Benny and his family were on vacation in Orlando when a severe headache and vomiting landed him in the ER. A simple CT scan revealed he had a tumor in the back of his brain.
Abby was first diagnosed with Ph+ ALL, a rare and aggressive type of leukemia, in February 2011. Soon, Abby was on a unique combination chemotherapy treatment available to her because of St. Baldrick’s-funded research.
Emily’s nickname as a camp counselor is “Sunshine,” and for good reason.
Diagnosed with acute promyelocytic leukemia in April 2016, Emily has kept a sunny attitude, despite a devastating diagnosis and a risky treatment plan.
It started with a swollen eye that wouldn’t get better. Then, Princeton’s parents found a large, hard lump on the side of his head. In late December 2011, at 2 years old, Princeton was diagnosed with stage 4 neuroblastoma.
Want to see someone tough? Look no further than Ike.
Rocky and Rambo have nothing on this childhood cancer fighter who just finished treatment for acute lymphoblastic leukemia.
We may be welcoming new Ambassadors soon, but not before we give our 2016 Ambassadors a chance to share some final thoughts about the past year. Read on to find out just how much the St. Baldrick’s community means to these amazing kids and their families.
Ambassador Alyssa celebrates two birthdays every year — one for herself, and one for her leg. Today, the anniversary of Alyssa’s first big surgery for childhood cancer, her mom remembers that day and shares how far Alyssa has come.
A joyful Alyssa is cradled by (left to right) her mom Michella, sister Kalie, dad Harold, and brother Jacob.
Someone recently asked me why December 16 is hugely significant to us as a family.
It’s the day my 11-year-old daughter Alyssa had a major surgery that changed her life forever.
It’s the day my sweet girl got a new leg.
Tina and Carlos’ childhood cancer journey didn’t begin with their son Phineas’ diagnosis in 2013. It began seven years earlier with their second child, Althea. On the 10th anniversary of Althea’s death, Tina shares how she continues to honor her daughter’s memory.
Althea and her mom.
December 1. I can feel it in my bones days before it arrives. Late fall, Thanksgiving leftovers gone, dead leaves, frost, Christmas coming, my daughter dying in my arms.
A fact of my life for 10 years now — my daughter Althea died of cancer when she was 2 years old.
When 2010 Ambassador Sara was diagnosed with Wilms tumor in 2008, it was a birthday surprise her family did not expect. The now healthy 11-year-old and her family are still committed to fundraising for childhood cancer research, and they recently took a trip to Northwestern University to visit the St. Baldrick’s researcher her Hero Fund is helping support. Her mom tells the story below.
Sara, bottom left, and her family at a St. Baldrick’s event in 2013.
I feel sick with guilt looking at this picture of our daughter Sara blowing out her fourth birthday candles.
29 days later, cancer barged into our home and attacked Sara.
We talk a lot about how childhood cancer affects the family. But what about the siblings, specifically? Ambassador Cheyenne’s mom opens up about how her 5-year-old son, Tristen, copes with his big sister’s childhood cancer journey, and how she and her husband balance their children’s needs.
It’s September. This is a big month for those of us in the childhood cancer community.
If you know anyone impacted by childhood cancer, I am sure your Facebook feed is blowing up with heart wrenching facts about how underfunded the research is and how rare childhood cancer ISN’T.
One thing that tends to be forgotten is how childhood cancer impacts the rest of the family. Most specifically, the siblings.
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