Insights from recent episode analysis
Audience Interest
Podcast Focus
Publishing Consistency
Platform Reach
Insights are generated by CastFox AI using publicly available data, episode content, and proprietary models.
Est. Listeners
Based on iTunes & Spotify (publisher stats).
- Per-Episode Audience
Est. listeners per new episode within ~30 days
1 - 1,000 - Monthly Reach
Unique listeners across all episodes (30 days)
1 - 5,000 - Active Followers
Loyal subscribers who consistently listen
1 - 500
Market Insights
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Reach across major podcast platforms, updated hourly
Total Followers
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* Data sourced directly from platform APIs and aggregated hourly across all major podcast directories.
On the show
Recent episodes
22. Zoe Chung: Raising a Baby with CMS While Facing Breast Cancer
Apr 26, 2026
50m 24s
21. Clare Best: Raising Deaf Children Bilingually
Apr 5, 2026
38m 04s
20. Courtney Hibbard: Trusting Your Instincts in a Cerebral Palsy Journey
Mar 22, 2026
28m 18s
19. Makayla Jensen: The Sibling Perspective After Brain Injury
Mar 8, 2026
31m 56s
18. Mel Garcia - Living one day at a time with Epilepsy
Feb 25, 2026
39m 26s
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| Date | Episode | Description | Length | ||||||
|---|---|---|---|---|---|---|---|---|---|
| 4/26/26 |  22. Zoe Chung: Raising a Baby with CMS While Facing Breast Cancer | 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 still in hospital with Sophia, Zoe was also diagnosed with breast cancer, beginning treatment while continuing to care for her daughter. This is a conversation about facing the unexpected on multiple... | 50m 24s | ||||||
| 4/5/26 | 21. Clare Best: Raising Deaf Children Bilingually | 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 child has the opportunity to thrive. Clare is also passionate about connecting families with the deaf community and supporting parents to feel confident in their child’s journey. Resources mentioned: &n... | 38m 04s | ||||||
| 3/22/26 | 20. Courtney Hibbard: Trusting Your Instincts in a Cerebral Palsy Journey | 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 love to connect with other families with a similar diagnosis. Resources mentioned: The Centre of Movement – https://www.centreofmovement.com.au NAPA Centre – https://napacenter.org Disability Ad... | 28m 18s | ||||||
| 3/8/26 | 19. Makayla Jensen: The Sibling Perspective After Brain Injury | 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 week he spent in a coma, and the long, uncertain road of rehabilitation that followed. She speaks honestly about the fear, the waiting, and the shift from being “just a sister” to becoming part of hi... | 31m 56s | ||||||
| 2/25/26 | 18. Mel Garcia - Living one day at a time with Epilepsy | 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 strength it takes to live one day at a time. Knowing firsthand how quickly the emotional and financial pressures mount when a child is in and out of hospital, Mel and her husband Rafa created 1 in 25 — a... | 39m 26s | ||||||
| 2/19/26 | Season 3 - Welcome Back | 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 connect with us here: Website : The Long Road Podcast Lisa McKelvey xx | 7m 02s | ||||||
| 8/24/25 | 17. Silver Linings: Sam Carroll on Life Beyond Childhood Cancer | 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 Speech - https://www.facebook.com/share/v/171Z9mAd6J/ Tour de Cure Website | 36m 25s | ||||||
| 8/10/25 | 16. Sparkle in the Storm: Julie Cross’s Story of Living and Loving with Autism | 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 Lisa McKelvey. Show notes: To find out more about Julie and her book "Living and Loving with Autism": www.juliecross.com.au | 32m 40s | ||||||
| 7/27/25 | 15. Grit and Grace on the Land: Sasha Stanton’s Journey After Her Son’s Farm Accident | 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 rebuilt her world, and the powerful ways she now supports other rural mums facing isolation and hardship. A heartfelt conversation about resilience, values, and finding strength and community in the... | 31m 03s | ||||||
| 7/6/25 | 14. When the Road is Rare: Molly Bell on Parenting Through Uncertainty | The Long Road - Episode 14 Guest - Molly Bell Hosted by - Lisa McKelvey In this episode, Molly Bell — a pharmacist, wife, and mother of two from Toowoomba, QLD chats about her family’s journey. Molly and Nathans youngest son, Alfie, was diagnosed with an extremely rare neuro deficiency disorder (PPP2R1A), which affects his gross motor skills and causes moderate intellectual disability. Molly shares some of the challenges she has faced, of raising a child with additional needs, the uphil... | 31m 39s | ||||||
