“I Lost Both Of My Legs Because Of A Tampon”, Lauren Wasser Defied the Odds and Became a Prominent Model

Lauren Wasser is a model and activist who has overcome incredible odds to become a prominent figure in the fashion industry. In 2012, Wasser lost both legs due to toxic shock syndrome (TSS) caused by a tampon. Despite this devastating setback, Wasser refused to let it define her. She has since become a vocal advocate for women’s health and safety, using her platform to raise awareness about the dangers of TSS and the need for better menstrual product regulation.

Lauren Wasser grew up in a family of models.

Lauren Wasser was born into the fashion industry in California on March 2, 1988. Her parents were both professional models, and she first appeared in Vogue alongside her mom when she was just 4 months old. Unsurprisingly, the young girl would be drawn to this career path.

She lived a full and active life until she became ill.

Lauren Wasser was a talented basketball player who even received a prestigious athletic scholarship. However, she decided to pursue her modeling career instead. Even so, she maintained an active lifestyle for several years.

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Her world was turned upside down at the young age of 24.

AtThe Diary of a CEOpodcast, Lauren Wasser, age 35, shockingly revealed her harrowing experience by saying, “I lost both of my legs because of a tampon.”

The syndrome results from an overgrowth of Staphylococcus aureus bacteria in the body, which can produce a deadly toxin in the bloodstream. TSS first caught public attention in the United States in the late 1970s when several young women became gravely ill. By the 1980s, the syndrome was infecting people at a rate of approximately 6 in 100,000.

It all started with flu-like symptoms, followed by renal failure and, ultimately, two heart attacks, all due to the rare and life-threatening syndrome. With a slim chance of surviving, doctors had to put Wasser into a medically-induced coma to save her life.

After regaining consciousness a week and a half later, Lauren Wasser shared in a poignant interview, “I woke up a week and a half later and had no idea what had even happened. They pumped me full of 80 pounds of fluid.” Tragically, her situation worsened as gangrene spread, causing her right leg and left foot to be engulfed in searing pain. “From there, my feet were on fire, and gangrene set into my right leg and my left foot. There was no option. I had to amputate my right leg.” Then, in 2018, she faced another heartbreaking setback as her left leg had to be amputated.

Lauren Wasser advocates for TSS awareness and safer menstrual products.

As she spoke out about the dangers of TSS, Lauren Wasser emphasized the harmful constituents of tampons, stating, “[They] are made using chlorine bleach, dioxin, and synthetic fibers, which create the perfect storm in our bodies.”

“I have been working with a mother who lost her teenage daughter to TSS when she was 18 — Madeline Mosby. Through the darkness and trauma of that, we have joined forces in wanting to change the world.”

She returned to modeling and became the “girl with the golden legs.”

“My whole job has been to show that you are enough, and you’re beautiful in the skin you’re in and highlighting your scars and the things that you hate most.” With this resolution in mind, Lauren Wasser decided to return to the modeling industry and started looking for gigs again. While many of her colleagues supported her decision to return to modeling, some doubted whether she could make a successful comeback.

Wasser decided to choose gold-toned prosthetics instead of prosthetics that matched her skin color after entirely accepting her new condition. “Making it my own and giving it life, so to speak, changed my perception,” she said, explaining her choice in an interview. Thus, she became the “girl with the golden legs” and started walking for famous designers again.

Currently, she’s still taking the fashion world by storm and fighting for more inclusivity.

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Following the amputation of her left leg due to chronic pain, the model is now able to lead a more active lifestyle. She has resumed playing basketball, which is her passion and is even preparing for a marathon shortly. Additionally, Wasser’s modeling career is flourishing as she walked for Gabriela Hearst and Louis Vuitton in 2022 and was featured in Lacoste, Furla, and Shiseido campaigns.

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In addition to her thriving modeling career, Wasser remains dedicated to advocating for inclusivity and acceptance of individuals with disabilities and diverse conditions within the fashion industry. Her activism and contributions to the fashion world have earned her a spot on Harper’s Bazaar’s special-edition Women of the Year 2022 covers, alongside other inspiring women.” I’ve worked so hard to be myself and never take ‘no’ for an answer,” is how Lauren Wasser sums up her success.

