UMDF/MitoAction – Voice of the Pyruvate Dehydrogenase Complex Deficiency (PDCD) FDA Listening Session

The U.S. Food and Drug Administration (FDA) has just confirmed a virtual FDA listening session, co-hosted by the United Mitochondrial Disease Foundation and MitoAction, focused on Pyruvate Dehydrogenase Complex Deficiency (PDCD). The session, The Voice of the Pyruvate Dehydrogenase Complex Deficiency (PDCD) Patient Community, will be held virtually on Friday, September 8, 2023 from 1:00pm to 2:30pm ET. FDA listening sessions […]

Energy for Life Walk: Indianapolis

Coxhall Gardens Children's Pavilion 11677 Towne Road, Carmel, IN

Energy for Life Walkathon: Indianapolis 2023   When: September 9, 2023 Where: Coxhall Gardens Children's Pavilion 11677 Towne Road | Carmel, IN 46032 Contact: events@umdf.org Schedule of Events 10:00 am - Walk Registration 11:00 am - Opening Ceremony 11:15 am - Walk Starts Register Today Register today Donate now Register to walk with us by […]

Energy for Life Walk: Chicago

Katherine Legge Memorial Park 5901 County Line Road, Hinsdale, IL, United States

Energy for Life Walkathon: Chicago 2023   When: September 10, 2023 Where: Katherine Legge Memorial Park 5901 S County Line Road | Hinsdale, IL 60521 Contact: events@umdf.org Schedule of Events 9:00 am - Walk Registration, Music, & Activities! 10:00 am - Opening Ceremony 10:30 am - Walk Starts 11:30 am - Picnic and Closing Ceremony […]

Energy for Life Walk: Delaware Valley

Pennington Park 801 Creek Road, Delanco, New Jersey

Energy for Life Walkathon: Delaware Valley 2023   When: September 10, 2023 Where: Pennington Park 801 Creek Road | Delanco, NJ 08075 Contact: jordan.rogers@umdf.org Schedule of Events 10:30 am - Walk Registration 11:30 am - Opening Ceremony 12:00 pm - 1 Mile Walk Starts Register Today Register today Donate now Register to walk with us […]

TK2d Awareness Day

Join us as we mark the second global TK2d Awareness Day. Thymidine kinase 2 deficiency (TK2d) is a rare genetic mitochondrial disease that causes muscle issues often severely impacting a patient's motor skills, breathing, and eating. TK2d is caused by inherited mutations in TK2, a nuclear gene responsible for making a mitochondrial enzyme called thymidine […]