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Celebrating 20 years: NorthStar a ‘shining light’ for people living with Duchenne muscular dystrophy
September 7, 2024
Read Celebrating 20 years: NorthStar a ‘shining light’ for people living with Duchenne muscular dystrophy
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We’re investing £1.7m into new research
August 29, 2024
Read We’re investing £1.7m into new research
Children living with muscle wasting conditions rally together at charity sport event
August 28, 2024
Read Children living with muscle wasting conditions rally together at charity sport event
We’re delighted to launch our new employability helpline
August 20, 2024
Read We’re delighted to launch our new employability helpline
Planned improvements to patient registries for the muscle wasting community
August 17, 2024
Read Planned improvements to patient registries for the muscle wasting community
Andy Fletcher appointed as our new Chief Executive
August 15, 2024
Read Andy Fletcher appointed as our new Chief Executive
A researcher in a lab
Our research impact
August 9, 2024
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CIFFERO clinical trial for DMD gene therapy cancelled
July 31, 2024
Read CIFFERO clinical trial for DMD gene therapy cancelled
Using MRI to tell dysferlinopathy apart from other genetic muscle wasting conditions
July 19, 2024
Read Using MRI to tell dysferlinopathy apart from other genetic muscle wasting conditions
Calling for more fully accessible toilets
July 19, 2024
Read Calling for more fully accessible toilets
What do the Work and Pensions Secretary’s priorities tell us about the new UK Government’s plans for supporting people into work?
July 15, 2024
Read What do the Work and Pensions Secretary’s priorities tell us about the new UK Government’s plans for supporting people into work?
What do the Secretary of State for Health’s priorities tell us about the new UK Government’s plans for health and social care?
July 11, 2024
Read What do the Secretary of State for Health’s priorities tell us about the new UK Government’s plans for health and social care?

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