Actor Address Williams tragically passed away after a horrific motorcycle accident, and numerous celebs sent their condolences to his family via social media.
The 71-year-old calendar man passed away as a consequence of the party, according to a statement released by his agent Barry McPherson on Monday, June 13.
John Travolta, who reminisced their Broadway adventures in the musicals Grease and More Than Here, was among the first to pay their respects to the late actor.
He recalls, “Treat Williams and I started together in NYC by appearing in two Broadway productions, More than Below and Grease.”
“I’m really sorry, treat. You and your family are on my mind. You’ll be missed by us. Greetings, John.
The Phantom, a 1996 movie starring Williams and Catherine Zeta-Jones, was tweeted with the simple message “R.I.P. Dearest Handle Williams.” Zeta-Jones shared a still from the movie.
Kim Cattrall, an actress and mother of two who costarred with the late actor in the 1999 television movie 36 Hours to Die, tweeted, “I’m in shock!”
“Farewell, Pricey Ensure. My sympathies go out to Pam, Gille, Ellie, and the family. a fantastic actor and friend.
“Sad information, relax in peace, brother,” Sharon Stone tweeted beside a screenshot of a news article claiming his death.
Mark Hamill shared a picture of them from the established with the caption, “Just got the terrible news that the globe has missing @Rtreatwilliams.” Mark Hamill was an uncredited storm base warrior with him in The Empire Strikes Back (1980). Such a wonderful individual, such a skilled actor, and such a cherished close friend. It breaks my heart. #RIP_Pal.”
“The numerous instances we worked collectively was generally remarkable and I was usually enthusiastic for the next time,” stated Emily VanCamp, the actress who portrayed Williams’ co-star in the film Everwood, with a picture of the actor in his youth. I’m offering my best wishes to your family, Deal with. Go get it, my dear friend.
“Treat and I spent months filming As soon as On a Time in America in Rome,” said James Woods, his co-star in the epic criminal offense drama from 1984.
“A long shoot can make traveling very lonely, but his constant sense of humor and amazing sense of humor have been invaluable. I’m saddened by his passing because he was someone I truly appreciated. #TreatWilliams, Godspeed.
Billy Baldwin penned a lengthy tribute to the celebrity in which he extolled his qualities as a clever, skillful, charming, witty, successful, attractive, and kind person. “Heart of gold.”
“A terrible loss,” he continued. He fought tirelessly to improve the climate and advance social fairness. We won’t get to see you. Manage your leisure time peacefully.
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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