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Published on Jan 29, 2020
The annual IFOPA Family Gathering is a chance for those living with FOP, families, caregivers, and experts to learn about the latest in research, meet with experts and connect with each other.
The International FOP Association is a 501c3 non-profit organization supporting medical research, education, and communication for those afflicted by the rare genetic condition Fibrodysplasia ossificans progressiva (FOP).