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Education & Information

A comic published in 1997 predicted online schooling in 2021 with eerie accuracy

A comic published in 1997 predicted online schooling in 2021 with eerie accuracy

In 1997, we used the internet primarily for email and for the novelty of being able to look things up on the "worldwide web." The internet as we know it wasn't even 10 years old and was a tiny fraction of one percent the size it is now. Speeds that seemed fast then would make us throw our laptops at the wall now. There was no Google, no social media, no Zoom. This is what the top search engine looked like:

Wayback Machine

We knew the internet had some potential, but we had no idea how reliant we would become on it for pretty much everything. Our vision of what the future might hold still looked like the Jetsons in many ways. Flying cars. Bulbous architecture. Inexplicably pointy clothing. Some kind of cool communication devices that would allow us to see one another's faces in real-time.

And yet, Archie Comics got one thing eerily right in a 1997 Betty comic titled "High School 20201 A.D." Virtual, online school.

Of course, it wasn't happening due to a pandemic, but was simply the way school happens in their imagined future.

"Kids today are SO lucky! They're able to go to school in their own home!" says Betty's Dad. "They never have to carry books to school...and they never have to worry about the weather!"

Flashback to this winter, when schools contemplated whether or not to have "snow days" for kids doing school at home.

"'Scue me, folks!" says Betty. "Class is about to begin!" She sits in front a definitely-not-2021-accurate computer with a hilariously huge camera atop it, but the basic gist is spot on. Especially when we see the sign on the wall that reads "VIDEO MONITOR MUST REMAIN UNCOVERED AT ALL TIMES."

Kids turning off their cameras was one of the hundreds of challenges teachers have had to deal with through the 2020-2021 school year. Phew.

Screenshots of the first page of the comic have gone viral on social media as people point out how bonkers it is that the comic pinpointed this year for their online, at-home schooling idea. Snopes had to do a fact-check as people asked if it was real, and Archie Comics themselves wrote up a page on their site about the prescient comic.

They wrote:

"The 6-page story, originally titled 'Betty in High School 2021 A.D.' was written by George Gladir, with art by Stan Goldberg, Mike Esposito, Bill Yoshida, and Barry Grossman. In this story we find Betty and her friends in Riverdale dealing with the struggles of virtual home schooling!

When this story was reprinted in 2015, the year in the title was changed to '2104 AD' (probably because we didn't have flying cars yet) but rest assured, the original story was published in 1997 and eerily predicted elements of virtual home schooling now commonly found across the world!"

Archie Comics went ahead and shared the rest of the comic on Facebook, and it's fun to see what was eerily accurate and what was hilariously not.

"My video phone is flashing!" Betty thinks, as her pink magic-mirror-looking phone rings. Remember, most people didn't have cell phones at this point, and smartphones with cameras were a more futuristic idea than flying cars, oddly enough.

And as bizarre a year as it's been, I don't think any schools have instituted "closet detention" for at-home schoolers.

Betty's friends' "special video screen" she puts behind her to make her feel like she's not alone in class is pretty funny, and not terribly unlike the Zoom backgrounds we can virtually put behind ourselves.

They actually overshot a little with the super short skirts, as the micro-mini actually made a comeback in the early 2000s.

And yep, there's the good ol' futuristic flying car. Is there anything we've been more wrong about than the likelihood of flying around in cars by now? I don't think so.

The rest of the comic is the teens checking out the old high school museum, where they could see the cafeteria and bulletin board and "an actual classroom."

And Betty ultimately saying she wished she could "go back to the days of our old and obsolete high school."

Yep. That part's accurate for a lot of actual 2021 students as well.

Virtual schooling has been a mixed bag, with some kids thriving at home without the pressures and social drama of in-person school, while others have struggled without the structure and social stimulation of it. But no one was prepared for the sudden shift to online learning. The past year has been one long stretch of trial and error, forced flexibility, and constant adaptation. And it definitely wasn't the future—or present—any of us had hoped for.

Hopefully, we'll get those flying cars one of these days. In the meantime, we'll settle for basic in-person schooling and some semblance of normalcy.

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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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