Solving Kids' Cancer
Solving Kids' Cancer
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Solving Kids' Cancer UK Christmas Concert 2024
In December 2024, we packed out Holy Trinity Church in Sloane Square, London for an unforgettable evening of hope and celebration.
We were treated to incredible performances by Ella Henderson, London Show Choir and Louis Moorhouse. We also presented our very special Hero Awards to those in the community who made a real difference in 2024.
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Solving Kids’ Cancer UK is fighting for a future where no child dies of the childhood cancer neuroblastoma or suffers due to its treatment.
About Neuroblastoma:
Solving Kids’ Cancer works to support children with the aggressive childhood cancer neuroblastoma and their families.
Neuroblastoma is an aggressive and rare childhood cancer that affects around 100 children in the UK each year. Most children are diagnosed below the age of five and treatment can be intensive and gruelling, including chemotherapy, surgery, radiotherapy and immunotherapy. Sadly, neuroblastoma has a high rate of relapse, meaning that even after successful treatment, the cancer can come back. If it does, survival rate drops to a devastating 1 in 10.
Solving Kids’ Cancer is fighting for a future where no child dies of neuroblastoma or suffers due to its treatment.
They offer family support, to be there for families of children affected by neuroblastoma throughout their cancer journey. They also provide access to treatment, offering impartial information to help families navigate the complex medical landscape and choose treatment options for their child. They fund innovative clinical research bringing kinder and more effective treatment options to the UK for children fighting neuroblastoma now, and in the future.
COVID- 19 presents more challenges than ever to children with neuroblastoma and their families. Children in frontline cancer treatment or who have recently finished their treatment are at their most vulnerable and are going to have to self-isolate for 12 weeks or longer. Parents isolating with their children may have to sacrifice their jobs or stop working all together. In this time of unprecedented uncertainty, Solving Kids’ Cancer is dedicated to supporting families throughout their cancer journey to overcome any challenges that may arise and as such would like to offer all families of children with low, medium or high risk neuroblastoma the opportunity to access emergency hardship relief funds.
To find out more visit www.solvingkidscancer.org.uk
มุมมอง: 13

