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Democracy

12 real stories that show why ruthless immigration laws are the wrong move.

Immigration policies that rip families apart are a travesty.

12 real stories that show why ruthless immigration laws are the wrong move.

This article originally appeared on 03.02.17


If there's ever been a particularly bad time to be an undocumented immigrant, it's right now.

President Donald Trump, who launched himself into the 2016 presidential race with his support for a multibillion-dollar border wall, has been cracking down on immigration as promised. In addition to tightening border security, he's pledged to remove 2 to 3 million undocumented immigrants "immediately." And he appears to be keeping his word.

Deportation is nothing new, but Trump's plans are unprecedented. Photo by Scott Olson/Getty Images.


It's a scary climate we're facing, but unfortunately, it's not just Trump and it's not just America. All over the world, people are more concerned with their countries' borders than seemingly ever before.Nations all over Europe, for example, are tightening up immigration rules and/or ramping up deportations themselves.

Amidst all the noise and rhetoric — every "radical Islamic terrorist" attack that gets waved about by politicians with something that eerily resembles pride, every horrific crime committed by white Americans that's met with deafening silence, every press conference faux pas — there are real people and real families being ripped apart in the name of patriotism.

Their stories are terrifying and heart-wrenching, but they're massively important.

1. A DREAMer gave a powerful speech about deportation. Moments later, she was arrested.

Daniela Vargas, who has lived in the U.S. since she was 7 years old, spoke at a news conference in Jackson, Mississippi, about the importance of the DREAM Act, which aims to help immigrant children who have lived in the U.S. for more than five years and graduated high school receive permanent legal status.

After the event, Vargas and a friend were pulled over and arrested by immigration agents.

2. A Sri Lankan student studying in North Wales was saved from deportation only by a last ditch effort hours before her flight.

Shiromini Satkunarajah, an electrical engineering student at Bangor University, was nearly sent back to Sri Lanka earlier this year. Despite having lived in the U.K. since she was 12 and being only three months shy of graduation, Satkunarajah was only allowed to stay after receiving an outpouring of community support.

3. A woman living in Great Britain was sent back to Singapore without being allowed to say goodbye to her husband and two children.

Irene Clennell had lived in the U.K. since 1988 but was abruptly sent back to Singapore after having her indefinite leave to remain revoked. Clennell is married and has two children with her husband but was not afforded the chance to see them one last time.

4. A mom living in Phoenix was sent back to Mexico. Her children would later face Trump as he addressed a joint session of Congress for the first time.

Guadalupe Garcia de Rayos' children were reportedly in attendance as Trump addressed Congress. Photo by Jim Lo Scalzo/AFP/Getty Images.

Guadalupe Garcia de Rayos was sent back to Mexico in January this year for having a criminal record. Her crime? Working under the table to provide for her young children.

5. A beloved restaurant manager in a deep-red town in Illinois was arrested, and now the community is reeling.

Most of the people in West Frankfort, Illinois, voted for Trump. They never thought anything would happen to Juan Carlos Hernandez Pacheco, the friendly restaurant manager who seemed have done at least one kind deed for everyone in the community. Now, he's been detained by ICE and is currently waiting to find out if he'll be sent back to Mexico.

6. A Kuwaiti man and father of two living in Ann Arbor, Michigan, on the other hand, was miraculously spared from deportation because it would cause his family too much hardship.

Yousef Ajin has lived in the United States for 18 years with his wife, with whom he has four children. He reportedly met with immigration officers frequently, but on Jan. 30, 2017, he was suddenly detained.

In February, a judge granted a deportation waiver in order to spare Ajin's family from hardship. Many other immigrants aren't so lucky.

7. One man was caught trying to cross the border and returned to Tijuana. He appears to have jumped to his death shortly after.

The man, Guadalupe Olivas Valencia, had reportedly worked in the U.S. before to provide for his family back home before being deported multiple times. Caught trying to enter the country once again, he seemingly decided jumping from a bridge was his only option.

8. A single mother in California was sent back to Mexico, leaving her two young children in peril.

Photo by Jose Cabezas/AFP/Getty Images.

On Feb. 7, María Robles-Rodríguez was nabbed by U.S. Border Patrol and sent back to Mexico, leaving her twin 18-year-old daughters to fend for themselves.

9. Gay men being deported from Britain to Afghanistan are being told to pretend they're straight.

The British government's advice to gay men being sent home to Afghanistan, where they can be freely persecuted for their sexual orientation? Just don't act gay and everything will be fine!

Seriously.

10. Jose Escobar was detained after a routine meeting with immigration officers. He's a husband and father of three.

Escobar, who has lived in the United States for 16 years, had a deportation scare a few years back but was told he'd be safe if he checked in with immigration agents every year. Only this year, an agent reportedly told his wife, "We're just doing what President Trump wants us to do with the new rules."

Escobar will likely soon be deported.

11. A Mexican man living in Idaho was deported. His wife and the mother of his children could be next.

Tomas Copado ran his own auto body shop in Idaho Falls until he was sent back to Mexico earlier this year. His wife, for the sake of their children, recently had her own deportation deferred.

For now.

12. Some undocumented immigrants may be deported to Mexico even if they're not from there.

Photo by John Moore/Getty Images.

According to several reports, the Department of Homeland Security plans to send anyone who crosses illegally over the southern border of the U.S. back to Mexico, even though they may be citizens of another country.

Needless to say, this is horrendous and possibly in violation of international law.

Statue of LibertyPhoto by Guzmán Barquín on Unsplash

Every modern nation needs smart, empathetic paths to citizenship. Any immigration policy that tramples on human rights and rips families apart is a travesty.

It's time to bust the narrative that foreigners primarily come to our country — or any country — to do harm. They come mostly to find opportunity, to escape persecution, or to be with family.

If we can't come to see them as human beings rather than inanimate outsiders, finding the money to pay for a giant wall will be the very least of our problems.

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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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