+
Most Shared

Emma Watson’s Met Gala gown sent a bold message to the fashion industry.

Sustainability, FTW.

Emma Watson knows how to rock a red carpet, and the Met Gala on May 2, 2016, in New York City was no different.

Photo by Larry Busacca/Getty Images.


The event's theme was "Fashion in an Age of Technology," and Watson totally nailed it.

Photo by Dimitrios Kambouris/Getty Images.

Not only was her gown stunning in and of itself, it was also created using sustainable products.

Photo by Dimitrios Kambouris/Getty Images.

As Watson explained, the gown combined "creativity, technology, and fashion" to send a bold message about curbing waste.

"I am proud to say it is truly sustainable and represents a connection between myself and all the people in the supply chain who played a role in creating it," she wrote on Facebook.

Photo by Dimitrios Kambouris/Getty Images.

According to Watson, the fabrics of the dress were woven from recycled plastic bottles — "one of the biggest pollutants on the planet," she noted. The cotton used in the design was organic — not the conventional kind that uses chemicals to grow and thus damages the earth and puts workers' health at stake. Even the zippers were crafted from recycled materials.

Watson has no plans to keep the gown locked away in a closet forever either.

"It is my intention to repurpose elements of the gown for future use," she wrote. "The trousers can be worn on their own, as can the bustier, the train can be used for a future red carpet look … I’m looking forward to experimenting with this. Truly beautiful things should be worn again and again and again."

Watson wasn't the only star committed to going green on the red carpet. Lupita Nyong’o wore a jade sequin dress that showed style and sustainability can totally go hand-in-hand.

Can we take a moment to appreciate that amazing hair style? Photo by Timothy A. Clary/AFP/Getty Images.

"The dress is a celebration of craftsmanship and truly reflects the theme" of the gala, according to Eco-Age, the brand consultancy group that partnered with the celebs.

Margot Robbie also joined the duo in celebrating Eco-Age's #GreenCarpetChallenge.

All three wore designs by Calvin Klein.

Watson, Robbie, and N'yongo. Photo by Mark Sagliocco/Getty Images.

Sustainability, FTW.

The global fashion industry isn't exactly known for its ethical treatment of people or the planet. But there's been a push for change in recent years.

"When we think of pollution, we envision coal power plants, strip-mined mountaintops, and raw sewage piped into our waterways," as Glynis Sweeny wrote for AlterNet last August. "We don’t often think of the shirts on our backs. But the overall impact the apparel industry has on our planet is quite grim."

From our reliance on cotton (a thirsty crop that needs more than its fair share of water to grow) to an over-dependence on shipping materials cheaply from around the world, thus increasing carbon footprints, Big Fashion really hasn't prioritized environmentalism (like, at all).

That's just part of what makes the #GreenCarpetChallenge designs Watson, Nyong'o, and Robbie, wore on the Met Gala red carpet such an important statement.


Photo by Timothy A. Clary/AFP/Getty Images

Livia Firth, who co-founded the Green Carpet Challenge, is looking at the future of the fashion industry with hope.

"'Fast fashion' will slowly die as we will start realizing they have taken us for a ride for too many years, addicting us to buying too fast and too cheaply," Firth told Conscious Living TV of an industry that sacrifices the Earth and workers' well-being to produce cheap clothing.

"2016 is going to be the year where we will take fashion back for what it is: beautiful clothes made with love and quality," Firth predicted.


Photo by Dimitrios Kambouris/Getty Images.

Watson, Nyong’o, and Robbie can't revolutionize the fashion industry by themselves, but their red carpet looks can inspire us all to be a little bit more critical of our own closets.

And that's the best way to be fashion forward.

Photo by Timothy A. Clary/AFP/Getty Images.

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.

Joy

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.

Keep ReadingShow less

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.

Keep ReadingShow less
Joy

Street artist creates delightful 3D scenes in walls and walkways for everyone to enjoy

David Zinn's characters bring joy to the lucky folks that happen to come upon them before they wash away.

David Zinn creates art from what he sees everywhere he goes.

Street artists are a special breed. While "the art world" can sometimes be a snooty, elite place for those with means, street art is made for everyone. Sometimes that means large public murals, but street art can be small, too. In fact, some of the best street art is so small you might miss it if you're not paying attention. But those who are can discover some delightful surprises.
Keep ReadingShow less

A size 21 Nike shoe made for Tacko Fall.

A local reporter at Hometown Life shared a unique and heartfelt story on March 16 about a mother struggling to find shoes that fit her 14-year-old son. The story resonated with parents everywhere; now, her son is getting the help he desperately needs. It's a wonderful example of people helping a family that thought they had nowhere to turn.

When Eric Kilburn Jr. was born, his mother, Rebecca’s OBGYN, told her that he had the “biggest feet I’ve ever seen in my life. Do not go out and buy baby shoes because they’re not gonna fit,’” Rebecca told Today.com. Fourteen years later, it’s almost impossible to find shoes that fit the 6’10” freshman—he needs a size 23.

Keep ReadingShow less

Dramatic flying squirrel makes it look like the broom fell on it. Spoiler: It did not.

Animals can be far cleverer than we give them credit for, especially creatures we don't think of as having distinct personalities. Most of us expect cats and dogs to do show us their unique quirks, but what about a flying squirrel?

A video is making its way around the internet that has people giggling over the dramatic antics of a large pet flying squirrel. It includes no narration explaining what's happening and no context—it just shows a flying squirrel repeatedly faking its own death by broom.

That's right. Death by broom. And from the way it looks, the little bugger came up with the idea on its own and made multiple attempts to create a convincing crime scene.

This is one you just have to see.

Keep ReadingShow less