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| 6/22/25 | 13. One Breath at a Time - Congenital Diaphragmatic Hernia (CDH) | The Long Road – Episode 13 Guest – Mel Nicol Hosted by – Lisa McKelvey In this episode, Mel shares what life was like raising four children while living remotely on Cubbie Station in Dirranbandi, QLD. Their journey took a complex turn when their youngest child, Will, was born with congenital diaphragmatic hernia (CDH). Mel speaks openly about the challenges, the heartbreak, and the strength it takes to be a medical mum — and how, at its core, it’s all about navigating and advocating for your... | 39m 22s | ||||||
| 6/4/25 | 12. Caroline Kiefer - A Mother’s Fight: Rare Disease (GAND) and Breast Cancer | The Long Road – Episode 12 Guest: Caroline Kiefer Hosted by: Lisa McKelvey A Mother’s Fight Caroline Kiefer is a mother of two from Melbourne, Victoria. In this episode, Caroline shares her remarkable story of strength and resilience after her only daughter, Alana, was diagnosed with a rare condition—GATAD2B-associated neurodevelopmental disorder (GAND). Together with her husband Chris and eldest son Bailey, Caroline has spent the past 17 years dedicated to giving Alana the best quality of l... | 49m 21s | ||||||
| 5/18/25 | 11. A Race Against Time: Toni Bloor’s 15-Year-Old Son James and the Life-Saving Gift of a Double Organ Transplant. | The Long Road Podcast - Episode 11 Guest - Toni Bloor Hosted by - Lisa McKelvey A Race Against Time Toni Bloor, a mother of two from Melbourne, shares her family’s extraordinary journey through heartbreak and healing. Her eldest son James survived Burkitt lymphoma at just five years old—only to face the unimaginable once again as a teenager, needing a life-saving heart and lung transplant. In this powerful episode, Toni opens up about the transplant process and the priceless gift... | 41m 35s | ||||||
| 3/30/25 | 10. The Mystery Girl. Susan Crains 11 year old daughter, Isabella and her severe case of Post Viral Myalgia Arthralgia | The Long Road Podcast - Episode 10 Guest: Susan Crain Hosted by: Lisa McKelvey In this episode of The Long Road Podcast, we welcome Susan Crain as our Episode 10 guest. Susan, a mother of three, opens up about the lasting impact of a traumatic period in her family's life when her children were young. What began as a terrible virus affecting all three kids turned into an exhausting ordeal. Like many parents, she pushed through the sleepless nights and stress, expecting the illness to pass. H... | 28m 08s | ||||||
| 3/16/25 | 9. From Heartbreak to Research: Karlie Ross on Medical Trauma, and her daughters Leukemia journey. | In this episode of The Long Road Podcast, host Lisa McKelvey sits down with Karlie Ross from Toowoomba, QLD, to discuss her family’s deeply personal journey through childhood trauma. Karlie and her husband, Mason, faced an unimaginable challenge when their daughter, Ellie, was diagnosed with Leukemia just before her second birthday. At the same time, they were navigating the complexities of raising their son, Leo, who has non-verbal autism outside the home. Through it all, they’ve fought to f... | 47m 08s | ||||||
| 3/2/25 | 8. A Father’s Story: How One Tragedy Changed a Family Forever (Jeff McPaul Story) | In this powerful episode, host Lisa McKelvey sits down with Jeff McPaul to reflect on a tragedy that changed his family's life forever. 25 years ago, Jeff’s four-year-old son, Matty, was hit by a car in a devastating accident. Matty’s recovery has been a lifelong journey, shaping the resilience, strength, and love within their family. Jeff shares his insights on grief, hope, and the lessons they've learned along the way. #thelongroadpodcast #traumaticbraininjury #strength #l... | 34m 04s | ||||||
| 2/16/25 | 7. The apple doesn't fall far from the tree - Emma Rennison's children both have her genetic condition Multiple Epiphyseal Dysplasia (MED) | Emma Rennison chats with host Lisa McKelvey about the difficulties her mum went through with getting medical assistance for what was originally thought to be hip dysplasia for herself as a child. Then years later, as a mother, Emma sits in medical appointments and by her childrens bedside, while they have extensive orthopedic conditions as well. The Rennisons now have a diagnosis of the genetic condition - Multiple Epiphyseal Dysplasia (MED) Emma is a wonderful mother, wife, writer, s... | 1h 12m 53s | ||||||
