Has your child been affected by neuroblastoma? Call 020 7284 0800 for help and information.

Latest News

Press Announcement of CEO Appointment

A new Chief Executive is to head the childhood cancer charity, Solving Kids’ Cancer (Europe), based in the UK. Having spent the last seventeen years working for Macmillan Cancer Support, Stephen Richards has extensive experience in the field and will focus on driving the charity’s aims of supporting children and families affected by childhood cancer

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Thank you Anya for being my inspiration

“On the 9th Sept 2012 I completed my 4th half marathon  and planned to try a full marathon the following year. Less than 6 weeks later my family had all of our plans and dreams destroyed as we were told our baby girl – our precious 17mth old bundle of joy Anya – was being

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Thank you to our Volunteers

This year, National Volunteer Week (NVW) runs from 1st-12th June. For Solving Kids’ Cancer, NVW means celebrating our volunteers and highlighting the crucial role that they play in supporting our work to help children and families. Solving Kids’ Cancer works with some truly amazing volunteers. They dedicate their free time, around busy schedules, to share

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Jack Brown – a remarkable little boy with a remarkable legacy

It’s been 7 years since beautiful Jack passed. Jack was diagnosed with neuroblastoma in 2005 when he was aged 3 years old. The neuroblastoma landscape was quite different back then, particularly for children who relapsed, like Jack did. His Mum and Dad, Richard and Yvonne, were devoted to researching and learning the science behind the

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Vanessa accesses a pioneering vaccine trial in New York

With the help of Solving Kids’ Cancer and the oncologists at Great Ormond Street Hospital Vanessa Moss is now in New York receiving a pioneering vaccine that hopes to prevent her cancer from returning. This is part of a clinical trial being conducted at Memorial Sloan Kettering Cancer Centre and will see Vanessa receive 7

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New genetic testing for children with neuroblastoma

Scientists at the Institute of Cancer Research and Royal Marsden Hospital have developed a new genetic test that will be given to children with solid tumours in an effort to analyse genetic changes in 81 cancer genes, with funding from Christopher Smile. This is the first stage of an initiative to bring these tests to

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Blindfolded fundraising run

The family of 7-year-old Oliver from Minster-on-Sea is doing a blindfolded fundraising run to honour Oliver’s bravery and highlight his daily struggle with blindness since he lost his sight fighting cancer. Oliver was diagnosed with neuroblastoma before his 1st birthday and has been fighting the disease ever since. Side effects from his treatment have also meant

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We’re planning the Neuroblastoma Parent Education Conference 2016

Planning is well underway for our 5th annual Neuroblastoma Parent Education Conference.  This event is focused entirely on supporting families affected by neuroblastoma to grow their knowledge and understanding of the disease, and the treatment options and clinical trials which may be available for their child now and in the future.  The conference brings a range

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We provided support to families affected by neuroblastoma

Our Family Coordinator Vicky is a dedicated resource, and the main point of contact within our organisation, for families affected by neuroblastoma. She works closely with other members of our Care and Connect team, each of which is passionate about supporting families throughout their journeys. Whether it’s an issue, concern, difficulty or question related to: neuroblastoma

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Vitality British 10k London Run

Twenty-six runners have already secured their charity places for this world’s greatest road race route for Solving Kids’ Cancer. On 10th July runners will take to London’s stage for our biggest third-party event. You can be part of this special event for £25 with a pledge to raise £200. For more information visit the 10k

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Solving Kids' Cancer

Tel: 020 7284 0800

CAN Mezzanine
49-51 East Road
London
N1 6AH

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