Neuromuscular Disease Foundation’s Dr. Kelly Crowe Presented with $20,000 Research Grant from Uplifting Athletes Rachel Leib2023-01-14T20:09:34-08:00January 14, 2023|
NDF’s Secret Weapon in Raising GNEM Awareness Is a Team of Motivated Young Professionals Who Are Leading the Way to A Healthier Tomorrow Through Genetic Screening Advocacy Rachel Leib2022-11-30T16:46:53-08:00November 30, 2022|
Accessibility: Where are we still falling short? Where can accommodations for disabled persons be improved? Rachel Leib2022-11-23T08:34:13-08:00November 20, 2022|
The Beverly Hills Rotary Club Renewed its Support of The Neuromuscular Disease Foundation Rachel Leib2022-10-14T05:26:07-07:00October 13, 2022|
Rich Horgan Talks Gene Therapy, How He Feels about Egos in the Lab, and Guiding NDF to the Head of the Pack in Developing a Cure for GNEM Rachel Leib2022-10-12T08:38:56-07:00October 11, 2022|
NDF’s Research Program (IGTDP) Moves Closer to a Cure for GNE Myopathy (GNEM) Rachel Leib2022-09-12T10:47:14-07:00September 9, 2022|
Family Planning? Have You Considered Genetic Screening? Rachel Leib2022-09-09T15:58:01-07:00August 22, 2022|
Life with GNEM: Voices from around the World Lift the Veil on the Patient Experience – Part 2 Rachel Leib2022-08-17T12:40:25-07:00August 17, 2022|
Media Messaging on Inter-abled Relationships: What Are We Saying to The Disabled Community? Rachel Leib2022-07-25T12:03:49-07:00July 24, 2022|
Life with GNEM: Voices from around the World Lift the Veil on the Patient Experience – Part 1 Rachel Leib2022-08-17T12:38:33-07:00July 14, 2022|