How ironic that in the week before Dementia Action Week, this year themed around social care reform, the latest Queen’s Speech yet again failed to provide detailed plans to address the issues that have plagued the care system for years.…
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.
Making meaningful conversation
“When was the last time you really engaged with a person living with dementia?” This was a question I posed during a recent online training session I ran with a small group of social care staff. Some of the…
Regrets, I’ve had a few…
Listening to the radio recently, Frank Sinatra’s ‘My Way’ came on. These two lines really stood out for me: “Regrets, I’ve had a few. But then again, too few to mention.” They got me thinking, as I so often do…
Intergenerational lessons from the (home education) classroom
I’m probably going to put myself into a very small group of parents with my opening comment for this blog, but I’m so glad I’ve had the chance to home school our daughter. Whilst I know many parents have struggled…
Five things I’m glad we bought my dad
A question I’m often asked is what would I recommend buying a person with dementia? This has become even more pertinent with so many family members unable to see relatives with dementia during the pandemic, and looking for ideas of…
Resolve to not put off until tomorrow what you can do today
As we come to the end of a year that I’m sure no one expected to turn out the way it has, most of us are probably feeling that our coping skills have been sorely tested. The exponential rise of…
When eating just isn’t happening
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,…
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…
