In this episode of ListenABLE, Angus sits down with Spencer Connelly for a conversation that is confronting, inspiring and incredibly human.

Spencer shares his lived experience after surviving a traumatic fire as a child, spending months in hospital, and learning to navigate the world with visible scars and amputations. He reflects on memory, trauma, recovery, self-image, the complexity of forgiveness, and why he now sees his scars as signs of strength rather than weakness.

The conversation also explores disability identity, facial difference, confidence in public, representation in film, and Spencer’s growing dream of building a career in acting. That dream has already taken shape, with Spencer landing a speaking role in Furiosa: A Mad Max Saga, and he has publicly credited the KIDS Foundation with helping build his confidence after his injuries.

If this episode resonates, share it with someone who needs to hear a story of resilience, perspective and hope.

Key Topics:

• surviving severe childhood burns

• trauma and memory

• hospital recovery and rehabilitation

• living with facial difference

• disability identity

• scars and self-acceptance

• therapy and healing

• public perception and staring

• confidence and resilience

• acting, representation and Furiosa

  
  

The Story:

00:00 Childhood trauma and the memory that stayed
01:00 Spencer’s story and entering the disability community
05:45 Living with disability and visible difference
07:20 Recovery, surgeries and life after hospital
11:10 Returning to school after trauma
14:50 The truth about what happened
17:40 Differently abled, disability and identity
19:00 Staring, confidence and moving through the world
20:40 Looking in the mirror after trauma
23:15 Forgiveness, healing and moving forward
27:20 Acting dreams and losing one career path
28:20 Meeting Sean Millis and working on Furiosa
35:30 Facial difference and representation in film
37:50 Halloween, scars and public perception
40:10 The bowl of uncomfortable
44:25 Life from here and what’s next

When Joshua Ruff’s heart stopped for three minutes, everything changed.

Living with Duchenne Muscular Dystrophy (DMD) since childhood, Joshua had already navigated a lifetime of disability, adaptation, and resilience. But in 2020, a sudden cardiac arrest during the early days of COVID forced him into a profound reckoning with mortality, fear, and what actually matters.

Unable to speak and communicating only through his eyes, Joshua was told he might never return home. Instead, that moment became the catalyst for a new way of living. One centred on human connection, creative purpose, and letting go of fear.

In this powerful conversation, Joshua shares how surviving cardiac arrest reshaped his outlook on life, relationships, and ambition. He opens up about growing up with DMD, the emotional toll of teenage years, and the quiet pressure to always appear positive as a wheelchair user. We explore how gardening became both therapy and vocation, leading to the creation of Henle Gardens, a lavender farm producing oil, products, and community experiences.

This episode is about disability, yes. But more than that, it is about meaning, independence, love, and choosing to live fully without apology.

Key Topics Covered

• Surviving a cardiac arrest and communicating only through eye movement

• Living with Duchenne Muscular Dystrophy and challenging early life expectancy narratives

• Letting go of fear after facing death

• Gardening as purpose, therapy, and business

• Building an accessible lavender farm and producing lavender oil

• Independence, support systems, and redefining success

• Why people with disability are elite problem solvers

• Relationships, self-worth, and rejecting the idea of being a burden

• Positivity, grief, and the danger of masking emotions

  
  

  Notable Moments

• “The most important thing is human connection. Everything else doesn’t matter.”

• “My heart stopped for three minutes, and somehow that freed me.”

• “I didn’t believe I deserved a relationship. That belief almost cost me one.”

• “People with disability are the best problem solvers because life never gives us the easy path.”

• “Independence for me is choice, not doing everything alone.”

About Joshua Ruff

Joshua Ruff is a gardener, lavender producer, and founder of Henle Gardens in regional Victoria. Living with Duchenne Muscular Dystrophy, Joshua has transformed personal adversity into creative expression, community connection, and entrepreneurship.

After surviving cardiac arrest in 2020, he committed to building a life driven by purpose rather than fear. Today, his lavender farm produces oil, dried lavender products, and hosts garden visits, festivals, and community groups, proving that accessibility and beauty are not mutually exclusive.

Colin Judge was born with one arm and no legs, and today he is a Paralympic table tennis player, speaker, and analyst living in Dublin.

In this episode of ListenABLE, Colin opens up about dating with a disability, rejection, and why you do not need to prove your worth to the wrong people. He shares the moment a short video about dating stopped the scroll online, and how learning to value the people who choose you changed the way he sees relationships and confidence.

Colin also takes us through his journey to the Paralympics, the hidden grind of elite sport, and what people do not see behind the scenes of Paralympic competition. From being excluded as a teenager, to finding his sport, to navigating reclassification and identity, this conversation explores resilience, adaptability, and self-belief in a way that goes far beyond disability.

