The Deep C

Snack Labs
  • 5.0 (4)
  • 育儿
  • 一周一更

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.

  1. 5天前

    Naturopath Dr. Jackie on Integrating Alternative Practices into her Son's High Risk ALL Treatment

    Today I speak with Dr Jackie, a naturopathic doctor and mom to 3 beautiful boys. Jackie’s life was completely upended when her youngest son Spencer was diagnosed with high risk ALL at 13 months old. And when I say her life, I mean her entire foundation. As a naturopath, Jackie was consciously raising her family in alignment with her practice - this meant using things like natural remedies, tinctures, supplements and diet to not only help her kids through fevers, bumps and bruises, but to also work preventatively to prepare their little immune systems for a long healthy life. So when Spencer was diagnosed, Jackie had to embrace a type of intervention that was the complete opposite of what she had built her family and practice on. Western medicine and pharmaceuticals don’t typically have a place in a naturopathic practice, and within hours her baby was needing them to survive. Jackie talks about the rapid switch she had to make, which of course she did, and how it felt to accept and even find peace with what was needed to save Spencer's life. In our chat, Jackie shares the simple and gentle practices she brought into Spencer's treatment, and how she advocated and worked alongside their team to provide him with the support he needed. This is such a great episode for families, much like mine, who were raising their kids with natural and holistic treatments and had to instantly pivot and embrace the most toxic and harsh medicines being administered to their child’s body. I learned so much from Jackie's confidence and calm, assured belief that cancer is more than a physical disease and it's equally important to heal the body as well as our mind, soul and spirit. You can find Jackie at www.doctorjackie.ca and/or IG @doctorjackieND Hosted on Acast. See acast.com/privacy for more information.

    37 分钟

  2. 7月16日

    The Shame of Having Cancer as a Kid with Childhood Cancer Survivor & Oncology Mom Lindsay Craig

    Todays talk with my friend Lindsay hit so close to home, in many ways. I first connected with Lindsay because our kids were diagnosed with the same cancer, rhabdo. It felt really good to talk to another parent who knew all the same things I knew - like meeting someone in a foreign country who spoke the same language AND also knew all the same people. She was comfortable, familiar and we instantly connected. So it was a matter of minutes before Lindsay told me that ON THE SAME DAY she found her son’s cancer, 32 years prior when she was 7 yrs old, SHE was diagnosed with Wilms. Lindsay was now a child cancer survivor AND a cancer mom - I don’t need to highlight what a unique and complicated journey it’s been for Lindsay, but also a journey where her insights are already baked in, giving her a vantage point that not many of us have. I had a million questions for Lindsay about what it’s like ushering your child through a treatment you yourself had, and this is where our chat got even deeper, because hearing Lindsay share her memories of treatment, especially integrating back into her life post treatment, felt like I was listening to my own daughter share her exact same experience. Lindsay talked about the shame of having cancer and what it felt like to be different from her peers, and how she went to extreme lengths to hide her scars and bald head - and it was all just the same for us. Hearing Lindsay share her stories of shame and wanting to hide her cancer went straight to my core because not only was I witnessing this exact same struggle with my child, but I knew there had to be other parents out there feeling the same helplessness watching their child desperately try to blend in post treatment. This prompted our episode today where Lindsay goes deep into her feelings of being different, of looking sick and getting sad pitiful eyes from strangers, and how complicated it was to feel embarrassed about her cancer when everyone was telling her it was something to be proud of. This talk will resonate so deeply with parents whose kids were a little older during treatment or maybe more self aware and who struggle with the whole idea that children with cancer are celebrated as being brave and warriors when really, they want to blend in and not be recognized at all - until, as you’ll hear Lindsay say, she came through her teen years and realized that she was, in fact, tremendously brave and she decided to truly embrace her cancer. But that had to be on her terms, in her own way, and not because everyone told her so. Hosted on Acast. See acast.com/privacy for more information.

