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Health

No, the CDC did not mandate kids get the COVID-19 vaccine to go to school

Loads of misinformation keeps floating around about COVID-19 vaccines.

vaccines covid-19 immunization cdc
Photo by CDC on Unsplash

States set immunization requirements for school entry, not the CDC.

It's hard to log onto social media these days without being hit with a firehose of misinformation, especially when it comes to COVID-19. Getting accurate information during a global pandemic with a novel virus that keeps mutating is a challenge, and people's (sometimes understandable) distrust of the government, the media and various institutions certainly doesn't help.

But that doesn't mean there's no such thing as accurate information. A lot of what's floating around out there about COVID-19 is simply and verifiably wrong. As Kaiser Family Foundation President and CEO Drew Altman said, “It just isn’t enough for us to be in the business of putting out good information. We have to now also be in the business of countering misinformation and deliberate disinformation as well."

Unfortunately, studies of Facebook and Twitter have found that misinformation and disinformation spread faster and are more likely to be shared than true information. So, let's sort through some of the myths and facts about one of the biggest topics out there right now—COVID-19 vaccines and children.

Myth: The CDC is adding the COVID-19 vaccine to the mandated vaccine schedule for kids who attend school.


Fact: The CDC’s Advisory Committee on Immunization Practices (ACIP) recommended updating the 2023 childhood and adult immunization schedules to include additional information for approved or authorized COVID-19 vaccines. That is not the same as adding the vaccine to school vaccine requirements. The immunization schedule is a best practice recommendation, not a requirement.

In fact, the CDC can't require kids to get vaccines. State and local jurisdictions decide what vaccines are required for school entry, not the CDC. States do look to the CDC's recommendation for guidance in making decisions, but just because a vaccine is recommended by the CDC doesn't mean schools will automatically require it. (For example, flu shots aren't required for most schools even though they're recommended by the CDC for school-aged children. And the HPV vaccine has been on the CDC's recommended schedule since 2006, yet only four states require it for school.)

Myth: The CDC added the COVID-19 vaccine to the Vaccines for Children program, which means kids will have to get it.

Fact: The ACIP unanimously voted to add the COVID-19 vaccine to the Vaccines for Children program, but that doesn't mean it's required. Vaccines for Children is a program that provides free vaccines to kids from low-income and uninsured families. Adding the COVID-19 vaccine just means it's included in that free program so more parents who want their kids to get it will be able to.

Myth: The COVID-19 vaccine is dangerous and kids are dying from it.

Fact: No, they're not. Let's look at the specific claims on this front.

First, the myocarditis question. Let's go to the experts at the American Heart Association for that one. According to its website, the most recent studies have shown that the risk of myocarditis from the vaccine is low and the risk from myocarditis is very low (all cases were considered mild and all recovered). But most importantly, studies have shown that the risk of myocarditis from COVID-19 infection is higher than it is from the vaccine.

If parents are concerned about the risks of myocarditis from the vaccine, they hopefully have even more concern about the risks of it from COVID-19 itself, since we know that COVID-19 can damage the heart.

Second, the "young people are dying suddenly at an alarming rate" claim. There are multiple ways in which this rumor has spread multiple times, so it's hard to tackle all of them at once. But if you've heard that vaccines are causing SADS (Sudden Arrhythmic Death Syndrome, which some have erroneously referred to as "Sudden Adult Death Syndrome"), read this fact check and the accompanying links. Also, note the fact that the SADS Foundation—an organization literally dedicated to this syndrome—recommends everyone with conditions linked to SADS get the COVID-19 vaccine.

People don't need to trust the government or the media to not fall for misinformation and disinformation about the COVID-19 vaccines. The most telling thing to me is that every reputable medical organization and association in the U.S. that I've checked recommends the COVID-19 vaccine. Every single one.

In fact, in July, the American Medical Association, the American Academy of Pediatrics and the American Academy of Family Physicians issued a joint letter urging families to get the vaccine for kids ages 6 months and up. These organizations are not the government or the media or the pharmaceutical companies. They are the nation's top experts on medical care for families. They're the ones we should be looking to for guidance on medical decisions, not politicians, social media influencers or cable news hosts.

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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.

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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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