Cancer and Blood Disorders

All Articles in the Category ‘Cancer and Blood Disorders’

Travis Pays it Forward

Travis, Turner and Tynan Patterson (from left to right) packed the car for last year’s toy drive for Children’s.

Travis, Turner and Tynan Patterson (from left to right) packed the car for last year’s toy drive for Children’s.

This month, Travis Patterson and his 16-year-old son, Turner, are spearheading their seventh annual holiday toy drive for patients at Seattle Children’s.

It’s just one way the Pattersons give back to the place that saved Turner’s life and changed Travis’s forever.

Nearly 11 years after Travis first walked through Children’s doors, holding tight to a very sick Turner, he is a grateful parent, a dedicated volunteer and – since earlier this year – an engaged employee.  In February, the journeyman electrician joined the Plant Operations team.

And he’s not the only family member working at Children’s. His older son (and Turner’s big brother), Tynan Patterson, works in the Nutrition Department.

When Travis makes his hospital rounds to work on the emergency generator or fulfill Fix-It requests, Travis brings the tools of his trade and something else – a type of compassion that can only come from been-there, done-that experience.

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Shopping for a cause this holiday season at Bargain Boutiques

Bargain BoutiquesWith frost appearing on our windshields and temperatures dropping, we find ourselves again nearing the height of the holiday season. And with only one week left to go before Christmas, holiday shoppers are on a tight deadline to find the latest deals and steals before time runs out. But there’s no need to worry because at area Bargain Boutiques, the deals are not only good for your pocketbook, they also benefit children.

There is little doubt that there is a tremendous amount of shopping that goes on during December. According to the American Research Group the average American spends nearly $1000 on gifts around the holidays each year.

What you might not know is that that this increased spending is also accompanied by an increase in giving around the holidays each year. If you talk to Eva Campbell from Seattle Children’s, she’d probably tell you that shopping for gifts and donating to a worthy cause don’t need to be done separately.

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Wedding wish becomes a reality for patient family thanks to cancer care team

The Olivera's wedding day

Photo courtesy of Soulumination

Tuesday was a day that the Olivera family will never forget – It was a beautiful day of unity, celebration and joy. It was a bright spot in what has been one of the most challenging years of their lives.

Oct. 22 was the day that Saul and Alejandra Olivera were finally able to get married after three years of being engaged. “Making it official” was something they were very excited to do and something their 9-year-old daughter, Miranda, had wished for.

From a limo, cake, caterer and photographer, to a chocolate fountain (the most important element for Miranda) – the big day was complete. And it all became a reality, within one week’s time, thanks to three members of Miranda’s cancer care team at Seattle Children’s who made it happen with the help of the community.

“It was the most amazing day and we couldn’t have asked for anything more,” said Alejandra. “Everything was perfect and Miranda was so happy to be there and be a part of the celebration.”

Now, this wasn’t just any wedding – it was extraordinary. And in order to understand its significance, it’s important to understand the family’s journey, as well as the people that were behind the important day.

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Patient Voices: Kat becomes titanium girl, makes a difference for future cancer patients

Hello my name is Kat Tiscornia and up until March of 2013 I was your typical 8th grader. I loved horseback riding, eventing to be more specific, skiing and spending time with friends and family. Then it all changed. I went to the doctor to have a large bump on my thigh checked out.  I was told what I thought might be a bad bruise had a high probability of being cancer.

After many tests, two biopsy surgeries for my lung and my leg, and a stressful couple of weeks, I was diagnosed with a rare form of bone cancer called Ewing sarcoma. There are approximately 200 new diagnoses of the disease in the U.S. each year. Read full post »

Patient voices: At age 27, Hunter puts his life on hold to fight cancer

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.

At 27 years old, Hunter Storey had a great life in Sun Valley, Idaho. He worked as a fireman, enjoyed spending time with his girlfriend of eight years, and was an avid skier and ski instructor.

However, last December things started to change.

It was ski season and he was coaching ski racing to a group of high school students when, one day, he noticed a painful lump on his shin that didn’t seem right. He decided to see a doctor.

After what was first thought to be a broken bone, seven months later, he learned it was cancer – Ewing sarcoma to be exact. Ewing sarcoma is a bone cancer that mainly affects children and adolescents between the ages of 10 and 20 years old, but there are cases that occur at all ages.

“It was of course very shocking when I was diagnosed,” said Hunter. “But I was really lucky because I had caught it early.”

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Patient voices: Hunter Schroeder celebrates two years cancer free

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.

Hunter Schroeder OBK at Ballpark 8.25.13On Sept. 19, 2013, 8-year-old Hunter Schroeder celebrated one of the biggest milestones of his life – it marked his second year cancer free.

“He’s perfect.”

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 »

All for one and one for all in the battle against childhood cancer

collaborate

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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Patient voices: Stacy celebrates 10 years cancer free, reflects on being chemo Barbie

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.

My name is Stacy Helton and I am a 10-year cancer survivor. I celebrated this momentous milestone in July by flying to Florida to be with my family. We reflected upon how far we’ve come over the years and how much we’ve grown together.

Before sharing where I am today, it’s important to describe what has got me here.

I was diagnosed with Hodgkin Lymphoma when I was 16, the day before Christmas break my junior year of high school.

It was by happenstance that I learned I had cancer. I had slipped getting into my car, hitting my chin and chest on my steering wheel, and so my mom and I went to urgent care where I got a chest X-ray. Surprisingly it showed a tumor. Later I learned it was cancer.

It might sound funny, but when I got the news my biggest question was if I could start treatment after junior prom. I had already purchased my dress and had been looking forward to prom for months. Of course to my disappointment, I couldn’t wait and had to start treatment immediately.  

While everyone else was making last minute plans for the holiday break, I was on a flight from Anchorage to Seattle Children’s Hospital consumed with feelings of uncertainty. I was hopeful that treatment would go well because doctors said my cancer had a high survival rate, but I didn’t know what was in store for me.

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Patient voices: Jake beats cancer, starts new life at college

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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One mother’s creation provides a valuable tool for tiny cancer patients

Robin in her Hickman HiderOn July 13, 2012, Robin Ulness was diagnosed with leukemia at just 9 months old.  Gayle Garson, Robin’s mother, said the diagnosis was a complete surprise and it all came on very quick.

“Getting the news was devastating,” Gayle said. “It was like getting kicked in the stomach by a horse. It was so surreal; I just kind of went numb.”

Robin was diagnosed with infant acute lymphocytic leukemia (ALL), which arises from white blood cells called lymphocytes that do not mature properly. While ALL is the most common type of cancer in children, infant ALL is very rare.

Robin’s diagnosis marked the beginning of two years of treatment. Robin came to Seattle Children’s Cancer and Blood Disorders Center and began six weeks of inpatient care. She then had four more rounds of chemo, which required a number of inpatient stays.

While Robin was inpatient, Gayle came up with an innovative idea for something that would not only help her daughter but would also help other children going through treatment.

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