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A man grossly misjudged how to speak to girls and got expertly handled by a Girl Scout

"No. Walk away."

A man grossly misjudged how to speak to girls and got expertly handled by a Girl Scout

This article originally appeared on 03.09.20


Somewhere in Salt Lake City, a Girl Scout is getting allll the good mojo from The People of the Internet.

Over the weekend, Eli McCann shared a story of an encounter at a Girl Scout cookie stand that has people throwing their fists in the air and shouting, YES! THAT'S HOW IT'S DONE. (Or maybe that's just me. But I'm guessing most of the 430,000 people who liked his story had a similar reaction.)


"I just saw the most wild thing!" McCann wrote on Twitter. "A man started walking toward the Girl Scouts cookie stand in front of the grocery store and he yelled 'My bitches are BACK' and this Girl Scout just yelled 'No. Walk away.' AND HE DID."

So simple. So straightforward. But it gets even better.

McCann wrote out the full story on his blog, It Just Gets Stranger, offering some extra details to his tweets.

"It was truly jarring," he wrote of the man's exclamation. "Like, it was sort of the last thing I expected anyone to say. My mind suddenly rebooted. The six or so other people who were all standing around in front of the grocery store froze and looked at him. I opened my mouth to say something, but then really didn't know what to say."

"It was unclear who he was calling 'bitches,'" he continued. "If it was the Girl Scouts, well obviously that was terrible. If it was the cookies, I mean that's kind of funny (don't @ me), but totally inappropriate to say to a bunch of 12 year olds (is that how old Girl Scouts are?). Either way, he shouldn't have said it and I don't know what could have possibly made him think this was a fine way to approach a group of Girl Scouts."

McCann said the girl's response was immediate, and it floored everyone. "Her tone was so full of confidence and sass," he wrote. "It was the most perfectly delivered line I have ever heard."

"This dude completely froze. He just stopped walking. His face went bright red. His mouth was sort of gaping open. He did this very awkward and stilted nod, almost apologetic, abruptly turned around, and shuffled back to his car at like 6-minute-mile pace. The girl just death stared him all the way through his walk of shame."

McCann says it took him a bit to digest what he'd just seen.

"I ended up walking into the store and the entire time I was shopping I was just trying to process what had happened. I kept replaying it over and over and wondering if I had misheard or misunderstood something," he wrote.


"Who was this guy? Did he just make the biggest miscalculation of his life? Is he going to move away and start a new life now? Is that girl going to be president one day? Can I adopt her? Can she adopt me? Can I start a cult to follow her?"


As he was leaving the store, he went up to the girl to compliment her—then got another perfectly delivered line from the intrepid Girl Scout.

"Two adult women were standing behind the girl (the troop leaders, I assume)," he wrote. "I said to the girl, 'I saw how you handled that man earlier. That was really really impressive. Your troop is pretty lucky to have you.'"

"And this girl. This Goddess of a human. The one I'm for sure going to worship if ever she starts a religion. Without stuttering. With perfect comedic timing. She responded:

'You gotta be pretty tough if you're gonna go out in THIS outfit.'"

OMG.

Let's all give this girl a virtual high five for her gumption and wit. It takes a lot of courage to say something to an adult when you're a kid, especially a man who is doing something inappropriate. The fact that she seemed to have been perfectly prepared for that moment, shutting him down so immediately and decisively that everyone in the vicinity stopped to take note, is so dang impressive.

This is what happens when you teach girls their true worth and encourage them not to accept anything less than respect and dignity. Gotta love it.







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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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