

Peter
150 posts

@CureDMCharity
Cure DM exists to help those with Myotonic Dystrophy, their families and carers. We Raise Awareness, Provide Family Support and Facilitate Research.



Muscular Dystrophy Canada is offering a special program that provides access to myotonic dystrophy genetic testing and counselling at no cost. While provincial systems may cover testing, long wait times to see a neurologist, geneticist, or counsellor can delay answers. This program helps fast-track access and includes expert support to help you understand what your results mean for you and your family. If you have a clinical diagnosis but no genetic confirmation, or a family history of DM1, this is an opportunity to get clear answers without waiting. To take part or learn more about this special program, reach out to research@muscle.ca or call 1-800-567-2873 x5401 #InternationalMyotonicDystrophyAwarenessDay


Ginny cares for her husband Tim, who has myotonic dystrophy. She works part-time, on top of caring for him every day. Now, under the Government’s PIP changes, they face losing £12,000 a year. Today I asked the Prime Minister: what does he expect carers like Ginny to do?

🧬 Today is International Myotonic Dystrophy Awareness Day — a global effort to raise visibility and understanding of this condition. To show our support, we’re offering 20% off standard registration for the TREAT-NMD® Conference throughout September! 👉 buytickets.at/treatnmd/16721…

























