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After Sammy de Laszlo was diagnosed with Duchenne muscular dystrophy in 2012, parents Oliver and…
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We heard concerns arising because of the pandemic, such as continued delays to accessing critical…
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There are lots of exciting changes happening at the Muscle Diseases Unit at Salford Royal. The…
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As I’m getting ready to leave hospital following a short admission my respiratory consultant…
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Our Muscle Group meetings are hugely important to MDUK, as it’s a great way to bring people…
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As well as being the chair of the Milton Keynes Muscle Group, Patricia supports others as a peer…
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He said:
Being actively involved with MDUK for nearly 30 years has, I hope, allowed me to do…
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Every day counts when you’re living with a rare, progressive condition. At MDUK, we’re here for…
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Today marks the first day of Volunteers Week so it seems the perfect time to introduce myself! I…
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My daughter Jessica was so buoyed up by caring friends and our company staff after her painful…