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Issue title: Spina Bifida, Part 1
Article type: Research Article
Authors: Walker, Jr., William O.
Affiliations: University of Washington School of Medicine, Seattle, WA, USA
Note: [] Address for correspondence: William O. Walker, Jr. MD, Division of Genetics and Developmental Medicine, Seattle Children's Hospital (M/S A-7938), 4800 Sandpoint Way NE, Seattle, WA 98105, USA. Tel.: +1 206 987 3664; Fax: +1 206 987 3824; E-mail: [email protected]
Abstract: The contributions of primary care providers to the successful care of children with spina bifida cannot be underestimated. Overcoming systemic barriers to their integration into a comprehensive care system is essential. By providing routine and disability specific care through the structure of a Medical Home, they are often the first line resource and support for individuals and their families. The Medical Home model encourages primary care providers to facilitate discussions on topics as varied as education and employment. Knowledge of specific medical issues unique to this population allows the primary care provider to complement the efforts of other specialty clinics and providers in often neglected areas such as sexual health, obesity and latex sensitization. As individuals with spina bifida live into adulthood, and access to traditional multidisciplinary care models evolves, these skills will take on increasing importance within the scope of providing comprehensive and coordinated care.
Keywords: Spina bifida, medical home, children with special health care needs, disability
Journal: Journal of Pediatric Rehabilitation Medicine, vol. 1, no. 4, pp. 337-344, 2008
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