Home News Football star, ALS activist Rob Burrow dies at 41

Football star, ALS activist Rob Burrow dies at 41

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Rob Burrow, a brilliant rugby player who overcame his small stature with agility and ferocious physique to become an eight-time English Premier League champion and who was later praised for raising awareness of motor neurone disease after being diagnosed with it in 2019, died on Sunday at the age of 41.

He died from MND, a neurological disease that includes amyotrophic lateral sclerosis, also known as ALS, also known as Lou Gehrig’s disease. Leeds Rhinoshe played for the English club for his entire 17-year career. The report did not reveal where he died.

Burrow was met with skepticism despite his small stature — he was about 5-foot-5 and 150 pounds — but he became a star, earning nicknames like “The Giant Atom” and “The Pocket Rocket” in the British tabloids.

However, in 2017, just two years after his retirement, he was diagnosed with a neurological disease at the age of 37, which curtailed his physical gifts.

Despite an incurable disease that has left his muscles atrophying and even making eating and breathing an ordeal, Burrow teamed up with his friend and former teammate Kevin Sinfield Raising millions of dollars for MND research and support for people with the disease, including setting up a Nursing Center Leeds is located in the north of England.

In a high-profile fundraising challenge last December, Sinfield ran seven marathons in seven days in seven cities, adding a 27th mile to each marathon to encourage people to “go the extra mile” for a friend in need.

“My feet look like they’ve been run over. Lawn mower” Sinfield told the BBC.

These efforts have caught the attention of the British royal family. In January this year, Prince William appeared at Headingley Stadium in Leeds to present Burrow and Sinfield with the Commander of the Order of the British Empire (CBE) for their “Extraordinary”Charitable efforts.

Prince William posted on social media on Sunday that Burrow was a “legend” in British rugby, adding: “He taught us, ‘In this world full of adversity, we must Dare to Dream“”.

In the sporting world, Burrow is best known for his outstanding performances for Leeds United, where he was a prominent member of the club’s so-called golden generation, winning several cup titles and eight Premier League titles.

He has twice won the Harry Sunderland Trophy for Best Player in the Premier League Final. victory His performance culminated in a touchdown against St Helens in 2011, which was considered “ The most beautiful everThe British newspaper The Daily Telegraph reported that “with lightning speed he dodged, weaved and ducked past stunned defenders. Long distance running

exist A statement Following his friend’s death, Sinfield wrote on social media: “I always said you were the toughest player I ever played with, and since you were diagnosed with cancer you have become the strongest, bravest man I have ever met.”

Robert Geoffrey Burrow was born in Pontefract, West Yorkshire, south-east of Leeds, on 26 September 1982. He was the youngest of three children of Geoffrey Burrow, secretary of the British trade union GMB, and Irene (Bateman) Burrow.

He leaves behind his parents, his wife Lindsey Burrow, daughters Maya and Macy, son Jackson and sisters Jo Hartshorne and Claire Burnett.

Burrow was an active child growing up in nearby Castleford and started playing rugby at the age of 7. He attended Aire Valley High School and played for two amateur clubs before signing for Leeds United in 1999.

He made his professional league debut in 2001 and was named Super League Young Player of the Year. “Rob was given the number 7 shirt, which has become iconic; Never look backDaryl Powell, one of his former coaches at Leeds United, said after his death.

The first signs of Burrow’s illness came months before his diagnosis in December 2019, when his family noticed he was slurring his speech.

“The next big thing was, when I was speaking in the clubhouse, someone came up to me and asked, ‘Am I drunk?'” Burrow said. 2020 Video Interview However, he added that he remained optimistic following the diagnosis.Stephen Hawking “I’ve lived with it for 55 years,” he said.

By the second year, his condition had worsened. He could no longer speak and could only rely on Sighta technology that allows people to communicate using cameras that track eye movements.

Still, he remained undaunted, telling The Guardian, “I think you never know your Inner Strength Until you are told you are going to die.”

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