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Culture

People share useless facts that simply won't leave their heads

random facts, viral reddit
Photo by Sean Benesh on Unsplash

Some facts are only useful for trivia contests.

Ah, useless facts. Random knowledge that serves no purpose other than to take up space in our brains, and maybe, just maybe, win a trivia game (yeah right) or kill time at a party (I’ve forgotten, what’s a party?).

Leave it to Ask Reddit to resurface all things odd and amusing, though. People shared their own useless facts that live rent free in their heads. And though they might be pointless, they are certainly entertaining.

Without further do:


  Mitochondria is the powerhouse of the cell.

Yep, this useless fact has stayed with us since elementary school On the bright side, it’s been the source of many a fun meme.

Vending machines are more deadly than sharks.

animation domination lol GIF by gifnewsGiphy

Think about this next time you go to retrieve a Snickers bar: Between 2002 and 2015, the National Electronic Surveillance System reported that vending machines caused four deaths per year in the U.S. Mostly due to people tipping the machines onto themselves.

Compare that to the shark-related deaths averaging out to just 0.6 deaths per year. Not sure how only about half of a person is considered dead, but math was never my strength.

This statistic might need to be taken with a grain of sea salt however, given that those in landlocked states have next-to-zero chances of experiencing a shark attack. But there you have it, a useless fact to use when you’re at the beach.

Snails have teeth.

horror finger GIF by absurdnoiseGiphy

“They’re not big enough teeth to hurt humans. That’s what makes it a useless fact to know. & it won’t leave my head because it’s juuuuuust disturbing enough to make me rethink my entire opinion on snails.” – ghosts-go-boo

But cows do not.

At least, no upper front teeth. Makes chewing—and dentist visits—easier I suppose.

The Sun is about 400 times bigger than the Moon but also about 400 times farther away from Earth. So they look to be about the same size.

File:Solar eclipse 1999 4.jpg - Wikimedia Commonscommons.wikimedia.org

This explains how the sun can be completely blocked in an eclipse.

Pigeons and doves are in the same bird family.

Happy Animation GIF by sahlooterGiphy

Columbidae is a subspecies of birds that are stout bodied, with short necks, and primarily feed on seeds, fruits and plants. Though one lives on as a symbol of peace and love, and the other is often considered a flying rat, the names are practically interchangeable.

However, thinking about Stevie Nicks singing, “just like a white-winged pigeon” doesn’t have quite the same ring to it.

The length of a jiffy…

back to the future great scott GIFGiphy

According to ScienceFocus.com, physicists use a “jiffy” to define how long light takes to travel one femtometer (which is a tiny fraction of a millimeter). In layman’s terms, one jiffy equals one-fiftieth of a second.

So next time you say, “be back in a jiffy,” know that you better return really, really, really fast.

Most corn is inedible for humans.

corn on teal surfacePhoto by Charles Deluvio on Unsplash

1% of the corn grown in the USA is sweet corn (the corn you eat as corn). The other 99% is field corn (or dent corn), which is fairly inedible raw and needs to be processed before human consumption. This field corn is also what they use for non-edible corn products, like ethanol, paint, cosmetics, etc. Yes, most corn goes to livestock feed. Ethanol and High Fructose Corn Syrup are up there as well. Yes, if you're driving on a highway and are passing fields of corn, you very likely cannot eat it.” – Kat_lbltko1pl

Infants have flexible bones.

stretching GIF by AFV BabiesGiphy

Ever wonder why toddlers seem so much more flexible? This is because a baby’s skeleton if very different from an adult's. Babies are born with about 300 bones (94 more than adults) that are joined together with pliable cartilage to make that whole birth thing possible. As they get older, the bones will fuse together. And suddenly that toe touch is nothing but a distant dream of the past.

Numbers from 1-999 don't have the letter "a" in word form.

white printing paper with numbersPhoto by Mika Baumeister on Unsplash

Some vowels just don’t get the respect they deserve.

John Wilkes Booth and Lee Harvey Oswald are both known by three names. And each full name is composed of 15 letters.

surprised season 4 GIFGiphy

Actually, this is not entirely correct. Oswald’s full name was not used until after Kennedy’s assassination, due to his habit of adopting false names.

Cockroaches molt.

Unlike a reptile shedding it’s skin, cockroaches molt out of their entire exoskeleton. Out crawls a soft, fleshy, ghostly-white creature that will turn brown over a few hours. You’re welcome for the nightmare fuel.

There you have it. Gems of wisdom no one asked for. They say knowledge is power. But in this case, I’d say knowledge is unnecessary. But still fun!

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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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