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The Spina Bifida Association (SBA) serves adults and children who live with the challenges of Spina Bifida. Since 1973, SBA has been the only national voluntary health agency solely dedicated to enhancing the lives of those with Spina Bifida and those whose lives are touched by this challenging birth defect. Its tools are education, advocacy, research, and service. Through its network of chapters, SBA has a presence in more than 125 communities nationwide and touches thousands of people each year. Lives are changed by the programs SBA has created, the services the organization provides, and the accomplishments of its advocacy efforts. Understanding Through Education The quest for new information, the celebration of lives being lived to their fullest, and the unity of a community built on caring and compassion are embodied through SBA's National Conference held in June. SBA also supports all efforts to bring together leaders in health care and representatives of the Spina Bifida community. In 2003, a research agenda was defined at a ground breaking conference entitled "Evidence-Based Practice in Spina Bifida." This agenda is gaining momentum and yielding first fruits. Our Message of Hope and Prevention Nurturing Our Next Generation of Leaders If you are interested in supporting SBA in its efforts, please click here.
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