Lynda Wiesmeier was an actress who made a splash with a few notable films.
Yet, it’s a particular image of her that has gained attention in recent years, capturing something that feels like a glimpse into a bygone era…
Her journey began in Bitburg, Germany, where her father served as a doctor in the U.S. Air Force. The family moved around quite a bit before Lynda finally landed in sunny Los Angeles. She also spent some time in Bound Brook, New Jersey, where she became a regular sunbather at the Jersey shore.
Starring in zombie movie
Lynda loved working and keeping busy, balancing three careers: modeling, acting, and clerical work in a medical office.
In 1982, her beauty caught the eye of Playboy, and she was featured as the centerfold Playmate in their July issue. After becoming a Playmate, Lynda entered a whirlwind phase in her show business career, starring in films that showcased her stunning natural physique. She appeared in movies like Real Genius (1985), Teen Wolf (1985), Malibu Express (1985), and R.S.V.P. (1984).
Final movie
But it was her final film that might just be the one to put Lynda Wiesmeier on the map. In 1987, she was cast as Dianne in the zombie horror flick Evil Town.
The film starred none other than the legendary Dean Jagger, who took on the role of a mad scientist on a quest for eternal youth. His method? Synthesizing a drug from human pituitary fluid, of course. As he extracted the fluid, things took a turn for the worse — the process resulted in mindless zombies created from the unfortunate donors.
By an interesting twist of fate, Evil Town also featured Keith Hefner, the younger brother of Playboy founder Hugh Hefner. With both Lynda and Keith on board, the film had quite the Playboy connection.
The film was set to hit theaters on June 3, 1987, but excitement was so high that many theaters started showing it a day early, on June 2. However, despite the buzz, Evil Town didn’t quite live up to expectations.
Critics panned it, calling it a “silly horror film.” Cavett Binion of All Movie Guide pointed out that the movie was a mishmash of scenes from earlier films, including an unfinished project from the 1970s, and added that it was “spiced up with some gratuitous nudity courtesy of former Playboy Playmate Lynda Wiesmeier.” Ouch!
Luckily, Lynda Wiesmeier was destined for a bit of a comeback. Somehow, a particular scene from Evil Town has gone viral in the years since its release.
However, it’s not for the reasons some might assume.
Lynda Wiesmeier photo
In this memorable moment, Lynda shares the screen with the nearly unknown actor Scott Hunter.
At first glance, this looks like your classic 1980s snapshot. In front of a Dodge car, a young man and woman strike a pose, both rocking quintessential ’80s attire. But take a closer look, and you might uncover something unexpected!
The man sports dark shorts and a gray hoodie splashed with colorful motifs, while Lynda shows off high-waisted white shorts paired with a bright red top, artfully knotted at the waist. Short shorts were just the style back then, and Scott wore them with corduroy shirts, which everyone seemed to have.
Their retro outfits scream ’80s fashion, making it a delightful throwback to the era for many. And that’s exactly what has people falling in love with this image.
Fashion in the 1980s was big, bright and bold – and we embraced a mix of styles, including punk, glam rock, and preppy looks.
We could play with colors, hair, makeup and lots of plastic jewelry and other crazy accessories. And sometimes, all it takes is a simple image from a lesser-known film to transport us back to this fantastic era – thanks for that, Lynda and Scott.
Left the industry
After leaving the film industry, Lynda embraced family life, marrying and welcoming two wonderful children —a son and a daughter— from her first marriage.
According to Joyce’s Take, the family settled in Lafayette, Louisiana, where Lynda took on the role of records manager in a law office.
However, life took a turn, and after a divorce in 2004, Lynda packed her bags and headed to sunny California, ready to start anew. Even as she moved on, Lynda cherished her connection with her fans. She became a familiar face at various fan conventions, like Glamourcon, The Hollywood Collectors Show, and WonderCon, where she shared her stories and signed autographs.
Cause of death
Sadly, Lynda’s journey was cut short when she passed away at just 49 in December 2012, following a brave battle with a brain tumor.
It’s bittersweet to think about what she might have shared about her time in films like Evil Town — a charming piece of cinematic history that captures a different era.
But even in her absence, we can still celebrate Lynda’s legacy and the joy she brought to her fans. Share this article if you also miss the 80s!
Mom of Boy with Rare Condition Shares Their Life, People React Differently
Logan Pacl stands out among teenagers. At 17, he faces a rare illness known as Sanfilippo syndrome. Often called “childhood Alzheimer’s,” this cruel disorder gradually takes away a child’s cognitive skills, mirroring the effects of Alzheimer’s in older people. But he keeps fighting and uses social media to spread awareness about his condition.
