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This feminist's comedy show didn't allow men. Now a man is suing her for it.

It was supposed to be a funny, lighthearted evening of comedy for women. And it was — until some dudes made it about them.

In November 2016, comedian Iliza Shlesinger hosted a women's-only comedy night at the Largo in Los Angeles. The event, Girls Night In, "was a singular evening that encouraged women to get together, talk and laugh about the things we go through as well as donate some money to Planned Parenthood," Shlesinger said in a statement.

Photo by Brandon Williams/Getty Images for International Myeloma Foundation.


Two men — George St. George, 21, and a male companion — decided to buy tickets to the show anyway. Staff at the theater told the men it would be best to sit in the back row for the event prominently advertised as being "no boys allowed," then later denied them entry altogether.

Now St. George is suing Shlesinger for discrimination, claiming he was not allowed to attend due to his gender.

This is not the first time St. George's attorney, Alfred Rava, has filed lawsuits essentially claiming "reverse sexism."

Rava sued after not receiving the Mother's Day promotion at an Oakland A's game and sued Club Med for a women-only promotion. He's done this dozens of times, both as the plaintiff and the attorney on the cases.

But this lawsuit isn't exactly subtle: In the 14-page lawsuit, Rava even compares St. George being asked to leave to the "...Montgomery City Lines bus company in Montgomery, Alabama circa 1955 morphing into the Woolworth’s department store lunch counter in Greensboro, North Carolina in 1960."

And before you ask: No, St. George was not publicly humiliated, pelted with food, or dragged away and arrested for trespassing. He was simply offered a refund and asked to leave.

We have yet to know if a judge will determine that St. George's claims hold water in the courts. But they simply don't hold water in the real world, and here are three reasons why.

1. Despite his attempt to appeal to ideas of fairness and equality, St. George is filing a case to solve a problem that simply doesn't exist: reverse oppression.

Reverse oppression (be it sexism, racism, or what have you) is not a thing and never has been.

In 2015, Melissa A. Fabello over at Everyday Feminism did a great job breaking down exactly why, but here's the part everyone (especially dudes like St. George) needs to read:

"...yes, all people can experience stereotyping (assumptions that all people in one group are similar), prejudice (dislike toward a group based on those stereotypes), and discrimination (refusing access to resources based on that prejudice).

However, only oppressed people experience all of that and institutionalized violence and systematic erasure."

There you have it. When the Largo didn't allow St. George and his companion into the space to make a mockery of an event, this action was not reverse sexism — or in any way akin to the suffering endured by those in the civil rights movement.

These men have every right to feel hurt or bummed out that they were not allowed to attend (though let's remember: they got a refund), but since no one in the history of time has ever mounted a successful campaign to violate, subjugate, disenfranchise, harm, or forever silence men because of their gender, this incident is by no means oppression.

Please, tell me more about the systemic oppression and erasure of men. I am genuinely curious. Photo by Brendan Smialowski/AFP/Getty Images.

2. If St. George wanted to truly stand up for men that day, he could've. But he didn't.

He could have supported organizations that support male survivors of sexual assault, or he could have spoken out against toxic masculinity and the dangerous attitudes and traditions that don't always allow for boys and men to express a full range of emotions. Hell, he could've raised money to support prostate or lung cancer research, the most common cancers among men.

Of course he didn't do that because he's not really interested in bettering the lives of men. He just wants to silence, shame, and disrupt the work of women. Men like St. George and Rava are cowards in activists' clothes.

[rebelmouse-image 19346257 dam="1" original_size="750x499" caption="If he isn't already, St. George's time may be better spent signal boosting the voices of male survivors who have shared their stories of sexual assault and misconduct, like Terry Crews, Anthony Rapp, and countless others. Photo by Frazer Harrison/Getty Images." expand=1]If he isn't already, St. George's time may be better spent signal boosting the voices of male survivors who have shared their stories of sexual assault and misconduct, like Terry Crews, Anthony Rapp, and countless others. Photo by Frazer Harrison/Getty Images.

