Zachary Butterfield

Zach spends most days protecting and serving his community, now he needs your help.


In April of this year, while Zach was spending time in Tulsa with family, he woke up in the middle of the night with extreme pain in his right chest and arm. So much so that I drove him 2 hours all the way back to Mercy Rogers emergency room. They did some tests and found a substantial amount of fluid in Zach’s lung and high amounts of certain proteins/Vitamin D. Zach was sent to Highland’s Oncology for further testing on the abnormal cells they found from CT and PT scans. The abnormality shown on the scans was a 7cm mass between his right lung and his heart  along with some smaller anomalies. A biopsy was scheduled and performed, as well as draining his right lung. (Which would later have to be performed again, as they did not get large enough specimens) After further testing of the biopsy, Zach was diagnosed with Large B-Cell Lymphoma. Before starting treatment, Zach went through a surgery to have a chemotherapy port put in the left side of his chest. While doing this procedure, they also drained more fluid off his right lung.  Zach’s chemotherapy treatment consisted of 6 rounds of week-long chemotherapy that lasted from May until the end of October. During these treatments, Zach was too weak to stand, let alone work. The first week of every treatment was the roughest. The white blood cell shot they gave him after his treatments, made his body ache, which caused pain and lack of sleep. The chemotherapy itself caused nausea, hair loss and loss of appetite. After the first treatment, we found a blood clot in his neck and arm. He was issued blood thinners, which he has continued to take as the blood clot is still there (side effect of the lymphoma). Half way through chemotherapy (3 treatments down), Zach had his midway round of scans. PT scan, Ultrasound, CT scan and Xray. Great news, the masses had shrunk from 7cm down to 3cm! Blood clot was still there, along with some of the smaller masses, but the scans showed no lighting, which was a great sign. Zach still had pain in his chest, and some fluid buildup, but those were deemed as side effects of treatment. Zach was getting used to the loss of hair and shortness of breath, and painful chemo weeks. We all stayed hopeful though, as the recent scans were positive in our favor.
During this time of need, so many people showed us how much Zach means to them. Rogers PD, Rogers FOP, my work, our friends, and some family, have gone above and beyond for our family.

Fast Forward to the last weeks of treatment and he got the clear from Dr to go back to work, light duty. He loved this news as he had run out of vacation/sick/fmla. He loves his work family, and to see everyone on a regular basis again was a reason to hope again. 

Zach finished his treatments and had to wait several weeks before he could rescan to see if the cancer was gone for good. Everyone was hopeful, especially us. Why wouldn’t it be gone? Doctors said it was pretty cut and dry. It was shrinking like it was supposed to, he had his strength up, a little chest pain but to be expected with all the scar tissue. The day of the scans we were ready for the Dr to give us great news and for him to ring the cancer bell. However, that’s not how it happened. The cancer had grown again, closer to his heart and a little higher. The scans showed up bright in the picture meaning it was active. Two different specialists said they had never seen anything like this. The lymphoma was residual and needed a different treatment option. Another biopsy was scheduled. The surgery was supposed to take an hour, but ended up taking 4 hours because of all the scar tissue his lungs already had on them from previous biopsies. What was supposed to be a 12 hours in the hospital, ended up being 3 days. His treatment is being transferred to UAMS in Little Rock. His treatment is now proton and Car T cell therapy. Proton therapy lasts 2 weeks in patient awhile waiting on the Car T Cell therapy. This means being either in the hospital or at a nearby facility but monitored on the daily. Away from family, away from friends, doing treatment.We begin this track next week with our first appointment at UAMS in Little Rock. Cancer moves quickly and gives us no time to think but only react. Expected time to be out is at least 2 more months depending on how this treatment goes. Could be longer, but let’s hope not. Being out of Sick time, vacation, or resources is going to be very hard for our family. Any and all help is appreciated
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