In this episode, I share my conversation with Dawn Pickering. Dawn is the mother of two remarkable kids. Her son Ollie was diagnosed with cancer at the age of seven. He endured many rounds of treatment, one of which caused blindness in both of his eyes. Dawn’s daughter Abby, stepped up to be Ollie's stem cell donor when she was just 11 years old. Dawn tells us the story of her amazing family, how they overcame the unimaginable and how they continue to persevere despite the long-term side effects of everything they’ve been through. Dawn has since become a fierce advocate for childhood cancer, as well as for the CNIB.

Here are the links to the organizations that Dawn mentions in the episode can be found here:

Dawn Pickering:

https://www.instagram.com/pickeringdawn/

Ollie's Hope:

https://www.instagram.com/cnib_ollies_hope/

ACCESS / Acces:

https://www.instagram.com/access_acces/

Golden Moms Ottawa:

https://www.instagram.com/goldenmomsottawa?stkn=a2NoeGcyajhzaWpq

September 21, 2026 - Golden Moms on the Hill

https://www.goldenmoms.ca/event-details/gold-on-the-hill-a-national-strategy-for-kids-with-cancer

And finally, here is where you can find Templates to write your MP to ask for a national pediatric cancer strategy:

https://www.strongerthancancer.ca/access-advocacy/access-action

If you would like to share your story, please reach out at nccpod@gmail.com.

I know you'll enjoy this episode.

In this episode, I’m joined by Dr. Matthew Seftel, Medical Director of the Stem Cell Program at Canadian Blood Services. At this moment, there are patients in need of a stem cell transplant. For many, finding a matching donor is their greatest challenge. The Canadian Blood Services Stem Cell Registry recruits volunteer donors who can provide stem cells to patients in need.

Dr. Seftel explains what stem cell transplants are, why patients may need them, who is eligible to join the registry, and how to register. He also walks us through what the donation process involves if someone on the registry is selected to become an anonymous donor.

It is all very remarkable and this is such an interesting conversation. Please listen, and encourage the 17-35 year olds in your life to visit Blood.ca to join the Stem Cell Registry.

https://www.blood.ca/en/stemcells/donating-stemcells/stem-cells-questionnaire

In this episode, I share my conversation with Ambika. Ambika is the mother of Arya, who was 5 in 2024 when he was diagnosed with T-cell Acute Lymphoblastic Leukemia. Ambika and her husband Abhinav reached out to me because they hoped to share their family’s story and wanted the opportunity to talk about all the ways theirr child’s cancer impacted their family.

Ambika discusses the unique way her family rallied to support her and her husband while they shared the caregiving responsibilities for their two young children. She also shares some of the challenges they faced along the way, such as the isolation that comes with parental identity loss, how to relate to friends and colleagues when your world is upside-down, and how to handle nutritional challenges when your child simply cannot tolerate most of the foods he used to love. In Ambika's words, "We hope our story can offer comfort and connection to other families and caregivers who may be walking a similar path."

If you would like to share your story, please reach out at nccpod@gmail.com.

I know you'll enjoy this episode.

In this episode, I share my conversation with Zack Sandor-Kerr. Zach is the father of 3 boys, including 10 year old Jasper, who was diagnosed with leukemia in June of 2023. Zack tells us about his experience as a Dad, who has been the primary caregiver for his child throughout his treatment, and what that has been like for him, and his wife Kaitlin. He rightfully raises the issue of inclusive care in both the hospital environment, and in our communities. His perspective is both considerate of others, and an important reminder to all of us to check our assumptions, and consider our words. As a super creative person, Zack also had an interesting way to prepare family and friends for visits to the Sandor-Kerr home during the early days of his son's treatment. If you would like to see a copy of the Tip Sheets that Zack describes in this episode, please email me at nccpod@gmail.com.

You can learn more about Zack's art on Instagram, or at storypanda.ca.

In this episode, I’m sharing my conversation with Alexx Friesen. Alexx is a Child Life Specialist who works in Toronto. She has worked with families in hospital settings, as well as in hospice and palliative care. She also has experience in oncology, both as a professional, as well as a patient. She herself is a childhood cancer survivor. Her experience as a patient when she was a child led her to this career and it gives her such a unique perspective and skill set to work with families in these extremely difficult scenarios. She is a kind and happy person who is so creative and insightful into the experiences of children. She is also so well-equipped to be doing this very important work.

You can find Alexx online at @childlifealexx.

In this episode, I share my conversation with Michelle Da Costa. Michelle is the mother of three girls. Her youngest daughter is a childhood cancer survivor. Michelle is also a Parent Liaison with @OPACC Ontario Parents Advocating for Children with Cancer. I had the fortune of meeting Michelle at a parent drop-in while my own child was in treatment, and our conversation had a deep impact on me. Michelle tells the story of her daughter's experience with cancer, and how it inspired her to become a support and a resource to other oncology parents. It is remarkable how Michelle has turned her own struggle into purpose, and how she shows up week after week, in service of all the families who are now walking the path she travelled so many years ago.

In today's episode, I am speaking with two representatives from Make-A-Wish® Canada.

You are very likely familiar with Make-A-Wish Canada. This is the charitable organization that grants wishes to children with critical illnesses. But you may not be aware of some of the interesting facts about Make-A-Wish Canada that I learned from this conversation:

• In 2023, Make-A-Wish Canada brought wishes to 1,389 wish kids and their families across Canada.
• A wish might be a chance to travel, to meet a celebrity, to have an experience, or to have an item or piece of equipment. And some kids are hoping to realize other dreams like recording a song or writing a book. The wish coordinators are so thoughtful and creative at helping kids to uncover their wishes and bringing them to life.
• Nearly 50% of children in Canada waiting for a wish have been diagnosed with Cancer. Wishes are considered to be an essential part of treatment and can even improve outcomes.

In the words of Make-A-Wish Canada, “Wishes are transformative, replacing fear with confidence, sadness with joy, and anxiety with hope. Make A Wish believes that through these experiences, children can discover that anything is possible.”

If you are interested in getting involved with Make-A-Wish Canada, either to donate, to fundraise or to volunteer, you can find them online at makeawish.ca.

In this episode, I have the honour of sharing my conversation with Jessica Hill. I first learned of Jessica, and her daughter Addy, in September of 2023, when Sick Kids Hospital posted a story about a new initiative called Precision Child Health.

The post featured an enormous crystal ball that was filled with colourful mist. At the unveiling, beside the crystal ball, stood a family who spoke about the young teen who inspired the campaign. That teen was Addison Hill, or Addy, as she is affectionately called.

I watched Jessica’s speech, and I was in awe at how a grieving mother could demonstrate such strength and hope, I needed to know more, so I followed along. I went on to learn about Addy’s experience with childhood cancer, and the work that her family has done since Addy's death to raise awareness for angiosarcoma, and to fulfill Addy’s wish to raise funds for cancer research, specifically for the work of Addy’s oncologist and his team, in order to do more for all the other kids out there with this disease.

Jessica herself is a force. She is tireless, committed, so well-spoken, and approaching this situation with so much grace and compassion. I feel so fortunate to have met her, and it is my great honour to share her story with you here.

You can learn more, and watch the documentary about Addy at https://www.teamaddy.ca/addys-story
https://www.instagram.com/teamaddy8/