
People with ME have been neglected by the government and society for too long
I have been ill since I was nine. I am largely housebound and I’ve had periods of being bedbound. There has not been a day in the last decade where I have been free from bone-crushing fatigue and pain. At times, I lost access to my education. I have had to fight for care and to be listened to by doctors. I lost my teenage years to Myalgic Encephalomyelitis (ME).Despite three years of delays hampering the publication of a promised cross-government delivery plan on ME/Chronic Fatigue Syndrome (CFS...