It’s not easy to be a parent of a haughty, disrespectful adolescent, and parents use numerous strategies to discipline their kids.
A mother named Heidi Johnson shared a handwritten letter she penned to her son Aaron on Facebook. She had no idea the post would become very popular. She had no intention of making the post public at all. Although it was only intended for her friends to see, she is not sorry that she posted it online.
Johnson chastised her 13-year-old son for treating her like a “roommate” in a letter to him. She continued by giving him an itemized bill totaling more than $700 for food, rent, and other expenses. She would treat him like a roommate if he was going to treat her like that rather than his mother.
Johnson wrote, “Love Mom,” on the note, and she genuinely does adore her son. She wrote a second post in response, giving some more information on the circumstances. “I am not going to put my 13-year-old on the street if he can’t pay his half of the rent,” she promised parents who were condemning her. I don’t want him to make any payment. I want him to value the blessings and gifts we have, and to take pride in his house and surroundings.
She went on to say that she never meant for Aaron to cover the cost. Rather, she desired that him “acquire an understanding of what things cost.” Johnson wanted her kid to know “what life would look like if I was not his ‘parent,’ but rather a ‘roommate,’” so she penned the note. It was from the start a lesson in appreciation and decency.
Johnson added that her son had lied to her before she wrote the note about finishing his homework, and that he had said, “Well, I am making money now,” in response to her warning that she would be limiting his internet access. She clarified that the money he was talking about was a small amount of money he was earning from his YouTube channel, not nearly enough to cover his rent and food expenses.
Johnson’s relationship with her son has not been harmed by the public statement. “He and I still talk as openly as ever,” she clarified. He has expressed regret several times.
Since she sent the note to her kid, Johnson has also been asked for guidance by parents. As she puts it, “People feel comfortable coming to me and asking for advice, venting, or even just having someone bear witness to their experience by listening, opening up, and sharing a piece of myself in return. It seems like my post has opened a door.”
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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