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.periodicparalysisnetwork.com .
Serene Forest
Sunday, February 23, 2014
Over 150 Members Now!!!
I wanted to let everyone know
that the Periodic Paralysis Network (PPN) now has over 150 members!!!!
Congratulations to us all!!!! Thank you all for your support!!!!
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