine or post infection.
Please can someone tell me what blood tests do I need to ask the doctors for in order to prove that I have this. I have been told I have long covid. I am / was very fit and healthy. I have eaten a vegetarian-vegan diet for 20+ years. Pre covid I was hardly ever ill. Since it I am ill so much. I feel there is no help out there for me. Where do I look for support? I will do anything to not feel like this any more. I run my own business and am struggling to keep going due to dipping into illness so much.
Hi Charles - sorry to hear about how much you have been affected by this! There are investigations your doctor can do to screen for autoimmunity, however, in my experience many of those come back inconclusive for people - narrowing down and diagnosing autoimmune disease can be tricky due to the principles discussed in this video. There are private labs that can offer comprehensive panels which I discussed in a video specifically on testing which you can find on our channel. I would advise you to work with someone who can direct your on testing options and solutions rather than doing it yourself though as you could spend alot of money on tests which are not actually appropriate... A functional medicine practitioner is a good option - you may also reach out to us for support via the link in our channel bio if you would like to. Kind regards.
COVID vaccine gave me an autoimmune condition. I went from 205 lbs bench pressing 275 lbs to 140 lbs unable to walk after taking the vaccine
I always had skin psoriasis. I've got the jabs and was ok. But then, I've got covid. Skin psoriasis turned into psoriatic arthritis, spondility ankylosis, brain fog...
How about all the issues from the V?
Technically Rachael Maddow lied about it being what we used to call a "V". Check the patent holders on the "T's" Did they exist before the wet market "B's" ? Gain of function is proven, so was Ivermectin, so is and was censorship of the "Science."
Yes, autoimmunity can be triggered post vaccination.. Spike protein from vaccine or infection - they both trigger the immune system and in the right situation (as described in this video) can lead to an autoimmune phenomenon.. What we may/may not find out with time is whether there is a difference in the immune activity in reaction to either source of the spike protein - both post vax and post infection long haulers have very similar symptoms so it's not clear at the moment..
@@drjamie_drjudith However, aberrant or excessive production of pro-inflammatory cytokines is associated with uncontrolled local and systemic inflammation, resulting in cell death and often irreversible tissue damage.
infection has shown to cause cytokines, vaccines do not prevent infeciton or replication cycle and would not prevent cytokines, covid 19 is known to cause multi organ damage, known to cause cytokines, known to provoke a immune response and even asymptomatic infection still lands individuals with long term symptoms, so even asymptomatic disease with no symptoms provokes enough cytokines to cause significant damage.
@@drjamie_drjudith wouldn't it make sense for a controlled group then? The un V who have had COVID-19 compared to the V. We know so many people that are very sick all the time and also know people personally that have developed aggressive cancers and they are V. The medical community is not looking at both groups here and that raises serious questions.
I already fought Multiple Sclerosis. Nobody knew what COVID-19 would do to someone with MS. A very long bout of fatigue was to be expected according to my doctors. But then I got the vaccine and it was a repeat of the original infection but more intense and 2 years later I’m fighting all sorts of stuff. Fibromyalgia, possible POTS, blood pressure yo-yo, palpitations. My MS doctor said that those aren’t MS. I agree. But all of my other doctors want to blame MS.
