Kurt Vogel Russell is an American actor.At the age of twelve, he made his screen debut in a western series.Russell’s portrayal in Mike Nichol’s Silkwood earned him a nomination for a 1983 Golden Globe for Best Supporting Actor.Massachusetts’ Springfield is where Russell was born.Bing, his father, was an artist as well.His mother is ballerina Louise Julia Russell.Kurt Russell reportedly has a virulent flesh-eating sickness, according to The Globe.The 65-year-old actor from Hateful 8 is said to have had unattractive ulcers under his lower lip, which are a result of Peutz-Jeghers Syndrome (PJS), a condition that has been connected to colon cancer.Cancer.According to Net, “people with PJS may have a lifetime risk of cancer of up to 93%.”Dr. Stuart Fischer, who does not treat Kurt, described the ulcers as “precancerous lesions that can become aggressive and dangerous if not treated immediately and properly.”
Immunologist and Maryland resident Dr. Gabe Mirkin concurs that Kurt “needs immediate testing” and thinks PJS could be the cause of the ulcers.He needs to start counseling right away.We must pray for Kurt Russell. The Globe also claims that Kurt recently got into a fight with Goldie Hawn, his 71-year-old longtime partner.In October, Kurt was supposed to be honored into Oklahoma City’s Hall of Great Western Performers.The Hollywood Walk of Fame already bears his name.Kurt, though, is unable to attend because of a “surprise medical issue.”The actor insisted in a statement that he need surgery, which his doctor stated was a necessary treatment that couldn’t be put off.
The Oklahoman reports that he is scheduled to undergo hip replacement surgery.”My doctors say it needs to happen in September, but I thought it could wait.”As much as I would have hoped to be there this year, I am pleased that the museum has decided to postpone our honor until 2022 so I can accept this wonderful prize in person, Russell stated in the statement.We applaud Kurt Russell on being inducted into the Hall of Great Western Performers!We hope that his treatment later this month goes well and he recovers quickly.
Bottom line: Despite having his name already on the Hollywood Walk of Fame, Kurt ought to be admitted into Oklahoma City’s Hall of Great Western Performers.Kurt, though, is unable to attend because of a “surprise medical issue.”The actor, 64, was spotted in New Orleans sporting cuts and bruises on his face and arms.Kurt Russell has a fatal flesh-eating sickness, according to The Globe.
A Man Who Was Called “The Tree Man” Was Able to Hold His Daughter Again After Many Surgeries
“The Tree Man” is a man whose life has been defined by a rare malformation in his hands. Once dubbed for his distinctive condition, he has undergone numerous surgeries, overcoming tremendous challenges on his journey. Now, with unwavering determination and the skilled hands of medical professionals, he has reclaimed a simple yet profound joy—holding his daughter once again.
Abul Bajandar has a rare condition called ’Tree Man’ Syndrome.
Abul Bajandar, a man hailing from Bangladesh, is afflicted with an extraordinary and rare condition known as ’Tree Man’ Syndrome. This hereditary condition, though non-contagious, is unfortunately incurable, and surgical interventions offer only temporary relief. Abul is not alone in his struggle, as there are others worldwide grappling with the challenges posed by this syndrome.
This syndrome manifests through the development of wart-like skin growths that bear a striking resemblance to tree bark. These growths, while initially small, have the potential to grow significantly in size, resulting in considerable disability for those affected.
He has it from a young age.
The onset of his condition began during adolescence, with small warts appearing on his body at the age of 13-14. Regrettably, as he advanced in age, the affliction rapidly escalated, affecting various parts of his body.
After 16 surgeries he was able to hold his daughter again.
After undergoing a series of 16 surgeries between 2016 and 2017 at Dhaka Medical College Hospital in Dhaka, Bangladesh, Abul Bajandar achieved a poignant milestone—he could once again hold his daughter. The surgical procedures aimed to remove the bark-like lesions from his hands and feet, offering a glimmer of hope in his battle against Tree Man Syndrome.
Bajandar shared the profound joy he experiences spending time with his daughters, emphasizing, “If I recover from this, I want to work again, to build a small business to help my daughters in her studies and to give them a good life.” These words reflect not only his determination to overcome the challenges posed by his rare condition but also his unwavering commitment to providing a better future for his family.
Throughout Abul Bajandar’s challenging journey with Tree Man Syndrome, he draws strength from the unwavering support of his wife and mother. In the face of the condition’s recurrence, their steadfast presence provides him with comfort and encouragement. Bajandar reflects on the transformative power of fatherhood, sharing, “When my daughter was born, she brought me the hope of life again. I didn’t want to leave her as an orphan. I felt like I must live for her.”
Abul Bajandar’s condition returned but he remains hopeful.
Despite facing the disheartening recurrence of his condition, Abul Bajandar maintains a resilient sense of hope. Doctors, initially uncertain about the possibility of the condition’s return, witnessed its reappearance. Undeterred, Bajandar expresses his unwavering optimism, declaring, “My only dream is to recover from this situation and live a healthy life.”
His poignant words reflect not only the personal challenges he endures but also a universal desire for health and well-being. Bajandar’s enduring hope shines through as he states, “All I can say is that I truly believe and hope that a cure exists for this disease.” In the face of adversity, his spirit remains unbroken, embodying the strength of individuals confronting rare and challenging medical conditions.
Another person born with a rare condition has defied societal norms and emerged as a symbol of extraordinary resilience. Meet the girl affectionately referred to as “Voldemort” due to being born without a nose.
Preview photo credit Tansh / Alamy Stock Photo, ZUMA Press, Inc. / Alamy Stock Photo
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