Episode 036 - Passing a Non Discrimination Law, and How to Pray about a Diagnosis

Episode 040 - Adopting a Baby with Down syndrome

Ellie Sanazaro is a mom to three, one of which has an extra chromosome, and is the author of the new book Image Bearer! [https://www.imagebearerbook.com]  In today's episode Ellie shares about the adoption process when adopting a child with Down syndrome.  Through all of the pitfalls and uncertainties, Ellie knew God would bring them through, and he truly blessed their Upside Down family with their son, Finn!

Episode 039 - Celebrating World Down Syndrome Day

Season one of The Upside Down Family Podcast is coming to a close on Thursday!  In today's episode we share how we celebrated World Down syndrome Day this year, and share one big take away from season one.  Thank you for being part of the Upside Down Family!

Episode 038 - Art of the Heart: Building Bonds and Making Music

With his life already feeling chaotic, Jesse learned that his new baby girl not only has Down syndrome, but would also need a heart surgery.  It was a tailspin, and he found himself struggling to connect with his daughter.  But as he cared for her, he determined he would fight for her. This resolve led to Jesse writing and recording an album about this  journey, and how he and his daughter built bridges.  Listen in to my conversation with Jesse Norell! Visit https://jessenorell.bandcamp.com

Episode 037 - The Value of Your Story

Phil Martin (Kyle's Dad) speaks and writes about life and business principles, and to celebrate his new book "Take the Stage: 64 Essential Leadership Lessons Learned from Theatre" I interview him on some (not all 64) of those principles.  He dives into the importance of your story, going beyond communicating to truly connecting, to inviting the audience into the story, and finally defining success. Dad has a rich and storied history, and I'm so glad I get to share him with you.  Enjoy this conversation with Phil Martin!

Episode 036 - Passing a Non Discrimination Law, and How to Pray about a Diagnosis

People with disabilities were often denied access to transplant lists... Until superheroes like Rachel Anderson came along!  Calebs law is helping people with differing abilities have equal rights to organ transplant lists, and its amazing work.  Rachel shares this and more in todays episode!