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Sarepta Therapeutics, Inc. (NASDAQ:SRPT), the leader in precision genetic medicine for rare diseases, today announced that ...
Health Secretary Neil Gray has been furiously condemned for failing to ensure access to a new muscular dystrophy drug for ...
Irish Examiner on MSN2d
Parents plead for approval of 'vital drug' to slow down their son's muscular dystrophyParents of seven-year-old boy are calling for a drug which improves muscle repair to be made available here as it is in some ...
Duchenne muscular dystrophy (DMD) in India faces challenges in diagnosis, treatment, and support, highlighting the urgent ...
Chronic illness affects 40 percent of school-aged children. Learn how caregivers can help reduce the stress and depression ...
Children with a rare form of muscular dystrophy have been promised access to a groundbreaking drug after the Sunday Mail highlighted their plight. Around 30 boys could have their lives extended by ...
Families say it's 'completely frustrating' that children with Duchenne Muscular Dystrophy are being denied access to free drugs that will slow its progression. | ITV News Granada ...
The symposium took place on 18 th March 2025, as part of the Muscular Dystrophy Association (MDA) Clinical & Scientific ...
WATE 6 On Your Side on MSN11d
Golf tournament in Rockfort to raise funds for young burn victims, muscular dystrophyIn June, an inaugural golf tournament being held by the Knoxville Fire Fighters Association will be raising funds to help two nonprofit organizations that benefit young burn victims and ...
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