Hi, I’m Detty — a mum, a wife, a crocheter, a tea-lover, and someone living with Functional Neurological Disorder (FND).
I created The FND Podcast as a place to have real, honest chats about life with this condition — the parts that are scary, the parts that are frustrating, and the parts that are still full of light.
Here, you’ll hear from people with lived experience, carers, professionals, and advocates who all bring their stories, their insights, and their heart to the table. We talk about what it’s like to be diagnosed with FND, what recovery can really look like, how to manage flare-ups, navigate work, raise a family, and just keep showing up — one breath, one step, one day at a time.
This podcast isn’t about perfection. It’s about connection.
It’s about making space for every part of this journey — especially the parts that often get left out of the conversation.
Whether you’re living with FND, supporting someone who is, or just trying to understand it better — you’re welcome here.
So, grab a cuppa, get comfy, and join me for conversations that are warm, raw, and real.
You’re not alone.
💛 Detty
We are happy to announce that we are FND AUS Podcast series.
Please support:
FND AUSTRALIA SUPPORT SERVICES INC: www.fndaus.org.au
Together lets talk FND.
All content for The FND Podcast is the property of Odettecreates, Detty, Odette Placido and is served directly from their servers
with no modification, redirects, or rehosting. The podcast is not affiliated with or endorsed by Podjoint in any way.
Hi, I’m Detty — a mum, a wife, a crocheter, a tea-lover, and someone living with Functional Neurological Disorder (FND).
I created The FND Podcast as a place to have real, honest chats about life with this condition — the parts that are scary, the parts that are frustrating, and the parts that are still full of light.
Here, you’ll hear from people with lived experience, carers, professionals, and advocates who all bring their stories, their insights, and their heart to the table. We talk about what it’s like to be diagnosed with FND, what recovery can really look like, how to manage flare-ups, navigate work, raise a family, and just keep showing up — one breath, one step, one day at a time.
This podcast isn’t about perfection. It’s about connection.
It’s about making space for every part of this journey — especially the parts that often get left out of the conversation.
Whether you’re living with FND, supporting someone who is, or just trying to understand it better — you’re welcome here.
So, grab a cuppa, get comfy, and join me for conversations that are warm, raw, and real.
You’re not alone.
💛 Detty
We are happy to announce that we are FND AUS Podcast series.
Please support:
FND AUSTRALIA SUPPORT SERVICES INC: www.fndaus.org.au
Together lets talk FND.
What happens when your body stops functioning? And the neurologist simply says " Deal with it".. Suggesting its all in your head?
In this powerful episode, Brad shares his personal journey from collapse and confusion to finding his voice in the FND community. Diagnosed with functional Neurological disorder after a barrage of symptoms and no clear answers, Brad was left to navigate the system alone. But instead of staying silent he took action:
We talk about
*The moment it all started
* The trauma of misdiagnosis and dismissal
*Brads current petition to improve FND care
The emotional Toll of FND and how it reshapes identity
The importance of community support and speaking out
This is a story of courage, advocacy and refusing to be invisible. If you live with FND or love someone who does this ones for you.
In this insightful and compassionate episode of The FND Podcast, Detty is joined by Jason Kreuzman, a pediatric occupational therapist based in St. Louis, Missouri, who specialises in treating children with Functional Neurological Disorder (FND).
Together, they explore what occupational therapy really is, how it differs from physiotherapy, and the powerful role it can play in helping children and teens with FND rebuild their lives — one meaningful activity at a time. Jason shares how he adapts therapy for young people, how to support kids returning to school, and why building confidence and safety is key to long-term recovery.
Whether you’re a parent of a newly diagnosed child, a healthcare professional wanting to understand FND better, or someone looking for practical tools and real hope, this episode is full of heart, helpful insights, and supportive guidance.
✨ Topics covered: – What occupational therapy looks like for FND – Explaining FND to children in age-appropriate ways – Supporting school transitions and daily life – Creating personalised care plans for families – Raising awareness in the healthcare system – Free resources now available for pediatric FND care
This one’s a must-listen for families, carers, educators, and therapists — and a powerful reminder that support for kids with FND does exist.
