“Our founders, Nic and Jen, were both mothers of young children living with secondary breast cancer.
They met at a cancer event and quickly bonded over the shared challenge of how to talk to their children about their diagnosis, how much to say, and in what way. They agreed that secrecy could only lead to confusion and sadness in young, curious minds, and that openness, in an age-appropriate, guided way, was best. Drawing on their professional backgrounds, Jen as a teacher and Nic as a nurse, they created a set of A–Z flashcards covering cancer and healthcare topics, each with activities and discussion points designed for primary-aged children.
The cards were immediately welcomed by families and professionals alike. For the rest of their lives, Nic and Jen devoted themselves to developing more resources and reaching as many people as possible.
Jen passed away in 2022, and Nic in 2023. After their loss, a small group of family and friends gathered to reflect on their legacy and the future of The Little C Club. We have committed to pursuing charitable status, so their work, born from friendship, courage, and love, continues to ease this painful challenge for families everywhere.”
“To support adults who face the difficult and heart-breaking task of talking with young children about cancer and its impact.”
“We are currently working towards charitable status so we can expand our reach and make our resources more widely available.
Our cards are already used by some NHS trusts, and we regularly donate to charities and organisations who support families.
The flashcards can also be purchased through our website at www.littlecclub.com, and you can contact us directly at hello@littlecclub.com.
This is an exciting time of growth for us, and while change is underway, our focus remains the same: supporting families and easing the burden on young minds.”
A big thank you to The Little C Club for their inspiring work and taking the time to share more about how they support people affected by cancer.
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