Valentina: Living with Pediatric Low-Grade Glioma

This story was originally published in May 2022 and has been updated to reflect Valentina’s current age

In June 2018, Valentina was diagnosed with a pediatric low-grade glioma with a BRAF mutation. At the time, she was only one year old. Surgery was not an option, so her family had two choices for treatment—traditional chemotherapy or an experimental treatment suitable for her type of mutation.

Valentina’s family originally chose to try chemotherapy for her treatment; however, after three days of infusions, the port didn’t work because it was impossible to access. The only other treatment option was an experimental treatment.

While Valentina’s parents, Jocy and Marcelo, and her older brother Mauricio weren’t prepared for this news, they are grateful to have been able to turn to communities like the Pediatric Brain Tumor Foundation’s for resources and opportunities to connect with other families.

Today, Valentina is a sweet seven-year-old who loves art, baking and swimming, just like her favorite princess Ariel. Like many other low-grade glioma patients, though, she faces the possibility of chronic relapses and significant challenges. Her brain tumor is currently steady, but she still must receive treatments to stop it from growing.

“A child with any kind of illness is a fighter. And it’s a fight that’s worth fighting alongside them,” says Valentina’s mom Jocy.

Because of the Pediatric Brain Tumor Foundation community, families like Valentina’s have hope. When you donate, fundraise, or volunteer with the Pediatric Brain Tumor Foundation, your support accelerates the development of safer ways to diagnose and treat pediatric brain tumors and provides families with the resources they need.

Ready to change kids’ lives? Check out our Get Involved section for ways you can make a difference today!