There’s something magical about Cyndi Lauper, the lively artist behind the 1983 hit “Girls Just Want to Have Fun,” a song that quickly became a global anthem, encouraging women everywhere to embrace fun and freedom.
Lauper is the definition of cool. Her quirky, carefree personality, playful fashion, and colorful hair inspire people with her message to always be yourself.
However, behind the playful voice that spreads joy to her listeners, Lauper battles a severe skin condition called psoriasis. At one point, it was so intense that, as she described, “It looked like someone threw boiling water on me.”
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The legendary pop star, now 69, recently opened up about her ongoing battle with psoriasis—a chronic skin condition that has no cure—since she was first diagnosed in 2010.
Psoriasis can cause severe pain, itching, discomfort, and rough, scaly patches on the skin. About 8 million people in the U.S. and 125 million globally live with this condition.
Lauper’s symptoms started as scalp irritation and general discomfort, which worsened over time.
Initially, she thought her itchy scalp was from frequently coloring her hair, but the symptoms continued, causing both physical pain and emotional strain for the award-winning musician.
The “Time after Time” singer is a busy mother, touring pop star, and activist.
Inspired by her sister Ellen, who is a lesbian, Lauper has become a strong supporter of LGBT rights, working tirelessly to advocate for the community.
Her 2005 song “Above the Clouds” was written in honor of Matthew Shepard, a 21-year-old gay student who was beaten to death in Wyoming. Lauper also started the “True Colors” concert tour in 2007-2008, which raises support for local and private LGBT charities and organizations.
Besides her advocacy, Lauper has an impressive career as a singer, songwriter, and actor. Over the past forty years, she has received many awards, including a Tony Award, two Grammy Awards, an MTV Music Video Award, and an Emmy Award for her role in a 1995 episode of the TV show *Mad About You*.
She also has a star on the Hollywood Walk of Fame, is a member of the Songwriters Hall of Fame, and in 2013, her humanitarian work earned her a special invitation to attend President Barack Obama’s second inauguration.
Despite her diagnosis, Lauper continues to stay strong. She is committed to not letting psoriasis hold her back and works on managing stress to avoid triggering flare-ups.
When she was first diagnosed and dealing with severe psoriasis, Lauper wrote the music and lyrics for the Broadway musical *Kinky Boots*, which won her a Tony Award for Best Original Score. She became the first woman to win a Tony in that category on her own. The show also won five more Tony Awards, including Best New Musical.
In a conversation with the American Academy of Dermatology (AAD), Lauper openly shared her experience living with the autoimmune skin condition, hoping her story might help others.
“I’ve never been able to really manage stress,” she admitted, explaining that she now takes a holistic approach to healing and stress relief both at home and on the road. She learned reiki, a Japanese technique for relaxation, saying, “That helps me.”
Along with reiki, Lauper works to stay grounded by meditating, practicing yoga, or taking walks in the fresh air with her dog and her husband, David Thornton, whom she married in 1991. The couple has one son, born in 1997.
“It’s not a bad thing to take care of yourself,” Lauper said, urging people to always “make a little time for you.”
She encourages starting small. “How about five minutes for you?” she added.
Lauper speaks with resilience about her experience, explaining that “when psoriasis gets really bad, it’s really hard to get up again.” She shared that at times, she couldn’t regulate her body temperature, leading to chills that could result in hypothermia. Even when resting, her condition only worsened, and hearing people dismiss it as “just a rash” added to her struggles.
“You don’t have to suffer,” Lauper said. Treatments, such as topical and oral medication or injections, can help ease the often unbearable symptoms of psoriasis. For Lauper, she found relief with Novartis’ Cosentyx, and as a spokesperson for the medication, she happily shares that she’s been “four years clear.”
In 2017, Lauper spoke with HealthDay about managing her psoriasis.
“It’s funny—you start wearing gloves, or this and that, hoping [psoriasis] is invisible, but it’s not. I didn’t show it off, like, ‘Woo-hoo, check this out!’ Doesn’t everyone try to hide it? You’d be surprised how many people have it and don’t talk about it. It’s one of those invisible things, so it’s good to talk about it.”
She shares more about it on her podcast *PsO in the Know*, where she talks with celebrities, advocates, and everyday people who offer insights on living with psoriasis.
The show is now in its third season and is available on Apple Podcasts, Spotify, Google Podcasts, Pandora, and Stitcher.
Lauper isn’t the only celebrity with psoriasis. Kim Kardashian, now 42, was diagnosed at 30 and is open about her challenges. Her mom, Kris Jenner, 67, had her first outbreak in her late 20s and said it was “life-changing.” Other celebrities with psoriasis include musician Art Garfunkel, 81, actor Jon Lovitz, 65, and Jerry Mathers, 74, known as “The Beaver.”
Jase and Missy Robertson’s journey: Overcoming obstacles and finding strength
Mia Robertson, the youngest daughter of Duck Dynasty’s Jase & Missy Robertson, has been born with a condition known as cleft lip and palate, a gap in the upper lip that can involve the gum as well.
The U.S. Centers for Disease Control and Prevention shares that about one in every 1,600 babies is born with a cleft lip with a cleft palate in the U.S.
Because of her condition, sweet Mia, who is now 18 years old, has been forced to undergo 13 surgeries, with the 14th taking place just recently. The family truly hopes this would be Mia’s last procedure before her problem is finally solved.
Throughout every surgery, the young girl remains positive. What’s most, she hopes she serves as inspiration for other young children who are born with the same condition. On her own initiative and with the help of her family, Mia established the Mia Moo Fund in order to assist in making certain that each and every child wears a smile on their face.
“One of the functions of the Mia Moo Fund is to spread awareness of the cleft lip and palate journey,” Missy Robertson told Christian Post. “The other one is to help with medical funds for the parents and the families living right here in America.”
On his podcast Unashamed, Jase Robertson shared an update on Mia’s condition and said that his daughter is recovering well.
“She’s doing great. She’s turned a corner,” he said, and then added, “Everything seems great, seems to be fine.”
“Surgery went a little longer than expected, but she is home and recovering,” the loving father told his podcast listeners. “Thank you for praying for her and for our family. She is a champion!”
Before the surgery took place, Missy spoke of her daughter’s condition and explained that she had been constantly asked about the number of procedures Mia would need to undergo in the future. “There is never any other response than ‘We just don’t know,’” Missy said. She then added that they rely on God for assistance. “Since she is 18 now, she is taking the lead in all the discussions and medical forms. It’s been a little strange,” Missy wrote. “But it’s just another reminder to lean on the Lord and that I’m not in control.”
Mia also hopes that she’s at “the finish line.”
“Hopefully the last time I’ll see my doctors in this setting! It’s been a long road but we are at the finish line,” brave Mia said.
The Robertson’s have also been preparing for a new addition to the family as they open the doors to their hearts and home for a child whose mother was unfit to take care of.
We wish Mia speedy recovery.
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