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What comes to mind when you think of undocumented immigrants? Probably not Julissa Arce.

This young woman proves there are no barriers — physical or otherwise — when it comes to achieving your dreams.

When you first meet Julissa Arce, you might assume she's like lots of other ambitious young women just looking for her own slice of humble American pie.

And she is. But she also lived with a huge secret for years.

Image by Julissa Arce, featured with permission.


Julissa was an undocumented immigrant who became a citizen two years ago.

She came to Texas from Taxco, Mexico, when she was 11, in 1994. Her parents got her a tourist visa, but when it expired three years later, she didn't go back to Mexico. Instead, her parents enrolled her in school. As Julissa notes in her book, her parents never addressed the expiration of her visa until it was too late.

Today, Julissa is 33 years old. She became an executive at Goldman Sachs before age 30, which might make her seem like a 100% success story. And she is. But her fight to get to where she is today shows us a lot about living as an illegal immigrant, too.

Her life story will hit home for anyone who says undocumented immigrants are only here to steal U.S. jobs.

(Just tell them to read her new book, "My (Underground) American Dream.")

"There’s so much that hasn’t been told ... and I really need to tell the whole story," she said about writing her book."I need to tell not just the victories, but also people need to understand the suffering and all the pain that went into getting to where I wanted to get and I couldn’t think of a more timely time to tell the story."

Julissa first realized the severity of her position while in college.

Julissa was a strong student in high school, but she still experienced a roller coaster of emotions when it came to attending college. Because she was an illegal immigrant, it was entirely possible that she wouldn't be able to attend at all.

Then she read about House Bill 1403 and was told to call then Sen. Rick Noriega's office. Her grades earned her a signed letter from the senator to the University of Texas in Austin asking them to consider Julissa's application. She was in.

But it wasn't smooth sailing from there.

She had purchased fraudulent papers with a fake Social Security number because she was so nervous about staying in America without correct documentation. Her parents and younger brother had decided when she was 18 that it made more financial sense for them to go back to Mexico, but because she wanted to go to college, she stayed, alone. How would she pay for her apartment or her tuition or her books? Julissa got a job and got to work. She manned a funnel cake stand, and she worked at a call center, taking any job that would pay the bills.

In her book, Julissa explains her heightened anxiety during college. She couldn't risk presenting any sort of ID at a bar or club, so she rarely went out. Driving meant risking a traffic stop that could potentially lead to deportation because she didn't have a driver's license.

Julissa speaking at The Berkeley Forum. Image by Julissa Arce, featured with permission.

There were also the more obvious sacrifices, like the comfort of family. Julissa couldn't visit her family once they went back to Mexico. She couldn't risk attempting to come back into the U.S. with fake papers. There was too much at stake. That also meant she had to spend holidays (including Christmas) alone.

This is one of my favorite pictures that I share in "My (Underground) American Dream". I dedicated the book to my mom, Luisa, and my dad, Julio. Today marks the 9th anniversary of my dad's passing and not a day does by that I don't wish I had been by his side in his last hours. It hurts just as much as it did on day one. In his honor, in his memory, I share my journey. My biggest wish is that not a single daughter, father, son, mother would have to be separated. The cost of my American Dream was too high. I share some painful moments about my relationship with my dad in the book, but the way I will always remember him is by his smile, his laugh, his jokes, his silliness! He used to call me Juliana. So today call me Juliana.

A photo posted by julissaarce (@julissaarce) on

Julissa's grades in college were stellar, and she also became involved in the Hispanic Business Student Association, serving as president in her final year. Her work ethic and grades were so impressive, she managed to land one of a few coveted internships at Goldman Sachs before her senior year. She left such a positive impression with them that she secured a job as an analyst with the financial firm before graduation.  

She met a guy in Manhattan, and they got married. That's what got the ball rolling on her path to becoming a U.S. citizen. But when it came time to take the oath in August 2014, it was an understandably emotional moment for Julissa.

In her book, Julissa writes that as she looked around the courtroom, she knew every person in there had worked hard for this moment. "America is still the shining beacon of the world. I kept wiping away my tears, simply overwhelmed to think that this day was finally here, and that never again would I have to live in fear of being deported from the country I loved. Never again would anyone be able to question that I was American."

What does this once-undocumented immigrant think about immigration reform?

She thinks we need a path to citizenship for the millions of undocumented immigrants who already live in America. But she also points out that much can be done at a state and local level, too. Local governments can give people access to driver's licenses, and they can allow for in-state tuition costs for undocumented students as well.

When it comes to 2016 Republican presidential nominee Donald Trump, Julissa admits she's disappointed that we've given him a platform: "The problem is that whether he wins or loses — the damage has already been done, and we have a lot of work to do to repair the damage that he has done over the last 18 months that he’s been running his campaign."

Julissa's future isn't slowing down either, which excites her.

Her father died nine years ago, in 2007. She was climbing her way to the top at Goldman Sachs at the time. She recalls in her book slipping into a conference room to cry before composing herself and walking back out to face her coworkers.

Now that Julissa is a citizen, she can visit her family in Mexico whenever she wants to. But she also says she's found her true calling — and it's not on Wall Street. She wants to help other people like her looking for a path to citizenship. She has come out the other side of her incredible struggles a successful woman and wants to share the wealth of her knowledge with those who need it the most — undocumented immigrants who want to earn their way into the country.

During one week in October 2016, Julissa was in New Orleans on Monday, hosted a talk at Berkeley on Tuesday, was invited to the White House on Wednesday, and pitched a TV show on Friday. She's currently working on a TV show inspired by her book, too. America Ferrera is producing the series, making the rounds with Julissa in L.A. as they pitch the show.

Julissa with America Ferrera. Image by Julissa Arce, featured with permission.

Julissa says talking about her story is cathartic, but it's also incredibly important for other immigrants.

In fact, she has a simple yet powerful message to all the young, undocumented immigrants living here now: There's always a way.

"You can’t give up and that the road is tough but, at the end of the road, is your goals and your dreams," Julissa said. "You just can’t give up. You’ve gotta be really strong in your convictions and you gotta know that all of your sacrifices are … your dreams are worth your sacrifices."

I can't wait to see what Julissa does next, and as a fellow Latina, I'm thankful for her perseverance in chasing her dream in spite of the unimaginable obstacles, for the way she's reached such impressive heights at such a young age, and — most importantly — for how she is coming forward to share her powerful story to help others obtain their American dream. Every story matters.

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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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