3d training videos24

Sue Barker thanks all our wonderful supporters for the courage of signing up to do a skydive, which will support funding for vital research into muscle-wasting conditions. To find out more and sign up: http://bit.ly/1jyQyBw

Muscular Dystrophy UK Ambassador, Jack Wilshere, has launched the Move a Mile for Muscles competition for the ‘most creative mile’. Send us your pictures and videos of the different ways you’ve completed your mile this summer, and you could win this amazing prize.

Advocacy Ambassadors are ready to give you all the support. In this video Gemma Rose give us top tips for applying for home adaptations:

1.- Work closely with your occupational therapist
2.- Stay positive!
3.- Make sure you know what you are entitled to

Share the bauble, spread the word.
http://www.musculardystrophyuk.org/yo...

‘This Christmas I hope you will join me in taking a stand for other families living with muscular dystrophy. Let's show them that they're not alone.' Liz Keenan, whose three sons have Duchenne muscular dystrophy.

Liz is asking you to join her this Christmas, by spreading awareness of muscular dystrophy by sharing the Christmas bauble below with your friends on social media.

MDUK Ambassadors and Paralympics GB Boccia players, talk about the benefits of playing sport.

This video featuring people affected by congenital muscular dystrophy and specialist neuromuscular health professionals is an introduction to the main facets of congenital muscular dystrophy and the support that is available from Muscular Dystrophy UK.

Marina di Marco, Principal Neuromuscular Physiotherapist, talks about the Scottish Muscle Network and the value of multi-disciplinary support for families living with muscle-wasting conditions

The Jackson family, stars of our Christmas Appeal this year, say thank you for all your support.

Dr Shuko Joseph at the University of Glasgow has been awarded an MDUK-funded clinical academic training fellowship to study bone health and how it changes in boys with Duchenne muscular dystrophy

This Valentine's Day, hear from members of Muscular Dystrophy UK's Trailblazers as they discuss all things dating including embarrassing moments and awkward questions.

Find out more about our mental health matters project from Suzanne and Sadie who are two members of our expert steering group

Advocacy Ambassadors, are here to support you. Hear about Andy’s experiences of being in the network and get tips about applying for care packages. Find out more: http://bit.ly/1Gczh6e

As part of Trailblazers dating diaries marking Valentine's week, we look at dating discussions in more detail. In this video Trailblazers discuss some of the pros and cons of being single and being in a relationship.

What do you think?

Ravi give us top tips when applying for the PIP

1.- Get supporting evidence from your GP or health professionals.
2.-Keep a diary of your daily activities.
3.- When you are filling out the forms, take your time.

This video featuring people affected by facioscapulohumeral muscular dystrophy and specialist neuromuscular health professionals is an introduction to the main facets of facioscapulohumeral muscular dystrophy and the support that is available from Muscular Dystrophy UK.

Dr Jarod Wong, from the Royal Hospital for Children in Glasgow, talks about research into bone health in boys with Duchenne muscular dystrophy

This video featuring people affected by spinal muscular atrophy and specialist neuromuscular health professionals is an introduction to the main facets of CMT and the support that is available from Muscular Dystrophy UK.

Marina di Marco, Principal Neuromuscular Physiotherapist, talks about how the Scottish Muscle Network supports families living with muscle-wasting conditions