Did She Really Go Bald? Fans Are Convinced After Jennifer Hudson’s Stunning AMAs Appearance!
This past weekend, during the American Music Awards 50th Anniversary special, Jennifer Hudson enthralled the crowd. Even though she gave her typical amazing singing performance, her haircut was the one that really got people talking.
It may be puzzling that a celebrity’s new hairdo would create such a sensation, but Hudson’s look had nothing to do with a daring new cut or color for the occasion. Rather, admirers of the 43-year-old vocalist conveyed their conviction that she had entirely shaved her head. We can confirm that, contrary to what many social media users thought, Jennifer Hudson has not truly gone “bald,” even though we are convinced she would still look amazing.
Legends like Mariah Carey, Nelly, and Nile Rodgers performed on Sunday night (October 6) to commemorate the American Music Awards’ 50th anniversary.
Fans’ confusion about the current artists’ lack of recognition during the ceremony dominated much of the conversation around the event. The simple answer is that the normal AMAs will now take place in March 2025 instead of as scheduled. As the name suggests, Sunday’s event was an anniversary special celebrating the awards’ half-century of relevance in the music business.
The surprises didn’t stop there, as Jennifer Hudson, 43, attracted a lot of attention with her presence.
For the occasion, the Dreamgirls actress chose a figure-hugging, glossy gown that emphasized her silhouette and exuded elegance.
One of the night’s most watched videos saw Hudson introducing Mariah Carey to the AMA stage. People on social media reacted angrily to her appearance in the clip, believing that she had cut off her hair.
On Instagram, someone wrote, “Not me thinking she went bald although she would look stunning.”
To the same post, another person replied, “Same. But she looks good in it. If she ever does, that is.
“Me too! I thought I was the only one haha until I saw the pony tail [sic],” a third person said.
“What made me believe Miss Hudson was bald? However, I think that would look fantastic,” remarked a fourth user.
“Jen, I thought you went bald for a minute,” a fifth person said.
One commenter said, “Lord thank God [..] she didn’t go bald.” Another said, ” “I thought she was rocking the bald look,” said another person.
It’s possible that fans remember Hudson’s 2015 bald hairdo. The singer at the time captioned a selfie she had uploaded to Instagram with her hair pulled back, saying, “Who needs hair when you’re serving face!”
Recall that the centerpiece of Hudson’s AMAs performance ought to have been her stirring rendition of “I Will Always Love You,” a smash song made popular by Whitney Houston in the 1992 movie The Bodyguard.
Prior to her amazing performance, Hudson was questioned about her relationship with the late Whitney. “What is my connection to Whitney Houston?” she asked in response. The gospel, you know, the presence, is a gift, in my opinion. I was just struck by it at a young age. I doubt that there was ever a moment when I was unaware of Whitney.”
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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