Hey hi thank you for your message I am having such a struggle oh my God I can't I can't even believe this oh goodness yes I have been seeing my doctor and I saw her I think it was a month ago went in and when she had listened to my heart that time before she detected that there was my heart was like skipping beats so she had me where a heart monitor that was on my body that I wore for a week and it was like it's some little computer light situation and then when the week was up put it in the envelope and mail it to the lab and and they do the analysis of it and it showed that I have an arrhythmia. I I don't completely know all the information about that I haven't checked in about all of that and then my blood pressure absolutely was crazy as could be it's all over the place low extremely high and so she wanted to put me on a medication and and the migraine has been constant since October. it's just weird!!! she put me on another inhaler thinking that it was just my asthma acting up everything was just you know being absolutely crazy so in a way as it on one side it's good to know what is happening what's going on and there's also like I I don't want to be like this I want to be up I have things to do that I want to do! I can get from my bed to the bathroom and I'm absolutely exhausted and gasping for breath it's just absolutely insane absolutely insane I can't believe I absolutely was ADAMANT and I WAS NOT TAKING THE SHOT AT ALL!!! I got pressured to get the shot by a person in my life... I caved in and I got the shot and I got horribly horribly ill I was so ill from that shot so sick it was horrible absolutely horrible and I was like oh my God !!! I thought it's done over and then it came up that they were saying you had to get a booster shot and I was like there's no way I am not getting the booster!!! NO WAY IN HELL!!!…. once again I caved into pressure from someone and got the shot and again I was horrible absolutely horrible so ill.
sorry...but you are too easy to influence......do what your feelings tells you.
Can somebody recomend any cleanses they can do for toxins ect. Ive been on aip for a while but every now and again i will eat out and have a flare up because they cook everything in fucking rapeseed oil. I still have pain in my lungs every now and again, especially when ive been stressed with work. Love the way this guy delivers my nervous system feels super safe.
I’ve had Covid at least twice, possibly three times. I’ve not had a “vaccine “. Now I’ve had three bouts of painful, itchy splotchy breakouts.
The spike protein is also in the virus but at least you aren't getting shots over and over and getting the whole spike injected into you multiple times. Or have side effects from the shot.
Omg same
There is another source of the spike protein that should be considered.
The spike protein is the entire problem. Covid virus was just the transport vessel. The vaccine was the transport vessel, the damage and all the problems are caused by the spike proteins, why? Because it's man made it's not of this world. The body doesn't know how what to do. Plus they are so small they are damaging the mitochondria etc.. Detox and block the spike that is the key.
I have pericarditis. And I had pots. My pots has mostly resolved. Both are concerning to me since it involves my heart.
Ecg echo and crp levels are all ok.
Also my d dimer is high 612.
And I feel very breathless. 😭 unvaxxed 34 years old.
Sorry to hear about your current situation Carmella - that must be driving alot of anxiety for you! If we can be of any assistance, please do contact us via our website.
Try vinponcitine. & methel blue..
All the way from kenya 🇰🇪 Africa am experiencing heart palpitations and stomach issues,more so bloatin,constipation.Dizzines,joint pains and excessive farting
What can I do Doc
My head feels.like it is going to explode so woozy stomach pains headaches now black eyes sore eyes pressure in head sinus pain .had none of this before shots horrible 19months
Covid activated Narcolepsy in me. I have a normal sleep study that was done just 2 months prior to my first covid infection. Got covid/covid pneumonia and within 1 month could not stay awake in the daytime. 2 sleep studies later i have narcolepsy 2.
Sorry to hear about your situation!I did a video on sleep and Long COVID specifically if you search our channel - it focussed mainly on insomnia, but perhaps you can pull some useful things from it?
How do you detect autoimmune response to long covid with a test available in a typical clinical setting? All I got was an ANA blood test but I'm guessing that is not enough. I've suffered head compression and paresthesia on the LHS of my face since Sep 2021 and no doctor can tell me why or what's wrong with me. I do have elevated ctokines: IL-10, SCD40L, IFN_GAMMA, and VEGF. Maybe more, but those are the ones I have had tested that are elevated. Any of that point to autoimmunity? Is there anything in the literature that speaks to this?
