The Childhood Cancer Blog
The Childhood Cancer Blog
by Eli Talley, ALSF
When I was 4 years old in August 2005, I was diagnosed with stage IV neuroblastoma. Thirteen years later, I’m still fighting every day and I don’t intend on stopping any time soon.
Since I was so young at diagnosis, I did not really know what was going on. All I knew was that I was going to the hospital so the doctors could look at me and figure out why my leg was hurting. After performing tons of tests and taking lots of blood, they told me that I was sick and had something called cancer. They also said that they were going to do everything they could... Read More
Alexandra “Alex” Scott said it best: “I think if we all work together, we can do it.”
This is ALSF’s Formula for Cures. It starts and ends with the inspiration of supporters, heroes and researchers.
Alex Scott inspired supporters everywhere to make a difference—from stand hosts to corporate partners to children to adults to researchers—each of us has a contribution to make towards cures.
To maintain our dedication to rigorous scientific review, the Crazy 8 Initiative will create a roadmap to tackle the most pressing problems facing researchers.
Each year, ALSF-funded Young Investigators gather to share their research, network and collaborate on ways to innovate their research.
Accelerating breakthrough research for hard to treat cancers like DIPG is critical. ALSF-funded researcher, Dr. Michelle Monje, recently discovered that a type of immunotherapy shows promise in the treatment of this deadly brain tumor.
Willow’s family needed to make a 1,000 mile road trip every three months for her treatment for a rare brain tumor. The ALSF Travel for Care program was able to provide her with immediate financial support to receive her treatment at a facility far from home.
There is enough publicly available disease data at the National Institute of Health to fill up several hundred Libraries of Congress and through ALSF’s investment in technology, the Childhood Cancer Data Lab is translating that data into one consistent format for researchers to access and use.
Supporters, like the Lemonettes, take a stand every day for cures. The sister duo has raised more than $15,000 since 2012.
The inspiration for all the work we do begins and ends with our supporters. Dr. Glen Samuels and his patient, Malina, worked together to identify a biomarker for Ewing sarcoma. Dr. Samuels used Malina’s donated blood sample in the lab to study what happens in the blood when a child has Ewing sarcoma.
by Trish Adkins
Starting with her very first lemonade stand, Alexandra “Alex” Scott, Alex’s Lemonade Stand Foundation (ALSF) founder, sparked a movement—a movement not only to help sick kids get better and find cures for childhood cancer; but one that would inspire and call on each one of us to work together.
Over the last 13 years, childhood cancer heroes and their families, donors, volunteers, and of course, researchers have come together for one goal: cures for childhood cancer.
At ALSF, we have learned that curing childhood cancer is not just a product of... Read More
You can rack up the miles this September and together, we can find cures for childhood cancer!
Get your dog in on The Million Mile tracking fun!
Lace up those sneakers and get ready to track some miles.
You can join The Million Mile anytime in September and track your miles during the biggest childhood cancer awareness challenge!
by Trish Adkins
September brings new beginnings to families everywhere. It’s a new school year and sports, dance and other extracurricular activities begin. It’s also Childhood Cancer Awareness Month, and around the hallways of Alex’s Lemonade Stand Foundation (ALSF), it is time for The Million Mile, a month-long awareness campaign. In honor of Childhood Cancer Awareness Month, supporters everywhere join together to track the miles that they walk, run and cycle. ... Read More
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