Read Lynda Rogers personal journey with Fragile X Syndrome.
March 5th & 6th, 2018
National Fragile X Advocacy Day - D.C.
April 21st, 2018
6th Annual TXFX Awareness Walk
June 23rd, 2018
12th Annual Splash Day
July 11th - 15th, 2018
16th International Fragile X Conference
September 22th, 2018
7th Annual Fragile X Symposium
October 6th, 2018
11th Annual Fall Festival
December 1st, 2018
(Date to be confirmed soon)
TXFX North Pole Express Train Ride
More Event Info
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.