This Girl Became a Successful Child Star after Bio Parents Gave Her up to Family Who Had ‘No Plans’ to Adopt

When she was a newborn, his celebrity’s biological parents placed her for adoption.

Because their occupations meant more to them than raising a child, the star’s birth parents didn’t want her when she was born.

Up until the truth was revealed, the actress’ adoptive parents had been lying about her background.
The French Hospital in Los Angeles, which is now defunct, was the hospital where the future celebrity was born on May 8, 1964. The actress was adopted by Barbara Crane and Paul Gilbert, who took her in when she was just 24 hours old.

Paul Gilbert, their daughter, and Barbara Crane at the 4th Annual People's Choice Awards on February 20, 1978 | Source: Getty Images


Jonathan, her younger brother, was also adopted by the couple. Barbara was a twentysomething actress whose career was cut short, and Paul was a stand-up comedian, actor, and dancer who began as an aerialist with a family circus from Buenos Aires. Barbara and Paul parted ways when the young child was six years old, but his daughter remembered him with affection, saying:

“I have never known a more brilliant, energetic, humorous, loving, and fair person than my father.”

When Paul passed away in 1976, many believed he had suffered a stroke while in bed. Her adoption was made public. The celebrity claimed in her book “Prairie Tale: A Memoir” that she was informed when she was a young kid that her father, David Darlington, had been a Rhodes Scholar and that her biological mother, Kathy Wood, was a prima ballerina.

Her birth parents reportedly had no desire to give up their occupations in order to raise her, according to her adopted parents. The timing of the celebrity’s birth was allegedly incorrect, and as a result, they had to give up their daughter because her father was in the middle of a project.

She learned the whole truth about her biological parents when she was old enough. Although not a prima ballerina, her birth mother was a dancer, and David was a stock car racer and sign painter.

Kathy and David had three children between them when they were first married to other people. After running away, becoming pregnant, and moving in with their kids, the couple realized they couldn’t support a seventh child.

Parents Who Adopted Her Didn’t Want Her

The actress was stunned to learn more about her adoption after the death of her adopted father. Mitzi, her godmother, talked about the day she was picked up from the hospital by her adoptive parents.

She acknowledged that when the Gilberts returned with their new baby, it came as a shock. This astonished the actress, who looked to Barbara, along with other family members, and she confessed:

“Well, we weren’t planning on adopting a kid.”

When Barbara and her husband received a call informing them that the little girl will be available, they replied they weren’t seeking for a kid. When the celebrity’s adoptive mother phoned her out-of-state spouse, he instructed her to “go get it.”

She said to the journalist that she wouldn’t subject her kids to the burden of such a dark secret.
She was taken aback to hear herself referred to as a “it,” but Barbara clarified that she hadn’t even been born yet. Later, after learning of her upcoming arrival, Barbara revealed to her that they had been attempting to conceive.

Barbara claims that although the Gilberts were undergoing fertility treatments, they had not brought up the subject of adoption until they got the call. The actress discussed the secrecy of her adoptive family in an interview from July 2020.

The Secrets of the Family
The famous person disclosed to “CBS Sunday Morning” that she learned at the age of 11 that her father had passed away due to a stroke. But she found out at 45 that he had committed suicide.

The actress concealed the secret from everyone in her life, even herself. She informed the interviewer that she would never subject her children to the harm that such deep secrets do to families.

To learn the truth about what had happened to her adopted father, the actress engaged a detective. The detective learned that the deceased World War II veteran had threatened to take his own life while receiving care from the VA and was in excruciating pain.

An actress seen at the Santa Monica Bowling Alley in Santa Monica on January 23, 1982 | Source: Getty Images

She fought the anguish of losing her father in this way for approximately six months after learning the truth about Paul. During that time, she was unable to eat or sleep. She has since come to terms with it, though, and now works to preserve his memory by supporting mental health awareness and suicide prevention.

On January 23, 1982, an actress was spotted in Santa Monica at the Santa Monica Bowling Alley | Source: Getty Images
The actress also accepted and forgave Barbara for her decision to conceal the truth, even though she had been angry and betrayed for a long time. The next chapter reveals the celebrity’s name and her current way of life.

Who Is the Star Who Got Abandoned and Went on to Become a Famous Actress?
Melissa Gilbert is the actress, best known for her role as Laura “Half-Pint” Ingalls Wilder on the adored television program “Little House on the Prairie,” which ran from 1974 to 1983. She published her memoir, “Back to the Prairie,” in July 2022, and she is currently spending time with her family.

The celebrity acknowledged that she is “blessed” and mentioned that she is in a different place from her deceased adoptive father. She wants Paul to have felt the happiness that comes with having grandkids and the value of having a life partner who makes you feel listened, safe, and loved.

Timothy Busfield, Melissa’s third husband, and she became grandparents to a total of eight grandchildren in May 2022. While going through his second divorce, Busfield observed the actress waiting for a buddy at an empty pub in 2012.

Melissa Gilbert and her husband Timothy Busfield at a photocall during the 62nd Monte Carlo TV Festival on June 20, 2023, in Monte-Carlo, Monaco | Getty Images

On June 20, 2023, in Monte-Carlo, Monaco, Melissa Gilbert and her spouse Timothy Busfield attended a photocall for the 62nd Monte Carlo TV Festival | Getty Images
In April 2013, the pair got married in an intimate ceremony in Santa Barbara, California, with Melissa donning a dress by Morgane Le Faye. When Barbara’s daughter couldn’t determine what she wanted, Barbara suggested the brand’s Santa Monica store.

She disclosed in her book “Back to the Prairie” that Busfield, dressed in a blue suit, was alone at the private event; no guests were present. After nearly a lifetime in Hollywood, the famous person had her first kid, a son named Dakota Paul Brinkman, from her first marriage to the actor Bo Brinkman.

Michael Garrett Boxleitner is Melissa’s second child, born after her marriage to Bruce Boxleitner. Along with being a father, Busfield raised three children: Wilson, Daisy, and Samuel. He and his wife currently reside peacefully in a 14-acre cottage in the Catskill Mountains of New York.

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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