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Solving Kids' Cancer UK

@skc365

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Fighting for a future where no child dies of neuroblastoma.
💙 Supporting families
🔬 Funding research
📣 Driving change for children and families

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When your child has cancer, sometimes you just need someone who gets it.

Each member of our Family Support Team knows what it’s like to care for a child with neuroblastoma. They understand the uncertainty, the questions, and the challenges families can face.

Because no family should face childhood cancer alone.

This Childhood Cancer Awareness Month, we'll be sharing the stories and voices of families, and showing how their experiences have helped shape the support we provide today.

Join us throughout September as we shine a light on the realities of childhood cancer and the power of support.

#ChildhoodCancerAwarenessMonth #CCAM #Neuroblastoma #ChildhoodCancer #FamilySupport by @skc365

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2 months ago

You've lived through something no family should have to face. Now, your experience could help make things better for the next child or young person diagnosed with cancer.

Engage is the new lived experience platform from CCLG and Solving Kids' Cancer UK for parents, survivors and family members affected by childhood and young people's cancer 💛

By joining Engage, you can share your experience in ways that shape research, improve services and influence decisions at every level.

Your voice matters, and it has the power to create real change.

Sign up today using the link in our bio.

💬 What's one thing you wish people understood about cancer in children, teenagers or young adults? Share your thoughts in the comments below. by @skc365

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2 days ago

“Families like ours cannot live a life under the dark cloud of childhood cancer without knowing our child’s experience was not in vain. We feel strongly that good has to come from our experiences. We want to be heard and seen, and to know that we can help make a difference. It gives us hope when, for some of us, hope was taken away by cancer.”- Lisa Radcliffe, mum to George, who was diagnosed with rhabdomyosarcoma aged 3

You’ve lived through something no family should have to face. By sharing your insights, you can help shape a brighter future for children and young people diagnosed with cancer.

Through Engage, you can share your experience in ways that shape research, improve services and influence decisions at every level.

Your voice can help change the future. Sign up today using the link in our bio 🔗 by @skc365

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4 days ago

What a fantastic team! 🎉

We’re so proud of our amazing Royal Parks runners who crossed the finish line yesterday!

Your dedication and hard work have helped raise an incredible £25,760 (and counting) to fund potentially life-saving childhood cancer research and provide vital support for families affected by neuroblastoma. 💛

A huge thank you to each of you and to everyone who supported the team along the way! by @skc365

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4 days ago

A massive GOOD LUCK to all our amazing runners taking on @royalparkshalf tomorrow! 🌟

After months of hard work training and fundraising, it’s finally time to take on this iconic run for an incredible cause – raising crucial funds for ground‑breaking neuroblastoma research and vital support for children and families facing this disease. 💛

We’ll be cheering you on every step of the way. 💪

Keep an eye out for us between miles 6 & 7.

Let’s all show our support and send lots of encouragement to the team – you’ve got this! by @skc365

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6 days ago

Looking for a festive challenge with a difference?

Take the leap for Solving Kids' Cancer UK and experience the thrill of a tandem skydive from 10,000ft.

Pull on a Santa suit or Christmas jumper, tick a bucket-list experience off your list, and raise vital funds to help children with neuroblastoma and their families.

🎄 Jump from 10,000ft
✈️ Reach speeds of up to 125mph
📍 Choose from locations across the UK

This Christmas, don't just spread festive cheer. Take it to 10,000ft.

Sign up using the link in our bio 🔗 by @skc365

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15 days ago

As Childhood Cancer Awareness Month draws to a close, we want to take a moment to say thank you. 💛

This September, we’ve been privileged to share the voices and experiences of children and families affected by neuroblastoma.

Their stories are at the heart of our work, reminding us why it matters to stand alongside families throughout their journey, provide support when they need it and continue working towards kinder and more effective treatments for every child.

Whether you’ve followed and shared our stories, worn your gold ribbon with pride, or supported our work in other ways, thank you.

No family should face childhood cancer alone. 💙

#ChildhoodCancerAwarenessMonth #CCAM by @skc365

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16 days ago

Alfred loved tending his vegetable garden. He dreamed of becoming a farmer one day. But at just four years old, he was diagnosed with high-risk neuroblastoma.

Despite everything that followed, Alfred found joy in playing hide and seek, trips out with his family, and potting plants in his beloved garden. 💛

From the earliest days of Alfred’s diagnosis, our Family Support Team were there to provide practical guidance and emotional support to his family.

When Alfred relapsed in early 2025, we were there to support his family through the emotional weight of that news and the difficult decisions that followed.

Devastatingly, Alfred passed away in August 2025. But our support didn't stop. We stood beside his family through their grief, helping them navigate the unimaginable pain of losing their little boy.

Our support doesn’t end when a family’s world falls apart. That’s often when it matters most.

This Childhood Cancer Awareness Month, your donation could help us be there for another family when they need us most (🔗tap our bio link).

