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Talking about all the things with The Rare Life's Madeline Cheney

Talking about all the things with The Rare Life's Madeline Cheney

FromConfessions of a Rare Disease Mama


Talking about all the things with The Rare Life's Madeline Cheney

FromConfessions of a Rare Disease Mama

ratings:
Length:
82 minutes
Released:
Mar 26, 2024
Format:
Podcast episode

Description

This week I sit down with founder and host of The Rare Life, Madeline Cheney. She started her podcast in 2020, but the seed was planted 3 years prior—when doctors found troubling results at her 20-week ultrasound that pointed to a rare syndrome during her pregnancy with her second child. She and her husband Juston have two beautiful children, their 7-year-old daughter Wendy, and their now 5-year-old son Kimball. I have been a long time fan of the Rare Life, so I was so excited to talk with Madeline and learn more about her and her family's unique journey. We talk about ALL the things including what is was like during her pregnancy knowing her son had a rare condition, our not so great first encounters with Palliative Care, the family dynamics between a disabled and non disabled siblings, family planning/IVF, and so much more. We also touch on a few of my favorite episodes of The Rare Life which are linked below for you all to check out! Happy listening, ya'll!https://therarelife.org/https://www.instagram.com/the_rare_life/?hl=enhttps://www.facebook.com/p/The-Rare-Life-Podcast-100039719031110/ Episode 130: Fearful of Child Loss/Anticipatory GriefEp. 95: The Parable of the Pain ScaleEp. 99: Family Planning When You Have a Medically-Complex Child w/ Amanda Griffith-AtkinsEp. 19: The Story of Clairehttps://www.confessionsofararediseasemama.com/Learn more about my children's fight with ASMD and donate to our cause:https://www.saveromanandstella.com/Follow on instagram: https://www.instagram.com/confessionsofararediseasemama/
Released:
Mar 26, 2024
Format:
Podcast episode

Titles in the series (47)

Join me every week as I navigate the ups and downs, and everything in between of the crazy stressful, but always beautiful life of being a rare disease parent.