She has received backlash, meanwhile, for a recent social media post that many have referred to as “tone-deaf” that she made while in Greenland.
When the 82-year-old posed for the Sports Illustrated Swimsuit issue in May of this year, she garnered a lot of good attention; but, the same kind of excitement wasn’t sparked by her most recent Instagram post.
On Tuesday, August 29, Stewart shared a photo of herself during a voyage that included a view of Greenland’s east coast. The TV personality and businesswoman is shown in one of several photos, one of which has the caption:
As we approach a magnificent fjord on the east coast of Greenland, Swan Hellenic Cruises’ inaugural Zodiac cruise draws to a close. Indeed, for our cocktails this evening, we were able to grab a tiny bit of iceberg.
Fans were instantly incensed at Stewart for using the “small iceberg” as a symbol for her drink, even though it was most likely not her intention for the post to offend.
Stewart’s mention of a little iceberg in relation to the “ice caps melting” in her comments section quickly drew criticism from many.
The ice caps are melting, Martha, according to one Instagram user. Keep them out of your drink.
“In general, I adore Martha and her excesses because she’s all about gorgeous houses, gardens, and food, but drinking iceberg cocktails while the world burns seems a little tone deaf,” another person commented.
So while the planet heats due to the wealth of a few thousand individuals, millionaires travel to the melting icebergs, scoop them up, and use them to keep their cocktails cold. That line seems like it belongs in a dystopian novel. A third said, “Can’t make this shit up, haha.”
We still need glacier ice for cocktails, despite global warming and the melting of ice caps? Talk about tone def. Been a devotee for years, but recently, I’m out when I can’t afford food because I’ve seen enough caviar,” remarked a fourth individual.
When Stewart bravely posed in provocative swimsuits for Sports Illustrated’s cover in May, she made history. The 81-year-old revealed her previous stringent health routine as well.
Stewart stated, “I didn’t starve myself, but I didn’t eat any bread or pasta for a couple of months,” in an interview with Today.
“It was incredible that I attended Pilates twice a week, and I continue to do so because it is so beneficial.” Either way, I live a clean lifestyle with a balanced diet, consistent exercise, good skincare, and other practices.
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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