+
Heroes

Surfer writes names of people's lost loved ones on his surfboard so they can ride 'one last wave'

surfing, grief, newport, rhode island

Dan Fischer takes people's lost loved ones out surfing for "one last wave."

Dan Fischer understands grief. He also has some idea of how to cope with it—and how to help others through it as well.

Fischer has experienced tremendous loss in the past few years, losing both his father and his best friend. As a surfer, he's a believer in what he calls "the transformative power of the ocean." Originally from Montreal, Canada, Fischer has found healing riding the waves off Newport, Rhode Island, where he's lived for the past seven years.

Now he wants to share that healing power of the waves with others.


"After one of those faithful sessions, where I had written my dad's name on my board," he tells Upworthy, "I decided to throw out an open invitation on TikTok to others who were struggling with loss." On January 4, he shared a TikTok video inviting people to share the name of a loved one who has passed and said he would write their name on his board and take them out into the ocean.

"It felt right and I wanted to help," he says. "I knew how healing surfing had been for me, and I wanted the opportunity to share that with others in hopes of inserting some positivity into their lives."

@paradrenaline

Comment a loved one who you’d like me to include. #love #memories #dreams #surfing #oceanlover #saltlife

People started sharing the names and stories of lost loved ones in the comments, and Fischer started writing down names. A dozen soon turned to 100, which turned to 500, which turned to more than 1,000.

In just over a week, the one TikTok blossomed into a full-fledged movement Fischer has dubbed the One Last Wave Project.

"Something we always say out there is, 'one last wave,'" Fischer says. "There's always one last wave to catch and I wanted to give that to others. There have been so many stories shared about loved ones who always wanted to learn to surf, or how the ocean was their happy place and unfortunately, their families weren't able to get them there in time. I committed to ensuring that they got out there for that one last wave."

Fischer gets emotional sharing what the project means to him.

"I've spent many nights sitting out there alone at sunset, connecting with the beauty of nature to heal," he says. "Now, I have thousands of loved ones joining me…it's truly hard to explain just how truly moving that is for me. I just hope to help in some small way."

Right now, the project is just a one-man show, with Fischer spending hours a day connecting with people in the comments and writing down names. He knows he's going to need help collecting names and stories as the list grows, and he's already looking into getting more longboards to accommodate more names.

"It is important to me that every single person's story is told," he says. "I would love to see it expanded where surfers from around the world can join in the movement and take loved ones out into the ocean from wherever they are."

Fischer says people keep asking if it's too late to get their loved one's name on his board, and he wants people to know it's never too late. He's in this for the long haul.

One Last Wave Project isn't Fischer's first project impacting people's lives in creative ways. He works as an MBA admissions consultant, but he also founded Step Up for the Cure, a charity fundraiser for cancer research. He credits his mother's influence for his impulse to use whatever he has to give back to others in a meaningful way.

"When I founded Step Up for the Cure, I was trying to create a symbolic struggle—we ran marathon distances up stairs for 24 hours straight—to align those involved with those facing such harsh adversity," he says. "One Last Wave has a bit of a different vision. While surfing, trying to harness the sheer power of the ocean for a few fleeting moments in order to ride the open face of a wave is extremely challenging; however, this movement is more about the peace and healing that results when you do, letting go, immersing yourself in the sea.

"Surfing is one of my great passions," he continues. "It has changed my life, and I'm grateful for the opportunity to be sharing that love with others in a way that provides hope and healing."

Fischer says he never imagined his project would resonate so deeply with so many people, but he's grateful that it has.

"I am deeply affected by every single story shared," he said. "Heartbreaking doesn't even begin to describe it, but when I connect with these people, we are bonded, and the board feels very much like a beacon of hope that their loved ones are set free to enjoy and shine once again. It's a way for them to be forever memorialized in a place they loved.

"I can't tell you how many times I've cried reading the stories, writing the names, and feeling them etched on the board as I paddle through the waves," he says.

Many of the commenters are parents sharing the names of children they've lost. Some of them loved the ocean, and some of them loved it but never got to see it. One commenter recently asked for her own name to be put on the board, as she's in hospice and the ocean has always been her peaceful place.

The simple act of reaching out, connecting with others, making an offering of what you have and bringing some measure of comfort to people who are in mourning is such a beautiful thing.

Fischer is working on getting the One Last Wave website up so that he can direct people to one central place if they want to add a loved one or find out how to help, but in the meantime, you can find him on these social media pages:

Tiktok: @OneLastWave

Twitter: @OneLastWave

Instagram: @OneLastWaveProject

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.

Joy

Sorry, Labradors. After 31 years, America has a new favorite dog.

