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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
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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.
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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.
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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/
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In this chat, Scott Walker shares his family's journey through his teenage daughter's cancer diagnosis of rhabdomyosarcoma and treatment. He discusses the shock of receiving the diagnosis, the protective 'armor' parents wear, and the importance of finding moments of release. Scott emphasizes the significance of approaching treatment in phases, coping with the hair loss phase, and the vital role of team sports and community support in their journey. Scott shares the profound impact of team dynamics and community support during his daughter Peyton's cancer treatment. He emphasizes the importance of mutual support within teams, the significance of billeting, and the courage required to let go as a parent. The discussion highlights the role of community in fostering resilience and the emotional journey of navigating treatment while maintaining a sense of normalcy for Peyton. The conversation emphasizes teamwork, resilience, and the power of community in navigating difficult times.
March 31- April 4th is Adolescent and Young Adult Cancer Awareness Week. Here are some links to learn more:
https://www.childrenscancercause.org/ayaweek
https://acpmp.org/aya-cancer-awareness-week/
https://www.uhn.ca/PrincessMargaret/Clinics/Adolescent_Young_Adult_Oncology
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This conversation spans the epic journey of Shara and her wife Karen navigating their son's stage IV osteosarcoma diagnosis while immigrating to Canada. Friends from childhood, Shara and Karen grew up together in the Philippines. Their paths went in different directions, Shara to Canada where she’s a nurse, and Karen to becoming a psychologist, marrying and becoming a mother. Years later, when Karen was a single mom to Tim, still in the Philippines, she reconnected with Shara, and it didn’t take long for these lifelong friends to realize there was more to their connection. They fell in love, and you’ll hear Shara say, falling in love with Karen also meant falling in love with Tim, who was 7 at the time they reconnected.
As many families who are immigrating do, Karen immigrated to Canada first to be with Shara while they worked endlessly to get Tim’s paperwork approved so he could join them. It was one day over a FaceTime call that Tim told his moms that he banged his knee and there was a sore lump. After tests and scans, Shara and Karen were told over facetime from the Philippines that their son had stage IV osteosarcoma. Like all of us, their lives were instantly fractured and they were forced to navigate treatment on the other side of the world.
This conversation emphasizes the importance of hope, community support, and the unconditional love that drives parents to fight for their children's well-being. Shara's resilience and determination shine through as she recounts the struggles and triumphs of their journey, ultimately showcasing the power of love in overcoming adversity.
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Hosted on Acast. See acast.com/privacy for more information.
Hosted on Acast. See acast.com/privacy for more information.
In today's conversation, Sarah Bailey shares her emotional journey as a single mother navigating the challenges of her daughter's leukemia diagnosis. The discussion covers her life before the diagnosis, the shock of receiving the news, the transition into a new reality, the importance of connection and support, and the complexities of parenting during treatment. Sarah emphasizes the loneliness of her experience and the significance of sharing her story to help others feel less isolated. Sarah discusses the overwhelming responsibilities of being both a medical parent and a regular parent, the emotional toll it takes, and the coping mechanisms she employs. The dialogue explores the importance of maintaining a sense of normalcy, the challenges of navigating the healthcare system, and the healing power of nature and movement. Sam and Sarah discuss how nature serves as a metaphor for resilience and healing, the importance of self-care for parents, and the lessons learned through hiking. Sarah shares her journey of dedicating hikes to raise awareness for childhood cancer and the significance of supporting siblings of cancer patients. The conversation emphasizes the healing power of nature and the importance of community support.
If you would like to follow along with Sarah and Bellamy's hikes, or have one dedicated to your child, you can reach out to Sarah on instagram at @bellamywillwin
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From the publisher's feed
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,…
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.
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