No Spoons to Give

This conversation with Matt Brown—a Spoony user all the way from Canada—left us feeling all the feels. Matt shared what it was like to be diagnosed with cancer just before the first major COVID lockd…

AI—it’s the buzzword on everyone’s lips. Is it going to blow up the planet? Take all our jobs? Or could it actually do something good—like improve healthcare for the people who need it most?

That’s ex…

All the way from the UK, the lovely Zara Beth joined us for a chat about growing up disabled, navigating friendships, and finding her people through online communities. We talked about disability adv…

There’s a lot of misinformation, confusion, and unclear research when it comes to chronic and invisible illnesses. So we sat down with someone who lives and breathes this work every day to help cut t…

In this episode, we’re joined by Carter—creator of the Touched Out podcast—for an honest, funny, and deeply relatable chat about parenting (and also just *life*)  while neurodivergent.

We dive into t…

A little takeover episode, if you will. This week on the pod, we sat down together to have a bit of a deeper chat and connect over our shared lived-experience with neurodivergence, chronic illness an…

To all the ADHD’ers in our Spoony community — we see you, we hear you, and we know there are a lot of you! You asked for an expert who *gets* ADHD, and we’ve delivered. 🎧

This week, we’re joined by th…

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…

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 gr…

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 b…

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 …

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—a…

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, w…

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 w…

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 vibra…

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 Mel…

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 Under…

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 th…

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 live…

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/in…