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A radiologist is flawlessly recreating famous celeb photos to help cancer patients.

Sometimes, a photo is worth a thousand words — and an amazing tool in helping cancer patients.

A patient broke down in front of Mark Udovitch and her tears changed his life forever.

She'd just lost her hair after undergoing chemotherapy and it was downright devastating for her — so much so, in fact, the patient said it was worse than losing her breast to cancer.

"This was a really profound thing to say," Udovitch, a radiologist from Australia, explained to Upworthy.


So he came up with an idea.

Udovitch decided to grow out his own hair so he could help people like her. Because — as the woman had explained — most of the wigs she had access to were itchy and looked fake. 

He wanted his hair, in some small way, to make a difference.

It wasn't long before Udovitch started getting comments about his longer, luscious locks.

Because apparently, he had some celebrity look-alikes.

Many folks started chiming in: Udovitch looked like the lead the singer of Creed, some said. And the lead singer of Nickelback, others noted. He got Kenny G too.

"Even Jesus," Udovitch added.

This sparked another idea: What if this funny celebrity intrigue over his hair could further help patients who could use it? 

Thus, a new campaign was born. And the (hilarious) evidence has spread all across the internet.

Udovitch decided to snap pics of himself recreating famous celebrity photos.

He did it to help benefit the charity Dry July — and the results are ... amazing.

Dry July is a group doing a whole lot of good benefitting cancer patients in ways that are often overlooked when we think about their quality of life. 

The nonprofit has helped fund worthwhile products and services at the Liverpool Cancer Therapy Center, where Udovitch works on the radiation oncology team. A few years ago, for instance, Dry July helped the center purchase much more comfortable chairs for patients undergoing chemotherapy — a treatment that entails sitting in one place for several hours — Udovitch explained.

Udovitch's hilarious photos are helping draw attention to Dry July's online fundraiser.

So far, members of his fundraising team — which also joined in on the photo fun — have raised over $20,000.

It's clear from his photos that Udovitch has his finger on the pulse of pop culture, too. Just look at his "Game of Thrones" re-creations.

He can also pull off "Star Wars."

I mean, he's got the lightsaber down and everything.

And he's basically part of the Kardashian-Jenner family now.

Move over, Kimye.

"Staff [at the cancer therapy center] loved that I managed to make a garbage bag, kitchen gloves and a Diet Coke-Mentos explosion look so good," he said.

The photos are lighthearted and fun, of course. But the underlying motivation behind Udovitch's re-creations is about far more than a few laughs.

"Working as a radiation therapist for the past eight years has given me incredible perspective on life and has taught me that you cannot take your health for granted," he said. 

"The idea that a charity like Dry July exists — and that their sole mission is to provide support and comfort to cancer patients across Australia — was one that I was very keen to support."

Soon, Udovitch's wavy locks will be gone. But there's still time for you to make a difference.

Udovitch will shave his head on July 29, 2016, at the Dry July Shave Off. (Unfortunately, the celebrity doppleganger remarks may disappear along with that long, brown hair.)

But you can still help his fundraising team do big things. They want to raise enough money to provide services like wireless music to patients during treatments — that way, patients can have customized playlists to help with their anxieties — and decorative artwork to give the department a splash of color (and look less like a cold, sterile clinic), Udovitch said.

To Udovitch, drawing attention to this campaign has been quite a ride.  "The entire experience has been overwhelming," he said. 

But it's certainly been worth it.

"Obviously our message is resonating well with everyone," he said. "And it is so great to see the general public get on-board with us so that we finish our fundraising campaign strong!"

If you're interested in supporting Udovitch's team, check out their fundraising page and learn more about their efforts on Facebook.

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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.

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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.

CGI characters speaking Old English, Old Japanese and Hittite.

Given that language evolves so rapidly, it’s hard to imagine what people sounded like 200 years ago, let alone 500 or a thousand. Even when we watch movies about ancient civilizations, the characters usually speak in a language similar to the audience, giving us a false sense of what people in those times were like.

