Tom Cruise, one of the most well-known American movie actors, became well-known at a very young age. When he acted in the now-classic film “Top Gun,” the actor was just 24 years old.
Fans might not be aware, though, that Cruise was given a dyslexia diagnosis when he was just seven years old. The actor has also been a longstanding follower of the Church of Scientology, and he attributes their help in helping him overcome his dyslexia.
Mimi Rogers, Cruise’s first wife, introduced him to the faith. Since her father was a member, he introduced Cruise to his faith and extended an invitation to a meeting at the Hollywood Scientology facility.
Cruise is a member of the Hollywood Educational Literacy Project’s board of directors. With the use of this learning tool, adults and children can receive free one-on-one instruction.
Cruise claimed that even with many tutors’ assistance, he had made every effort to comprehend the reading material, but he was unable to retain what he had read.
Cruise wasn’t able to acquire the assistance he need until he discovered L. Ron Hubbard’s Scientology study tools.
The actor greatly appreciates H.E.L.P. technology because it enabled him to overcome his learning problem by placing the object he was studying in front of him. The idea is to “have an airplane in front of you, if at all possible, while you’re studying an airplane.”
The airplane example is appropriate as Cruise has acknowledged to others that he has always wanted to become a pilot. Despite getting to pretend to be a pilot in “Top Gun,” his dyslexia prevented him from pursuing a career in aviation.
Instyle magazine claims that Cruise and Rogers first spoke in an interview with Rolling Stone in 1986. However, the actress was seeing his friend at the time, so she was powerless to stop it.
Nonetheless, Tom claimed that her “extreme brilliance” piqued his interest. Things moved swiftly once they grew close, and they soon started discussing marriage.
It was not an easy effort, nevertheless, to marry one of the most well-known guys in Hollywood; according to Instyle, they hid the wedding by referring to it as “the project.” The project was carried out in 1987. They seemed to have had a lovely, private ceremony.
The actor claimed that Rogers improved him as an actor and that he couldn’t see himself with anyone else. He continued, saying:
“My wife is the most important person in my life. My best friend is her.
According to Andrew Morton’s unofficial biography of Tom Cruise, the actor filed for divorce on December 9, 1989.
But Mimi gave a detailed account of the circumstances behind her marriage’s dissolution in an interview. She acknowledged that it “bothers” her that her age is frequently mentioned in the media. Tom Cruise was six years her junior.
The well-known actress Rogers maintained, though, that their separation had nothing to do with Scientology, celebrity, or Cruise’s jealously.
The actress disclosed that Cruise had given serious thought to becoming a monk, a career choice that would not work with a married life. As a result, their marriage failed.
Although Cruise maintains the privacy of his personal life, Instyle reports that there are speculations circulating that he dated his “Mission Impossible” co-star Hayley Atwell from 2020 to mid-2022 and is currently unmarried.
Regarding Rogers, she wed producer Chris Ciaffa in 2003; the couple is parent to two kids, Charlie and Lucy.
Following their divorce, Cruise and Rogers announced that the actress had quit Scientology. He continues to be an involved member of the church, for his part.
According to some sources, the church of Scientology played a role in the breakup of Cruise’s two marriages—the first to Rogers and the second to Nicole Kidman.
The actor, who still attends his church, feels that Scientology was a major factor in his success and in helping him get over his dyslexia.
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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