エピソード

  • Disability, Resilience & Real Stories | Golden Threads Podcast Trailer

    Disability, Resilience & Real Stories | Golden Threads Podcast Trailer
    2026/04/06

    Golden Threads: Stories of Disability & Resilience

    Golden Threads is a Kintsugi Heroes podcast hosted by Daniel Dougherty, sharing honest, lived-experience conversations with people navigating disability, identity, and inclusion.

    This series explores what it really means to adapt, persevere, and live fully in a world still learning what accessibility and inclusion look like in practice.

    Each episode brings forward real stories — not focused on labels, but on people, relationships, and lived experience.

    Topics covered:

    disability, resilience, lived experience, inclusion, accessibility, identity, mental health, community, personal stories

    About Kintsugi Heroes

    Kintsugi Heroes is an Australian not-for-profit dedicated to strengthening wellbeing through lived-experience storytelling.

    We create safe, respectful spaces where stories can be shared with dignity — helping people feel seen, heard, and connected.

    Learn more or support the work:

    https://www.kintsugiheroes.com.au

    https://www.kintsugiheroes.com.au/donate/#donate

    Mentioned in this episode:

    Kintsugi Heroes

    Follow the show, share it with someone who needs it, or share your own story at kintsugiheroes.com.au. Your story matters.

    Support Kintsugi Heroes

    Kintsugi Heroes is a not-for-profit, and every story we share is free for the people who need it. If this show has meant something to you, you can help us keep going. Visit kintsugiheroes.com.au and click donate. Every contribution helps us keep telling these stories, and it's tax-deductible.
    続きを読む 一部表示
    3 分
  • Leanne Watson: Three Acts, a Diagnosis, and a Life Built on Community

    Leanne Watson: Three Acts, a Diagnosis, and a Life Built on Community
    2026/05/04
    Leanne Watson sees her life in three acts — and the third one started the day a freshly minted GP finally took her seriously.For nearly a decade, doctors fobbed her off. Lose weight. Build glutes. You've had three kids. One specialist had her parade in her bra and undies and said she "looked fine." She was 42 when she was finally diagnosed with limb girdle muscular dystrophy (LGMD) — a rare, progressive neuromuscular condition that's been quietly dismantling her muscles ever since.In this Episode 1 of Golden Threads, host Dan Dougherty sits down with Leanne — now 60, podcaster, former community radio host, and one of the warmest advocates you'll meet — to talk about what it's actually like to become disabled in slow motion. The optimism. The grief that doesn't announce itself. The husband who decided this happened to both of them. The strangers who pray over her in hotel lobbies. And the barista at Chadstone who looked her in the eye and changed how she felt that whole day.This is a conversation about disability, inclusion, marriage, motherhood, advocacy, and the simple radical act of saying hello.Key Takeaways- A life in three acts. Leanne maps her 60 years into three chapters — the privileged childhood and young marriage, the family-building decades, and the third act that began the moment she was diagnosed at 42.- The cost of being dismissed. Nine years of being fobbed off by doctors before a young GP ordered the right blood test. A reminder that women, especially, get told their bodies are "just changing."