For people suffering from Orthostatic Intolerance, Postural Orthostatic Tachycardia, Mast Cell Activtation or EDS. Follow me as I document my struggle towards better health.

Pens of Glory » The Race of Life

Here is an interesting creative post I found written by someone with POTS:

If you have a story you would like to share with other POTS or OI sufferers, please send me an email at  It's nice to know we're not alone!


  1. Hi,
    Thank you for making this blog- there aren't very many sites that I have found for understanding POTS- and of course- you probably know that most doctors and specialists aren't much help in that quest either!
    I'm hoping to follow your lead with Dr. Levine's physical therapy- (if I'm able!)
    Time will tell~

  2. Zoe-Very best of luck with the exercise protocol. It seems to be working for is TOUGH in the beginning. I find that I can do very little else except the treatment and sleep. But keep with it and I'm sure you'll start to feel better! :-)