Special Needs Diaries
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 window into the world of disabilities, genetic conditions, and medical families.
I’d love to hear your thoughts and feedback along the way. So feel free to reach out to me on social media at My kabuki Girl, or on the website www.mykabukigirl.com
Let’s celebrate the love, strength, and stories that make this journey unforgettable. 💚
Special Needs Diaries
Celebrating My Daughter’s Journey with Communication Delays
Use Left/Right to seek, Home/End to jump to start or end. Hold shift to jump forward or backward.
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 words! But as any parent in our community knows, milestones can be a double-edged sword.
I’ll share a personal moment of Googling how many words a typical 2-year-old speaks (spoiler alert: it wasn’t what I expected) and explore how I’ve learned to reframe comparisons. We'll chat about how milestones can help guide us, but also how they sometimes miss the mark for special needs families.
Let’s rethink what progress looks like, celebrate our kids’ wins on their terms, and discuss why it’s time to develop inclusive benchmarks that reflect diverse journeys.
Join me for a conversation filled with insights, lessons, and a few laughs as I learn to be proud of Beatrice’s incredible progress—no matter the number. 💖
👉 Next Episode Teaser: Storytime: My mum is with me
Did you like this episode? Let me know! 💕
Don’t forget to subscribe for more stories of love, strength, and Kabuki Syndrome.
Follow me on TikTok, Instagram and YouTube @MyKabukiGirl and share your thoughts!
Check the website www.mykabukigirl.com for merchandise and so much more!👀
Stay safe, ciao! ☺️