    39 分钟

  3. 6月21日

    Running Towards the Pain - Bereaved Dad Matt on the Healing Power of Endurance Running

    My conversation today with Matt got so deep, so fast, and I think it’s because he’s worked really hard at clearing the path towards the place he holds his pain and grief around losing his son Landon. When Landon was 10.5 years old he passed away from medulloblastoma, leaving Matt with a choice to follow his grief in a bad, destructive direction, or in a powerful and healing direction. A friend challenged him to run for 21 days to start a habit and hopefully give Matt an outlet for his grief, and so he started to run. And run, and run, and run for miles and miles. At first around his neighborhood, and then through the trails near his home. The more he would run, the more pain his body would endure, the closer he would get to feeling his grief - and to feeling his son. Running became his catharsis, and his direct path to connecting with Landon. He pulled from all the mental endurance he learned during treatment and applied it to long distance running, and then ultra running - and then to running 140 miles to raise money and awareness for childhood cancer. Matt documented his run and made it into a film called No Finish Line because, this isn’t a spoiler, at the end of Matt’s 140 mile run, he DNF’s which stands for Did Not Finish - because as Matt knows, and as we all know, childhood cancer doesn’t end. It’s a loud message to everyone watching that kids in treatment are up against a heck of a lot more than the physical and mental strain of running 140 miles, and his message lands. This conversation today is really bold, really honest and has so many meaningful takeaways on processing pain, choosing the ultimate good vs the ultimate bad, our dragons, our grief, and what it’s like to live - truly live - when the biggest fear in your life happens. How does that change the trajectory of your path, how do you run it, and most importantly, how far can you go when you aren’t running from the pain, but running purposefully, and with great intention, towards it. So, let’s dive deep, with Matt. No Finish Line can be watched here https://www.youtube.com/watch?v=QL6irMXCIM8 Hosted on Acast. See acast.com/privacy for more information.

    34 分钟

  4. 6月3日

    The Sibling Experience - A Brother Shares His Perspective Of His Sister's Treatment 20 Years Later

    Today I speak with Alex, who was 7 yrs old when his sister was diagnosed with leukemia 20 years ago. We discuss the profound impact of childhood experiences related to a sibling's cancer diagnosis and dive deep into themes of loneliness, emotional neglect, and the long-term effects on mental health. Alex shares his personal journey of navigating his sister's illness, the feelings of being sidelined, and the eventual realization of the need for support and therapy. Our discussion highlights the importance of recognizing the sibling experience in the context of family illness and the lasting emotional scars that can result from such experiences. Alex shares his journey of confronting deep-seated anger related to his sister's cancer diagnosis and the impact it had on his family dynamics. Through therapy, he navigates feelings of abandonment and the complexities of healing relationships with his parents. Our discussion highlights the importance of communication, understanding, and the efforts made to mend familial bonds. Alex's current work in oncology reflects his personal experiences, driving his passion for cancer research and patient advocacy. Hosted on Acast. See acast.com/privacy for more information.

    36 分钟

  5. 5月24日

    The Golden Moms

    Today I talk with five incredible oncology moms who met during their kids treatments and felt the need to create a collective for cancer moms to come together, feel seen, supported and less alone. Katelyn, Sarah, Amanda, Nicole and Lindsay discuss the importance of having a support system of other oncology moms, the emotional challenges they face, and how they found strength in their shared experiences. Our discussion highlights the birth of the Golden Moms community, the significance of connecting with others who understand our journey, and the role of social media in fostering these relationships. Each mom shares their personal story, emphasizing the importance of community, shared experiences, and the need for emotional support. They discuss the discomfort that often arises in friendships during crises, the healing power of connecting with others who understand, and the necessity of caring for caregivers as well. To find the Golden Moms, visit their instagram @goldenmoms05, and the Ottawa Golden Moms group @goldenmomsottawa Hosted on Acast. See acast.com/privacy for more information.

