Rare Like Us: Taylor Kane
Вставка
- Опубліковано 20 сер 2024
- Meet 'the girl who changed the dictionary', Taylor Kane. She's not only a rare disease carrier, but an advocate, entrepreneur, author, speaker, and hero to many.
In this episode we cover:
-Adrenoleukodystrophy (ALD)
-What it's like to lose your father to a rare disease
-How to build the community you wished you had
-Why teens aren't 'future leaders', but 'present leaders'
And MORE.
What's the ONE takeaway from this episode? What's one thing you can put into action? One thing that inspired you? Or one thing that you think someone else needs to hear right now?
Maybe the Jack Kerouac quote of ‘being the author of your own page’ really resonated with you.
Please please drop a comment below. Be sure and hit the subscribe button on UA-cam and turn on notifications for our Impactivist group on FB… that’s where the magic is happening right now.
Get involved. Join our FB community and lets work together to make our world something that’s good for all of us. Let’s make an impact together.
----------------------------------------------------------------
Connect with Taylor @ www.taylorkane.com
Get her book: www.amazon.com...
DON'T FORGET to hit the SUBSCRIBE button :)
Do you FACEBOOK? Join our Impactivist group (it's FREE) and connect with other creative, inspiring people who are changing the world.
Got questions? Leave a comment below!
Great interview with Taylor Kane, I'm a guy over 35 with a rare genetic disease which affects my liver and metabolism. It's called Tyrosinemia Type 2. I'll check out her book. Watching from the UK 🇬🇧 P.S I love Jack Kerouac. Maggie Cassidy is my favourite book.