Explore every episode of the podcast I'm Disabled... So What?

In this episode of I’m Disabled… So What?!, Lauren and Heather (she’s back!) take to the skies with Chris Wood MBE — the powerhouse behind Flying Disabled, Air4All, and Rights on Flights.

Chris shares his incredible journey from frustrated passenger to leading global advocate for accessible aviation. From campaigning for wheelchair-securement systems on commercial aircraft through Air4All, to lobbying airlines and regulators with Rights on Flights, Chris is leading the charge to make flying safer, easier, and more inclusive for disabled travellers everywhere.

We discuss:
✈️ Why accessible flying is a human right, not a luxury
🧳 The dream of staying in your own wheelchair onboard
📣 What it’s like to go head-to-head with airlines and win
💬 How change is finally happening — and what’s next

Whether you fly regularly or haven't dared to try, this one will leave you feeling inspired and informed.

🎙️ Out now on all major platforms. Tune in and share your travel stories with us!

In this episode of I’m Disabled… So What?!, Lauren is flying solo as co-host Heather was unwell during the recording, but don't worry, the energy is still top-tier!

We’re joined by none other than David Smith OBE, Paralympic boccia legend and proud Team GB athlete. From his instantly recognisable tricolour hair to his unforgettable medal-winning performances, David opens up about his incredible journey through elite sport, living with cerebral palsy, and the mindset that’s helped him dominate the court across multiple Games.

We also chat about disability identity, public perception, and what life is really like behind the podium. It’s inspiring, heartfelt, and just the right amount of chaos — much like David himself.

🎧 Stream it now on all platforms — you won't want to miss this one!

is week on I’m Disabled… So What?!, we’re joined by Nick Hardman, the creator behind 3D Toy Shop, home to what’s been called “the best teddy hospital in the world.”

Nick and his team create brand-new, one-of-a-kind teddy bears and soft toys that bring comfort and joy to children and families across the UK. These teddies aren’t restored or repaired — they’re carefully chosen and crafted to become treasured companions from the start.

With a two-month waiting list and huge demand, Nick shares the incredible journey of 3D Toy Shop, why these teddies mean so much to children, and the heartwarming stories behind his work.

🎧 Listen now wherever you get your podcasts and prepare to smile!

Donate to 3D Toy Shop: https://www.gofundme.com/f/help-3dtoyshop-grow?utm_campaign=p_lico+share-sheet&utm_medium=copy_link&utm_source=customer

#ImDisabledSoWhat #3DToyShop #NickHardman #TeddyHospital #DisabilityJoy #AccessibleToys #DisabledAndProud #PodcastEpisode #ToyRepair #EmotionalSupportTeddy

In this episode of I’m Disabled… So What?!, Lauren and Heather are reunited and joined by disability advocate and writer Hannah Deakin for an honest and deeply relatable chat.

They dive into the overwhelming world of disability life admin, from medical forms and benefit assessments to the mental toll of constantly proving your needs. But the conversation doesn’t stop there…

Hannah also shares her experiences of public interactions as a wheelchair user, including unsolicited comments, social barriers, and the pressure to constantly educate others.

It’s a powerful discussion about boundaries, resilience, and the everyday realities disabled people face—both behind closed doors and out in the world.

🎧 Available now on all streaming platforms!

#ImDisabledSoWhat #HannahDeakin #DisabilityLifeAdmin #AccessMatters #DisabilityAwareness #DisabledAndProud #PodcastEpisode #AdvocacyInAction

In this vital episode of I’m Disabled… So What?!, Lauren is joined by disability advocate and founder of Chronic But Thriving, Sara Bugg, for an honest and urgent conversation about the Welfare Reform Bill and what it really means for disabled people in the UK.

As proposed cuts and policy shifts threaten vital support systems, Sara helps unpack the complex (and often confusing) realities behind the headlines. From Personal Independence Payments (PIP) to work capability assessments, this episode explores how these reforms impact disabled lives, independence, and mental health.

If you’ve felt anxious, confused, or unheard during this political shift, you’re not alone. This is your breakdown of the bill, straight from lived experience and advocacy.

🎧 Available now on all streaming platforms.

#ImDisabledSoWhat #WelfareReformBill #DisabilityRights #ChronicButThriving #SaraBugg #DisabledAndProud #DisabilityAdvocacy #PolicyMatters #PIPReform #BenefitsCuts #PodcastEpisode

Sex and disability, two words that society rarely puts together, but it’s time to change that. In this candid and empowering episode of I’m Disabled… So What?!, Lauren is hosting solo as Heather is currently unwell (sending her lots of love 💜).

Joining Lauren is Jennie Williams, CEO of Enhance the UK, an organisation breaking down stigma around disability, relationships, and sexuality.

Together, they dive into the myths, taboos, and real experiences of having sex while disabled. From accessibility in intimate spaces to body confidence and the right to pleasure, Jennie brings expert insight and refreshing honesty to a topic too often left unspoken.

🎧 This episode is bold, funny, and absolutely essential listening.

#ImDisabledSoWhat #EnhanceTheUK #SexualityAndDisability #JennieWilliams #DisabledAndProud #BreakingTaboos #DisabilityAwareness #IntimacyMatters

In this lively and thought-provoking episode of I’m Disabled… So What?!, Lauren and Heather are back together to welcome the amazing Cassidy Huff, a U.S.-based disability advocate, content creator, and singer-songwriter.

The trio dives into the realities of dating as a disabled person in the United States, from inaccessible venues and ableist assumptions to celebrating the moments of connection and joy that make dating worthwhile. Cassidy opens up about her own experiences while highlighting the changes still needed to make dating truly inclusive.

With honesty, humour, and a sprinkle of sass, this conversation shines a light on love, advocacy, and accessibility - Stateside style.

