A journey with CNF | Interview with Simone Eyles
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Hi guys, I'm Minie, #Italian special needs mum from #Sydney! 🇮🇹🇦🇺Welcome to our channel, where I share our daughter’s journey with #Kabukisyndrome.
In this podcast episode, I interview Simone, a mum and entrepreneur who shares her son's journey with Congenital Nephrotic Syndrome of the Finnish type.
The interview touches the complexities of kidney transplants on babies, the relationship between siblings, the creation of an agency aimed at raising awareness on disabilities and more.
Are you a special needs parent? Are you interested in being interviewed on How We...Special Needs? Let me know in the comments! 👇
You can find Simone here:
➡️ https://www.disinfluencer.co
➡️ https://www.instagram.com/disinfluencer.co/?hl=en
Send me a feedback!
Support the show
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If this episode resonated with you, please subscribe and leave a review on Apple Podcasts or Spotify — it helps other families find us when they need it most. 🙏 Share it with a fellow mum, carer, or anyone who might feel less alone after listening. 💚
🎧 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: ...