In 2011, Catherine, Princess of Wales, wore a second stunning wedding dress to celebrate her marriage to Prince William. But only 300 guests saw it.
Thirteen years ago, Kate Middleton captivated the world as she walked down the aisle with her father, wearing a breathtaking wedding gown designed by Sarah Burton for Alexander McQueen.
While her first dress made global headlines, Kate also wore a second dress at a private evening reception. According to a royal expert, this dress reflected how she truly wanted to express herself. Kate chose the British McQueen brand for its craftsmanship and respect for traditional workmanship.
The Palace stated at the time that she wanted a gown that combined tradition and modernity with the artistic vision of Alexander McQueen. The first dress, made of elegant French Chantilly and English Cluny lace, cost a staggering £250,000 and became an iconic symbol of her wedding day. However, her second dress, though less publicized, was just as special.
Stylist and royal fashion expert Miranda Holder explained that some royals change into a second wedding dress after the ceremony. This allows them to leave behind formalities and fully express themselves. Speaking to The Express, she said that having a second dress allows brides to show who they really are and how they want to feel after the formal ceremony and official photos.
Kate’s second look, while still formal, was simpler and more relaxed. Holder described it as “simple and sweet,” with a “very pretty” cardigan, but noted that Kate didn’t seem to have the chance to fully relax.
Which dress do you prefer? Here’s where you can find the secret message Princess Catherine hid in her look during her first public appearance after cancer treatment.
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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