Raymond and Cynthia’s Vow – ‘Facing things together’
Raymond and Cynthia James have been married for 55 years. They share the story of how they met and how their relationship has helped them face his diagnosis
Raymond and Cynthia James have been married for 55 years. They share the story of how they met and how their relationship has helped them face his diagnosis
Stevie Morris, talks about his diagnosis of motor neurone disease (MND). Put your questions to Stevie & hear about the MND-SMART trial in our livestream today.
Ananga and Jo Moonesinghe discuss all things life, from how they met, to their experience with Ananga’s Alzheimer’s disease diagnosis and hopes for the future
Need a reminder as to why your research is important? Take a look at Tracy and Steve’s story shared from the Dementia UK website
Christine talks about life as a Dementia Carer and finding the Support she needed – a new short film from Alzheimer’s Society reminding us why research is vital
Trina was diagnosed with Posterior Cortical Atrophy in 2012, 4 years after she initially visited the doctor & 6 since starting to have problems with vision
Alzheimer’s Society have an emergency appeal to help support them to continue with companion calls, and to fund important research.
Themiya’s father Gunasena was always very independent, so it worried her when he began to experience hallucinations and falls.
In 2017, Laura found out she carries a rare gene which means she will develop early-onset Alzheimer’s disease. Now she’s using the Dementia Revolution to speak out about her diagnosis.
Tracey, 51, who was diagnosed with frontotemporal dementia, talks about her dementia journey from diagnosis to the support she has received from Alzheimer’s Society.
Mum-of-two Carla Bramall began showing the symptoms of dementia at just 30-years-old, and she was diagnosed with early-onset Alzheimer’s at just 36. Now 39, Carla is bedbound in a care…
“There’s no connection between the brain and my eyes. The connection has been broken.” Dementia isn’t all about memory loss. Watch Trina’s story about her life with posterior cortical atrophy,…