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What's wrong with aging? Here are 17 pleasures people only started to enjoy as they got older.

Don’t let the youngsters fool you. There’s nothing wrong with a quiet night in and a good night's sleep.

aging, ask reddit, youth culture

A lady happily spends time with herself.

American culture has always been obsessed with youth and vitality. It feels like after you reach the age of 35 you become invisible. That’s why we fret over gray hair and wrinkles and spend nearly $17 billion a year on cosmetic surgery.

The funny thing is that studies show people get happier as they age.

So why are we obsessing over being young when we should just relax and enjoy the self-acceptance and wisdom that comes with aging?

As people age, they also start to enjoy things that they previously didn’t like or hadn’t experienced. Older people are better at slowing down, being present and appreciating the world around them instead of looking to see what’s coming around the corner. They develop an instinctual knowledge that joy comes from being in the moment.


As people age, they develop a refined sense for food, drinks and the arts. Older people also have a lot less tolerance for other people’s baggage and appreciate healthy relationships.

A Reddit user by the name of fgfy4454 asked the online forum “What did you start liking the older you got?” and the responses showed an appreciation for the richness of life. The conversation also had an undercurrent of appreciation for the gifts that come with aging and a healthy disdain for the foolishness of youth.

Here are 17 of the best answers to the question, “What did you start liking the older you got?”

1.

"Spending time alone with myself." — NobodyCool2844

EvilBosch added:

"I am very happy with my own company. Not a shut in at all, but certainly don't feel compelled to always be chasing social contact. A weekend with nothing to do, and no social commitments sounds to me like a rare treat! But all folks are different. I've also known people who are basically the human equivalent of Labrador dogs - contantly needing attention and stroking, and who get sulky and cross (and bitey) when they don't get it. We all exist on a continuum of introversion/extraversion, and that's fine. But it's the extravert's fallacy that anyone who is happy with their own company must be somehow unfulfilled or leading a lesser life. Some of us prefer to quietly read a book."

2.

"Sleeping." — bletusibebusi

3.

"Comfy, quality socks." — wildcard520

4.

"Myself." — Sea-Professional-953

5.

"Quiet time." — Pepperrr01

AteUrGrandma added:

"Sitting outside and doing nothing. As a kid, I always wondered why adults would do that."

6.

"A new dish scrubber." — 18gsir

IAmNotABritishSpy added:

"I was doing the washing up recently and realised I have a favourite pot to cook with, as it always washes out so easily."

7.

"Not drinking alcohol. Hangovers feel worse, it’s an expensive habit, and it’s not as fun as it used to be." — wicked-vibes

PasGuy55 added:

"Absolutely. A hangover now lasts until about 7pm. Nothing fun about spending the day feeling queasy."

8.

"Tea instead of coffee. I used to pound coffee. But now it aggravates reflux and generally upsets my stomach more. A nice cup of tea especially earl grey with milk really does the trick." — wormholeweapons

9.

"Vinegar. I absolutely HATED pickles, olives, and vinegar chips as a kid. I am now at the “extra pickles and banana peppers” phase of my sandwich journey through life." — SickAssFoo_69

10.

"Compound interest." — FatOldRugbyDude

11.

"Mustard. What a great condiment." — Hei2

12.

"Old songs. Younger me always followed whatever is mainstream." — Duschkopfe

13.

"Art museums. Used to think they were pretentious and boring growing up. Over time, thought about the process and effort it really takes to make that kind of work. Whole new perspective." — bdruid117

14.

"Scented candles. I used to avoid "feminine" things because it's not 'manly' to have nice stuff. But a couple of months ago I started lighting candles in my new apartment and now I can't get enough from trying new scents. Currently, my favorite is apple cinnamon. Apparently being manly is bullshit and having nice stuff is fun." — MemChoeret

15.

"People who don’t create or have drama in their lives or mine. At least not on purpose. Simple quiet relationships." — themermaidbrain

16.

"I began falling for large women they became so much more attractive to me." — DrGoldy2

17.

"Staying home on the weekends or just going to a friend's house for a couple of beers instead of going out clubbing." — No1_Knows_Its_Me

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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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Sorry, Labradors. After 31 years, America has a new favorite dog.

The American Kennel Club has crowned a new favorite.

via Pixabay

A sad-looking Labrador Retriever

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Mzansi Youth Choir received a Golden Buzzer for their cover of Nightbirde's "It's OK."

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Back in 2021, Nightbirde arrived on the stage with only a 2% chance of surviving a third round of cancer. But still, she kept to her philosophy of "You can't wait until life isn't hard anymore before you decide to be happy." She passed away in Feb 2022, but not before sharing her beautiful heart with the world.
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