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, the holiday season is almost here! 
 
As the crisp autumn air gives way to the chill of winter, we find ourselves in a season of transition - a time to reflect, prepare and embrace the warmth of community. The changing seasons remind us of resilience and renewal, much like the spirit of the MitoCommunity.
 
As the days grow shorter and the nights longer, we're here to share updates, resources and stories that inspire hope and keep us connected through the months ahead.
 
NEW - Mito in the Classroom for Educators!
 
MitoCanada has developed a suite of resources to help educators better understand the unique challenges faced by MitoStudents and create an informed, supportive learning environment that empowers them to thrive.
 
These resources include a teacher resource guide, an accommodations checklist, educational animations, teaching modules and more!
EXPLORE MITO IN THE CLASSROOM
 
Honouring Evan: A Legacy of Joy, Strength and Inspiration 
We are deeply grateful and thank the mitoCommunity for the outpouring of love and support for the Penny family following Evan's passing. 
 
Evan showed us the true meaning of living fully and finding joy even in life's most challenging time. Evan's legacy will always be woven into the fabric of MitoCanada, inspiring our mission to support and advance research for Canadians living with mitochondrial disease.⁠
REMEMBERING EVAN
 
Faces of Mito: A family bound by resilience in the shadow of mitochondrial disease
 
“I often think of my life in two parts,” says Jodi Young. “There was ‘before my mom got sick’ and then there’s everything after.”
 
For Jodi, childhood took an unexpected turn in 2008 when her mother, Brenda, a devoted nurse and parent, began experiencing a series of inexplicable health challenges at just 44 years old. A stroke, seizures, and a series of worsening symptoms led to a life changing diagnosis of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS), a rare and complex mitochondrial disease.
READ MORE ABOUT JODI YOUNG AND FAMILY
 
One Donation, Twice the Impact
This holiday season, your donation will be matched dollar-for-dollar by a generous supporter, doubling the impact of your generosity! Every dollar you give will go twice as far!
DOUBLE YOUR DONATION 
Make a Tribute Donation
Celebrate the life of a loved one this holiday season and help their memory live on. Or honour someone special by making a donation in their name.
 
MAKE A TRIBUTE DONATION
Start a Facebook Fundraiser today!
Facebook Fundraisers are a quick, impactful and powerful way to celebrate a special occasion or remember someone dear, all while raising funds and awareness for mitochondrial disease.
START A FACEBOOK FUNDRAISER
 
Mitochondrial Replacement Therapy (MRT) Survey
Have you heard about mitochondrial replacement therapy (MRT)? This groundbreaking IVF procedure offers families hope by reducing the risk of mito inheritance in children. While MRT is not yet available in Canada, it is being used in other countries.
 
We value your input! Take our quick 4-minute survey to share your thoughts and contribute to research that shapes and supports our community.
LEARN MORE AND TAKE THE SURVEY
Tisento Study | Teen MELAS Interview Study 
Our partners at Tisento are looking for teens aged 12-17 with MELAS to participate in an interview study to share their lived experiences with MELAS.  Together, we can contribute to the development of future treatements for MELAS.
 
Participants are asked to take part in two 45-minute interviews and can receive up to $150 for their time.
LEARN MORE ABOUT THE TISENTO STUDY
MitoCanada is Energizing Lives. Our foundation is dedicated to creating a world where all lives are powered by healthy mitochondria.