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Culture

Brits share the most 'bizarre' things Americans do that seem unbelievable across the pond

united states, united kingdom, british, pledge of allegiance

From an outside perspective, the pledge of allegiance seems "culty."

You know how you were raised in a household where things were done a certain way, and then at some point, you went to other people's houses and saw that other people's families lived completely differently and it sort of blew your mind? Different rules, different standards, different consequences, different habits—all of which were considered normal to them? Some of those differences may have made you thank the heavens for your parents, or they may have made you realize your own family had some issues you didn't recognize.

The same thing happens when you are born and raised in a specific culture. Your sense of what's normal is molded by it—so much so that you may never even think to question whether certain things are actually rather bizarre.

That's why it's nice to have some outside perspective sometimes.

A Reddit user asked "What is the most bizarre thing Americans do that feels unbelievable by British standards?" and the answers are eye-opening.


Pledging allegiance to the flag

The first response was "Having kids pledge allegiance to the flag in school. Seems culty."

Most adult Americans were trained as young children to place our hands over our hearts, face the flag and recite the pledge every morning at school. Every single morning. Swearing our allegiance to our country and its flag, out loud, in unison.

"I went to an American school while I lived in Italy; I was one of the only English kids there. The pledge of allegiance was indeed every morning, and it felt as culty as you think. They called my parents when I wasn't joining in ffs," wrote one commenter.

"Never mind seeming culty, it just flat out is," wrote another.

And another: "As an expat, I can confirm that having to pledge allegiance to the American flag was definitely one of the weirdest things that contributed to the culture shock."

Let's be real. If we saw children from any country deemed unsavory to American sensibilities (let's say Russia, China, North Korea, for example) being required to stand in unison and recite a pledge of allegiance to their country's flag every single morning, we'd consider it brainwashing.

There's a reason that first comment got more than 5,500 upvotes.

The way we do healthcare

The comment "Going bankrupt because you needed your broken leg realigned. Being homeless as a result of needing to pay for cancer treatment" garnered 2,000 likes because the U.S. approach to healthcare is genuinely bizarre.

Everything Americans accept about healthcare is asinine: the for-profit health insurance industry, the fact that health insurance is tied to employment (but not all employment, because that would make too much sense, apparently), the fact that we pay way more for healthcare than other wealthy nations and yet have worse health outcomes, the fact that virtually no one understands how their health insurance works because it's so complicated, the fact that medical bankruptcy is a thing, etc.

And on top of that, the fact that there is a baffling number of Americans who actually defend this system when all evidence points to the superiority of universal healthcare is absolutely mind-blowing.

How we don't do guaranteed paid parental leave

"No paid maternity/paternity leave and new mothers having to go back to work within two weeks of giving birth. Insane," wrote one commenter.

After Americans tried to say this wasn't true because their company offers paid leave, the commenter clarified that the U.S. doesn't require paid leave. It's up to the discretion of companies, which is, indeed, insane.

"I've always thought this was barbaric but since having my baby it horrifies me even more," someone wrote in response. "My baby is 12 months old next weekend and I'm still on leave. My mat leave is just finishing and I'm about to start annual leave which will see me through until January. I've been on around half pay for the year which has been tough financially but I wouldn't give up this time for anything.

"At 2 weeks I could still hardly sit (episiotomy), my boobs were painfully full and leaking all the time, I was barely managing to get dressed, my baby was wanting to be held at all times day and night... I was hardly functioning.

"We don't separate kittens and puppies from their mothers that early, how can it possibly be okay to separate babies from their mothers."

School shootings and the active shooter drills that go along with them

Well, yeah. Not exactly a point of pride.

It's not that other countries never ever have school shootings, but the U.S. is in a league of our own here.

"My cousins in America do school shooting practises every term," wrote one commenter. "It's awful that that's a thing they need. Scary."

"You can buy bulletproof school bags," wrote another. "It's nuts."

To be fair, most Americans would agree that school shootings and active shooter drills are bizarre. We just can't agree on what to do about it.

Our lack of electric kettles, apparently

One commenter wrote:

"On a less serious note, boiling water in a pan (or microwaving it!) for a cup of tea or coffee. I've seen it when watching regular people do videos, not just on tv or whatever. Where are all the kettles??(There are a lot about guns and stuff, so I thought I'd do one that's less sad.)"

Others chimed in:

"I'm a Brit living in the US and my electric kettle is viewed by some of my American friends as a revelation. I buy them as gifts."

"Both times I've been to America, I would go down to reception at the hotel and ask for a kettle. The receptionist would look at me dumbly and ask what a kettle was. And this wasn't once or twice. This was multiple times."

Some people explained some reasons for kettles being rare-but-not-unheard-of, ranging from the voltage being different in the U.S. to the fact that microwaving water is quick and easy. But there's also this:

"British/American living in the US... No one I know really drinks tea with enough regularity to warrant a kettle, specially living in tiny apartments with limited kitchen space. Coffee makers are a lot more common because coffee is more popular than tea that I've seen."

This is the truth. (And I do know a lot of people with electric kettles, but it apparently varies from region to region.)

We don't walk when we can drive

Several commenters pointed to Americans' resistance to walking anywhere that's farther than a block or two, as well as our lack of sidewalks and walkways to even make it possible:

"No pavements/sidewalks in some places. I went to Dallas for work some years ago, and was dismayed to find that I couldn't just 'go for a walk' from the hotel."

"Yes! Nobody there walks ANYWHERE. I have a friend who is from Iowa but lived in London for a few years. When she went back she said she really misses walking. I asked what she meant, she said if she just went on a random walk she'd definitely get people stopping for her thinking she's not okay, not okay in the head or just homeless."

"I was reading a book the other day that described a woman walking two miles to then get a bus home as a 'hike'. I mean, that's just walking? Sure it was alongside a road not on a pavement but it's still just walking!"

"Yep, that's really weird. I went to an IT conference in Orlando back in the late 1990's. The hotel was only about a kilometre from the conference centre, so obvs we walked as the weather was nice. Not only was it tricky due to the lack of any footpath, people thought we were mad. Also you can't just cross the road where you want to."

Sorry, Brits. Our land is big and our gas is cheap compared to yours. And also, you know we're notorious for our unhealthy habits.

Sales tax tacked on at the end of a purchase

"Taxes put on at check out," wrote one commenter.

Wait, what? This isn't normal?

Apparently not.

"The taxes infuriate me," wrote one commenter. "I was in Canada last week and they do the same thing. I kept thinking I was being overcharged until I remembered that advertised prices don't include taxes, and that you're expected to tip for pretty much everything."

"I only found out about the tax thing recently and it f*cking blew my mind," wrote another. "How tf do you know how much cash you'll need? Americans must be really good at mental arithmetic if they have to add tax every time they add something to their basket."

Spoiler: We're not all that good at mental arithmetic. We just know we need about 10% more money than what a thing actually costs.

Agreed, though. It's weird and annoying.

This isn't an exhaustive list, by any means. Other "bizarre" American habits include circumcision (just the messenger—please don't send me hate mail), televangelism, prescription drug commercials and spray cheese.

Definitely some food for thought as we consider what's "normal" and what's not. Different or even "bizarre" isn't necessarily bad, but we could certainly do some national soul-searching with some of the things on this list.

(And hey, British friends—the way you say "aluminum" is weird. So there.)

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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.

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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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