Cora Faith’s Story

Site created on June 4, 2020

Cora's journey with Leukemia will be a long road but we hope you stay here to join with her and us in the journey. We are using this as our go-to place to keep family and friends updated and appreciate your prayers and words of hope and encouragement. Please post, comment and interact here as it will become our primary source of updates and information. We love you all and appreciate you lifting up our sweet Cora Faith to the Father in Prayer. **Please Note that CaringBridge has a section for "Tribute Donations" which is their own non-profit fundraising  for their 501c(3) and is not a donation to us or this cause. 

The first 48 Hours: 
June 1st, 2020 was a totally normal day until Cora got a fever. That night she woke up with extreme pain in her back and we battled that with her all night long. In the morning (June 2nd) we got in to see her Pediatrician where they did a quick blood test during their visit. Those initial results came back with a lot of things out of whack, so they did a blood draw and sent it off to a lab STAT just in case. About 4 hours later after the lab reviewed her blood and a Pathologist studied it to confirm, her doctor called Kelly personally and informed us that they found positive signs of Leukemia. Just like that, the world changed and within 4 more hours, we had Cora admitted to Medical City Children's in Dallas. 


June 3rd - After many more tests and a long night full of high fevers, pain, and fear we got confirmation that she was positive for Acute Lymphoblastic Leukemia (Pre-B Cell). Another long day and night full of pain for Cora and more information than Kelly and I could take in, coupled with the hospital rules where only one parent can be on the floor at a time and we came to June 4th. - Day 1 of Cora's Battle. 


Please follow along as her journey continues. We post semi-regular Journal updates as well as connect with people via a private Facebook group here: https://www.facebook.com/groups/corafaith 

Newest Update

Journal entry by Kelly Brewer

Cora had surgery on Monday to remove her mediport! The port has been sitting under the skin in her upper right chest with a line fed into her external jugular vein. We are so relieved that the surgery went smoothly. The same expertly skilled hands of the surgeon who put her port in on June 4, 2020 were the same hands to safely remove it. She had the same anesthesiologist this time as well. Sitting in the same spot of the hospital surgery waiting room, I couldn’t help but feel how full circle the moment was. I also felt deep gratitude for sitting there with something to celebrate instead of grieving what was just beginning.

Cora was so brave about the whole thing. After many trauma-inducing, painful failed attempts to get an IV started that very first evening of admission following her diagnosis, Cora quickly learned to view her port as a faithful friend that spared her excess pain during every blood draw, anesthesia, chemo, or other med infusion. She was initially not very excited to learn that it was time to have her port removed, especially since she will still be having frequent blood draws for years to come. But in true Cora fashion, she quickly accepted this next step and found a way to look forward to it. Shortly before her surgery, she declined the “goofy juice” from the anesthesiologist that is normally given to help kids relax and not care about the separation from parents and all the unusual experiences of entering the OR and being put to sleep. Cora said she was excited about the moment and wanted to remember everything. And she did!

Cora’s still really sore from the procedure, so today is a good rest day to spend all day in the car heading to the mountains for her last dose of chemo celebration. She currently has only one more dose of methotrexate to take tomorrow evening and 3 more daily doses of 6MP, with her last chemo pill to swallow on Saturday morning! Bell ringing in 3, 2, 1…
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