The pixie-like Cyndi Lauper, whose 1983 hit song “Girls Just Want to Have Fun” became a global anthem and encouraged women of all ages to follow its advice, has a certain allure.
Lauper epitomizes style. Her message of self-empowerment stems from her colorful hair, unique fashion, and funny, carefree personality.
But the performer is really dealing with a serious skin ailment called psoriasis, which at one point was so aggressive that “it looked like someone threw boiling water on me.” This is hidden behind the comical voice that makes her listeners feel happy.
The 69-year-old pop icon recently talked about how she has been fighting psoriasis, an incurable chronic skin ailment, since her diagnosis in 2010.
The symptoms of psoriasis might include scaly patches, extreme pain, itching, and discomfort. The skin condition affects an estimated 125 million people globally and 8 million people in the United States.
When Lauper first started experiencing symptoms, such as general pain and scalp irritations, these got worse with time.
The celebrated performer experienced both physical and mental distress as a result of the outbursts, which she initially blamed to her frequent hair dyeing.
The singer of “Time after Time” is an activist, a touring music sensation, and a busy mother.
As an advocate for human rights, motivated by her lesbian sister Ellen, Lauper dedicates her life to helping the LGBT community.
“Above the Clouds,” a song she wrote in 2005, was dedicated to Matthew Shepard, a gay student who was killed by beating in Wyoming in 2005. Additionally, she started the “True Colors” concert tour in 2007–2008, which raises money for LGBT foundations and charities in the community and beyond.
Apart from her advocacy work, Lauper has a strong background as an actor, singer, and songwriter. Over the course of her four-decade career, Lauper won multiple accolades, including the Tony Award, two Grammy Awards, an MTV Music Video Award, and an Emmy Award for her 1995 cameo in a Mad About You episode.
In 2013, she was invited as a special guest to U.S. President Barrack Obama’s second inauguration for her humanitarian endeavors. She also has a star on the Hollywood Walk of Fame and is inducted into the Songwriters Hall of Fame.
Despite her illness, Lauper is a true force to be reckoned with. The True Colors singer is learning how to control her stress, which can cause a flare-up, in order to prevent her psoriasis from taking control of her life.
She composed the music and lyrics for the Broadway hit musical Kinky Boots, which won her a Tony Award for Best Original Score, while suffering from severe attacks of psoriasis at the time of her diagnosis. Lauper is the first female Tony winner in that particular category. Five further Tony Awards were won by the production, including Best New Musical.
In an effort to assist others, Lauper shares her honest story of living with an autoimmune skin disorder in an interview with the American Academy of Dermatology (AAD).
“I’ve never been very good at handling stress.” She continued, saying that she has healed and reduced stress both at home and while traveling using a holistic approach. She researched reiki, a Japanese method of relaxation and stress relief, and stated, “That helps me.”
Apart from reiki, Lauper deliberately tries to maintain her groundedness through yoga, meditation, and outdoor walks with her dog and/or husband, David Thornton, whom she wed in 1991. Born in 1997, the couple has one son.
“Taking care of oneself is not a bad thing,” Lauper declared, urging others to “make a little time for you every day.”
You can begin modestly. She went on, “How about five minutes for you?”
Resiliently, Lauper states that “it’s really hard to get up again when psoriasis gets really bad.” She occasionally had chills due to an inability to control her body temperature, which can result in hypothermia. Even when she rested, the pain persisted, and the discomfort was exacerbated by others who downplayed the severity of the issue by stating that it was merely a rash.
You don’t have to go through pain, Lauper stated. Psoriasis can be treated with topical, oral, or injectable medications to decrease its often-intense effects. Lauper claims to be “four years clear” after using Novartis’ Cosentyx, which provided her great relief.
In 2017, Lauper discussed her psoriasis management with HealthDay.
It’s strange how you start wearing gloves or other items in the hopes that your psoriasis won’t show, but it doesn’t. I didn’t wear it with a sense of excitement or admiration. Everyone hides it, don’t they? The number of people who have it but keep it a secret could surprise you. It’s a topic worth discussing because it’s one of those things that is somewhat invisible.