3. In fact, it's because of men like this that women need a space to feel safe, encouraged, and supported in the first place.

Living as a woman comes with the emotional burden of sexual harassment, the constant threat of gender-based violence, microaggressions, and a substantial wage gap.

Not-so-shockingly some women just want a space, without men, to celebrate, talk, share, and commiserate, even if just for one night. To the men who understand and support this: Thank you. To the men who can't wait to shit on something that doesn't center them: Do better.

Photo by Araya Diaz/Getty Images for Hollywood Wilshire YMCA.

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Three women, three MS journeys: How multiple sclerosis looks different for everyone

Gina, Nathalie and Helga share their reactions to being diagnosed with MS and how they stay informed and positive in the face of ever-changing symptoms.

Courtesy of Sanofi

Helga, Nathalie and Gina all have MS, and their experiences show how differently the disease can manifest.

True

It’s been 155 years since neurologist Jean-Martin Charcot gave the first lecture on a mysterious progressive illness he called “multiple sclerosis.” Since then, we’ve learned a lot. We know MS causes the immune system to attack healthy tissue, including damaging the brain and spinal cord. Resulting symptoms can be debilitating and include fatigue, blurred vision, memory problems and weakness. Huge advancements in our understanding of MS and its underlying causes, as well as treatment advances, have been made in the past few decades, but MS remains a complex and unpredictable reality for the 2.8 million+ people diagnosed around the world.

Ironically, the only real constant for people living with MS is change. There’s no set pattern or standard progression of the disease, so each person’s experience is unique. Some people with MS have mild symptoms that worsen slowly but sometimes improve, while others can have severe symptoms that drastically alter their daily lives.

All people with MS share some things in common, however, such as the need to stay informed on the ever-evolving research, find various lines of support and try to remain hopeful as they continue living with the disease.

To better understand what navigating life with MS really looks like, three women shared their MS stories with us. Their journeys demonstrate how MS can look different for different people and interestingly, how the language used to talk about the disease can greatly impact how people understand their realities.

woman with horse, woman riding horseGina loves riding her horse, Benita.Courtesy of Sanofi

Gina—Hamburg, Germany (diagnosed with relapsing multiple sclerosis in 2017)

When her youngest son was 4 months old, Gina started having problems with her eye. She’d soon learn she was experiencing optic neuritis—her first symptom of MS.

“Immediately after the diagnosis, I looked up facts on MS because I didn’t know anything about it,” Gina says. “And as soon as I knew what could really happen with this disease, I actually got scared.”

As her family’s primary income provider, she worried about how MS would impact her ability to work as a writer and editor. Her family was afraid she was going to end up in a wheelchair. However, for now, Gina’s MS is managed well enough that she still works full-time and is able to be active.

“When I tell somebody that I have MS, they often don't believe me the first time because I don't fulfill any stereotypes,” she says.

Overwhelmed by negative perspectives on living with MS, Gina sought support in the online MS community, which she found to be much more positive.

“I think it’s important to use as many positive words as you can when talking about MS.” It’s important to be realistic while also conveying hope, she says. “MS is an insidious disease that can cause many bad symptoms…that can be frightening, and you can't gloss over it, either.”

To give back to the online community that helped her so much, Gina started a blog to share her story and help others trying to learn about their diagnosis.

Though she deals with fatigue and cognitive dysfunction sometimes, Gina stays active swimming, biking, riding horses and playing with her sons, who are now 11 and 6.

Cognitive dysfunction is common in MS, with over half of people affected. It can impact memory, attention, planning, and word-finding. As with many aspects of MS, some people experience mild changes, while others face more challenges.

Gina says that while there’s still a lot of education about MS needed, she feels positive about the future of MS because there’s so much research being done.

woman in wheelchair holding medal, woman rowingNathalie is an award-winning rower with multiple international titles.Courtesy of Sanofi

Nathalie — Pennes Mirabeau, France (diagnosed with relapsing-remitting multiple sclerosis in 2002)

Nathalie was a teenager and a competitive athlete when she noticed her first symptoms of MS, but it would take four years of “limbo” before she was diagnosed.

