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The vision of the AMDF is to cure mitochondrial disease. Its mission is to fund mitochondrial disease research, provide support to sufferes of mitochondrial disease and their families, and to educate the general public and medical profession regarding mitochondrial disease.
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THE CHILDREN'S MITOCHONDRIAL DISEASE NETWORK | UK C/EMDN is a registered charity in the UK dedicated to providing information and support for all mitochondrial disorders.
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Energy4All is commited to find a cure for energy metabolism disorders through funding research. Energy4All supports people who are affected by energy metabolism disorders by sharing knowledge and organizes carefreedays for patients.
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FOUNDATION FOR MITOCHONDRIAL MEDICINE | USA The mission of the Foundation for Mitochondrial Medicine is to support the development of the most promising research and treatments of the many forms of mitochondrial disease. We’re funding a path to the cure, making connections to other related diseases and leading our stakeholders to the best answers.
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INTERNATIONAL MITO PATIENTS | International IMP’s mission is to increase quality of life for people with mitochondrial disease by facilitating cross-border cooperation and collaboration among national patients’ organisations. In order to achieve this we have national patient organisations involved in mitochondrial disease as members; from Belgium, France, Germany, the Netherlands, the United Kingdom and the United States.
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The Lily Foundation is committed to finding a cure for Mitochondrial Disease and other metabolic disorders through funding research and providing support to those involved and affected by metabolic disorders.
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The mission of MitoAction is to improve quality of life today for all adults, children and families affected by mitochondrial disease through support, education and advocacy initiatives.
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Our mission is to promote research and education for the diagnosis, treatment and cure of mitochondrial disorders and to provide support to affected individuals and families.
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Förderschwerpunkt für seltene Erkrankungen des Bundesministeriums für Bildung und Forschung.
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The aim of NZMito is to raise the profile of mitochondrial disease, and support those affected. NZMito also aims to raise funds to enable further research.
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Our mission is to promote research and education for the diagnosis, treatment and cure of mitochondrial disorders and to provide support to affected individuals and families.
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We welcome the participation from other mitochondrial disease related organizations around the world. Help us raise the profile of this debilitating disease. To get involved, please contact us.
