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.
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 .
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