“The PAINFUL Truth About Living With Erythropoietic Protoporphyria”

Written By CAP/ACP

CAP on Rarely Discussed Podcast

CAP’s President, Michelle Capon, appeared on the Rarely Discussed podcast to discuss her journey with Erythropoietic Protoporphyria - or EPP. In her quest to find answers, she found community and a way to support other patients living with this rare disease.

CAP/ACP
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Porphyria Advocacy Around the World