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United Kingdom

Mum’s desperate plea as son, 7, diagnosed with rare muscle-wasting disease

News RoomBy News RoomJuly 24, 2025
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Evan Winter’s family has recently raised thousands of pounds to build a safer future for their seven-year-old son, Evan, who has been diagnosed with Duchenne muscular dystrophy (DMD). DMD, a progressive genetic disorder affecting muscle tissue, is the most common muscle-destitute disease in children, with estimates suggesting only 2,500 individuals worldwide are affected in the UK. Evan’s diagnosis came after his early years with autism were discovered, leading to a搜救 incident where Laura Winter, Evan’s dad and sister, identified him as autistic due to his padding walking. However, Evan was not recognized as autistic until later stages of his condition.

Evan Winter, who had been slow to progress, began walking only at two-and-a-half months of age and was initially described as “a little bit lazy.” His guitar string tremors suggested he was doing something voluntary, but his family concluded he appeared disabled. Eventually, his legs cramps triggered for ages ended up becoming a life-changing experience, leading to his diagnosis with DMD on March 25, 2025. Laura Winter, a disclosure risk assessor from Maidstone, Kent, revealed the diagnosis after a car ploughed into her house. She described DMD as a mysterious and often misunderstood condition, stating she had only ever seen one affected child in her career as a doctor.

Evan’s family is desperate to raise funds for their son’s future. During the initial stages of his condition, Evan’s mobility decreased significantly, and his family sought gig economy opportunities in the automotive industry. Laura Winter, the disclosure risk assessor, noted the economic hardship due to his limited mobility and the potential for a warriorship environment once he starts treatment. Despite initial hesitance, Laura urged them to proceed.

Since the diagnosis, Evan’s world has dramatically changed. He now uses his wheelchair for trips, which he learned in a jackhammer toy from his father. His treatment plan includes steroid therapy, which aims to slow the disease’s progression. Laura explained that he initially anticipated a change in his quality of life due to DMD but dismissed lack of understanding for his condition as doubting himself.

Evan Winter’s recovery, however, is a testament to the power of others. Laura wrote that their families had continually pushed Evan to imagine a better future, acceptingAnalysisEach section of this response has been condensed into a few sentences, with the maintain to address the requested content concisely while conveying the narrative’s progression and emotional impact.

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