Spring into Action and Celebrate 15 Years of MitoCanada!
Spring is a time of renewal, energy, and new beginnings – and this year is even more special as we celebrate 15 years of fuelling hope and empowering the mitoCommunity across Canada!
To mark this milestone, we’ve been sharing 15 Stories for 15 Years – featuring inspiring voices from beneficiaries, volunteers, and donors who have shaped our journey. We’re deeply grateful to everyone who has made our work possible!
In this Spring edition of MitoNews, we’re excited to launch our 2025 mitoScholars program, showcase a new Community Corner feature, and celebrate the launch of our new French website!
There’s no shortage of events and initiatives taking place this year. Join us as we step into spring with excitement and momentum – and energize lives together!
Empowering Futures! Apply now for the 2025 mitoScholars Program!
At MitoCanada, we believe every student living with mitochondrial disease (mito) deserves the opportunity to pursue the education and, ultimately, the careers they dream of. That’s why we’re excited to announce that applications are now open for the 2025 mitoScholars Program!
Since 2022, our mitoScholars program has been helping Canadian students living with mito – and those with a parent or sibling affected – overcome the unique hurdles they may encounter in their educational journey. Our scholarships help ease financial barriers, allowing students to focus on their studies and future goals.
This year, we’re proud to award three scholarships to young adults living with mito. The application portal is open now and will close on Monday, June 30, 2025, at 11:59 pm.
Apply today and take the next step toward your future!
Community Corner: Adam’s Story
What does it mean to live with mitochondrial disease?
For Adam and his family, it meant navigating the unknown, facing challenges with resilience, and finding joy in the everyday moments. Diagnosed with Leigh syndrome at age three, Adam defied expectations, embracing life with quiet determination. Now 29, he continues to carve his path, proving that a diagnosis does not define a person.
Read his inspiring journey, shared by his mother, Alison, and discover the power of perseverance, connection and hope.
Expanding Access: Our French Website is Live!
We’re thrilled to announce that our French website officially launched on Friday, February 28th — Rare Disease Day!
This milestone reflects our commitment to inclusivity and accessibility, making it easier for more Canadians to access the support and information they need.
2025 Education Events
MitoCanada is proud to connect you with the latest educational events hosted by a variety of health organizations – designed to support Canadians living with rare disorders, including mitochondrial disease.
Explore our curated list of online education events taking place in 2025 – available in both English and French!
Share Your Thoughts on MitoTransplantation
MitoAction and MitoCanada are teaming up to keep patient voices front and center as mitochondrial science evolves.
Our new article explores mitochondrial transplantation, its challenges and its potential.
Read the article and share your thoughts in our quick survey. Your input will help shape the conversation.
Become a mitoAmbassador!
At MitoCanada, we share a bold vision: a world free from mitochondrial disease. Our mitoAmbassadors are essential in turning that vision into reality. As passionate volunteers, they raise awareness, build local connections, and inspire change in their communities.
If you’re driven to make a difference, we invite you to apply and join this incredible network. Applications open April 7!
