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Joy

10 things that made us smile this week

Here, have a round of joy. It's on us.

joy smiles
Alexas_Fotos/Canva

Upworthy's weekly roundup of delights.

When headlines and social media seem to be dominated by the negative, we all need reminders that the world is full of wonderfulness. Joy connects and inspires us and can be found everywhere—if we keep our eyes open and look for it. One of our goals at Upworthy is to make that search a little easier by telling stories that highlight the best of humanity and sharing the delights, large and small, that unite us.

Each week, we collect 10 things that made us smile and offer them to you to enjoy and share with others. We hope this week's list tickles your heart and brings a smile (or 10) to your face as well.

1. Tico the parrot is a master vocalist. Not even an exaggeration.

@ticoandtheman

On a dark desert hwy, cool wind in my hair…

We've shared some delightful parrots in these roundups before, and each one somehow seems to out-entertain the last. I did not see Tico's vocal skills coming, though. The intonation! The vibrato! Even my music major daughter was blown away by this singing bird.


You can see more of Tico singing with guitarist Frank Maglio on YouTube and TikTok.

2. Mom navigates adorable toddler questions about her pregnancy.

@kadynsmithsmith

😂🥰🤍 #pregnant #momtok #momsoftiktok #toddlertok #toddlersoftiktok #baby

Three-year-old Blakely is going to be a big sister for the second time, but this time she has questions. Every parent felt that weighty pause when she asked how the baby got into Mommy. (You just never know when that question is coming, so it's hard to be prepared with the right answer for the age and maturity of the kid asking.) Little Blakely sure is a doll, though. Read the full story—and get some expert tips for how to field kids' questions in an age-appropriate way—here.

3. People are sharing simple ways to practice kindness daily.

kindness

Simple ways to show kindness to others.

Canva/Upworthy

A Reddit user asked for ideas of kind acts people can do every day, and people shared their thoughts. Some of the ideas were profoundly simple, and not necessarily things we might think of, like being aware of how we're impacting those around us or leaving a place a little better than we found it. See the whole collection of acts of kindness here.

4. Woman finds out her best friend named her baby after her and it's a roller coaster of emotion.

Meeting a brand new human being is always a special moment, and when it's a loved one's baby it's even more special. But Mireya meeting her best friend Morgan's baby pushed special into a whole other stratosphere when she found out she'd become a namesake. That second when it sunk in and then the disbelief. "What? No, you did not." Oh yes, she did. So much love here.

5. Little chimpanzee kiddo is greeted with hugs from his new family.

Oh, the hugs for Beckley! This is almost too much sweetness for one video.

It was shared by Liberia Chimp Rescue & Protection, a sanctuary and conservation center in Liberia that rescues baby chimps from the illegal bushmeat and pet trades. While most of the chimpanzees the workers rescue and rehabilitate aren't able to be returned to the wild, they do get to live their life in a protected forest with other chimps. You can read more about their work here.

6. The Onion filed an amicus brief with the Supreme Court and it's seriously hilarious.

supreme court the onion parody satire

The Onion used parody to defend parody before the Supreme Court.

Photo by Jimmy Woo Man Tsing on Unsplash

It's a real brief with a real argument for a real First Amendment case, but it's unlike any other court filing you'll ever read. The satirical news site is petitioning the Supreme Court to review a case of a man who was arrested and prosecuted for creating a Facebook page parodying the Parma, Ohio, police department. After the man was acquitted by a jury, he sued the police for violating his constitutional rights, but his case was thrown out because the police were granted "qualified immunity." In defense of the man's—and everyone's—First Amendment right to parody, The Onion filed a 23-page brief utilizing the very parody it's defending, and it's a brilliant and hilarious read. I mean, who else could call the federal judiciary "total Latin dorks" while making a solid argument? Read the full story here.

7. Kids casually chatting with scientists is the cutest thing everrrr.

Kids are naturally curious, which makes them the perfect people to ask questions about science. Upworthy and Pfizer have been inviting kids to chat with scientists and there's just no way to predict where their conversations will go. Precious Marcelo here with his "I've got like 27 more years" to think about a career while chatting with virologist Vidia Roopchand was just so delightfully real. You can find more of these kid chats on our Instagram channel.

8. Four-year-old sings The Isley Brothers with his whole soul.

Goodness. "Driftin' on a nemberee…all we need is candlewight…" He's putting his entire self into singing that song. Beautiful voice from her, too.

9. The Rock's daughter pranks him with a water balloon as he's waking up.

"Good Morrrnniiiiing!" HA. She knows how to get her dad good.

Not gonna lie. I would not have the good-natured patience of The Rock if my child broke a water balloon over my face in bed. But this isn't the first time he's played the "Daddy, close your eyes!" game, so he knew something was coming. See more of Jazzy's pranks on her pops here.

10. Let's welcome the weekend with the exuberance of this ball-fetching doggo.

Even without the bouncing in anticipation, the tail wag says it all. Pure joy. Bring it.

That's it for this week! Come back next week for another round of joy on us. And if you'd like more stories like this in your inbox, subscribe to our free newsletter, The Upworthiest, here.

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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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