Miranda Meldrum, 13, hopes to be home for Christmas after making a rare recovery from “locked-in” syndrome caused by a brain haemorrhage.
The family of a young boy living with cerebral palsy are trying tirelessly to raise enough money for a rare operation which could help him to walk unaided.
Sally, aged 10, from Liverpool, attends conductive education classes at cerebral palsy charity Stick ‘n’ Step. Recently, she received a Mo Salah shirt, thanks to the kind actions of a Widnes businessman. Operations Director of Yield UK Ltd, Tony Gibbons…
A new study into the impact of stem cell therapy on symptoms of cerebral palsy potentially offers new hope to children living with the increasingly common condition.
The Steve Morgan Foundation has revealed that £60,500 will be granted to children with Down’s syndrome and their families to ensure they are provided with greater educational support.
Scientists and researchers all over the globe are working tirelessly to find a way of combating Duchenne muscular dystrophy (DMD) – a condition widely considered to be the most common fatal genetic disorder in children.
October is Rett Syndrome Awareness Month – and a number of people all over the world are taking part in fundraising activities and charity appeals in their efforts to raise awareness of the condition.
A four-year-old boy living with Duchenne muscular dystrophy had the surprise of a lifetime last week, after a prominent charity informed him he’d be going on a dream trip to Disney World.
Bakers are being called upon across the nation this October to help raise vital funds for Muscular Dystrophy UK.
A young girl living with cerebral palsy has received £3,500 towards potentially life-changing surgery, following a successful charity event organised in her local community.