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

Happiness is not worrying about POTS & OI

Hi Folks
Yes, it has been quite some time since I last posted on this blog.  My apologies to those of you who thought I had some terrible relapse and so was incapable of writing.  I have, in fact, been feeling very well.  Since undertaking Dr. Levine's exercise protocol I have been gradually improving to the point where I feel (mostly) completely normal.  Since about 3 weeks ago I have been able to put in a full day's work.

So how have I been spending my time?  Primarily on a charity fundraiser to raise money for military wounded and their families. I am pleased that this black-tie event for 400 people and $200 a plate is now sold out.  Yay!

As Dinner Chair for the event I will have to say a few words of thanks to all of the people who have made the dinner a success.  I only hope that the adrenalin rush of speaking in front of such a crowd does not cause me to faint. has been known to happen.  I don't do adrenaline very well which I am sure other persons suffering from POTS can relate to.

I do intend to continue my writing on this blog and I thank you for reading...I hope you find it useful, amusing, annoying or at least something.  Stay tuned for more Yellow Wiggle adventures as I WILL follow up on Greg's offer to be interviewed!