Reasons To Be Joyful with Gaby Roslin
Reasons To Be Joyful with Gaby Roslin

Reasons To Be Joyful with Gaby Roslin

Spiritland Productions

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Gaby Roslin wants to spread joy and THAT is what this podcast is all about.Each week, she welcomes a famous face to the studio to find out what makes them smile, chuckle and belly laugh.We find out what brings them joy in their lives and, in our bonus Show & Tell episode, get a glimpse into their lives as they tell us about an object they love, & why.Subscribe and follow the podcast, from your platform of choice, so you never miss an episode! (And follow Gaby on instagram and twitter)

Recent Episodes

Jordan Adams (The FTD Brothers)
MAR 24, 2026
Jordan Adams (The FTD Brothers)
<p>Gaby is joined by Jordan Adams - one of the FTD Brothers - who tells us all about his journey with dementia and the importance of finding the joy in things every day. </p><p>Jordan and his brother are on a mission to cure dementia before it takes their own lives. They have raised an amazing amount of money so far - and continue to do so, through running! </p><p>You can find out more about what they're doing on their <a href="https://www.instagram.com/theftdbrothers/">instagram </a>- and - donate to via their<a href="https://www.gofundme.com/f/theftdbrothers"> go fund me page</a>. </p><p>And here's a little more about Jordan and his family's journey:<br><br>"After our mum’s passing, our sister Kennedy felt a burning need to know whether she would inherit the same illness. Through family connections in Ireland, she arranged an appointment at the Dublin Neurological Institute with Professor Tim Lynch, who had researched familial FTD within our family.</p><p>Kennedy underwent research studies and genetic counselling before receiving her test result in 2018. She had inherited the normal copy of the gene from our dad — meaning she would not develop FTD.</p><p>For the first time in years, we had good news.</p><p>Kennedy was able to move forward, start a family, and live without the shadow we had all been carrying. Her bravery gave Jordan the courage to follow the same path. In September 2018, Jordan received his result: a carrier of the faulty MAPT gene, meaning he will develop the same form of dementia as our mum.<br><br>Jordan describes that diagnosis as a 'licence to live'. Knowing what lies ahead has sharpened every decision since — including the decision to ensure this disease is not passed on further. Tragically, earlier this year, Jordan and his partner Agnès learned during a pregnancy that their child had also inherited the faulty gene, and they were unable to continue. Their journey to start a family continues."</p>
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38 MIN