Hi, I’m Minie, an Italian special needs mum based in Sydney.
My daughter has a rare genetic condition called Kabuki syndrome and on My Kabuki Girl I share our journey throughout medical issues, disabilities, therapies and lovely family moments.
But here’s the thing: there are so many traumas, so many aspects of special needs parenting and motherhood in general that are completely ignored by society or, even worse, treated like tabus, and that instead I feel we should talk about.
I believe that, if one of us is experiencing certain emotions, many others are feeling the same way but have not reached out yet.
And so I created this podcast, where I will share with you the tears, the laughs, the questions I have or that you have and I’ll interview many other special needs parents, in order to get to know a bit better each other’s roadblocks and victories.
We are a community and we are stronger together. So if you want to join, please follow the podcast on your favourite platform and get ready for this hopeful, emotional, crazy ride in the world of special needs and special people.
I’ll do my best to post a new episode weekly or fortnightly and I look forward to reading your comments and feedback.
Stay safe. Ciao.
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🎧 LISTEN TO SPECIAL NEEDS DIARIES
▶️ Apple Podcasts: https://podcasts.apple.com/au/podcast/special-needs-diaries/id1782035233
▶️ Spotify: https://open.spotify.com/show/2zp384wlxzIZyYAEEEqZlh
⚠️ CONTENT WARNING
This episode may contain discussions of [medical challenges/grief/diagnosis/mental health]. Please listen with care if these topics are sensitive for you.
📍 CONNECT WITH MINIE
🌐 Website: https://www.mykabukigirl.com
▶️ YouTube: https://www.youtube.com/user/mykabukigirl
📘 Facebook: https://www.facebook.com/profile.php?id=100090362986609
📸 Instagram: https://www.instagram.com/mykabukigirl
🎵 TikTok: https://www.tiktok.com/@mykabukigirl
💼 LinkedIn:...