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We asked about the best presents you've ever given. The answers will make you smile.

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Hershey's

The holidays are here, which means that gifts are on everyone's minds.

Sure, you're probably dying to know what your friends and family got you (we hope it's what you've wanted all year). However, when it comes down to the actual gift exchange, you might find that giving leaves you feeling better than receiving.

Whether you're gifting jewelry to your wife, a bag of Hershey's Kisses to a work colleague, or a sweater covered in dachshunds that your friend will show off at every holiday party this year, there's just something about giving that warms all of our hearts.


In order to prove this theory, we asked real people about a time in their life when giving a gift was better than anything they could have found under the tree. Take a second to grab a tissue before you read these responses.

1. Tracey Carnazzo calls her best friend Noelle her "soulmate." For her, there was no greater gift than buying the gown the woman she loves most would be married in.

Tracey and Noelle. Photo courtesy of Tracey Carnazzo.

"Noelle's been my best friend for over 20 years," says Carnazzo. The pair, who live in New York,  do everything together — from traveling to hosting a popular podcast. When Noelle's mother couldn't make it wedding dress shopping with her daughter, Carnazzo (who also served double duty as both officiant and maid of honor)  took the reins.

"She was planning on buying the dress herself," explains Carnazzo, "but your mom is supposed to buy your dress! I bought it for her because I am her 'other mom,' even though she's three years older than I am."

"It made her feel loved and taken care of. It made me feel great to be able to give her something that she really deserves. Seeing her walk down the aisle in it was better than any gift I’ve ever received. I really love her. To see her happy is when I'm truly happy."

2. David Pardo said 'thank you' to a mentor who had helped him through so much.

Photo by Lucas Lenzi on Unsplash.

"I had a mentor who, when my life was difficult, spent a couple years effectively playing my therapist by phone every week or two, even though he was 1000s of miles away," writes Pardo in an email. His mentor was training to be a counselor, but wasn't comfortable accepting anything in return for his guidance. That didn't stop Pardo from repaying him down the road, though.

"About 4 years after we last spoke, my finances improved along with my mental state, [so] I gave him $1000 as a bit of a start on paying him back," he continues. "He'd been living in his van while finishing his PhD. A divorce while in grad school wrecked his finances. He didn't have a place for his son to live with him."

"After getting the money, he was able to get a place where he could live with his young kid. Being able to fix the thing that is most hurting someone brings a special type of satisfaction."

3. Martha Miller gave a memory that will endure for more than a lifetime.

Photo courtesy of Martha Miller.

"My father-in-law, Hubert, was turning 80 right before Christmas and certainly didn't need a single thing," writes Miller in an email. "I was trying to think of something meaningful we could give him and it finally struck me. He waited a very long time to become a grandfather and was thrilled when two grandsons were born just six weeks apart."

"I got the idea of giving him a photo shoot with them as a present. My sister-in-law and I took Hubert and our boys dressed in Notre Dame jerseys Grandpa had given them for the photo session the next week. My father-in-law wanted several sets of pictures so he could send them to his six brothers and sisters."

"When Grandpa passed away at 88, my son, then 10 years old, spoke at the funeral. He said his favorite memory of Grandpa was having the picture taken with his cousin and Grandpa in the jerseys Grandpa had given them. I tear up just thinking about it. We have the picture placed prominently in my son's room so he will be reminded of his wonderful Grandpa who loved him dearly and the fun time he had with Grandpa and his cousin. I love that this present was so meaningful to Grandpa, and that it is still bringing joy to us and to our son."

4. For Lisa Umar, bringing all of her mom's friends together for her birthday showed her that there's no better gift than making someone happy.

Photo courtesy of Lisa Umar.

"I was living in Washington, D.C. at the time while my family lived in Phoenix," Umar says. "For my mom's birthday, I decided to plan her a surprise party. I managed to track down a bunch of her friends, another friend donated their house for the evening and I sent out printed invitations and everything."

"I also flew home the day before so I could help set up the party and surprise her. She was totally surprised and cried a lot. I may have cried a little too. It felt awesome to pull the entire thing off as a complete surprise, and I was able to get so many of her friends all together in one room.

"There's really no better feeling than making someone that happy. Then, of course, she's reminded me every single year that no gift I ever give her will ever top it. Worth it!"

5. Rachel Toburen gave her mother a very different gift — one of a heartwarming companion.

Photo of Petal via Rachel Toburen.

"I fostered a litter of puppies, and my mom (two time zones away) fell in love with one," says Toburen. "She was trying to figure out some way to adopt the puppy, but coming to Colorado wasn't a possibility."

"To surprise her, we paid Petal's adoption fee, and flew to Michigan to deliver a 12-week-old puppy to my mom for Mother's Day. We told her about it in advance so she would be prepared and have her house ready. It was a lot of work on our end, but seeing my mom fall in love with this puppy from across the country, and then getting to have her...that was pretty awesome."

6. Jess Keegin gave a child the gift of education.  

Photo courtesy of Jess Keegin.

"I started sponsoring Tasila through Children International in 2012 when she was five years old," writes Keegin. "Zambian children typically start school when they're seven, but when I got Tasila's family report at age eight, it said she didn't attend school because her family (which consists of a single mother — her father is deceased — as well as four other siblings) can't afford it."

"I immediately knew I was going to change that, so I reached out to Children International to see what the costs would be to get her in school. She started school in January of 2014."

"She went from a child who looked constantly grumpy and unhappy to one whose smile could light up a room. When I asked CI what her school costs would be for 2017, I received a note that said she was 1st in her class."

"Her education will cost $171 in 2019. It's the best money I'll spend all year."

7. And David Pemberton proves that you can make people feel loved and special no matter how much or how little you spend.

Comic courtesy of David Pemberton.

"When I lived in Denver, I had absolutely no money, and my parents had to scrape together what they could to buy me a ticket back home to Tennessee for the holidays," says Pemberton.

"I have a big family — my present list that year was in the teens — and I knew that I wouldn't be able to buy anyone anything. So I got a ream of computer paper, some pencils, and a few sharpies from the office and I drew a one-page comic for everyone in my family. Each comic was inspired by my favorite memory with them. I bought several $1 frames from the local Goodwill to frame them."

"That year, as we all sat around to open gifts, it was always the comics that made people cry. And I mean everyone cried. Why does that make it better than receiving a gift? Well, I think it's because it let me know that everyone cherished these memories just as much as I did."

This holiday season, the best present you can give is one that you've wrapped with love. The joy you get in return will last you all year long.

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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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