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Pop Culture

Embrace your inner coziness: Mozy 22 is the ultimate wrap for comfort, warmth, and convenience on the go

It's over 500% warmer than a typical stadium blanket.

Embrace your inner coziness: Mozy 22 is the ultimate wrap for comfort, warmth, and convenience on the go

Editor's Note: Upworthy earns a fee for purchases made from items listed in this article.


Imagine you're working from home, attending a Zoom call, when you suddenly feel a chill in the air. Or maybe you're out exploring nature, taking in the beauty of the great outdoors, but the temperature starts to dip, and your jacket just isn’t enough. Wouldn’t it be nice if there was a simple solution to keep you warm and comfortable that was also lightweight and mobile? That’s where the Mozy 22 comes in. It provides warmth, comfort, convenience, and mobility, making it the perfect companion for video calls, outdoor adventures, and everything in between.



Meet Mozy's best seller!
Mozy leg jacket
The Mozy 22 Leg Jacket
From $74 at Mozy


The Mozy 22 isn't just any ordinary wrap; it's a game-changer. Whether you're snuggled up on the couch with a good book, taking your dog for a walk, or cheering at your child's soccer game, Mozy 22 literally has you covered. With its lightweight, super-soft design and adjustable hook closure, you can easily wrap yourself up and stay warm in those cooler temperatures.

The Story Behind Mozy

The journey to create the Mozy 22 began with its founder, a busy dad who found himself shivering at his kid's games and realized there had to be a better alternative to the traditional stadium blanket. This problem sparked a relentless pursuit to develop a superior solution that provides warmth, comfort, and mobility. Through countless trials and iterations, the team behind Mozy explored over 40 different designs, fine-tuning the details to create the ultimate wrap. It wasn't just about creating a better stadium blanket but revolutionizing how we keep warm in everyday situations, from virtual meetings to outdoor leisure activities. After numerous tests and refinements, the Mozy 22 was born.

Mozy 22’s Innovative Design

The Mozy 22’s groundbreaking approach to warmth and comfort sets it apart from other products. With its patented technology, this extraordinary wrap is truly a one-of-a-kind solution for those looking to stay warm, no matter the occasion. Extensive testing using thermocouples has proven that the Mozy 22 is over 500% warmer than a typical stadium blanket. With one patent issued and another pending, its innovative design effectively blocks convective heat loss.

What sets Mozy 22 apart from traditional warmth solutions is its innovative design that reduces convective heat loss. Compared to jeans, which offer minimal protection and allow heat to escape all over the legs, or stadium blankets, which still lose heat through gaps and around the back of the legs, Mozy 22 efficiently retains warmth. This design ensures that cool breezes don't penetrate the wrap, keeping your legs toasty and comfortable. The science behind Mozy 22's impressive warmth retention lies in its ability to minimize molecular convective heat loss. By effectively maintaining a layer of warm air molecules close to the exterior of the jeans while keeping cold air molecules outside, Mozy 22 ensures you stay warm even when the temperature drops. This intelligent design creates a microclimate around your lower body, making it the perfect choice for those cooler days.

Controlled engineering tests were conducted on the Mozy 22, using a warmed test dummy and thermocouples to compare its performance against jeans and stadium blankets. The results were clear: Mozy 22 excelled at retaining heat, proving that its groundbreaking design truly lives up to the promise of keeping you warm and comfortable.

Features and Benefits

One of the standout features of Mozy 22 is its mobile and hands-free design. It allows you to move freely without sacrificing warmth. Whether you're hopping up to cheer at a game or simply going for a walk, Mozy 22 stays securely fastened around your waist, ensuring your blanket won't fall to the ground, and you'll never have to fumble with it while on the go. Another fantastic benefit of Mozy 22 is its adjustable hook closure, which provides a customizable fit for users of all shapes and sizes. The wrap is easily pressed closed along your left side as snugly as you'd like, and the snag-free hook and loop border creates a seal that's both easy to adjust and open, keeping you dry and comfortable.

Mozy 22 also features two easy-to-reach pockets and a carabiner clip, making securing all your outdoor essentials a breeze. From water bottles and keys to hats, gloves, and even your phone, Mozy 22 has room for everything you need while out and about. Comfort is key with Mozy 22, and its plush fleece interior offers an added layer of warmth and coziness. As you wrap yourself in this soft, heavyweight fleece, you'll feel instantly snug and ready to face cold weather.

A Fit For Every Size

But Mozy 22 isn't just a one-size-fits-all solution. Its infinitely adjustable warmth allows you to adapt quickly to changing weather conditions. You can wear Mozy 22 higher up on your torso, just at your waist, sealed halfway down, or fastened snugly over your ankles. With Mozy 22, you're always in control of your level of warmth, making it a versatile and essential addition to your wardrobe.

Mozy 22 is designed to cater to various body types, ensuring everyone can enjoy its warmth and comfort. With size options available for both youth and adults, there's a Mozy 22 for everyone. The Size 120 is best suited for youth with hip sizes ranging from 20" to 27", while the Size 140 is ideal for adults with hip sizes between 28" and 46". For those with hip sizes of 47" to 58", the Size 160 is the perfect fit. To choose the best size for your needs, simply measure your hip size and refer to the recommendations provided. By selecting the proper size, you'll ensure that your Mozy 22 fits comfortably and securely, providing optimal warmth and coziness as you go about your day. So whether you're attending a chilly outdoor event or just looking for that extra layer of comfort during a Zoom call, Mozy 22 is the perfect fit.

Act Now

With the unbeatable combination of comfort, warmth, and convenience, the Mozy 22 is a must-have for anyone seeking an adaptable and stylish solution to staying warm on the go. Act now, and embrace your inner coziness with Mozy 22! Grab yours today and join the revolution in staying warm and cozy, no matter where life takes you.


Meet Mozy's best seller!
Mozy leg jacket
The Mozy 22 Leg Jacket
From $74 at Mozy
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.

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