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Armed with a Sharpie and rocks, this guy is lifting people's spirits every day.

They're rocks with faces, but they're so much more.

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Airbnb

The best parts of the world are those that are full of random acts of kindness.

In the wake of Ferguson and Black Lives Matter, the St. Louis area has a reputation for being a segregated hot bed of neighbor-against-neighbor rage. That's what we've seen on the news.

But what if you were there?


You'd get to see how people actually live every day. You'd see neighbors of all kinds talking together, playing together, and helping each other out.

That's exactly what artist Bryan Payne is doing — and he's showing us we're all connected.

He's a local artist who's hiding treasures. What? Yes. Image by Jarred Gastreich.

Bryan is the guy behind a unique treasure-hunting project: Doodlestones.


Round 3 of doodlestones starts today!
A photo posted by @doodlestones on


"This constant impulse to want to connect. I feel like everyone's got this," Bryan says.

So what, exactly, are Doodlestones?

Bryan is an artist and amateur urban archaeologist and treasure hunter, and he's putting his passions to use by creating small stones decorated with friendly faces. He hides them in places where people cross paths as a way to help make his town a friendlier, kinder place. By geotagging and using location clues in the images he posts on Facebook and Instagram, he leaves behind a trail of tiny, happy artworks.


The 75 year old Kingshighway bridge is being torn down and with it goes the infamous diy skate park that is underneath it. Bug Chaser played a show here yesterday to send it off and tons of people were getting their last skate session in. I did a little memorial with the objects found on site, by next week it will all be gone.
A photo posted by @bryancharlespayne on


"I wanna find a way to connect all people. Not just an art crowd or a certain scene. It crosses all boundaries." Bryan says.


#doodlestone @pdianegs #cherokeestreet thank you @bryancharlespayne @flowersandweeds
A photo posted by Jennifer McComb (@mccombhoney) on
A photo posted by @doodlestones on


Each stone comes from a river in his home state of Missouri. On each stone, he writes "#doodlestone," the date, and "finders keepers."

Thumbs up. Image by Jarred Gastreich.


Breakfast time?
A photo posted by @doodlestones on


A quick glance at its Facebook page shows just how many folks agree and are joining in.

"People following the clues are starting to find them," Bryan says. "They're all geotagged. You can click on the map and see them on the map, whatever the satellite proximity is."

Images via Doodlestones' Facebook and Instagram.

Bryan wants everyone to be on a hunt for treasure, whether that be for Doodlestones themselves ...


Got three doodle stone fans at the farmer's market, so I gave them each treasures to take home. They told me they paint on stones with their grandma.
A photo posted by @doodlestones on

...or a new small business they find while hunting for Doodlestone treasure...


Found my first #doodlestone! I'm leaving it behind because it fits so perfect. Hint: Egghead can be found at the best place to get grilled cheeses on a Saturday morning.
A photo posted by It is Alright, Ma. (@itisalrightma) on

...or a kind moment with a neighbor they might not have known.


Portrait of an artist being super friendly. Image by Jarred Gastreich.

That very thing has already started happening around the St. Louis area. One of the Doodlestone treasure hunters found him on Facebook, and they met up.

"The family in the photograph contacted me after finding the two Doodlestone ghosts in their planter. ... I ended up giving them each a Doodlestone of their choice from my newest batch as a thank you for their willingness to engage in the project in a new way," Bryan said. "What I got to experience with them is a huge part of what it's about for me: hearing stories, looking at treasures, and finding a new way to connect with the community."

Bryan hiding stones. Image by Jarred Gastreich.

One small idea is turning into a discovery ground for an entire town.

Bryan notes, "This is the first way that I've been able to use my resources to create some sort of community, building to bring people from across barriers together."

Images via Doodlestones' Instagram.

Helping humans connect with their surroundings and tap into their community. It's an innately positive pursuit. How does it not help to direct somebody to a new coffee shop or a new park?

"I think both things help in different ways, it's all connected," he says. "Taking people outside their comfort zone and leading them somewhere else that's safe … or fun or adventurous."



"I'm an artist, and this is my take on how to build community. I realize now that's my job, to build community."

And from the looks of it, this artist's hope to be a small part of creating more joy and connection and kindness is already working.

I can't wait to see it grow.


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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.

@thehalfdeaddad/TikTok

Dad on TikTok shared how he addressed his son's bullying.

