Neuromuscular Disease Foundation Earns 2019 GuideStar Platinum Seal of Transparency ndf2023-02-04T09:52:06-08:00March 22, 2019|
Neuromuscular Disease Foundation Announces $700K in Awards for GNE Myopathy (HIBM) Research & Programs ndf2023-02-04T09:53:02-08:00March 12, 2019|
7 Ways To Support Those with GNE Myopathy on Rare Disease Day, February 28th ndf2023-02-04T09:54:39-08:00February 21, 2019|
Neuromuscular Disease Foundation Announces Monthly Patient HUDDLEs for Those Affected by GNEM ndf2023-02-04T09:55:26-08:00January 31, 2019|
Rare Disease Foundation takes on 2.5 Million challenge grant to fund Gene Therapy ndf2023-02-04T09:56:58-08:00October 24, 2018|
Neuromuscular Disease Foundation (NDF) Launches Whole Genome Sequencing Research for Rare Muscle Disease ndf2023-02-04T09:57:43-08:00December 21, 2017|
Lalé Welsh Appointed New Executive Director of The Neuromuscular Disease Foundation ndf2023-02-04T09:59:23-08:00March 26, 2015|