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Also did you have dysautonomia issues after Lyme or it's co-infections or was it after? Has treatment helped with dysautonomia or the infections symptoms? Has treatment helped with breathing issues if you had them? Thanks!
Just curious to see if there's any sort of link here. I know it was mentioned in another thread that someone's neurologist said they weren't any more likely to develop Parkinson's than any other person. BUT I can't help but wonder as my grandfather had and died from Parkinson's, and I also have tremors from time to time. Both of my grandparents on my father's side had dementia in their final years as well. Since I had the tremors starting in my teen years, I had intentionally skipped any careers (surgery) which required fine dexterity just in case it struck me.
I was just recently diagnosed with POTS, and in the process of starting my career. I am finding it hard to keep up with the duties of my job and chosen career choice. I would like to know if it is possible for people with POTS to have successful active careers, either by sheer will, and/or by proper treatment? Thank you for your time.