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Men's Rugby Union Rugby star Slater stays positive by ‘living in the present’ after MND diagnosis

ED SLATER has said that living in the present is helping him face the challenge of his motor neurone disease (MND) diagnosis.

The 34-year-old revealed last month that he had been diagnosed with the devastating degenerative condition that fellow former sports stars Doddie Weir, Rob Burrow and Len Johnrose are also battling.

Gloucester rugby player Slater announced his retirement from the sport last month after receiving the news following months of tests.

“It was month after month, my arm got weaker and weaker, my grip became weaker, and I went to Oxford and was diagnosed with MND,” Slater told the BBC.

“Part of me had prepared for that, partly because of the weakness and partly because of the symptoms. I know very close friends of mine who have lost a family member to it, was able to speak to them about his experiences and so I prepared myself.”

Slater, who has three young children, has already begun recording his voice in anticipation of the condition affecting his speech.

He is determined to stay positive, saying: “I’m not saying that makes it easier when you’re diagnosed — it absolutely doesn’t — but in some ways it had been 11 months of torment: different symptoms, not knowing, looking for different reasons, and to have definitive diagnosis — it sounds strange to say this — but at least it gave me an answer.

“It’s not an answer I wanted, but I can’t change it. My attitude is to get on with things. There are difficult things in life, not many things harder than that, but you have to face challenges head on.

“I don’t think too far into the future and I take each day as it comes. I find that’s a peaceful place for me and keeps me in best spirits as I can.”

In July former Leeds and GB rugby league star Burrow accused the government of having blood on its hands over delay in delivering on a pledge to fund efforts to find a cure for the disease.

“I have 100 things to say to this government but I will keep it to one,” he said.

“People with MND don’t have the luxury of time to wait. It is as if there is no rush to give our scientific researchers the opportunity to join the race to find an effective treatment while six people die each day from motor neurone disease.

“There is blood on your hands, this government and the civil servants, with the red tape you are putting up.”

A Department of Health spokesman said at the time: “We remain committed to spending at least another £50 million to help find a cure, and researchers can apply for funding at the National Institute for Health & Care Research and UK Research & Innovation.”

In June 2021 a pioneering University of Sheffield study reported that frequent strenuous exercise increases the risk of developing MND in individuals with a predisposing genetic profile.

The neurodegenerative condition affects about 5,000 people in Britain.

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