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Pop Culture

'Rainbow Bridge' poem has long comforted grieving pet parents. Finally, the author is revealed.

For years, the creator of this beloved piece has been shrouded in mystery.

rainbow bridge author, losing a pet, pet grief
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For years, 'Rainbow Bridge" seemed to simply exist without an author.

For grieving pet parents, few words come closer to providing some sort of comfort than those of “Rainbow Bridge.” After all, the poignant and wildly popular poem offers a slice of hope, promising a reunion with our furry loved ones in a magical paradise of the afterlife. Even for those who aren’t so theologically inclined, the imagery can be soothing after irrevocable loss.

For so long, “Rainbow Bridge” has seemingly existed as its own entity, being handed out by vets or shared in condolence cards and online sans a credited author. However, thanks to the tireless sleuthing of historian and author Paul Koudounaris, that mystery has been solved.


According to an interview with National Geographic, Koudounaris had first become enticed to find the unknown creator of “Rainbow Bridge” after encountering it several times while working on his book about pet cemeteries (fitting). Wanting the person who wrote what he described as “a text with monumental importance to the world of animal mourning” to receive some well-deserved acclaim, Koudounaris began his search.

He discovered that “Rainbow Bridge” first came to notoriety through the long syndicated advice column “Dear Abby,” where in 1994 the poem was printed along with a warning for readers to “grab their hankies.” However, there was still no writer’s name attached. Koudounaris would have to compile two dozen names with even the slightest connection to the poem, and one by one cross them off the list until he landed on just one—a woman in Scotland by the name of Edna Clyne-Rekhy.

“What initially would have seemed like the most unlikely candidate in the end turned out to be the most intriguing candidate and, of course, the actual author,” Koudounaris told National Geographic, noting that Clyne-Rekhy was the only non-American on the list.

Koudounaris reached out to Clyne-Rekhy, who was not only shocked that he had found her but completely unaware that her poem had touched millions of hearts.

As Koudounaris details in his own story, Clyne-Rekhy was only 19 years old when she first put her words to paper. The year was 1959, and she had just lost her beloved Labrador named Major. Her only ambition (or more accurately—compulsion) at that time was to memorialize him and surrender to the “warm feeling” that seemed to be inspiring her to write.

Even when it was but a messy draft full of crossed-out words and scribbles, people knew the poem was special. At least, the few people who were shown it knew. Despite her husband’s encouragement, Clyne-Rekhy never sought to publish but would share a copy from time to time, always without her name written on it.

Here is the poem in its entirety:

The Rainbow Bridge

By Edna Clyne-Rekhy

"Just this side of heaven is a place called Rainbow Bridge. When an animal dies that has been especially close to someone here, your pet goes to Rainbow Bridge. There are meadows and hills for all of our special friends so they can run and play together. There is plenty of food, water, and sunshine, and friends are warm and comfortable. All the animals who have been ill and old are restored to health and strength, those who were hurt are made better and strong again, like we remember them before they go to heaven. They are happy and content except for one small thing, they each miss someone very special to them who had to be left behind. They all run and play together, but the day comes when one suddenly stops and looks into the distance, his bright eyes are shineing (sic), his body shakes. Suddenly he begins to run from the herd, rushing over the grass, his legs carrying him faster and faster, and when you and your special friend finally meet, you cuddle in a happy hug never to be apart again. You and your pet are in tears. Your hands again cuddle his head and you look again into his trusting eyes, so long gone from life, but never absent from your heart, and then you cross the Rainbow Bridge together."

By the early 90s, “Rainbow Bridge” made its way to a few animal lovers’ groups in America and then to the 1 million readers of “Dear Abby.” Sixty-four years after its creation, now we see its words engraved on countless pet gravestones and recited during mourning groups. Clyne-Rekhy had no idea.

And though she wasn’t thrilled that several people attempted to take credit for something she poured her heart into—including one who, according to Koudounaris, insisted it was originally performed by a Native American shaman—more than anything, she was touched to learn that it made such a positive impact on others.

As for any further advice for grieving a lost pet? Clyne-Rekhy, now 82, says get another one. While she agrees that no two animals are alike, she told Koudounaris, “There’s no reason to deny yourself…your previous pet certainly wouldn’t have wanted you to live without it.”

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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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