- "This has happened to the both of us." Leanne's husband Gary's quiet philosophy — and what it teaches us about love, partnership, and refusing to make disability a solo project.- Inclusion is small, daily, and specific. From the strangers who pray over her uninvited to the barista who simply looked her in the eye — Leanne unpacks what real inclusion looks like in everyday Australian life.- Community is non-negotiable. Why she joined Women with Disabilities Victoria, started a radio show, and now hosts her own podcast — and why one phone call to a community group can change everything.Guest BioLeanne Watson lives on the Bellarine Peninsula in Victoria with her husband Gary. She is the eldest of four, a mum of three, and grandparent to a growing family. After a career at Westpac and decades of part-time work and community volunteering, Leanne was diagnosed with limb girdle muscular dystrophy (LGMD) at 42. Today she is the host of You, Me and Muscular Dystrophy, a former presenter of Rolling Through Wednesdays on Pulse FM, and an active member of Women with Disabilities Victoria (Barwon Hub).Find Leanne:- Website: Leanne's Wheel Life — leanneswheellife.com - Podcast: You, Me and Muscular Dystrophy (YouTube, Spotify, Apple Podcasts)- Instagram: @leanneswheellife Resources Mentioned- Limb Girdle Muscular Dystrophy (LGMD) — overview via Muscular Dystrophy Australia: mda.org.au- Women with Disabilities Victoria (WDV) — wdv.org.au — Leanne is a member of the Barwon Hub- Women with Disabilities Australia (WWDA) — wwda.org.au- From the Outskirts — WDV's podcast featuring women with disabilities going about their lives- Rolling Through Wednesdays — Leanne's former weekly spot on Pulse FM (community radio, Bellarine), supported by Loretta Hart- You, Me and Muscular Dystrophy — Leanne's current podcast (YouTube, Spotify, Apple) Timestamps- 00:00 Cold open + welcome to Golden Threads- 01:01 Meeting Leanne — and the breathing tube on the desk- 02:42 What limb girdle muscular dystrophy actually is- 03:53 A life in three acts: childhood in Melbourne's east- 06:11 Meeting Gary in Year 11 — and a life built early- 08:19 Marriage, motherhood, and a quietly privileged life- 08:49 Something starts changing at 35- 09:46 Nine years of being fobbed off by specialists- 11:43 The blood test that finally cracked it open- 12:11 Diagnosis at 42 — and the third act begins- 13:35 The slow inventory: high heels, toilet frames, stairs- 17:58 "Each time I thought, this is it. It's not going to get worse."- 19:21 Optimism, pragmatism, and protection- 20:15 Gary's philosophy: "this has happened to the both of us"- 22:08 Parenting through progression- 23:07 What end of life looks like from here- 25:30 Loneliness, community, and being seen- 25:52 What it's like being treated as "different"- 27:46 The strangers who pray over her uninvited- 30:30 The wheelchair "speed jokes" — and why they sting- 31:54 What Dan got wrong, and what real inclusion looks like- 34:30 Choice, consent, and being pushed without permission- 34:56 The Chadstone barista who got it right- 36:32 Anatomy of LGMD — what it does muscle by muscle- 40:22 Why Leanne started You, Me and Muscular Dystrophy- 41:18 The power of community — book club, WDV, Pulse FM- 44:00 The radio show, the illness, and finding podcasting- 45:26 "Just make one phone call."- 47:48 Final reflections: we are only as strong as our weakest link- 50:08 ...
    続きを読む 一部表示
    51 分
  • Julie Fisher: A Mother's Advocacy, Down Syndrome, and the Glue That Holds a Family Together

