<H1> Let’s give Fragile X a voice. </H1> |
<H1> </H1> |
<H1> For more information and support </H1> |
<H1> Mailing Address </H1> |
<H1> DONATE NOW </H1> |
<H2> FRAGILE X FOUNDATION OF CANADA </H2> |
<H2> Mission: </H2> |
<H2> Transforming the lives of individuals with Fragile X, their families, and the networks of professionals who serve them. We are a volunteer-based organization that facilitates community education, awareness and advocacy, as well as basic and clinical research into treatments of Fragile X and it’s related conditions. </H2> |
<H2> Vision: </H2> |
<H2> A world where Fragile X is recognized and supported in all aspects of health and social care, with effective and accessible treatments. </H2> |
<H2> COLLABORATIVE RESEARCH FUNDING </H2> |
<H2> The Fragile X research Foundation of Canada recognizes the exponential impact of building partnerships around the world. In collaboration with FRAXA Research Foundation we are thrilled to share that Dr. Raymond Turner and Dr. Xiaoquin Zhan have been awarded a $100,000 research grant to continue to develop a ground breaking approach to treat Fragile X syndrome. </H2> |
<H2> </H2> |
<H2> Xpressions Newsletter </H2> |
<H2> In each issue, you will find articles, stories and information for and about the Fragile X Research Foundation’s research, members, families and friends. </H2> |
<H2> Click here for the summer 2023 issue </H2> |
<H2> </H2> |
<H2> Click here for the Spring 2023 issue </H2> |
<H2> </H2> |
<H2> Click here for the Winter 2023 issue </H2> |
<H3> info@fragilexcanada.ca </H3> |
<H3> 777 Tapscott RoadScarborough Ontario M1X 1A2 </H3> |
<H3> Thank you for choosing to donate to our Foundation. </H3> |
<H4> Transforming the lives of individuals with Fragile X, their families, and the networks of professionals who serve them.We are a volunteer-based organization that facilitates and supports community education, awareness and advocacy, as well as basic and clinical research into treatments of Fragile X and it’s related conditions. </H4> |
<H6> – A community comes together to raise awareness </H6> |
<H6> – Fragile X-Associated Primary Ovarian Insufficiency I FXPOI </H6> |
<H6> – Discovering the prevalence of the FX gene in the Jewish population </H6> |
<H6> – How an X-traordinary family raised awareness through a golf tournament </H6> |
<H6> – The unique challenges for females with Fragile X syndrome </H6> |
<H6> – Researcher Spotlight </H6> |
<H6> – Metformin trials for individuals with Fragile X syndrome </H6> |
<H6> – X-traordinary people </H6> |
<H6> – Toolbox trips and tricks </H6> |
Social
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Cost and overhead previously rendered this semi-public form of communication unfeasible.
But advances in social networking technology from 2004-2010 has made broader concepts of sharing possible.