MitoAction
2024 Member
About MitoAction
MitoAction is a nonprofit organization founded by patients, parents, and Boston hospital healthcare leaders who had a vision of improving quality of life for children and adults with mitochondrial disease. The organization began in 2005 as an idea and has evolved from a small New England support group to a dynamic, active service organization helping thousands of patients and families. Despite the growth of the organization, the mission remains the same.
Related Rare Diseases:
- Pyruvate Dehydrogenase Complex Deficiency
- Primary Mitochondrial Myopathies
- Maternally Inherited Leigh Syndrome and NARP Syndrome
- Cytochrome C Oxidase Deficiency
- Short Chain Acyl CoA Dehydrogenase Deficiency
- Very Long Chain Acyl CoA Dehydrogenase Deficiency (LCAD)
- MERRF Syndrome
- MELAS Syndrome
- Mitochondrial Neurogastrointestinal Encephalopathy
- Pyruvate Carboxylase Deficiency
- Alpers Disease
- Medium Chain Acyl CoA Dehydrogenase Deficiency
- Leber Hereditary Optic Neuropathy
- Leigh Syndrome
- Kearns Sayre Syndrome
- Deficiencia de acil-CoA deshidrogenasa de cadena muy larga (LCAD)