    Julie Fisher: A Mother's Advocacy, Down Syndrome, and the Glue That Holds a Family Together
    2026/05/18
    Two years before Julie Fisher fell pregnant with her third child, the universe set her up.She'd just become friends with a woman named Tina, whose daughter Amy had Down syndrome. Julie had never met anyone with Down syndrome before. She watched Amy in the playground. She asked questions. And one of the answers — about how hard a postnatal diagnosis can be when nobody warned you — quietly rewrote what Julie would do if it ever happened to her family.It did. At 12 weeks pregnant, an ultrasound flagged a marker. At 15 weeks, an amniocentesis confirmed it. Then came five appointments with two different doctors pushing termination — until Julie yelled at them at 25 weeks that she wasn't going anywhere.In Episode 2 of Golden Threads, host Dan Dougherty sits down with Julie — author of five books, weekly radio host, motivational speaker, founder of an annual disability expo, and mum to 19-year-old Darcy — to talk about advocacy that starts before a baby is born, the fear-based stares that turned out not to be stares at all, and the signature line she takes everywhere: "Give people a chance and watch them shine."This is a conversation about motherhood, disability, inclusion, the slow work of changing minds, and the kind of family glue you don't see coming.KEY TAKEAWAYS- Advocacy that started before birth. How a friendship with another mum and a single conversation about postnatal diagnosis prepared Julie to say "we want to know" — and to push back hard against five appointments of termination pressure.- "He came into the world like a rock star." Born five weeks early with a roomful of doctors and students waiting to see how he'd cope, Darcy entered screaming. He's been entering the world that way ever since.- The Darcy effect on a family. Two older brothers, a busy house, and the third child who became the glue. Why Julie's other boys argue with him, stir him up, and treat him exactly like a brother — and why that's the win.- From defence mode to smiling back. Julie's honest account of being in mama-bear mode at every stare in the supermarket — and how learning to smile first changed her, her son, and a lot of strangers.- "Give people a chance and watch them shine." Julie's signature quote, plus the five books, the radio show, and the annual expo it now powers.GUEST BIOJulie Fisher is an Australian author, motivational speaker, weekly radio host, community organiser, advocate, and mum of three. She lives in Victoria with her family and her son Darcy, 19, who has Down syndrome. Julie is the author of five books, including "The Unexpected Journey", "The Magic of Inclusion", "From the Hearts of Mums" (gold award winner), the children's book "Big School", and her latest, "The Adolescent Journey". She hosts a weekly disability-focused radio show (now over 100 episodes deep) and founded her local disability expo. Her signature quote — "Give people a chance and watch them shine" — has become a small movement in itself.RESOURCES MENTIONED- "The Unexpected Journey" — Julie's first book about Darcy's birth and early years- "The Magic of Inclusion" — Julie's second book on community and acceptance- "From the Hearts of Mums" — anthology of 13 mothers of children with Down syndrome (gold award winner)- "Big School" — Julie's children's book- "The Adolescent Journey" — Julie's latest, on the teenage years and the practical side (Centrelink, NDIS, functional capacity assessments, tax file numbers)- Down Syndrome Victoria — dsav.asn.au- Carers Victoria — carersvictoria.org.au- Carers Australia — carersaustralia.com.au- NDIS — ndis.gov.auTIMESTAMPS- 00:00 Cold open + welcome to Golden Threads- 00:32 Meeting Julie Fisher — author, advocate, mum- 01:28 The friendship that set everything up — meeting Tina and her daughter Amy- 02:59 Pregnant with Darcy: the ultrasound, the nuchal fold, the question- 04:03 Walking into the obstetrician already knowing- 04:34 The amniocentesis result — and what it actually felt like- 05:13 Five appointments, two doctors, and the 25-week yelling match- 05:50 The mixed reactions of family and friends- 06:40 Tina's support group: 10 mums, every fortnight- 08:23 Where mother-bear advocacy actually comes from- 09:51 Mapping out a primary school life before he was born- 11:21 Darcy enters the world like a rock star- 12:33 Family life with three boys — and a baby in special care- 13:53 The brothers' protective instinct, and why she'd just sit back and watch- 15:34 Dual schooling: four days specialist, one day mainstream ("Darcy Day")- 16:41 Why high school had to be specialist — and why Darcy thrived- 18:01 Life after school: performing arts and the working farm- 19:05 The one thing she sometimes wonders about- 21:25 Worry, vulnerability, and the world getting better- 23:01 Going out in the community — stares, smiles, and learning to smile first- 26:15 Why "if you want to ask, ask" is part of the message- 27:41 The fear that drives a lot of awkward ...
    続きを読む 一部表示
    59 分
  • Paul Jamieson: Nine Years After the Wakeboard, the Mango, and the Hand Squeeze That Said He Was Still There

