If you’re interested in what it’s like to live with CFS/ME then this might be a useful read. Fair warning though, it is Loooong. This is part of the appeal submission when my Disability Benefit (SLP) application was declined. The full appeal document was over 10,000 words long. I’ve edited it, added bits that I … Continue reading What it’s like to be me, living with ME/CFS
Living with a chronic illness, such as ME/CFS, often feels like life is a placeholder without meaningful content. We're not really living a life, more just holding the space.