이 팟캐스트 소개 🔗
The Deep C Podcast is for families, caregivers, friends and community who are supporting a child through a cancer diagnosis.
While every ounce of your being is used to carry your child, this podcast is here to carry you.When you're bedside at the hospital, sitting in a waiting room for the millionth appointment, or just need to feel like you're not alone in this dark place - come find us.
Our conversations will match the ones you're already having in your head. No topic is off limits, no fear is kept hidden. We speak to parents and caregivers at every stage of a diagnosis - families who are NED and families who are bereaved - diving deep into their reflections and personal accounts of how they walked (sometimes crawled) through their child's cancer diagnosis.
This is not a medical podcast, we don't discuss chemo cocktails or treatment plans. You already talk about that enough. This podcast is where you come for conversations between people JUST like you: scared, tired, determined, and fierce as hell.
Hosted on Acast. See acast.com/privacy for more information.
진행자:
업데이트 빈도:
every 20 days
평균 오디오 길이:
44 minutes
게스트 인터뷰
영어
미국
에피소드 69 개
2024년 1월 30일부터
episodic
최신 에피소드 🔗
What do our children discover about themselves when they go through cancer treatment?
On The Deep C, I usually talk to parents about the strength, hope and love we discover deep within ourselves when our child is diagnosed with cancer. But for this episode, I wanted to hear about that experience fr…
이전 에피소드 🔗
What happens when the person who usually delivers the diagnosis suddenly becomes the parent receiving it?
In this powerful episode, Sam sits down with Dr. Raksha Hemanth Raheja, a pediatrician and cancer mom whose son Rian was diagnosed with leukemia and later relapsed. Raksha shares her unique per…
In this Mother’s Day episode, Sarah Bartosz joins Sam for a deeply honest conversation about motherhood, grief, survival, and the question every cancer parent has heard: “I don’t know how you do it.”
Sarah is Jack, Annie, and Tommy’s mom, the Executive Director of the Beat Childhood Cancer Fou…
In this episode, Sam sits down with her close friend, award-winning songwriter and bestselling author Tara MacLean to explore the importance of parents telling their own story in the context of childhood cancer.
This conversation moves beyond the clinical version of events—the timelines, …
Infant cancer is rare—so rare that many physicians may never encounter it, especially outside of major centres. And because of that, parents are often required to step into a role they never expected: becoming the voice for a baby who can’t speak, and advocating within a system that is still learni…
When Kerri Steele’s husband was diagnosed with terminal cancer, she was at home with three young children—just two, four, and six—trying to navigate his care, her own grief, and the impossible task of helping her kids understand what was happening. What she quickly realized was that their words and…
When your child is diagnosed with cancer, everything changes — instantly. And when your teen wants to move on while you’re still trying to process it, the experience can feel isolating, overwhelming, and surreal.
In this episode, I sit down with my friend Kelly Stein-Marcus, an extraordinary mom an…
Today I speak with Susan, founder of OPAAC (Ontario Parents Advocating for Childhood Cancer), about the development of parent-led advocacy in pediatric oncology. Susan shares how her daughter’s diagnosis in 1995 led to her becoming a parent liaison at SickKids Hospital and eventually establishing O…
Today I'm privileged to chat with Recreational Therapist and owner of Flow Recreation Therapy and Consulting, Danielle Scarlett, about the hard conversations no parent wants to have with their children. We work through every topic from how to tell our kids they have cancer, what to say when somethi…
I absolutely adore my guest today, Kirsten — and I know you’re going to feel the same way. Kirsten is a three-time childhood and young adult cancer survivor with so much honesty and insight to share about what survivorship really feels like.
Kirsten was first diagnosed with ALL at age 10, spending …
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