After Janine and Kirsten were diagnosed with #PPP, they felt isolated not knowing where to turn for support. Connecting with others living with PPP was life-changing for them both.
When Janine attended our annual conference, she realized she had finally met “her people.” And when Kirsten talked to someone through the PPP Mentor Connect™ Program, she finally felt seen.
Hear Janine and Kirsten describe the value of attending our annual conference and the impact PPP Mentor Connect, established by Xeris Pharmaceuticals®, has had in their personal journeys.
To learn more about the PPP Mentor Connect program or to talk with someone like Janine or Kirsten, visit: bit.ly/3PfQlpw. #Sponsored
#PeriodicParalysis #TemporaryParalized #PPA
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 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
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.
________________________________________
Connect with us on social:
Facebook: / periodicparalysisassoc...
Instagram: / periodicparalysis
________________________________________
If you liked this video, please hit the like button, subscribe to our channel and hit the bell button to receive future videos.
#PPA #NotFaking #paralyzed
________________________________________
0:00 -