what we do
We fund research and provide comprehensive resources for the community, including a global patient registry for Leigh syndrome, an educational website AboutLeighSyndrome.com, Leigh syndrome healthcare providers directory, annual Leigh syndrome virtual symposium, family planning guide, support resources for patients, and opportunities for free genetic testing, among other initiatives.
MEET OUR KIDS
ABOUT LEIGh sYNDROME
AboutLeighSyndrome.com is a first of its kind informational website about Leigh syndrome with resources and support for both families and healthcare professionals.
RECENT NEWS
You can help advance research today.
Our Foundation’s effort to find a cure for Leigh syndrome and other mitochondrial diseases is accomplished by funding the efforts of doctors and researchers who share our passion and relentless drive to fight this devastating disease. 100% of your donations are tax-deductible and will go directly to research dedicated to mitochondrial diseases. Cure Mito Foundation is a 501(c)(3) nonprofit organization led by parents who volunteer their time to search for a cure.
We thank you for your support!