Skip over main navigation
  • Log in
  • Basket: (0 items)
Solving Kids' Cancer
  • Twitter
  • Facebook
  • Instagram
  • LinkedIn
Shop Contact us Donate
Menu
  • About Neuroblastoma
    • About Neuroblastoma Home
    • What is neuroblastoma?
    • Symptoms
    • Diagnosis
    • Risk Groups and Staging
    • Clinical Trials
    • Treatment for Neuroblastoma
  • Find Support
    • Family support
    • The Big Love Fund
    • Access treatment
    • Neuroblastoma Parent Education Conference
      • Neuroblastoma Parent Global Symposium 2021
      • See past conferences
    • Other sources of help
  • Research
    • Our research
    • Scientific Advisory Board
    • Research Funding
      • Funding award process
      • Grant Award Calls
    • Projects
    • Funding partners
    • Research policies
    • Research blog
  • Get Involved
    • Help Us Today
    • Support The Big Love Fund
    • Shop
    • Ambassador Programme
    • Corporate partnerships
    • Challenge events
    • Set up a fundraising page
    • Gaming
    • Fundraising resources
  • Children’s stories
    • Stories
    • Children’s campaigns
    • In memory
    • Named funds
  • About us
    • What we do
    • Meet the team
      • Trustees
      • Our team
    • Patrons
    • Parent Involvement Forum
    • Join our Team
    • Annual reports
  • News
    • News
    • Blogs
  • Admin
    • Log in
  • Basket: (0 items)
  • The Big Love Fund
  1. Find Support

The Big Love Fund

The Big Love Fund is here to support you - the fund has been created for families across the UK and Ireland to support a child or young person's physical or emotional welfare (up to £250 per year) and to support families in bereavement with funeral and associated costs (up to £500). 

To apply for the fund, follow this link The Big Love Fund Application Form

About the Fund 

This special fund has been inspired by Luke Wiltshire's story. Luke was diagnosed with neuroblastoma when he was 14 years old, in 2021 Luke and his family received the devastating news that there were no more curative options for him. Having faced years of aggressive and toxic cancer treatment, Luke found solace and comfort in the world of Marvel and gaming and had a special wish to play the, not yet released game, Marvel’s Midnight Suns from 2K and Firaxis Games. 

His wish to play this game sparked a remarkable series of events and a groundswell of support across social media from the gaming community, which resulted in Luke’s wish coming true.  Incredibly, 2K – the game’s publisher –reached out to Solving Kids’ Cancer UK and a member of the 2k team visited Luke with a special in-development version of the game, making Luke among the first few people in the world to have the chance to play. He is now forever immortalised in the game with a special tribute – his name engraved on a tree within the game.  

Luke’s sister, Claire, said of the fund, “Luke was someone so special – I can’t wait for the fund to be launched so that other children and young people can be helped like he was. He would have given everything to ensure others were okay. His journey is our inspiration and his legacy will live on – he will be recognised just how he wanted to be.” 

Luke sadly passed away in 2021 at the age of 23. The Big Love Fund has been inspired by his legacy to help us reach and provide support, via a grant, to more families of children and young people affected by neuroblastoma and help their physical and emotional welfare. The fund is available to families across the UK and Ireland. 

To find out more about the fund please contact us [email protected]

Published: 28th April, 2022

Updated: 10th June, 2022

Author: Anne Denman

Share this page
  • Email
  • Facebook
  • Twitter

Latest

  • Cross-party MPs back calls for a UK-led vaccine trial to help children with cancer

    Cross-party MPs back calls for a UK-led vaccine trial to help children with cancer

  • Cycle SWFC to MK Dons

    Cycle SWFC to MK Dons

    Jude’s dad, Arron, made his SWFC debut in a win against MK Dons. So it feels very fitting that this should be the match of choice for a cycling challenge - the team will begin at SWFC ground and finish at MK Dons stadium.

  • Kathryn's RSR for Jude

    Kathryn's RSR for Jude

    To help Jude's family reach their fundraising target.

  • St Mary Magdalene - Y5 and Y6 Ticket Sales

    St Mary Magdalene - Y5 and Y6 Ticket Sales

Most read

  • Beau's Campaign

    Beau's Campaign

    Beau was diagnosed with high-risk neuroblastoma, an aggressive childhood cancer that has a 40-50% chance of long-term survival at diagnosis, in December 2020. Her family are appealing for your help to raise £317,000 by May 2022.

  • Flora's Campaign

    Flora's Campaign

    In January 2021 Flora was diagnosed with Autism Spectrum Disorder, and just three months later her parents were given the devastating news she had high-risk neuroblastoma. Her family are appealing for your help to raise £252,000 by August 2022 for Flora to enrol on the Bivalent Vaccine clinical trial in New York that aims to stop her neuroblastoma from coming back.

  • Joseph Yeandle

    Joseph Yeandle

    We are devastated to share the news that beautiful Joseph has sadly passed away.

  • Jude's Campaign

    Jude's Campaign

    Jude is a Dinosaur and animal-loving three-year-old. In July 2021 Jude was diagnosed with high-risk neuroblastoma, a rare and aggressive childhood cancer that has a 40-50% chance of long-term survival at diagnosis.

  • Maysaa's Campaign

    Maysaa's Campaign

    Four-year-old Maysaa was diagnosed with high-risk neuroblastoma, an aggressive childhood cancer that has a 40-50% chance of long-term survival at diagnosis, in March 2021. Her family are asking for your support to raise £106,000 by August 2022 for Maysaa to enrol on the DFMO study in Charlotte that aims to stop her neuroblastoma from coming back.

  • Chloe’s Journey

    Chloe’s Journey

    Beautiful Chloe passed away on the 4th of February 2022.

  • Eden's Campaign

    Eden's Campaign

    Six-year-old Eden was diagnosed with high-risk neuroblastoma, an aggressive childhood cancer that has a 40-50% chance of long-term survival at diagnosis, in April 2021.

  • Kayla's Campaign

    Kayla's Campaign

    Three-year-old Kayla was diagnosed with high-risk neuroblastoma in May 2021. Kayla’s parents are asking for your help to raise £221,000 by November 2022 for Kayla to enrol on the bivalent vaccine clinical trial in New York that aims to stop her neuroblastoma from coming back.

  • Peter's Campaign

    Peter's Campaign

    11-year-old Peter was diagnosed with neuroblastoma in early 2019. Devastatingly he relapsed in August 2020 after being clear of disease for 6 months. Thanks to your incredible fundraising and support, Peter was able to enrol on the DFMO study in Charlotte at the end of January 2022.

  • Dulcie's Campaign

    Dulcie's Campaign

    In December 2021, five-year-old Dulcie was diagnosed with high-risk neuroblastoma, a rare and aggressive childhood cancer that has a 40-50% chance of long-term survival at diagnosis.

Sign up for our newsletter

Please enter your first name
Please enter your last name
Please enter your email address Please enter a valid email address (e.g. [email protected])

Contact us

Solving Kids' Cancer UK
Coram Campus
41 Brunswick Square
London
WC1N 1AZ

Phone: 020 7284 0800

Follow us

  • Twitter
  • Facebook
  • Instagram
  • LinkedIn

  • Jobs
  • Media enquiries
  • Sitemap
  • Accessibility
  • Terms & Conditions
  • Safeguarding Statement
  • Privacy Policy

Solving Kids’ Cancer UK is a registered charity in England and Wales (1135601), and in Scotland (SCO45094). It is a company limited by guarantee in England and Wales (7208648). The charity and company is currently operating as Solving Kids’ Cancer.