“Ultimately, the diagnosis was more of a relief, than a shock,” she says. “Because when you have signs and you don’t know why, it’s worse than knowing, in the end, what you have.”

However, learning more about the disease—and the realities of disease progression—scared her.

“That glimpse of the future was direct and traumatic,” she says. Her neurologist explained that the disease evolves differently for everyone, and her situation might end up being serious or very mild. So, she decided to stop comparing herself to others with MS.

She said to herself, “We’ll see what happens, and you’ll manage it bit by bit.”

By 2005, Nathalie’s MS had progressed to the point of needing a wheelchair. However, that has not dampened her competitive spirit.

Nathalie began her international rowing career in 2009 and has won multiple world titles, including two Paralympic medals—silver in London and bronze in Tokyo. Now, at 42, she still trains 11 times a week. Fatigue can be a problem, and sometimes hard workouts leave her with muscle stiffness and shaking, but she credits her ongoing sports career for helping her feel in tune with her body’s signals.

“Over the years, I’ve learned to listen to my body, letting my body guide when I need to stop and take breaks,” she says.

Nathalie explains that she used to only look backwards because of the initial shock of her diagnosis. In time, she stopped thinking about what she couldn’t do anymore and focused on her future. She now lives in the following mindset: “Even when doors close, don’t miss out on those that open.” Instead of focusing on what she can’t do, she focuses on the opportunities she still has. Right now, this includes her training for the 2024 Paralympic Games in Paris, where she will compete for another rowing medal.

“I only go forward,” she says. “Well, I try, anyway…It’s easy to say, it’s not always easy to do. But that’s what I try to do.”

woman exiting water after swimming, woman with great daneHelga's Great Dane has become a helpful and beloved companion.Courtesy of Sanofi

Helga—Johannesburg, South Africa (diagnosed with relapsing multiple sclerosis in 2010)

When Helga first started having balance issues and numbness in her feet, she chalked it up to her training as a runner. But when the numbness moved to her face, she knew something was wrong. She never guessed it was MS.

“When I was diagnosed, I felt completely overwhelmed and clueless,” Helga says. “I felt that I had nowhere near enough information. I did not know anything about the disease…I had no idea that it was going to be a process of continually monitoring and adjusting your lifestyle.”

In the beginning, Helga’s symptoms developed slowly, and she didn’t appear ill to others. She was even able to run for a few years after her diagnosis, but she couldn’t do marathons anymore, and she began to fall frequently due to balance issues and right-foot dragging. Then her cognition issues became more problematic, especially in her job as a trainer in a printing company.

“My executive function, decision-making and short-term memory were affected to the point that I was eventually medically unfit for work,” she says. She stopped working in 2017.

However, she didn’t stop living life. Even though she could no longer run, she continued to swim competitively. She got a Great Dane puppy and trained him as a service dog to help her walk. She also serves as vice chair of the patient support organization Multiple Sclerosis South Africa, and she advises others who have been diagnosed to join a patient advocacy group as soon as possible to get reliable information and meet others with MS.

Helga says she is “hopeful” about the future of MS. “I must say that I am so grateful that we have all the new medications available, because my life would not be the same if it wasn't for that,” she adds.

Part of how she manages her MS is by looking at the positives.

“If I could tell the world one thing about MS, it would be that MS is an incurable disease of the nervous system, but it's also the greatest teacher of valuing your health, family, friends, and managing change in your life,” she says. “My life is diversified in a way that I never, ever thought it would, and MS has been honestly the greatest teacher.”

Each MS journey is unique – with each person impacted experiencing different struggles, successes, and feelings as they manage this unpredictable disease. But the common thread is clear – there is a critical need for information, support, and hope. We are proud to participate in World MS Day and share these incredible stories of living life while living with MS. To learn more about MS, go to https://www.sanofi.com/why-words-really-matter-when-it-comes-to-multiple-sclerosis.

MAT-GLB-2301642-v1.0-05/2023

This article was sponsored by Sanofi. Participants were compensated when applicable.

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