International Fibrodysplasia Ossificans Progressiva Association (IFOPA)

The International FOP Association is a 501(c)(3) non-profit organization supporting medical research, education and communication for those afflicted by the rare genetic condition Fibrodysplasia Ossificans Progressiva (FOP). Our mission is to fund research to find a cure for FOP while supporting individuals and their families through education, public awareness and advocacy. Our vision is a cure for FOP.