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Special Needs Diaries

Hosted by My Kabuki Girl · kids · EN-AU

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About this Podcast:

Welcome to Special Needs Diaries. Previously called How We... Special Needs , this podcast aims to open conversations around the world of Special Needs and how it transforms people, carers, families and communities. I’m Minie Minarelli, an Italian special needs mum living in Sydney, sharing my personal diary as I walk alongside my daughter’s journey with Kabuki Syndrome. But this podcast isn’t just about us - it’s about us . Through heartfelt stories, sometimes interviews with other special needs parents, and honest conversations, we’ll explore the challenges, victories, and emotions that come with raising extraordinary children. Together, we’ll share the tears, the laughter, and the questions we might be too afraid to ask. Whether you’re part of the special needs community or simply curious about this roller coaster called life, you’re welcome here. This podcast offers a raw, relatable, and unconventional w

Pitch Analysis

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Contact path

Public web form

Booking probability

23%

Guest openness

Selective

80/100
Required Score

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Questions about Special Needs Diaries

What is Special Needs Diaries about?

Welcome to Special Needs Diaries. Previously called How We... Special Needs, this podcast aims to open conversations around the world of Special Needs and how it transforms people, carers, families and communities. I’m Minie Minarelli, an Italian special needs mum living in Sydney, sharing my personal diary as I walk alongside my daughter’s journey with Kabuki Syndrome.

Who hosts Special Needs Diaries?

Special Needs Diaries is hosted by My Kabuki Girl. The show has published 19 episodes to date.

What has Special Needs Diaries covered recently?

Recent episodes include "‘Hospital Talk’ | 8 Things Every Parent Needs to know" (14 March 2026, 13 minutes), "She got an ASD Diagnosis | Our daughter's developmental assessment" (6 March 2026, 29 minutes), and "New Year, New Podcast" (14 January 2026, 8 minutes).

How often does Special Needs Diaries publish?

Special Needs Diaries publishes roughly monthly, with episodes averaging 22 minutes across 19 episodes.

How hard is it to get booked on Special Needs Diaries?

Booking probability for Special Needs Diaries is 23%, and the host is rated Selective on guests. Special Needs Diaries requires a Pod Score of 80 or higher. Special Needs Diaries's contact route on record: public web form.

Who should pitch Special Needs Diaries?

The strongest fits for Special Needs Diaries are Family & Social Services. Special Needs Diaries has a kids audience.

About the host

My Kabuki Girl hosts Special Needs Diaries, a kids podcast with 19 episodes published.

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Recent episodes

Our AI reads these to draft pitches. Use them as grounding for a pitch that cites a real guest and a specific topic.

  • Episode #19

    ‘Hospital Talk’ | 8 Things Every Parent Needs to know

    Mar 14, 202613 minS2

    <p>In this podcast episode, I share how I address the "hospital talk" every time our daughter has a regular check-up or hospital visit.</p><p>I got lots of positive comments on this topic, on the social media of My...

  • Episode #18

    She got an ASD Diagnosis | Our daughter's developmental assessment

    Mar 6, 202629 minS2

    <p>In this unscripted episode of Special Needs Diaries I share with you our newest updates: our child got an autism diagnosis and moderate developmental delays, on top of her rare syndrome.</p><p>I want to share with...

  • Episode #17

    New Year, New Podcast

    Jan 14, 20268 minS2

    <p>For the second season of the podcast “How we…special needs”, I thought of keeping the tone a bit more conversational, talking about topics that matter to us (me and you guys!) the most, sharing with you the blog...

  • Episode #16

    A journey with CNF | Interview with Simone Eyles

    Oct 13, 202540 minS1

    <p>Hi guys, I'm Minie, #Italian special needs mum from #Sydney! 🇮🇹🇦🇺Welcome to our channel, where I share our daughter’s journey with #Kabukisyndrome.<br/>In this podcast episode, I interview Simone, a mum and...

  • Episode #15

    A journey with Auto inflammatory disease | Interview with Sharon Kensell

    Sep 12, 202541 minS1

    <p>Hi guys, I'm Minie, #Italian special needs mum from #Sydney! 🇮🇹🇦🇺Welcome to our channel, where I share our daughter’s journey with #Kabukisyndrome.<br/>In this podcast episode I interview Sharon, my first guest...

