Living with Periodic Paralysis: The Blog

This blog was created and designed to educate the world about Periodic Paralysis a rare, inherited, hard to diagnose, debilitating and cruel mineral metabolic disorder. I have two variants of this condition and my life is filled with constant challenges as I attempt to manage my symptoms to stay alive. My husband and I are co-founders of the Periodic Paralysis Network, Inc. This blog is an extension of our educational and support network at www.periodicparalysisnetworkinc.com .

Showing posts with label Rare Disease Day Photo. Show all posts

Tuesday, March 1, 2016

Rare Disease Day Photo

We wanted to share our observation of Rare Disease Day by sharing a picture of us with our new Periodic Paralysis Awareness T-shirts!!
Thank you all for your support!!!
Calvin and Susan Hunter Co-Founders, Co-Creators and C-Managers of Periodic Paralysis Network.

Serene Forest

Tuesday, March 1, 2016

Rare Disease Day Photo