    Paul Jamieson: Nine Years After the Wakeboard, the Mango, and the Hand Squeeze That Said He Was Still There
    2026/06/01
    For almost two years after his brain injury, Paul Jamieson could not eat or drink anything. When his speech pathologist finally decided he was ready to try, she asked him what he wanted. He said mangoes. He still remembers exactly what it tasted like.Nearly nine years ago, Paul was wakeboarding on a lake in Victoria when a fall headfirst into the water caused a severe brain bleed. He was helicoptered to the Alfred Hospital, where surgeons drilled a hole in his skull to relieve the pressure. The surgery saved his life, but the brain injury had already happened. In the weeks that followed, Paul was absent from his own body, existing but not present, with doctors at one point considering palliative care. Then, without explanation, he started to get better.Host Daniel Dougherty sits down with Paul to trace the nine years since: the speech pathologist who worked on his swallowing muscles for months before the mango was possible, the physiotherapist who pressed her body weight onto his knees to get one revolution on a stationary bike, the ex-partner who sat beside him every day when he could not respond, and the hand squeeze that told that partner he was still in there. Paul also talks about moving into his own apartment in Brunswick, training for a 40-kilometre bike ride, co-authoring a research paper, and pursuing motivational speaking and allied health work. He is, by his own account, happier now than he was before the accident. He knows how that sounds.This is a conversation about acquired brain injury, rehabilitation, independent living, the people who make recovery possible, and what it means to appreciate the smallest things.Key Takeaways- Recovery is measured in small, specific milestones. From one revolution on a stationary bike to a 30-kilometre ride on an electric tricycle, Paul's progress has been built on incremental goals set by a team of therapists who had a vision for him that he could not always see himself.- The people beside you matter as much as the therapy. Paul's family, his ex-partner Adam, and his support workers Rachel and Isabelle each played a distinct and named role in his recovery. He is specific about what each of them gave him, and careful to credit them.- Positivity, for Paul, is not a choice but a condition. Paul describes the brain injury as having knocked the negativity out of him. Before the accident he was struggling. After it, something shifted. He does not frame this as inspiration; he describes it as something that happened to him.- Independent living is a system, not a solo act. Paul's apartment in Brunswick has 24-hour on-site support staff. He calls them when he needs them and does not when he does not. That structure is what makes his independence possible, and he is clear about that.- Contribution is part of the recovery. Paul is pursuing motivational speaking, a traineeship at Jigsaw, a short course in medical reception, and a co-authored research paper. He sees each of these as a way of giving something back, not just as personal milestones.Guest BioPaul Jamieson is a Melbourne-based speaker and advocate who sustained a severe acquired brain injury in a wakeboarding accident nearly nine years ago. After an extended period of rehabilitation that included relearning to speak, swallow, and move, he now lives independently in Brunswick with on-site support. He has produced a five-part podcast series about his recovery, Beyond the Impact, available on Spotify, and speaks at universities and workplaces about resilience, positivity, and life after brain injury. His website is pauljamieson1.com.Resources Mentioned- Beyond the Impact, Paul's Recovery Story, https://open.spotify.com/ (Paul's five-part podcast series on Spotify featuring his speech pathologist, OT, and physiotherapist)- Paul Jamieson's website, http://pauljamieson1.com (Information on Paul's motivational speaking services and background)- Jigsaw (Organisation where Paul is completing a traineeship in preparation for allied health reception work)- Walter and Eliza Hall Institute (WEHI), https://www.wehi.edu.au (Medical research institute where Paul worked in the breast cancer lab prior to his accident)- The Alfred Hospital, https://www.alfredhealth.org.au (Melbourne hospital where Paul received emergency surgery following his brain injury)- Kintsugi Heroes, https://kintsugiheroes.com.au (Tax-deductible donations to support the podcast)Chapters00:00 Introduction and welcome01:47 The wakeboarding accident03:14 Surgery at the Alfred, and the brain injury07:02 Life since the Beyond the Impact podcast08:52 Moving into his own apartment in Brunswick13:56 Being absent from his own body15:47 The therapists who changed his recovery17:34 Two years without eating, then the mango20:01 The stationary bike and the electric tricycle25:20 Adam, the hand squeeze, and a friendship that held30:38 How the brain injury changed his relationship with negativity32:47 Motivational speaking and the website38:27 The 40-kilometre ...
    続きを読む 一部表示
    56 分
  • Ian Harvey: Unlocking Experiences and Rewriting What's Possible in Disability

