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Mark was forced to give up the many sports that he enjoyed, but started coaching football. He did…
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M’s application for Disability Living Allowance (DLA) was initially rejected. He contacted a…
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Jennie’s daughter, Gayle– who also has myotonic dystrophy – used to support Jennie with things like…
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Jenson has a form of muscular dystrophy, but has not yet received an exact diagnosis. Genetic…
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A new date has been set for the major On Farm event planned by the Royal Northern Agricultural…
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This Changing Places Awareness Day we’re delighted to share the exciting news of a brand new…
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May Macleod met Cara when she applied for a support role as a carer. They have been friends for two…
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Lincoln man who lives with muscular dystrophy has pushed his limits as far and high as they would go
This has been the most difficult thing I have ever done – all in a great cause.
Oliver booked the…
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Becoming an admin member of the CMT Facebook group and connecting with MDUK has proved a life-…
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After an international study, The IMP has released updated guidance on the medicines that should be…