Reba McEntire won the Country Music Association’s “best singer” award four times in a row following her breakthrough in the late 1970s and early 1980s. Naturally, she is also honored with a star on the Hollywood Walk of Fame.
However, Reba has also had her fair share of personal traumas, so life has not always been easy for her, even with her amazing profession and wealth.
Reba’s mother Jacqueline, at 93 years old, lost her fight with illness in 2022.
She was completely prepared to pass away and had lived a lovely, long, and healthy life. The country music performer posted on social media, “The cancer may believe it has won the fight, but we’re giving God all the credit for choosing the time for her to go home to Him.”
Jacqueline McEntire’s desire of becoming a professional country singer was always realized when she taught Reba to sing, fulfilling her dream via her daughter.
We all know how much she loved us, and she left knowing how much love she had.Reba remarked, “We have so many amazing memories, but we’re going to miss her.
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Reba is well aware of the suffering associated with loss and grief.
Thirty-two years ago on March 16, she lost her tour manager in a horrific plane crash after a concert, along with seven other band members.
I recall that 1991 day. I heard about the crash on the radio as I was heading to work. I felt my heart skip a beat, thinking that Reba was on the plane too.
She wasn’t, though.
After playing in San Diego on March 16, 1991, Reba and her band were on their way to Fort Wayne, Indiana, for their next tour stop.
At the airport in San Diego, two flights were waiting; Reba, her husband, and manager spent the night in San Diego, while the band members and tour manager traveled on ahead.
Ten miles east of the airport, the first aircraft tragically met its demise.
Reba has frequently honored her deceased friends throughout the years.
She opened out about the day her band broke up in an emotional 2012 interview with Oprah Winfrey.
“Everyone on board was killed when the airplane’s tip struck a rock on the side of Otay Mountain,” McEntire said to Winfrey.
“Our pilot was contacted, and Narvel, Reba’s manager, went to meet with him to inform us of what had occurred. When Narvel returned to my hotel room at two or three in the morning, he informed me that one of the planes had crashed. I said, “Are they okay?” In his words, “I don’t think so.” “But you’re not sure?” I asked. I don’t think so, he said.
Reba remembered the events of the disaster, tears welling up in her eyes.
“Narvel was calling from room to room while holding a phone,” she started, stopping when tears welled up in her eyes. “I apologize, but even after 20 years, it seems like it will never stop hurting,” she remarked. But that chamber is visible to me. Narvel is moving back and forth, as I can see.
It’s been 32 years since the crash. She recently recalled the terrible events of that day by sharing a picture of her band on Instagram.
She shared another homage to her friends in 2020.
“I lost my pals in a plane tragedy 29 years ago today. It seems fitting that Mama passed away on that anniversary,” she writes.
“I am aware that they are all together in Heaven, looking out for one another. Let’s continue to look out for one another while we’re still on this planet and never take a moment for granted to spend with our loved ones.
Soon after, Reba’s admirers rallied behind the country music icon.
Many folks sent prayers and good vibes.
“Reba I’ve always admired your music, our mutual love of horses, and now that I follow you on Instagram.May God bless you and your mother. A fan wrote.
Reba showed once more this year, in 2023, that she still grieves the terrible loss of her pals and that she will never forget them.
She posted a video of the group performing together along with the message, “Their love for music and the stage gives us all the strength to go on.”
I apologize, Reba. You are an amazing woman; stay strong. You make so many people happy that there is a reason God has preserved you on this planet. Keep grinning!
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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