🎙️ The JJ Segment: Catching Up with Jess – Working, Writing, and Living with FND
In this deeply honest and joyfully heartfelt episode of The FND Podcast, Detty sits down with the wonderful Jess for a long-overdue catch-up on the JJ Segment. From moving states, to getting married, to navigating life with FND while diving headfirst into a blue-collar job — Jess shares it all with her trademark humour, grit, and glowing resilience.
Together, we unpack what it’s really like returning to work with Functional Neurological Disorder, from workplace seizures and flare-ups to pacing, planning, and the importance of telling your employer. Jess opens up about her journey from overdoing it to finding a more manageable balance — and how she's learned to adapt rather than fight her FND.
But that’s not all — Jess is also a published author! We chat about her newest fantasy release "Woman of Wolves", her passion for storytelling, and how she balances creative life with chronic illness. You’ll laugh, nod, maybe even tear up — and definitely walk away feeling inspired.
✨ In this episode:
– Jess’s journey with FND & employment
– Coping with seizures at work
– The emotional evolution of living with FND
– Why communication with employers matters
– Writing through chronic illness
– Creating a fantasy world… and lifting 3 tonnes of flour a day?! 💪
– The gift of self-acceptance and finding your pace
📚 Want to support a fellow FND warrior? Check out Jess’s books on Amazon and follow her on TikTok @jessmcfarlane – links in the show notes!
A massive thank you to Jess for being so open and shining your light. And to our listeners: you’re not alone. Your journey with FND is your own, but we’re right here beside you.
Stay safe, love hard, and peace — see you on the flip side 💛
In this heartfelt episode of The FND Podcast, Detty welcomes back the inspiring Tiarne, who bravely shares her personal journey of returning to work while living with Functional Neurological Disorder (FND). From the early days of navigating symptoms and mobility aids to finding the balance between part-time work and self-care, Tiarne opens up about the realities, challenges, and victories of employment with a chronic condition.
Whether you’re considering re-entering the workforce, looking into volunteering, or simply curious about how others manage FND in the workplace — this conversation is filled with honesty, insight, and encouragement. Tiarne reminds us that pacing, self-awareness, and finding supportive environments can make all the difference.
We also talked about
– Flexible working arrangements
– Managing symptoms on the job
– Advocating for your needs
– What really matters when you’re living with FND
– The power of purpose and doing what you love
A huge thank you to Tiarne for being so open and sharing her lived experience working with FND
Don’t forget to check out the show notes for helpful resources and past episodes, including Tiarne’s My FND Reality and our insightful chat with Katherine Gill from FND Australia Support Services on returning to work.
As always — stay safe, love hard, and peace. See you on the flip side
To work or not to work with FND that is the real question. It's a hard one to gauge and safely decide and its definitely not for everyone. Here's a short conversation we have with Katherine Gill from Australia Support Services and also a sneak preview to the upcoming episodes.
On this episode we talk to Haseel Bhatt who is a specialist Neuro Physiotherapist specialising not only in FND but in other movement Disorders. Join us as we talk FND but also Neurophysiotherapy. Thankyou so very much for talk to us Haseel grateful and very much appreciated we hope you can join us again. Thankyou for all that you do .
Happy FND Awareness day. To celebrate, we are honored to be speaking to one of the biggest FND advocates in Australia. Dr. Katherine Gill has returned to speak about FND and FND Awareness. Thankyou for talking on the FND Podcast it’s always amazing to hear your perspective and insights about FND as well as what services FND Australia support services does.
It's been 3 years since we last talked all the way back in March 2023 and finally back in 2025. Checking in and saying hello and being grateful for the continued FND awareness that has grown since we last talked.
Warning: this episode contains sensitive topics which can be triggering to some listeners. Please be advised.
