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RARE MAMAS RISING- EPISODE 013
10 Minutes with a Rare Mama
Catherine Oh - Congenital Nephrotic Syndrome Mom
Introducing "10 Minutes with a Rare Mama!"
"10 Minutes with a Rare Mama" is a bite-size serving of all the warm, nourishing goodness you love about Rare Mamas Rising—learning from each other, uplifting one another, and walking away feeling empowered. Each episode is filled with hearty ingredients to help you grow! But let's be honest, sometimes mama ain't got time for a full meal! So,"10 Minutes with a Rare Mama" is meant to give you an easily-digestible, snack-sized episode that can actually FIT into your day! In this episode, we hear from Catherine Oh, a veteran Rare Mama whose son Shawn is now a teenager living with an extremely rare variation of congenital nephrotic syndrome. Catherine highlights all the major life events that unfolded at the same time as Shawn's diagnosis, how she embraced life post-diagnosis, what she's learned about herself, where she finds hope, and her best piece of advice to other rare mamas. Check out this episode and grab a splash of inspiration, a little helping of hope, and a bite of bravery to get you through your day. This episode will fill you up in the best possible way!
LINKS & RESOURCES MENTIONED
Catherine Oh
www.catherineoh.com
CONNECT WITH NIKKI
https://www.facebook.com/RareMamas1/
https://www.instagram.com/Rare_Mamas/
Website
https://raremamas.com/
By Nikki McIntosh5
2929 ratings
RARE MAMAS RISING- EPISODE 013
10 Minutes with a Rare Mama
Catherine Oh - Congenital Nephrotic Syndrome Mom
Introducing "10 Minutes with a Rare Mama!"
"10 Minutes with a Rare Mama" is a bite-size serving of all the warm, nourishing goodness you love about Rare Mamas Rising—learning from each other, uplifting one another, and walking away feeling empowered. Each episode is filled with hearty ingredients to help you grow! But let's be honest, sometimes mama ain't got time for a full meal! So,"10 Minutes with a Rare Mama" is meant to give you an easily-digestible, snack-sized episode that can actually FIT into your day! In this episode, we hear from Catherine Oh, a veteran Rare Mama whose son Shawn is now a teenager living with an extremely rare variation of congenital nephrotic syndrome. Catherine highlights all the major life events that unfolded at the same time as Shawn's diagnosis, how she embraced life post-diagnosis, what she's learned about herself, where she finds hope, and her best piece of advice to other rare mamas. Check out this episode and grab a splash of inspiration, a little helping of hope, and a bite of bravery to get you through your day. This episode will fill you up in the best possible way!
LINKS & RESOURCES MENTIONED
Catherine Oh
www.catherineoh.com
CONNECT WITH NIKKI
https://www.facebook.com/RareMamas1/
https://www.instagram.com/Rare_Mamas/
Website
https://raremamas.com/

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