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I contacted the helpline a couple of years ago, before I worked here, about my housing situation. I…
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I grew up seeing the affect muscular dystrophy had on my grandma and my whole family as she…
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All through life I struggled with everyday things and couldn’t understand why. I couldn’t do sit…
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A career in science and muscular dystrophy I’ve always had a brain for science as opposed to…
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This Disability History Month, we really wanted to give people an opportunity to share what they…
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Jack: The theme of this year’s UK Disability History Month is childhood and youth, and my colleague…
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Did something frustrating happen today? Or funny? Or annoying? Writing it down could help you keep…
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Carmela, who was diagnosed with LMNA congenital muscular dystrophy in 2017, is the subject of a new…
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Living with CMT has limited areas of my life. Some of the everyday things that people without my…
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On Sunday 15 October Angela, with her husband Brian, will officially start Bidwells Cambridge Town…