We also talk about fear of rejection, finding your voice on social media, taking initiative when it feels uncomfortable, and why accessibility is often more about mindset than infrastructure.

This is a powerful, honest conversation about confidence, self-worth, and becoming more than the labels placed on you.

Follow Colin Judge on Instagram: @colinjudge100

What happens when you finally get the diagnosis that explains your whole life… and what doesn’t it change at all?

In this powerful episode of ListenABLE, Angus sits down with disability advocate and podcaster Kelly Berger, who shares her journey living with an ultra-rare form of congenital muscular dystrophy, Collagen 6. After years of misdiagnosis, Kelly received her genetic confirmation as an adult, a moment that brought clarity, community and a new sense of direction, without changing who she fundamentally is.

Kelly speaks candidly about the emotional weight of diagnosis, navigating healthcare systems, building community, and what real accessibility actually looks like in daily life. From the realities of infrastructure in the US to the gaps between performative inclusion and genuine integration, this conversation goes well beyond awareness and into what meaningful change requires.

We also dive into Kelly’s podcast 'Wheel Talk', her advocacy work, and how she’s helping reshape how disability, rare disease and identity are spoken about in public spaces.

This is a conversation about resilience, identity, leadership and how visibility changes everything.

• Living with Collagen 6 congenital muscular dystrophy

• The emotional impact of finally receiving a genetic diagnosis

• Rare disease advocacy and disability representation

• Accessibility in infrastructure and public spaces

• Navigating healthcare systems and misdiagnosis

• Disability identity and pride

• Building community with and without disability

• Language, inclusion and allyship

• Performative vs meaningful disability representation

• Creating podcasts within the disability community

• Why visibility matters

Kelly Berger is a disability advocate, podcaster and rare disease community leader living with Collagen 6 congenital muscular dystrophy. She is the co-host of Wheel Talk, a podcast exploring disability, identity and lived experience through honest, accessible conversations. Kelly works actively in advocacy, accessibility awareness and rare disease representation.

ListenABLE is a podcast created to amplify disability voices, challenge stereotypes and explore what inclusion actually looks like in practice. Hosted by Angus O’Loughlin alongside Dylan Alcott, the show brings real stories, lived experience and meaningful conversations into the mainstream.

Podcast: Wheel Talk with Kelly and Averyhttps://www.instagram.com/thewheeltalkpodcast/

Episode out Tuesday!

In this episode, Elizabeth Wright shares her journey from being a Paralympic swimmer to becoming a sports journalist. She discusses the challenges and triumphs of her career, the importance of representation in media, and her personal experiences with disability. Elizabeth emphasises the need for more coverage of Paralympic sports and the significance of embracing one's identity and pride in the face of ableism. The conversation highlights the evolving landscape of disability representation in journalism and the importance of community support.

Connect with Elizabeth

Instagram: https://www.instagram.com/elizabethlwright/?hl=en

LinkedIn: https://www.linkedin.com/in/elizabeth-wright-ply-300610129/

Website: http://www.elizabethwright.net/

What we cover:

• Elizabeth Wright transitioned from Paralympic swimmer to sports journalist.
• She emphasizes the need for more representation of disabled individuals in media.
• The Sydney 2000 Paralympics were a turning point for public support of para sports.
• Elizabeth faced challenges in her identity after retiring from swimming.
• She found empowerment through photography and art.
• Living with a disability requires daily practice of self-acceptance.
• Elizabeth advocates for more coverage of Paralympic sports.
• She reflects on the ableist perceptions in society.
• The importance of community pride in disability is highlighted.
• Elizabeth aims to inspire more disabled individuals to pursue journalism.

Chapters

00:00 Introduction and Background

02:58 Elizabeth Wright's Journey in Sports Journalism

05:51 Reflections on the Paralympic Games

09:05 Life After Competitive Swimming

11:51 Exploring Identity Through Art and Photography

14:54 Understanding Disability and Personal Experience

21:19 The Journey of Adaptation

22:34 Prosthetics: Tools of Empowerment

26:54 Disability Pride: A Daily Practice

31:10 The Future of Disability Representation in Journalism

33:43 Confronting Ableism: Personal Experiences and Growth

See omnystudio.com/listener for privacy information.

In this episode of ListenABLE, Dylan and Angus sit down with Storm and Holly, the founder and brand ambassador of ByStorm Beauty, a trailblazing inclusive beauty brand designed for people with disabilities.