    Ian Harvey: Unlocking Experiences and Rewriting What's Possible in Disability
    2026/06/15
    SUMMARYA diving accident on a Boxing Day cricket trip changed everything — for an 18-year-old named Jason, and for Ian Harvey, the young rugby coach standing beside him. In this episode of Golden Threads, host Daniel Dougherty sits down with Ian — National Foundation Manager for the WhatAbility Foundation in Perth — to trace a 20-year journey from fitness manager to one of Australia's most quietly powerful advocates for inclusion. Ian shares two friendships that reshaped his life (Jason and Doug, both quadriplegic after sudden injuries), the lessons they taught him about honesty, friendship, and fun, and his work today gifting tickets, experiences, and joy to families living with disability across Australia.EPISODE PILLARSThe phone call that changed everythingIan unpacks the day Jason — a 17-year-old he coached — broke his neck diving into a wave, and how that single moment rewired his understanding of disability, friendship, and luck.Friendship as the real teacherThe lesson Jason gave a mental health nurse from a hospital bed — "I feel fine, I've got my mates here" — and what 20+ years of friendship has taught Ian about showing up, honesty, and not turning away from hard conversations.Why fun is the missing piece in disability supportIan explains why WhatAbility is built around joy, jet skis, footy and four-wheel-driving — and why "fun" is too often the first thing stripped from disability service models.Like Santa Claus every dayInside the WhatAbility Foundation: gifting up to six tickets a month per family, and partnering with the Australian Grand Prix, the Australian Open, Fun Lab and Bounce to unlock experiences usually out of reach.One million experiences by 2035Ian's bold goal — and why his vision for an inclusive Australia means building events so good that people without disability in their lives feel like they're missing out.GUEST BIOIan Harvey is the National Foundation Manager at the WhatAbility Foundation, based in Perth, Western Australia. After two decades managing health clubs and gyms across Australia, Ian pivoted into the disability sector — drawing on more than 20 years of personal experience supporting two close friends, Jason and Doug, both of whom acquired spinal injuries in their late teens and early twenties. Ian leads the Foundation's national mission to unlock one million inclusive experiences for people with disability and their families by 2035.LINKSWhatAbility Foundation — https://whatabilityfoundation.org.auWhatAbility (NDIS provider) — https://whatability.com.auRESOURCES MENTIONEDRiding for the Disabled Association (RDA) — https://www.rda.org.auAustralian Grand Prix sensory pit-lane toursAustralian Open accessibility programmingFun Lab and Bounce inclusive sessionsNDIS — https://www.ndis.gov.auTIMESTAMPS00:00 Welcome to Golden Threads00:43 Meet Ian Harvey01:21 What is the WhatAbility Foundation02:43 The fitness years04:50 COVID burnout and the career pivot05:41 "Two Steves" — meeting WhatAbility07:38 First experience with disability — Jason09:09 The diving accident12:06 The phone call and the guilt13:41 Mum's volunteer work with RDA14:06 Doug's accident in Canada16:08 Standing on the family's doorstep20:00 The 20-year journey with Jason22:18 "I feel fine" — what Jason said in hospital24:27 Jason today — chartered accountant via voice control27:39 The true value of friendship30:02 Beyond physical reciprocity33:25 Hidden disabilities and being comfortable with hard questions36:31 Feeling like you get more than you give40:09 Like Santa Claus every day40:42 The Australian Grand Prix collaboration42:42 Inside the WhatAbility model46:06 No such thing as a barrier49:22 Meeting WhatAbility — the night at the footy52:18 Society and hidden disabilities53:55 The future — 1 million experiences by 203555:34 Building a one-stop platform for inclusion58:40 Closing words and gratitudeCALL TO ACTIONIf this episode moved you, please follow Kintsugi Heroes on Apple Podcasts, Spotify or your preferred app, leave a rating or review, and share it with someone who needs to hear it. To support our not-for-profit mission to share more stories like Ian's, visit kintsugiheroes.com.au and make a tax-deductible donation, or get in touch about partnering with us.THE KINTSUGI CONNECTIONWatch every episode on YouTube — https://www.youtube.com/@kintsugiheroesIf this story resonated, explore more from our Disability Series — honest conversations with advocates, carers, and people with lived experience reshaping what inclusion looks like in Australia.ABOUT KINTSUGI HEROESKintsugi Heroes is a not-for-profit storytelling platform sharing real stories of resilience, disability and transformation. Inspired by the Japanese art of kintsugi — repairing broken pottery with gold so the cracks become the most beautiful part — we believe every life can be made more beautiful through what it has survived.PARTNER WITH USWe work with NDIS providers, advocacy organisations,...
    続きを読む 一部表示
    1 時間 2 分
  • Jeff Parker: From Weightlifter to Blind Advocate — 36 Years of Showing Up

