Charlotte's Journey

 Good morning village: our friend Elijah could use your prayers today. After his 3rd relapse with Neuroblastoma, his disease is progressing despite treatment. Tumor has infiltrated his jaw. He is having a scan this morning to determine the extent of disease but his family is reporting their greatest fear—that his cancer could be resistant to treatment and that they may be running out of options. Elijah and his mom recently came from their home in Ohio to Charlotte, NC for new treatment options, with a brand new baby brother whom Elijah adores more then anything. My hope and prayer today is that the scans and their new team of doctors here who specialize in precision therapy that targets tumor genetics, can find a way. That Elijah’s journey is partly to make a way. That there would be therapy to slow down this progression while still allowing for a good quality of life and TIME for a cure to be developed as there is so many new and exciting advancements happening. That his parents do no

Joy and Pain in this moment I want to update all of you who have been loving our family and cheering for our Charlotte all this time, but I am having a hard time writing this. (We have returned from MSK where Charlotte received her 7th and final NB vaccine shot on this clinical trial, had 4 bone marrow biopsies (returned clear), and met with survivorship team for tests and exam and to establish care for long term follow up appointments.) Yesterday, on the same day that our Charlotte received what we pray was truly her final cancer therapy treatment, our Poppy took his last breath while holding his wife’s hand. We loved this man so so much and there are just no words at this time that can be said as we try to process this sudden and unexpected loss of our stepfather, father-in-law, and grandfather who was such a special soul and presence in our lives. Neal and Schuey have been here supporting and holding us since diagnosis and now, it’s our turn to hold them close and surround Nana Schu

 Quick update to let you all know that Charlotte remains CLEAR with no evidence of Neuroblastoma! Now that Charlotte is growing older amid all of this, one of the truly special and remarkable parts of has been watching her reaction when we tell her the news. She can genuinely feel the joy I think because she knows some of what it has cost her to get this news. She immediately beams that smile and seems to light up. Although Brian and I try to never let the children see the weight this is on us, the worry, the fear, she feels it too. She wants this to be behind her too. She asks us what will happen if her scans showed that the cancer has started to grow again. We tell her that we would fight it off once again. That we would keep fighting it off. And honestly, that is what we are doing right now in this clinical trial. So now we turn towards NYC and trying to find a way or MAKE a way for her to keep having access to what could make all the difference not just for her, but for so many chi

 Starting today, Charlotte has some big appointments. We start off at Duke for 3 scans over today and tomorrow for her routine disease evaluations. Then Sunday, we leave for NYC for appointments there. She will have a 4 location bone marrow biopsy and the 7th shot for the Neuroblastoma Vaccine trial. We actually do not know if we are wrapping up this trial at this appointment or if she will be offered a continuance as we hope and pray for. Charlotte is doing amazing but she is still in the window for reoccurrence and we want to do everything possible to help continue to keep her clear. So, my anxiety is at a high as we await what will be possible...of course we need these scans to be clear first. I wish we felt at peace and could welcome the finality of finishing this clinical trial once again. But we simple do not and cannot. We are also under discussion about arranging a consultation with another Neuroblastoma expert who has just relocated to Levine’s Children’s hospital in Charlotte