On this episode of the JJsegment Jess talks about how life has been this past year and about Mental Health. We are grateful that she has shared how she has been. Thankyou Jess for sharing. In the meantime she is an incredible author and you can support Jess also by reading her wonderful book! Follow Jess on Instagram @functionallyjess
Following on the episode "Hello Mr. Tom Plender" we talked about the Inform the Doctor campaign that FND ACTION has. With Toms permission we were able to record his explanation he had on this campaign and encourage you wherever you are in the world to utilise this campaign/information. It is a worldwide campaign and it's to help spread the awareness of the advancements of FND. To find out more head to FND ACTION website: www.fndaction.org.uk , follow Tom on his instagram : @tplender and have a look at his website at www.tomplender.com
Come hang out with me and Jake on this episode of Uniting FND it's certainly been a while and well overdue. Talking FND and listening to Pink and Kelly clarkson from Youtube. Follow jake on his podcast Itsmeitsmeitsfnd as well as youtube channel @punkchef41
On this episode of the FND Podcast we are talking to Mr. Tom Plender who is a massive Campaigner for FND. We talk to him about FND and he brings up what we need to do to help FND Awareness and talk about FND. Thankyou so much for your time and for talking to us Tom it's been an amazing conversation with you, food for thought, inspiration and just so valuable. To follow Tom on instagram : @tplender. He has a website: www.tomplender.com and also FND ACTION: www.fndaction.org.uk
An announcement for FND awareness day , especially for caregivers and Parents who are looking after child/children with FND there is an amazing even happening today. To check it out please look at the FND ACTION UK website. https://www.fndaction.org.uk/fnd-awareness-day-uk/
On this episode we are proud to talk to Dr. Katherine Gill president and founder of FND Australia Support Services. For those newly diagnosed in Australia we describe what FND Australia Services does and provides and hearing about a new FND wellbeing course that is going to be available. We thankyou Katherine Gill for giving us the opportunity to talk to you again. Check out the website and the app.
On this episode of the Deb and Detty Show we are joined by a special guest Jess (as Deb said the famous author) I ask questions in relation FND 1. Why is it so important to raise awareness for FND 2.What difference would it have made if you received proper treatment from the very beginning? 3. What message would you give to those who are newly diagnosed? 4.how do you deal with new symptoms?
Episode 161 Hello there and welcome to the FND Podcast. Today we will be posting up our episodes throughout the day to participate in FND awareness day. To all of you out there Happy FND awareness day and watch this space. Stay safe Love Hard and Peace. xoxo
In this episode of the FND podcast we are talking to chucky who unfortunately had an accident with his ankle. Or he was attacked by a ninja step! His experience with the emergency and how it all played out and what to do in an emergency. It’s important to prepare for emergencies especially with FND.
On this episode of Maggies corner we talk to Maggie on how she’s been doing. We split this episode into two parts as there is so much to catch up on. Maggie has done amazing podcast episodes with @zoopnetwork @ the #9for9 real talk series. Maggie on Instagram @Maggie.Chapman and her creatively on @maggiesa.creative we congratulate her also on finishing the challenge #9for9 29 days in cold water and for you guys raising money towards youth mental health.
On this episode Chrissie talks about two wonderful articles that she has found that leads to discussions on FND. They are amazing reads and are linked and will be included in the resources for future episodes of the podcast. Please check them out! Also a recent article on the MJA published this month on FND. Follow Chrissie @chrissiejbutler.
Trigger warning : this episode has sensitive topics that may trigger some. It is in relation to a post made in the past which had emphasised and claimed that covid vaccinations causes fnd. This is our opinions we encourage you to speak to your own gp and specialists seek medical advice in regards to this topic in regards to your own fnd and health in regards to this topic. At present the fnd society has a media statement in regards to this matter. We also talk about the awkwardness of FND especially when flares present themselves. Follow Jess on Instagram @functionallyjess , her Instagram for her creative writing @jessmcfarlaneauthor and link to her new book for pre order link below. Shoutout to Michael! Hello
Hi, I’m Detty — a mum, a wife, a crocheter, a tea-lover, and someone living with Functional Neurological Disorder (FND).
I created The FND Podcast as a place to have real, honest chats about life with this condition — the parts that are scary, the parts that are frustrating, and the parts that are still full of light.
Here, you’ll hear from people with lived experience, carers, professionals, and advocates who all bring their stories, their insights, and their heart to the table. We talk about what it’s like to be diagnosed with FND, what recovery can really look like, how to manage flare-ups, navigate work, raise a family, and just keep showing up — one breath, one step, one day at a time.
This podcast isn’t about perfection. It’s about connection.
It’s about making space for every part of this journey — especially the parts that often get left out of the conversation.
Whether you’re living with FND, supporting someone who is, or just trying to understand it better — you’re welcome here.
So, grab a cuppa, get comfy, and join me for conversations that are warm, raw, and real.
You’re not alone.
💛 Detty
We are happy to announce that we are FND AUS Podcast series.
Please support:
FND AUSTRALIA SUPPORT SERVICES INC: www.fndaus.org.au
Together lets talk FND.