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Heroes

Polar bears are stealing booze and candy from humans, and it's really not as funny as it sounds.

Polar bears are largely known as the poster-pets of environmentalism, and it's easy to see why.

They're like giant, adorable, white-but-not-actually-white teddy bears who could just as easily cuddle you as kill you.

Also they've spent the last half-century dwindling near extinction and are still considered threatened under the Endangered Species Act.


The new rap music video from Polar B. GIF via John Downer Productions/YouTube.

And that's exactly why we should be using mass surveillance to keep them safe.

After all, it works with people, right?

"Oh hello there Mr. Spy-Drone-Video-Camera-Thing Disguised as a Giant Snowball, how are you today?" — this polar bear, probably. GIF via John Downer Productions/YouTube.

See? Polar bears love being spied on — just like us!

...Oh wait.


GIF via John Downer Productions/YouTube.

OK, so they might not appreciate the snooping. But we have good reason for keeping tabs on our fuzzy Arctic friends.

According to a new study in the scientific journal PLOS ONE, human-polar bear interactions are on the rise, now that the bears' homes and food sources are melting away.

Or, as they put it in the abstract:

"Polar bears are increasingly using land habitats in some parts of their range, where they have minimal access to their preferred prey, likely in response to loss of their sea ice habitat associated with climatic warming. [...] Projections of continued sea ice loss suggest that polar bears in the Chukchi Sea and other parts of the Arctic may increasingly use land habitats in the future, which has the potential to increase nutritional stress and human-polar bear interactions."

For all we've done to cut down on hunting all across the globe, polar bears must still contend with threats of starvation and a rapidly shrinking habitat — both of which are symptoms of the larger issues of climate change.

As a result, polar bears are wandering from their natural habitats and walking right into our backyards — with alarming frequency.

It's like when an ant shows up and ruins your picnic. Except in this case, that ant can kill you with one swipe of its massive claw.

"Draw me like one of your French girls. Then let me claw your face off." GIF via John Downer Productions/YouTube.

For example, there's the polar bear who stole a steak and wine dinner from a BBC film crew in Norway.

After a long day shooting on location for an episode of David Attenborough's "The Hunt," Sophie Lanfear and her team came home to their rented cabin in Svalbard to find a drunken polar bear passed out on the lawn, having gorged himself on their stash of wine and the 55 pounds of meat they brought along for their trip.

The polar bear returned three more times over the course of two days — but of course, there wasn't any more food for him to eat.

"Huh? What? I'm awake. You guys wanna do shots?" GIF via BBC Earth Unplugged/YouTube.

All kidding aside, the idea of a drunk polar bear stumbling through your home is pretty horrifying, to say the least.

Meanwhile, in Manitoba, Canada, polar bear wrangling is a full-time job.

Authorities actually have to police the streets on Halloween to stop polar bears from beating up little kids and stealing all their candy. There's even a dedicated bear cell at the local precinct house.

"Give us all your Kit-Kat Bars and no one gets hurt." Photo by Payton Chung/Flickr.

(Other polar bears have recently been caught trying on human pants and disco-dancing with a whale carcass, but I'm not including those photos here because they both make me uncomfortable.)

So as much as it pains me to say — maybe spying on polar bears isn't such a bad thing?

That snowball-lookin' drone in the GIFs above was one of five specially-designed spycams created as part of a BBC program called "Polar Bear: A Spy on the Ice" — until the polar bear came along and gleefully crushed it, anyway.

These spycams allow filmmakers and researchers to get up-close-and-personal with polar bears, and gather information on their movements, habits, and behaviors.

As the show's director, John Downer, explains in an interview with Mongabay:

"Some of our small Snowcams were designed to operate autonomously, they would power up and record once a bear came within 20 metre range of it. These could be left for up to one week in the extreme cold. They even contained a satellite phone that would automatically call us on sensing a bear. [...] They were strengthened to withstand the bears' crushing body weight and powerful jaws. Icebergcam was able to follow bears hunting on the sea ice and track alongside them from just a paw swipe away. The close proximity of the cameras provided viewers with an engaging and fresh experience of polar bears that was far removed from the solitary cold killers as they have been traditionally portrayed."

Data collection alone won't help us stop climate change any more than it helps stop terrorism (which is not at all). But if we're not going to pay attention to the damage that we're doing to the planet — and we really should — then we're going to need to figure out how to coexist with our furry new neighbors.

"Do you have a moment to talk about your Lord and Savior — hey wait come back!" GIF via John Downer Productions/YouTube.

But despite their increasingly erratic behavior, things are (mostly) looking up for the polar bear population.

It's hard to get an exact count, but the general consensus is that the polar bear population has at least doubled since its lowest point in the late-1960s. And thanks to those handy polar bear wranglers, no one in Manitoba has been mauled by a bear in more than 30 years. That's a win on both sides, right?

But none of that changes the fact that they're still in danger — and so are we, as long as their homes continue to melt away.

So let's demand that our world leaders take action now to protect our planet's climate, or else we'll have to deal with a lot worse than polar bears drinking all our booze and ruining Halloween.

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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.

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