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25 clichés that are actually true and how they could change your life.

Sometimes we need to remind ourselves of the things we’ve learned, over and over again.

Socrates, considered to be one of the founders of Western philosophy, was once called the wisest man on Earth by the Oracle of Delphi.

When Socrates heard that the oracle made that comment, he believed the statement was wrong. Socrates said, "I know one thing: that I know nothing."

How can the smartest man on Earth know nothing?

I heard this paradoxical wisdom for the first time from a teacher when I was 14 or 15. It made such an impact on me that I used Socrates’ quote as my learning strategy from then on.


"I know nothing" means, to me, that you might be an educated person, but still you can learn from everything and everyone.

One thing I like better than learning from my own mistakes is to learn from other people’s mistakes. Over the years, I’ve been blessed to have great mentors, teachers, family, and friends who have taught me about life. Of course, I learn from my own life too. But learning from others is often faster and deeper.

Plus, while we might learn things quickly, we often forget those things at the same rate. Sometimes we need to remind ourselves of the things we’ve learned, over and over again.

So here’s my list of 25 things about life that other people have taught me.

These are things that have changed my life completely and that I wish I’d known about 10 years ago.

1. Struggle is good.

Never say, "I can’t take it anymore." Say, "Bring it on!"

2. Don’t complain.

Complaining is the biggest waste of time there is. Either do something about it, and if you can’t, shut up.

3. Spend time with the people you love.

That’s your family and best friends. If you don’t have a family, create one (in whatever way that means to you). Most people in life are only visitors. Family is for life.

Photo via iStock.

4. Don’t start a relationship if you’re not in love.

I’ve done this more than once. You kind of like someone and think, "We might as well give it a shot." Not a good idea. You’re either in love, or you are not. Don’t fool yourself. It’s not fair to you and the other person.

5. Exercise daily.

I didn’t get this until recently. A healthy body is where you have to start everything in life. If you can’t build a healthy and strong body, what CAN you build in life?

6. Keep a journal.

No, keeping a journal is not for children. It helps you to become a better thinker and writer. "I don’t want to be a writer," you might think. Well, how many emails and texts do you send a day? Everybody is a writer.

7. Be grateful.

Say "thank you" to everyone and everything. "Thank you for this beautiful day." "Thank you for your email." "Thank you for being there for me."

8. Don’t care about what people think.

We all die in the end; do you really think it matters what people think of you?

9. Take more risks.

Don’t be such a wimp.

Photo via iStock.

10. Pick an industry, not a job.

If you want to become good at something, you need to spend years and years doing that. You can’t do that if you hop from industry to industry. Pick an industry you love and start at the bottom. You will find the perfect role for you eventually.

11. Lead the way.

When you find yourself in a situation where everyone looks at each other, it’s time for you to lead. You‘re a leader when you decide to become one. There’s no initiation or a title. Just a decision.

12. Money isn't important.

It really isn’t. But you have to train yourself not to care about money. Don’t become too dependent on the stuff you own — otherwise, the stuff will own you.

13. Be nice.

I don’t mean you should be a pushover. You can be someone that doesn’t take shit and be nice about it. Just don’t insult people, think you’re better than them, or act like an idiot.

14. Learn every day.

You’ve got to train your brain to stay alert. You don’t have to read a book a day to learn every day. Learn from your mistakes. Learn from the people around you — be open to what they can teach you.

Photo via iStock.

15. Rest before you are tired.

Even if you love your job and every day seems like a holiday, you need to take time to rest. You’re a human and not an android; never forget that.

16. Don't judge.

Just because people make different choices than you, they are not stupid. Also, you don’t know everything about people, so don’t judge them — help them.

17. Think about others.

Just be mindful, that’s all. We all have families, bills to pay, and our own issues. Don’t always make everything about yourself.

18. Give without expecting something in return.

Don’t keep score. You will become a bitter person if you do that. Give solely for the joy of giving. If you get something in return, great, and if you don’t, great.

19. There's no end game.

We, as a species, just are. Don’t try to figure it all out. Enjoy your journey.

20. Enjoy small things.

I like clichés because they are (usually) true. Especially this one. You know why? Everyone says they know it, but no one lives up to it. They just chase big things.

Photo via iStock.

21. Don't take yourself so seriously.

Yeah, yeah, you’re an individual, and people have to take you seriously. I get it. But at the end of the day, we’re all a bunch of ants trying to chase the same things. Lighten up.

22. Don't blame people.

What’s the point? Do you want to punish them? Also don’t blame yourself — you’re only human.

23. Create something.

Not to leave a legacy (you won’t be here to see it anyway), but to be of use. Make music, write a book, build a table, anything. You’ll feel good about yourself, plus you give something back to people to use or enjoy.

24. Never look back for too long.

Reflecting on the past is only good for one thing: learning.

25. Take action.

Don’t just sit there; do something. Without action, there is no outcome.

Photo via iStock.

You might know a lot. But like Socrates, you and I also know nothing at all. So we have to keep learning.

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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