As part of our foundation’s mission to raise awareness, we would like to recognize the brave pediatric warriors who are battling cancer. Starting this month, our Warrior of the Month program will share one courageous journey or story each month.
If you would like to share your story, please contact us via social media or Breanna@bryson12sunshine.org.



Ezekiel was diagnosed with acute lymphoblastic leukemia on November 5, 2019 at 21 months old. He is now about to celebrate his third birthday! He did not reach 0% minimal residual disease at the prospective time (have no cancer cells in body) so he was moved to the "high risk" bracket and he reached 0% MRD (no cancer cells) on March 13, 2020. Although he is considered to be in remission, his battle continues for approximately 2 more years to ensure that every single leukemia cell is destroyed. If even one cell is hiding in the body, it can quickly multiply and cause a relapse. Through all the bumps along his journey, he always smiles and pushes through. He has just finished Frontline treatment, the most invasive part, and entered maintenance. This means his 4x a week chemo infusions at the hospital have been decreased to 2x a month with most of his chemo taken at home. To Ezekiel’s family, it seems like a never ending tunnel to maintenance but also the fastest 11 months of their lives. They are so happy to be here because it means they are one step closer to ringing the bell and being free of this monster.

With Ezekiel's father being a Hodkins Lymphoma survivor, their family is definitely resilient and tough. Together, they plan to overcome this and walk away stronger than ever.

If you would like to continue to follow Ezekiel’s journey, you can check out @ezekiels.battle (on instagram)! 


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Rosie Jane Rosell turned 3 years old when she stopped walking. It took her family a month with many doctor appointments to figure out what was wrong. On July 6th, their whole world changed with a blood test. Immediately, she had two transfusions followed by a bone marrow biopsy, a port inserted in, and started chemotherapy.


From there, she started to experience side effects of her treatment as well. Hair loss, nausea, neuropathy, muscle and leg pain, and steroids became Rosie Jane’s world. Rosie Jane almost spent two months in the hospital due to low counts followed by a bacterial infection and a common cold.  Rosie Jane didn’t walk for 13 weeks but through physical therapy and the encouragement of her three older siblings, Carly, John John, and Reed, she learned to walk again and even has started to run! 


Her world now consists of constant appointments through out-patient visits with oncologists, psychologists, neurologists,  and many trips to the ER because of her compromised immune system. She takes multiple pills a day and tries so hard to be good even when she doesn’t feel well. 


Just as her mother, Emily, says, “We are so proud of Rosie Jane and will be right by her side for the two years of treatment.  Rosie Jane, we love you baby girl, you can do it!” 


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Ryan was diagnosed with stage 4 Wilms tumor of the kidney in August of 2020. The tumor grew from her right kidney and began to spread up through her vein towards her heart. She underwent two months of chemo to shrink the tumor, mainly from that vein.

Unfortunately, the tumor only shrunk in her kidney, not the desired vein. As a result, she had a 12 hour surgery to have her right kidney removed, as well as the tumor from the vein that was leading up to her heart. The surgery was a success! Soon after, she underwent 6 treatments of radiation and two more months of chemo. Ryan’s last chemo treatment was this past March 12th!

She has a few more CT and X-Ray scans to determine the next steps in her healing process!



On Mother’s Day of 2020, Alex’s family got the heartbreaking news that he (3 years old) had been diagnosed with High Risk Stage 3 Neuroblastoma. As most cancer families know, hearing "Your child has cancer” are the most devastating words a parent can hear. For Alex’s family, it felt like their world was crashing down.

Since then, Alex has fought and persevered through his treatments, including 6 rounds of aggressive chemo, liver failure that left him on life support for 2 weeks, a 15 hour tumor removal surgery, relearning how to walk, 2 stem cell harvests, a bone marrow transplant, and 14 rounds of radiation. Also, during this time, Alex’s brother, Dominic, was born.

Now, Alex and his family continue the rough journey against cancer, working through the lowest lows and highest highs. While they dearly miss their life before Alex’s cancer diagnoses, they are extremely proud of how far Alex’s come and how he continues to give this fight his all! We are all cheering for you Alex!

