Our Mission
Read Lynda Rogers personal journey with Fragile X Syndrome.
Donations Welcomed!
February 25th & 26th, 2019
National Fragile X Advocacy Day - D.C.
April 27th, 2019
7th Annual TXFX Awareness Walk
July 20th, 2019
13th Annual Splash Day
September 2019
8th Annual Fragile X Symposium
October 12th or 26th, 2019
12th Annual Fall Festival
December 7th or 8th, 2019
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.
Personal Story
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.
Upcoming Events
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.