viggster
Senior Member
- Messages
- 464
I am pretty sure I have POTS/NMH but it has not been formally diagnosed (CFS/ME has been diagnosed by two specialists). I'm wondering if anyone has gone to Vanderbilt, and if so, was it useful? Did you end up with treatments for your POTS/NMH that were helpful? It seems like they really try to isolate the problem.
http://www.mc.vanderbilt.edu/root/vumc.php?site=adc
http://www.mc.vanderbilt.edu/root/vumc.php?site=adc