What do you do when you find out your kid bullied someone? For many parents, the first step is forcing an apology. While this response is of course warranted, is it really effective? Some might argue that there are more constructive ways of handling the situation that teach a kid not only what they did wrong, but how to make things right again.

Single dadPatrick Forseth recently shared how he made a truly teachable moment out of his son, Lincoln, getting into trouble for bullying. Rather than forcing an apology, Forseth made sure his son was actively part of a solution.


The thought process behind his decision, which he explained in a now-viral TikTok video, is both simple and somewhat racial compared to how many parents have been encouraged to handle similar situations.
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Should babysitters be expected to clean?

When it comes to babysitting, you can hit the jackpot with someone who not only enjoys hanging out with your kiddos but also cleans out of boredom. The only babysitter I've had that experience with is my mom, but I do hear they do exist. While walking into a spotless house after a much-needed night out would be amazing, it's not really part of a standard babysitting package.

Typically, whoever babysits for you is solely there to focus on the well-being of your children. They feed them snacks, play games with them, and follow their bedtime routine to the letter. Then they hang out on your couch reminding Netflix that they're still watching and wait for you to return. Sure, they clean up dishes from dinner and whatever toys were pulled out during their time with your kids, but they don't typically clean your house.

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Man lists things millennials grew up with that Gen Z would be outraged by

"Imagine telling them that their free unlimited minutes only started after 9:00 and on the weekends."

Things Gen Z would be outraged by that were normal for millennials.

There will likely always be some kind of playful generation war going on between older and younger generations. This time it's a millennial throwing what some may deem as truth bombs at Gen Z, seemingly unprompted. (Well, it could be that he's upset that Gen Z is getting all the credit for being tech savvy since the majority of his complaints were technology related.)

Dwight Thomas uploaded a video to TikTok listing things that millennials grew up with that the generation below him would be outraged by. As someone who would be considered an elder millennial by some people, I'd have to agree. The man makes some valid points about things we experienced as teenagers that would likely make teens today aggressively send out Change.org petitions.

"These new-age kids will never understand the struggle. Imagine telling them that their free unlimited minutes only started after 9:00 and on the weekends," Thomas says into the camera.

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The 1990s was a magical time.

If you grew up in the '90s then you were part of the last generation of kids who lived without being constantly connected to the internet. You lived during that last gasp of the analog era where most of your entertainment came on tape and if you wanted a new pair of Guess jeans or LA Gear shoes, you had to drive to the mall.

Also, if you wore parachute pant, aka "Hammer Pants," people actually thought you were cool.

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Pappas Pärlor's fantastic street art.

Anyone who grew up in the late '80s and early '90s—Gen X, I’m looking at you—grew up in a world that was dominated by 8-bit graphics. Back in the day, computers and video game systems had a limited amount of processing power so the graphics had to be simple.

That meant the heroes that we played with such as Mario from Super Mario Brothers or Link from The Legend of Zelda, had to be super simple looking and we had to fill in the rest with our imaginations.

Video graphics have come a long way over the past 30-plus years, but people still love the old designs because it takes them back to a simpler time. This has led to an 8-bit movement where people use their creativity to make art within the confines of the limited medium.

Some people also use the limited 8-bit soundscape to create music that’s reminiscent of the old games. Sure, computer game music may be much more sophisticated these days, but is there anything better than the soundtrack to the original Tetris? Would Super Mario Brothers be the same with a sophisticated soundtrack? I think not.

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Mom shares her autistic son's 'sensory friendly' movie experience and how to find them

"Nobody is looking at you weird because all the families are there for the same reason."

Camille Joy shared her excitement at getting to take her son to a movie showing that worked for him.

Going out to see a movie is a classic fun family activity, but for some families, it's an outing that causes far more stress than it's worth. When you have a child who needs to move or make sounds in order to function, sitting quietly through a two-hour movie simply isn't going to happen.

That's why major movie theater chains have started having dedicated "sensory showings" of feature films for families with autistic members or others who have sound and movement needs that don't mesh well with traditional moviegoing etiquette.

Camille Joy of the Moments of Joy Podcast shared a video her son, Maison, enjoying a sensory showing of Disney's "The Little Mermaid." Maison can be seen walking up and down the aisle stairs during the film in the post, with Joy sharing how the experience went.

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