Thomas’s Story

Site created on December 28, 2020

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A brief overview of our journey: 
While visiting family in Portland for Christmas, Thomas went to the children's hospital (it was recommended to take him in due to a large mass near his liver).  He was immediately diagnosed with Hepatoblastoma (pediatric liver cancer) on December 22nd. We did the biopsy there to confirm the diagnosis, and soon left to head home. Thomas went directly to Phoenix Children's Hospital, and surgery was scheduled for January 2nd. The surgeons were able to remove a mango sized tumor off the lower right side of his liver. They discovered the tumor had ruptured in two places, which required more chemotherapy than planned.  He requires six total "big" treatments with 4 different types of chemotherapy (Doxirubicin, Cisplatin, F5, and VinChristine) every three weeks, but two weeks in between he receives VinChristine each Friday. The "big" treatments require that he is admitted to the hospital for the weekend, because he gets two doses of the Doxirubicin (24 hours apart). Thomas has had approximately 10 transfusions (blood and platelets). He has admitted due to fevers 5 times. He struggles with pain from mucositis (sores that run from his mouth, down his throat through his organs, and on his bottom), which are extremely painful. He doesn't like to eat already as chemo changes the taste of food, and meds are hard to get down, so we opted for a feeding tube to help offset the struggle of nutrition and medicines. He struggles with nausea, overall fatigue, and several side effects such as drowsy eyes and being off balance. He will no longer walk on his own, but maybe a few steps here and there. He is very hard to understand, so it is a constant battle deciphering what he is trying to communicate. This journey is far from over, because we expect him to decline on the last half of chemo. The Carrolls are doing the best they can to persevere through all of this. Prayers have certainly been their source of strength through all of this. THANK YOU to all of you who follow the journey and support them in SO many ways.  Please keep praying and supporting them as they endure such hardship.

Newest Update

Journal entry by Teresa Carroll

I know many people have been awaiting an update regarding Thomas, and I cannot believe how long it has been. It has been so very busy I cannot believe it. Thomas finished his last two chemotherapy appointments. The last one was while he was admitted due to his counts dropping per usual from the prior "big" chemotherapy (the one with all four chemos at once). He stayed the last time from May 21st to June 1st. It was particularly long because he got "C diff" during his stay, which was likely caused by so many antibiotics. This is extremely contagious, so it was very stressful and time consuming try to keep everything clean. The last day, June 1st we got the "end of treatment" tests. He got his hearing test done (this is needed, because the Cisplatin chemo causes hearing loss). He has some high frequency hearing loss in his left ear, and it can continue to worsen overtime. He needed an EKG and ECHO, because the Doxirubicin chemo is particularly hard on the heart. It came back normal! He lastly had his scans done to confirm that the cancer did not show. The scans also showed no signs of cancer! We got the confirmation that he was cancer free on June 4th at clinic. He was able to ring the bell! Our family had a very small celebratory photo session, thanks to a good friend Lexy Popa (some photos below). Thomas will have an outpatient surgery June 30th to remove his port. We also should get an update on how many more meds he still needs to take. The feeding tube will stay for a few more months while he is still taking medicine. Although Thomas has regained a lot of strength back to his body, he is not expected to walk for a few more months. The side effect of a prescription (Gabapentin) has very harsh side effects including balance issues, dizziness, and many others. He must continue to take this due to his neuropathy. We hope to lower the dosage soon and quickly.

Our family has been together since that day, and Thomas is doing better than I expected. His spirits are up, and he enjoys being home with his brothers. He turned 3 on June 12th, and he had a wonderful co-celebration with his brother Andrew (also had his fifth birthday). Two firetrucks and 6 firefighters surprised the boys at our house. The boys all loved the visit, and it will be a memory for a very long time! Adjusting to a new "normal" has not been easy, but we continue to truck along slowly. We have learned so much on this journey, and we are so incredibly grateful for community and especially for our faith in Jesus Christ. He has certainly not left our side in this tough journey. Thank you so so much for continued prayers. Please keep us in mind as we will have follow up scans every 3 months for a year, and 6 months to a year following until he turns 18. 
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