The question of what is going on behind closed doors at Windsor is one of the most asked questions during the last couple of months, or better said since Kate Middleton‘s last public appearance.
The Princess of Wales had undergone a “planned” abdominal surgery in mid-January and ever since, her exact health state or whereabouts haven’t been discussed by the Palace except for the statement which came as a for of reassurance that she was “doing well,” and that they won’t be sharing any details except when they feel something truly significant takes place.
The people of Britain, as well as those from around the world who closely follow the situation involving Kate and the rumors surrounding her state, were given a glimpse of hope when the Minister of Defense confirmed that she would be attending the Trooping the Colour dress rehearsal ceremony on June 8, ahead of the main event on June 15.
However, it later turned out that it was a mistake and that Kate’s potential return to royal duty event has been deleted from an Army website. As per GB News, Kensington Palace was “not consulted” regarding the Princess of Wales’ appearance.
“It seems the MoD jumped the gun with this announcement and that Kensington Palace was not consulted…we will have to wait to see if the PoW will be well enough to attend,” Telegraph royal reporter Victoria Ward posted on X.
What’s most, the event’s overview mentioned Kate’s presence multiple times.
“Trooping the Colour reviewed by Her Royal Highness The Princess of Wales is identical to Trooping the Colour reviewed by His Majesty The King,” “Trooping the Colour reviewed by Her Royal Highness The Princess of Wales also includes 250 soldiers from the Foot Guards,” and “The soldiers will be inspected by Her Royal Highness The Princess of Wales, Colonel Irish Guards.”
The site removed every information related to Kate and the event as well as her photo on the site’s landing page.
Kate hasn’t been seen in public for a long period of time, which is very unusual for a royal of her rank.
The public could last see her on a photo taken by TMZ, which some claimed was staged.
She also posted a photo herself on Mother’s Day on which she could be seen together with her children, but it was later determined the photo had been edited at parts which led to the news agencies to issue “kill notices,” which are advisory notices to remove or not use a specific photo.
“It appears that the source has manipulated the image,” the Associated Press notification read.
They also released a statement, saying, “The Associated Press initially published the photo, which was issued by Kensington Palace. The AP later retracted the image because at closer inspection, it appears that the source had manipulated the image in a way that did not meet AP’s photo standards. The photo shows an inconsistency in the alignment of Princess Charlotte’s left hand.
Although the Palace didn’t comment on the edited photo, Kate herself decided to explain why the image had “flaws.”
On her and William’s official X account, she wrote, “Like many amateur photographers, I do occasionally experiment with editing. I wanted to express my apologies for any confusion the family photograph we shared yesterday caused. I hope everyone celebrating had a very happy Mother’s Day. C.”
Kensington Palace has later confirmed it “would not be reissuing the original unedited photograph of Kate and her children.”
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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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