This Christmas, you have the power to bring hope and joy to families living with the daily challenges of muscular dystrophy. By giving a gift today, you can provide essential support to those facing this difficult journey.
Meet Jack’s Family
“Christmas is a big deal in our family and I treasure every single one we have together.
“I’ve always loved Christmas – decorating the tree, getting everyone together and doing turkey with all the trimmings. But best of all is seeing my boys’ faces light up as they open their presents. And ever since my older son, Jack, was diagnosed with Duchenne muscular dystrophy, these moments are even more precious to me.
You see, Duchenne is a severe muscle wasting condition and, sadly, there isn’t a cure for it. In the 10 years since his diagnosis, Jack’s decline has been dramatic and we just don’t know what the future holds for him – or how many Christmases we’ll have as a family.
“But what keeps me going and gives me hope is the support of Muscular Dystrophy UK (MDUK), who’ve been with us every step of the way. They’ve provided us with practical help, information and advice through the toughest of times. And they help fund the research that could bring about the next big medical breakthrough and add years to the lives of young people like Jack. ” – Emma Gauder, Jack’s mother
Why is this important?
Over 110,000 people are living with a muscle wasting and weakening condition in the UK – and we’re determined to be there for them and their families.
When someone is diagnosed with a muscle wasting condition, it can be an overwhelming, confusing and distressing time for everyone concerned. Life will never be the same again and the stress, exhaustion and loneliness can often be unbearable.
That’s why we do everything we can to provide practical and emotional support through our helpline, website and support groups. But right now, we’re busier than ever – and we rely on supporters like you to keep running these life-changing services.