Childhood Cancer Heroes

You are here

Drew Herrell

  • Rhabdomyosarcoma

Click the images to see them larger above!

Learn more about
Rhabdomyosarcoma

Get the facts about Rhabdomyosarcoma and how our research projects are making a difference.

Learn More »

Drew is a witty and funny 9-year-old who always makes his family laugh. He loves LEGOs, going to the arcade, seeing movies, and having a boys’ night out with his dad.  

In 2019, after a few weeks of Drew experiencing vague symptoms like fatigue, a fever, pain opening his mouth and pain in his leg, Drew’s family noticed a lump on the right side of his jaw. His mom, Emily, took him to the ER, where doctors found a five-centimeter tumor in his jaw. On May 10, Drew was diagnosed with stage 4 embryonal rhabdomyosarcoma, with primary site of the right jaw muscle and metastatic sites of his lungs, lymph nodes, spine, pelvis, and the long bones of his arms and legs.  

Drew put on a tough face for his following 42 weeks of frontline chemotherapy and six weeks of proton radiation. He then had an additional week of proton radiation to his lumbar spine and right hip before starting six months of maintenance chemo. He and his family were ecstatic when his port was removed in February 2021.

Drew had an eventful spring in 2023, first going through the removal of some swollen lymph nodes that were thankfully not cancerous, and then dealing with an abscess that formed where his surgery was, being inpatient for four days. He is now all recovered and enjoying his summer. He's also grown 5% in height from taking a growth hormone for eight months. 

Drew is his family’s hero because he rarely complained about his situation, and never asked “why me”. He took it all head-on. His frustration with having cancer is always short-lived, which has been a good lesson for Emily. His empathy and love for others is also inspiring. 

Emily dreams that her son is not defined by his cancer and the limitations his treatment has caused. She prays that he gains confidence in himself and knows how amazing he is, and that he continues to have his witty and hilarious personality. 

“This is the hardest thing ever,” said Emily about all families facing a childhood cancer diagnosis. “The only way is through – one day at a time.” Foundations like Alex’s Lemonade Stand Foundation give her hope that we are getting close to a cure! Emily, Drew, and their family held a lemonade stand during Lemonade Days in 2023 and raised $560 to help move that research forward.

“If you don’t know what to do, do something nice for someone else.” - Drew 

Information provided by Emily H., Drew’s mom
Updated June 2023

Next Hero

Donate in Honor of Drew 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
Jason is a high school student who plans to get a PhD in mathematics. When he was 2 years old, he was diagnosed with Ewing sarcoma. He had a rotationplasty, a surgery that saved Jason's leg, and his life. He's been able to remain active 13 years later!
Kaitlyn is a determined girl who is a bright light in a dark room! After what her family thought was a volleyball injury, Kaitlyn was diagnosed with osteosarcoma of her left femur. Recently, Kaitlyn sadly relapsed with the cancer in her lung.
McKenzie is a big prankster – while in the hospital, she would often silly string her nurses and doctors! She was diagnosed with both Hodgekin lymphoma and Supraventricular Tachycardia and went on a 15-week treatment plan. Today she has reached remission!
Kno’lan is a little guy with a BIG personality. He was diagnosed with Langerhans cell histiocytosis (LCH), a rare cancer-like disease, and has relapsed three times. Today, his family is traveling to Texas in search of his cure.