In a picture-perfect self-portrait shared just last Friday from her beach vacation during the festive season, she proudly displayed the unmistakable beauty she inherited from her mother.
Resembling her mother, Catherine, during the iconic era of “The Darling Buds of May”, the 20-year-old actress captured the spirit of her mother’s portrayal as Mariette in the beloved 1990s series. This marked the inception of Catherine’s remarkable acting journey.
Amidst her holiday celebrations, Carys donned a stylish brown bikini, showcasing her radiant beauty in a casual selfie. Additionally, she treated her followers to a sneak peek of her cozy cabin retreat, giving insight into her literary preferences, including a focus on Kahlil Gibran’s masterpiece “The Prophet”.
Earlier in the current year, Carys captivated her audience with a collection of videos showcasing her musical prowess. From her impressive vocal range to her adept piano playing, she earned accolades from none other than her mother, who lauded the interpretations as “captivating” and “remarkable”.
Carving her unique niche in the world of entertainment, Carys is gracefully treading her own path while embracing the legacy of her illustrious parents. In a recent captivating video, she took center stage alongside the Honky Tonks, the resident band at Hus Mals og Menningar bar in Reykjavik, Iceland.
The performance was met with such admiration that one of the band members even knelt before Carys, expressing heartfelt praise as the act reached its conclusion. Posting the video on Instagram without any caption, Catherine couldn’t contain her pride, leaving a comment that resonated with joy, saying: “Carys!!!! Incredible! Wish I could be there. Love you. Have a blast, my darling”. Sibbi, the lead singer of the band, acknowledged Catherine’s comment, affirming Carys’s amazing talent and shedding light on their nightly renditions of “Shallow” featuring different guest singers.
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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