Hi guys! In this episode, we answered questions about how our girls with Congenital Disorders of Glycosylation (CDG) go to school. You guys asked us on Instagram about how that works, how it's affected them and what our plan is moving forward so we dove right in! Raising awareness about CDG is important to us and we are happy to talk about it. Let us know in the comments if there are any other questions you have!

Learn more about the Summer Boot Camp here! ▶ https://bit.ly/FMMSummitReg23

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YouTube ▶ https://www.youtube.com/@WillardsonFamily


#FamilyMade #podcast #marriage #IVF #babies #family #kids #pregnancy #children #couples
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Hi guys! In this episode, we answered questions about how our girls with Congenital Disorders of Glycosylation (CDG) go to school. You guys asked us on Instagram about how that works, how it's affected them and what our plan is moving forward so we dove right in! Raising awareness about CDG is important to us and we are happy to talk about it. Let us know in the comments if there are any other questions you have! Learn more about the Summer Boot Camp here! ▶ https://bit.ly/FMMSummitReg23 Follow us here! Instagram ▶ https://www.instagram.com/shannonwillardson/ YouTube ▶ https://www.youtube.com/@WillardsonFamily #FamilyMade #podcast #marriage #IVF #babies #family #kids #pregnancy #children #couples Learn more about your ad choices. Visit megaphone.fm/adchoices

how our daughters with CDG go to school & feel included

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!

Parenting

Kids & Family

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!

Family Made Media presents “Don’t Judge, Just Love“ with Shannon and Chase Willardson!&nbsp;A podcast where you can come as you are and find joy amidst the chaos of everyday life.&nbsp;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&nbsp;both have&nbsp;an extremely rare genetic disease called Congenital Disorder of Glycosylation&nbsp;(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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how our daughters with CDG go to school & feel included

how our daughters with CDG go to school & feel included

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