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.periodicparalysisnetwork.com .

Tuesday, October 21, 2014

Periodic Paralysis Awareness GoFundMe

Hello All,

We, at the Periodic Paralysis Network, Inc, would like to share our Periodic Paralysis Awareness Project. This is 'Invisible Disease Awareness Week' the perfect time to launch our fundraiser. Even if you cannot donate, please read about Periodic Paralysis and share this link with others. We need to share the facts and bring awareness to the world about this rare condition. Thank you.
http://www.gofundme.com/ftnr50

Until later...

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Living with Periodic Paralysis: The Blog

Serene Forest

Tuesday, October 21, 2014

Periodic Paralysis Awareness GoFundMe

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