Provides parents of children with Fragile X syndrome, believed to be the genetic cause of mental retardation, with information on diagnosis, education, daily care, and related legal issues.

About the Author

Jayne Dixon Weber is the parent of two children; the oldest is an eleven-year-old who has fragile X syndrome. She is an advocate in her community and the author of Transitioning "Special" Children (1994). She and her family live in Boulder, Colorado.

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