At first, everything seemed normal.
Logan Pacl’s life is a battle against time. Diagnosed with Sanfilippo syndrome, often known as “childhood Alzheimer’s,” the 17-year-old from Silverdale faces a relentless genetic disorder that viciously strips away the very essence of childhood. Caused by a single defective gene, this neurodegenerative disease attacks the brain and spinal cord, leaving behind a cruel wake of lost abilities, seizures, and constant pain. It’s a ticking time bomb, as most children with this terminal illness don’t survive beyond their mid-teens.
For Logan’s family, the heartbreak began early. Born in 2007 with his twin brother Austin, Logan seemed like any other healthy baby. Both boys hit their developmental milestones—until Logan began to fall behind. A year in, the red flags emerged: while Austin was speaking, Logan remained silent. The difference between the brothers grew, signaling the start of a devastating journey.
Sanfilippo syndrome doesn’t just rob children of their future—it erases their past.
Then the news of the diagnosis hit the parents, something no one could have anticipated.
As Logan’s condition worsened, with chronic infections and a noticeably swollen belly, Noelle and William were left searching for answers. In January 2010, they learned that Logan had Sanfilippo syndrome, a terminal illness with no cure or treatment, and a life expectancy that typically extends only into the late teens. “I’ll never forget the day we got the phone call. The genetic counselor on the other end went on and on, and all I thought was, well get to the part on how we fix this. Then she said it, ’This disease is terminal, and there is no cure or treatment,’” his parents recall.
Noelle recalled her initial reaction, grappling with the news that the disease was terminal. The weight of the diagnosis was overwhelming, leaving her with a heart that felt as though it had dropped into her stomach. The severity of the situation rendered her unable to process much beyond the devastating reality.
Noelle described the experience of mourning not just the child she had but the life she had envisioned for him, a life that was abruptly stolen away. The medical advice they received was minimal and unhelpful, simply advising them to take Logan home and cherish their time with him. This lack of concrete guidance only deepened their sense of helplessness.
In their search for hope, Noelle and William discovered an experimental stem cell transplant through online research. Inspired by the success of another mother’s child, they decided to pursue the same treatment for Logan. So, Pacl went through a tough three-month treatment that was basically a bone marrow transplant. He had to endure chemotherapy to wipe out his immune system so it could accept the new stem cells. It was a risky procedure, but it seems to have helped with some of Logan’s physical symptoms.
His mother uses social media to spread awareness about his condition.
At 17, Logan’s life is very different from that of most teenagers. Losing his ability to speak at a young age was tough for him and his family, but over time, he’s become more easygoing. “Life with Logan is anything but typical. Each day is a battle to maintain the skills he still has,” his mother Noelle said.
Since 2020, Noelle has been a vocal advocate for Sanfilippo syndrome, using TikTok to share her family’s story. Her videos have reached a global audience, raising awareness about the disorder and encouraging other parents to seek early diagnosis for their children.
Although Logan’s future is uncertain, the Pacl family is committed to making the most of their time together. Noelle and William used to avoid thinking about what lies ahead, but now they focus on cherishing every moment with Logan and ensuring he enjoys his time to the fullest. Noelle notes that among Sanfilippo parents, there’s a bit of a joke that all their children seem like siblings, sharing similar features like bushy eyebrows, a low nasal bridge, and large, round stomachs.
Even with the demands of caring for Logan, Noelle keeps life as normal as possible for Logan’s siblings, Austin and Aidyn. She acknowledges that having a brother with special needs can bring its own set of benefits.
As for sharing Logan’s journey online, Noelle remains thoughtful about what she posts. While she plans to continue sharing, she’s careful to respect her family’s privacy. “We just live in the moment,” his mother said. “And if something comes up, and we’re like, we can make that, we’ll do it.”
People in comments react differently.
Mostly people express support and empathy.
- You take the most wonderful care of him. You are the greatest mom. © lauralang1108 / Instagram
But some show a bit of skepticism.
- Genuine question, what is your plan when you are gone? © devin_abq.505 / Instagram
- I just wanna know why it’s necessary. People have to publicize their children’s conditions. Why do people think that we all wanna know what’s wrong with your child? I feel sorry for the parents, but I don’t know why you want to put this all out there. I’m sure you have support group publicizing putting your child out there like this. © marlawomble / Instagram
Today, conversations about living with disabilities are becoming more open, especially on social media. Celebrities are sharing their experiences as parents of children with special needs, helping to normalize these discussions and inspire others. This shift fosters understanding and empathy, creating a more inclusive environment for everyone.
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