Dear Friends, Partners, and Supporters of the Cure Mito Foundation,
February is Rare Disease Month — a time to raise awareness, share stories, and shine a light on families affected by Leigh syndrome and other rare diseases. We invite you to follow us on social media throughout the month as we share patient stories, educational posts, and ways our community is making a difference.
This month, we highlight a new blog post detailing our journey to develop a SURF1 gene therapy — the first in a new series designed to make our research more accessible and understandable for our community.
You’ll also see how our community continues to show up with compassion — from dedicated family fundraisers to supporters making a difference in creative and meaningful ways.
You’ll find all the details in the sections below. Thank you for being part of our mission and for your continued support.
With gratitude,
The Cure Mito Foundation Team
