International Women's Day - TWO Episodes!
With it being International Women's Day, we decided to produce two separate episodes, discussing how women with a disability can often...
Words of Advice from Manjula Gohil at the Action Duchenne Conference
Catch one of Peter's recent interviews from the Action Duchenne, with the mother of one of our co-editors, Vivek Gohil. #peterduffy...
Muscle Owl Talks Ep81: Duchenne After 18; Avoiding Infantilisation of Condition
In our latest episode of Muscle Owl Talks, Vivek chats with Peter about the way Duchenne muscular dystrophy is often perceived in adults....
Muscle Owl Talks Ep80: Charcot Marie Tooth!
For a long time we've been looking to produce an episode on the uniquely named neuromuscular condition, Charcot Marie Tooth! Finally,...
Muscle Owl Talks Ep67: Duchenne - Just Children?
Duchenne muscular dystrophy.... A childhood condition? After reading a number of posts from around the community, Peter and Vivek respond...
Muscle Owl Talks Ep65: SMA Awareness Month 2017 (August 2017)
August is SMA Awareness Month - you may have noticed from our frequent posting! We all know spinal muscular atrophy is a form of muscular...
Muscle Owl Talks Ep60: Trains, the London Tube, and Accessibility!
Zoe was taken an hour out of her way last week, when her tube train decided not to stop at the station without prior warning! All this...
What is EAMS and how could it help men with Duchenne muscular dystrophy in the UK?!
In episode 59 of our weekly chat show Muscle Owl Talks, we hosted Action Duchenne CEO, Diana Ribeiro, to discuss the Early Access to...
Muscle Owl Talks Ep58: ADAPT Protest & Senate Vote on Revised Healthcare Act
The senate vote on the latest US healthcare bill is upcoming, and many Americans are fearful it will finally pass. Watch Steve and...
Muscle Owl Talks Ep54: Charlie Gard & Patient/Parental Consent
Charlie Gard is a young child who is currently being cared for at Great Ormond Street Hospital in London; he is currently on life support....