| 12/1/24 | 6. A thank you note - Elisa Spano's 12 yr old son, Rafferty and his long road with Perthes Disease | In episode 6 of The Long Road podcast, we sit down with Elisa Spano, a dedicated mother of 2, to discuss her son's journey with Perthes Disease. Elisa shares her story, shedding light on the emotional, physical, and medical hurdles their family has faced since the diagnosis. From the initial signs, Elisa offers insight into what it's like to advocate for a child with a rare and often misunderstood condition. This episode is a must-listen for anyone touched by chronic illness or seeking inspi... | 45m 19s | ||||||
| 11/10/24 | 5. From Day One. Aylish Mahers son has a severe cardiac condition and 22q. | In Episode 5 of The Long Road Podcast, host Lisa McKelvey will speak with Aylish Maher a wife, to Mick Maher and mother to two beautiful children Miley and Monty. The Maher family begun their long road on day one of Montys life. Monty has a severe cardiac condition and was diagnosed with 22q deletion. Monty is currently 4 years old, and Aylish speaks about the whirlwind of the first year, time in the Queensland Childrens hospital and life as they know it now. Please enjoy the li... | 1h 03m 55s | ||||||
| 10/27/24 | 4. Just Keep Swimming-Tamara Lloyds journey with son Kai and his high functioning Autism. | Tamara Lloyd, together with her husband Jono are raising 3 beautiful children. Life definitely has its challenges with their eldest Kai (13 yo) having high functioning autism. Kai is non verbal, and in her 13 years of raising Kai, Tamara has never heard him say the words I love you. Only a handful of times has she heard him say the name "mum". Yet their bond is so so special. Tamara chats with host, Lisa McKelvey about raising Kai, family life in Goondiwindi QLD and all things a... | 51m 50s | ||||||
| 10/13/24 | 3. A Healing Heart - Sarah Moorcrofts baby "Hunter" diagnosed with Myocarditis at 6 weeks old. | Sarah Moorcroft had always dreamed of having children, and after meeting her husband John and having her first born, soon found out, its not always as straight forward as you would imagine. Sarah chats on the podcast with host, Lisa McKelvey, about her second born son Hunters time at the Queensland Childrens Hospital with inflammation of his heart muscle - Myocarditis, life since, and some of the things she has learnt on this precious journey. Enjoy the listen! Kids Heart... | 33m 22s | ||||||
| 9/29/24 | 2. Choosing Happiness - Jen Drummonds son, Rafferty's devastating severe traumatic brain injury | Jen Drummonds son, Rafferty (2) was tragically struck by a car while riding his balance bike, with his family while they were walking their dogs. Rafferty devastatingly sustained a severe traumatic brain injury. Jen chats with host, Lisa McKelvey, about family life since the life changing accident. Jen and her husband Dylan have chosen to pick happiness and make the most of the life that they do have with their family, although its not always easy. Putting one foot in fron... | 43m 05s | ||||||
| 9/15/24 | 1.Riding Lifes Waves - Brooke Colless and a rare AVM Spinal Injury effecting her eldest, Kai. | What do you do when your on an adventure of a life time overseas with your husband and 5 kids, when your eldest son becomes increasingly unwell, and after seeking out medical help, you hear the diagnosis - he has a rare AVM on his spinal cord? Brooke Colless has lived this incredible story. Its one of love, hope and faith. Show Links: Brooke Colless - Blonde Nomads - https://www.instagram.com/blondenomads?igsh=Mzd2cmx0bTc2OWJv | 48m 08s | ||||||
| 9/8/24 |  Trailer - Welcome | Hi and welcome to The Long Road. Hosted by Lisa McKelvey, a mother of 5 children ranging in age from 16 - 5 years old. She lives with her husband Steve in Goondiwindi, QLD. On boxing day 2021, Lisas second eldest son Beau, had a motorbike accident which resulted in a Spinal Cord Injury, at just 12 years old. Lisa has gained so much by speaking with other parents who also have experienced a life changing trauma with their young person. She shares some of those stories with you on The L... | 4m 30s | ||||||
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Chart Positions
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Chart Positions
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