Last year, I went for a PIP assessment, which I failed. Apparently, my “high level of intelligence” excludes me from being disabled (epilepsy, anxiety, being autistic… yeah, none of those incringe on my life at all, apparently). As for the ME/CFS… “I wish I could stay in bed all day.” This was actually said to … More ME/CFS Awareness: Not A Lifestyle Choice!
Disclaimer: The following post contains photographs of a spider, and a possibly distressing photograph of myself in intensive care, at death’s door. I don’t know how to hide them, and so I thought I ought to warn you.
It’s that time of year again, when the lovely people at Epilepsy Action start their drive to raise awareness of epilepsy. This year they asked members to contact them and tell them what epilepsy means to sufferers as individuals – because no two epileptic patients are affected in the same way, and this needs to … More March 26th: Purple Day For Epilepsy
“Go on then, just one.” That’s what I always say. And I always mean it, I truly do. The problem is, that I know I’m kidding myself: I can never have “just one” of anything. A multipack of crisps; a favourite cheese; a bottle of gin; a jar of herring in mustard; a box of … More “Go On Then, Just One”
I want my life back. I have spent a year trying to work things out with you, and I just can’t do it any more. You and I are through, but I’m a kindly soul and feel that the least you deserve is an explanation. In the beginning you delighted me. You’re a pretty shade … More Dear Amitriptalyne…