Miranda Lambert seemed to have no regrets about embarrassing one of her fans, even in the face of the criticism.
The country music star is currently the main attraction at a Vegas residency slot, as Mamas Uncut previously revealed. Additionally, she abruptly ended her performance last week to yell at a fan at one of her shows.
Lambert reportedly noticed a fan who had paid to attend her event snapping a “selfie” as she was singing her song “Tin Man.” In front of the whole audience, Lambert used the occasion to call out the paying fan.
“I’m going to stop for a minute,” she declared. The woman she was gesturing to was then told by Lambert to stop taking selfies rather than enjoying the music.
I’m a little annoyed that these females are preoccupied with their selfie and aren’t listening to the song. I’m sorry, but I really dislike it. Tonight, we’re here to listen to some country music. I’m performing some damn country music.
Lambert resumed his performance as the woman put her phone aside. Fans of Lambert were eager to applaud her when she called out the “selfie-takers” during the performance.
After her most recent performance, Lambert halted her show once more when she noticed a fan sporting a t-shirt that said, “Shoot tequila, not selfies.” Lambert apparently liked the shirt.
The crowd was informed by Lambert that her blouse read, “Shoot tequila, not selfies.” “I didn’t do it; she did!”
Lambert’s decision to add salt to the wound has now angered people even more. “Whoa! One commenter commented, “It’s unbelievable that this is how she’s responding to her rudeness.”
Some social media users were equally supportive of Lambert’s behavior as the other concertgoers appeared to be. One Twitter user remarked, “How to humiliate and shame your devoted fans who love you.” She could have made fun of them, posed for the selfie, and then urged them to live in the present. Not cool.
“The goal of attending a concert is to make memories and have an experience. Another Twitter user commented, “Anyone should be able to take a picture to record that memory.”
Since then, the alleged “self-taker” has released the pictures she shot and offered a response to Lambert’s behavior. When asked how long it took to take the photo before they went back to their seats, Adela Calin responded, “It was 30 seconds at most.” She also added that they “took the picture quickly and were going to sit back down.”
But Miranda Lambert has already called them out before they can reach that stage. Calin acknowledged that she was “appalled” by Lambert’s denigration of them in front of thousands of people.
She remarked, “It felt like I was back at school, with the teacher telling me to sit down again in my place and reprimanding me for doing something wrong.” “… She seemed intent on making us appear youthful, conceited, and immature. However, we were merely mature women in our 30s to 60s attempting to capture a photo.
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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