About Us
The Mission of the Spina Bifida Association is to build a better and bright future for all those impacted by Spina Bifida.
The Spina Bifida Association (SBA), founded in 1973, is the only national voluntary health agency solely dedicated to serving people affected by Spina Bifida.
SBA Chapters and clinics serve more than 125 communities nationwide. SBA touches thousands of people each year through research, clinical care, education and support, network building, and advocacy.
What We Do
We are committed to serving the Spina Bifida community through our five pillars
Research, Clinical Care, Education and Support, Network Building, and Advocacy
Staff, Board, and Leadership
Meet our staff, our Advisory Councils, and our Board of Directors
We dedicate our time and energy to supporting the mission of the Spina Bifida Association.
SBA History
Read about SBA's rich history.
Since its early days, the Spina Bifida Association has devoted itself to responding to the needs of those whose lives have been touched by Spina Bifida, the most frequently-occurring, permanently disabling birth defect that is compatible with life in the United States.
Governance and Policies
SBA holds itself accountable to its donors, volunteers, people with Spina Bifida and their families, and the public. Learn about our governance and policies.
Reports and Financials
Learn about our accomplishments in research, education, advocacy, community support and fundraising.