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  • Episode #14

    A journey with Hirschsprung Disease and ASD | Interview with Mari Suzuki

    Jun 6, 202546 minS1

    <p>In this podcast episode I interview Mari, an amazing mum - and Zumba instructor - who shares on socials Kai's (her son) journey with Hirschsprung Disease and ASD (autism).<br/>The interview spans from the...

  • Episode #13

    Stop Telling Mums to Take Care of Themselves

    May 9, 202512 minS1

    <p>“You should take care of yourself!” </p><p>“Go get a massage!” </p><p>“Don’t forget to rest!”</p><p> Have you ever heard these well-meaning but *completely useless* pieces of advice? I did—over and over again—when I...

  • Episode #12

    The Lantern Against All Fears | A Special Needs Story that Stirs

    May 2, 202516 minS1

    <p>I was invited to speak on the theme "expansion" at the event @Storiesthatstir, on the 24th February 2025. I know the lovely organiser, Monica, and I was honoured when she invited me to talk about our...

  • Episode #11

    Two Countries, One Date | What 25 April Means to Our Family

    Apr 25, 20257 minS1

    <p>What happens when one date—April 25th—means two completely different things depending on where you live?</p><p>In this reflective episode, I read a blog entry I wrote about Anzac Day and Liberation Day, and what they...

  • Episode #10

    Life with a SWASH Brace | What Parents Should Know

    Apr 18, 202519 minS1

    <p>🎙️ <b>Life with a SWASH Brace: What Parents Should Know</b></p><p>When my daughter was prescribed a SWASH brace, I didn’t expect to cry—but I did. In this episode, I’m sharing our honest experience with this...

  • Episode #9

    A journey with Kleefstra Syndrome | Interview with La Toya Redman

    Apr 11, 202551 minS1

    <p>In this podcast episode I interview La Toya, a sweet and strong mum who shares on socials Luna's (her daughter) journey with Kleefstra Syndrome.<br/>La Toya shares Luna's and her family's roller coaster with such...

  • Episode #8

    Storytime | The Butterflies in Our Kitchen

    Jan 10, 20257 minS1

    <p>It's story time!<br/>In this episode I will share with you the story behind the lovely butterflies that for two years have populated our kitchen and dining room, and why it's so hard to say goodbye.<br/>What should I...

  • Episode #7

    A journey with Menkes Disease | Interview with Ana Romanow

    Jan 3, 20251h 1mS1

    <p>This is my first interview and it couldn't have been with a better guest: Ana Romanow. She's a super mum and super woman who's sharing her son's journey with Menkes Disease.<br/><br/>Although Philip is not here with...

  • Episode #6

    Our 2024 Recap | Chat & Cooking Gnocchi di Patate

    Dec 27, 202416 minS1

    <p>We recorded this episode on Christmas Eve and we made gnocchi di patate (potato gnocchi), while recapping what happened in our 2024. Check the YouTube video to see the cooking part! Have you ever tried gnocchi? Let...

  • Episode #5

    The nurse I hated on Christmas Day

    Dec 20, 202412 minS1

    <p>🎙️ Episode 5: Forgiveness and a Christmas to Remember</p><p>This week on How We...Special Needs, I share a deeply personal story from Christmas 2022—our first Christmas as a family, spent in a hospital ward with our...

  • Episode #4

    BONUS Storytime: My mum is with me

    Dec 13, 20247 minS1

    <p>When our therapy centre unexpectedly increased their charges, I was overwhelmed, frustrated, and at a crossroads. But on a tearful drive to yet another therapy session, an unexpected moment changed everything—a sign...

  • Episode #3

    Celebrating My Daughter’s Journey with Communication Delays

    Dec 6, 202410 minS1

    <p>In this episode of How We…Special Needs, I’m diving into a topic we all know too well: milestones. My daughter Beatrice, who has Kabuki syndrome, has made incredible strides with her communication—she can now say 20...

  • Episode #2

    A Message for My Daughter’s second Birthday

    Nov 29, 202410 minS1

    <p>Welcome to the first episode of How We...Special Needs! 🌟 I dedicate it to my beautiful daughter, Beatrice, as she celebrates her 2nd birthday. I reflect on the challenges and triumphs of her first two...

  • Episode #1

    Trailer of How We...Special Needs

    Nov 27, 20241 minS1

    <p>Hi, I’m Minie, an Italian special needs mum based in Sydney.</p><p>My daughter has a rare genetic condition called Kabuki syndrome and on My Kabuki Girl I share our journey throughout medical issues, disabilities...

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