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: 

Resources & Support

Connect With The Fibrous Dysplasia Foundation

Patient Worthy Posts on Fibrous Dysplasia

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