Scientists have yet to see the money
“I have 100 things to say to this Government but I will keep it to one,” Burrow told the PA news agency.
Burrow’s stance is supported by his wife and full-time carer Lindsey, who said: “I am hopeful that one day a cure will be found but we need the UK Government to support people with MND and provide more funding for research into the disease. “For example the funding has supported clinical trials of a repurposed drug, Triumeq, which has shown promise at reducing a type of virus in the brain thought to kill motor neurons.
Burrow, who was given two years to live at the time of his diagnosis, says his condition has not worsened since he started taking an immunotherapy drug used in clinical trials for various types of cancer.
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