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.
Nobody’s prepared for this challenge. Not emotionally, not financially, not in any sense. I think one of the things we are super grateful for is we had family, friends, community and organizations that were able to support us when we needed it the most. I know at the beginning of this it takes everybody by surprise. Marcelo, Valentina's Dad
