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Pop Culture

Here are 17 things people really miss the most about living in the '90s

the 1990s, Kurt Cobain, Bill Clinton

Kurt Cobain, Blockbuster Video, Bill Clinton.

The 1990s was a sweet spot in American history. The stifling Cold War with the Soviet Union had just come to the end in 1989 and it would still be 12 years before a new era of fear after the 9/11 attacks.

The 1990s was also a time of prosperity that lifted up Americans across the socioeconomic spectrum and an era that saw unprecedented peace in the world. In fact, things were going so well in America that President Clinton managed to have a budget surplus four years in a row.

The '90s was also the last gasp of the analog era when people couldn't contact you 24/7 and did things for the pure joy of it instead for the likes and shares.

To say that the '90s was the last great American decade may be looking back with rose-colored glasses but it's obvious that as we've entered this new era dominated by technology, we left behind a lot of things that brought us joy. Many of us wouldn't mind having them back.

A recent Reddit thread asked "What do you miss about the '90s?" and the answers will take you back to a time that most of us remember fondly. Will people ever say that about the 2020s? Only time will tell.


1. You made plans without having to text people.

"Before we had mobile phones, my wife and I would plan to meet at a certain street corner at a certain time after work. We sometimes had to wait for the other person to show up, but we knew they would." — i_will_be_dead

2. The world was clearly changing for the better.

"There was a period between the Cold War and the War on Terror when it seemed like there was hope for the world." — igetasticker

3. Friday nights at home with the family.

"Blockbuster/Pizza Hut on Friday nights." — EdwardPackard

4. People left you alone.

"Not being contactable 24/7. Peace of leaving school/work and not having to deal with their nonsense till tomorrow." — Soma_Tweaker

5. Air travel without the stress.

"Did you know that before 9/11, it wasn't a massive pain in the ass to go fucking anywhere?! Loved ones could walk you right to the gate. You could bring snacks, sandwiches, and drinks onto the plane with you. The prices at Hudson News were perfectly reasonable, because if they weren't, you could just walk out of the terminal and grab something." — GavinBelsonsAlexa


6. The mall.

"Malls were awesome, and I hate that the strip mall style has taken over. Especially up in Canada, where it gets to -40 in the winter. Back in the day you could legitimately spend hours wandering the mall, indoors and warm. Now it is depressing. Maybe the big malls like Mall of America or West Edmonton Mall are still okay, but the ones in my city are shit." — Lexi_Banner

7. Following a scene.

"In the '90s I would walk to my local record shop and talk to the guy. He would recognize me and ask about my thoughts on the Offspring album I bought last time I was in, and then recommend something that just came in from some guys called Green Day.

I'd then give a listen on the wall-mounted headphone player and take it home. Then, the whole next week would listen to nothing else... It was kind of great." — Koro

8. A genuine good time.

"I think people are more concerned with posting something and going viral now. I really hate that you can just be minding your business, doing something with family or friends and enjoying yourself, and somebody will randomly record what you're doing so they can call you 'corny' and get likes and views." — Enviornmental-Bank81

9. Magazines.

"Everyone had their favorites for whatever hobby or interest you had. For me it was 'Guitar World,' picking up the issues with bands I loved and plinking along to the tab on my crappy electric guitar! For my wife it was 17, checking out the most recent trends!" — JackFairy80

10. Hanging out.

"Honestly the thing I miss the most, and the thing that is so hard to explain to modern kids, is 'hanging out.' Before cell phones, people used to just go to each other's homes, or to some public space, and just spend time together." — Vambot5

11. Making mix tapes.

"It was so much fun to make them, carefully trying to fit as much as you could in the limited amount of time that you had, but still making each song work with the next. Getting one was just as thrilling, especially if you just put it on without looking at the tracklist (if whoever made it included one) and being surprised by each new song." — Edgar

12. Music mattered more.

"Music felt more special because you kind of had to take some risks when buying a cd. At best you could listen to it at one of the stations in the store, but other times you might have heard a song on the radio or watched a music video on MTV. I bought some albums where only the song I liked was good, but still tried to appreciate it all." — plentyfunk66

13. Less pressure to be perfect.

"Nowadays due to social media, especially sites like Instagram, so many young people feel like it's necessary to always be dressed well, always wear a full face of make-up, etc. Sure, we had unrealistic beauty standards and plastic surgery before, but to me it feels like it's gotten much, much worse and also much more uniform than before." — Owezara

14. No 24-hour news cycle.

"Maybe I'm in a minority, but I for one REALLY miss NOT having a 24-hour news cycle. Once that became a thing, it basically prevented journalists from actually doing thorough research before splitting 'information' on TV to satiate their corporate owners." — Minerva_Madin

15. People talked to one another.

"I miss going to coffee shops or bars and being able to meet new random people. I made some of my best friends that way. Now folks just leer up from their phones more often than not." – Shiller_Killer

16. People watched concerts instead of filming them.

"Concerts weren't a sea of phones in the air. People are so concerned with people knowing they were at a concert via social media, that they don't even pay attention or experience the show. It's so dumb." — thebestmike

17. Brick-and-mortar stores.

"I still think this is underrated. Yes now we have a much much wider selection of stuff available instantly, but it used to be extremely fun to go out on a Sunday, go to a record store or video rental store with your friends, discuss options and settle on one." — Humble Shoulder

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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