In 2010 My Mum was diagnosed with MND a condition I knew little about. Over the next 18 months she changed from the happy outgoing bubbly Mum I knew to a dribbling quadraplegic unable of doing anything herself before she sadly passed away in 2011. During that time I got to know many others like her, all of whom were crippled by this horrible debilitating disease. There is currently no cure or even much help to ease or slow down the disease. 

Much money is needed for research but also in the care required by sufferers. MNDA  supports not only the sufferers but those around them. They provide the funding for families to make the necessary changes to their homes to cope. 

Please give generously.