National Fragile X Foundation

Start Fundraising

Approximately 100,000 individuals in the United States have fragile X syndrome, many of them undiagnosed.
More than 1 million people have or are at risk of developing a Fragile X-associated Disorder.


The National Fragile X Foundation supports and connects families affected by Fragile X, providing educational and emotional support, promoting public and professional awareness, and advancing research toward improved treatments and a cure for Fragile X.

What is Fragile X?

  • fragile X syndrome (FXS), the most common cause of inherited intellectual disability; it causes behavioral disorders and speech and language delays that manifest in early childhood.
  • fragile X-associated tremor/ataxia syndrome (FXTAS), an adult onset neurological disorder causing tremors, balance and memory problems, and cognitive decline.
  • fragile X-associated primary ovarian insufficiency (FXPOI), a condition that causes irregular menstrual cycles, infertility, and premature menopause in females of reproductive age.

The NFXF needs your help!

Help us carry out our wide-reaching mission by raising money through your own personal fundraising page!

For more information about supporting the NFXF, contact fundraising@fragilex.org

 

We cannot do this work without the support of generous donors. Thank you for taking the time to make a big difference for those affected by Fragile X!

 

 

Just click the "Get Started" button at the top of this page. It's fast, easy, and totally secure!