Hi Brad. Yes, this is an unclear area right now in mainstream healthcare and will take some time for any specific diagnostic testing to be established in mainstream guidelines in relation to specifically Long COVID. I have seen a number of clients who have had ANA come back as negative or positive but not significant enough to be diagnostic for an autoimmune diagnosis so they are in this grey zone. It can commonly take time for that to happen as any potential autoimmune disease takes time to manifest in a clear way to then be placed in a diagnostic category.. Monitoring through a rheumatology department is part of that process, or Immunosciences Lab by Aristo Vojdani offers comprehensive autoimmune panels, but I would caution against ordering these without working with a practitioner/doctor to guide you on results etc. There are clearly things going on with your immune system and elevated cytokines indicate an inflammatory process, but this can happen independent of any autoimmune process. Whether that is related to the paraesthesia you are experiencing, it is hard to say. I would imagine you have had brain scans done for those symptoms, and so if they are clear for pathological causes, the problem usually relates to inflammation and more functional causes. Hope that helps, but please feel free to contact us via our website should you have any further questions.
However, aberrant or excessive production of pro-inflammatory cytokines is associated with uncontrolled local and systemic inflammation, resulting in cell death and often irreversible tissue damage
@@brianpancotto8829 I, too, am concerned about the downstream affects of uncontrolled inflammation, especially around the brain. This can't be good.
If you are vaccinated no doctor will tell you the truth.
After Covid vaccine my 8 year old got Alopecia Areata. Is there anyway we can reverse the condition or Covid vaccine mess from body?
for Alopecia check out Chinese medicine. My friend lost all of her hair on her head... so Chinese medicine 6 months later her hair is all back. It is grown back! Try to find herbs and Chinese medicine.
The video is very nice and explains a ton of information. But honestly, people just want a cure. But no one knows a cure. I want people to understand that those who are having long covid like me I am trying different supplements to try and help reduce the pain. Let me know what you have tried also. But here is a list of things that can help with the pain. Please try it out and let me know if it helped you also. Listen to your body as your body and you are the best doctors.
1. Heat Sauna or hot water with Epsom Salt Try to do it 2 or 4 times a week. Your skin may be sensitive so you might want to be extra careful with the Hot water bath with Epsom Salt 2 to 5 cups depending on your tub size and do it for 40 minutes. For Dry Sauna for those who are sensitive to water then 20 to 40 minutes. Do drink water and take breaks. 40 minutes is a long time in a sauna.
2. Supplements
1. Magnesium 100 mg - can help with muscle pain take low amounts and increase slowly
2. vitamin B1 100 mg - can help with energy production
3. CoQ10 60 mg - helps with energy production
4. Boswellia Root powder - helps with joint pain and inflammation
5. Ginger root - Can help reduce pain in muscles
If you are having trouble with Mood because of the pain such as Depression try the following.
1. CBD - you can get drops or a drink. Do not take much and test yourself on it. The CBD can reduce inflammation and help with the pain.
2. GABBA - helps with depression
3. Ashwagandha - helps with depression
3. Exercise - if you can do it good for you. If you can not. Try only 4 minutes and build up your strength. But listen to the body if you can't do it don't do it. Because if you overdo it you'll crash and can't get out of bed.
DIET CHANGES:
1. No bread or grain.
2. No sweets or candy or anything like it
3. No coffee
4. No beer
5. smoking
A diet that you can change to help with pain
1. KETO - veggies and meat
Try fasting 1 time a week for 12 to 14 hours.
I have tried so many drugs from the doctor and none of those drugs helped. Tried over 20 drugs and they made me sick. Maybe you can try drugs with Western medicine but honestly, they made me sicker.
Try Chinese Medicine to get better.
If you found a supplement or something that has helped you please let me know. because we need a cure for this and a way to get better. Sadly in my area, I am on my own. Doctors don't know and don't study it and most just do not care. If you have a nice doctor very good for you. Because I live in an area where they do not care if you die.
I had Covid once not vaccinated I admit it wasn’t pleasant however I had worse head colds
How do I fix it, reverse this
whole fooods is a good start heal the gut flora, Over Eating, Drinking stop smoking can trigger it more environmental Less Stress
Karen Kingston, DR.ANA MIHALCEA.
Were these people vaccinated?