ABOUT THIS PODCAST 🔗

Update frequency:
every 18 days
Average audio length:
40 minutes
Guest interviews
English
United States
25 episodes
since Sept. 8, 2024
episodic

LATEST EPISODE 🔗

In this episode of The Long Road Podcast, Lisa sits down with Heidi McIntosh to share the story of her son, Benaiah Roi, and the profound impact of neonatal loss on her family. After a healthy pregnancy, Heidi and her husband Caleb received unexpected news at 37 weeks that their unborn son was crit…

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In this episode, I’m joined by Zoe Chung, a mum to her daughter Sophia, who was diagnosed with Congenital Myasthenic Syndrome (CMS) after a complex start to life. Zoe shares her experience navigating the NICU, receiving a rare diagnosis, and adjusting to life with a medically complex child. While s…
Clare shares her journey raising her 5-year-old son Frank, who is deaf, and what it has looked like navigating diagnosis, early intervention, and raising him bilingually using Auslan and spoken English. We talk about advocacy, language access, and the importance of creating a world where every chil…
Courtney shares her journey raising her 3-year-old son Larry, who lives with cerebral palsy and complex medical needs. We talk about advocacy, trusting your instincts, and embracing that every child develops in their own time. Larry also has a rare genetic mutation called CBX1, and Courtney would l…
In this episode of The Long Road, I sit down with Makayla Jensen to share the story of her younger brother Beau, who survived a life-threatening drowning accident just days after his 17th birthday. Makayla takes us back to the moment her family received the call that Beau was being given CPR, the w…
In this episode of The Long Road, Lisa sits down with Mel Garcia to share the moment everything changed — when her eight-month-old daughter experienced a prolonged seizure that led to a diagnosis of Dravet Syndrome. Mel speaks openly about the fear, hospital stays, constant vigilance, and the stren…
Welcome back to Season 3 of The Long Road. This podcast was created to remind families facing childhood trauma, disability and adversity that they are not alone. I’ve missed these conversations — and I’m so excited for what’s ahead this season. Thank you for being here. Find all episodes and connec…
At 9 years old, Sam Carroll was diagnosed with a rare childhood cancer. Now 21, he reflects on his journey through treatment, recovery, and the silver linings he’s discovered along the way.  A story of courage, resilience, and hope.  Hosted by: Lisa McKelvey Show Notes:  Video of Sams Tour De Cure …
Julie Cross shares the hardest chapter of her life — losing her husband Flash after a stroke, parenting two young boys, and navigating her youngest son Thomas’s autism diagnosis.  Through heartbreak and challenge, Julie has mothered through the storms with sparkle, humour, and wisdom.  Hosted by Li…
When Sasha Stanton’s 3-year-old son, Logan, lost his leg in a devastating farm accident (2018), life changed in an instant. What followed was a period of deep trauma, reflection, and ultimately, personal growth.  In this episode, Sasha shares the raw truth of parenting through crisis, how she rebui…
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