They explore the challenges of inaccessible makeup, the importance of representation in beauty, and how ByStorm is creating products that empower the disability community while building a profitable, inclusive business. Storm shares the journey from co-designing accessible tools to collaborating with major brands, while Holly reflects on the personal impact of independence, confidence, and visibility.

Discover how thoughtful design, community consultation, and advocacy are reshaping the beauty industry—and learn why accessibility benefits everyone.

Connect with Holly and Storm:

• Storm: https://www.linkedin.com/in/storm-menzies/
• ByStorm: https://bystormbeauty.com/
• Holly: linkedin.com/in/holly-sultana-b37410212

Chapter Titles & Timestamps

• 00:00 – Intro: Welcome to Listenable

• 00:01 – Accessible Makeup Inspiration: How breaking a hand led to a new approach

• 01:40 – Meet Storm & Holly: Founders and ambassadors of ByStorm Beauty

• 03:00 – Empowerment Through Representation: How ByStorm impacts the disability community

• 06:10 – The Problem With Inaccessible Beauty: Everyday struggles and barriers

• 07:27 – Normalizing Struggle: Holly’s perspective on accessibility and independence

• 08:33 – Overcoming Ableism in Beauty: Challenges convincing others accessibility matters

• 12:12 – Building a Disability-Led Business: From prototypes to a thriving brand

• 16:20 – What is Accessible Makeup?: Tools, attachments, and co-design

• 18:08 – Collaborations & Industry Impact: Celeste Barber and mainstream engagement

• 19:43 – Representing ByStorm: The ambassador experience and social impact

• 25:08 – Community & Advisory Board: Lived experience shaping product development

• 27:00 – Retail & Global Expansion: Inclusion in stores and future plans

• 31:04 – Time & Independence: How accessibility saves time and fosters autonomy

• 33:06 – Product Design Details: Shapes, grips, and user experience

• 34:52 – Packaging & Unboxing: Accessibility beyond the product itself

accessible makeup, inclusive beauty, disability advocacy, disability-led business, ByStorm Beauty, makeup for disabilities, co-design products, empowerment, representation in beauty, inclusive product design

See omnystudio.com/listener for privacy information.

Australian Senator Jordon Steele-John joins Dylan Alcott and Angus O’Loughlin to share what life is really like inside Parliament as a wheelchair user and one of the few disabled politicians in Australia. From rushing to Senate votes without extra time allowances to reshaping accessibility in politics, Jordon gives a candid and inspiring look at how inclusion, policy, and representation intersect in Australia’s most powerful building.

The conversation spans his journey from a 23-year-old Greens candidate from WA to a national advocate for accessibility, neurodiversity, and disability rights. Jordon opens up about moments of misunderstanding on the campaign trail, how his ADHD and cerebral palsy shape his leadership, and why true inclusion starts with “getting our own house in order.”

This episode is full of insight, humour, and practical advice for anyone—disabled or not—who wants to create change in their community.

Connect with Jordon:

• https://www.instagram.com/jordonsteelejohn/?hl=en
• https://www.linkedin.com/in/jordon-steele-john-656ba917a/

Key Topics

• Life as a Senator with disability

• Accessibility barriers in Parliament House

• Ableism in political systems

• How Parliament handles (or doesn’t handle) disability inclusion

• The power of lived experience in politics

• Jordon’s journey to the Senate at age 23

• Disability pride and representation

• ADHD, cerebral palsy, and leadership

• Advice for young people with disability wanting to enter politics

• Building collective action for change

Quotes

“If Parliament is going to make laws that fix accessibility in the community, we’ve got to literally get our own house in order first.” – Jordon Steele-John

“People thought I was collecting for charity, not running for office. That moment showed how deeply society equates disability with needing help, not giving leadership.” – Jordon Steele-John

“Politics should represent every voice—including people with intellectual and cognitive disabilities. The system can and should be rebuilt to meet everyone’s access needs.” – Jordon Steele-John

About Jordon Steele-John

Jordon Steele-John is an Australian Greens Senator for Western Australia and the youngest person ever elected to the Australian Senate. A proud disabled man with cerebral palsy and ADHD, Jordon has been a leading advocate for disability rights, climate justice, and inclusive reform since 2017. His work includes helping establish the Disability Royal Commission and pushing for systemic accessibility across Australian institutions.

Jordon Steele-John, Dylan Alcott, Angus O’Loughlin, ListenABLE podcast, Australian Parliament accessibility, disability politics Australia, cerebral palsy, ADHD, Greens Senator WA, disability representation, ableism in politics, Disability Royal Commission, inclusion, accessibility reform, disabled leaders, advocacy Australia

See omnystudio.com/listener for privacy information.