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
You may have noticed that I was quiet in 2016. I really just wasn’t feeling my muse, and I only write when I have something cohesive to say. Besides, I wanted to see how the year would end, after the dark days of benefit deprivation, celebrity deaths, Brexit and Trump. I can safely say that … More 2016: The Year That Was (Or, Why Sweden Is Wonderful)