Kayla’s Neuroblastoma Journey

Urgent Appeal!!! Our beautiful 4year old Granddaughter has been diagnosed with stage 4 high risk neuroblastoma. We have to raise £221,000 by November to get her further treatment in New York America. Kayla is a typical 4year old and absolutely loves Minnie Mouse, and all things pink! She still smiles and it’s a beautiful one 💗and she takes the treatment as it comes, shes so brave, and she certainly teaches us adults a thing or two! Our family have been totally devastated by this diagnosis so have teamed up with Solving Kids Cancer to raise these funds. Neuroblastoma is the most aggressive form of childhood cancer. In almost 50% of children with this the cancer returns and if it does the chances of survival drops to only 10%. By sending her to America to get her the Bivalent Vaccine which is not available here in the Uk, her chances of the the neuroblastoma not returning increase to 91%. Given the urgent nature of this fundraising and the short time frame to raise these funds, we as a family would be very grateful for you support. We have to give Kayla every chance we can for long term survival. We are doing lots of fundraising events, fetes, bucket collections, concerts, sponsored events all the time and if anybody would like to do a fundraiser for Kayla and her campaign then please do, we will be more than grateful for your help and support. You can read more about Kayla and her journey at https://solvingkidscancer.org.uk/appe... You can donate on that page as well or you can text by sending the word KAYLA followed by any whole amount ( up to £20 ) to 70085. For example texting KAYLA 5 would cost £5 plus standard network charge. You can do multiple texts. Thank you all for reading this, we thank you from the bottom of our hearts 💕 We are Kayla’s Army!!! and we will with your help, get her on that plane✈️