Have you ever tried explaining your MS symptoms to people who don’t have MS? Giving honest accounts of my symptoms can be a bit like advertising a circus of bizarre ailments…
This one’s going to be tough. I want to confront a topic that has slowly but steadily invaded my mind and now occupies dark corners of my self-image, my confidence, and my sense of, well, ‘me’. Does my partner consider himself to be my carer?
