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← Return to COVID vaccines and neuropathy
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I understand that everyone reacts to information differently, but I could not have navigated 14 months of vaccine injury without the information and support provided by the Neuro V Long-Haulers Facebook group. Just this week, a member posted a peer-reviewed Harvard study that was helpful in understanding my condition. My outstanding neurologist agrees the likely cause of my sudden sensory and motor polyneuropathy was the vaccines. There is a need for transparency about vaccine injuries on the part of the media, pharma, and government.
Replies to "I understand that everyone reacts to information differently, but I could not have navigated 14 months..."
I’m glad you found the Facebook group helpful. I found it to be full of fearmongering, politics, and crazy theories but it’s very possible I was “there” at a time when things were different. It’s unfortunate that we have to look for support groups and do our own research and can’t depend on our medical system to figure this out and help us. I have finally spent so much money and undergone so much mental anguish trying to figure things out with minimal interest or help from my physicians that I finally decided to just do the things I know are right and good for me and not even seek help for this anymore unless something new and/or more serious/debilitating occurs. I do not plan to ever again take a COVID vaccine if I can possibly avoid it. Best of luck to you!
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are you able to share that post here or the title? Good research is always valuable!
Sorry about the V/I btw.