Lol. I just find it very weird that I got them after treatment..My heart is really effected and thats my only symptom.
Thanks for the replies
-------------------- [IM] Posts: 64 | From Calgary | Registered: Jun 2010
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POTS is Lyme, no doubt. If it isn't Lyme then it's one of the Co's.
I had a variant of it. My BP didn't drop, but my HR would go from 60 to 160 from sitting to standing.
This was at it's worse before treatment. Much much better now. Still taking a beta blocker as I havn't got it all yet, but I can tell you that I have been treating Lyme and Bart only, so it has to be one of those.
Getting ready for Babs now....
Sad thing is that there is a Dysautonomia site called POTS Place, or something like that where the folks there all talk about their POTS, and they are all doing "bandaid" treatments such as salt, hydration, and some other things, but they don't know they have Lyme.
I tried to tell them a while back, but they all told me they were tested for Lyme and were negative. A few though did listen to me and came back thanking me as they tested pos.
I tried to tell them about the bad testing, etc., but they got tired of hearing me and I got booted.
I tried :-)
BTW, FYI, there is a Hopkins pediatrician treating POTS with Minocycline and getting results. I read an article on this a while back. I guess in a few centuries or so, the other Dr.'s will catch on.