posted
Anyone have any articles on POTS and lyme? I know many of us have POTS, but I can't find any articles to give my neurologist. Any info would be helpful. Thanks
Posts: 561 | From eastcoast | Registered: Aug 2006
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WildCondor
Unregistered
posted
DO a search on here for NMH or Neurally Mediated Hypotension, it will provide you with all the old posts and links...
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posted
I did- there were just anecdotal stories-no articles. I need some "scientific proof" for my neurologist.
Posts: 561 | From eastcoast | Registered: Aug 2006
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posted
If your neurologist is giving you a hard time, you may need to find a new one. I've been to 4 different neuros in my time, and only one had a clue about how much Lyme can freak out your nervous system. None of the others were helpful in understanding my vertigo either.
So, if your neuro is uninformed and not interested in learning/researching more, be cautious about staying with someone who can lend a bad attitude to your care.
Posts: 168 | From Delaware | Registered: Aug 2005
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