Foundation for Mitochondrial Medicine

AA

A A
Foundation for Mitochondrial Medicine
7th of March 2018

The Thing About Loss

Share List The Thing About Loss Susan Schreer Davis, contributing writer and Voice of Hope for the mito community and all those seeking inspiration in their day-to-day lives. Follow along each week at www.hopeflies.org, and on social media. While perusing Facebook this morning, I read a post by a grieving mom. She lost her young […]

Read More

1st of March 2018

I Can’t Imagine

Susan Schreer Davis, contributing writer and Voice of Hope for the mito community and all those seeking inspiration in their day-to-day lives. Follow along each week at www.hopeflies.org, and on social media. “This one looks interesting,” my husband suggested. “Are you sure?” I asked, not wanting to waste time on the wrong movie. “I think […]

Read More

21st of February 2018

Hope Flies with Fashion on Rare Disease Day!

Share List Draper James Atlanta hosts FMM on Rare Disease Day Y’all, don’t miss this fun event for a great cause. Please join the Foundation for Mitochondrial Medicine on Wednesday, February 28, 11-2 at the new Draper James boutique at the Shops Around Lenox in Atlanta. Come check out southern style at its best created […]

Read More

20th of February 2018

The Great Big Why

Susan Schreer Davis, contributing writer and Voice of Hope for the mito community and all those seeking inspiration in their day-to-day lives. Follow along each week at www.hopeflies.org, and on social media. Share List The nurse sounded as uninterested as my sister at a football game, “You need the results of a recent EMG?” “Yes…” […]

Read More

26th of January 2018

#Give28on28 for Rare Disease Day – Learn More

via GIPHY What is #Give28on28? The Foundation for Mitochondrial Medicine launches its annual fundraising campaign #Give28on28 to mark Rare Disease Day. Our goal is to have each supporter have 28 friends donate $28 by February 28th. It’s easy to help and it’s all via social media. You can help by posting today and making posts throughout the […]

Read More

8th of January 2018

Mitochondrial Organizations Launch Pilot Phase of the Mitochondrial Care Network

Major mitochondrial disease organizations join forces to create Mitochondrial Care Network to improve standard of care for those with disease The Foundation for Mitochondrial Medicine (FMM), MitoAction, the Mitochondrial Medicine Society (MMS), and the United Mitochondrial Disease Foundation (UMDF) jointly unveil an revolutionary new initiative to create a Mitochondrial Care Network (Network). The priorities for […]

Read More

21st of December 2017

Hope Flies® with Gratitude for the Holidays

Hope Flies® with Gratitude for the Holidays During this holiday season, we reflect back on the year with gratitude for all of our volunteers, supporters, families and friends. Many thanks to each and every one of you for your contributions of time, energy and resources, helping us on our journey to raising awareness for mitochondrial […]

Read More

1st of October 2017

Hope Was Flying on September 22nd!

8th Annual Hope Flies Catch the Cure a Smashing Success Thank you to Hope Flies® Catch the Cure event co-chairs, Kyle Hinson and Anne Worrell and Committee Members, Caroline Chisholm, Mandi Coogle, Miller Jackson and Abby King for leading the way to another fantastic evening of friends, fun and fundraising for awareness and research for mitochondrial […]

Read More

18th of September 2017

Global Mitochondrial Disease Awareness Week 9/17

SHARE THE WAYS MITOCHONDRIA MATTER THIS WEEK September 17-23 is Global Mitochondrial Disease Awareness Week. Mitochondria are in every cell of our body, except red blood cells, and are tiny cellular powerhouses, essential for energy creation in organ systems, like brain, heart and muscles. Approximately 1 in 2,500 adults, teens and children are affected, making […]

Read More

24th of July 2017

UMDF, MitoAction, Foundation for Mitochondrial Medicine Statement Charlie Gard

July 28, 2017. Our heartfelt condolences to the family and friends of Charlie Gard. Rest in peace. July 24, 2017. The thoughts and prayers of the entire mitochondrial disease community are with Charlie Gard and his mother and father, Chris Gard and Connie Yates. They have decided to withdraw their request to have little Charlie […]

Read More

Stay Connected with FMM

  • This field is for validation purposes and should be left unchanged.
Translate »