She discusses it on her podcast, PsO in the Know, where she interviews psoriasis sufferers, advocates, and celebrities who share their experiences with the disease.
Currently in its third season, the show may be downloaded from Stitcher, Pandora, Google Podcasts, Spotify, Apple Podcasts, and Pandora.
Not all celebrities, including Lauper, have psoriasis. Kim Kardashian, 42, was given a diagnosis at the age of 30, and she is candid about her difficulties. Kris Jenner, her mother of 67 years, experienced her first breakout in her late 20s and described it as “life-changing.” A few more well-known people with psoriasis are musician Art Garfunkel, 81, actor Jon Lovitz, 65, and Jerry Mathers, 74, also known as “The Beaver.”
We are really lucky to have role models like Cyndi Lauper who use their platform to support others in overcoming obstacles. We can’t fathom a world without her gifts and journey—what a courageous woman she is!
A Man Born With No Jaw Finds Love, but Their Relationship Sparks Heated Controversy: “She Can’t Kiss Him!”
In a profoundly inspiring story of love and determination, Joseph Williams defied seemingly insurmountable odds to find not just love, but an enduring and unbreakable connection with Vania. Their journey, marked by initial uncertainties and obstacles, ultimately led to a heartwarming union in 2020.
Williams encountered many challenges and faced repeated rejections.
Born with otofacial syndrome, Williams endured a lifetime of bullying and isolation until he found the love of his life. Despite ongoing criticism, the couple is now happily married and has emerged from these challenges even stronger. Unable to speak or chew due to his disability, Williams communicates through sign language and relies on a feeding tube.
The love he experiences with his wife has reignited his self-esteem following years of feeling worthless. This has motivated him to advocate for embracing life despite differences. He expressed fervently, “I understand that I am different and that some people will think I am ugly and not accept me, but I am still a person who has a heart, feelings, and a brain. I should be treated with respect, just as anyone else should be.”
During difficult times, love persists.
Joseph prefers to receive questions rather than stares regarding his condition. He emphasizes the importance of independence, as he experienced excessive protectiveness during his youth. His adoption stemmed from his birth mother’s surprise at his condition, yet he remains steadfast in not letting it define or limit him.
Despite enduring difficult treatments such as bone and skin grafts along with jaw reconstruction, Joseph faced self-esteem challenges in his youth, fearing a life of isolation. However, in 2019, he met Vania, who would become his wife. Their relationship started as friends and evolved into a deep and meaningful love story.
Curiosity blossomed into a deep love that bound them together.
When Vania first encountered Williams at her workplace, she was intrigued but uncertain about how to approach his condition. Eventually, she learned about it through someone else. Williams had faced various reactions to his condition, from curious stares to people avoiding him out of discomfort.
Despite these challenges, Joseph and Vania forged a deep bond. Their friendship gradually evolved into a romantic relationship, though Vania initially struggled with feelings of embarrassment. Over time, she fully embraced him for who he was. They communicate using a text-to-speech app and sign language. When Vania’s mother, Janice, first met Williams, she was initially surprised but curious about his condition.
Despite initial uncertainties, their love triumphed.
Vania’s mother expressed her admiration, saying, “He’s a remarkable man. He does things that, you know, normal men don’t do. He’s a hard worker, for one, he’s attentive to Vania. He cares about her, he loves her, and she loves him.”
Despite initial doubts, Williams and Vania got married in 2020, supported by her parents and his loved ones.
Their relationship has sparked various opinions from people, with many making assumptions about them. Some have commented, “She can’t kiss him,” or “She must be cheating on him.” However, their unwavering determination and deep love for each other have never stopped them from pursuing their dreams, proving that love conquers all and prevails above all else.
Their story is a testament to the immense power of love to overcome obstacles and defy societal expectations. Through highs and lows, doubts and triumphs, they have forged a remarkable bond that will endure a lifetime.
Countless other stories similarly demonstrate that love is an unstoppable force capable of conquering any adversity.
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