Our Mission

Our mission is to provide emotional support, quality of life programs, and financial assistance for children and their families affected by childhood cancer.

40 Faces

The 40 Faces of Candlelighters chronicles and shares the stories of individuals and their families who have benefited from the support of Candlelighters Childhood Cancer Foundation of Nevada.

In 2018, the nonprofit organization observes 40 years of service in Las Vegas. Each Forty Faces of Candlelighters story represents one year of the nonprofit’s operation, providing just a small glimpse of the significant impact the organization has made in improving the lives of families in our community.

Justin Burkhardt

Justin Burkhardt

This is the story of Justin Burkhardt:

In early 2009, Justin Burkhardt was just 10 years old. A natural born athlete, even at that tender age, Justin fit the description of what many might describe as “the strong, silent type.” Never one to fuss, he had been complaining to his mom, Tonya, about a stomachache for a couple of days.

“He wanted to stay home from school one day,” Tonya recalls. “I said if you’re going to stay home, we’re going to the doctor and he agreed; so, we went to the doctor.”

At the doctor’s office, Tonya remembers, the physician ordered bloodwork to check for mono. When the results came in, all three of his blood cell lines were very low.

“The doctor said we needed to go to Sunrise [Hospital] immediately because they were expecting us.”

On February 6, 2009, Justin was diagnosed with leukemia.

“In hindsight, there were vague symptoms,” says Tonya. “He was taking naps in the afternoon which was unusual for him. I thought he might be faking it to get out of school. I know now that he did have what is somewhat of a commonality in these cases: he had a growth plate injury from playing basketball. In doing more research, there is a theory that a traumatic injury – when all of these things line up – can be the trigger for leukemia to present itself. He had a growth plate injury and cast on at the time of diagnosis.”

Justin’s care protocol, which included both in-patient and out-patient treatment, lasted for three and a half years.

“It was hard with Justin because he held so much in,” says Tonya. “It was difficult for me to figure out how much to talk about and how much to just let him be. I wasn’t sure if talking about it made it worse for him. He wasn’t very outward with his emotions, though every once in a while, he would break down and tell me he wanted to go home.

“I don’t really know exactly what his emotions were when he heard the diagnosis. We were very careful with our words and very cognizant of him being a child and trying to frame speaking in a way that would be less scary for Justin. I’m not sure at that age if he knew how serious it was. We tried to keep our emotions in check when we were with him and would break down in private. I was very cautious with how we reacted to things.”

Candlelighters was a support to the Burkhardts during this time.

“They were very respectful of Justin and took cues from him,” Tonya remembers. “Candlelighters respected the space he needed. The team knew which kids wanted to be engaged and which kids weren’t quite ready for it. Candlelighters always achieved that with Justin and respected the boundaries he needed, yet were always there for us.

“At the clinic or hospital, the Candlelighters team were familiar faces that we could count on whenever we were stressed, upset, or just needed that calming presence. It was a group of people we could depend on to help us through our journey without pushing anything on us, and they always took their cues from Justin.”

One of the most difficult parts of treatment for Justin was his inability to continue to play all of the sports he had played before diagnosis.

“When he was diagnosed, he was a major sports guy,” Tonya says. “He was the fastest guy in soccer. It was hard for him that he didn’t have those things when treatment started.”

One sport Justin was able to complete and excel at during treatment was bowling. He started bowling in the Red Rock youth league and was able to bowl throughout his treatment. In fact, Justin became so good at bowling he made the varsity bowling team in his freshman year at Palo Verde High School.

Justin completed treatment just ahead of entering ninth grade, and the Burkhardts celebrated with an end of treatment party. “He did not want his party to have any reference to cancer. We had a dodgeball party at the park. The slogan was, ‘Grab life by the ball.’ We had a blast.”

Now 19, Justin graduated from Palo Verde in 2016 and is studying at the College of Southern Nevada thanks to a Candlelighters scholarship.

“With Candlelighters' help, we haven’t had to pay a dime for his education,” Tonya says. “We are so grateful not to have to carry that financial load. His bowling scholarship, Candlelighters, and the Millennium Scholarship keep him going. The scholarship puts things into perspective for him and encourages him to keep up with his studies.”

Always strong and steady, Justin has a lot more living to do and will no doubt “Grab life by the ball.”

Photo Credit: Denise Truscello

Comprehensive Cancer Centers is proud to sponsor Forty Faces of Candlelighters.

  • children under 19 diagnosed with cancer each year
    children under 19 diagnosed with cancer each year

    15,780

  • survivors face chronic health condition
    survivors face chronic health condition

    66%

  • families experiencing financial hardship
    families experiencing financial hardship

    83%

  • US childhood cancer survivors
    US childhood cancer survivors

    270,000 +

Facts pulled from American Childhood Cancer Organization

This is the story of Jeremy James Floyd

By all accounts, 37-year old Jeremy James Floyd shouldn’t be with us today. His five-month-old daughter, Gwen, is an even greater miracle. The odds were stacked against Jeremy surviving his childhood cancer diagnosis, let alone one day becoming a father. Yet, despite the odds, here they are today, thriving.

“We always just call him our miracle baby,” says Jeremy James’ mom, Carey.

While so many years have passed since Jeremy James beat his diagnosis, recalling the journey is still difficult for Carey and her husband, Kevin. “Jeremy James was born with craniostenosis. The bones in his head were fused together, and he had corrective surgery when he was 10 weeks old. He lost over half of his blood supply and developed complications. His kidneys shut down, and we almost lost him. Because of that surgery and the complications, he had regular doctor check-ups, much more than was usual for most kids. He started out life with lots of problems."