Brooks was only 5 years old, but he had a passion for life! He loved dance parties, Hot Wheels cars, monster trucks, Legos and video games.
His favorite holidays were Christmas and the Fourth of July, and his favorite sports were baseball and soccer. Brooks knew every pizza joint in town and loved salami sandwiches. He enjoyed taking walks to look for rocks or shells on the beach.
When you meet Julia, you know right away there’s something special about her. Perhaps it’s her bright smile or her exuberant joy and compassion for others. But this 11-year-old girl is super!
In fact, that’s her family’s favorite nickname for her — “Supergirl Julia” — given in honor of her courage and determined spirit during her cancer journey.
Zach is a cancer warrior. He is courageous, strong and has fought cancer three times.
Diagnosed when he was 6 years old, Zach beat cancer for the first time after nearly four years of treatment. Then, at age 11, he knew it was back. Zach powered through almost three more years of treatment with a positive attitude.
Maya describes the day she was diagnosed with Wilms tumor as “the worst day ever.”
It was July 6, 2016, one month before her seventh birthday. Doctors immediately scheduled surgery to remove her left kidney, where the tumor was located. Two weeks later, Maya began her treatment plan, which included radiation and chemotherapy. But shortly after treatment started, more aggressive cancer cells were found in her tumor and Maya was placed on a more intensive chemotherapy plan.
With an irresistible laugh and the face of a cherub, 5-year-old Kellan wins the hearts of everyone he meets. No one even notices his wheelchair.
We asked Ambassador Cheyenne who her heroes are. Her answer? “My mom and dad.” So today, for National Parents’ Day, we asked her to tell us why — and she gave us 10 great reasons. (Number 10 is our favorite!)
Cheyenne with her mom and dad, Amy and Levi.
Today marks the end of an era for Joe Bartlett and Chuck Chamness as they complete their terms on our board of directors. Read 2012 Ambassador Sarah’s heartfelt letter thanking them for all the hard work they’ve dedicated to kids with cancer.
Joe Bartlett (left) and Chuck Chamness hold their goodbye gifts at their final St. Baldrick’s board meeting.
Dear Mr. Bartlett and Mr. Chamness,
I want to thank you for all you have done as members of the St. Baldrick’s Foundation’s board of directors.
Ambassador Isaac finished treatment for medulloblastoma almost four years ago. But today, on the five-year anniversary of his diagnosis, the effects of childhood cancer are still evident in his everyday life. Read what his mom, April, has to say about what survivorship looks like for Isaac.
People often say to me, “Move on. Let it go. He’s cancer free. We’re sick of hearing about it.”
Yes, it has been some time since Isaac finished treatment for medulloblastoma on August 24, 2012. He has made tremendous strides, and let’s face it — he’s still here and cancer free.
So why don’t I forget it? Why do I seem forever trapped in this cancer nightmare?
On June 13, we learned that 2013 Ambassador Avery passed away.
In loving memory of sweet Avery, forever 13.
“She was peaceful and calm,” wrote her mom, Stephanie, on the Fabulous Team Avery Facebook group earlier today.
Even though we knew Avery was on hospice, the words felt like a sucker punch to the gut. No amount of preparation could have prepared us for the news that childhood cancer claimed the life of a fabulous kid like Avery.
In our last update on 2013 Ambassador Avery, she was participating in a clinical trial to treat her brain tumor. Today, she’s off the trial and back home on hospice care. Here’s an update on the next chapter in Avery’s story.
2013 Ambassador Avery was diagnosed with a brain tumor in 2011.
At the end of last year, after living with a stable brain tumor for two and a half years, 13-year-old Avery was back in the fight against childhood cancer.
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