Lynn Gilderdale: a life reMEmbered …
Lynn Gilderdale (20.09.1977~04.12.2008)
was a healthy teenager in the UK who enjoyed swimming, sailing and cycling when she was struck by myalgic encephalomyelitis at age 14. The disease left her bedridden, partially paralysed, unable to talk or drink along with acute cognition problems and horrific pain. She leaves her mother, Kay, who was an advocate for ME and her father Richard, both who cared for her. One journalist who wrote a story about Lynn said “I have seen African children suffering from starvation, met people dying of AIDS, patients paralysed from the neck down, others in the last stages of terminal cancer, but I had never seen a living person as desperately ill as Lynn Gilderdale.”
fragmented_ME
My birth name is Denise, but I’m know as Bella to those who love me. I have a first class honours degree in education & psychology and a strong passion to keep learning and educating others ... I have severe ME/CFS and lots of other chronic illnesses and I started this blog as an expansion to my instagram page, where I advocate for chronic illness. I am married and have two grown up boys, or should I say young men. I have three gorgeous grandchildren, one boy and two girls. And despite being chronically sick and housebound I am mostly happy. 🥰
