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.
THIS ITALIAN TEEN’S 2006 DEATH COULD MAKE HIM THE FIRST MILLENNIAL SAINT!
Think about saints, and you might picture people who lived a long time ago. But there’s big news: the world might soon have its first millennial saint, someone who lived not too long ago!
Carlo Acutis, an Italian teenager, could become the first millennial saint. He passed away in 2006 when he was only 15 years old. Carlo is special because he’s known as the patron saint of the internet. He was really good with computers and used them to talk about his faith.
Carlo was born in London, but his family moved to Milan when he was little. He loved Catholicism from a young age. His passion for the religion was so strong that it even inspired his mom, Antonia Acutis, to rejoin the church. Even as a kid, he went to church every day.
From a young age, Carlo felt a strong calling to help others. He did things like giving to homeless people to make a difference. Before he died, Carlo used his computer skills to create a website to help others.
After he passed away, his mom got messages from people all over the world. They told her about miracles that happened after they prayed to Carlo. Some said they got better from cancer or became able to have children.
Carlo’s mom said he was like a light in the darkness of the internet. Some people even called him an “influencer for God” because they admired him so much.
Carlo’s mom, Ms. Acutis, believes her son’s life shows how the internet can be used for good things.
In 2020, the Diocese of Assisi, where Carlo’s family had property, asked the Vatican to make him a saint.
In February 2020, Pope Francis said a sick boy got better after touching Carlo’s shirt.
To become a saint, Carlo needs one more miracle. The Vatican says a Costa Rican student got better after her mom prayed to Carlo.
The Pope might call a meeting to talk about making Carlo a saint, but there’s no date for the ceremony yet.
It will be interesting to see Carlo become the first millennial saint! What do you think? Let us know in the comments and share this news with your friends and family.
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