#ChildhoodCancerAwarenessMonth #CCAM by @skc365

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17 days ago

When Beatrice was diagnosed with low-risk neuroblastoma at just 10 months old, her family suddenly found themselves navigating a new and uncertain world.

Soon after, they contacted Solving Kids’ Cancer UK and found a community of people who understood what they were going through.

From meeting other families at our Neuroblastoma Parent Symposium to staying connected with our Family Support Team and joining us at our Family Fun Day, that support has continued throughout their journey.

As Beatrice’s parents told us:

“Connecting with the other families in similar situations to us definitely gave us a sense of belonging in this nasty neuroblastoma world.”

Now two and a half, Beatrice has scans every three months, and her most recent results showed that her neuroblastoma remains stable.

For Beatrice’s family, and families like hers, having someone there who understands can make a real difference.

If you’d like information and support for families affected by low-risk neuroblastoma, visit the link in our bio.

#ChildhoodCancerAwarenessMonth #CCAM by @skc365

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18 days ago

When a child is diagnosed with neuroblastoma, life can change in an instant.

Last year, our Family Support Team provided ongoing one-to-one support to 230 families affected by neuroblastoma.

Every member of our Family Support Team has experience of caring for a child with neuroblastoma, so they understand the realities families are facing.

From treatment information and practical help to emotional support and simply having someone to turn to, we're here throughout the journey.

This Childhood Cancer Awareness Month, we're shining a light on the support families need.

No family should face childhood cancer alone. 💙

#ChildhoodCancerAwarenessMonth #CCAM #Neuroblastoma #ChildhoodCancer #FamilySupport by @skc365

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19 days ago

This month is Childhood Cancer Awareness Month. Here at Boogie Beat we have been helping children to feel less alone.

Imagine being a child and having to spend time in hospital or isolate at home before starting cancer treatment.

Days can feel long. You may miss your friends, your school, your usual activities and simply being able to play and have fun.

That’s why we’re incredibly proud to have created a special 𝗕𝗼𝗼𝗴𝗶𝗲 𝗕𝗲𝗮𝘁 𝗠𝘂𝘀𝗶𝗰 & 𝗠𝗼𝘃𝗲𝗺𝗲𝗻𝘁 𝘃𝗶𝗱𝗲𝗼 𝗳𝗼𝗿 𝗰𝗵𝗶𝗹𝗱𝗿𝗲𝗻 𝘀𝘂𝗽𝗽𝗼𝗿𝘁𝗲𝗱 𝗯𝘆 𝗦𝗼𝗹𝘃𝗶𝗻𝗴 𝗞𝗶𝗱𝘀’ 𝗖𝗮𝗻𝗰𝗲𝗿 𝗨𝗞. 🎶

Our video gives children the opportunity to join in with music, movement and imagination - wherever they are.

Because sometimes, something as simple as a song, a story and a chance to dance can bring a little bit of joy to a difficult day. 💛

We’re also fundraising to support the amazing work of Solving Kids’ Cancer UK.

𝗜𝗳 𝘆𝗼𝘂 𝗰𝗮𝗻, 𝗽𝗹𝗲𝗮𝘀𝗲 𝗵𝗲𝗹𝗽 𝘂𝘀 𝗺𝗮𝗸𝗲 𝗮 𝗱𝗶𝗳𝗳𝗲𝗿𝗲𝗻𝗰𝗲 𝗽𝗹𝗲𝗮𝘀𝗲 𝗗𝗼𝗻𝗮𝘁𝗲 £𝟮 𝗼𝗿 £𝟱
👉 Donate here: https://www.justgiving.com/page/boogie-beat-music-and-movement-ltd-3?utm_medium=FA&utm_source=CL

𝗘𝘃𝗲𝗿𝘆 𝗱𝗼𝗻𝗮𝘁𝗶𝗼𝗻, 𝗯𝗶𝗴 𝗼𝗿 𝘀𝗺𝗮𝗹𝗹, 𝗵𝗲𝗹𝗽𝘀. 💛

#BoogieBeat #SolvingKidsCancerUK #ChildhoodCancer #MusicAndMovement #MakingADifference #Fundraising #KidsCancer by @skc365

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21 days ago

On Wednesday, we were honoured to stand alongside colleagues from @josephssmileuk, @latchwales and @younglivesvscancer at the Kids Get Cancer Too Senedd reception, raising awareness of the impact childhood cancer has on families across Wales.

We highlighted the vital importance of research and why the upcoming Cancer Strategy for Wales must include dedicated commitments for children and young people.

This means investing in research and innovation, recognising that childhood and young people’s cancers are unique, and ensuring families across Wales have fair access to the latest opportunities in care and treatment.

Every child and young person with cancer deserves to benefit from progress in research and innovation – wherever they live in Wales. 💛 by @skc365

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