A happy mom recently told the story of how her little girl said goodbye to a birthmark on her forehead, even though they initially faced some criticism from doctors.
A very uncommon birthmark.
© viennarosebrookshaw / Instagram, © viennarosebrookshaw / Instagram, © viennarosebrookshaw / Instagram
Here’s the story of Celine Casey and her two-year-old daughter, Vienna Shaw. Vienna was born with a rare birthmark called congenital melanocytic nevus (CMN) on her forehead, which only occurs in one out of every 20,000 newborns.
When Celine learned about the birthmark, she felt worried and wondered if she had done something wrong during her pregnancy. She didn’t know what the birthmark would mean for Vienna but was determined to remove it so that her daughter could grow up without feeling different.
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Even though the birthmark didn’t affect Brookshaw’s physical health, Casey knew it could impact her daughter’s mental well-being as she grew older and interacted with other children who might be curious about her condition.
Celine shared that the family sometimes used to hide Vienna’s birthmark by covering her face when they went out. She said, “We went out daily with her and got a few stares.”
The surgery was challenging.
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When they sought help from the NHS, the family received disheartening feedback. Doctors couldn’t go ahead with the surgery to remove the birthmark, categorizing it as a cosmetic procedure.
However, the parents viewed it differently. They were genuinely worried about potential teasing from other kids, which could affect their daughter’s mental well-being at a young age. Casey was also concerned that if they didn’t remove the birthmark, her daughter might grow to resent her and her partner.
© viennarosebrookshaw / Instagram, © viennarosebrookshaw / Instagram, © viennarosebrookshaw / Instagram
The parents took matters into their own hands and privately raised the required funds. Through crowdfunding, they managed to gather $52,000 within 24 hours. However, due to increased hospital costs in 2020, they had to raise an additional $27,000. With a new funding request, they eventually reached their goal.
They encountered difficulties with doctors.
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Disagreements between the medical team and the parents have led to differing opinions. Vienna’s parents wanted the birthmark removed through surgery, but the surgeon refused to perform the procedure. The surgeon’s stance is rooted in the belief that the child should make the decision once she reaches an appropriate age.
After this controversy arose, Daniel Brookshaw, Vienna’s father, expressed his dissatisfaction with the doctor’s viewpoint. The doctor also consulted with a dermatologist who concurred with the surgeon, emphasizing that the birthmark doesn’t threaten Vienna’s health and is not cancerous.
The surgery was completed successfully.
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Vienna is now two years old, and her doctors have successfully removed her birthmark, leaving only a faint scar between her eyebrows. Casey regularly shares updates on Shaw’s scar and recovery process on her social media, and followers often comment on how beautiful her little girl looks.
Despite the birthmark being gone, Casey mentioned that they still have to travel between cities to check the healing of the scar and see if any additional procedures are needed beyond the three she has already undergone. Shaw is now enjoying the typical life of a two-year-old.
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This little girl’s case with her birthmark brings attention to the delicate balance between parental advocacy and a child’s autonomy in medical decisions. While her parents aimed to secure her social acceptance and well-being, medical professionals stressed the importance of respecting Vienna’s future autonomy over her own body.
This story serves as a reminder of the intricate ethical considerations that arise when navigating the boundaries of parental authority and individual autonomy, prompting broader reflections on the rights of minors in the medical realm.
Bruce Willis: A Remarkable Life
Fast forward to the present, and there’s a renewed interest in Bruce Willis’s career, specifically his iconic role in the 80s TV show “Moonlighting.” The show, also known as “Maddie & David,” has made a comeback on a streaming platform, thrilling fans worldwide. Glenn Gordon Caron, the creator of the series and a close friend of Willis, shared some touching insights about their recent interactions.
Glenn revealed that he has seen Willis’s health decline rapidly. Despite this, Willis remains enthusiastic about the comeback of “Moonlighting.” Glenn confessed that he tries to maintain regular contact with his dear friend and his family, acknowledging the significant impact the illness has had on Willis’s life.
Although Bruce Willis’s condition has affected his ability to communicate verbally, Glenn acknowledges that the essence of Willis remains intact. Glenn marvels at Willis’s recognition when they meet and describes him as a truly remarkable individual. Though he may have lost some linguistic abilities, Glenn emphasizes the enduring spirit of Bruce Willis.
In an interview with the New York Post, Glenn shared his admiration for his friend, highlighting the immense joy for life that Willis possessed. Each day brought enthusiasm and a zest for living to the fullest. It is this spirit that captivated those fortunate enough to spend time with him.
A Journey Filled with Love and Compassion
Bruce Willis’s wife, Emma Heming Willis, has been a pillar of strength throughout his battle with illness. In a recent appearance on the Today show, she bravely discussed the impact of dementia, both on the person diagnosed and their loved ones. Emma, who has two daughters with Bruce, emphasized that receiving a dementia diagnosis is a challenging experience for the entire family.
Emma admits that uncertainty clouds Bruce’s awareness of his illness. However, she finds solace in being the primary caregiver and having a comprehensive understanding of the disease. While it is undoubtedly painful, Emma sees it as both a blessing and a curse – a way to navigate this difficult journey alongside her husband.
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