Wyva
Senior Member (Voting Rights)
Alice Hattrick is an author who lives with ME/CFS and has recently published the book "Ill Feelings".
“Society is ableist”: Alice Hattrick on gender, chronic illness and long Covid
Alice Hattrick was aged eight when their mother collapsed with mycoplasma pneumonia. The author – who prefers the gender-neutral pronoun “they” – found her on the kitchen floor at their home in Brighton. Their mother was in her early thirties. She experienced flu-like symptoms – fatigue, headache, chest pain and fever – from which she never recovered. It took two years before she was diagnosed with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS).
In their book Ill Feelings, a blend of memoir, literary criticism, and analysis into the social effects of chronic illness, Hattrick, now 34, transposes their mother’s account of that day: “‘Alice witnessed this,’ she later wrote, as if I had observed a crime and needed a new identity.” Hattrick started to develop their own symptoms, which bore a striking similarity to their mother’s. They experienced stomach aches and headaches that lasted all day; they felt like sleeping during school break times; they felt pain in their arms and legs after PE. Later, Hattrick too would be diagnosed with CFS, by a doctor at a children’s hospital. “I remember feeling almost pleased with my diagnosis, even if I was not entirely convinced by it,” they write. “It made me feel closer to my mother.”
Full article: In their book Ill Feelings, a blend of memoir, literary criticism, and analysis into the social effects of chronic illness, Hattrick, now 34, transposes their mother’s account of that day: “‘Alice witnessed this,’ she later wrote, as if I had observed a crime and needed a new identity.” Hattrick started to develop their own symptoms, which bore a striking similarity to their mother’s. They experienced stomach aches and headaches that lasted all day; they felt like sleeping during school break times; they felt pain in their arms and legs after PE. Later, Hattrick too would be diagnosed with CFS, by a doctor at a children’s hospital. “I remember feeling almost pleased with my diagnosis, even if I was not entirely convinced by it,” they write. “It made me feel closer to my mother.”
“Society is ableist”: Alice Hattrick on gender, chronic illness and long Covid