Living with LPSVS (long post-COVID vaccination syndrome)
Has anyone experienced long-covid symptoms from the vaccines. I have been searching for 10 months now for the cause of my severe fatigue. I have been sent to an ENT, a cardiologist, a hematologist and undergone so many tests/scans. My doc told me a few days ago that he is stumped. No idea. Come back in a month. I pace myself to get through a day. Is this LPCVS? Is there something to do besides pace oneself? Should I ever get another covid vaccine?
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Have not found a doctor yet. On number 19
Adda b12 injection
Me too in and out
https://www.cureus.com/articles/127662-a-case-report-long-post-covid-vaccination-syndrome-during-the-eleven-months-after-the-third-moderna-dose#!/
I totally understand. I am one year after my last Covid shot. It has changed my life also. I too was very active. It is very frustrating when no one understands how it just sucks the life out of you! I am so glad to have people who understand on this support site
No
I too, am a vaccine victim. First Moderna shot just fine, second one 4 weeks later and within 24 hours I am a cripple now. That was in April 2021. I have lost my balance and unable to walk like normal people. I am utterly and totally dizzy all the time except when laying down. My eyes are blurry and watering and my sense of balance is in total disarray - everything is swaying and moving up and down unless I am sitting or laying still. On top of that I have to deal with the endless fatigue, brain fog, constant coughing so that I am close to needing treatment for GERD, and not being able to use my legs and my torso like I should when normal people walk. All I have left in my lower body is something like pudding that just flops around uselessly. And all that is because the second vaccine was so necessary to keep us healthy!! Yes, right!!! Thanks so very much .... ;-(
@www3 first, my apologies for taking too long to respond to your question. As many of us have experienced, we all stood in very long lines, waiting to see different specialists in our own home area. One of those specialists was able to connect me with Mayo Rochester after being rejected by Mayo, Jacksonville and Vanderbilt. Before going to Mayo was lucky enough to find a couple of medical professionals that had an idea about how to help me and those ideas involved acupuncture multiple supplements and cranial sacral treatments. These were all aimed at affecting the autonomic nervous system and calming it down. I had a tilt table test near home that showed some level of autonomic dysfunction, which is a clue in LC because LC affects the nervous system. I had so many different tests done at Mayo Rochester that included blood tests, a second tilt table test multiple interviews by doctors and other medical professionals and the only thing noteworthy was that the second tilt table test showed that my autonomic nervous system was back to normal the medical professionals there said that was a sign that my body was healing. What seemed like hundreds of different blood tests showed everything normal. Mayo was looking for markers that they were aware of that pointed to LC. My primary symptoms were exercise intolerance, brain fog, and post exertion malaise. The most noticeable symptom that I experienced soon after my first booster was a feeling of swaying, not so bad that I felt like I was going to trip and fall. In fact, I’ve never tripped and fallen, but just a rocking swing sensation.
More specifically to your question, mayo, set me up with months of virtual coaching with nurses and exercise people. I also took a course of Cymbalta and Naltrexone which have been shown to be helpful for LC sufferers. Through the home virtual coaching phase, I had access to medical professionals at Mayo Rochester to ask any questions that I had. To make the story short today I feel better, I would say I know how to manage the symptoms that still remain, and with time my symptoms seem to diminish. Now it’s been nearly 3 years since my first and last Moderna booster so we will see how things go from here. I will say that my body has deconditioned which I don’t like at all and I’m fighting like hell to get back in better shape. In order to keep symptoms at bay Mayo coaches, moderation of physical exertion, which has limited my exercise sessions to basically 15 minutes of cardio and resistance exercise three days a week where I used to do 60 minutes six days out of seven.
I refused to take any more boosters. I refused to take any vaccines for almost two years because I didn't trust them. Now, I make it a point to ask directly if a vaccine that they want to give me is traditional or mRNA.
Sorry for the late reply. I've only managed to get one week in the last 3 years where I was 95% functional over the last 3 years. I'm not sure what I did, but my attempts to recreate it have been unsuccessful.
I used to be more active too. I used to walk 4 miles a day, go hiking and scouting for new hunting spots. I was active in my local sports leagues. Now, I'm in the worst shape of my life and could probably give Gabriel Iglesias a run for his money for the Fluffy moniker. Any type of physical activity will trigger a massive flare of symptoms. The worst part of it is that I had to cancel a dream elk hunting trip in Colorado... I doubted that I could physically do it and live to tell the lies about my hunting prowess.
I've been struggling to keep my own advice and keep from asking the Oracle at Google about LPCVS... I will continue to adminently deny being a member of the "Tinfoil Hat Brigade", but when I went looking for answers to give me hope I was amazed at some of the theories out there. I usually take information on the internet with an ocean full of salt... but let's just say that I can understand why some people have started folding.