Join us in making a difference! In our community, there are always people we can help. Ataxia Canada – Claude-St-Jean Foundation is a community of people of all ages, genders, and origins affected by a hundred forms of ataxia. The ATAXIA CHALLENGE will take place on Sunday, August 16th, 2026 in...
Dear member, You are cordially invited to attend the annual general meeting of Ataxia Canada-Claude St-Jean Foundation, which will be held on Sunday, December 7, 2025, via videoconference. In addition to being the governing body, this meeting is an opportunity for you to learn about the Association’s financial results, its...
Register and participate in the webinar this Thursday Unlock Expert Insights on Friedreich Ataxia exploring how FA affects the heart Register Now! Date: Thursday, October 2nd, 2025 Friedreich Ataxia (FA) doesn’t just affect movement, it also impacts the heart. We’d like for you to join us for an informative webinar exploring...
Join Us in Making a Difference! Purchase your tickets and donate to support those living with ataxia. Your generosity directly impacts their lives, bringing hope and funding research and programs! We are thrilled to invite you to our inaugural pickleball tournament, a fundraising event dedicated to supporting the Ataxia Canada Foundation’s...
Dear members, You are cordially invited to the annual general meeting of Ataxie Canada-Fondation Claude St-Jean, which will be held on Sunday, December 1st, 2024 by video conference. In addition to being the governing body, this meeting is an opportunity for you to learn about the financial results of the...
Join us for an unforgettable day dedicated to making a lasting impact. On September 7th , we’re gathering at Central Park in Burnaby to raise crucial funds for those affected by ataxia A Day of Impact, A Day to come together For a few years now, the metro Vancouver Ataxia...
Together, Manon, Trine and I share the hope of a treatment for present and future generations! Although we have no doubts about the research in progress, our mission for the moment is to make family, friends and colleagues aware of the rare Friedreich Ataxia’s disease.