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Do these 6 holiday stress hurdles sound familiar? Here's how you can avoid them.

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Hallmark

Many people say the holidays are the happiest time of year. (And they should be!) But for others, the season is also the most stressful time of the year.

Whether you’re dealing with family, time, or money issues — or all three — it can get very overwhelming very quickly.

Luckily, Hallmark has some simple, effective tips on how to spread smiles, not stress, over the holidays. Check out some of their suggestions to show you #CareEnough this time of year:


Holidays have you stressed? Here are some helpful tips on caring for yourself and others. #CareEnough

Posted by Upworthy on Saturday, December 17, 2016

Where does all that holiday stress come from in the first place? And what exactly can we do about it?

Sometimes, a little outside perspective is just what the doctor ordered. We enlisted the help of Dr. Sharon Kelly, a clinical psychologist, and Dena Patton, a certified life and business coach, to break down what causes holiday stress, what we can do to manage it, and how to keep the spirit of the season strong.

Here are six different hurdles that many people find themselves facing:

1. Feuding with the family.

Where it comes from: “I think most people that I see, there’s some family triggers, family history, family dynamics, interpersonal conflicts. That creates a lot of anxiety for people,” says Kelly. There's no doubt that our disagreements and attitudes towards family can get in the way of the celebration. And the more we hold on to them, the more we allow them to reach a boiling point.

What you can do: It all starts with you. “Choose to bring joy, not stress, to the party,” Patton writes in an email.

“The opportunity is in your hands,” adds Kelly. “You change the meaning that you attach to [the holidays], you change your response to it, you change your intention for the day. If you know that a certain person is going to really get under your skin, how do you go into that situation?”

2. Money, money, money! (For gifts, gifts, gifts.)

Where it comes from: “There’s all this anxiety around what to get people,” says Kelly. “Is this the right gift? Are they going to like this? Is this going to show how I feel about them?" When that stress hits, some people think an expensive gift will do the trick. Kelly adds, "They actually spend more even if it’s not something that you want.”

What you can do: “Have a budget and stick to it,” writes Patton. “Do not go into debt out of feeling obligated.” When it comes down to it, simply being prepared and knowing ahead of time how you’re going to plan your attack will ease all your emotions.

3. Holiday party obligations piling up.

Where it comes from: First off, there can be too many parties this time of year. And second, many times, these parties become more about impressing others and less about the actual gathering. “I know people that have these big, beautiful parties because they’re really good at it,” says Kelly. “But it’s, like, way over the top, and they have all this anxiety, no one appreciates it.”

What you can do: If throwing or going to a big party brings you joy, go for it! Just remember to do it for the right reason. “Pick your battles here,” writes Patton. “Practice your boundaries and don't say yes to every party. Make this year the [one] you are doing things that really bring you joy and cut out the things that bring you stress.”

4. HUGE crowds and looooong lines.

Where it comes from: The stress that long lines bring boils down to one simple idea: waiting until the last minute. Holiday crowds and shopping are a totally different animal, and remembering that will save you so much time in the long run.

What you can do: “Shop online or go shopping in off peak hours when crowds aren't present,” writes Patton. “Planning ahead in this area really helps.” Plus, the beauty of the modern world is that we can do all the holiday shopping we need without ever leaving the house.

5. All that food around you!

Where it comes from: If you’re cooking the food, it’s pretty easy to see how all the stress can creep in. As the number of diners rises, so does the pressure to get things right. If you’re just eating, though, try not to overdo it. All that indulgence and excess may come back to stress you out later on.

What you can do: “Have a plan and work the plan!” writes Patton. “If the plan is to indulge, then go for it, but if you promised yourself not to gain 10 pounds then never go to a party hungry.”

6. More-than-full to-do lists.

Where it comes from: “The bottom line is that we are busy — actually we are over-scheduled!” writes Patton. “We pile on more things to our schedule, our money and our emotional state and we go into overload.”

What you can do: If you're feeling overwhelmed, Kelly has a simple suggestion. "I would have them just step back in a quiet moment on their own," she says. "Really think about if they were really happy and [if] they really were going to enjoy the season ... how would they design it? What choices would they make?"

Whichever combination of hurdles apply to you, address the stress by taking a breath, planning ahead, and really thinking about what the holiday spirit means for you.

Ultimately, if we understand what brings us joy and make a conscious effort to really pay attention to that, then good things will follow. In fact, take a breather once in a while if you need to. If there's one S-word that should describe the holidays. It's special — not stress.

"Remember that this season isn't about gifts, stress, or social media," notes Patton. "It's about faith, family and making memories. Sometimes we get so wrapped up in the busy-ness that we forget what really matters."

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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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