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The Osteogenesis Imperfecta (OI) Foundation is the only voluntary national health organization dedicated to helping people cope with the problems associated with osteogenesis imperfecta (OI). The Foundation's mission is to improve the quality of life for people affected by OI through research to find treatments and a cure, education, awareness, and mutual support.
Osteogenesis imperfecta is a genetic bone disorder characterized by fragile bones that break easily. Compared to healthy bone, the bones of a child or adult with OI are like chalk. Changing a diaper or putting on a T-shirt can cause a fracture. Your support will help the OI Foundation respond to more than 6,000 inquiries each year, produce new information resources, fund research, and facilitate the operation of support groups across the country
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