May is M.E./CFS Awareness Month and I had been planning to write at least one but hopefully three blog posts as well as many Instagram posts. However, ironically I have been too fatigued to do so. I have been sat here for at least a week trying to give you the facts and figures to raise awareness for M.E./CFS. Although facts and figures are important and they can share a certain amount of information with you, what they can’t do is tell you what living with M.E./CFS is really like, they don’t tell you how it actually affects peoples lives. So please excuse my foggy brain as I try to…