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Dominic's Sunshine Trust

Following the devastating diagnosis of Duchenne muscular dystrophy when their son Dominic was just four years old, Nikita and Dan set up Dominic’s Sunshine Trust.
Following the devastating diagnosis of Duchenne muscular dystrophy when their son Dominic was just four years old, Nikita and Dan set up Dominic’s Sunshine Trust.

The John Walton Muscular Dystrophy Research Centre

Newcastle has long been a world leader in the treatment and management of muscle diseases. The John Walton Muscular Dystrophy Research Centre is part of the Institute of Translational and Clinical Research, within Newcastle University. It is recognised by Muscular Dystrophy UK as an adult and paediatric centre for research and clinical excellence for inherited neuromuscular diseases.
Newcastle has long been a world leader in the treatment and management of muscle diseases. The John Walton Muscular Dystrophy Research Centre is part of the Institute of Translational and Clinical Research, within Newcastle University. It is recognised by Muscular Dystrophy UK as an adult and paediatric centre for research and clinical excellence for inherited neuromuscular diseases.

I'm in for Will

I’m in for Will is a family fund set up by Caroline and Robert after their son William was diagnosed with Duchenne muscular dystrophy in 2015. William loves playing on his X-Box, building Lego and spending time with his little sister Rosie and despite his condition he never stops smiling
I’m in for Will is a family fund set up by Caroline and Robert after their son William was diagnosed with Duchenne muscular dystrophy in 2015. William loves playing on his X-Box, building Lego and spending time with his little sister Rosie and despite his condition he never stops smiling
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