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Can we all agree that slashing $7.1 billion from education is asinine?

Can we all agree that slashing $7.1 billion from education is asinine?

Of all of the hair-brained, short-sighted budget proposal ideas, removing billions of dollars from education takes the cake.

If there's anything that people of all political persuasions should be able to agree on, it's the importance of education.

A well-educated citizenry is the chassis that supports everything we need to keep moving forward—a thriving economy, safer communities, advances in science and technology, strong international standing, and more.


And as the top-performing educational systems in the world prove, a well-funded, equitable, government-funded school system is the most reliable engine humans have designed to keep the machine of civilized society running.

However, the 2020 budget proposal coming from the White House includes cutting $7.1 billion from the Department of Education. On the chopping block include summer and after school programs in low-income areas, Public Service Loan Forgiveness programs, and subsidized Stafford loans for higher education. And while those programs would be cut, more funds would go to charter and magnet school initiatives.

Why? Because public education doesn't require money, duh! College graduates can pay soaring tuition rates with their bootstraps, don'tcha know? And nobody needs after school or summer programs, especially not kids in high poverty areas, right? Nah. We just need to make sure that for-profit charter schools get a bigger piece of the taxpayer pie, because government-funded capitalism is totally the way to make sure everyone has equal access to quality education.

Or maybe we don't actually need to know the best way to educate our diverse and growing populace, because guess what— funding for scientific educational research is on the chopping block too!

(Sorry, sometimes sarcasm is the only reasonable response to absurdity.)

Federal fund allocations are complicated. But this part shouldn't be.

I know the arguments about education being funded locally instead of federally. I understand the sorta-nice-on-paper idea of "school choice." But we have models of successful educational systems around the world, and the vast majority of top-performing systems are government funded with a small percentage of parents choosing private education.

Considering how many schools in America struggle and how many teachers have to pay for materials out of their own pockets, I see very few scenarios where cutting money from education could be considered wise. Even if an educational program is ineffective, it makes more sense to funnel that money into expanding and increasing programs that are working rather than cutting funding altogether.

Call me crazy, but I think education should get every last drop of money we can throw at it. I attended public schools and I've taught in public schools. I know what a challenge it to meet the needs of all students. I chose to homeschool my own kids but still vote yes on every single public school funding measure that comes across my path. I've seen how money makes a difference in what schools are able to offer, and I prefer to live in a well-educated society.

It's not like we don't have the money for more books, when we clearly have the money for more bombs.

What really chaps my hide is that this budget proposes cutting $7.1 billion from education while adding $8.6 billion for a border wall and a 5% increase in defense spending (which equates to an extra $30 billion plus). I can get behind the proposed military pay increase of 3.1% because military families make enough sacrifices as it is, but do we really need to increase defense spending by that much?

We are already the most powerful military force on the planet and we spend more on defense than the next seven countries combined. At what point do we decide that the hundreds of billions we already spend on defense and destruction is enough, and start investing more heavily in the education and health of our people?

The vast majority of educational professionals I know believe that our current administration is taking education in the wrong direction, and this budget proposal highlights why. Both the president of the American Federation of Teachers and the president of the National Education Association—the country's largest teacher unions—denounced the budget cuts. AFT president Randi Weingarten said in a statement:

“This budget doesn’t fund the future; it does quite the opposite, forfeiting children by yet again cutting the education budget while safeguarding the tax cuts given to the wealthy last year. President Trump and Secretary DeVos have made a choice with this budget—enriching those who are rich and who don’t want for anything, on the backs of our children. Even their so-called priorities, career and technical education and child care, aren’t funded in a meaningful way. By eliminating the Public Service Loan Forgiveness program, they are sending a message that public service doesn’t matter..."

“Rather than increase funding for kids with special needs or for those who live below the poverty line in both rural and urban America, or addressing the issues raised in their own safety report, DeVos once again seeks to divert funding for private purposes in the name of ‘choice.’ However, if they listened to parents, they would hear that, overwhelmingly, parents want well-funded public schools as their choice. By assaulting public education again, Trump and DeVos are defying the will of parents, educators and the American people who continue to march, rally and even strike to secure the investment our children and their public schools desperately need."

Let's bring this privatized war on public schools disguised as educational reform to an end.

It's time to put actual educational professionals with actual teaching experience in charge of education, provide them with enough funding to make our public education system what it could be, and then get out of their way.

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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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