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Hoyt’s parents just recently found out their 9 month old little boy has neuroblastoma. It all started just by taking him to his regular checkup…his parents brought up concerns about a “knot” in his belly at his 6 month checkup. The doctor brushed it off as him either being constipated or him having an umbilical hernia and showed no concerns about it. A few months went by and his parents kept an eye on said “knot”. The knot had grown a little so his parents decided to bring it up at his nine...
Ambrea was diagnosed in July 2015 with a stage 4 Wilms tumor. So far, she has had two surgery’s and six chemotherapy treatments. As long as her scans come back with no new masses, Ambrea will be done with treatment in January 2016. Ambrea loves her Mickey Mouse clubhouse and playing with her older brother. Every child who has been diagnosed with childhood cancer inspires us to Rally On to find better treatments with fewer long-term side effects and, ultimately, cures. Please join us in the...
Amanda is a 23-year-old proud childhood cancer survivor. She was diagnosed with stage 4 Wilms Tumor when she was 5-years-old. The prognosis was not good as she had a right nephrectomy, 2 rounds of chemo, radiation treatment, and a bone marrow transplant over the course of 2 years. She has now been cancer free since 1997! Today, Amanda loves Braves baseball, live music, shopping, and cooking. “It is by the grace of God that I am here to share my story today,” Amanda says. Every child who has...
Every child who has been diagnosed with childhood cancer inspires us to Rally On to find better treatments with fewer long-term side effects and, ultimately, cures. Please join us in the fight against childhood cancer by making a donation or setting up your own Rally fundraiser today.RALLY WITH US!MEET MORE RALLY KIDS
Ansley was diagnosed with Neuroblastoma at age 2 1/2 yrs. old. After several years of treatment, she reached NED status twice for almost 5 years each time. She relapsed in 2009 and has been in the fight since that time. Enduring multiple trial therapies, numerous surgeries, MIBG therapies, stem cell transplants, multiple radiation visits, tests, scans and pokes resulted in her being rushed to ICU in February 2017 and placed on a ventilator for almost 3 weeks. This was her first experience in...
Anna’s parents write, “We adopted Anna Corinne in November of last year. One week later, we discovered she had multiple tumors in her brain. We were in the watch and wait until a ambulatory EEG presented with over 55 seizure spikes in a 24-hour period. She suffers from seizures on a daily basis.” Every child who has been diagnosed with childhood cancer inspires us to Rally On to find better treatments with fewer long-term side effects and, ultimately, cures. Please join us in the fight...