Spina Bifida

Youth and parents’ experiences of a new inter-agency transition model for spina bifida compared to youth who did not take part in the model

Sally Lindsay, Ph.D., Melissa Fellin, Ph.D., Heather Cruickshank, B.A., Amy McPherson, Ph.D., Joanne Maxwell, M.Sc. Disability and Health Journal, Volume 9, Issue 4 Published online: May 27, 2016 DOI: http://dx.doi.org/10.1016/j.dhjo.2016.05.009 Background Young adults with spina bifida are underserved in health care and are at risk as they transition to adult health care. A pediatric rehabilitation hospital and […]

Read More »»