Michael Jackson’s Friend ‘Knew the Real Reason’ He Wore Single White Glove on Right Hand
Michael Jackson’s single white glove became one of his most famous fashion choices during his career. According to actor Cicely Tyson, she knew the real reason why he wore it. Tyson shared that she had been aware of what motivated Jackson to make this iconic glove a part of his look.
Michael Jackson Wore His Famous White Glove to Hide a Skin Condition, Says Friend
Michael Jackson’s iconic white glove became a signature part of his look during his career. According to a friend, the glove was originally designed to hide signs of vitiligo, a condition that causes patches of skin to lose color. Jackson, who passed away in 2009, often wore the glove on his right hand.
Vitiligo affects the skin, especially on the face, neck, and hands, and is caused by a lack of melanin, the pigment that gives skin its color. It affects about 1 in every 100 people.
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Late actor Cicely Tyson, who knew Jackson, shared this detail about his glove during his 2009 memorial service.
A single white glove became a signature accessory for the late Michael Jackson throughout his career. The glove, often worn on his right hand, was part of his iconic style. It was originally created to help cover the effects of vitiligo, a skin condition that causes patches of skin to lose their color. Jackson, who passed away in 2009, used the glove to make a fashion statement while also concealing the condition. Vitiligo affects around 1 in 100 people and is caused by a lack of melanin, the pigment that gives skin its color.
Late actor Cicely Tyson talked about Michael Jackson’s famous white glove in 2009 after his death.
Cicely, known for movies like *Sounder* (1972) and the TV show *How to Get Away with Murder*, spoke to CNN’s Don Lemon in an interview. She mentioned that she and Michael shared the same fashion designer in the 1980s, who worked on creating the glove.
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Cicely remembered the designer saying, “I’m doing this glove for Michael,” explaining that Michael was starting to develop vitiligo, a skin condition, on his hand. She said, “The glove was to cover it. That’s how it came about.”
When asked how she knew, Cicely replied, “I was there when he was creating it.”
Michael first wore the white glove in 1983. He later said, “I felt that one glove was cool… wearing two gloves seemed ordinary.”
Michael Jackson talked about his skin condition during a 1993 interview with Oprah Winfrey, likely referring to vitiligo, a condition that runs in his family.
Oprah asked him about the noticeable change in his skin color and addressed rumors about him possibly bleaching his skin, asking, “Is your skin lighter because you don’t like being Black?”
Michael, unaware of skin bleaching, explained, “I have a skin disorder that destroys the pigmentation of the skin. It’s something I cannot help.” He added, “When people say I don’t want to be what I am, it hurts me.”
He mentioned that he first noticed his skin changing after releasing *Thriller* in 1982. Michael said he used makeup to manage the blotches but denied bleaching his skin.
Oprah later remarked that in 1993, many people didn’t understand vitiligo and noted that it was a sensitive topic for Michael.
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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