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Our Mission:

Advocate. Educate. Empower.

Connecting families and sharing information on research, therapies, and care for Bardet Biedl Syndrome.

 
 
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Family Resources

The Bardet Biedl Syndrome Foundation and Family Association is dedicated to improving the lives of individuals and families affected by BBS. Our mission is to provide a community of support for individuals and families; information about BBS; and promote science and research to improve the lives of individuals with Bardet Biedl Syndrome.

Learn More

 
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Stay Up to Date

Sign up with your email address to receive news and updates on how
to get involved and the latest research.

 
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Our Impact to Support Research & Advocacy.

Great strides have been made toward improving the lives of families affected by Bardet Biedl Syndrome through information, support and by advancing research and therapy in the last decade. The syndrome is accurately and promptly diagnosed much more often; the genetics of the syndrome have been deeply explored; and progress is being made in understanding the molecular basis of symptoms and in possible treatment for retinal degeneration.

12+

Years Serving the BBS Community

We are proud to serve our community to make a daily impact on the lives of those affected by Bardet Biedl Syndrome.

$680K+

Raised

Over the past five years, the Bardet Biedl Syndrome Family Association has raised over $681,000 to further research into treatment and care for people affected by BBS as well as education and outreach to families, physicians and educators.

$425K+

Given

through grants to support Bardet Biedl Syndrome research.
 
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Make a Donation

 Donations to the Bardet Biedl Syndrome Foundation will support research into treatment and care for people affected by
BBS as well as education and outreach to families, physicians, and educators.

 
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