I have been living with Myalgic Encephalomitis (aka ME/CFS) since 2006. It has taken away my job, my independence, my social life, my confidence and for the most part left me housebound.

People with ME's abilities vary. Some are bedbound relying on others to carry them around, others can work a bit. But there are still doctors who don't believe in ME!

ME is still very misunderstood and research and funding is desperately needed, so that people like me can hopefully one day have a better treatment or even a cure.

Please help us raise money and awareness so that this dream can be a reality.