- Fragile X-associated Disorders
- Treatment & Intervention
- Public Policy & Legislative Advocacy
- Support the NFXF
Each week over the past month, we’ve shared a story with you representing the many families who have gained hope and inspiration through the NFXF. We hope you’re pleased to see the faces of but some of the families that you’ve helped out with your donations to the Annual Fund.
Thank you so much for donating, and also for spreading the word about our campaign!
Please share with on Facebook and Twitter or tell them to check out the videos online at annual.fragilex.org.
From the Forward Thinking video series
We’d never heard the word “Fragile X” until Elijah was 4 years old. Sara was 2 then, and her testing showed she has fragile X syndrome, too. (Daniel doesn’t.) We had to decide how and what to tell all our relatives. It took a while to figure out the best course of action. No matter who you are, you need something to hold onto. It tested our faith—and made us better people. Going to our first International Conference made a huge difference. To be with so many other families who shared so much with us really gave us hope. We’ll always be grateful to the National Fragile X Foundation for making it all happen. What the foundation does in advocacy and research funding not only helps kids with FXS, but it advances the whole disability field.