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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.
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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.
