When we hear the phrase “Catwoman”, we imagine that very attractive comic book heroine. But today we decided to talk about another woman, who is also called that.
Jocelyn Wildenstein was born in 1940 in Switzerland. As many of her acquaintances say, the girl had an incredibly attractive appearance: blond hair, big eyes and sophisticated facial features.
Due to this appearance, she often enjoyed success with men.
All her life, Jocelyn was looking for a status gentleman for herself. So she decided to try to find one in Paris.
The girl managed to find an interesting man who worked in the field of cinema.
Over time, he introduced his girlfriend to many people from this area, and she completely immersed herself in the world of glamour. Jocelyn suddenly wanted to change something in herself, despite the fact that she was a real beauty.
From that moment, her journey of transformation began.
When it comes to such changes, everyone immediately understands that it will not do without the intervention of a plastic surgeon.
It all started with the most ordinary braces, which were not supposed to change the girl much. But it frequently happens that the body is not going to accept such an intervention, so Jocelyn’s appearance has changed dramatically.
In order to somehow get out of this situation, our heroine began to position herself as a new Catwoman. She was not going to cause any admiration for her new look, and in fact no one was going to do this.
In the future, each attempt by Jocelyn to correct herself only aggravated the situation. Now she herself realizes that she did a great stupidity.
Today’s plastic has taken several steps forward in development, but this story is an example. Therefore, before taking such a step, think not 7 times, but all 100.
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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