The Long Road

Lisa McKelvey
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Sharing stories of parents who have a young person who has experienced a life changing trauma in Australia. Hosted by Lisa McKelvey. 

  1. 7. Juni

    23. Heidi McIntosh: A Family Forever Changed by Neonatal Loss

    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 critically unwell. What followed was a journey of hope, fear, love, and heartbreak as they stayed in Brisbane for specialist care and welcomed Benaiah into the world. Benaiah lived for six precious days before unexpectantly passing away due to a sepsis infection.  With remarkable honesty and vulnerability, Heidi reflects on navigating grief as a mother, supporting siblings through loss, the challenges of life after trauma, and learning to hold both joy and heartbreak at the same time. Together, Lisa and Heidi discuss the realities of neonatal loss, the importance of acknowledging grief, and the ways families can continue to honour the children they carry in their hearts. This conversation contains discussion of neonatal loss, infant death, grief, and trauma. Please listen at your own pace. Resources mentioned in this episode: • Red Nose Australia – support and resources for families affected by stillbirth, miscarriage, and newborn death. Join A Support Group | Red Nose Australia • Red Nose Bereavement Support Community (Facebook Group) • SANDS Queensland (Stillbirth and Neonatal Death Support) http://www.sands.org.au/ Books:  - A Grief Observed – By C.S. Lewis  - It's OK That You're Not OK: Meeting Grief and Loss in a Culture That Doesn't Understand. By Megan Devine - How To Carry What Cant Be Fixed. A journal for Grief. By Megan Devine  If this episode has brought up difficult emotions for you, please reach out to a trusted support person or professional support service. To keep up to date with The Long Road Podcast, follow along on Facebook and Instagram or visit thelongroad.au. Thanks for being here, Lisa McKelvey xx

    1 Std. 9 Min.

  2. 26. Apr.

    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 fronts, the reality of medical motherhood, and what it looks like to keep moving forward through it all. As always, this episode is a reminder that even in the hardest seasons, you’re not alone. Show Links: Very Special Kids - Providing holistic palliative care for children and young people across Victoria. Medical Mums Australia (of kids with complex medical needs): https://www.facebook.com/share/g/18WsAxGBhu/ Zoes Instagram account  https://www.instagram.com/zoefromtiktok?utm_source=ig_web_button_share_sheet&igsh=ZDNlZDc0MzIxNw== Thank you for being here, Lisa xx

    50 Min.

  3. 5. Apr.

    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:  Deaf Connect – https://deafconnect.org.au Deaf Australia – https://deafaustralia.org.au Expression Australia – https://expression.com.au Follow Clare on Instagram: @raisingbilinguals Thanks for being here, Lisa McKelvey x

    38 Min.

  4. 22. März

    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 Advocacy Network Australia (DANA) – https://www.dana.org.au Follow Courtney on Instagram: @court.a.ney Thanks for being here, Lisa McKelvey x

    28 Min.

  5. 8. März

    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 his care and recovery. This is a beautiful conversation about trauma, resilience, and the unseen experience of siblings when everything in a family changes overnight. If you’ve ever wondered what that side of the story feels like, this episode is for you. Hosted by: Lisa McKelvey Show Notes: Bring it 4 Beau Insta Link - https://www.instagram.com/bringit4beau?utm_source=ig_web_button_share_sheet&igsh=ZDNlZDc0MzIxNw==

    32 Min.

  6. 25. Feb.

    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 — an advocacy initiative raising awareness and funds to support families affected by epilepsy. The name reflects the statistic that 1 in 25 Australians will experience epilepsy in their lifetime. Website: 1IN25.co Thank you for walking this road with us. Lisa McKelvey x

    39 Min.

  7. 19. Feb.

    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

    7 Min.

  8. 24.08.2025

    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

    36 Min.
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Sharing stories of parents who have a young person who has experienced a life changing trauma in Australia. Hosted by Lisa McKelvey. 

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  • Erstellt von
    Lisa McKelvey
  • Jahre aktiv
    2024 - 2026
  • Folgen
    25
  • Bewertung
    Unbedenklich
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    © 2026 The Long Road
  • Sendungswebsite
    The Long Road

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