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Families are now facing a postcode lottery over who gets the drug givinostat, which can slow progress of Duchenne muscular ...
Tahira Mathur, 31, from London, volunteers for Muscular Dystrophy UK, the leading charity for more than 110,000 children and ...
LONDON, ON, May 19, 2025 /CNW/ - On May 25, Canadians are walking, running ... to raising awareness and funds for Duchenne muscular dystrophy. Duchenne is a rare, life-shortening genetic disorder ...
Scientists present current evidence for a new gene therapy for Duchenne muscular dystrophy called delandistrogene moxeparvovec. AAN Evidence in Focus articles highlight the strength of the current ...
This symposium was held at the Muscular Dystrophy Association (MDA ... I could still maintain myself, but I was using a walking stick more and more. Then, my health really started to decline, and I ...
The university has been awarded a £1m grant from LifeArc and Muscular Dystrophy UK Researchers from University College London (UCL) are aiming to develop potential treatments for congenital muscular ...
This suggests that claimants with conditions such as epilepsy, multiple sclerosis, muscular dystrophy ... and co-founder of Cool Crutches and Walking Sticks, Amelia Peckham, is hopeful that ...
It means claimants with epilepsy, multiple sclerosis and muscular dystrophy ... and co-founder of Cool Crutches & Walking Sticks, Amelia Peckham, is hoping these changes will improve PIP applications.
Two posters presented at the 2025 Muscular Dystrophy Association Clinical ... were in need of mobility aids like walking sticks or canes, and 42% still lived with moderate-severe symptoms ...
Duchenne muscular dystrophy (DMD) is a rare neurological condition that causes severe muscle weakness and intellectual disability. DMD is an inherited (passed down) disorder. The condition is ...
A 12-year-old boy with a severe form of muscular dystrophy has said it is "cruel ... could avail of this that some of them might not be walking next year? "Time is muscle when it comes to Duchenne.
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