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Monthly Mito Expert Series

by kira@mitoaction.org
Join us on Friday, April 6, 2018 at Noon EST/9 a.m. PST as Dr. Richard Boles discusses "Spectrum Needs, a New Comprehensive Nutritional Therapy for Autism, Functional Conditions, and Mitochondrial Disease"  

 Talking points include:

Mar 23, 2018 Comments: 0
by Shawney7491
Top-line data expected by the end of 2018

Mar 06, 2018 Comments: 0
by admin

IRVING, Texas, March 01, 2018 (GLOBE NEWSWIRE) -- Reata Pharmaceuticals, Inc.

Mar 01, 2018 Comments: 0
by Shawney7491
Join us on Friday, March 2, 2018 at Noon EST/9 a.m. PST as Dr. Mary Kay Koenig discusses "The Evolution of Leigh Syndrome"

 Talking points include:

Understanding the history of Leigh SyndromeUnderstanding Leigh Syndrome, andCurrent treatment
Feb 20, 2018 Comments: 0
by admin

ATLANTA, January 8, 2018 -- The Foundation for Mitochondrial Medicine (FMM), MitoAction, the Mitochondrial Medicine Society (MMS) and the United Mitochondrial Disease Foundation (UMDF) collectively announce an important new initiative to create a Mitochondrial Care Network (Network).

Jan 08, 2018 Comments: 0
by GingerD
Join us on Friday, Feb. 9, 2018 at Noon EST/9 a.m. PST as Dr. Fran Kendall of VMP Genetics discusses "Is it really Mito? When an alternative diagnosis should be considered."

Talking points include:

Clinical red flags that suggest an alternative diagnosis should be considered;Why that option should be entertained;Tools utilized to reanalyze patients classified with mitochondrial disease.
Jan 06, 2018 Comments: 0
by GingerD
Angela Runs 4 JBI Run 4 buddy match turns into family

It started as a runner-buddy partnership through I Run 4 and grew into family.There was an instant connection. “We talk once a week through Facebook,” said Brooke Smith. “She’s like a part of our family.”Angela Messer runs for JB (short for Jeremiah Blake) Smith, a boy who has mitochondrial disease.

Dec 31, 2017 Comments: 0
by GingerD
‘She’s a gift to everyone who knows her’Ellie Kovalcik celebrates Sweet 16

Sweet 16. The Kovalcik family didn’t think they’d see this day. “Sixteen is a big deal, especially when we were told we’d lose [Ellie] between 7 and 8 years old,” said mom Kris. 

Dec 26, 2017 Comments: 0
by GingerD
Matthew Harty’s memory inspires donations

“There is no footprint too small to leave an imprint on this world.”Matthew Harty lost his battle with mitochondrial disease shortly after his 8th birthday in 2013, but he is still leaving an imprint today.“Matthew continues to make a difference,” said Angela Harty, Matthew’s grandma. “People still think about him. I feel like he’s not forgotten.”

Dec 15, 2017 Comments: 0
by GingerD
Matthew Harty Scholarship update: Erica Blanchette

Erica Blanchette was honored to be the first Matthew Harty Scholarship recipient. “I hope it inspires others with Mito,” she said at the time of the award in 2015. “This proves you can go to college and do other things that people never thought you could do."The daughter of Loree and Ralph Blanchette of Peabody, MA, has one year left on her early childhood degree from North Shore Community College in Danvers, MA.

Dec 15, 2017 Comments: 0

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