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 all the sports day videos across Facebook, we decided to reminisce on sports days gone by. We ask what is best for young children with a physical disability, and how best to adapt races!
Tune in here and on iTunes, and as always, feel free to like, share, and comment below! #disability #children #parents #school #duchenne #sma #musculardyst
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 years old and has Duchenne muscular dystrophy. However, unlike many other boys with the condition, Fraser has never been able to walk. So Shelley decided to embark on a mammoth hike and fundraise over £11,000 for research into Duchenne muscular dystrophy while she was at it! #duchenne #musculardystrophy #fundraising #shelleysimmonds #children #p