Don't Judge, Just Love

4,9 (47)
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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!

См. все (19)

4,9

из 5

Оценок: 47

Very helpful

8 мая

Packnplay

I’ve gone through this unfortunately. How you got your diagnosis, dealing with the medical professionals and getting support from the community… it all resonates with me. I think the medical system is not set up to help rate disease patients and that needs to change but it’s going to have to start with a voice.
Great podcast

19.06.2023

9htr4

This is a keeper! Such a real check in with chase and Shannon. I love it and look forward to listening
LOVE

29.04.2023

kyliekuz

I love this podcast and family! 🩷 I must add, Chase’s laugh might be my favorite part of the pod 🤣
Obnoxious

05.06.2023

Beth7609

Tried to listen to the latest episode but the nine year old son is too obnoxious.

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!