Show Notes
In this episode Beth discusses finally receiving an FTD diagnosis for her mum and all the emotions that came with it...
If you're struggling with anything discussed in this podcast, there are a number of helplines available. Visit alzheimers.org.uk for the dementia support line.
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More from FTD - Navigating The Cr*p
This week I’m joined by Sam, whose son Andre was diagnosed with FTD at just 22. Sadly, he passed away at 24.
Last week we heard from Suzi, who is living with FTD. This week her husband, Colin, joins me to share the other side of their story.
This week I'm joined by Suzi Barton - the FTD Warrior. Suzi was diagnosed with FTD at just 50 and has been living with it for 11 years. She's a former social worker, a mum, a nana to 11, a rock chick and a miniature maker, and she's proof that a dementia diagnosis doesn't mean life has to stop.
Series 3 kicks off in FTD Awareness Week 2026 with Emily Harris. Her mum, Andrea, was a nurse for 35 years. She was first diagnosed with young onset Alzheimer's at 56, until a genetic test showed she actually has MAPT FTD.
In this special bonus episode of FTD: Navigating the Crap, Beth is joined by Natalie Carter, host of the Dementia Dialogues podcast.