At times, our bodies seem to sense when something isn’t quite right. Actor Mark Ruffalo shared a fascinating story during his recent talk on a podcast. He got a bad dream that turned out to be unwanted reality.
Bad news came when they were expecting their first child.
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Back in 2001, while busy filming The Last Castle, doctors discovered a harmless brain tumor behind his left ear. What’s intriguing is that Ruffalo had a strange dream before this, almost like a warning. He felt compelled to see a doctor urgently after the dream, even though he didn’t have any obvious symptoms except for a minor ear problem.
«It wasn’t like any other dream I had had. It wasn’t even a voice, it was just pure knowledge: ’You have a brain tumor, and you have to deal with it immediately,’» Rufallo shared.
Ruffalo had to make a hard decision in order to protect his wife.
Ruffalo was hesitant to worry his wife, who was about to have their first child, so he kept the news to himself until after the birth. When he finally told her, she was understandably upset saying, «I always knew you were gonna die young!»
Ruffalo underwent surgery to remove the tumor, but it wasn’t without risks. There was a chance he could lose his hearing or have facial paralysis. Sadly, he did lose his hearing in left ear permanently.
«Take my hearing, let me keep the face, and just let me be the father of this kid,» The Incredible Hulk actor recalled thinking at the time.
Despite these challenges, Ruffalo didn’t let them hold him back. He continued his acting career and even received his fourth Academy Award nomination. Alongside his professional success, he treasures his role as a father to his three children: Keen, Bella Noche, and Odette.
Mark Ruffalo’s heartfelt tribute to his wife, Sunrise, reflects their enduring love story. Despite humble beginnings, Ruffalo’s rise to Hollywood stardom was accompanied by Sunrise’s unwavering support and companionship. She played a significant role in his life journey, standing by him through thick and thin, showcasing the strength of their bond and partnership.
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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