The folks at Equator AI are giving people a realistic idea of what people in ancient civilizations sounded like by recreating the languages of 15 languages that haven't been heard in centuries. In the video, the languages are spoken by computer-generated recreations of people who lived in that era.

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'Ted Lasso' excelled at portraying platonic love. Here are the show's Top 6 'love stories.'

We all love a romantic love story, but it's just as fulfilling to witness these platonic love stories play out.

Ted and Rebecca's friendship is one of the best things about the "Ted Lasso" series.

"Ted Lasso" has wrapped up its third and final season, leaving people analyzing and debating and feeling all kinds of feelings about the series and its characters.

Since watching the final episode, I've been thinking about what I've loved most about the show, because seriously, there's a lot to love. Ted himself, of course. The quirky cast of characters. The humor. The triumph and redemption. Roy Kent's grumbles. Sam Obisanya's everything.

Then there are the relationships, which is where the show really shines. Not so much the romantic relationships—those were somewhat meh in the end—but the way the show portrayed genuine platonic love in its various hues. Considering how many shows (over)utilize romance and sex for dramatic effect, it was refreshing to see multiple relationships develop and deepen over three seasons without any romance involved.

Here are (in my humble opinion) the six best platonic relationships on "Ted Lasso."

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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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Farmers are pretending their chickens are 'armies' and battling it out on TikTok

The "Chicken Wars" might be the most wholesome online trend ever.

#chickenwars/TikTok

The battle has begun.

TikTok has no shortage of silly trends, but this one is so clucking cute.

In a bizarre phenomenon dubbed the “chicken wars,” farmers have begun posting videos of themselves hyping up their flocks, which they call “armies,” and bragging about how their army would “win” in a theoretical battle against another flock.

According to Insider, the trend began on May 27, after a farmer named Dylan (@dylan_bezjack) posted a video of himself strutting in front of his feathered friends and doing some playful trash talking.
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Joy

Meet the 11 outstanding nonprofits that took home this year’s Classy Awards

Each organization has gone above and beyond to make our world a better place.

All images provided by the Classy Awards, used with permission

Give these organizations all the awards

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Since 2009, the Classy Awards have celebrated nonprofits for their unique approaches to making our world a better place for everyone. Winners are given a platform to amplify their cause and showcase the positive impact of their programs.

This year, we are proud to announce that the Classy Awards have partnered with Upworthy, and we are thrilled to shine a spotlight on the 2023 winners.

From championing gender equality, to massively reducing food waste, to providing trade-based skills training to the neurodivergent community, each organization has made an incredible contribution to the betterment of our world.

Collectively through their efforts, nearly 1.5 million people and animals were served across 34 countries worldwide last year alone. That’s a win in itself.

Check out the 11 winners for 2023 below:


​412 Food Rescue

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In an effort to address the growing concern of food waste, hunger, and environmental sustainability, 412 Food Rescue uses an innovative app to match volunteers, aka Food Heroes, with other organizations that might have a surplus of perfectly good but unsellable food that would otherwise be wasted and redirect it to people who need it.

Food Heroes has redirected 137 million pounds of edible food from landfills to the people who need it most.

Arnold Schwarzenegger in São Paulo, Brazil, 2019.

At 75, Arnold Schwarzenegger is thinking about the big questions of life. He opened up about his thoughts on the afterlife in a conversation with his “Twins” co-star Danny DeVito for Interview Magazine.

Devito asked “The Terminator” star, “What's in the future for us?" and he gave a thoughtful answer to a question that philosophers, scientists and religious leaders have grappled with since the dawn of humanity.

"It reminds me of Howard Stern's question to me. 'Tell me, governor, what happens to us when we die?' I said, 'Nothing. You're 6 feet under,'” he told DeVito.

"I said, 'We don't know what happens with the soul and all this spiritual stuff that I'm not an expert in, but I know that the body as we see each other now, we will never see each other again like that,'" continued Schwarzenegger.

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