วีดีโอ

Natalie Cassidy - BBC Radio 4 Appeal
มุมมอง 654 หลายเดือนก่อน
We are delighted to share that actress Natalie Cassidy will be presenting our BBC Radio 4 Appeal in September 2024 to raise vital funds for our work in supporting children and families affected by neuroblastoma. You can listen live to our appeal on Sunday 15 September at 07:54 and 21:25 and again on Thursday 19 September at 15:27. Please spread the word and encourage others to listen in, share,...
Join our #CrochetForKidsCancer challenge
มุมมอง 2425 หลายเดือนก่อน
Join the #CrochetForKidsCancer challenge with Kellie Bright, Patron of Solving Kids' Cancer UK! Kellie is spearheading this campaign to raise crucial awareness and funds for the charity. Get involved by crocheting a 'granny square' - each one will be transformed into a beautiful blanket by Kellie, featuring a special square made by a celebrity. Solving Kids’ Cancer is fighting for a future wher...
Kids Get Cancer Too Campaign Film
มุมมอง 2647 หลายเดือนก่อน
Solving Kids’ Cancer is fighting for a future where no child dies of the childhood cancer neuroblastoma or suffers due to its treatment. Text SKCFestival to 70085 to donate £5 About Neuroblastoma: Solving Kids’ Cancer works to support children with the aggressive childhood cancer neuroblastoma and their families. Neuroblastoma is an aggressive and rare childhood cancer that affects around 100 c...
Solving Kids' Cancer UK Brand Film (2024 version)
มุมมอง 3209 หลายเดือนก่อน
Watch our brand-new charity film showcasing the work that we do for those affected by childhood cancer. You'll hear from some of the amazing families that we have supported over the years as well as powerful words from staff and trustees, some of whom have lived experience of neuroblastoma. It is thanks to Solving Kids’ Cancer UK Patron, Carl Cavers, and the incredible Sumo team that we have su...
Neuroblastoma post-treatment coaching - feedback
มุมมอง 3710 หลายเดือนก่อน
Helen gives her thoughts and feedback after she participated in the pilot phase of the post-treatment coaching programme launched by Solving Kids' Cancer UK in partnership with Life After Cancer, specifically with oncology parents like Helen in mind. Solving Kids' Cancer UK is passionate about the importance of ongoing support post-treatment and is proud to begin planning for this. It is active...
Solving Kids' Cancer Christmas Carol Concert 2023 (Highlights)
มุมมอง 47711 หลายเดือนก่อน
This event is an evening of hope and celebration, and always a night to remember. In December 2023, we packed out Holy Trinity Church in Sloane Square, London, and over £25,000 was raised for children and their families affected by neuroblastoma. We had a brilliant of performers, including the renowned London Show Choir, the incredible Louis Moorhouse, the cast and crew of EastEnders, as well a...
Louis Moorhouse and Sirine Jahangir - River (Solving Kids' Cancer UK Christmas Carol Concert 2023)
มุมมอง 1K11 หลายเดือนก่อน
Louis Moorhouse and Sirine Jahangir perform River (Joni Mitchell cover) at the Solving Kids' Cancer UK Christmas Carol Concert at Sloane Square Church, London, in December 2023. Louis was diagnosed with stage 4 neuroblastoma when he was 18 months old. He had a primary tumour on his adrenal gland and another tumour in his nasal cavity. The tumour in his nasal cavity crushed his optic nerve leavi...
Introducing Ruben Hage, Solving Kids' Cancer's newest partner
มุมมอง 60ปีที่แล้ว
Find out more about Solving Kids' Cancer UK's newest partner as he takes you behind the scenes on race weekend. Solving Kids’ Cancer is fighting for a future where no child dies of the childhood cancer neuroblastoma or suffers due to its treatment. Text SKCFestival to 70085 to donate £5 About Neuroblastoma: Solving Kids’ Cancer works to support children with the aggressive childhood cancer neur...
Luke's Legacy (2023 version)
มุมมอง 108ปีที่แล้ว
