Insights on Access from the Rare Disease Community
Released Thursday, 12th October 2023
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Insights on Access from the Rare Disease Community
Insights on Access from the Rare Disease Community
Thursday, 12th October 2023
Good episode? Give it some love!
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IFOPA Podcast Series
The International Fibrodysplasia Ossificans Progressiva (FOP) Association (IFOPA) serves families living with the ultra-rare genetic disease fibrodysplasia ossificans progressiva, as well as researchers and health care providers studying and treating this disease. The IFOPA is a US-based nonprofit organization whose mission is to fund research to find a cure for FOP while supporting, connecting and advocating for individuals with FOP and their families, and raising awareness worldwide. You can find us online at ifopa.org.Join Podchaser to...
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