IFOPA

About the International FOP Association

The International FOP Association (IFOPA) was founded in 1988 by Jeannie Peeper, who sought to connect individuals affected by fibrodysplasia ossificans progressiva (FOP). This organization has become a vital resource for FOP families, offering advocacy, education, and support.

Impact of IFOPA

Through its programs, the IFOPA provides hope and essential resources to individuals and families impacted by FOP, while actively funding research aimed at finding a cure.

Why Donate?

Your contributions are crucial in funding research for new treatment options and ultimately discovering a cure for FOP. Every dollar raised directly supports scientific advancements and pain management strategies.

Join the Fight Against FOP

Support the mission of the IFOPA by donating cryptocurrency or cash today. Together, we can make a difference in the lives of those affected by this rare condition.