Muscle Owl Talks Ep69: No Wheelchair on the First Day of School?!
Today is World Duchenne Awareness Day. It was also 4 year old Fraser's first day of school! However Fraser - who unlike many with DMD,...
World Duchenne Awareness Day 2017 - Our Community's Balloons!
It’s World Duchenne Awareness Day 2017! Here is our annual Duchenne Awareness Day animation, featuring facts about the condition, and ALL...
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 Ep61: Accessible Gaming with Ian Hamilton and Vivek Gohil
This week on Muscle Owl Talks, we spoke to gaming expert, Ian Hamilton. He and Vivek discussed how the gaming industry is making games...
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 Ep57: Sports Day for Children with a Disability?
We hope you're enjoying the heat wave - depending on where you are in the world! With it being Summer in the northern hemisphere, and...
Muscle Owl Talks Ep55: Shelley's DMD Snowdon Challenge: DONE!
It's a week since Shelley Simmonds took her son, Fraser, up Snowdon on her back! Tune in as we chat about how it went! Fraser is 4...
Muscle Owl Talks Ep 37: Behind the Scenes Chat on Drugs & Treatments
Join us for Muscle Owl Talks Episode 37! It's a special behind the scenes episode, recorded before a filmed discussion a few weeks back....
Muscle Owl Talks Ep36: Rare disease, diagnosis, and self identity
Tune in to our second Muscle Owl Talks episode for Rare Disease Day 2017! This week, Steve, Vivek, Sulaiman, and Peter discuss the vast...