    Jeff Parker: From Weightlifter to Blind Advocate — 36 Years of Showing Up
    2026/06/29
    SUMMARYAt 25, Jeff Parker was a weightlifter in country New South Wales. A week later, he was paralysed from the waist down by a tumour in his spinal cord no doctor had seen coming. In this episode of Golden Threads, host Daniel Dougherty sits down with Jeff — now 61, blind, an NDIS advocate, YouTube creator and self-described "advocate, activist, or troublemaker" — for an unflinching conversation about three decades of acquired disability, the friend who saved him 18 months of bureaucracy, the wife who refused his three offers to leave, and why it has to be easier for the people who come next.EPISODE PILLARSA tumour, a paralysis, a promiseJeff walks us through 1989 — the gym session, the slow loss of his legs, the astrocytoma at L3, and the promise he made to walk out of St Vincent's that the doctor said wouldn't happen.Steve — the friend who knew the wayThe man in a wheelchair who phoned a week after Jeff got home, brought every form he'd ever need, and saved him 18 months of bureaucratic dead ends. Why peer mentorship is the most underrated support in disability.The impossible choice — sight or mobilityAfter six years of escalating prednisone for MS, Jeff's bones started fracturing from the medication. His GP gave him an impossible choice: keep your sight and stay bedridden, or lose your sight and walk again. The conversation he and his wife had at the kitchen table.Three hats — advocate, activist, troublemakerHow a 10-year fight with Armidale Council over the CBD path of travel turned Jeff into a national NDIS advocate, a YouTube creator (Blind Advocate, 145+ videos), and the person other people across Australia ring when the system has stopped listening.We're all in this togetherWhy Jeff's wife of 31 years, his support workers, and Australia's invisible army of carers (saving the government an estimated $100 billion a year) are the unsung heroes of every disability story — and why "you don't have to do it alone" is the message he most wants you to take from this episode.GUEST BIOJeff Parker is a long-time disability advocate based in Armidale, NSW. He acquired his first disability — paralysis from the waist down — in 1989 at age 25, following a spinal cord astrocytoma. Since then he has lived with MS, blindness, medically-induced osteoporosis, eight fractured vertebrae, and chronic pain. He runs the YouTube channel Blind Advocate, sits on his local access committee, contributes to NDIS reform conversations nationally, and has been married to his wife for 31 years.LINKSBlind Advocate (YouTube) — search "Blind Advocate" on YouTubeEmail — blindadvocate007@gmail.comRESOURCES MENTIONEDNational Disability Insurance Scheme (NDIS) — https://www.ndis.gov.auCarers Australia — https://www.carersaustralia.com.auAustralian Human Rights Commission (Disability Discrimination Act) — https://humanrights.gov.auJAWS screen reader — https://www.freedomscientific.com/products/software/jawsNVDA screen reader (free, Australian-made) — https://www.nvaccess.orgApple VoiceOver — built into macOS / iOSTIMESTAMPS00:00 Welcome to Golden Threads02:00 1989 — A Tumour at 2509:30 Walking Out of the Hospital12:35 Steve — The Friend Who Knew the Way15:40 MS, Prednisone, and an Impossible Choice23:00 Losing a Friend, Falling into Depression33:05 Becoming an Advocate, Activist, or Troublemaker49:50 Why Carers and Support Networks MatterCALL TO ACTIONIf this episode moved you, please follow Kintsugi Heroes on Apple Podcasts, Spotify or your preferred app, leave a rating or review, and share it with someone who needs to hear it. To support our not-for-profit mission to share more stories like Jeff's, visit kintsugiheroes.com.au and make a tax-deductible donation, or get in touch about partnering with us.THE KINTSUGI CONNECTIONWatch every episode on YouTube — https://www.youtube.com/@kintsugiheroesIf this story resonated, explore more from our Disability Series — honest conversations with advocates, carers, and people with lived experience reshaping what inclusion looks like in Australia.ABOUT KINTSUGI HEROESKintsugi Heroes is a not-for-profit storytelling platform sharing real stories of resilience, disability and transformation. Inspired by the Japanese art of kintsugi — repairing broken pottery with gold so the cracks become the most beautiful part — we believe every life can be made more beautiful through what it has survived.PARTNER WITH USWe work with NDIS providers, advocacy organisations, community partners and brands who share our values. To explore partnership, visit kintsugiheroes.com.auDONATEKintsugi Heroes is a registered not-for-profit. Donations over $2 are tax-deductible. Visit kintsugiheroes.com.au to support future episodes.CONNECTWeb: kintsugiheroes.com.auYouTube: @kintsugiheroesInstagram: @kintsugi.heroesRemember — we're all in this together.Mentioned in this episode:Support Kintsugi HeroesKintsugi Heroes is a not-for-profit, and every story we share is free for the ...
    続きを読む 一部表示
    1 時間 5 分
  • The weight of letting go | Naomi O'Byrne | Golden Threads

