Fans call Goldie Hawn, 78, “ugly” in swimsuit photos, Kurt Russell defends her, says she’s beautiful

With an unwavering sense of confidence, Goldie Hawn consistently dazzles her fans with grace, even in the face of online negativity. The actress acknowledges the realities of aging in Hollywood but remains unfazed by trolls and their hurtful remarks.

As one of Hollywood’s most beloved figures, Goldie, alongside her partner Kurt Russell, exudes a resilience that comes from decades in the spotlight. Delve deeper into why Goldie Hawn faces criticism online as we explore her remarkable journey!

Goldie Hawn stands as a formidable matriarch of a renowned acting dynasty, including Oliver (47), Kate Hudson (45), and Wyatt Russell (37). Her down-to-earth charm has secured her iconic roles in films such as “Private Benjamin” (1980), “Overboard” (1987) alongside Kurt Russell, her partner since 1983, and Steven Spielberg’s “The Sugarland Express” (1972).

Before meeting Russell, Goldie navigated through two divorces, opting to skip marriage with Russell in favor of a committed partnership. As she told Woman’s Day in 2007: “We’ve done perfectly fine without getting married. I feel committed already, isn’t that the essence of marriage?”

Kate Hudson, herself a Golden Globe nominee, praises their union, describing them as a perfect match. “Mom is a free spirit, always on the move, while Kurt cherishes his home and family”, she shared. “When they’re together, it’s a powerful dynamic”, she added, referring to their actor son and their strong family bond.

Goldie Hawn, with her trademark golden locks and enduring charm, remains radiant after over five decades in the limelight, embracing the natural process of aging. “Aging is part of life. Embracing it fully means recognizing life’s continuous transformations”, she shared with People. “Growing older? It means you’re still alive!”

Despite her positive outlook, Goldie Hawn acknowledges the ageism entrenched in Hollywood. “Women will always fight this battle”, she remarked to Bazaar. “You don’t expect Hollywood to embrace you when you hit forty-five and show them you’re still desirable and marketable. It’s a specific world”, she added, remaining unfazed by the industry’s narrow standards.

Though she embraces her age gracefully, Goldie Hawn isn’t immune to the onslaught of online abuse. Even during their idyllic 2022 getaway to Greece, where photos showed them enjoying the sun and sea, the internet wasn’t always kind. Critics criticized their appearance, dismissing their enduring love and confidence as they age gracefully.

Despite the negativity, many fans rallied around the couple, especially after their endearing appearances together in films like “The Christmas Chronicles,” where they portrayed Mr. and Mrs. Claus. “They look amazing! There will always be trolls, but their love shines through”, defended one supportive fan.

Goldie’s lifelong companion, Kurt Russell, has always been her staunchest supporter. Recalling their Hollywood Walk of Fame ceremony in 2017, where they received stars side by side, he declared his love publicly: “Goldie, I owe my incredible life to you. There’s no one else I’d rather be next to”, he affirmed, encapsulating their enduring bond.

At 78, Goldie Hawn continues to captivate and inspire, navigating fame and aging with grace. Share this story and let us know your thoughts.

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.

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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