The American Kennel Club has crowned a new favorite.

via Pixabay

A sad-looking Labrador Retriever

The sweet-faced, loveable Labrador Retriever is no longer America’s favorite dog breed. The breed best known for having a heart of gold has been replaced by the smaller, more urban-friendly French Bulldog.

According to the American Kennel Club, for the past 31 years, the Labrador Retriever was America’s favorite dog, but it was eclipsed in 2022 by the Frenchie. The rankings are based on nearly 716,500 dogs newly registered in 2022, of which about 1 in 7 were Frenchies. Around 108,000 French Bulldogs were recorded in the U.S. in 2022, surpassing Labrador Retrievers by over 21,000.

Keep ReadingShow less
Photo by Tod Perry

A recreation of the note left on Brooke Lacey's car.

If you are having thoughts about taking your own life, or know of anyone who is in need of help, please call the National Suicide Prevention Lifeline at 1-800-273-TALK (273-8255) or text "HOME" to the Crisis Text Line: 741741.


There’s an old Hebrew saying that if you “save one life, you save the world entire.” Who knows if Brooke Lacey, 22, had that lofty goal when she began a campaign in 2020 to help uplift people’s spirits during the first COVID-19 wave.

But her kind efforts may have done just that.

Lacey has struggled with mental health issues throughout her life and she knew that people like her were going to have a really hard time during COVID-19 lockdowns. A study from May 2021 found that the New Zealand population had “higher depression and anxiety compared with population norms.” The study also found that “younger people” and “those most at risk of COVID-19 reported poorer mental health.”

Keep ReadingShow less

Drew Barrymore speaks during the FLOWER Beauty launch at Westfield Parramatta on April 13, 2019, in Sydney, Australia.

Drew Barrymore, 48, has been in the public consciousness since she starred as Gertie in 1982’s mega-blockbuster, “E.T.: The Extra-Terrestrial,” a performance that earned her an Oscar nomination for Best Supporting Actress. So, it makes sense that many people of a certain age feel as if they’ve grown up with her.

Now, she’s an even more significant part of people’s lives as the host of “The Drew Barrymore Show,” which runs every weekday on CBS.

On May 25, the show’s Instagram page posted a touching video of an off-the-cuff moment between Barrymore and a fan during a taping of her show. In the clip, Barrymore realizes that someone in the audience is crying. So, instead of ignoring the fan, she jumps to action to see what is the matter.

Keep ReadingShow less
@geaux75/TikTok

Molly was found tied to a tree by the new owners of the house.

Molly, an adorable, affectionate 10-year-old pit bull, found herself tied to a tree after her owners had abandoned her.

According to The Dodo, Molly had “always been a loyal dog, but, unfortunately, her first family couldn’t reciprocate that same love back,” and so when the house was sold, neither Molly nor the family’s cat was chosen to move with them. While the cat was allowed to free roam outside, all Molly could do was sit and wait. Alone.

Luckily, the young couple that bought the house agreed to take the animals in as part of their closing agreement, and as soon as the papers were signed, they rushed over to check in.
Keep ReadingShow less

The young Mealy family was blown away by the instant kindness of their new neighbors.

If you're looking for a reminder of the good in people, we've got some sweet evidence for you.

Madison Mealy and her husband Blake recently moved to a rural area in the Blue Ridge Mountains and are new to country living. Mealy shared a video on TikTok showing her husband mowing the lawn with their baby in a backpack.

Cute, right? The only problem is they have a humongous lawn and her husband was mowing it with the teeniest push mower.

To be fair, if you've never had a big lawn, you may not realize how long it takes to mow and that not all lawn mowers are created equal. (They make riding lawn mowers for a reason, and it's not because of laziness.)

Mealy shared her amusement at having sent her husband out to buy a mower and seeing him come back with the tiny mower. It was going to take him hours to mow their grass.

Keep ReadingShow less
Pop Culture

Woman was mocked online for calling an $80 purse a 'luxury item.' Her response went viral.

"I'm so grateful that my dad was able to get me one. He worked so hard for that money.”

@zohtaco/TikTok

Zoe Gabriel, showing off her new purse from Charles & Keith

Insults of any kind are painful, but jabs towards someone’s financial status are their own breed.

In January 2023, Singapore-based Zoe Gabriel was on the receiving end of this particular flavor of mockery when she posted a TikTok about a purse from local retail brand Charles & Keith—a gift bought for her by her father.

In her excitement, the 17-year-old called the bag, which costs around $80, a “luxury” item as she unwrapped it. Her excitement was sadly cut short by some of the negative comments she received.

One comment seemed to stand out above the rest and prompted Gabriel to post an emotional response video.

Keep ReadingShow less