Rare Disease Advocate Shares Family Story | A Rare Adventure EP 06

This is Teresa. She has Hypokalemic Periodic Paralysis, a rare disease that renders a person paralyzed for long episodes of time for a variety of different reasons. She tells how she has adapted to her rare disease over the years as well as other topics on her blog at https://findingyourself.blog/

#Advocate #PeriodicParalysis #ARareAdventure

Periodic Paralysis is an extremely rare disease and you may have a lot of questions, a great resource to help find answers can be found at the PPA website at https://www.periodicparalysis.org

We'd love to hear from you. Comment below on your experience with PP or with questions about the condition.

You can also donate at
https://www.periodicparalysis.org/donate
Your donation will help with Dr. Cannon's genetic research or a list of other extremely helpful options. The great thing is you can decide how you want your donation to be used.

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Instagram:   / periodicparalysis  

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#DayInTheLife #MyLife #misdiagnosed #diagnosed #PPA #PeriodicParalysisAssociation #NotFaking #paralyzed #PPAttack #PPA #PMC #HypoPP #HyperPP #RareDisease

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