We have some BIG news to share!

Gift from LivJoy Foundation Funds Postdoctoral Fellowship at University of South Carolina  to Study Females with Fragile X Syndrome

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A NEW GRANT

ADVOCATE. SUPPORT. FUND.

Founded by a family of girls with Fragile X, The LivJoy Foundation is dedicated to finding and funding resources that enable girls with Fragile X Syndrome to live a life full of joy. We do so by financially supporting well-managed, high-performing organizations that align with our areas of focus.


WHAT WE DO

PARTNERS
& REsources

We aim to support medical research into treatments for females with Fragile X. More research is necessary to understand how this genetic disorder effects females from infancy through adulthood into old age. This includes fertility studies, an important area of advocacy.

Support for females with Fragile X needs to start early and continue throughout adulthood. The right school, camp, or social group can be life-changing for a girl with Fragile X. We identify and fund programs that add joy and normalcy to their lives—from meeting friends and trying new experiences to improving executive function and having access to new therapies.

Support Life-spanning SUPPORT Services

Fund Medical Research

Build Awareness & Advocacy

It is imperative that the world learns more about Fragile X in females, as many often go undiagnosed. In addition to increasing awareness of the disorder, we support organizations that advocate for and enable genetic testing at early ages.

OUR AREAS OF FOCUS

WHAT WE CARE ABOUT

OUR MISSION

The LivJoy Foundation’s mission is to find, fund, and share programs that enable girls with Fragile X Syndrome to live a life full of joy.


WHAT WE BELIEVE