Michael Strahan’s daughter, Isabella, recently talked openly about her ongoing fight with brain cancer. In a heartfelt video on her YouTube channel called “Vlog 8: Recovering from Chemo at home,” the brave 20-year-old described the intense physical pain she’s going through during her treatment.
Isabella explained how agonizing the pain is, comparing it to a “heart attack.” She talked about trying to ease her headache by using an ice pack on her newly shaved head. She honestly shared, “Everything hurts,” and mentioned how her eyes, mouth, and jaw feel strained.
Isabella bravely shared about the intense pain she’s experiencing. She described her eyes feeling strained and painful when she looks to the sides. She compared the discomfort in her mouth to having all her teeth pulled out without replacements, saying even her jaw and tongue hurt when she drinks water.
Isabella admitted she would rather have radiation or brain surgery than endure chemotherapy because of the extreme pain it causes her. She called this journey the toughest and longest she’s faced, expressing worries about possible complications like heart pain, vision loss, or tooth decay.
Despite these challenges, Isabella is grateful to be home and sleeping in her own bed after being in the hospital. While she felt safe there, she finds comfort in familiar surroundings. Her vlog also showed moments from her hospital stay and special times with her father, Michael Strahan, and her twin sister, Sophia.
Isabella shared this update after she and her father talked about her illness on Good Morning America. She explained how she first noticed headaches and feeling sick, but didn’t worry until she woke up one day throwing up blood. Doctors later found out she had a serious brain tumor called a medulloblastoma. Michael Strahan was away from Good Morning America for more than three weeks because of “personal family matters,” though he didn’t say exactly what was happening.
Even with all these challenges, Isabella is staying strong. She finished her last round of radiation treatment in January after freezing her eggs because of her illness. Our thoughts are with Isabella and her family during this difficult time.
Despite the danger: a woman with dwarfism boldly poses with her baby belly on the beach.
Most married couples get asked “when,” but Charli Worgan and her husband Cullen frequently received “why” questions.
The parents, who live in Sydney, are frequently in the spotlight due to their unique forms of dwarfism, most notably when Charli got pregnant with their first child.
After giving birth to their first child, the content Australian mother created a social media account to share updates on their family life with others. Little did she know how well-liked her account would become.
With two stunning daughters under their belt, Charli has amassed over 300,000 Instagram followers.
Charli recently revealed that she was fourteen weeks pregnant with her third child, but the announcement was bittersweet.
Charli has had to undergo thorough genetic testing during each pregnancy. Experts warn that if Charli and Cullen’s offspring inherit just one type of dwarfism, inherit both forms, or are of average height due to their genetic problems, the results might be fatal.
Charli expressed her disappointment at not being able to celebrate her pregnancy’s 12-week mark with her family, as most mothers do.
But at 12 weeks, I was preparing for a procedure called Chorionic Villus Sampling (CVS), which is similar to an amniocentesis, whereas most individuals are pleased to be able to announce their pregnancy. To check the embryo’s genetic composition, a big needle is placed into my abdomen to extract a sample of the placenta, which has a 2% miscarriage rate.
Their two daughters, Tilba, 4, and Tully, 2, each have one of the two varieties of dwarfism, so they waited to find out which of the four possible dwarfisms Charli’s third child would have.
In an Instagram post, Charli explained, saying, “Our child would be of ordinary height.”
Our child would have achondroplasia and be dwarfed similarly to me.
Our child would have geleophysic dysplasia, the same type of dwarfism that Cullen has.
As a result of inheriting both genetic defects, our child would be born with “double dominant dwarfism,” which is fatal according to every expert medical assessment. In the event that this had occurred, I could have decided to terminate the pregnancy or to go on and see how things turned out.
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