Susan Lieu’s story is anything but ordinary. She’s the daughter of Vietnamese refugees, a truth-seeker, and the author of The Manicurist’s Daughter, a memoir about family, loss, and the impossible beauty standards. In this episode, Susan opens up about losing her mother to a botched surgery at age 11, uncovering the secrets no one wanted to talk about, and how she found strength in the messiness of grief and resilience. It’s raw, authentic, and a conversation you don’t want to miss.

Find Susan Lieu:

🌟 Get the book: https://www.susanlieu.me/the-manicurists-daughter

🌟 Watch the one-woman show: https://susanlieu.vhx.tv/products/140-lbs-how-beauty-killed-my-mother

Find Heather and Jake’s Help from Heaven:

❤️ APOY Instagram: https://www.instagram.com/aplaceofyespodcast/

❤️ Heather’s Instagram: https://www.instagram.com/heathersstraughter/

❤️ Jake’s Help from Heaven: https://jakeshelpfromheaven.org/

❤️ Jake’s Help from Heaven IG: https://www.instagram.com/jakeshelp/

❤️ Facebook: https://www.facebook.com/jakeshelpfromheaven

❤️ Our YouTube Channel: https://www.youtube.com/@APlaceofYesPodcast

 

Listen on Apple Podcasts | Spotify | iHeartRadio

FIND HEATHER & JAKE’S HELP FROM HEAVEN ⬇️

❤️ Heather’s Instagram: https://www.instagram.com/heathersstraughter/

❤️ Jake’s Help from Heaven: https://jakeshelpfromheaven.org/

❤️ Jake’s Help from Heaven IG: https://www.instagram.com/jakeshelp/

❤️ Facebook: https://www.facebook.com/jakeshelpfromheaven

❤️ Our YouTube Channel: https://www.youtube.com/@APlaceofYesPodcast

Connect with us on social media:
• Heather’s Instagram
Jake’s Help from Heaven
Jake’s Help from Heaven IG
Facebook
• Our YouTube Channel

Keep scrolling for the episode transcript.

Checkout our other episodes

 

 

What No One Tells You About Special Needs Parenting

What No One Tells You About Special Needs Parenting

Behind every rare disease diagnosis lies a story of heartbreak, resilience, and unshakable love. Heather sits down with Effie Parks, award-winning host of Once Upon a Gene and mother to Ford, who lives with CTNNB1 syndrome.

Together, they uncover the raw truths of parenting a child with special needs—from the moments of joy to the isolation no one talks about. Effie’s journey is a testament to the power of advocacy, community, and finding light in the darkest days. This episode will leave you inspired and deeply moved by the resilience of families navigating the rare disease world.

My Son Outlived His Life Expectancy: Microlissencephaly & Our Fear of Losing Miles

My Son Outlived His Life Expectancy: Microlissencephaly & Our Fear of Losing Miles

What happens when a 2-5-year life expectancy stretches into a decade of miracles, fear, and unconditional love? In this profoundly emotional episode of A Place of Yes, Heather talks with David Robinson, father to 10-year-old Miles, who has Microlissencephaly. Against all odds, Miles continues to rewrite the narrative of his condition, bringing joy and gratitude to his family while challenging them to face the ever-present grief and fear of the unknown.

David opens up about what it means to live in the tension of hope and heartbreak, sharing powerful lessons on resilience, love, and celebrating every moment. This is a story you won’t forget.

Glioblastoma: Losing a Parent to One of the Deadliest Cancers

Glioblastoma: Losing a Parent to One of the Deadliest Cancers

Kate Snedeker was still in college when she faced the unimaginable: losing her father to glioblastoma, one of the most aggressive and deadly cancers.

In this episode, she opens up about navigating profound grief, the life-changing moments that shaped her, and how she turned her pain into purpose by founding Gray for Glioblastoma. This isn’t just a story of loss—it’s a story of finding hope, even in the darkest times.