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See science come alive with a little help from these amazing illustrations.

Rachel Ignotofsky's book sits at the intersection of art, science, and history.

Name five women scientists you learned about in school. Go ahead, I'll wait.

GIF via "Sherlock."


I got to three very quickly but had to think for a moment to get to five. It's not because these researchers, explorers, and innovators don't exist; I simply didn't learn about their work and contributions to history in school. It just wasn't a large part of the curriculum. And, sadly, my experience isn't unique.

You can't be what you can't see,which may be why women remain underrepresented in science, technology, engineering, and mathematics (STEM) roles. Just 25% of computer and mathematical science professionals and a mere 13% of engineers today are women.

But one woman is doing her part to help change that. And she's doing it with comics.

Seriously, comics.

Rachel Ignotofsky is a Kansas City-based artist and designer whose first book is an illustrated look at 50 game-changing women across centuries of scientific discovery and inquiry.

Unless otherwise noted, all images reprinted with permission from "Women in Science," copyright 2016 by Rachel Ignotofsky, published by Ten Speed Press, an imprint of Random House LLC.

But why comics? It's the medium that changed her life.

Ignotofsky had a difficult time learning to read and grew frustrated until she found her secret weapon.

"The only thing that ... got me through it was educational comic books and cartoons," Ignotofsky said. "It gave me this push to learn information that was for the 'smart kids.'"

Ignotofsky grew up loving comics, design, and science. (If a career as an artist didn't work out, medical school was young Rachel's backup plan.) So she channeled her passions into "Women in Science: 50 Fearless Pioneers Who Changed the World." The book is a beautifully curated collection of personal narratives from female scientists from a wide variety of backgrounds and disciplines, with a dash of whimsy thrown in.

Ignotofsky hopes it will open doors to kids and adults interested in learning more about the women who shaped not only science, but history. And after her childhood struggle with reading, she knows firsthand how well comics can deliver information.

"I feel like there's a real struggle with scientific literacy, especially in this country," Ignotofsky said. "You have to win people over. And you can convince anyone to do anything with illustration."

Check out a few of the courageous women in science profiled in Ignotofsky's book.

1. Edith Clarke, who worked as a human calculator and became General Electric's first female electrical engineer.

She's also a Badger. On, Wisconsin!

2. Marie Curie, the two-time Nobel Prize winning physicist and chemist who discovered polonium and radium.

3. Paleontologist and fossil collector, Mary Anning, who at age 12 discovered an intact dinosaur skeleton. Though respected in the field, Anning was never allowed to publish her work because she was a woman.

4. Patricia Bath, a physician, professor, and inventor who brought eye care to people in need and developed the laser probe used to treat cataracts.

5. Rosalind Franklin was a pioneering chemist and x-ray crystallographer who discovered the double helix shape of DNA.

6. Sylvia Earle, a celebrated marine biologist and aquanaut, who explored the recesses of our oceans to study the plants and animals found in the depths.

7. Hypatia, one of the earliest recorded female mathematicians and teachers who was also an expert philosopher.

But even with the amazing women she highlights in her book, Ignotofsky still remembers the women she had to leave out.

Women like pioneering Indian botanist Janaki Ammal, paleoanthropologist Mary Leakey, accomplished physicist and astronaut Sally Ride, and Irene Joliet-Curie, daughter of Marie and Pierre Curie and a talented chemist in her own right. But for this collection, Ignotofsky had to make some tough calls and let variety be her guide.

"I could've had 50 women in chemistry if I wanted to, but I really wanted to have a diverse group."

Physicist Sally Ride became the first American woman in space in 1983. Photo via NASA.

But, luckily, for Ignotofsky — and all of us who love women in science — there are plenty of women in science for another book or two ... or 20.

Women are earning just over half of the undergraduate degrees in STEM fields, and we're re-writing history and making groundbreaking discoveries every day. The future belongs to these rising stars, and they have these courageous pioneers to thank.

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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.

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.

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