
The 19-year-old daughter of former NFL player Michael Strahan, Isabella, recently gave an update on her valiant fight against cancer. Isabella broke down in tears as she announced on social media that she would only need four chemotherapy sessions as opposed to the six that were initially scheduled. She was overcome with delight at hearing this unexpected news, which was a big step in the right direction for her recuperation.
Isabella was given a medulloblastoma diagnosis last year. This kind of cancer is found near the base of the brain. In January 2024, she courageously revealed her experience during an interview on Good Morning America, which made her diagnosis public. Isabella is resilient and unflappable in spite of her struggles.
“I feel fantastic. Not too awful,” Isabella said in the January interview, demonstrating her fortitude in the face of difficulty.

October 2023 marked the start of Isabella’s journey as she enrolled in her first year of college at the University of Southern California in Los Angeles. She sought medical attention when she began to experience recurrent headaches. As the symptoms worsened, nausea and trouble walking straightened out. When Isabella woke up one day in late October and started vomiting blood, her condition took a sharp turn for the worse. At first, her problems were thought to be caused by vertigo. She contacted her sister, who then alerted their entire family, as soon as she realized something was really wrong.
Isabella has fought cancer with incredible strength since learning of her illness. She gave a positive update in a recent YouTube video, revealing that she will only require four chemotherapy cycles as opposed to the original six. Knowing that Isabella is halfway through her therapy, the burden on her shoulders began to ease, and she shed these happy tears.
I’ll finish up in May. Isabella grinned and said, “And I can kind of try and have a summer to feel better.” And I’m overjoyed since I had assumed I would be finished by the end of July. My goal was to complete six rounds in all. After that, I would actually have to return to school immediately. I’m overjoyed.
’’We Got Stares’’, Parents Choose to Remove Baby Girl’s Rare Birthmark to Avoid Rude Reactions
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.
© viennarosebrookshaw / Instagram
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.
© viennarosebrookshaw / Instagram
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.
© viennarosebrookshaw / Instagram
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.
© viennarosebrookshaw / Instagram
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.
© viennarosebrookshaw / Instagram
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.
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