A diagnosis of a muscle wasting or weakening condition shouldn’t define anyone’s story.
That’s why we’re funding groundbreaking research that will make long term treatments – and even cures – a reality.
For over 60 years, we’ve helped people to stay independent, grow careers and start families. We’ve come a long way, but it’s not enough.
Together, we can change the story for good. Leave a gift in your Will.
Request our straightforward guide to leaving a Gift in your Will, covering all you need to know about leaving a gift to Muscular Dystrophy UK.
Having an up-to-date Will ensures everyone close to you knows your wishes. Here are some of the main things you need to consider when writing your Will.
Request a referral to make or a amend a simple Will for free with a local solicitor.
Professor Laurent Servais of the MDUK Oxford Neuromuscular Centre tells us how these special types of gifts have the power to change the story for future generations.
Teenager Joe Driffield lives with Duchenne muscular dystrophy. See how a gift in your Will can help families like his.
Bob and Irene Glover lost their son, Stuart, to Duchenne muscular dystrophy when he was just 16 years old. Find out why they have chosen this special type of gift to honour Stuart’s memory.
Sheila Hawkins was diagnosed with FSHD when she was 31 and has been actively involved with our community for many years. Watch Sheila tell us why it was important for her to pledge a gift in her Will to us.
If you have any questions our friendly and knowledgeable team is here to help. Call us on 0300 012 0172 (Monday – Friday, 9am-5pm) or email legacy@musculardystrophyuk.org.
