Alzheimer's Society blog

Read real stories from people affected by dementia, and find out about the latest dementia news, research and campaigns.

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Real stories
Real stories
Alex’s dad, Dave, was diagnosed with early onset dementia eight years ago at the age of 60. Alex reflects on how her dad came to terms with his diagnosis, and how the coronavirus pandemic has affected their relationship.
Real stories
Real stories
Tracey, a retired nurse, was diagnosed with early-onset dementia and posterior cortical atrophy (PCA) when she was in her mid-forties. Despite the challenges coronavirus has brought, Tracey is determined to keep her mind and her body active with a variety of activities and hobbies.
Real stories
Real stories
When Rachel's dad Paul started acting differently, she and her sisters convinced him to visit his GP. Eventually, Paul was diagnosed with frontotemporal dementia (FTD) or Pick's disease. He now lives in a residential care home that suits his needs.
Real stories
Real stories
May was always a kind, strong, independent woman. But following her diagnosis of vascular dementia, May's behaviour started to change. Her granddaughter Michelle is determined to raise money to help other people affected by dementia.
Real stories
Real stories
As the sole carer of a relative with dementia, making the decision to move them into residential care can be a very difficult time. But extra challenges can arise when other family members question your decision and your motives. Here, a sole carer of a person with dementia shares their story.
Real stories
Real stories
Suzanne knew that selling her mum’s house to pay care home fees was always going to be sad. But going through her parents’ belongings brought back the strong bond she’d had with them both before dementia came along.
Real stories
Real stories
Georgina, 21, has written a poem inspired by her Grandad Brian, who sadly died of dementia. It's about his favourite bird, a robin. Whenever she sees one now she smiles and thinks of him.
Real stories
Real stories
At 35, Hannah Mackay was told that she carries a rare gene which means she will go on to develop a form of Frontotemporal dementia. She explains why, for her, it was better to know, and how she’s now determined to raise funds for dementia research.

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Would you like to write a blog post? We're always looking for real stories to share on our blog. If you don't want to write a post yourself, you can also share your story with us, and get involved in our press and campaigning work. Find out more about both options.

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