The FD/MAS Alliance

The FD/MAS Alliance (incorporated as the Fibrous Dysplasia Foundation) is a community-driven 501c3 nonprofit that fosters the development of evidence-based treatments for Fibrous Dysplasia and McCune-Albright syndrome (FD/MAS). We advance research, provide education and channel the voices of individuals and caregivers with FD/MAS.

Our Vision

• To ensure that individuals with FD/MAS receive the best possible treatments for their many challenges.
• To accelerate the discovery of cutting-edge treatments—and ultimately, a cure for FD/MAS—over the next 5-15 years.
• Together, we can realize this vision and create a future where everyone affected by FD/MAS can thrive.

What We Do

• Foster the development of improved, evidence-based treatments for FD/MAS by advancing research
• Provide education
• Channel the voices of individuals with FD/MAS and their caregivers