Neuroblastoma UK

🚨 Exciting Opportunity: Senior Fundraising Officer at Neuroblastoma UK 🚨 We’re looking for a Senior Fundraising Officer to help us raise vital funds and fight for a cure for neuroblastoma. This is an incredible opportunity to make a real impact at an exciting time for the charity. The Senior Fundraising Officer is responsible for managing our portfolio of events and liaising with our community fundraisers to maximise their fundraising, as well as managing our individual supporters and fundraising admin. If you’re proactive, passionate, and ready to help us take our fundraising to the next level, we’d love to hear from you! 📍 Flexible working arrangements 💼 30 days annual leave 📝 Learn more about the role and how to apply: https://lnkd.in/dD-34JCV #FundraisingJobs #CharityJobs #NeuroblastomaUK #JoinOurTeam #MakeADifference

Mark your calendars for Go Gold Day, a special event dedicated to raising awareness and funds for Neuroblastoma UK. We’re encouraging everyone to participate in gold-themed fundraisers of your choice and help spread the word through turning social media gold. Here are a few ideas on how you can get involved ➡️ 📅 Thursday 26th September 🔗 Sign up to let us know your plans: https://lnkd.in/d58RrWpg

Most parents first hear the word 'neuroblastoma' during their child's diagnosis. Let's raise awareness and help more families recognize the signs early! 🌟 We believe in #AFutureTheyDeserve. Our mission is to fund ground breaking research to develop more effective treatments and, ultimately, find a cure. Help us continue our vital work by making a donation today: https://lnkd.in/dh-WyiNt! #ChildhoodCancerAwarenessMonth #Cancer #Neuroblastoma

Tilly was diagnosed with Stage 4 Neuroblastoma in November 2021 and sadly passed away in September 2022 at the age of four. Tilly’s dad, Jonathan, shares her story here… “The plan was for Tilly to undergo chemo, then surgery and then a stem cell transplant. She went through about 12 rounds of chemo, but her response to the chemo was deemed inadequate, meaning the treatment had failed to have the intended effect on her tumours. This was hard to comprehend. A few extra rounds followed and these seemed to do the trick. By mid-July, she would undergo surgery. Between the end of her treatment and her surgery, we were able to take a family holiday. We agonised over whether this was the right thing to do, but the medical team made sure that we had that time together and that it would not jeopardise Tilly’s health. In hindsight, this was a special experience and an opportunity for us to be together as a family, creating memories. Tilly had a wonderful time. She was able to horse-ride and paddle in the sea. It was a truly positive experience and none of us realised what was just around the corner.” Read Tilly’s full story here: https://lnkd.in/gz_67BSk

📣 📣 Go Gold on September 26th and help us spread awareness and raise funds for Neuroblastoma UK. Go Gold Day is a chance for you to host your own gold-themed fundraising event! You can get creative with gold-themed activities from bake sales to gold dress-up days, all in support of Neuroblastoma UK. Learn more about how to get involved here ➡️https://lnkd.in/d58RrWpg #GoGold #AFutureTheyDeserve #ChildhoodCancerAwarenessMonth #Cancer

Why is #ChildhoodCancerAwarenessMonth important? Here are just a few reasons why continued support and awareness is vital to see more cures and effective treatment for childhood cancers🎗️💛 #AFutureTheyDeserve

"I live in hope that children who are diagnosed in the future are offered better treatment options and better chances of survival, that they won’t suffer like Cara did.” After experiencing a lack of appetite, temperatures, lethargy, sickness and numerous trips to the GP, Cara was diagnosed with neuroblastoma. Despite 19 months of treatment, Cara relapsed three months after completing front-line treatment. She was just three years old when she passed away in February 2020. Four years after Cara’s passing, her mummy Isobel is training for the South East Coast Ultra Challenge in memory of Cara, to raise funds for Neuroblastoma UK. Read Cara’s full story - https://lnkd.in/d3acztYc

🌟 Introducing our 2024 Limited Edition Gold Ribbon! 🌟 Wear our new limited edition pin badge and show your support for children with neuroblastoma and their families this Childhood Cancer Awareness Month. Your purchase can help fund crucial research into neuroblastoma, a rare and aggressive childhood cancer. Get yours now and make a difference! 🎗️💛 👉 https://lnkd.in/eb5Antux #ChildCancerAwareness #GoldRibbon #AFutureTheyDeserve

Every child deserves a future filled with golden moments joy, whether that is learning to ride a bike, experiencing their first day at school, or enjoying sleepovers with friends. 🌟 However, cancer is stealing these precious moments away from too many children. The harsh reality is that every week in the UK, two families receive the devastating news that their child has neuroblastoma. This rare and often aggressive cancer not only claims young lives but also subjects children to gruelling treatments that can affect them well into adulthood. We believe in #AFutureTheyDeserve. To turn this belief into reality, we are dedicated to funding ground breaking research that can lead to more effective treatments. Our mission is clear: we must improve treatment options and ultimately find a cure. Together, we can give these brave children the future they deserve. 🎗️ To learn more about how you can support Neuroblastoma UK this September, from going gold to sharing our message visit: https://lnkd.in/dQccQtG3

📅Mark Your Calendars!📅 Every week, two families in the UK hear the devastating news that their child has neuroblastoma. Join us in bringing awareness to childhood cancers this September.🎗️ To find out how you can get involved visit our website - https://lnkd.in/dQccQtG3