The Big Love Fund has been inspired by Luke Wiltshire. Luke was diagnosed with neuroblastoma when he was 14 years old. He sadly passed away in 2021 at the age of 23. Luke would have given everything to ensure others were okay, which is what inspired this fund to do just that. The Big Love Fund has been created to help us reach and provide support, via a grant, to families of children and young ...
Children's message of hope
มุมมอง 1.4Kปีที่แล้ว
Hear from Charlie, Reuben, Eva, Isla and Anya; incredibly brave children who have been supported by Solving Kids' Cancer UK throughout their journey with neuroblastoma. They explain what life has been like since their neuroblastoma diagnosis and how Solving Kids' Cancer UK have helped them. Special thanks to the brilliant Sumo team for all their help in producing this film. Solving Kids’ Cancer...
Solving Kids' Cancer Care & Connect Support Bags
มุมมอง 1552 ปีที่แล้ว
We are delighted to launch our Solving Kids’ Cancer UK Care & Connect Family Support Bags. These support bags have been carefully created, with help from the neuroblastoma parent community, to ensure they contain just the right items for children and their families to support them during hospital visits, and connect them to other families and to our Family Support Team. The support bags are for...
Luke's Legacy
มุมมอง 8K2 ปีที่แล้ว
We are privileged to launch the BIG LOVE FUND, inspired by the story of Luke Wiltshire, on what would have been Luke’s 24th birthday. Solving Kids’ Cancer UK has launched this new fund to help support more children and young people like Luke. The Big Love Fund has been created to help us reach and provide support, via a grant, to families of children and young people affected by neuroblastoma. ...
Butterfly Relay 2021 - Georgina and Andy's 5k a day in May
มุมมอง 303 ปีที่แล้ว
Solving Kids’ Cancer is fighting for a future where no child dies of the childhood cancer neuroblastoma or suffers due to its treatment. Text SKCFestival to 70085 to donate £5 About Neuroblastoma: Solving Kids’ Cancer works to support children with the aggressive childhood cancer neuroblastoma and their families. Neuroblastoma is an aggressive and rare childhood cancer that affects around 100 c...
SIOPEN High-Risk Neuroblastoma 2 Trial- Q&A with Dr Emma Pond
มุมมอง 1113 ปีที่แล้ว
SIOPEN High-Risk Neuroblastoma 2 Trial- Q&A with Dr Emma Pond
Solving Kids' Cancer Patron Rob Brydon announces the Butterfly Relay
มุมมอง 603 ปีที่แล้ว
Solving Kids' Cancer Patron Rob Brydon announces the Butterfly Relay
SKC International Neuroblastoma Research Initiative 2019- Q&A with Leona Knox and Emily Hall
มุมมอง 753 ปีที่แล้ว
SKC International Neuroblastoma Research Initiative 2019- Q&A with Leona Knox and Emily Hall
Solving Kids' Cancer ButterflyRelay
มุมมอง 183 ปีที่แล้ว
Solving Kids' Cancer ButterflyRelay
Solving Kids' Cancer Thank You 2020
มุมมอง 1974 ปีที่แล้ว
Solving Kids' Cancer Thank You 2020
Solving Kids' Cancer Christmas Raffle Prizes
มุมมอง 704 ปีที่แล้ว
Solving Kids' Cancer Christmas Raffle Prizes
Rob Brydon, SKC Patron
มุมมอง 1114 ปีที่แล้ว
Rob Brydon, SKC Patron
Solving Kids' Cancer Butterfly Relay 2020
มุมมอง 2094 ปีที่แล้ว
Solving Kids' Cancer Butterfly Relay 2020
Solving Kids' Cancer Neuroblastoma Parent Education Conference 2018
มุมมอง 2495 ปีที่แล้ว
Solving Kids' Cancer Neuroblastoma Parent Education Conference 2018
About Solving Kids' Cancer
มุมมอง 3255 ปีที่แล้ว
About Solving Kids' Cancer
Q & A - Prof. Andy Pearson
มุมมอง 916 ปีที่แล้ว
Q & A - Prof. Andy Pearson
Role of Surgical Intervention - Biopsy and Resection, Mr Hany Gabra
มุมมอง 1506 ปีที่แล้ว
Role of Surgical Intervention - Biopsy and Resection, Mr Hany Gabra
Updates from St. Jude incl. Chemoimmunotherapy, Dr. Wayne Furman
มุมมอง 1136 ปีที่แล้ว
Updates from St. Jude incl. Chemoimmunotherapy, Dr. Wayne Furman
Hu3F8, Vaccines, and hu3F8-Bispecific Antibodies, Dr. Nai-Kong Cheung
มุมมอง 8716 ปีที่แล้ว
Hu3F8, Vaccines, and hu3F8-Bispecific Antibodies, Dr. Nai-Kong Cheung
COG and NANT studies incl. Chemoimmunotherapy, Dr. Rajen Mody
มุมมอง 836 ปีที่แล้ว
COG and NANT studies incl. Chemoimmunotherapy, Dr. Rajen Mody

