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Betsy DeVos is our education secretary. Here's what to do next.

On Feb. 7, 2017, Betsy DeVos was confirmed as America's next education secretary.

Resistance to her nomination was of historic proportions. Last week, two Republican senators — Susan Collins of Maine and Lisa Murkowski of Alaska — broke ranks and announced they would oppose DeVos, leaving the GOP-controlled Senate at a 50-50 stalemate (all 48 Democrats opposed her nomination). Vice President Mike Pence cast the tiebreaking vote.

Photo by Drew Angerer/Getty Images.


If you attended or have kids in public schools, DeVos' nomination may be a tough pill to swallow. DeVos, a Michigan billionaire born into wealth, has never attended or worked in a public school — although her family has given the Republican Party about $200 million over the years. She's also been a big proponent of school choice — a controversial free-market education method that allows public funds to be siphoned off to private, parochial, and even for-profit schools. It's a strategy many education advocates have criticized, claiming it uses already scarce public school funds to benefit mostly upper-middle class and wealthy families, leaving the most vulnerable students and schools in even worse shape.

Admittedly, it was not a good day for many public school advocates. But now more than ever, American kids and schools need our help.

Here are 20 ways you can turn your anxiety over the future of public education into real action:

1. First and foremost, don't feel hopeless.

Let your frustrations fuel your advocacy. Among President Trump's controversial cabinet appointments, DeVos' agenda may be the least popular among Americans. The resistance to her plans is alive and well.

2. Help fund a project that will make a difference on Donors Choose.

The platform gives teachers a place to crowd-fund classroom projects, allowing individuals (that's you!) to help students, whether it be giving art supplies to students in California or providing iPads to kids in Brooklyn to boost their linguistic and social skills.

Photo via iStock.

3. If you can, get involved in the National Education Association.

The focus of NEA — the largest professional employee organization in the country — is to make public education high-quality and accessible to every student. There are many ways for prospective, current, and former public education professionals to join the cause.

4. Come midterm elections, don't forget which senators voted for DeVos — many of whom received campaign donations from her family:

Steve Daines (Montana), John Thune (South Dakota), Ron Johnson (Wisconsin), Richard Burr (North Carolina), Jeff Sessions (Alabama), Roger Wicker (Mississippi), Roy Blunt (Missouri), Bob Corker (Tennessee), Michael Enzi (Wyoming), John Barrasso (Wyoming), Dean Heller (Nevada), Rob Portman (Ohio), Bill Cassidy (Louisiana), John McCain (Arizona), Richard Shelby (Alabama), Mike Lee (Utah), Ted Cruz (Texas), Dan Sullivan (Alaska), Cory Gardner (Colorado), Rand Paul (Kentucky), Deb Fischer (Nebraska), Lindsey Graham (South Carolina), James Inhofe (Oklahoma), Jim Risch (Idaho), James Lankford (Oklahoma), Jerry Moran (Kansas), Patrick Toomey (Pennsylvania), Joni Ernst (Iowa), Tom Cotton (Arkansas), Michael Rounds (South Dakota), Thad Cochran (Mississippi), Mitch McConnell (Kentucky), Michael Crapo (Idaho), John Hoeven (North Dakota), Pat Roberts (Kansas), Shelley Moore Capito (West Virginia), Orrin Hatch (Utah), John Kennedy (Louisiana), Thom Tillis (North Carolina), Todd Young (Indiana), Jeff Flake (Arizona), Tim Scott (South Carolina), Ben Sasse (Nebraska), Marco Rubio (Florida), David Perdue (Georgia), Johnny Isakson (Georgia), Charles Grassley (Iowa), John Cornyn (Texas), John Boozman (Arkansas), and Lamar Alexander (Tennessee).

5. Think local.

You know your own community best. What local or regional organizations do the crucial work unique to the problems facing the public schools in your city? Reach out and ask them how you can get involved.

6. Donate to No Kid Hungry.

The nonprofit helps feed American schoolchildren so they can stay full and focused in the classroom. One $10 gift can provide up to 100 meals to a kid who could use it.

7. Support after-school arts programs.

There's probably at least one group in your area helping teach art to kids outside the classroom — an opportunity that could help them in many ways for years to come. In Pittsburgh, for instance, free after-school art classes at Manchester Craftsmen’s Guild Youth & Arts teach any kids in the Pittsburgh public school system skills in ceramics, design, photography, and more.

