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The National Fragile X Foundation is a 501(c)3 tax-exempt organization (Tax ID# 84-0960471), and your donation is tax deductible within the guidelines of U.S. law. Please keep your receipt as your official record. We'll email it to you upon successful completion of your donation.

Fishing for a Cure 2026

SEGMENT 1: October 17-21, 2026
SEGMENT 2: October 21-25, 2026 

Your gift today helps raise awareness, speed up diagnoses, and support life-changing research for Fragile X syndrome and the Fragile X premutation.

How your gift at every level
makes an impact beginning today.

The Randi

A gift of $5,000 helps advance research and improve treatments for individuals living with Fragile X syndrome and Fragile X-associated conditions.
 
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The Mouse

A gift of $3,000 helps bolster future generations of Fragile X professionals through support of younger researchers and clinicians.
 
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The Tracy

A gift of $2,000 helps launch virtual peer-to-peer support groups for caregivers of individuals living with Fragile X syndrome and FXTAS.
 
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Team Hagerman

A gift of $1,500 provides scholarships to help send first-time attendees to the NFXF International Conference.
 
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The Craig

A gift of $1,200 helps support NFXF Advocates on Capitol Hill to share their story with their member of Congress, to help secure funding for research.
 
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The Liz

A gift of $1,000 helps expand our consortium of clinics that specialize in treating Fragile X syndrome and the Fragile X premutation
 
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The Linda and Natalie

A gift of $967.24 honors the amount Mitchell's sister Natalie raised in 2018 from a lemonade stand, cookie sales, and a Facebook fundraiser. Way to go Natalie!
 
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The Hilary

A gift of $500 provides valuable, on-demand educational content for families living with Fragile X across their lifespan, as well as the professionals who strive to serve them throughout their lifetime
 
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The Jay

A gift of $250 helps support NFXF Advocates on Capitol Hill to share their stories with their Members of Congress, to help secure legislation and funding for Fragile X research.
 
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Mrs. Rogers

A gift of $100 helps grow resources for Self-Advocates, like our new animated video series, "I Have Fragile X".
 
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Miller Time

A gift of $75 helps expand our clinical network serving individuals with FXTAS, through our partnership with the National Ataxia Foundation.
 
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The Solomon

A gift of $50 helps guide a newly diagnosed family like Solomon's - with knowledge, resources, tools and hope.
 
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“We finally recieved a diagnosis to explain our son's developmental delays — and with that knowledge came hope.”
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National Fragile X Foundation
1012 14th Street NW, Suite 500
Washington, DC 20005
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