A mother of four was shocked when New Hampshire’s DMV told her she had to give up the vanity plates she had for 15 years.
The plates were a playful reminder to her sons to use the bathroom before getting in the car. However, the DMV didn’t see it that way and decided the plates referred to “sexual or excretory acts.”
In 2019, Wendy Auger from Rochester, New Hampshire, was told by the DMV to turn in her vanity license plate after using it for 15 years.
“It would be a real shame if I lose it,” said Wendy, who often gets compliments on her funny plates.
Referencing the state’s motto, “Live free or die,” she added, “If I have to take it off, then I won’t be able to live free.”
Her plates read “PB4WEGO,” reminding her kids to “pee before we go” before getting in the car.
“What parent hasn’t said that to their kids before leaving the house?” she asks. “I’m not one to protest, but this is just ridiculous.”
However, the DMV sent her a letter saying the plates needed to be turned in because they believe the letters refer to “sexual or excretory acts.”
“I’m not a political activist,” she tells CNN. “But this plate isn’t offensive. It’s part of our family and who I am, and there was no reason for them to take it away.”
At the time, Auger had 10 days to return her plate and was allowed to pick another custom plate for free.
After getting the letter, she posted it on Facebook with photos of her plates.
Her post quickly went viral.
One person commented on Auger’s social media page, saying, “This is so ridiculous… It’s funny and cute, and it’s a great reminder!” Another person wrote, “What’s going on?! You’ve had that plate FOREVER.”
A third person suggested, “Maybe it should say Pee or Pay…??? lol”
Responding to those who encouraged her to fight the decision, Auger joked, “Live free or die my arse,” and added, “I might get a plate that says ‘dmv sux,’ but I might get pulled over a lot!”
Her post gained a lot of attention on social media and eventually caught the eye of New Hampshire Governor Chris Sununu. He sent her a message saying: “Hey Wendy, it’s Chris Sununu. Just wanted to let you know we fixed that issue. Sorry for the mix-up and the delay, but common sense won out in the end.”
On August 28, 2019, Auger shared a new Facebook message, announcing her victory.
“This Sassy Momma Has Her Plates!!!,” writes Auger.
What is the funniest license plate you’ve seen? Please let us know what you think and then share this story so we can hear from others!
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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