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What happens when your personal and professional lives collide in the most powerful way?
That's what happened to Geri Landman. A mother of three and a practicing pediatrician, Geri has taken on the fight against ultra-rare genetic disorders head-on. Her world was changed when her youngest daughter Lucy, was diagnosed with PGAP3 CDG, a rare genetic disorder. Turning tragedy into a mission, Geri, and her husband, who's also a doctor, established Moonshots for Unicorns, a nonprofit to facilitate research and find cures for similar single gene disorders. Their expertise and personal journey blend seamlessly to spearhead a path for rare disease treatment.
In this episode, you'll learn:
Find out more about Geri:
Website
Facebook
Instagram
Rate, Review, & Follow on Apple Podcasts
"This is my go-to podcast for inspiration and to discover new approaches to embrace the challenges in my life." If that sounds like you, please consider rating and reviewing my show! This helps me reach more people -- just like you -- find strategies and insights to do the things that feel undoable. Click here, scroll to the bottom, tap to rate with five stars, and select “Write a Review.” Then be sure to let me know what you loved most about the episode!
Also, if you haven’t done so already, follow the podcast. Follow now!
Sign up for my newsletter and learn more about these remarkable stories at www.jessicafeinstories.com
Order Jessica's memoir, Breath Taking: A Memoir of Family, Dreams, and Broken Genes
Watch Jessica's TedX Talk
Music credit: Limitless by Bells
5
8181 ratings
What happens when your personal and professional lives collide in the most powerful way?
That's what happened to Geri Landman. A mother of three and a practicing pediatrician, Geri has taken on the fight against ultra-rare genetic disorders head-on. Her world was changed when her youngest daughter Lucy, was diagnosed with PGAP3 CDG, a rare genetic disorder. Turning tragedy into a mission, Geri, and her husband, who's also a doctor, established Moonshots for Unicorns, a nonprofit to facilitate research and find cures for similar single gene disorders. Their expertise and personal journey blend seamlessly to spearhead a path for rare disease treatment.
In this episode, you'll learn:
Find out more about Geri:
Website
Facebook
Instagram
Rate, Review, & Follow on Apple Podcasts
"This is my go-to podcast for inspiration and to discover new approaches to embrace the challenges in my life." If that sounds like you, please consider rating and reviewing my show! This helps me reach more people -- just like you -- find strategies and insights to do the things that feel undoable. Click here, scroll to the bottom, tap to rate with five stars, and select “Write a Review.” Then be sure to let me know what you loved most about the episode!
Also, if you haven’t done so already, follow the podcast. Follow now!
Sign up for my newsletter and learn more about these remarkable stories at www.jessicafeinstories.com
Order Jessica's memoir, Breath Taking: A Memoir of Family, Dreams, and Broken Genes
Watch Jessica's TedX Talk
Music credit: Limitless by Bells
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