🎧 Listen now and join the conversation!

#ImDisabledSoWhat #CassidyHuff #DatingWithDisability #AccessibilityMatters #DisabledAndProud #DisabilityPodcast #StatesideChat

In this special U.S. edition of I’m Disabled… So What?!, Lauren takes the mic solo as Heather is off unwell this week (rest up, Heather! 💜).

Joining us from across the pond are two incredible guests—Kelly Berger in New York and Avery Roberts in Ohio—both living with Congenital Muscular Dystrophy (CMD) and using their voices to drive change.

We dive into the realities of living with CMD in America, including the harsh impact of recent cuts to Medicaid, accessibility barriers, and what it means to advocate for your basic needs in a system that often overlooks disabled people.

From healthcare injustice to personal resilience and the power of friendship, this episode is packed with raw truth, lived experience, and hope.

🎧 Out now wherever you get your podcasts.

#ImDisabledSoWhat #CMDCommunity #MedicaidCuts #DisabilityRights #KellyBerger #AveryRoberts #DisabledAndProud #RareDiseaseAwareness #DisabilityPodcast #HealthcareJustice

In this gold medal-worthy episode of I’m Disabled… So What?!, we’re joined by power couple Louise Hunt Skelley PLY and Chris Hunt Skelley MBE—both elite Paralympians with a shared passion for sport, advocacy, and each other.

We dive into their journey as athletes and partners, the reality of competitiveness (on and off the mat!), and what it takes to balance love, ambition, and disability in the public eye. From the Paralympic Games to life behind the scenes, Louise and Chris open up with honesty, humour, and heart.

This episode is all about pushing limits, lifting each other up, and proving that disability is never a barrier to greatness.

🎧 Tune in now and get inspired.
#ImDisabledSoWhat #Paralympics #LouiseHuntSkelley #ChrisHuntSkelley #DisabledAndProud #DisabilityPodcast #LoveAndSport #AdaptiveAthletes #ParalympianLife

In this inspiring (and hilarious) episode of I’m Disabled… So What?!, we’re joined by the unstoppable mother-daughter duo Carmela and Lucy Chillery-Watson, known for their fearless campaigning, big laughs, and the now legendary Poo Plod 🏅💩

Carmela lives with LMNA-CMD, a rare form of muscular dystrophy, and together with mum Lucy, they’ve raised awareness, inspired thousands, and even caught the attention of the royals (MBE alert! 👑).

We chat about living with a rare condition, the power of positivity, cheeky humour, and the strength of family—and of course, what exactly a Poo Plod is!

This episode is bursting with love, advocacy, and Carmela’s incredible spirit. Don’t miss it!

🎧 Streaming now.
#ImDisabledSoWhat #CarmelaChilleryWatson #RareDiseaseAwareness #DisabilityAdvocacy #PodcastGuests #PooPlod #DisabledAndProud #LMNACMD #MBE #DisabilityPodcast

In this powerful and eye-opening episode of I’m Disabled… So What?!, we’re joined by activist and Disability Rebellion member Mike O’Brien to unpack the harsh realities behind recent benefit cuts—and the devastating impact they’re having on disabled people across the UK.

From financial insecurity and mental health to systemic inequality, Mike shares lived experience, frontline advocacy, and the urgent need for collective action. This isn’t just policy, it’s personal.

If you've ever felt unseen by the system or want to understand what’s really at stake, this conversation is essential.

🎧 Listen now.
#ImDisabledSoWhat #DisabilityRebellion #MikeOBrien #BenefitCuts #DisabilityRights #DisabledAndProud #AdvocacyMatters #PodcastEpisode

In this inspiring episode of I'm Disabled... So What?, Lauren and Heather chat with the brilliant John and Jade Reynolds—content creators, disability advocates, and authors of the powerful book Able To Laugh.

John and Jade open up about their journey as a couple, their experiences navigating life with disability, and what led them to share their story with the world. From the highs and lows of parenting to the behind-the-scenes of content creation, they talk openly about love, resilience, and finding humour even in the hardest moments.

This episode is packed with insight, warmth, and lots of laughs—just like Able To Laugh itself. You won’t want to miss it.

#ImDisabledSoWhatPodcast #AbleToLaugh #DisabilityAdvocates #GuestInterview #ContentCreators #LoveAndDisability

Welcome to the very first episode of I'm Disabled... So What? 🎉

In this opener, hosts Lauren Mill and Heather Monger get real (and a little ridiculous) as they roll into your ears to share who they are, how they met, and why they decided to start this podcast. Expect plenty of laughs, candid chat about life with a disability, and a no-filter look at the realities of living unapologetically disabled.

We’re smashing stereotypes, one episode at a time — and it all starts here.
Grab a brew, buckle up (or don’t), and let us wheelie introduce ourselves! 🧡

#ImDisabledSoWhatPodcast #DisabledAndProud #MeetTheHosts #DisabilityPodcast

Think being disabled means living a limited life? Think again.

Welcome to *I’m Disabled... So What?*—the podcast where **Lauren Mill** and **Heather Monger** smash stereotypes and speak the unfiltered truth about life with a disability. In this trailer, you'll meet two women who refuse to be defined by labels, pity, or low expectations. Instead, they’re turning lived experience into loud conversations—with honesty, humour, and a healthy dose of sass.

From awkward dating stories and navigating inaccessible spaces, to the realities of education, friendships, careers, and everything in between, this show is here to explore what it really means to live unapologetically disabled.

We’re not your “inspiration” story—we’re the *main characters* in our own narrative.

If you’re tired of the same old disability tropes or just want to hear conversations that are real, raw, and relatable, hit play. This is the start of something different.

New episodes coming soon—subscribe now and get ready to rethink everything.