 MAY 2021: HYRUM

It has been nearly 600 days since a doctor walked into Hyrum’s hospital room just after 1:00 AM and diagnosed him with leukemia. While his family were no strangers to hospitals, it was the very first time in his 3 years of life he had gone to the ED not knowing what was wrong. 4 hours later, he was admitted for 34 days with a new diagnosis and a new focus: surviving cancer.

While their journey still has around another 600 days to go, it has taught them many things, mainly that priorities can be altered to more simple things. Social distancing saves lives and music is healing. Hyrum has faced so much adversity throughout these last 19 months. He has been admitted to the ICU over and over and over, always for breathing difficulty. He has had covid twice, a cyst in his brain, a thyroid that failed, kidney stones from steroids, and fractures in his feet from a depleted bone marrow. His family has learned that sunshine brings chemotherapy rashes, chemotherapy brings seizures, and that one can manage to survive without food for several days in a row and when hunger takes over, anything is allowed.

They have learned Hyrum's love language is music and cuddles, that sleep is more important than school, and that Hyrum's daily affirmations of, “I strong,” standing in front of a mirror while flexing his tiny toddler muscles carry a family trying to endure. They could have never imagined Hyrum having Dwayne the Rock Johnson as a personal fan or that he would receive prayers and well wishes from strangers around the globe.

But here they are, full of gratitude for the journey they are on. It has given them focus and a determination to live intentionally every single day. It has reminded them to have hope, especially on hard days and to choose joy because if Hyrum has taught them anything, it's that attitude matters!



On July 18th, 2020, Ellie’s parents received the devastating news that she had been diagnosed with Grade IV Glioblastoma. Ellie had been just shy of turning 11 months old.

As many cancer families know, a diagnosis affects the entire family, and suddenly, Ellie’s life revolved around countless scans, multiple surgeries and radiation treatments, and several rounds of chemotherapy. While the journey was filled with obstacles, she has remained strong and positive through it all. A true princess warrior!

Inspired by Ellie’s battle with cancer, her parents, Brittany and Jonathan Cogan, created the Ellie Ruby Foundation. They strive to raise childhood cancer awareness, fund cancer research, as well as offer support to other childhood cancer families. You can find more information about the Ellie Ruby Foundation @teamelliec !



On May 1st, 2020, Jayce was diagnosed with MDS (Myelodysplastic Syndrome), a type of Leukemia. After his first bone marrow transplant, Jayce relapsed and the MDS converted to AML (Acute Myeloid Leukemia). He then underwent a 2nd bone marrow transplant and multiple stem cell boosts and is currently hopeful for engraftment.

Jayce has had a rough journey from several rounds of chemo to radiation to two transplants. He spent most of his treatment inpatient, living in the hospital.

Dealing with this crazy lifestyle for half his life, he has been a true warrior. He continues to always smile and wants to give everyone knuckle bumps!!

You can continue to follow Jayce’s courageous battle @babyjayceg on instagram!



Kaine is a spunky and goofy 5 year old who likes to play outside. Recently, Kaine was feeling ill and his mother took him to the emergency room. After being there all night with a fever, they did not find anything wrong, so they gave him an ibuprofen and sent him and his mother home. His father, both a parent and a teacher, understood that kids got sick all the time, but this time felt different. About 1 hour after arriving to the hospital, they learned that he was going to be transferred to the children’s hospital in Milwaukee.

While they knew there was a chance that Kaine could have leukemia, they wanted to do more tests to be sure. When the results confirmed a B cell leukemia diagnosis, it was devastating for Kaine and his family. Kaine has been receiving treatment, and is currently in maintenance. He is scheduled to finish treatment in December!


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Alice was 10 months old when she was diagnosed with a brain tumor. At the time, it was not affecting her much so doctors monitored it with regular MRI’s for a year and a half. Two months ago, Alice started chemotherapy and a trial drug to try to shrink the tumor. Similar to a spiders web, the tumor had grown. They are currently unsure if surgery is possible.

Currently, she is having a really hard time with chemotherapy as she is terrified of the hospital. They are hoping things will get better in time. Keep fighting Alice!