2010 Patient Story: Olivia Schroeder
Olivia's story coming soon!
2009 Patient Story: Colton Sandhofer
Colton Sandhofer, now almost 14, was diagnosed with Rhabdomyoscarcoma, a tissue cancer, when he was 11 years old. His journey began when he found a lump in his wrist. Initially, Colton was sent to a physical therapist. Within weeks doctors realized his tumor was cancer and he was immediately sent to Seattle Children’s to start treatment.
Colton endured a year of chemotherapy, radiation and surgeries, and almost always had a smile on his face. Colton is now cancer free and continues quarterly checkups at Children’s. He is in the 8th grade at Tolt Middle School and is an avid athlete, excelling at both football and baseball. Colton lives in Duvall with his mom Tracie, dad Brian and younger brother Trent.
2008 Patient Story: Logan Lewis
Logan Lewis was diagnosed with stage 4 neuroblastoma cancer at the age of 5 in the summer of 2007. Neuroblastoma is a disease in which malignant cells form in nerve tissue of the adrenal gland, neck, chest and spinal cord. In the beginning of July, 2007, Logan began limping and running a fever which lead to several trips to Children’s hospital for a diagnosis. Throughout this time, Logan’s mom, Kelly, was due to give birth at the end of the month. A definitive diagnosis of neuroblastoma came on July 26, 2007. Logan’s baby brother, Peyton was born 4 days later on July 30
Dr. Julie Park supervised Logan’s treatments and numerous stays at Children’s Hospital. He endured 6 rounds of chemotherapy, surgery to remove the tumor, a stem cell transplant, radiation, and an experimental treatment. Logan always handled his treatments with a smile and a positive attitude.
Logan is now eight years old and is happy, loving, confident and full of life! Logan’s parents are thankful to the staff at Children’s for their amazing care.
For more information about Logan Lewis please visit his website
2007 Patient Story: Thomas Bailey
Thomas Bailey was diagnosed with stage 3 neuroblastoma cancer at the tender age of 8 months. Neuroblastoma is a disease in which malignant cells form in nerve tissue of the adrenal gland, neck, chest and spinal cord. The cause of the tumor is unknown and symptoms can vary. Often, children experience few symptoms until the cancer has spread to the bones and bone marrow making treatment prolonged and difficult.
Thomas' cancer was discovered during a routine exam for a bad chest cold. He was immediately admitted to Children's Hospital in August 2005 under the care of Dr. Julie Park. He initially spent 10 days in the Seattle Cancer Care Alliance wing where she determined his course of treatment would be several months of chemotherapy followed by surgery to remove the diminished tumor. Treatment went well, especially due to the advances in pediatric cancer, cutting-edge drugs to combat nausea, and the meticulous care of the Children's Hospital staff.
Thomas is now five years old and is completely cancer free.
2006 Patient Story: Kelty Pierce
Kelty Pierce has been a patient at Children's Hospital since she was a year old. At the time of her birth in December, 1997, she was diagnosed with Developmental Dysplacia of the Hip, the abnormal growth of the hip joint (DDH). After her first unsuccessful surgery at eight weeks-old, and a year of follow up treatment in Tacoma, Kelty came to see Dr. Mohammad Diab in Children's Orthopedic Clinic. He determined Kelty needed more surgery and she went in January, 1999 for the first of five surgical procedures. Between the ages of two months and five years-old, Kelty had six surgeries, each one followed by a body cast, cast changes and numerous hospital stays.
Dr. Diab left Children's in 2002 and Kelty is now under the care of Dr. Vincent Mosca. She sees him annually, and although she is stable and in no pain, more surgery is imminent. Kelty's hip sockets are not normal - never will be completely, so she is destined for dual hip replacements once she is fully grown. It is our hope to put that off long enough for technology to make that procedure less invasive and more permanent.

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