This week on the Mimosas with Moms Podcast, Abbey Williams kicks off Season 2 by welcoming Nadine Friedman-Roberts! In honor of Birth Defects Awareness Month, Abbey and Nadine talk about Nadine’s experience welcoming a son with a rare craniofacial condition and how that experience inspired her goals of sharing and normalizing the complexities of parenting a child with a diagnosis, and ending both systemic and everyday ableism. More importantly, it motivates her to be a model of empathy and inclusivity for a really fabulous kid. Professionally, Nadine Friedman-Roberts is a nonprofit specialist working in gender and racial equity. How has Nadine’s perspective as a mother and an individual evolved throughout her journey? Let’s talk about it, CHEERS!!
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You can find Nadine Friedman-Roberts:
IG @ubuwhaaaaaa
Interested in learning more about rare disease legislative advocates? Visit: https://rareadvocates.org/about-us/
And to get involved, stay updated, donate and more! Visit: Bc it’s a program created BY every life https://everylifefoundation.org
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FB /mimosaswithmoms
Email 2mimosamoms@gmail.com
