Admire The Survivors

Uintah Basin Healthcare, Urban Tulip Studios, Vernal Floral and Ooh La La & Friends invite you to “ADMIRE THE SURVIVORS” as we feature five local cancer survivors. We celebrate all cancer fighters and survivors here in the Basin and hope to raise awareness for all cancers. The purpose of this campaign is to educate men and women on the importance of preventative screenings and to inspire others to feel comfortable in their own skin.
In 2025, an estimated 2,041,910 new cases of cancer will be diagnosed in the United States and 618,120 people will die from the disease. To view statistics from the National Cancer Institute, click here.
Cancer screening tests aim to find cancer before it causes symptoms and when it may be easier to treat successfully. Because of the many types of cancer, there are many different tests used. (Click here to find out about them.) Call to schedule your annual check-up today. (Family Practice Roosevelt: 435.722.6130 | Family Practice Vernal: 435.789.1165 |  Women’s Health: 435.722.4652 or 435.781.2030  |  Women’s Imaging for Mammography: 435.725.2081)
DID U KNOW? We now offer Cancer Care Services in Roosevelt and Vernal. From chemotherapy to care planning, you’ll receive individualized support from our local cancer care team and Intermountain Healthcare oncologists via telehealth. Learn more!
Learn more about the cancer journey stories of these five incredible individuals…

Joyce Newberry

In January 2023, I started having constant pain in my lower stomach... [read more]

In January 2023, I started having constant pain in my lower stomach. Day after day it lingered—sometimes mild, sometimes intense—but never fully gone. Nothing I tried made it better. By February, I finally went to the doctor. He suggested a colonoscopy to rule out anything serious. I remember saying, “Why? I’m only 42, almost 43. There’s no way it’s cancer.” On April 27th, I had my colonoscopy. Afterwards, they brought me into a private room—the kind of moment when you know something isn’t right. That’s when I heard the words I never imagined: “You have cancer.” The very next day, I had blood work and scans. Then came the waiting—four of the longest, most terrifying days of my life. When the results came back, my doctor told me the cancer hadn’t spread to other organs, but some lymph nodes near the tumor looked suspicious. Two weeks later, I underwent surgery to remove a foot of my colon and 23 lymph nodes. Out of those, 4 tested positive. That’s when it became official: stage 3 colon cancer. From there, I had to be strong. I had a port placed, and on June 22nd, I began chemotherapy—four rounds of treatment plus two weeks of chemo pills. It wasn’t easy. Some days were harder than others, but I kept pushing forward. My last chemo infusion was on August 24th, and I finished my final chemo pills on September 7th. The turning point came on August 23rd, when my doctor shared the news I had been praying for: my CEA levels were normal. That meant I was cancer-free. Since then, I’ve gone to checkups every three months and scans every six months. And just recently, I celebrated my two-year anniversary of being cancer-free. Looking back, I never thought I’d hear those words—“You have cancer.” But I also never imagined the strength I’d find in myself, or the support I’d feel from those around me. If you’re going through this journey, know this: there is hope. There is healing. And there is life on the other side of cancer.

Hunter Keel

Hunter was four months when we started to notice that he was uncomfortable... [read more]
Hunter was four months when we started to notice that he was uncomfortable to sit, lay or stand. He was also spitting up all of his bottles. These are what led us to taking him into the dr. on the exact day that he turned five months old. All the routine tests came back negative. The dr was concerned about Hunter because when you pushed on his belly he would scream and cry. He ordered an ultrasound and that is where we found the tumor. The next morning we went out to Primary Children’s Hospital where it was determined by MRI that it was Wilms Tumor on his left kidney. We were then admitted into the hospital on the cancer floor. The next morning we met Hunters cancer team. The team consisted of his oncologist, surgeons, and doctors. They had made a plan that was best for Hunter at the time. They had also found an unnatural spot in his liver, so they wanted to do a biopsy to see if it was cancerous. The results were that it was benign. A day after the biopsy they took Hunter in for his surgery to remove his left kidney and the tumor. The tumor ended up being two pounds. Hunter went from weighing 18 pounds to 16 pounds
after surgery. After surgery and recovery, his oncologist set up his chemo plan. We started with 19 weeks of chemo going every Friday for 10 weeks. The other 9 weeks were every other third Friday. He got a dose of two different kind of chemo’s every time. While we were going every Friday Hunter ended up getting COVID in the middle of it. We were able to still give him his chemo while he ad COVID. A month after he had COVID he came down with a bacteria infection in his blood. We were hospitalized for a week while they gave him medication to clear the infection. We had to skip a couple of weeks of chemo because of the infection. Once the infection was cleared we were able to continue his chemo. We finished his chemo on May 29th of 2024. His port was then removed on June 7th. We started our three month checks. Each check consists of an ultrasound on his kidneys to make sure the empty pocket looks good and his right kidney is still functioning well and then x-rays of his stomach. We then have his oncologist visit right after that and they check his results and all his levels. We have just moved to four month checks. Hunter is doing really well and every check is a healthy growing boy.