    42 分钟

  6. 5月14日

    Post Treatment Healing for Parents - Oncology Mom Kayleigh on Somatic Healing & Processing Her Trauma

    In this conversation, Sam and mindset coach/oncology mom Kayleigh Kennedy explore the emotional landscape for parents post treatment and the profound impact of trauma on our mental and physical health. Kayleigh shares her personal experiences and insights on mending the broken heart her son's cancer treatment left her with, and the ongoing process of healing, highlighting the significance of setting boundaries and prioritizing self-care. One of the ways Kayleigh has approached her healing is through somatic therapy and integrated somatic trauma processing (ISTP). She discusses the healing power of breath work, the importance of releasing suppressed emotions, and the journey of letting go of control. The conversation highlights the physical and emotional challenges faced during therapy sessions, including intense releases of energy and emotions. Kayleigh emphasizes the significance of trusting oneself and exploring personal healing needs, while also acknowledging the discomfort that comes with the healing process. Hosted on Acast. See acast.com/privacy for more information.

    47 分钟

  7. 5月1日

    Did I Make It Too Fun? A Fascinating Talk on What it's Like When Your Child Thrives Through Treatment and Doesn't Want it to End

    My talk with Lily has really stuck with me. This is a mom who simply refused to let cancer define her family’s life. There was no way cancer was going to interrupt their normal, and there was no way it was going to interfere with her son’s growth and learning and development. Lily was determined to maintain Wyatt’s full and active life, and not only maintain, but better it. Cancer wasn’t something that would stop him, it was something that would make him stronger. When Wyatt was 5.5 yrs old, he was diagnosed with T cell ALL, and like all parents, Lily was floored when she was told the news over the phone after some routine blood work, But you’ll hear her say Wyatt’s diagnosis completely shifted her perspective and made her even more optimistic and less concerned and worried about the things in life that don’t matter. I’ve had a lot of talks with parents who come to those realizations, maybe after treatment, but for Lily, it was right off the bat, and she harnessed this optimism and perspective into making Wyatt’s cancer treatment an opportunity for growth and something that wasn't going to define him. One of the areas of our chat that will stick with me forever is when we talk about how Lily made treatment so positive for Wyatt that he legitimately mourned when it was over. This makes so much sense when you hear Lily’s story, but I mean, we can all agree it’s not the most common reaction coming from a little kid who’s just gone through 3 years of gruelling cancer treatment. But port removal and final lumbar punctures were devastating for Wyatt, and we go into how Lily is managing these really honest and deep emotions. We also talk about her other son Jack and how in many ways Wyatt’s cancer treatment was hardest on him. So much insight and deep conversations in this episode. I love Lily, she is incredible and so is this chat. I know it will stick with you too. So, let’s dive deep with Lily. Hosted on Acast. See acast.com/privacy for more information.

    32 分钟

  8. 4月17日

    Supporting Families & Siblings in Children's Hospice with Recreational Therapist Samantha Albert

    Sam Albert, a recreational therapist at Roger Nielson Children's Hospice, shares her experience supporting families and siblings through treatment and end of life care. Sam shares personal stories of growing up with a brother who had cancer, the impact of grief, and the importance of validating the sibling's experience. The conversation also emphasizes the significance of peer support among siblings and the creative ways they express their emotions. Sam explores the profound experiences of supporting families in palliative care, emphasizing the importance of creating lasting memories, the privilege of holding space for families during their hardest moments, and the unique emotional journey caregivers undergo. The discussion highlights the beauty found in love amidst grief, the impact of personal experiences on caregiving, and also touches on the examination of belief systems and the diverse needs of families after the loss of a child. https://www.rogerneilsonchildrenshospice.ca/ Hosted on Acast. See acast.com/privacy for more information.

    36 分钟
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关于

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.

信息

  • 频道
    Snack Labs
  • 创作者
    Snack Labs
  • 活跃年份
    2024年 - 2025年
  • 单集
    53
  • 分级
    儿童不宜
  • 版权
    © Sam Taylor
  • 节目网站
    The Deep C

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