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Pop Culture

Have you noticed your favorite shows don't look as good as they used to? This viral post explains why.

A fascinating look at quality versus quantity.

game of thrones, house of dragons, lotr costumes

One of these things is not like the other.

For fantasy fans, it truly is the best of times, and the worst of times. On the bright side—there’s more magic wielding, dragon riding, caped crusading content than ever before. Yay to that.

On the other hand, have you noticed that with all these shows, something feels … off?

No, that’s not just adulthood stripping you of childlike wonder. There is a subtle, yet undeniable decline in how these shows are being made, and your eyes are picking up on it. Nolan Yost, a freelance wigmaker living in New York City, explains the shift in his now viral Facebook post.

The post, which has been shared nearly 3,500 times, attributes shows being “mid,” (aka mediocre, or my favorite—meh) mostly to the new streaming-based studio system, which quite literally prioritizes quantity over quality, pumping out new content as fast as possible to snag a huge fan base.

The result? A “Shein era of mass media,” Yost says, adding that “the toll it takes on costuming and hair/makeup has made almost every new release from Amazon, Netflix, and Hulu have a B-movie visual quality.”

He even had some pictures to prove it.


Yost first addressed the Amazon Prime Series “The Rings of Power.” One of the many, many things that makes Peter Jackson’s “The Lord of the Rings” trilogy so iconic is the costumes. But that legacy was the direct result of dedication to detail.

“The production spent years hand-making every single piece of armor with real metal, hand-dyeing all-natural fiber fabrics, and designing distinct embroidery and hairstyles specific to each race in Middle Earth that had continuity through the story,” Yost wrote.

He added, “the natural dyes and dedicated layers of fabrics for elves, for hobbits, wool/dyes, and for men had a much more muted/medieval look, yet ethereal because of the slight detail you don’t really notice, but the depth draws your eye to every inch of the costume regardless.” This, he says, is why those three movies stand the test of time.

Compare this to the two images from “The Rings of Power,” below. In one photo “they barely scrapped together an unnaturally gilded scale mail breastplate and just screen printed a stretched long sleeve shirt to match underneath, all over a skirt in a single layer of a warped poly skirt.”

rings of power, house of the dragon

Now you too can look like you're from Middle Earth for the low, low cost of $10.99.

Nolan Yost/Facebook

The other image shows “they just saved money on an Elven wig altogether for a 2022 pompadour, with a velvet pleated priest smock (with crushed parts not even steamed out), and a neckline that isn’t tailored to fit like we’ve seen previously with Elrond or Celeborn.”


Yost then moved onto HBO’s “House of the Dragon.” Arguably even those who have never seen a single episode of its predecessor, “Game of Thrones,” would still recognize Daenerys Targaryen for her platinum white hair—an attribute that Yost notes was quite expensive.

got hbo

It cost big bucks to be a Khalessi.

Giphy

He explained that for the show’s final season alone, Daenerys’ wigs most likely cost tens of thousands, requiring human hair to be custom made into multiple wigs.

Luckily, there was only one character with that signature look in the show. For “House of the Dragon,” however, with a cast almost entirely made up of silver-haired brooding powerhouses, Yost surmises that due to budget constraints, the creators opted for synthetic wigs.

You can see below the problem this cost-cutting decision makes in terms of authenticity.

house of the dragon, house of the dragon wigs

Luckily, Matt Smith is such a good actor a few stray hairs are an easily forgivable.

Nolan Yost/Facebook

“Synthetic hair reflects light throughout the whole hair shaft and it tangles extremely easily,” Yost writes. “With any shot where a character isn’t actively moving or is performing dialogue and the hair isn’t being actively smoothed down every couple of seconds between shots, each flyaway is going to show up on camera if there’s any indirect lighting and look messy. Not only that, synthetic hair is also twice as thick per strand than human hair, so regardless of that the wigs are going to look bulky in an uncanny valley sort of way.”

This affects not just sci-fi and fantasy, but other genres meant to transport viewers into other worlds, like period pieces, which Yost points out with a picture from “Bridgerton” by Shonda Rhimes.

bridgerton

Yeah, this does look like they're wearing curtains. And not in a fun "Sound of Music" kind of way.

Nolan Yost/Facebook

“It’s obviously not meant to be historically accurate, which is totally fine,” he writes, but without important details or embellishments or even proper undergarments to make the clothes fit well, everything looks like a slightly more expensive Halloween costume.

Yost’s insightful post really shines a light on what audiences are having to trade off for the sake of constant output. The phrase “done is better than perfect” takes on a new meaning altogether as studios race to meet a deadline with whatever is easiest to mass produce. But if viewers are so easily taken out of these stories because of noticeable corner cutting, then perhaps it’s a sign that what we really want and need are stories worth waiting for, ones that truly pull us in and leave us captivated. This is no easy ask, for studio execs or customers alike (I too am a voracious binge-watcher), but as we can see in these examples, the most valuable experiences rarely, if ever, come from rushing.


This article originally appeared on 9.10.22

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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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via Pixabay

A sad-looking Labrador Retriever

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America's Got Talent/Youtube

Mzansi Youth Choir received a Golden Buzzer for their cover of Nightbirde's "It's OK."

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