FDMAS Alliance
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The FD/MAS Alliance, incorporated as the Fibrous Dysplasia Foundation, is the leading patient advocacy organization supporting individuals affected by fibrous dysplasia and McCune-Albright syndrome.
06/09/2026
is a NUMBERS game. If FD/MAS Alliance has taught me anything, it's that an ORGANIZED community can make a HUGE difference.
In past years, my goal has always been 100 supporters.
This year, we started late. We were focused on identifying our community's PRIORITIES for research and well-being advancments. We have a strategy and we have NO regrets about making time to focus on that.
NOW, we need you to show up and help us stand strong for Team FD/MAS.
Right now, we have 27 supporters. Will you help us reach 50?
A gift at any level counts. Let's work towards our priorities for research, advocacy, and education to support the communities vision of a future where everyone with FD/MAS can thrive!
www.tinyurl.com/teamfdmas2026
06/03/2026
It's ! Adaptive, stationary, imaginary, bedazzled--we love to see them all!
BUT right now we're MOST enthusiastic about Team FD/MAS and the Million Dollar Bike Ride! Bikes: Optional
You can also:
*walk (and chat with fellow team members)
*volunteer (to pass out race packets and snacks)
*DONATE to show your support for Team FD/MAS!
We now have 20 donors supporting Team FD/MAS and our work to advance research, advocacy, and education for the FD/MAS community. Will you help us get to 50?
www.tinyurl.com/teamfdmas2026
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Contact the organization
Website
Address
FD/MAS Alliance, 7315 Wisconsin Avenue Suite 400 W PMB 103
Bethesda, MD
20814
