Sheena Atkinson

My support for those with MND started many year's ago when I saw the result of the disease on a lovely, caring, vivacious aunt, mother of two teenage girls. On my last visit to her, before she died, she was unable to move and could only communicate by being shown words on a board which she acknowledged by blinking. It was heartbreaking. My aunt's grandson suffered from another genetic nerve/brain related disease, ALD & died aged around 7 years old. It was then that I wanted to remember them with a gift in my Will to support your work and research.