Childhood Cancer Heroes

You are here

Omari Lowe

Click the images to see them larger above!

Learn more about
Acute Lymphoblastic Leukemia (ALL)

Get the facts about Acute Lymphoblastic Leukemia (ALL) and how our research projects are making a difference.

Learn More »

Omari might be on the shy side, but when he steps onto a football field, he comes alive. Like most high school boys, Omari loves to play video games. Once he’s completed high school, Omari has dreams of attending a college where he can continue to play football.

During his junior year, Omari began feeling fatigued. He couldn’t seem to keep his food down and had two swollen lymph nodes beneath his chin. After a workout in July, Omari started vomiting, and his mom decided to take him to the emergency room, thinking it was a virus.

They waited hours for his blood test results to find out that, due to a high count of white blood cells, it was likely that Omari had acute lymphoblastic leukemia. He was transferred to St. Mary’s Hospital, where doctors discovered 70% of his white blood cells were already overtaken by leukemia. He had to begin chemotherapy immediately.

Now, Omari receives treatment once a week, but the COVID-19 pandemic has added some unprecedented challenges to an already difficult situation. In March, Omari’s mom was temporarily laid off. Luckily, Alex’s Lemonade Stand Foundation was there to help out by taking care of things like gas expenses. Omari’s mom, Tammy, expressed that her gratitude towards organizations like ALSF for the financial and moral support they provided in a particularly difficult time goes beyond words.

Information provided by Tammy Turner, Omari’s mom
Updated June 2020

Next Hero

Donate in Honor of Today!

Your donation helps to fund critically-needed research to find better treatments and cures for children with cancer.

Childhood Cancer Heroes

More Heroes

VIEW ALL HEROES
Katana was a creative spirit, sharing stories and developing movies in her head with her action figures. Her imagination ran wild and her heart was big. While she passed away at just 3 from leukemia, her parents continue to raise awareness in her honor.
At 15 months old, August was diagnosed with bilateral retinoblastoma. By the time her family found out, she was basically blind. ALSF's Travel For Care program helped August get to the treatments she needed, and today she is 3 years old and can see!
VIEW ALL HEROES