He was diagnosed 4 yrs ago while I was in hospital for a year with leukaemia. I only got out and he was told he has ALS 2 to 5 yrs to live. Couldn't believe our luck. We have 3 teenagers 2 disabled autism and prada willi syndrome. I researched online for months on end until I came across a doctor who's daughter was diagnosed with this too. He left his job and dedicated his life to saving his daughter and he did. She couldn't talk or walk but a few weeks into the Deanna protocol and she can talk walk and muscle was being regained not lost. It doesn't cure ALS but it slows it down dramatically and regains muscle speech and so much more. William was on this for a month as this was all we could afford and the change was like night and day. WE NEED THIS. Now he hasn't got it he is getting worse by the day. Am scared it's gonna be too late before we raise enough for at least 6 months it's about 300 pound a month to get it from usa. I'm hoping to raise 1800 enough for 6 months please please help us help him and also give others with this terminal awfully degenerative disease know there is hope. He is 49 a father a husband to be a brother a son a friend and importantly a human William brand if nothing else pray for him. There is o very much to our story and believe me you wouldn't believe Justhow muchad luck we've had lately. Please feel free to ask us anything as We r honest ppl and honesty we're scared time isn't on our side. And William has bug at the moment that makes his ALS 100% worse. Pls even if it's only a penny we appreciate anything. Thank you for listening

Jean and William