Learn about FXTAS

The Rose Family

Welcome to FXTAS.org, the National Fragile X Foundation’s site for those of you affected by Fragile X-associated tremor/ataxia syndrome, your families, the professionals you work with and all others who want to learn more about this and the other Fragile X-associated Disorders. On the left side of your screen you’ll find menu items about FXTAS. On the right are menu items about the NFXF as well as links for additional learning and ways to become involved. As you travel about this website, trying to learn everything you can about FXTAS, we encourage you to take your time. Slowly but surely Fragile X, and its many variations in disorders and symptoms, will begin to make sense. Whatever your situation, though, please don’t hesitate to contact us. We’re here to help. You’re not alone.

Robert M. Miller
Executive Director
National Fragile X Foundation

p.s. If you have any difficuty using a mouse to navigate this site, please use the “How to Navigate” link below for instructions on mouse-free navigation.