Destiny Mayfield

Starting in July 2017 Destiny woke up with a major headache... [read more]

Starting in July 2017 Destiny woke up with a major headache. She and her husband visited the emergency room, where medical staff referred her to Huntsman Cancer Institute in Salt Lake City. There, she was diagnosed with stage 3 Hodgkin’s Lymphoma. After completing her initial chemotherapy regimen of twelve treatments, it was determined that a second round would be necessary. When the subsequent chemotherapy was ineffective, radiation therapy was administered. Following radiation, she underwent an autologous bone marrow transplant, which provided partial improvement. A second bone marrow transplant of the allogeneic sort was performed using donated cells from her sister, Breanna, which finally managed to put her into remission. However, the cumulative trauma from these treatments led to stage 5 organ failure, including congestive heart failure and advanced kidney failure. She required dialysis for fourteen hours daily over a period of two and a half years. Placed on the kidney transplant list, her family members worked diligently through the donor evaluation process until a suitable match was eventually found from a deceased donor. The transplanted kidney has been functioning well, and she is currently recovering after eight challenging years. The selfless contribution of the donor and their loved ones is deeply cherished and appreciated. During her journey, she has demonstrated perseverance and managed challenges. We appreciate the support provided by Friends and Family in our community over the years. Donations contributed to Destiny’s ability to access treatment and begin her recovery after eight years. Her experience highlights aspects of hope, family relationships, and organ donation.

Colleen Lawson

This story starts the same as many other women’s… [read more]
This story starts the same as many other women’s. We are told at the age of 40 to get a mammogram done yearly. Which I had done, sometimes I would have to do follow ups either with biopsy or an ultrasound. They always came back benign. They were just cysts. On October 23, 2018, I went in for a yearly mammogram. The image was performed but instead of being asked to dress and I could leave. I was asked to dress and come into another room. The radiologist came into the room and said those words. “Cancer” My mind went in a million directions. “No” I thought this is just another one of those we will do an ultrasound or a biopsy, and it will come back benign, and I will be good until next year. The radiologist said he would like to have a left breast core needle biopsy. And it could be done later that day. I was numb, how could this be happening. I went to my car and called my husband. He could hardly understand me when I was balling. I told him what I had just found out and he finished up his day at work and came with me to have the biopsy. The result came in I had Lobular breast cancer. I had lumpectomy, and this showed a 1.8 cm ILC grade 2, ER/PR positive, HER2 with positive inferior and superior margins and associated extensive LCIS. 1/1 sentinel lymph nodes were positive with 0.5cm of metastatic cancer pT1pN1aMo-Stage la. I elected to have a double mastectomy, with tissue expander placement. This was November 27, 2018. December, I made the trip to Huntsman University. To find out what treatment I would be having. My oncologist was wonderful; she answered all my questions and my husband’s. Waiting for the call on treatments. She called and said I have some good news. You will only have to have 16 radiation appointments so don’t go crazy and cut your hair. I said, “Well too late I had done that. I started my radiation appointments February 1 st , 2019. I went into the radiology department. And finished up March 2019. Time to heal. I had implants put on June 24, 2019. After all the follow ups and treatments, I am almost 7 years clear. But there is never a day I don’t thank the man above for what he has given me. A loving and supportive family and beautiful grand babies to love and enjoy.

Chesney Mitchell

My name is Chesney and this is my breast cancer journey… [read more]

My name is Chesney and this is my breast cancer journey. After nearly a year of persistent symptoms and inconclusive scans that answered no questions, I underwent exploratory surgery and as a result, at the age of 36, I was diagnosed with Invasive Ductal Carcinoma in February of 2024, one day after my son’s sixth birthday. A cancer diagnosis at any age is intimidating, so confronting this at the beginning of a new career with two young kids at home, it rattled me but also sparked my determination. I was scheduled for a partial mastectomy and lymphadenectomy quickly after my diagnoses. A negative lymph node biopsy confirmed my cancer had not spread, so after a slow and complicated recovery I was able to start radiation treatment. I was fortunate enough to have a great radiation oncologist and team that made the experience the easiest part of the treatment thus far. Through each chapter of this ongoing experience, I have come to realize that cancer is a prolonged journey, not a singular event. Emotional wounds are profound and lasting and recovery isn’t just about healing physical wounds. From the beginning, I have had an army of earthly angels by my side. My family and friends were with me every step of the way and continue to be. I rely heavily on my Savior, trusting with certainty that prayers are heard and answered.
Being proactive about my cancer recovery meant educating myself on post-surgical medications. Last month marked a significant milestone-one year adhering to a medication designed to minimize the risk of recurrence, with four years remaining. Initially the decision was intimidating given the potential side effects I had been educated about. However, I didn’t fully understand until I went through it every day. I assumed taking a daily pill would be relatively effortless; instead, it has been a daily reminder of my battle with cancer and my dedication to ensuring it doesn’t return. As I reflect on this journey, my greatest hope is to empower YOU to act. Each person possesses a unique understanding of their body. If something feels amiss, heed your body’s signals and advocate for yourself. Thank you for reading my story.

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