Family Made Media presents “Don’t Judge, Just Love“ with Shannon and Chase Willardson! A podcast where you can come as you are and find joy amidst the chaos of everyday life. Shannon is a lifestyle blogger and digital creator who's best known for educating the community as a special needs mom. She and Chase have a son and two daughters who both have an extremely rare genetic disease called Congenital Disorder of Glycosylation (specifically CDG-1p), a condition that currently has no treatment and affects only 15 people in the world. Through the challenging seasons they’ve walked through, including their current sixth round of IVF, the Willardson’s are living proof that there's life after diagnosis. Their vulnerability, authentic conversations, and love for one another will bring a refreshing start to your week every Monday!
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Family Made Media presents “Don’t Judge, Just Love“ with Shannon and Chase Willardson! A podcast where you can come as you are and find joy amidst the chaos of everyday life. Shannon is a lifestyle blogger and digital creator who's best known for educating the community as a special needs mom. She and Chase have a son and two daughters who both have an extremely rare genetic disease called Congenital Disorder of Glycosylation (specifically CDG-1p), a condition that currently has no treatment and affects only 15 people in the world. Through the challenging seasons they’ve walked through, including their current sixth round of IVF, the Willardson’s are living proof that there's life after diagnosis. Their vulnerability, authentic conversations, and love for one another will bring a refreshing start to your week every Monday!
Hi guys! In this episode we want to talk about self care, what that looks like for us and how we make it a priority in our lives! Leave a comment below of what self care looks like to you :) We love hearing from you guys!! Until next week!
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Don't Judge, Just Love
Family Made Media presents “Don’t Judge, Just Love“ with Shannon and Chase Willardson! A podcast where you can come as you are and find joy amidst the chaos of everyday life. Shannon is a lifestyle blogger and digital creator who's best known for educating the community as a special needs mom. She and Chase have a son and two daughters who both have an extremely rare genetic disease called Congenital Disorder of Glycosylation (specifically CDG-1p), a condition that currently has no treatment and affects only 15 people in the world. Through the challenging seasons they’ve walked through, including their current sixth round of IVF, the Willardson’s are living proof that there's life after diagnosis. Their vulnerability, authentic conversations, and love for one another will bring a refreshing start to your week every Monday!