ความคิดเห็น

  • @LouisMoorhouseMusic
    @LouisMoorhouseMusic 8 วันที่ผ่านมา

    Was an absolute joy to be a part of this event, my second SKC Carol Concert. Thank you SKC for all the amazing work that you do.

  • @ShinyMew151
    @ShinyMew151 3 หลายเดือนก่อน

    Marvel Midnight Suns! That's how I found out about Luke's story! RIP man!😢

  • @SARAHSMITH-bg1rx
    @SARAHSMITH-bg1rx 4 หลายเดือนก่อน

    Yes yes I have squares where do I send

  • @toffeefawn5177
    @toffeefawn5177 5 หลายเดือนก่อน

    i will be joining!! i have so much spare wool laying around i can’t wait to get started and use it for a good cause 😊

  • @wendeeklein262
    @wendeeklein262 7 หลายเดือนก่อน

    Does transplant mean bone marrow transplant?

  • @dark__said
    @dark__said 2 ปีที่แล้ว

    Примите мои соболезнования! Все геймеры мира с Вами! 🤧

  • @epicworldradiotv
    @epicworldradiotv 2 ปีที่แล้ว

    Now Luke live in the paradise with Jesús,Amen..

  • @mickeymouse7726
    @mickeymouse7726 2 ปีที่แล้ว

    Nice

  • @michaelrevi7033
    @michaelrevi7033 2 ปีที่แล้ว

    Truly a champion he is, indeed. Thank you all, honestly, who made this possible

  • @POTIS1
    @POTIS1 2 ปีที่แล้ว

    RIP LUKE FROM GREECE...LIFE IS UNFAIR...:(

  • @commandernomad2817
    @commandernomad2817 2 ปีที่แล้ว

    2:20 you couldn't search the name on google to learn a little bit about it so you could have made your search a little easier? i mean you said you had no idea where to start, but the first thing i would have done is copy the name of the games he made his final wish to play into a search bar to find someone close to the project to get in touch with. Anyways, still an amazing story. Not many here will be familiar with games development so when i say those devs basically moved mountains to fulfill Luke's request I'm not exaggerating. Getting a build ready from scratch into a playable state that early and that quickly is insane, truly insane and impressive, and really shows the commitment by the team to do right by Luke.

  • @shawnkenneth5503
    @shawnkenneth5503 2 ปีที่แล้ว

    I know it doesn't change anything but I am sorry for your loss. He seemed wonderful.

  • @KerberosRS
    @KerberosRS 2 ปีที่แล้ว

    the MARVEL of being there, RIP Luke

  • @Ancient_Reboot
    @Ancient_Reboot 2 ปีที่แล้ว

    Stuff like this makes me always feel sad and happy. sad that uncureable diseases will take the Loved ones. Happy because there were people kind enough to give them their all to make one person happy even If the story do not have an happy end. Rest in peace my guy and to his family my condolences.i know how hard it is to see His Loved ones dying to an incureable disease

  • @dogsoldier123
    @dogsoldier123 2 ปีที่แล้ว

    Rest in peace Luke

  • @Sangor
    @Sangor 2 ปีที่แล้ว

    Rest in peace Luke.

  • @connorg189
    @connorg189 2 ปีที่แล้ว

    Soo beautiful, rest in peace you incredible ladd 👌🏻❤️

  • @tomhennessy7276
    @tomhennessy7276 6 ปีที่แล้ว

    "iron chelation in human neuroblastoma"

  • @steveynixon4995
    @steveynixon4995 6 ปีที่แล้ว

    Hello Dr handgretinger.if you read this or anyone does.this tenuous man did an ok that was controversially stopped and declared illegal in 2006 for my daughter who was only 6 months old when she contracted the horrible AML LEUKAEMIA ..An adult form very rare for her to get this.well I live in UK where his method was illegal AND STILL IS 12 YEARS LATER IN THE UK...!!!!! This tenuous of a man got my daughter into remission after 10days of landing in Germany.we never got her down past 28% blast cells in the royal Victoria hospital children's unit in Belfast northern Ireland. UK. This man did this exact I'm for my daughter using harvested stem cells from myself(HER FATHER)/.When we looked at his teqnique he used on baby Ava we couldnt believe the amount of drugs,work ,care,research and observation he used,he was so hands on himself. Well it's 2018 my daughter just had her 13 birthday and she's been on no medication since we left the hospitals in 2008.she never got graph vs host nor did she relapse.this man is my hero.i love you brother.i was only 23 bk then I'm now almost 36 and if I caused you any problems when I was young and stupid I'm very sorry to have gotten so stressed out on an occasion I remember and now mature your my all time hero Fiona her mum and Ava herself.she can weirdly recall a lot of events from that..haha 1 of them is she remembers that twojiiiìù

  • @MichaelWilliams-pr5pz
    @MichaelWilliams-pr5pz 10 ปีที่แล้ว

    Truly inspiring!!

  • @andrewwilliams9577
    @andrewwilliams9577 10 ปีที่แล้ว

    I want to be a nb hero

  • @andrewwilliams9577
    @andrewwilliams9577 10 ปีที่แล้ว

    brilliant. . I love the secret recipe. im doing cycling santa this year can't wait can you grt in contact with me arw301087@hotmail.co.uk