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

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Pioneering children’s cancer research role to speed up crucial clinical trials

We’re delighted to let you know about our funding of a ground-breaking role to enable more children with neuroblastoma to access potentially life-saving clinical trials more quickly. In the first dedicated position focusing on a single childhood cancer, Dr Emmanouela Gbandi was appointed as the Solving Kids’ Cancer Senior Trials Coordinator for Neuroblastoma at the

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Anti-GD2 Antibody Therapy Update, May 2018

Following the recent provisional decision by the National Institute for Health and Care Excellence (NICE) not to approve dinutuximab beta (Qarziba™) for use on the NHS in England and Wales, we have updated our briefing document. This was produced by Nick Bird (Parent, Research and Advocacy Trustee and member of the National Cancer Research Institute

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Urgent appeal for Kira Noble smashes target!

Thanks to enormous public generosity and huge fundraising efforts, as of today (8th May) more than £370,000 has been raised for 14-year-old Kira Noble’s life-saving cancer treatment in New York. Kira has been fighting neuroblastoma since she was just 11, and has endured years of gruelling treatment to try to get rid of her disease.

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Joint statement in response to NICE’s preliminary decision on Anti-GD2 antibody therapy dinutuximab beta for NHS clinical use.

From Solving Kids’ Cancer, Neuroblastoma UK, the Children’s Cancer and Leukaemia group, JACK, The Bradley Lowery Foundation, Hugs from Henry, Christopher’s Smile, Niamh’s Next Steps and Smile with Siddy. Charities and Clinicians that support children with high-risk neuroblastoma and their families have joined together in response to the decision not to recommend a life-saving drug

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Urgent appeal launched to help Kira Noble

Help us raise £340,000 by 10th May for 14-year-old Kira Noble’s life-saving cancer treatment in New York. Kira has been fighting neuroblastoma since she was just 11, and has endured years of gruelling treatment to try to get rid of her disease. Sadly, despite best medical efforts it was not possible to remove a growing

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Generosity of an anonymous donor benefits children with cancer

Thanks to an anonymous and generous donor, children’s cancer charities including Solving Kids’ Cancer have benefited from the sale of a valuable sculpture. Called ‘The Boy with the Dolphin’ by David Wynne it was auctioned recently at Christie’s for an amazing £80,000! The money will be split between our charity and other great causes Abbie’s

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Solving Kids’ Cancer wins charity of the month poll

Exciting news! We are delighted to announce that we won the My Favourite Voucher Codes March charity of the month poll. We’d like to say a HUGE thank you to everyone who kindly voted for us.  Your support will help us continue making a difference for children with neuroblastoma and their families, through funding ground-breaking

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Anti-GD2 Antibody Therapy Update, March 2018

A NICE committee hearing will be held on 11th April to discuss whether or not to recommend dinutuximab beta antibody therapy for NHS use. An application has been received from pharmaceutical company EUSA Pharma (who hold the European and UK licence). As we know, dinutuximab beta is an essential treatment that offers hope in the

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New partnership to help families travelling abroad for treatment

Many families travel abroad so that their child can have treatment to help them fight neuroblastoma. Visiting another country can seem overwhelming, so we help families prepare for this – from liaising with medical professionals to arranging flight tickets and accommodation. We’re delighted to let you know that we’re now working with the St George’s

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Urgent! New law means we need your consent to stay in touch

Say Yes to keep in touch here We know you care about our work for children and families affected by neuroblastoma. But when a new law comes into place on 25th May 2018, we won’t be able to keep in contact with you by email or telephone unless you’ve told us that it’s OK. Even

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