Save the date! Congenital muscular dystrophy community gathering and national youth club
Saturday, 10 August 2024. In-person at Muscular Dystrophy Ireland, 75 Lucan Road, Chapelizod.
Spotlight on members of our community living with neuromuscular conditions: Tania Quill
We began on Rare Disease Day, 29 February, to draw attention to the fact that rare disease isn’t just for one day. By sharing individual stories and information on their conditions, we want to raise awareness about the many neuromuscular conditions experienced by the diverse members of our community to whom MDI offers support.