Foundation for Mitochondrial Medicine

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Foundation for Mitochondrial Medicine
21st of December 2018

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Five weeks have passed since my back fusion. While my legs seem far more stable than before, my ankles swell like baseballs by day’s end. Ice packs might help, but since I just noticed the problem a few days ago, I haven’t opened my freezer yet. So, when friends ask if the surgery helped, I […]

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1st of November 2018

Mitochondrial Disease Advocacy Groups Launch Mitochondrial Care Network (MCN)

ATLANTA, October 30, 2018 – The Foundation for Mitochondrial Medicine, MitoAction, the United Mitochondrial Disease Foundation, and the Mitochondrial Medicine Society announce the formation of a first-of-its-kind Mitochondrial Care Network. The goals of this collaborative effort on behalf of patient advocacy groups and the Mitochondrial Medicine Society include formally unifying clinicians who provide medical care to […]

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20th of February 2017

#give28on28 stories – Jason

Stand with FMM in support of Rare Disease Day (Feb. 28), an international advocacy day to bring widespread recognition of rare diseases as a global health challenge. Share stories and #give28on28    

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#give28on28 stories – Lauren

Stand with FMM in support of Rare Disease Day (Feb. 28), an international advocacy day to bring widespread recognition of rare diseases as a global health challenge. Share stories and #give28on28 Mitochondrial disease is an energy production problem that primarily affects the muscular and neurological systems. A cure for mitochondrial disease could impact cures for […]

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#give28on28 stories – Chi Omega University of Georgia Chapter

Stand with FMM in support of Rare Disease Day (Feb. 28), an international advocacy day to bring widespread recognition of rare diseases as a global health challenge. Share stories and #give28on28 Mitochondrial disease is an energy production problem that primarily affects the muscular and neurological systems. A cure for mitochondrial disease could impact cures for […]

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19th of February 2017

#give28on28 stories – Caroline

Stand with FMM in support of Rare Disease Day (Feb. 28), an international advocacy day to bring widespread recognition of rare diseases as a global health challenge. Share stories and #give28on28

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18th of February 2017

#give28on28 stories – Abby

Stand with FMM in support of Rare Disease Day (Feb. 28), an international advocacy day to bring widespread recognition of rare diseases as a global health challenge. Share stories and #give28on28 If you live  near the Brood Brook, Connecticut area, check out the 2017 Walk for Abby! Click here for more info.       […]

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#give28on28 stories – Michaela

Stand with FMM in support of Rare Disease Day (Feb. 28), an international advocacy day to bring widespread recognition of rare diseases as a global health challenge. Share stories and #give28on28

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17th of February 2017

#give28on28 stories – Sheila

Stand with FMM in support of Rare Disease Day (Feb. 28), an international advocacy day to bring widespread recognition of rare diseases as a global health challenge. Share stories and #give28on28

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16th of February 2017

#give28on28 stories – Audrey

Stand with FMM in support of Rare Disease Day (Feb. 28), an international advocacy day to bring widespread recognition of rare diseases as a global health challenge. Share stories and #give28on28  

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