Read Lynda Rogers personal journey with Fragile X Syndrome.
February 22nd, 2020
8th Annual Fragile X Symposium
February 24th & 25th, 2020
National Advocacy Day, Washington D.C.
April 18th, 2020
8th TXFX Fragile X Awareness Walk
July 16th - 19th, 2020
National Fragile X Conference, Orlando, FL
July 25th or 26th or August 1st, 2020
December 12th, 2020
Christmas Event - TBD
February 20th, 2021
9th Annual Fragile X Symposium
We are here for you to answer questions or just to listen.
Click here for our email addresses or fill out the form to send us a note.
Our mission is to provide resources and guidance to families affected by Fragile X Syndrome. Increase awareness of Fragile X Syndrome in the community. Organize family activities, support meetings and educational programs. Promote research and treatment of Fragile X.
501(c)3 Non-Profit Organization
The Texas Fragile X Association is a 501(c)3 non-profit charitable and educational organization serving the Dallas Fort Worth Metroplex.
Fragile X syndrome (FXS) is a genetic condition that causes intellectual disability, behavioral and learning challenges, and various physical characteristics. As many as 1 in 130 women are carriers of the Fragile X mutation. Estimates vary and studies are ongoing.
Fragile X Syndrome is the leading known genetic cause of autism. Among the total population of those with autism, approximately 2-6% are diagnosed with Fragile X Syndrome as the underlying genetic cause. Approximately two thirds of all children with Fragile X Syndrome also have autism, an autism spectrum disorder or behaviors associated with autism.
Over one-million Americans carry a Fragile X mutation or are at risk for developing, a Fragile X-associated Disorder, including FXTAS (Fragile X-Associated Tremor Ataxis Syndrome) and FXPOI (Fragile X-Associated Primary Ovarian Insufficiency).
Over 100,000 Americans have Fragile X Syndrome, making FXS the leading cause of inherited intellectual disability.
Read Becky Cox Fragile X Story.