I picked this book up as a daily deal this month. Although it’s a horrendous topic to read about and I don’t say that lightly, I recently read Emma Hemming Willis’s book about caring for her husband Bruce, who was diagnosed with Frontotemporal Dementia, so my interest was somewhat peaked.
Fiona paints the picture, she was independent, stubborn, a workaholic, dependable, the perfect journalist. Then she started to notice things weren’t quite right with her mother, she seemed depressed, disinterested and beyond her age. Her mother was diagnosed with dementia in her early sixties, died and then somehow her father was soon diagnosed. It was unimaginable that two diagnoses and two essential death sentences in such a short space of time. Fiona tried to remain calm, presenting morning tv, driving back and forth to Wales and looking after a young family.
Fiona talks about coping, how the healthcare system treat people with Alzheimer’s and how things started to change for her.
We hear about the symptoms, the denial, the hope it was depression, menopause, long COVID, anything but Alzheimer’s.
We see the decline, the change and more of an input from Martin her husband as the book goes along. As he says, the pamphlets, the research and care homes are for the older audience, not people in their early 60s. Staying the ever professional journalists, this is Fiona’s last report, giving it her all and leaving no stones unturned so to inform, educate and personalise the story of Alzheimer’s