Bella's Compassionate Heart


Bella, 5, fighting hepatoblastoma

When 5-year-old Bella complained of incredible pain in her tummy, her parents were worried right away—Bella's not a complainer. Her dad, Travis, brought her to the emergency room where doctors assured them it was just constipation. Weeks later, Bella's mom, Tabitha, noticed a hard lump in Bella's abdomen, so at Bella's next checkup, she brought it up to the doctor.

"I could tell by the look on the doctor's face that something wasn't right," Tabitha says.

The next day Bella had a surgery, so doctors could get a piece of the mass and determine what it was. After the surgery, an oncologist sat down with Tabitha and Travis to give them the news that would change their lives. Bella had hepatoblastoma—liver cancer.

"My heart just dropped to my feet and I had tears streaming down my face and a lump in my throat—we just lost all sense of time in that moment," Tabitha says.

What came next was a flurry of X-rays, blood tests and other procedures. Bella had a port placed in her chest and began her first round of chemo just a few days after the diagnosis. For Tabitha, the hardest thing about Bella's cancer journey so far is watching the multitude of tests and procedures become her daughter's new normal.

"In the beginning, if Bella was going through a CT scan or X-ray or port access, she would give me this look of, 'Why are you doing this to me, Mom?'" Tabitha says. "She handles all of these things really well now, but that look still happens from time to time and it breaks my heart."

Since being diagnosed, Bella has had procedure after procedure, including a liver transplant that took doctors 11 hours. One thing that makes everything a little less scary is Bella's doll, Jessie. Jessie has had every poke and procedure that Bella has had, and she goes to every appointment. She even has a mini-ostomy bag to match Bella's—but Jessie's holds M&Ms, as Bella will tell you with a giggle. Tabitha says having Jessie helps Bella understand what's going to happen and makes everything a little less scary.

BellaBella is a girl's girl—she loves dressing up, the color pink and the TV show "Peppa Pig." Her laugh is so infectious that she has won the hearts of many doctors and nurses. But Tabitha's favorite thing about her giggly, upbeat daughter is her compassion for others. No matter what she's going through, Bella wants to check in with her family and friends to make sure they are all doing well.

"She thinks about everyone else before herself," Tabitha says. "If her little brother, Ian, isn't with her, she wants to know what he's doing and if he's OK. She's always thinking of her friends and cousins, and she makes art for them to tell them she misses them. She's an incredibly caring girl."

This difficult journey has brought Tabitha's attention to childhood cancer as a whole. She's amazed and frustrated by what she's found—that research into treatments for cancers like Bella's doesn't have enough support to move forward.

"Bella's cancer is rare, but it's on the rise in kids, and it's not really being researched enough. When I found that out, all I could think was, 'Why not?'" Tabitha says. "Why aren't we there yet? And it's because researchers don't have the funding."

The road in front of Bella and her family is still unclear, but their old "normal" is in the past. Bella will be on certain medicines for the rest of her life to make sure her body doesn't reject her new liver, and she'll have regular labs and appointments for the foreseeable future. Tabitha's hope for Bella is that she can do the normal things kids her age should be doing, like starting kindergarten and playing with her brother and friends, all free of worry and pain.

"She's a brilliant 5-year-old; she's done a lot of learning through this whole process," Tabitha says. "All I want now is for her to get to play like a 5-year-old should."

Help us continue our work to find new treatments for kids like Bella by making a gift to Children's Cancer Research Fund. Contact Amy Polski Larson at or 952-224-8486 to learn more.