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.
“She’s a real Thumbelina” – Meet the girl who’s only 99cm tall and defied all the odds
Kenadie Jourdin-Bromley, a Canadian child from Ontario, seemed ordinary at first glance.
She had high hopes for the future, loved sports and drawing, and went to school.
Nonetheless, one characteristic set Kenadie apart from her peers: her diminutive height of 99 centimeters.
Reports state that when Kenadie was born in February 2023, she weighed a mere 2.5 pounds. Her condition was quickly diagnosed by doctors as an uncommon form of cardiovascular disease, thought to affect only 100 people globally. The nurses dubbed her “Thumbelina,” quite fittingly.
Regretfully, Kenadie had slim chances of surviving.
According to reports, the girl’s condition can lead to complications like delayed mental development, respiratory issues, and digestive issues. Doctors at the hospital where the girl was born were concerned that she wouldn’t have much time to live due to her brain injuries.
Understandably, her parents were devastated. In order to give their little girl a name in case she passed away, they chose to christen her on the day of her birth.
“We thought we were going to take her home to die, because that’s what the doctors told us,” mom Brianne explained to Barcroft TV back in 2016.
Still, as the days went by, Kenadie steadfastly refused to give up. After she triumphed over all the challenges and hardships, her parents were able to dream again that she would survive. It was nothing less than a miracle for them.
Many years later, Kenadie still astounds everyone she encounters. She is only 99 centimeters tall, her arms and legs are still immature, and she struggles to learn new things, but she is a content young girl who enjoys life to the fullest.
Kenadie reportedly enjoys bowling and ice skating. Above all, she makes people happy that she meets.
“Kenadie makes me laugh. She’s very empathetic – if you hurt your finger she comes and gives you a hug. She’s got an infectious laugh that makes you want to laugh along with her,” Kenadie’s assistant Jessica Putnam mentioned to Barcroft TV in 2016.
Naturally, Kenadie and her family face many new challenges in their lives. Despite her loved ones’ best efforts to take each day as it comes, the young girl is continuously dealing with medical issues.
“My hope for Kenadie’s future– my biggest hope for her– is I want her to be happy. I want her to smile and be successful. If we can get through today, then we’ll see about tomorrow,” her mom said.
We are happy to share Kenadie’s inspiring story!
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