News

GuidanceSMApaper
Jul 06

New Publication Guidance on gene replacement therapy in Spinal Muscular Atrophy: a Canadian perspective

JND treatabolome
Jun 10

Treatabolome Project Designed to Shorten Diagnosis-to-Treatment Time for Patients with Rare Diseases

MDC_JJ
May 31

Neuromuscular Research Funding Announcements From Jesse’s Journey and Muscular Dystrophy Canada

newborn screeningMay
May 31

Muscular Dystrophy Canada Announce Phase 2 of Newborn Screening Initiatives with Call for Funding Proposals

EC Update
May 31

Early Career Working Group Update

LM_ECblog
May 14

Read Dr. Louise Moyle’s Early Career Blog

JJ_logo_EN
May 05

Jesse’s Journey Grants $1.7 Million to Duchenne Muscular Dystrophy Research

Bonnie Wooten profile pic
May 04

Introducing NMD4C Clinical Trial Concierge Bonnie Wooten

Our network brings together clinicians, researchers, and people with neuromuscular disease across the country.
May 04

Congenital Myotonic Dystrophy Trial Now Recruiting