In honor of Childhood Cancer Awareness Month, we are sharing a series of stories about some of our incredible patients who have overcome cancer or are currently fighting the disease.
On Sept. 19, 2013, 8-year-old Hunter Schroeder celebrated one of the biggest milestones of his life – it marked his second year cancer free.
That’s all his mother, Heather Schroeder, heard when the tests results came back from his two-year checkup. And with that, the weight of the world lifted off her shoulders. She was finally able to relax and breathe again.
He was healthy and perfect, exactly what she’d been praying to hear ever since her son was first diagnosed with acute myeloid leukemia (AML), a cancer of the myeloid cells, in 2011.
“It’s taken a while stop panicking about every bruise and every fever, and to see the hospital and not think his cancer has come back. But after two years, we’re finally getting there,” said Heather. “We’re finally getting back to normal, or at least adjusting to our new normal.”
She can, however, vividly remember the difficult time when the bruises on Hunter’s body did signify something very wrong with her little boy. Read full post »
It’s 9 a.m. on a recent rainy morning in Seattle. Julie Park, MD, has her shoes drying out by the heater in her office at Seattle Children’s Hospital. She’s on a conference call with doctors and statisticians from Germany, Canada, the U.S. and Europe, and they’re discussing neuroblastoma, the most common solid tumor in children younger than 1 year of age.
Park leads the Neuroblastoma Committee for the Children’s Oncology Group (COG), the world’s largest organization devoted to childhood and adolescent cancer research. COG is supported by the National Cancer Institute (NCI) and unites more than 8,000 experts at more than 200 leading children’s hospitals, universities and cancer centers across North America, Australia, New Zealand and Europe.
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In honor of Childhood Cancer Awareness Month, we will be sharing a series of stories about some of our incredible patients who have overcome cancer or are currently fighting the disease.
In the beginning of June 2012, Jake Steiner was on top of the world. At age 18, he had just graduated high school and was looking forward to working as a camp counselor at the Museum of Flight in Seattle over the summer. He would then be heading off to college at Santa Clara University in the fall. Life was good.
That is, until one week after graduation.
Jake had noticed a pain in his leg and he had a bump on the backside of hip bone that was about the size of his hand. He thought he had just pulled a muscle and a little TLC would take care of it, but his dad took him to a doctor because the bump was so large.
It was then that he got an MRI and received some of the worst news of his life: He was told that the bump was a malignant tumor, and after three weeks, he learned it was Ewing sarcoma. Ewing sarcoma is a bone cancer that mainly affects children and adolescents between the ages of 10 and 20 years old. It’s the second most common bone cancer in children, but only accounts for about 1 percent of all childhood cancers. There are about 200 new diagnoses of the disease in people younger than 20 years old in the U.S. each year.
“I didn’t know what my future was going to hold, but I knew I was not going to be able to go to college in the fall, which really bummed me out,” said Jake. “I was also very scared because I thought I caught it too late and I didn’t know if the cancer had spread. I thought I would die young, and that terrified me.”
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Headlines these days related to research funding are grim: “Seattle researchers fear federal cuts will costs lives and jobs” and “Show me the money: Is grant writing taking over science?” are two recent stories that ran in the Puget Sound Business Journal and The Guardian, respectively.
The federal government announced in May that the National Institutes of Health 2013 budget will drop by five percent, or $1.71 billion, to $29.15 billion, compared to 2012. The cuts are part of the effort to balance the budget and, based on what our researchers say, are part of the “new normal” moving forward.
But there’s a bright spot here at Seattle Children’s: Philanthropy for research is increasing, and it’s making a difference.
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Dishes, silverware, small appliances, sheets, towels. Home essentials like these appear on nearly all wedding gift registries. But for Shaquita Bell, MD, a primary care pediatrician at Seattle Children’s, and her fiance, Marc Stamm Boyer, giving their wedding guests a wish list of stuff for themselves just didn’t feel right.
“We are at a point in our lives where we have the things we need and the things we want,” says Boyer. “It seemed silly to say, ‘Hey, you know how we have all this silverware? We should totally get some more.’”
But knowing that guests might insist on giving a gift, they put their heads together to come up with another option: “registering” for donations to Seattle Children’s.
“If our guests want to spend money on our wedding, we’d rather it go toward something inherently good,” says Boyer. Read full post »