Neuromuscular Disease Foundation Earns 2019 GuideStar Platinum Seal of Transparency ndf2021-05-17T07:41:29-07:00March 22, 2019|
Neuromuscular Disease Foundation Announces $700K in Awards for GNE Myopathy (HIBM) Research & Programs ndf2021-05-17T07:41:30-07:00March 12, 2019|
7 Ways To Support Those with GNE Myopathy on Rare Disease Day, February 28th ndf2021-05-17T07:41:30-07:00February 21, 2019|
Neuromuscular Disease Foundation Announces Monthly Patient HUDDLEs for Those Affected by GNEM ndf2021-05-17T07:41:30-07:00January 31, 2019|
Rare Disease Foundation takes on 2.5 Million challenge grant to fund Gene Therapy ndf2021-05-17T07:41:30-07:00October 24, 2018|
Neuromuscular Disease Foundation (NDF) Launches Whole Genome Sequencing Research for Rare Muscle Disease ndf2021-05-17T07:41:30-07:00December 21, 2017|
Lalé Welsh Appointed New Executive Director of The Neuromuscular Disease Foundation ndf2021-05-17T07:41:30-07:00March 26, 2015|