No Spoons to Give is the official podcast of Spoony, the safe space for neurodivergent, chronically ill, and disabled people. Hosted by Spoony community team members Larissa and Maddy, who bring their own lived experience, we explore the highs, lows, and everything in between—chatting with voices from across our community and celebrating their stories. Find us at: Website - https://www.spoony.app/ TikTok - https://spoony.link/tiktok Instagram - https://spoony.link/instagram YouTube - https://spoony.link/youtube Facebook - https://spoony.link/facebook
Travel is meant to open up the world—but for millions of disabled and chronically ill people, it too often remains out of reach.
That’s something Jen Clark is determined to change. In this episode, we chat with Jen about Heartful—her new platform that's shaking up the travel industry by putting accessibility and social impact at the centre of the experience.
Heartful is a socially conscious accommodation booking site designed to make...
School is hard enough — now imagine navigating it with only 30% vision, in an environment that wasn’t built for you, all while trying to hide it from your peers. That was Chanelle Morris’s reality growing up. In this episode, Chanelle shares how those early experiences shaped her self-belief, how a trip to New Zealand helped her reclaim her identity as a proud disabled woman, and how she became a public speaker (and Spoony ambassad...
In this episode, we were thrilled to chat with the amazing Eliza Hull — a talented musician, proud disabled woman, passionate disability advocate, and all-round brilliant human. We talked about the barriers disabled artists face in the music industry, what it was like for Eliza to begin identifying as disabled later in life, and how powerful it is to find community with other disabled folks. ✨
Transcripts available here. 💜
In this episode, we sit down with Spoony’s founder, Nicholas Carlton, to hear the story behind Spoony. From his own experience with chronic illness to building one of the world’s largest communities for neurodivergent, chronically ill, and disabled people—Nicholas shares what inspired him to start Spoony, the highs and lows along the way, and his hopes for the future of the platform. A little BTS of Spoony, if you will! ✨
When Jane was diagnosed with cancer, she quickly discovered how limited clothing options were for people undergoing treatment and living with a chronic illness. Each day brought countless decisions—and choosing what to wear shouldn’t have to be one of them. She needed clothes that were comfortable, treatment-friendly, and still made her feel like herself.
So, she set out to change that, and Brighter Day was born: adaptive clothing t...
When Claire Jensz was diagnosed with Multiple Sclerosis (MS) at just 28, it was a life-changing moment she never saw coming—let alone something she'd one day turn into a hit Netflix film.
This week, we sat down with Claire to talk about her MS journey, from the early days of diagnosis to navigating friendships, rediscovering love, and channelling it all into her powerful film Take My Hand.
Claire opened up about the reality of l...
This week on the pod, we had the absolute pleasure of chatting with the lovely Carly Findlay. Carly is an appearance activist, writer, speaker, disability advocate, Spoony ambassador and all ‘round wonderful human (with the most wonderful and colourful wardrobe!). Carly shared her experiences of growing up disabled in a small country town, the importance of finding community, navigating a recent cancer diagnosis, and all things aut...
Ever wondered how Spoony transformed from just an idea into the brand it is today? Meet Anja & Emma from Shadowboxer—the powerhouse duo who helped shape our early thoughts and concepts into the vibrant identity you see now.
From day one, they’ve been behind the scenes, co-building Spoony alongside our community—listening, documenting feedback, ensuring accessibility needs are considered, and leaning into what people truly love.
I...
This week on the pod, we’re joined by Hayley and Kate—the dynamic duo from Melba Support—who are leading the charge in person-led disability support services across regional Victoria.
We dive into Melba’s human-rights framework, the importance of disability-led services, and the crucial role of intimacy and connection. Hayley and Kate also share how Melba stays at the forefront of innovation and what still needs to change in the dis...
Growing up as a neurodivergent child comes with challenges. So does raising one and advocating for their needs. But what if it didn’t have to be so overwhelming?
Meet Laetitia Andrac, founder of Understanding Zoe - an app designed to help parents navigate the flood of information, emotional overwhelm, and daily challenges of raising a neurodivergent child.
We chat with Laetitia about her lived experience as a neurodivergent parent, h...
Tired of adaptive clothing that feels medical, boring, or outdated? So were Emma and Molly - founders of JAM The Label, an adaptive fashion brand redefining accessibility with on-trend designs for the disabled, neurodivergent, and chronically ill community.
We chat with them about how they saw the need for JAM, who benefits from adaptive fashion, and how their clothing is making a real difference in people’s daily lives. It’s a good...
You may have seen our faces around the Spoony community - but we thought we should sit down and share our story! In this episode, Larissa and Maddy from the Spoony community team chat all things lived-experience, employment, and life as a Spoony.
Find our recommendations here:
'Take my Hand'-https://www.msaustralia.org.au/takemyhandthemovie/
Body Friend -https://www.goodreads.com/book/show/2002068...
Welcome to our brand new podcast - launching on February 12th, 2025.
Stay tuned!
Find us at:
Website - https://www.spoony.app/
TikTok - https://spoony.link/tiktok
Instagram - https://spoony.link/instagram
YouTube - https://spoony.link/youtube
Facebook - https://spoony.link/facebook
LinkedIn - https://spoony.link/linkedin
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An unlicensed lizard psychologist travels the universe talking to strangers about absolutely nothing. TO CALL THE GECKO: follow me on https://www.twitch.tv/lyleforever to get a notification for when I am taking calls. I am usually live Mondays, Wednesdays, and Fridays but lately a lot of other times too. I am a gecko.
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