Raman Bahal, Ph.D., a St. Baldrick’s Research Grant recipient at the University of Connecticut, Storrs, Connecticut, explains Burkitt Lymphoma symptoms, treatment options, and research opportunities.
Today, Feb. 15, 2019, marks this year’s International Childhood Cancer Day.
While the St. Baldrick’s Foundation might be thought of as just an American organization, the fact is that the research we fund has global reach – so we thought that we’d share a few snapshots of just how global our organization really is, and how our funding and your support are making a true impact for kids with cancer throughout the world.
February 4th is World Cancer Day. Established in 2000 at the World Summit Against Cancer in Paris, World Cancer Day promotes awareness, research, and services dedicated to helping people conquer cancer.
It’s an appropriate time, then, to reflect on the efforts of the St. Baldrick’s Foundation to fight childhood cancers around the world.
Founded in New York City and currently headquartered in Los Angeles, St. Baldrick’s has deep roots in the United States. But the organization has been very active beyond America’s borders, funding a variety of promising research projects that can help fight childhood cancers in the near and distant future.
Investing in the next generation of childhood cancer researchers — like researcher and St. Baldrick’s International Scholar Dr. Joseph Lubega — can change the lives of kids with cancer all over the world. Read on (and watch a video shot at the Uganda Cancer Institute) to learn more about the huge impact Dr. Lubega is making on kids with cancer in East Africa.
When Belinda heard, ‘leukemia,’ she was terrified.
She feared cancer. Belinda saw the impact it had on her family. In fact, she’d attended her cousin’s funeral in the spring. But cancer striking her 5-year-old daughter, Christa? How could that happen?
Last month, Ambassador Aaron finished his first semester at college and came home for a clinic visit to make sure he was still in remission. His mom, Dana, shares their good news and her hopes for 2016.
Aaron with his parents, Dana and Greg.
Joey was an energetic, mischievous kid who loved Legos and Spongebob. After he passed away from childhood cancer, his family attended their local St. Baldrick’s event to fight for a cure in his honor. Read on to learn how the event has come to be a cherished family tradition.
Joey on his fourth birthday, 10 months before he was diagnosed with childhood cancer.
Joey’s childhood cancer story is similar to others. He was a happy, active preschooler with a mischievous side and a love of Legos and SpongeBob. Everything was pretty normal until a few months before his fifth birthday when he developed flu-like symptoms that wouldn’t go away.
Two and a half years ago, Ambassador Aaron was just finishing treatment for non-Hodgkin lymphoma. He’s still in remission, and this week he’s starting his freshman year of college over 300 miles away from home. He shares this quick update.
Aaron stands with his family at his high school graduation ceremony.
Leslie shares her thoughts before her first shave last year with the 46 Mommas.
Leslie with her son, Brian, before shaving her head with the 46 Mommas. Brian is in remission from Hodgkin lymphoma.
Aaron was always the picture of health. Then at 15, the avid athlete was diagnosed with Burkitt non-Hodgkin lymphoma. Aaron wasn’t unfamiliar with childhood cancer. He had been a St. Baldrick’s shavee since the age of 11 and even created a team called the Bald Buddies.
Ambassador Aaron, his dad, Gregory, his mom, Dana, and his sister, Rita, proudly display the Team Aaron banner.