A relieved mother recently shared the heartening moment her baby girl bid farewell to a birthmark on her forehead. But not first facing criticism from the medical authorities.

Meet the story of Celine Casey and her two-year-old daughter, Vienna Shaw, who was born with a congenital melanocytic nevus (CMN) on her forehead, an uncommon birthmark that affects only one out of every 20,000 newborns. When finding out about the birthmark, Celine was filled with concern, feeling as though she might have somehow made a mistake during her pregnancy, with no understanding of what the birthmark would mean for her daughter. What she did know was that she wanted it eliminated, aiming for her daughter to grow up without feeling different.

Although the birthmark held no implications for Brookshaw’s physical well-being, Casey understood the potential impact it could have on her mental well-being as she matured and encountered other children who might be inquisitive about her condition. Celine mentioned that at certain points, the family used to conceal Vienna’s birthmark by covering her face, “We went out daily with her, and we got a few stares.”

When they approached the NHS for assistance, the family was met with discouraging feedback. Physicians couldn’t proceed with the operation to eliminate the mark as it would qualify as a cosmetic procedure.

But the parents didn’t see it like that. They were deeply afraid of other kids teasing her, impacting her mental health from a young age. Casey was also concerned that if they didn’t remove the birthmark, her daughter might come to resent her and her partner.

The parents decided to act on their own and raise the necessary money privately. After organizing crowdfunding, they raised $52,000 in 24 hours. However, hospital costs increased in 2020, and they needed to raise an additional US$27,000. With a new funding request, they finally met their goal.