Peer-Reviewed Medical Research Program’s FY 24 Funding Opportunities for Researchers — Webinar
Dr. Kathryn Argue share tips for applying for PRMRP funding with Fragile X professionals.
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Dr. Kathryn Argue share tips for applying for PRMRP funding with Fragile X professionals.
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.
The NFXF has continually adapted to the times when it comes to the best ways to communicate with the Fragile X community.
Join the NFXF Greater Chicago Chapter for a Sensory-Friendly morning at Lincoln Park Zoo.
Join us for an informational webinar about funding opportunities for FY24 on April 10th at 12pm ET with the Program Manager for the Peer Reviewed Medical Research Program (PRMRP).
Announcing FY 2024 federal research funding opportunities across six award categories available for all Fragile X-associated conditions and disorders.
Are you an adult with a family member who has been diagnosed with Fragile X syndrome (FXS) or with the FXS premutation? Help us learn about your experiences with the FXS screening process. Researchers [...]
Join the NFXF Heartland - Iowa & South Dakota as they host the 9th Bike to X Out Charity Bike Ride.
Join us for the NFXF Webinar Series - 10 Basic Financial Steps for Special Needs Caregivers with Kelly Piacenti to help caregivers get started in preparing for the financial future of their loved one with Fragile X.
Thankfully, we’ve come a long way since the day when FXS was jokingly referred to as “Fragile WHATSyndrome?!” In the 1990’s, many changes were taking place as a result of the increased scientific study of Fragile X and how the growing body of knowledge was impacting the work of the Foundation.