Meet Ryan
“I hope I can connect with somebody and give them information about a new clinical trial or to just give them an idea that there are people out...
Read: Meet Ryan“I hope I can connect with somebody and give them information about a new clinical trial or to just give them an idea that there are people out...
Read: Meet Ryan“We cannot control or predict the future, but we can control how we react. Take this time to appreciate the people in your little world...
Read: Meet Jennifer CoxEditor’s note: Jagger passed away from mitochondrial disease on April 20, 2024, with his family by his side. We turned to UMDF Associate...
Read: Meet JaggerWesley Slimp of Marietta, GA, has been interested in cars and racing for as long as he can remember and now it has become his passion. “I...
Read: Meet Wesley SlimpCole Salerno was just a few days old when his mom, Victoria, felt something was wrong. He wasn’t eating well, he was suffering from GI issues,...
Read: Meet Cole Salerno“UMDF has been a light in our life. They have supported my family in so many ways and have offered so much hope to me and to thousands of mito...
Read: Meet Hayley“It was that sense of accomplishment that has carried me to where I am today.” Charles ‘Chaz’ Davis remembers March 3, 2013 vividly. The...
Read: Meet Chaz Davis: Living With LHONIn honor of National Blindness Awareness Month, we feature LHON patient Joe McCormick. Joe was looking toward a bright future. While in high...
Read: Meet Joe McCormick, Jr.Every Wednesday night, you will find eight year old Harper Johnson in her seat at the Davis Arena in Louisville, KY. While she loves dance and...
Read: Putting Mitochondrial Disease Down for the CountLora Lacey was in her senior year of high school when she suffered a viral infection that affected her muscles. At the time, her mitochondrial...
Read: They’ve Been Walking for 20 Years