Fibrous Dysplasia Foundation (FDF)
The Fibrous Dysplasia Foundation (FDF) is a community-led nonprofit that fights back against fibrous dysplasia, McCune-Albright syndrome (FD/MAS), and related rare bone diseases. FDF serves people affected by FD/MAS through programs of research, education, and advocacy. FDF will create a better future for people living with FD/MAS by sponsoring efforts to find an effective treatment, improving education on how to manage FD/MAS, and building a strong network of patients, families, researchers and clinicians.
Condition Awareness & Advocacy
Here is a list of conditions this partner raises awareness and advocacy for: