Carol Burnett, the famous comedy legend, turned 91 in April!
After many years of making us laugh, Burnett still shines bright. NBC honored her amazing career last year with a special tribute called *Carol Burnett: 90 Years of Laughter and Love.*
Many of Hollywood’s biggest stars attended the event to honor Burnett, sharing their admiration on the red carpet.
**Birthday Tributes to Burnett**
One of the attendees was Julie Andrews, the legendary star of *The Sound of Music* and a close friend of Burnett. She joked, “She brings out the best in me, and I think I bring out the worst in her. I don’t know why!”
Andrews remembered meeting Burnett at a Chinese restaurant long ago: “When we met, no one else could get a word in. We bonded like that, and it has never changed,” Burnett said about their lasting friendship.
Music icon Cher also shared stories about her friendship with Carol Burnett.
“I would sneak out through the fence to go to the farmer’s market, and we played practical jokes on each other,” Cher said. “It was just easy and fun, and that’s all we wanted to do.”
Actress Jane Lynch remembered meeting Burnett for the first time: “I was firmly in love; she’s exactly the person you hope she would be,” she told the Hollywood Reporter.
The guest list for the tribute show, which was taped in March, included many big names from both the past and present. Stars like Lily Tomlin, Steve Carell, Laura Dern, Kristen Wiig, Maya Rudolph, Oprah, Michelle Obama, Steve Martin, Martin Short, Allison Janney, Jimmy Fallon, and Ellen DeGeneres all participated in celebrating Burnett’s remarkable career.
According to Playbill, some of Broadway’s biggest stars, like Bernadette Peters, Billy Porter, Sutton Foster, and Kristin Chenoweth, will perform musical numbers in honor of Burnett. She herself is a Broadway veteran, having received Tony nominations for *Once Upon a Mattress* and *Moon Over Buffalo*.
“I’m so excited NBC decided to throw me a birthday party and invited all of my closest friends,” Burnett said in a statement. “I can’t wait to look back at so many wonderful moments throughout my career. I feel so lucky to share this night with everyone.”
Carol Burnett is best known for her groundbreaking variety/sketch series, *The Carol Burnett Show*, which aired for 11 seasons on CBS. It was the first show of its kind hosted by a woman, and Burnett is widely seen as a trailblazer for female comedians.
She has recently received many lifetime achievement awards, including the Mark Twain Prize for American Humor and the Screen Actors Guild Life Achievement Award.
In 2019, the Golden Globes named their television lifetime achievement award after her, calling it the “Carol Burnett Award,” and she was the first person to receive it.
Last year, she returned to TV with an important guest role in the final season of *Better Call Saul*.
In an interview before her 90th birthday, Burnett shared that she doesn’t feel her age, calling herself a “late bloomer” compared to other performers.
“I can’t wrap my head around it,” Burnett told *People Magazine*. “I still feel like I’m about 11, but I’m amazed. It sure went fast. But I’m glad because I’ve got all my parts — my hips, my knees, and my brain, so I’m happy about that.”
As Carol Burnett celebrated her 91st birthday on April 26, the television legend was still making waves. She recently celebrated her role in the new miniseries *Palm Royale*, appeared on the cover of *Harper’s Bazaar* in March, and almost saw her playful birthday wish involving *Maestro* star Bradley Cooper come true during her appearance on *Jimmy Kimmel Live!* just days earlier.
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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