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With your help, we can fund research to develop more treatment options and, ultimately, find a cure for fibrodysplasia ossificans progressiva (FOP).
FOP is one of the rarest, most disabling genetic conditions known to medicine. It causes bone to form in muscles, tendons, ligaments and other connective tissues. In people with FOP, bridges of extra bone develop across joints, progressively restricting movement and forming a second skeleton that imprisons them in bone. There are no other known examples in medicine of one normal organ system turning into another. The mission of the International Fibrodysplasia Ossificans Progressiva (FOP) Association (IFOPA) is to:
Learn more about the IFOPA here.
Learn more about the In Pursuit of a Cure Day of Giving here.
Thank you for investing in a more hopeful tomorrow for everyone impacted by FOP!
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