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Vienna’s condition
The condition is rare and there was no way for anyone to tell how much the birthmark would grow as the little girl grew. Her mother was sure that she did not want her daughter to deal with that as she grew up.
Casey immediately asked doctors what could be done for her daughter’s birthmark. She said that she felt that if she did not get her daughter’s birthmark removed, she might resent her parents in the future.
The concerned mother said, “We love seeing her grow on her journey, and we can’t wait for the day that she does grow up and can speak for herself so we can hear her opinion, we’d love her no matter what, even if we did keep the birthmark.”
The reason for her ambition was that when their daughter was an infant, Casey, and her partner had already noticed that people were staring at her. She also saw that her baby was being treated differently than other babies and, hence, was even more motivated to get the birthmark removed.
The surgery was denied by the NHS and the mother had to find alternate sources for help. So, she began a crowdfunding campaign to raise funds for having the surgery done privately.
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