Sissy Spacek is best known for her role as the scary telekinetic teenager in Carrie (1976), where her big moment at prom has her covered in pig’s blood.
At that time, she was a beautiful 27-year-old off-screen, and she was so convincing in her scary role that fans still say, “she terrifies me to this day.”
While her character might bring up feelings of fear, fans are now praising the 74-year-old actress for aging naturally and not looking “weird from plastic surgery.”
keep reading to see what fans are saying about this talented Hollywood star!
Sissy Spacek was born Mary Elizabeth and grew up in a small town in Texas. She chased around her two older brothers, who called her “Sissy.”
Now, at 74, she is known all over the world and is likely best remembered for her Oscar-nominated role in Carrie, based on Stephen King’s story.
While filming Carrie, Spacek shared that she fully embraced her character by not brushing her teeth or her hair.
“I wanted to feel really bad about myself,” Spacek explained. “There’s nothing like not washing your face or brushing your teeth in the morning. I put Vaseline in my hair, and that made me feel really low. And that helped me get into character,” she told CBS.
In one of the scariest scenes ever, Carrie, who everyone thinks is dead, makes one last appearance at the end. Her bloody arm reaches out from her grave, grabbing the hand of a former classmate.
Speaking with NPR about her career, Spacek – whose cousin was the late Rip Torn – said she loved the fear factor of that scene: “I would go to theaters just to see the last five minutes of the film and watch everyone jump out of their seats.” She continued, “The film ends about eight times, as (director Brian De Palma) said. People get relaxed, the music is really nice and calming, and then suddenly that scene happens, and people just go wild.”
After several praised performances in other films, Spacek, who originally wanted to be a singer, was cast in her Oscar-winning role as Loretta Lynn in Coal Miner’s Daughter, where she sang songs made famous by the country star. Spacek also received a Grammy nomination for Best Country Vocal Performance.
Happy birthday, Sissy Spacek! The Oscar-winning actress turns 66 today. https://t.co/5T0dDF5jCK #Carrie #hbd pic.twitter.com/AdiKJo88ot
— IMDb (@IMDb) December 26, 2015
The star of The Help has played many roles, from a telekinetic teen to a killer’s love interest, a homewrecker, a single mom, and about 200 other characters, winning numerous awards, including three Golden Globes, over her more than 50 years of acting.
Throughout those 50 years, fans have watched her grow from a messy high schooler to a beautiful, mature woman.
In 2022, Schuyler was asked to take on her mother’s famous role in a new Carrie remake, but she said no, explaining that it “just didn’t feel like the right thing for so many reasons.”
“I feel like Carrie is such an epic film as it is. So, the idea of trying to do anything else to recreate it just didn’t feel necessary,” she said.
Beautiful mama Sissy’
In an Instagram post shared on March 12, 2024, Schuyler wrote, “It’s hard to sum up how special this was for me.” She talked about her excitement from “cheering on” her dad and being at the Academy Awards with her mom and sister.
Fans showed their joy at seeing the whole family together: “Wow. What a special moment in time. There’s nothing better than celebrating your people!”
One fan shared, “How extremely special!! You all look amazing! This is beautiful…all of you. Inside out.” Another fan wrote, “Absolutely stunning! The all-around best!”
Other fans praised Spacek and admired her beauty. One said, “And your beautiful mama Sissy, my favorite actress, iconic and legendary and one of the BEST ever.” Another added, “Sissy, you still look fabulous.”
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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