Born on March 7, 2019, Luna Tavares-Fenner instantly stood out with a rare birthmark across her face, earning her the nickname “Batman girl.” Behind the nickname was a serious medical concern—her congenital melanocytic nevus carried a high risk of melanoma.

Her parents, Caroline and Thiago, saw only her beauty, but they couldn’t ignore the stares, cruel comments, and potential health dangers. Determined to protect her, they sought treatment overseas with Dr. Pavel Popov, avoiding the harsher surgeries offered in the U.S. With help from loved ones and a generous anonymous donor, Luna underwent six operations to remove the mark.

The journey wasn’t easy—at one point she couldn’t close her left eye for months—but her spirit never wavered. At just two years old, she proudly declared, “My black spot is gone. I am a princess.”

In 2024, Luna’s story was published in a book to raise awareness and funds for ongoing procedures. That same year, she reached a huge milestone—starting public school. Worried about bullying, her mom worked with teachers to educate Luna’s classmates about her condition. The result? Luna comes home each day smiling and excited for school.

The road ahead still includes more surgeries, but Luna continues to face life with joy, courage, and the unwavering love of her family.