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.”
Wire Image
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.”
A tiny baby, who was kept in a sandwich bag for safety, is finally going home.
The parents of a baby named Robyn, who was born very tiny at just 11 ounces (328 grams), have finally brought her home after 18 months in the hospital.
Robyn was born five months early in March 2023 at Grange Hospital in Cwmbran, Torfaen, and she still needs special care all the time. Her parents, Chantelle (34) and Daniel (38) from Malpas, Newport, are raising money for her treatment. Chantelle said, “It’s like a dream come true to have Robyn home.”
Robyn was born at just 23 weeks and 2 days and was so tiny that she could fit in the palm of a hand. To keep her organs warm while she grew, she was kept in a sandwich bag.
After six months in the hospital, she spent another seven months in the pediatric intensive care unit at Noah’s Ark Children’s Hospital in Cardiff. She then returned to Grange Hospital until she was finally discharged in September.
Chantelle, who works part-time as an accountant, said, “It’s just so nice to do normal family things… and just all be together under one roof.”
Daniel, a self-employed bricklayer, mentioned that it’s much less chaotic at home now. He has had to cut back on work to focus on taking care of his daughter.
Robyn gets oxygen and nutrition through tubes in her nose and mouth, and her vital signs are watched all the time. She takes 30 doses of medication each day.
Her mom, Chantelle, explained, “She can’t cough, so we have to suction her mouth and nose throughout the day when she needs it.”
Daniel described Robyn as doing well and enjoying the “peace” of being at home. He added that they do a lot of physical therapy and play with her to help her senses.
Chantelle said it was tough to bond with Robyn in the busy hospital ward, with doctors and nurses always coming in and out.
“All you can do is sit next to her and watch,” she explained, “keeping an eye on the numbers on the screen and hoping she will be okay.”
“When Robyn was born, we weren’t sure if she would survive.
“As time went on, she grew bigger and stronger, but she still faced many problems. It became clear that her brain damage would have a big impact on her.”
‘We know nothing is impossible’
“We didn’t learn about her brain damage until about six months after she was born,” Daniel said.
“You have all these plans for how life will be, and then everything changes,” he added.
“But we try to stay positive.
“We know that nothing is impossible for Robyn because she has been told so many times that she wouldn’t be able to do things or even survive, but she keeps proving everyone wrong.
“She’s full of surprises, and I believe she will create her own story.”
Leave a Reply