I am Billy Allan's niece and I set this Fund up. For those of you that don't know in 2017 our family received the most devastating news possible, our beloved Husband, Dad, Brother, Uncle, Grandad, Great Grandad, friend and legend to many was sadly diagnosed with Motor Neurone Disease. 
He was diagnosed in May 2017 and given only 12 months to live and he sadly passed away on 6th November 2017. We must find a cure for this disease and stop it smashing other families to pieces like it has ours.

I can honestly say I have never witnessed a more horrific disease. It leaves people locked inside their own ever failing body, unable to move, talk and eventually breathe. To many of you this will be a shocking fact, to the Allan family and thousands of other families this was our awful reality. 

As a family and with our close friends, we will pull together and try and raise much needed funds to help find a cure for this horrific disease. Currently there is no cure and quite frankly there needs to be. Please help support 'The Billy Allan Tribute Fund' and donate what you can, no amount is too small. Let's smash this!!

Just so you know, 100% of the funds we raise will go towards research in to finding a cure.

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