It's hard to believe so much time has passed that has lead to this anniversary post. Looking back, it seems like an eternity ago and just yesterday all at the same time. It's been exactly one year since the moment when the resident came into our room to reluctantly admit that it was, in fact, cancer and that we were being transferred to MD Anderson. September 11, 2018, at 0946 will forever be burned into our memories. It's a part of who we are now, what's shaped us into the people we are today. I would have never imagined this would be our life today, and I wouldn't wish this on anyone. Honestly, I could write a J.K. Rowling length post on all of the negative aspects this year brought to my husband, myself, and our loved ones. This year has been grueling. However, we have been showered with immense amounts of love; outpouring love from people who've known us our wholes lives as well as love from complete strangers. This year has taught us to forever
September 11, 2018. Two years ago, today, our lives changed forever. There are so many things I could say within this post, but I’ll keep it short & sweet since Co doesn’t like it when I make a big deal out of things. But, today is a big deal. With a survival rate of roughly 20-30% at 2 years, today is an extremely big deal. Congratulations on blowing those statistics out of the water, Co. I have never met someone as strong and determined as you to push through each and every day. Despite everything you’ve been through, you still show up and love our little family with everything you have. Nine months of chemo, seven weeks of radiation, six different tubes out of your side, two transplant evaluations, one massive resection surgery, and post-op abscess turned sepsis, chest tubes, biliary tubes, stents, mediport placement, lab draws, IV’s, scans, waiting rooms, Houston traffic, Minnesota relocations, and all the things in between, you have overcome it all. I am so incredi
Co went under for a Cholangiogram (a procedure where they access his liver through his side and inject some fancy dye to light up the bile ducts like a Christmas tree and identify any narrowings or blockages). And, would you believe me if I told you they didn't find a blockage? That his surgical site looks good and isn't causing a fuss? Well, it's true. They didn't leave a drain, they weren't able to do much of anything because there's no specific blockage. Co is now scheduled for a liver biopsy tomorrow afternoon to look for an autoimmune disease that could be the culprit of his symptoms. His team is also investigating the medications he's taking to see if those might not be playing nicely with his baby liver. This process is long and tedious, but we have full faith in his care team at Mayo. I cannot begin to express how grateful we are for a team that truly cares about Cody's well-being and is openly communicating with us multiple times a day. Co is
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