About us:
The Rare Bone Disease Alliance is a new organization which works to educate physicians, expand research on rare bone disease and assist rare bone disease patients, patient organizations, and family members
The Alliance encourages professional, medical, and scientific societies to expand their educational programs on rare bone disease and will organize its own meetings and workshops.
The Alliance is built on the progress and success of The Rare Bone Disease Patient Network (RBDPN), a coalition of patient organizations which was founded in 2006.
Alliance participants include rare bone disease physician and scientific leaders, patient organizations, and pharmaceutical companies working in the rare bone field.