Dennis's Experience as a Patient Access Manager (PAM)
When Dennis experienced his first episode of full-body paralysis at 14 years old, receiving a diagnosis of primary periodic paralysis (#PPP) didn’t surprise him. After all, his great-grandmother, grandfather, and father lived with the disease. What Dennis didn’t know was whether he would pass #PPP along to his children who never once presented symptoms.
With the close support and guidance of Xeris CareConnection™ and its Patient Access Managers (PAMs), Dennis’ choice to pursue #genetictesting would help him discover answers to questions he’s wondered about ever since his diagnosis.
Dennis’ journey and his commitment to giving back to the community through the Xeris PPP Mentor Connect Program, inspires us all. Hear how his experience with PPP and giving back to others has kept him going.
To learn more about Xeris CareConnection™ or to connect with someone like Dennis through the PPP Mentor Connect program, visit bit.ly/3WVwBJe
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#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.
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#PPA #NotFaking #paralyzed
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