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 .
Read Our Stories ~ Meet Our Members
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Monday, October 27, 2014
300 Members!!!
Congratulations to us all at the PPN Support, Education and Advocacy Group!!! We now have over 300 members!!!!!!!! Thank you all for your support!!!
Our PPN Forum:
Please check out our PPN Members World Map: http://www.multiplottr.com/?map_id=55083
The following are the services and features of our PPN forum:
PPN Support, Education and Advocacy Group:
https://www.facebook.com/groups/periodicparalysisnetworksupportgroup/
PPN Website: www.periodicparalysisnetwork.com
PPN Book: "Living With Periodic Paralysis: The Mystery Unraveled"
(Found on our website)
PPN Blog: http://livingwithperiodicparalysis.blogspot.com/
PPN Book Discussion Group:
https://www.facebook.com/groups/periodicparalysisnetwork/
PPN Genealogy-Genetic Discussion Group:
https://www.facebook.com/groups/580168915344191/
PPN Website Facebook Page:
https://www.facebook.com/PeriodicParalysisNetwork
PPN Author's Page:
https://www.facebook.com/SusanQKnittleHunterauthor
Email: periodicparalysisnetwork@gmail.com
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