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Spina Bifida Association of America (SBAA)

Spina Bifida Association of America (SBAA) was founded to address the specific needs of the spina bifida community and serves as the national representative of more than 70 chapters nationwide. SBAA comprises individuals with spina bifida, family members, parents, professionals, and interested members of the general public. Its mission is to promote the prevention of spina bifida and to enhance the lives of all individuals and families affected by spina bifida. Services include an information and referral service, conferences and educational symposia, a scholarship fund, public awareness campaigns, a research fund, and individual & systems advocacy. Publications include SBAA brochures, guidebooks, videos, a bimonthly newsletter, and a biweekly legislative update. Information at the website, www.sbaa.org, provides information for health care professionals on how to help women reduce their risk of having a child with spina bifida.
http://www.sbaa.org


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NICHCY thanks our Project Officer, Dr. Judy L. Shanley, at the Office of Special Education Programs (OSEP), U.S. Department of Education.

Publication of this Web resource page is made possible through Cooperative Agreement #H326N030003 between the Academy for Educational Development and the Office of Special Education Programs of the U.S. Department of Education. The contents of this document do not necessarily reflect the views or policies of the Department of Education, nor does mention of trade names, commercial products, or organizations imply endorsement by the U.S. Government.

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