The Deep C

By: Snack Labs
  • Summary

  • 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.

    Sam Taylor
    Show More Show Less
activate_Holiday_promo_in_buybox_DT_T2
Episodes
  • In the Same Boat - Two Cancer Moms With Kids Who Have The Same Treatments Share How They Keep Each Other Afloat
    Dec 4 2024

    This conversation delves into the emotional and practical challenges faced by two mothers, Jenna and Alex, as they navigate their children's leukemia diagnoses. They share their experiences from the initial diagnosis to the ongoing treatment, highlighting the shock, fear, and isolation that accompany such a journey. The discussion emphasizes the importance of connection and support among parents in similar situations, illustrating how their friendship has provided strength and understanding during one of the most challenging times in their lives.


    In this heartfelt conversation, Sam, Alex, and Jenna explore the profound connections formed during the challenging journey of childhood cancer treatment. They discuss the anticipatory fears parents face, the importance of finding community, and the unexpected joys that can arise amidst the pain. The dialogue emphasizes the duality of experience, where sorrow and growth coexist, and highlights the significance of vulnerability in forging deep connections. As they share their stories, they reflect on the lessons learned and the hope that emerges from shared struggles, ultimately reinforcing the message that no one has to navigate this journey alone.


    Hosted on Acast. See acast.com/privacy for more information.

    Show More Show Less
    26 mins
  • When "I Don't Know" is The Answer - Parenting a Teen Through the Rare Diagnosis of Papillary Renal Cell Carcinoma
    Nov 22 2024

    In this episode, host Sam Taylor and parent Nicole talk about all the unknowns that come up when your child is diagnosed with a rare cancer that doesn’t respond to all the traditional treatments like chemotherapy and radiation. When Nicole’s son Hayden was 12 years old, he had a bad fall while snowboarding and complained of serious pain in his side that brought them to the hospital. After tests and ultrasounds, Nicole was told that Hayden’s fall had ruptured a15 centimetre tumor on his kidney, diagnosing him with a rare type of cancer called Papillary Renal Cell Carcinoma, typically only found in men over the age of 50. Treatment for Hayden’s cancer was surgery to remove the tumor, and 3 month follow up scans to check for recurrence.


    Nicole and Sam talk about Hayden’s rare diagnosis, and how difficult it is to resume a “normal” life when the lingering fear of Hayden’s cancer returning is always present. With no other treatments to try to eradicate his cancer, Nicole talks about how she moves forward with so many unknowns. Sam and Nicole also talk about Hayden’s age, and how he is old enough to understand his cancer and have a lot of questions about it, in particular, asking if he is going to die. This conversation is so important for families who also have rare diagnoses, non traditional treatments and families whose kids are old enough to experience all the unknowns alongside their parents.


    Hosted on Acast. See acast.com/privacy for more information.

    Show More Show Less
    34 mins
  • Zippaport Founder Julie Middleton On How A Good Idea Has Given Dignity and Normalcy to 5,000+ Kids With Cancer
    Nov 15 2024

    Julie Middleton, founder of Zippaport, shares her journey of her daughter's leukemia diagnosis and how it led to the creation of Zippaport, a charity that provides zippered shirts for kids port access. Our chat covers topics such as the challenges of treatment during the COVID-19 pandemic, the impact of Zippaport on families, and the process of ordering and receiving shirts. Julie also opens up about her own experience as a cancer mom and emphasizes the importance of community and giving back, and how it can be a healing process for parents. Julie also talks about the challenges of hair loss during treatment and the feelings of shame and embarrassment it can bring. She shares her own experience and the impact it had on her daughter. Finally, Julie discusses her daughter's relapse and the roller coaster of emotions that come with it, as well as the importance of self-care and taking time for oneself during treatment.


    You can learn more about Julie and her incredible work, and order a shirt, at zippaport.ca



    Hosted on Acast. See acast.com/privacy for more information.

    Show More Show Less
    49 mins

What listeners say about The Deep C

Average customer ratings

Reviews - Please select the tabs below to change the source of reviews.