New funding from Muscular Dystrophy UK

Extra funding for pioneering research projects

Muscular Dystrophy UK has announced that it is investing £1.5 million into 10 new pioneering research projects across England, Scotland and Wales.

The leading charity for more than 110,000 children and adults in the UK living with one of over 60 muscle wasting conditions, will be funding grants spanning one to four years in length.

This latest investment brings Muscular Dystrophy UK’s total current research commitment to over £10 million. Across more than 25 conditions, it’s now supporting 56 active projects that aim to deepen understanding, explore new treatments and make a meaningful difference to the lives of those living with muscle wasting by improving everyday quality of life.
 

Research into different muscle wasting conditions

Muscular Dystrophy UK’s portfolio of research spans the UK, with current research projects underway in all four nations, helping to reach more people and communities. This year, Muscular Dystrophy UK has awarded new funding to researchers in Cardiff, Glasgow, London, Newcastle and Nottingham.

The research projects cover a range of different conditions including Duchenne muscular dystrophy, facioscapulohumeral muscular dystrophy (FSHD), limb-girdle muscular dystrophies, ADSS1 myopathy and for the first time Carey-Fineman-Ziter syndrome and spinal muscular atrophy with respiratory distress.
 

Dr Kate Adcock, Director of Research and Innovation at Muscular Dystrophy UK, said:

“A key ambition of our ten-year strategy is to broaden our research portfolio and accelerate the development of new treatments.

“We’re delighted to continue our investment into funding research with the potential to transform the lives of those affected by neuromuscular conditions. With this latest research grant funding of £1.5 million we’re reaching new areas, investigating new conditions and supporting PhD students to become the next generation of scientists.”

Muscular Dystrophy Awareness Month

The announcement coincides with Muscular Dystrophy Awareness Month. Throughout the month of September, the charity is shining a spotlight on muscle wasting conditions to continue raising funds to support research and help those living with a condition and their families.

Advice and support for living well

As well as funding research, the charity also shares expert advice and support for the muscle wasting community to live well now, works with the NHS towards universal access to specialist healthcare and campaigns for people’s rights, better understanding, accessibility, and access to treatments.

More details and information on Muscular Dystrophy UK’s research projects: musculardystrophyuk.org/research (external link will open in a new browser tab or window)

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Further reading and resources

Philip Anderson’s daughters fundraising for Muscular Dystrophy UK in his memory

New treatment approved by NICE for Duchenne Muscular Dystrophy

Muscular Dystrophy UK and Whizz Kidz

Guest blog – living independently with muscular dystrophy

Do Muscles “Remember” Being Weak? New Research Suggests They Do

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