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"Earth-shattering."
That's how Nicole George described the news that her twin daughters, Scarlett & Kendall, had THG1L disorder, a mitochondrial disease that heavily disrupts energy production to the brain and muscles.
They're just one of the thousands of families that depend upon UMDF to support affected families, educate clinicians, advocate on Capitol Hill for mito-friendly legislation, and fund world-class research that will help unlock future treatments and cures.
Your donation today will help to ensure that our mission moves forward.
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About UMDF
For over 25 years, United Mitochondrial Disease Foundation has worked to promote research and education for the diagnosis, treatment and cure of mitochondrial disorders while supporting affected individuals and families. We are driven by a nationwide community of ambassadors solely focused on supporting patients and families affected by mitochondrial disease. Together, we are committed and energized to make a difference by funding the best science no matter where it is found in the world and providing critical programs and services to the patient families we serve.
UMDF's Mission
Promote research and education for the diagnosis, treatment and cure of mitochondrial disorders and to provide support to affected individuals and families.