i am afraid that I am not one to brush things under the carpet. Everyone I love and care about knows about me having Motor Neurone Disease and that half of those diagnosed with the same strain as me only live 14 months. It is daunting, devastating but there is nothing can be done There is no cure My sadness is for my daughters and the grandchildren, all of whom I adore, and of course, my new husband, Peter, who will adopt the role of the major carer. Family live three hours away in the car so we are quite isolated and so much grief will fall on his shoulders If the boot was on the other foot, I would look after him but it still is a dreadful scenario. But we have to soldier on and live every day as best we can! x