My daughter Lucy has Myalgic Encephalomyelitis (ME) sometimes known as Chronic Fatigue Syndrome (CFS).

I am virtually cycling the 1,083 miles from Lands End to John O’Groats over the 3 winter months to raise much needed funds and awareness for ME.

M.E. affects an estimated 250,000 people in the UK, and around 17 million people worldwide, and yet it is little understood and research very poorly funded, leaving many with a poor quality of life.

Please help Action for M.E. to achieve their vision of ‘a world without ME’.  

Many Thanks

Rob

We aim to end the ignorance, injustice and neglect experienced by children and adults with M.E.We're working to ensure children, young people, adults and families living with the illness are supported during this unprecedented time and beyond. Our dedicated team is here for anyone living with, or supporting someone with, M.E. of any age, anywhere in the UK.