FTD - Navigating The Cr*p

As a 30-something year old living in Lancashire in the North West of England, Beth has been living with the impact of her mum's diagnosis of early onset FTD (Frontotemporal Dementia) at the age of 65. For the last year she's been sitting down with a friend and a microphone to go over everything that's happened along the way. Loving someone with FTD is a club nobody wants to be a part of but Beth hopes that talking about it and sharing experiences helps others to feel less alone. This isn’t meant to be a shiny podcast that gives you all the answers. For a lot of us, the answers don’t exist - we’re just getting on the best we can. Hosted on Acast. See acast.com/privacy for more information.

FTD - Navigating The Cr*p is a health podcast hosted by Beth Jones, with 16 episodes on record and a Required Pod Score of 80. PitchCentric scores this show on Booking Probability, Listen Score, and live audience signals refreshed every 24 hours.

Beth Jones hosts FTD - Navigating The Cr*p, a health show with 16 episodes published.

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  Episode #11

  FTD Navigating the Cr*p X Dementia Dialogues

  Dec 15, 202544 minS2

  <p>In this special bonus episode of FTD: Navigating the Crap, Beth is joined by Natalie Carter, host of the Dementia Dialogues podcast.</p><br><p>Earlier this year, Beth shared her own family’s experience of Frontotemporal Dementia on Natalie’s podcast, and now the roles are reversed as she joins Beth to share her story and reflect on what she’s learned through years of honest conversations with carers and families affected by dementia.</p><br><p>Together, they talk about the shock of diagnosis and the devastating lack of follow-up support so many families face, the emotional weight...

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  Episode #10

  What This Year Taught Me About FTD: Season Two Reflections

  Nov 17, 202515 minS2

  <p>In this final episode of Season Two, Beth takes a moment to pause, look back, and share where life - and her mum’s dementia journey - are now.</p><br><p>She talks openly about the hardest moments of the past year: the sudden overnight decline that changed everything, learning to adapt to new routines with her dad and facing the reality that dementia is a progressive, life-limiting disease.</p><p>Beth also reflects on the powerful conversations she’s had throughout this series - from Helen’s genetic testing experience to Eleanor’s discussion on living grief - and ho...

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  Episode #9

  Living Grief and Unspoken Thoughts with Eleanor Connelly from Tide

  Nov 10, 202525 minS2

  <p>In this episode, Beth is joined by Eleanor Connelly from Tide (Together In Dementia Everyday) - a charity dedicated to supporting carers and former carers of people living with dementia. Eleanor opens up about her experience caring for her dad with vascular dementia, and how her own grief led her to the work she now does.</p><br><p>Together, we explore one of the hardest and most hidden parts of dementia: living grief. </p><p>The grief you feel while your loved one is still here - but changing. The weight of the lives you’re no longer li...

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  Episode #8

  When Nana’s Dementia Touched Us All: Lauren’s Story

  Nov 3, 202532 minS2

  <p>In this episode, Beth is joined by her friend Lauren, who shares the story of her Nana’s dementia diagnosis at 87, after years of slowly declining health. </p><br><p>Lauren explains how her Nana’s diabetes complicated symptoms, delayed a diagnosis and masked what was really going on - and how dementia still hit her family like a shockwave, even at an older age.</p><br><p>This episode is a reminder that dementia always hurts, no matter how old someone is. It still shakes families, it still changes everything and it still takes so much love, patience and...

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  Episode #7

  Facing The Future with Familial FTD: Helen’s Story

  Oct 28, 202550 minS2

  <p>In this episode, Beth is joined by Helen, whose family has been profoundly affected by familial FTD. </p><p>Helen first experienced the disease through her aunt, and later through her mum. When her mum was diagnosed, Helen was confronted with the reality that FTD could be genetic and that it might also shape her own future.</p><br><p>With honesty and courage, Helen shares what it was like growing up in a close, loving family, watching both her mum and aunt change through FTD, and eventually making the difficult decision to undergo genetic testing herself. </p><br><...

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