One of the topics I haven’t covered in depth on this blog is refusal to eat. So many of my blog posts are inspired by our experiences with my dad, and one thing he never did was refuse to eat,…
Author: Beth Britton
I'm an award-winning content creator, consultant, campaigner and speaker, trainer and mentor, specialising in ageing, health & social care. Until 2012 I was a carer to my dad who had vascular dementia for approximately the last 19 years of his life. I aim to provide support and advice to those faced with similar situations, inform and educate care professionals and the wider population, promote debate and create improvements in dementia care.
Knowledge is power
One of the loveliest parts of my work is being able to help people by sharing our experiences as a family, augmented by what I have learnt from my campaigning and consultancy in the 8+ years since my dad died.…
Demanding better for people with dementia
Ordinarily, September is dominated for me by World Alzheimer’s Month (or World Dementia Month as I prefer to call it), which in practice means 30 days of sharing all of the great content, ideas and initiatives that lots of fantastic…
A shrinking world
For the last five months I’ve written about different aspects of the coronavirus pandemic. For August, I want to think about the consequences of the required reduction in social interaction on people with dementia during lockdown. Is it all…
‘Old’ normal, ‘new’ normal or time to make a ‘better’ normal?
For the last four months I’ve written about different aspects of the coronavirus pandemic. For July, I want to think about life post-lockdown and pose these questions: What do we REALLY want ‘normal’ life to look like now? Is a…
Family carers and the coronavirus pandemic
For the last three months I’ve written about different aspects of the coronavirus pandemic. For June, I want to think about how family carers have been affected by lockdown and the ongoing coronavirus crisis. The pandemic has raised so many…
Living with dementia – It’s not postponed!
For the last two months I’ve written about the coronavirus pandemic. I want to continue with this theme since it is at the forefront of all of our minds, but also with a little nod to the significance of this month…
Coronavirus and being isolated from a loved one
Last month I wrote about the coronavirus pandemic and answered two questions families supporting a loved one are grappling with: How do we hand-wash more and how do we self-isolate? For families who aren’t in the same household, however, they…
Coronavirus and living with dementia – Coping in unprecedented times
It’s not easy to know where to begin with a blog on the current monumentally uncertain times that the world is facing, but I’m going to attempt to address the coronavirus disaster (I don’t think the word crisis goes far…
Who is really challenging?
As regular readers of D4Dementia will know, I’ve long been a supporter (including through the National Dementia Action Alliance Campaign ‘Dementia Words Matter’) of using respectful language – as defined by people living with dementia – when communicating about dementia. I…
Bothered and bewildered by the portrayal of dementia
The portrayal of dementia on TV and in the arts has undoubtedly risen since my dad was living with dementia. From major soaps to numerous stage plays, dementia – it seems – is popular subject matter. I’m not against portraying…
Resolve to ask people with dementia what THEY want
With over 200 blogs on D4Dementia, some of them now 7 years old, I’ve decided to spend my 2019 year of blogging by re-visiting some of the topics I’ve covered previously, throwing fresh light on why they remain relevant, and…
Together we can do SO much
With over 200 blogs on D4Dementia, some of them now 7 years old, I’ve decided to spend my 2019 year of blogging by re-visiting some of the topics I’ve covered previously, throwing fresh light on why they remain relevant, and…
