Community Impact
in FY19
%
Scientific Portfolio
%
Education & Support
%
Advocacy & Communications
%
Development
%
Administrative
2200 patients, parents and caregivers share data to advance treatments and therapies via the Mitochondrial Disease Community Registry
Enhancing the coordination of patient care across the country through the Mitochondrial Disease Care Network
$475,000 distributed in competitive research grants to fund the best science around the globe
Providing education for patient families, scientists and clinicians at the Mitochondrial Medicine International Symposium
$1,000,000+ invested in our Scientific Portfolio
Providing support through patient family meetings and a national network of more than 85 ambassadors