    The weight of letting go | Naomi O'Byrne | Golden Threads
    2026/07/13
    ⚠️ Content advisory: this episode discusses grief, which some listeners may find distressing.If you need support, you're not alone — help is available:• Lifeline (24/7 crisis support): 13 11 14 · lifeline.org.auNaomi O'Byrne's story spans 27 years of motherhood shaped by her daughter Sarah's complex disabilities. What began as discovering developmental delays at five months old became a journey of medical appointments, seizures, and challenging behaviours that made traditional day placements impossible. Naomi worked full-time throughout, determined to give Sarah a mainstream childhood despite systemic resistance. When Sarah reached adulthood, Naomi's health collapsed-she developed lymphoma while managing Sarah's escalating behaviours-forcing a crisis call to emergency services. What followed was Sarah moving into a group home, then her own supported unit. Naomi grieved the loss of her primary role, struggled with empty-nester syndrome, and eventually recognised she had been holding Sarah back. Now, two years later, Sarah is thriving in her own home with 24-hour support, and Naomi is finding her own life again, planning retirement and rediscovering herself beyond caregiving.Naomi O'Byrne is a mother, emergency management professional, and volunteer firefighter who has spent 27 years raising her daughter Sarah, who was born with intellectual and physical disabilities, genetic brain disorder, severe epilepsy, and scoliosis. She worked full-time throughout Sarah's childhood, navigated school systems and disability support services, and two years ago made the decision to help Sarah move into her own supported unit, fundamentally reshaping both their lives.In this Golden Threads conversation with Daniel Dougherty, Naomi shares the story behind the moments below.🎙️ IN THIS CONVERSATION:• Overprotection born from love can limit a person's independence and growth.🕒 CHAPTERS:00:00 Before Sarah: who Naomi was05:13 Sarah's diagnosis: discovering complexity12:41 Behaviour, judgment, and survival mode16:54 Mainstream school and the limits of integration21:05 Working full-time while caregiving: the dual life28:34 The NDIS and finding alternatives to day care33:07 Health crisis and the emergency call37:10 The separation: Sarah moves out41:17 Advice on asking for help43:18 Reading behaviour as communication46:19 The grief no one talks about54:23 What's next: retirement and reclaiming life🎧 If this story moved you, follow Kintsugi Heroes in your podcast app so you never miss an episode.━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ABOUT KINTSUGI HEROES━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━Welcome.We're glad you found your way here.Kintsugi Heroes was created from a simple belief: every person has a story worth sharing, and sometimes the story we need to hear arrives exactly when we need it most.Our name comes from the Japanese art of Kintsugi, where broken pottery is repaired with gold. Rather than hiding the cracks, they are honoured as part of the object's history. We believe people are much the same. The experiences that challenge us, break us, shape us, and help us grow are often the very things that connect us to one another.This channel is home to honest conversations about resilience, hope, grief, recovery, courage, love, and what it means to keep moving forward when life doesn't go to plan.Here you'll find six podcast series, each sharing stories through a different lens:• Kintsugi Heroes, hosted by John Milham• Animals & Us, hosted by Natalie Stockdale• Grit Diaries: From Grit to Grace, hosted by Simone Allan and Maryan Bova• From There to Here, hosted by Emma Bellamy-Dodd• Golden Threads: Stories of Disability & Resilience• Pride in Stories, hosted by John Dwyer (launching 31 July 2026)Every story shared here is offered with the hope that it helps someone feel a little less alone. A little more understood. A little more connected.Whether you're navigating a difficult season, supporting someone you love, or simply looking for meaningful conversations, you're welcome here.New episodes are released weekly across our series.If you'd like to help us keep these stories freely available to everyone, you can support our work here: https://www.kintsugiheroes.com.au/donateThank you for being part of this community.We help people tell the stories they need to share so others can discover the story they need to hear.━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━CONNECT WITH US━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━🌐 https://www.kintsugiheroes.com.au▶️ https://www.youtube.com/@kintsugiheroes📘 https://www.facebook.com/kintsugiheroes📸 https://www.instagram.com/kintsugi.heroes💼 https://www.linkedin.com/company/kintsugi-heroes#KintsugiHeroes #...
    続きを読む 一部表示
    59 分
  • Disability and Mental Health: How Daniel Searle Rebuilt His Life After Losing His Sight | Golden Threads