8. Share this video of Sen. Al Franken questioning DeVos' support of anti-LGBTQ causes — and hold her accountable to do better.

Let the record show: Dollars from the DeVos family have gone toward horribly anti-LGBTQ initiatives, including gay (to straight) conversion therapy — a practice that's  been deemed harmful by experts and is essentially a form of child abuse.

Despite her record, DeVos said during her Senate hearing that she never believed in gay conversion therapy and that she "fully embraces equality" for all students. Let's hold her accountable to that.

Earlier this evening, I questioned Betsy DeVos, President-elect Trump's nominee for Secretary of Education, and was deeply troubled by the fact that she seemed unfamiliar with some of the most basic issues in education today. Ms. DeVos repeatedly refused to answer questions, let alone offer specifics. That was not what the American people needed to hear. They deserved to see her demonstrate that she understands and can successfully address the profoundly difficult challenges ordinary families face every day when it comes to education: things like making sure their kids are prepared for the 21st century economy, addressing student loan debt, and ensuring kids feel safe in school.

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U.S. Senator Al Franken on Tuesday, January 17, 2017

9. Support your local libraries.

Libraries are great resources for our kids to learn outside the classroom (and they have so much more to offer than books). Get your library card, visit frequently, volunteer, and spread the word.

Speaking of libraries...

10. Create a Little Free Library in your own neighborhood.

Build a little library in your yard, stock it with some books, and let your neighbors enjoy. Ideally, it'll turn into a take-a-book, give-a-book situation.

Learn more about how to pull it off.

11. Fight for more affordable and free higher education at the ballot box.

Despite what you may think of DeVos' appointment, Americans increasingly support using public funds to ensure college is free or affordable to more students. Stanford University, for example, was cheered for guaranteeing students whose parents have a combined income of less than $125,000 would have free tuition. And San Francisco has also made waves for making City College free for residents.

Many state and local governments are also trying to make higher ed more accessible to more students. New York state may make its public colleges and universities free to attend for the vast majority of students. Stay plugged in to similar state and local initiatives in your own area.

12. Support the "nonpublic" schools in your area.

Nonpublic schools are, in fact, public schools for kids with moderate to severe disabilities that prevent them from attending a more traditional public school. The Individuals With Disabilities Education Act ensures schools like them exist for any family that needs it.

Considering DeVos' nomination has disability advocates worried, the nonpublic schools in your community could probably use your support. Many host regular fundraisers and even need classroom volunteers.

13. Support the Kids in Need Foundation.

The nonprofit provides thousands of backpacks filled with school supplies to students in need every year, giving them the tools they need to succeed in class. (There are lots of groups doing similar work, by the way — if you do some digging, you may find a more local option.)

Photo via iStock.

14. Don't forget that Open eBooks is a thing, and it's spectacular.

Former President Obama's ConnectED initiative helped get more than $250 million worth of fantastic children's e-books online, available to any young person who wants to dive into a good read.

Because not every kid gets that chance.

15. Donate to First Book.

This nonprofit provides new books and other learning materials to kids and families in need. Since it was founded in 1992, the group has given away 160 million books and education resources.

16. Help tackle crime, nutrition, and education ... with veggies.

The nonprofit Gardopia Gardens operates community gardens at schools in Texas, helping make nutritional foods more accessible to kids. It not only teaches them about nutrition and gardening, it lowers crime rates in the neighborhoods where it operates. Similar programs are offered at schools around the country — if your local school doesn't already have one, why not look into what it would take to start one yourself?

17. Help make lunchtime a little more stress-free.

18. Support Publicolor.

Kids in New York City who work in the after-school program Publicolor paint beautiful works of art in schools in order to bring a splash of color to the spaces they share, build relationships, and learn valuable skills like commercial painting and positive work habits.

19. Stand up for immigrant students by supporting United We Dream.

The group had already been rallying educators to stand up to Trump's agenda. Now, with DeVos' nomination, its Educators Toolkit may be even more necessary.

20. Take matters into your own hands and run for a position on your local school board.

All politics are local, right? Run for school board in your community and make a difference.

Let's not sugarcoat it: DeVos' nomination is a major setback for our public schools. But we can't get complacent.

In ways big and small, our resistance to her agenda can make a better tomorrow for kids everywhere.

Photo via iStock.

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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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