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People are sharing the weirdest things we accept as 'normal’ and it has people questioning reality

What will people say about us 50 years from now?

ask reddit, things that won't age well, healthcare
via Pexels

People living to work, not working to live.

If we looked 60 years into the past, there are a lot of things that were accepted as “normal” that today most people find abhorrent. For example, people used to smoke cigarettes everywhere. They’d light up in hospitals, schools and even churches.

People also used to litter like crazy. It’s socially unacceptable now, but if you lived in the ’70s and finished your meal at McDonald’s, you’d chuck your empty styrofoam container (remember those?) and soda cup right out of the window of your car and onto the street.



It’s hard to imagine that just 60 years ago spousal abuse was considered family business and wasn't the concern of law enforcement.

It makes me wonder when people in the future look back on the year 2022, which things will they see as barbaric? Almost certainly, the way we treat the animals we use for food will be seen as cruel. The racial divides in the criminal justice system will be seen as a moral abomination. And I’m sure that people will also look at our continued reliance on fossil fuels as a major mistake.

A Reddit user by the name u/MEMELORD_JESUS asked the AskReddit subforum “What’s the weirdest thing society accepts as normal?” and the responses exposed a lot of today’s practices that are worth questioning.

A lot of the responses revolved around American work ethic and how we are taught to live to work and not to work to live. We seem to always be chasing some magical reward that’s just around the corner instead of enjoying our everyday lives. “I’ll get to that when I retire,” we say and then don’t have the energy or the inclination to do so when the time comes.

There are also a lot of people who think that our healthcare system will be looked at with utter confusion by people in the future.

Here are 17 of the best responses to the question, “What’s the weirdest thing society accepts as normal?”

1. Work-life balance

"Working until you're old, greying, and broken then using whatever time you have left for all the things you wish you could have done when you were younger." — Excited_Avocado_8492

2. Rest in comfort

"That dead people need pillows in caskets." — Qfn4g02016

3. I.R.S. mystery

"Guessing how much you owe the IRS in taxes." — SheWentThruMyPhone

4. You get the leaders you deserve

"Politicians blatantly lying to the people. We accept it so readily, it's as though it's supposed to be that way." — BlackLetyterLies

5. The booze-drugs separation

"Alcohol is so normalized but drugs are not. It's so weird. I say this as an alcohol loving Belgian, beer is half of our culture and I'm proud of it too but like... that's fucking weird man." — onions_cutting_ninja

6. Stage-parent syndrome

"People having kids and trying to live their lives again through them, vicariously, forcing the kids to do things that the parents never got to do, even when the kids show no inclination, and even have an active dislike, for those things." — macaronsforeveryone

7. Priorities

"Living to work vs working to live." — Food-at-last

8. 'The Man' is everywhere

"Being on camera or recorded any time you are in public." — Existing-barely

9. Tragic positivity 

"'Feel-good' news stories about how a kid makes a lemonade stand or something to pay for her mom's cancer treatment because no one can afford healthcare in America." — GotaLuvit35

10. Credit score

"As a non-American, I am amazed at their credit score system. As a third-world citizen, credit cards are usually for rich (and slightly less rich) people who have more disposable money than the rest of us and could pay off their debt.

The way I see people on Reddit talk about it is strange and somewhat scary. Everyone should have a card of his own as soon as he becomes an adult, you should always buy things with it and pay back to actively build your score. You're basically doomed if you don't have a good score, and living your life peacefully without a card is not an option, and lastly, you'll be seen as an idiot if you know nothing about it." — BizarroCullen

11. The retirement trap

"Spending 5/7ths of your life waiting for 2/7ths of it to come. We hate like 70% of our life, how is that considered fine?" — Deltext3rity

12. Yes, yes and yes

"Child beauty pageants." — throwa_way682

13. That's not justice

"The rape of male prisoners. It's almost considered a part of the sentence. People love to joke about it all the time." — visicircle

14. Customers aren't employers

"Tipping culture in the US. Everyone thinks that it's totally OK for employers not to pay the employees, and the customers are expected to pay extra to pay the employees wages. I don't understand it." — Lysdexiic

15. Staring at your phone

"Having smartphones in our faces all day. This shit isn't normal...imma do it anyway...but it is not normal." — Off_Brand_Barbie_OBB

16. Homework on weekends

"Students being assigned homework over weekends and only having a two-day weekend. The whole point of a weekend is to take a break from life, and then you have one day to recover from sleep deprivation then one day to relax which you can’t because of thinking about the next day being Monday. And the two days still having work to do anyways." — MrPers0n3O

17. Kids on social media

"Children/young teens posting on social media sites. I’m not necessarily talking about posting on a private Instagram followed by friends, I’m talking about when kids post on tiktok publicly without parental consent." — thottxy


This article originally appeared on 03.11.22

Sponsored

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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