It is looking like POTS at least is a common symptom for ME, Lyme. EDS and of course POTsies ......when people finally get accurately tested for it.
It seems POTS and its significance has been widely overlooked due to ignorance of it and correct testing procedures - again I read the other day of doctors leaving people on tilt tables see if they fainted and using that as a diagnostic method!!!
There is no need to faint to have POTS and a good diagnostician can often diagnose it on symptoms alone..
There are lists of good POTS docs on some fb pages or go to a POT page/s on and request a recommendation to one in your area.
And no - POTS is not cureable at the moment but there are treatment that work well for many people with it.
Ally
This is really interesting to me at this moment in time.
I am having very strange things happening, including completely collapsing and fainting. My heart scan looks good apparently and the Dr said about a tachycardia perhaps. Reading about POTS I wonder if maybe it has something to do with it perhaps.