Lauren Wasser’s incredible journey from tragedy to triumph is just the beginning of a new era in modeling. Stay tuned to learn about 16 more unusual models who are revolutionizing the beauty industry.

Preview photo credit theimpossiblemuse / Instagramtheimpossiblemuse / Instagram

’’We Got Stares’’, Parents Choose to Remove Baby Girl’s Rare Birthmark to Avoid Rude Reactions

A happy mom recently told the story of how her little girl said goodbye to a birthmark on her forehead, even though they initially faced some criticism from doctors.

A very uncommon birthmark.

© viennarosebrookshaw / Instagram© viennarosebrookshaw / Instagram© viennarosebrookshaw / Instagram

Here’s the story of Celine Casey and her two-year-old daughter, Vienna Shaw. Vienna was born with a rare birthmark called congenital melanocytic nevus (CMN) on her forehead, which only occurs in one out of every 20,000 newborns.

When Celine learned about the birthmark, she felt worried and wondered if she had done something wrong during her pregnancy. She didn’t know what the birthmark would mean for Vienna but was determined to remove it so that her daughter could grow up without feeling different.

© viennarosebrookshaw / Instagram

Even though the birthmark didn’t affect Brookshaw’s physical health, Casey knew it could impact her daughter’s mental well-being as she grew older and interacted with other children who might be curious about her condition.
Celine shared that the family sometimes used to hide Vienna’s birthmark by covering her face when they went out. She said, “We went out daily with her and got a few stares.”

The surgery was challenging.

© viennarosebrookshaw / Instagram

When they sought help from the NHS, the family received disheartening feedback. Doctors couldn’t go ahead with the surgery to remove the birthmark, categorizing it as a cosmetic procedure.

However, the parents viewed it differently. They were genuinely worried about potential teasing from other kids, which could affect their daughter’s mental well-being at a young age. Casey was also concerned that if they didn’t remove the birthmark, her daughter might grow to resent her and her partner.

© viennarosebrookshaw / Instagram© viennarosebrookshaw / Instagram© viennarosebrookshaw / Instagram

The parents took matters into their own hands and privately raised the required funds. Through crowdfunding, they managed to gather $52,000 within 24 hours. However, due to increased hospital costs in 2020, they had to raise an additional $27,000. With a new funding request, they eventually reached their goal.

They encountered difficulties with doctors.

© viennarosebrookshaw / Instagram

Disagreements between the medical team and the parents have led to differing opinions. Vienna’s parents wanted the birthmark removed through surgery, but the surgeon refused to perform the procedure. The surgeon’s stance is rooted in the belief that the child should make the decision once she reaches an appropriate age.

After this controversy arose, Daniel Brookshaw, Vienna’s father, expressed his dissatisfaction with the doctor’s viewpoint. The doctor also consulted with a dermatologist who concurred with the surgeon, emphasizing that the birthmark doesn’t threaten Vienna’s health and is not cancerous.

The surgery was completed successfully.

© viennarosebrookshaw / Instagram

Vienna is now two years old, and her doctors have successfully removed her birthmark, leaving only a faint scar between her eyebrows. Casey regularly shares updates on Shaw’s scar and recovery process on her social media, and followers often comment on how beautiful her little girl looks.

Despite the birthmark being gone, Casey mentioned that they still have to travel between cities to check the healing of the scar and see if any additional procedures are needed beyond the three she has already undergone. Shaw is now enjoying the typical life of a two-year-old.

© viennarosebrookshaw / Instagram

This little girl’s case with her birthmark brings attention to the delicate balance between parental advocacy and a child’s autonomy in medical decisions. While her parents aimed to secure her social acceptance and well-being, medical professionals stressed the importance of respecting Vienna’s future autonomy over her own body.

This story serves as a reminder of the intricate ethical considerations that arise when navigating the boundaries of parental authority and individual autonomy, prompting broader reflections on the rights of minors in the medical realm.

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