    Disability and Mental Health: How Daniel Searle Rebuilt His Life After Losing His Sight | Golden Threads
    2026/07/27
    Daniel grew up sighted on an Australian farm, playing cricket and tennis, until his vision deteriorated over a few months at 16. Leber's optic neuropathy-a genetic condition affecting the optic nerve-meant no cure and no driving license. The initial years were marked by denial and shame; he rejected mobility aids and pushed himself to impossible academic standards. A failed Year 11 led him to accept help and split his final year of school. He pursued physiotherapy at Charles Sturt University, learning Braille and screen-reading software, gradually understanding that asking for help was not burden but reciprocal humanity. As a clinician, he connected deeply with patients living with chronic pain and mental health challenges, eventually working in a mental health ward where he could tell patients, "I've been here too." Today, he competes in blind cricket and triathlon, speaks publicly about disability and leadership, sits on boards, and advocates systemically through Guide Dogs to reshape how Australia includes people with disability.Daniel Searle is a physiotherapist, advocate, and guide dog handler who lost his sight to Leber's optic neuropathy at 16. Over two decades, he has rebuilt his life through sport, clinical work addressing chronic pain and mental health, and now leads social change advocacy at Guide Dogs Australia, working to reshape how society includes people with disability.In this Golden Threads conversation with Daniel Dougherty, Daniel shares the story behind the moments below.🎙️ IN THIS CONVERSATION:• Perspective shapes what we see as loss or gain.🕒 CHAPTERS:00:00 Introduction and the person before the break02:00 Growing up sighted: farm life, sport, and identity05:56 The fracture: vision loss over months and the diagnosis12:00 School support, technology, and the first camp18:00 Language, disability, and the social model24:00 Denial, shame, and the breaking point at university33:00 Anatomy labs, help, and learning reciprocity39:00 Travel, Quinlan, and navigating the world50:00 From physiotherapy to chronic pain to mental health57:00 Power and connection in healing spaces62:00 Public speaking, boards, and advocacy work65:00 Sport, purpose, and what's next🎧 If this story moved you, follow Kintsugi Heroes in your podcast app so you never miss an episode.📌 RESOURCES MENTIONED:Guide Dogs Australia: https://www.guidedogs.org.auVision Australia: https://www.visionaustralia.orgCharles Sturt University: https://www.csu.edu.au━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ABOUT KINTSUGI HEROES━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━Welcome.We're glad you found your way here.Kintsugi Heroes was created from a simple belief: every person has a story worth sharing, and sometimes the story we need to hear arrives exactly when we need it most.Our name comes from the Japanese art of Kintsugi, where broken pottery is repaired with gold. Rather than hiding the cracks, they are honoured as part of the object's history. We believe people are much the same. The experiences that challenge us, break us, shape us, and help us grow are often the very things that connect us to one another.This channel is home to honest conversations about resilience, hope, grief, recovery, courage, love, and what it means to keep moving forward when life doesn't go to plan.Here you'll find six podcast series, each sharing stories through a different lens:• Kintsugi Heroes, hosted by John Milham• Animals & Us, hosted by Natalie Stockdale• Grit Diaries: From Grit to Grace, hosted by Simone Allan and Maryan Bova• From There to Here, hosted by Emma Bellamy-Dodd• Golden Threads: Stories of Disability & Resilience• Pride in Stories, hosted by John Dwyer (launching 31 July 2026)Every story shared here is offered with the hope that it helps someone feel a little less alone. A little more understood. A little more connected.Whether you're navigating a difficult season, supporting someone you love, or simply looking for meaningful conversations, you're welcome here.New episodes are released weekly across our series.If you'd like to help us keep these stories freely available to everyone, you can support our work here: https://www.kintsugiheroes.com.au/donateThank you for being part of this community.We help people tell the stories they need to share so others can discover the story they need to hear.━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━CONNECT WITH US━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━🌐 https://www.kintsugiheroes.com.au▶️ https://www.youtube.com/@kintsugiheroes📘 https://www.facebook.com/kintsugiheroes📸 https://www.instagram.com/kintsugi.heroes💼 https://www.linkedin.com/company/kintsugi-heroes#KintsugiHeroes #LivedExperience #ResiliencePodcast #...
    続きを読む 一部表示
    1 時間 12 分