Spina Bifida Association

The Spina Bifida Association (SBA) is dedicated to building a better future for individuals affected by Spina Bifida through comprehensive research, advocacy, education, and support services. The organization provides essential resources and programs tailored to various audiences, including expectant parents, children, teenagers, and healthcare professionals. Their initiatives encompass educational offerings that connect families with medical experts and adults with Spina Bifida, ensuring critical knowledge is shared.

Advocacy efforts by the SBA focus on securing funding for essential programs, promoting disability rights, and ensuring access to affordable healthcare. In addition, the association is deeply involved in research, offering evidence-based guidelines for care and maintaining a national resource center that facilitates bilingual support and referrals. Through events like the Walk-N-Roll for Spina Bifida, community fundraisers, and volunteer opportunities, the SBA fosters a sense of community, encouraging participation and awareness.

Their unwavering commitment extends to enhancing the quality of life for all impacted by Spina Bifida