A PROUD dad has told how his brave daughter has battled to enjoy life despite her incurable disease.
Josie Chubb, seven, was diagnosed with Ullrich congenital muscular dystrophy, a rare and incurable muscle wasting condition, in 2021.
It took two years of medical investigations for the condition to be diagnosed. It leaves Josie, from Lewes, struggling to carry out her day-to-day life.
Her father James said: “Josie’s condition means she can’t run, jump, climb stairs or transition from seated to standing and everyday tasks are difficult without adult support.
“But she is a bright, fun-loving little girl who loves nature and being outdoors. Like most parents, the most important thing for my wife Charlotte and I is for our children to grow up happy and we strive to do everything we can to enable Josie and her brother, Harry, to fulfil their dreams.”
Since Josie’s diagnosis, James has been working to raise funds and awareness of the condition.
James said: “We knew nothing about muscular dystrophy before Josie’s diagnosis, but now we feel it’s our duty to raise awareness and promote understanding so that society as a whole can be more inclusive.
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“Charlotte and I want to raise awareness of Josie’s condition and the importance of research to find a treatment, but also feel it’s vitally important to make people understand that changes need to be made to enable a more inclusive life for those suffering with conditions like hers.”
In support of his mission, James, joined by friends Harry Collison, Ed Abis, Henry Lucas and Chris Owen, took on an 84-mile walk along the length of Hadrian’s Wall on August 31. They completed their challenge in 31 hours.
Together, The Chubb’s Crusade raised over £12,000 for Muscular Dystrophy UK, the UK’s leading charity for people living with one of more than 60 muscle wasting and weakening conditions.
Connal Kelleher, regional development manager at Muscular Dystrophy UK, said: “We’re so grateful to James and his friends for taking on this incredible coast-to-coast challenge.
“The Chubb family has raised so much for us and we really can’t thank them enough.
“But it’s not just about the fundraising, they also help to raise awareness of muscular dystrophy by talking about Josie and their family’s experiences.”
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