February 10, 2026 min
60 min
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What happens when a dementia diagnosis arrives – and the world starts treating you differently? In this episode of the Able to Care Podcast, Andy Baker is joined by Peter Berry (living with young onset Alzheimer’s) and Deb Bunt (writer, counsellor, and Peter’s close friend – often described as his “external memory”).
Together, they explore what it really means to live well with dementia – not through a clinical lens, but through story, humour, friendship, and the small practical adjustments that protect dignity and keep life meaningful.
Peter shares how, after diagnosis, he initially stayed quiet out of embarrassment and shame – and later realised that silence can make things harder for everyone. Deb speaks honestly about what it feels like watching people’s tone, body language, and attitude change the moment dementia enters the conversation.
Peter offers a powerful way to understand stigma: dementia can feel like wearing a shabby coat in public. People see the coat and respond to the label – not the person underneath. The message is simple and challenging: the coat may change, but the person wearing it is still the same.
Deb describes what “external memory” looks like in real life – not correcting or calling attention to what Peter can’t remember, but filling in the colour so he can stay part of the conversation with ease. Peter explains that while facts can disappear, feelings remain – and trust can be emotional and intuitive, even when memory is unreliable.
Peter’s cycling challenges – including riding a penny farthing – aren’t just headline-grabbing. They’re part of a bigger point: life doesn’t stop after diagnosis. Purpose, movement, and doing “your compass activity” can protect wellbeing and identity.
One of the most important takeaways is this: you may not be able to “make memories” together in the way you hope – but you can still make moments. And moments are what connection is built from, day by day.
Peter’s advice is direct and grounding: focus on what you can do, tell the right people what’s happening, don’t let shame isolate you, and live each day as it comes. Deb reinforces the human-first lens: they’re not “Tom with dementia” – they’re still Tom.
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