The sky often treats us to new wonders like meteor showers, intriguing planets, and captivating lunar eclipses. However, it’s not just about new arrivals in space — some things are saying their goodbyes and Saturn’s famous rings are on the way out. Scientists are closely monitoring this phenomenon.
Soon, Saturn’s rings are going to disappear from our view.
© NASA / JPL / Space Science Institute / Wikimedia Commons, © Public domain
Those iconic rings we’ve admired from Earth will no longer be visible in just 18 short months. These rings are composed of a mix of icy and rocky bits, often dust-coated, encircling the sixth planet in our solar system. But the reality is, even though it might not seem soon in human terms, they are on the path to becoming invisible to us by 2025, a cosmic blink of an eye. While the full disappearance will take millions of years, the show in the night sky won’t last much longer.
© NASA / JPL-Caltech / SSI / Wikimedia Commons, © Public domain
Here’s why this is happening: as Saturn orbits the Sun, its tilt angle will drop to zero on March 23, 2025. When this tilt reaches zero, it essentially means that Saturn will present itself perfectly on its side to us here on Earth. Saturn is about 746 million miles away from us at its nearest point, and when it’s sideways, we won’t see its iconic rings. This unique alignment will occur again on October 15, 2038, and then in quick succession on April 1 and July 9, 2039.
© NASA / ESA / A. Simon (Goddard Space Flight Center), M.H. Wong (UC Berkeley), OPAL Team / Wikimedia Commons, © Public domain, © NASA / JPL / Wikimedia Commons, © Public domain
After Saturn’s rings disappear in 2025, we won’t get a full view of them again until 2032. Saturn’s rings are tilted towards our planet at an angle of nine degrees. By next year, this tilt will reduce to only 3.7 degrees. We haven’t witnessed this disappearing act since September 2009; prior to that, it hadn’t occurred since February 1996. So, it’s a relatively rare event for skywatchers to witness.
NASA captured an image of an unusual celestial object resembling a question mark.
© Joseph DePasquale (STScI), Anton M. Koekemoer (STScI) / NASA, ESA, CSA
NASA’s James Webb Telescope has spotted a mysterious object shaped like a question mark. Although the true nature of this object is currently unknown, scientists have some speculations about it. This intriguing discovery has piqued the interest of astronomers and researchers eager to learn more about this enigmatic celestial feature.
© Joseph DePasquale (STScI), Anton M. Koekemoer (STScI) / NASA, ESA, CSA
The object is part of the Herbig Haro 46/47 star system, where two young stars orbit each other under the influence of gravity. These stars are located in the Vela Constellation, approximately 1,470 light-years away from Earth. The object’s distinct question mark shape is of a reddish hue, signifying it is more distant than the other stars in the image.
The true nature of this celestial entity remains a puzzle, but its unique shape and color provide some hints. It may represent a distant galaxy or even the result of two galaxies colliding, which gives it the distinctive question mark appearance. This interpretation is supported by experts at the Space Telescope Science Institute (STScI) in Baltimore.
The search for extraterrestrial life continues, and with technological advancements and our understanding of the cosmos, we may one day make significant discoveries. In the meantime, exploring the wonders of the starry sky through cosmic images can be a truly enchanting experience.
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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