Meet Our Donors
Our donors and fundraisers are dedicated and inspiring members of the community who are committed to ensuring that the National Fragile X Foundation is here to provide unwavering support to Fragile X families now and into the future. They know that life with Fragile X is often unexpected and sometimes incredibly challenging. They support our advocacy, awareness, and research programs, as well as our ability to provide timely educational resources and dedicated community support services that help Fragile X families each and every day.
Fishing for a Cure: The Christoffs Have Done it Again!
The annual Fishing for a Cure fundraiser, hosted by Joey Christoff in honor of his son Mitchell, was another great success in 2024! Check out the big fish and the big smiles.
Hope for the Future – Adult Resources
Learn how we are equipping families with resources needed to plan for the future with confidence, while we continue to work towards treatments for Fragile X.
The Bridges
The Bridges support the National Fragile X Foundation because of the life-changing opportunities they discovered for their daughter Caroline.
The Stedkes
For Kerry Stedke, creating awareness about Fragile X and becoming an advocate for individuals with intellectual disabilities is critically important.
Hope for the Future – Expanding Clinical Care
Learn how we are expanding our network of Fragile X clinics to better support individuals living with the Fragile X premutation.
Messages of Gratitude — Video
When we take a moment to reflect on what means the most to us in this season of gratitude and joy, the Fragile X community tops the list.
The Heymans
Gail and her husband Lyons have been supporters of the NFXF since 2005 when she helped host the NFXF International Conference in Atlanta.
The Sarups
Jordan Sarup is 12 years old and has Fragile X syndrome. Meet a family who goes the extra mile to help their son — and every child living with Fragile X.
The Souders
Anne discovered the NFXF early in her quest for support for her family after her son Alec was diagnosed with Fragile X syndrome at age four.
The Silvers
The NFXF was there at the beginning of their Fragile X journey, and the Silvers want to ensure it’s there for everyone’s journey.
Hope for the Future – NFXF Belonging Grant
Our NFXF Belonging Grant is already making an impact. Learn how we're expanding this program to reach even more families impacted by Fragile X!
Hope for the Future – Find Our People — Video Slideshow
We're on a mission to find and support EVERY family living with Fragile X
Marner Family Hosts 5th Annual Quad Cities Fragile X Golf Outing
The annual QC Fragile X golf outing, hosted by the Marner family, has been an incredibly inspiring demonstration of support. Thank you Andrea and Kevin - and your many supporters over the past five years!
Our 2024 NFXF Awardees
Our 2024 NFXF awards are in! Learn more about each award and the respective awardees.
The Greater Chicago Fragile X Families Raise Awareness at the Brookfield Zoo Tree Trim
The Greater Chicago Fragile X chapter families gathered on a sunny day in November to support the Brookfield Zoo and its annual Tree Trim event, and to raise awareness for Fragile X families everywhere.
Making Waves for Fragile X: The 7th Annual Fishing for a Cure Fundraiser
The annual Fishing for a Cure fundraiser, hosted by Joey Christoff in honor of his son Mitchell, was another great success in 2023! Check out the big fish and the big smiles.
Image (featured) by wagnercvilela from Pixabay