Support FMM this Holiday Season
Please Support FMM this holiday Season FMM’s mission is to accelerate the development of the most promising treatments and cures for the many forms of mitochondrial disease. As we continue our quest to fund cures and fuel connections, we thank our friends and supporters who make it all possible. Every donation – large or small […]Read More
Mitochondrial Myopathy Clinical Trial teleconference
12/6/2016 teleconference discussion of data from Stealth BioTherapeutics’ Mitochondrial Myopathy clinical trial. This summer, Stealth BioTherapeutics (Stealth BT) shared preliminary positive data from the MMPOWER study. The study purpose was to evaluate safety and efficacy of elamipretide (previously known as Bendavia) in adults with primary mitochondrial myopathy and genetically confirmed mitochondrial disease. Mitochondrial myopathy is primarily […]Read More
Alzheimer’s Drug Discovery Foundation and Foundation for Mitochondrial Medicine Partner to Support Novel Research for Mitochondrial-Directed Therapies
Research could lead to development of new therapies to treat a variety of mitochondrial diseases, including Autism, Alzheimer’s, Parkinson’s and Lou Gehrig’s disease ATLANTA and NEW YORK, February 26, 2014 – The Alzheimer’s Drug Discovery Foundation (ADDF) and the Foundation for Mitochondrial Medicine (FMM) announced today that they have awarded $200,000 in funding to James […]Read More
Planning to Run the Peachtree Road Race in Atlanta?
This year make your accomplishment something more by becoming a Hope Flies Athlete! In addition to helping raise funds and awareness for mitochondrial disease, you’ll have the opportunity to participate in Group Training Runs with elite athletes from the Atlanta Women’s Marathon League, including the winner of the 2013 Publix Marathon, Jill Horst. Group runs […]Read More
FMM Celebrates Newest Atlanta Braves Player, Kyle Wren!
Kudos to Kyle Wren, who was recently drafted to play baseball for the Atlanta Braves! As the son of FMM board member Frank Wren and the brother of FMM ambassador Colby Wren, Kyle is an integral part of the FMM team, and we are so very proud of his success. Best of luck to Kyle […]Read More
2012 Annual Report
On behalf of our Board of Directors, and the 1 in 2,500 affected by mitochondrial disease, we thank those who continue to support the Foundation for Mitochondrial Medicine. 2012 was filled with much success including research progress, 4 new regional fundraising and awareness events, the launch of our new Hope Flies Health Series and more. […]Read More
Become An All-Inclusive Multi-Event Hope Flies Partner
Hope Flies is the Foundation for Mitochondrial Medicine’s (FMM’s) signature fundraising program dedicated to celebrating hope and raising significant funds and awareness for the most promising mitochondrial disease research and treatments. Hope Flies fundraising events are held in various locations across the country and come in different shapes and sizes. Becoming an All-Inclusive Multi-Event Hope […]Read More