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19 fascinating pictures to remind us what polio used to look like.

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March of Dimes

My dad had weird feet.

He was born in 1942, and when he was just a few years old, he caught polio. He survived the disease, but it affected the way his legs and feet grew — one foot was always a shoe size or two smaller than the other one. I remember being fascinated by them when I was little.

Though polio affected my father, I myself have never been in danger of contracting it.

In fact, the disease has disappeared completely from the United States, and we're incredibly close to eliminating it worldwide.


But as much as we should celebrate its passing, we should also remember what it was like when polio affected people everywhere. And though these photos may be somber, they should also give us hope; they prove that we can overcome the worst obstacles and most pernicious infections. After all, we've done it before.

Check out these photos of what polio looked like when my dad was a kid.

Polio was a scourge. It could affect anyone. But it preyed most heavily on children.

A child paralyzed by polio in 1947. Photo by Keystone Features/Getty Images.

A young patient getting fit with a respirator in 1955. Photo by Three Lions/Getty Images.

Polio's actually a lot older than my father was. We even have paintings of it from ancient Egypt.

This over-3,300-year-old Egyptian stele is thought to depict a polio victim. Image via Deutsches Grünes Kreuz/Wikimedia Commons.

For most of that time, polio was content to remain quiet.

But in the 19th and 20th centuries, it became a killer. In 1952, an outbreak killed over 3,000 people and paralyzed over 21,000 in the U.S. alone.

Photo from Douglas Grundy/Three Lions/Getty Images.

Polio is a virus passed mostly through contaminated food and water. And as long as we humans were spread out, it never got the momentum to really become a problem. But as cities grew and, ironically, better sanitation came about and removed some of our natural exposure to it, polio suddenly found a weak spot in our defenses.

Children were most at risk of contracting the virus – hence one of its common names: infantile paralysis.

Photo by Sonnee Gottlieb/Hulton Archive/Getty Images.

In most cases, it's either harmless or mild, like a case of the flu. But in some people, polio can cause serious, sometimes permanent paralysis.

A paralyzed kid at London's Queen Mary's Hospital in 1947. Photo by George Konig/Keystone Features/Getty Images.

If the virus ends up in the central nervous system, it interrupts our body's ability to communicate with our muscles, causing paralysis. And if the paralysis lasts for a long time, the muscles themselves can start to waste away, a process known as atrophy.

This is already bad, but there's one more cruel twist to the disease. If a child is the one who gets paralyzed, the muscle atrophy can end up affecting the way their bones grow. That's what happened with my dad and why his feet looked so weird.

If the diaphragm was paralyzed, patients would need respirators to be able to breathe. Some respirators were portable, like this one.

A portable respirator from 1955. Photo by Hans Meyer/BIPs/Getty Images.

For a given value of "portable."

Others, like the iron lung, effectively trapped you inside.

An iron lung in 1938. Photo from London Express/Getty Images.

If you did recover, you may have still needed regular physical therapy to strengthen the atrophied muscles. Aquatic therapy was popular.

Photo by Juliette Lasserre/BIPs/Getty Images.

At its height, polio was one of the great public specters. People were terrified of it. Public pools were closed in a misguided effort to stop the spread. Houses were quarantined.

A board of health warning circa 1910. Image from National Library of Medicine/Wikimedia Commons.

There were public health campaigns and donation drives to help fuel research, like the March of Dimes.

A cartoon from 1943. Image from U.S. National Archives and Records Administration/Wikimedia Commons.

Still, nobody seemed safe. Even President Franklin Roosevelt had it, although he was careful about hiding his paralysis from the outside world.

A rare photograph of FDR in his wheelchair. Image from Margaret Suckley/Wikimedia Commons.

It was one of the great scourges of its time.

Then, in the early 1950s, Jonas Salk invented the first polio vaccine.

Photo by Three Lions/Hulton Archive/Getty Images.

Salk was a researcher and virologist who joined the fight against polio in the late 1940s. Initially tasked with identifying different strains of the virus, Salk and his team saw an opportunity to try to prevent the disease altogether, and their work paid off.

Manufacturers began to mass produce it.

Workers at England's Glaxo company in 1956. Photo from Fox Photos/Getty Images.

Suddenly, people could save their children from this awful disease.

Photo by Monty Fresco Jnr/Topical Press Agency/Getty Images.

As people became immunized against it, the disease had a harder and harder time spreading between populations. Numbers of infections started to fall.

And, slowly, polio transformed from a demonic specter into a manageable disease, then, eventually, into a distant memory.

A woman examines a gigantic model of a single polio virus capsule in 1959. Photo from Fox Photos/Getty Images.

Thanks to the vaccines created by Salk and other researchers, most of the world began to forget this disease.

Today, we're on the cusp of eradicating polio altogether. Its last holdouts are in Pakistan, Afghanistan, and Nigeria.

A child afflicted with polio in Afghanistan in 2009. Photo by Paula Bronstein/Getty Images.

We're really close. In fact, one of polio's three strains has already been eliminated.

Photo by A Majeed/AFP/Getty Images.

Which is why the U.N. switched to a two-strain vaccine in May of 2016.

In 2015, there were only 74 recorded cases of polio in the entire world. Just 74!

A Pakistani child receives the oral polio vaccine in 2016. Photo from Banaras Khan/AFP/Getty Images.

Polio has no natural reservoir. It has no place to hide. Once it's gone, it's gone.

We might never be able to eliminate the flu because it can hide in so many animals, like birds or pigs. But polio only infects humans. So when all humans are immunized, polio will disappear.

We're so close to eliminating a horrible disease thanks to researchers like Salk and workers dedicated to administering vaccinations. There are occasional setbacks, such as a recent shortage of the new vaccine, but researchers hope to completely eliminate the disease by the end of this decade.

We can overcome the worst demons. We have before. And we can do it again.

In the future, the only place where polio will exist is in picture archives like these. And the memories of my dad's poor feet.

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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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