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How 'Wintering' has changed my perspective and improved my mental health

How 'Wintering' has changed my perspective and improved my mental health
Photo by Mara Ket on Unsplash
person holding heart-shaped snow

Winter has always been a bit of a struggle for me. A long slog that must be endured. As soon as October comes around, my mental health takes a dip. I get a rebound in December with its cozy holiday vibes, but once the calendar flips to January, my mental health takes a major hit. I find myself counting down the days until March, wishing time away.

But lately, I’ve realized just how problematic this is for me. Not only does my mental health suffer, but as a result of my winter 'blahs,' my relationships also suffer. I’m shorter with my family. My motivation wanes, which in turn leads to feelings of shame and guilt, which decreases motivation even more. Rinse and repeat.



woman in gray hoodie sitting on brown wooden boat on lake during daytimePhoto by Boxed Water Is Better on Unsplash

For the past few years, I’ve been making more of a concerted effort to tend to my mental health during these seasonal changes. An introvert at heart, hygge is my jam. Snuggling under a blanket with a hot cuppa something? Yes, please.

What has really transformed my outlook on winter and helped my mental health in the process, however, has been the concept of wintering. Popularized by Katherine May in her book by the same nameWintering: The Power of Rest and Retreat in Difficult Times – wintering has not only changed the way I look at this season on the calendar, but also similar seasons of life.

Central to May’s book and the concept of wintering is adjusting our perspective of winter – whether the literal or metaphorical variety – from one of bleakness to one of renewal. Winters, after all, are essential to regrowth.

“Wintering brings about some of the most profound and insightful moments of our human experience, and wisdom resides in those who have wintered,” May writes.

Just reading these words last year – in the depths of a pandemic winter in the Upper Midwest, where cold isn’t just cold but downright frigid – brought comfort in this otherwise painful season. Instead of something to endure and wish away, winter started to feel almost honorable. And my newfound acceptance of it started to feel radical and rebellious. Instead of feeling like there was something wrong with me for feeling a bit sluggish, anxiety-ridden, and despairing, I felt an almost giddy ease, like I was in on a secret that these feelings were not only okay, but necessary.

body of water and snow-covered mountains during daytimePhoto by Tim Stief on Unsplash

At its core, wintering – to me, at least – is about changing my perspective and paying attention. “When you start tuning in to winter, you realize that we live through a thousand winters in our lives – some big, some small,” May writes. While this might seem like a pessimistic approach, there is comfort in knowing that we’ve made it through lean, hard, lonely times before, and we can do it again.

These winters of our life don’t need to be feared or avoided, but held with care and compassion. The past couple of years have felt like a never-ending winter for many of us, I suspect. Even when things seem reasonably “fine,” there’s a subliminal heaviness to my psyche. I feel stuck and confused, lethargic and antsy all at the same time. I want to heal.

Don’t get me wrong, wintering didn’t magically “fix” anything, but it did cause a subtle shift in me that snowballed (pardon the winter pun) into something more comfortable. Or at least less brutal.

So what does wintering look like for me, and how does it help my mental health?

person in orange jacket standing on snow covered groundPhoto by Boxed Water Is Better on Unsplash

Well, here are a few things I’ve tried to incorporate into my life during winter – whether they come in the months of December through February or some other time of the year:

Trust my intuition, and feel the feels. Once I accepted winters as a necessary, and perhaps even helpful part of life, I was able to accept them more easily. If I’m feeling sad or lonely, I let myself feel sad and lonely. Same thing with joy and comfort. We don’t need to ignore our sadness, or pretend it isn’t there; nor do we need to tamper our joy and contentment. We only need to trust ourselves. “Wintering,” May writes, “ is a moment of intuition, our true needs felt keenly as a knife.”

Give myself permission to rest – like, really, rest. Lying on the couch while my mind races with all the things I “should” be doing isn’t really resting. Nor is it resting if I feel guilty about how or when you rest. Wintering gives us permission to rest when and how we need. No questions asked. That means more sleep too. With darkness enveloping our home earlier, we might feel an almost circadian urge to sleep more. This is normal and good.

Get physical with wintering. In her book, May tells the story of cold water swimming (and by cold, I mean 37 degrees Fahrenheit cold). I was nearly shivering just reading about it, but there was something exhilarating about it too.

“Immersion in cold water has been shown to increase levels of dopamine, the neurotransmitter that stimulates the brain’s reward and pleasure centers, by 250 percent,” May notes in the book. “A recent study found that regular winter swimming significantly decreased tension and fatigue, as well as negative states associated with memory and mood, and improved swimmers’ sense of general wellbeing.”

person holding white ceramic mugPhoto by Alex Padurariu on Unsplash

I’m not going to start swimming in Lake Michigan in the middle of January, but this concept has changed my perspective. I’m more likely to blast the cold water at the end of a shower, and I was more eager to walk out into a cold mountain lake on vacation this summer, instead of sitting on the rocky shore as I would have done in the past. I feel energized and peaceful all at the same time, while also sensing a clarity that I can’t quite pinpoint. Bottom line: it feels good even if it feels uncomfortable.

Don’t be ashamed or embarrassed of the dark and difficult times. As May writes, “Everybody winters at one time or another; some winter over and over again.” In our glossy and edited social media culture, it can be easy to think that we are alone in our struggles, mental health challenges, and difficult times. But that just isn’t true.

Our inability to accept, hold space for, and even nurture our pain doesn’t come from a personality flaw or weakness, but simply because we weren’t given the tools to do otherwise. As May writes, “We’re not raised to recognize wintering or to acknowledge its inevitability. Instead, we tend to see it as a humiliation, something that should be hidden from view lest we shock the world too greatly.”

I’ve been open about my mental health challenges, but the concept of wintering has helped me be more open about these challenges in real time. I’m far more likely to say, “I am struggling” or “I’m dealing with a touch of depression right now,” than waiting until I “feel better.” And this distinction has been critical in getting the help and support so that I can actually feel better.

Wintering isn’t just cozy socks, glowing candles, and knitting while tucked under a quilt. Though it can certainly be those things too. Mostly it’s about seeing winter, and any hard or dark times in our life, for what they are – essential. Wintering is about shutting off the constant busyness and go-go-going of our lives that we sometimes use to mask our pain or anxiety or sadness so that we can recover, heal, and grow.

Christine is a writer who lives in the Chicago area with her husband, two sons, and rescue dog. You can find her on Facebook and Instagram.

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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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