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Sally Opie

My grandson Jonah was diagnosed with Stage IV high-risk neuroblastoma one week before Christmas 2014. He was 16 months old. With trepidation, I started researching neuroblastoma…amazed and saddened by what I was learning. Jonah was on the fence between a so-so survival rate and a good one. And so our journey began. Jonah had surgery on Christmas morning to have his port put in. He has had chemo, radiation, surgery, immunotherapy, and more in such a short time. So far, Jonah has shown No Evidence of Disease (NED). Scans are every 3 months and he continues immunotherapy (Neuroblastoma has a high relapse rate). I’ve become aware that childhood cancer is not rare and my goal is to make as many other people as possible aware as well. Please consider a donation to this organization to give kids like Jonah a fighting chance. Don't forget to also visit and join the #RunForTheWhiteHouse2017! Thank you for visiting. This cause is very dear to me, and I'll appreciate all the support I can get! Together we can make a difference! Best - Sally

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