“Do you guys see what I’m seeing?” wrote a TikTok user who had discovered something shocking at a nearby Chinese buffet. This user was shocked to see chicken nuggets fashioned like dinosaurs being served. The nuggets looked quite good with the sauce and sesame seeds on top. The user, however, was astounded by what they saw and chose to take a video in order to observe the reactions of others to this unexpected buffet provision.
The video was clear-cut and short. Using a variety of TikTok capabilities, the user concentrated the camera on the dinosaur nuggets coated in sesame seeds and produced a video that swiftly gained popularity. The first line of this article was narrated by the user via the text-to-voice tool. Then, the camera repeatedly focused in to provide a close-up of the nuggets, which were obviously obtained from the frozen food department of a grocery store and used for the buffet.
The video was shared on TikTok, Reddit, Twitter, and other websites. It received thousands of comments, over 100,000 likes, and over two million views.
That would surpass the severity of an infestation! One commenter screamed, “I mean, we can just buy them from the grocery store!”
Some appeared to be more understanding, stating that if they were the only thing available, they would happily eat them.
“No food over dino nuggets.” Another said, “I mean, they look pretty good too!”
After watching the video, someone even made a joke about going to get sesame seeds and dinosaur nuggets.
“I’m going to pick up some Dino nuggets.” Delicious! While we’re at it, I may as well purchase some chicken and sesame seeds. #satisfyinginmytummy
More than ten thousand people commented on the video, expressing their shock and amusement at the restaurant’s use of dinosaur nuggets. Someone said that if they happened upon the sesame seed dinosaur nuggets at the buffet, they would eat them all.
They said, “I would definitely eat dino nugget sesame chicken.”
A jubilant user said, “It doesn’t matter that they used dinosaur nuggets.” All I want to do is taste them.
Another TikToker joked, “Don’t be suspicious, don’t be suspicious.”
Another person responded, “Okay, but that really looks really good.”
Another commentator made the joke, “Chicken shortage so real that they replaced it with prehistoric meat.”
“You mean, not the dinosaur nuggets?” another person said.
One person brought up the point that customers, as well as businesses such as restaurants, are being severely impacted by supply chain problems and inflation.
“Dino nuggets, oh my god? They wrote, “This inflation is ridiculous.”
Some were worried that the chicken nuggets would be contaminated with maggots or other insects, while others anticipated the video to be offensive.
“I’m searching for maggots.” “Is that a dinosaur nugget?” inquired someone else.
Meet Twins with the Rare Benjamin Button Syndrome, Who Became Symbols of Resilience
In a small Brazilian town, there resides an extraordinary duo of identical twins named Elis and Eloá. Their story serves as a beacon of resilience and the remarkable power of the human spirit. Afflicted with Hutchinson-Gilford Progeria Syndrome, a rare and fatal genetic disorder causing accelerated aging, these twins confront their adversities with remarkable grace and strength, earning admiration from people worldwide.
Understanding Hutchinson-Gilford Progeria syndrome
HGPS stands as an exceptionally rare disorder, impacting roughly 1 in 20 million newborns globally. Marked by rapid aging from early childhood, individuals with progeria often display growth delays, diminished body fat and hair, prematurely aged skin, joint stiffness, and severe cardiovascular issues. Typically, those with HGPS have an average life expectancy of about 14.5 years, though some may extend into their late teens or early twenties. This syndrome gained public attention through the film The Curious Case of Benjamin Button.
The condition is caused by a mutation in the LMNA gene, which produces the lamin A protein responsible for maintaining the structural integrity of the cell nucleus. The mutation results in the production of an abnormal version of the protein, called progerin, which causes cells to become unstable and die prematurely.
Elis and Eloá’s journey
Elis and Eloá swiftly captured attention because of their distinctive medical condition. Despite the physical hurdles imposed by progeria, their contagious smiles and steadfast optimism have emerged as beacons of hope and inspiration. Guilherme and Elismar, the twins’ parents, have dedicated their lives to offering the utmost care for their daughters, striving to ensure they experience as normal a life as feasible within the confines of their condition.
The family’s path has been far from easy. Their daily life is filled with demanding medical routines, including physiotherapy, aimed at addressing joint stiffness and preserving mobility. Despite these challenges, Elis and Eloá approach each day with remarkable bravery and an unparalleled enthusiasm for life, which is truly remarkable.
A global community of support
Elis and Eloá’s narrative has touched hearts worldwide, sparking a surge of solidarity from individuals and groups committed to promoting awareness about progeria and backing research endeavors. The Progeria Research Foundation, a pivotal entity in this realm, has played a vital role in propelling research forward and furnishing assistance to families grappling with the condition.
Through social media platforms, the twins’ journey is shared with a broad audience, fostering a sense of community and solidarity. Their family’s updates, documenting both the highs and lows of their daily lives, provide invaluable insights into the realities of living with progeria, while also spreading a message of hope and perseverance.
Advances in research and hope for the future
In recent years, there have been remarkable advancements in comprehending and addressing progeria. A notable milestone occurred in 2020 when the U.S. Food and Drug Administration (FDA) granted approval for the first progeria treatment: lonafarnib. This medication has demonstrated efficacy in prolonging the lives of children with progeria by mitigating the accumulation of progerin in cells, thereby decelerating the disease’s advancement.
Though a cure remains elusive, ongoing research presents promising prospects. Scientists are delving into gene-editing methodologies, like CRISPR, as potential means to rectify the genetic mutation at its root. For families such as Elis and Eloá’s, these breakthroughs offer a ray of hope for the future.
And in our other article, we recounted the remarkable story of a girl born without a nose, affectionately dubbed “Voldemort,” who refuses to let her differences define her.
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