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Well Being

Anti-vaxxer Candace Owens was denied a COVID test, highlighting a big debate in medical ethics

Anti-vaxxer Candace Owens was denied a COVID test, highlighting a big debate in medical ethics
via Wikimedia Commons

The COVID-19 era was officially dubbed the "pandemic of the unvaccinated" by CDC Director Rochelle P. Walensky, MD last July and she wasn't kidding.

Unvaccinated people are 29 times more likely to be hospitalized than those who got the jab and studies show they now account for 99% of deaths from the virus.

It's terrible that people are dying of symptoms that are nearly 100% preventable. But it's also fair to criticize those who are unvaccinated because for nearly all of them it's a selfish decision. There are of course exceptions, primarily those who cannot get vaccinated because of overriding medical conditions. But those are relatively few and far between. Unvaccinated people are three times more likely to spread COVID-19 and on rare occasions, they can infect someone who did the right thing and got the shot.


The virus just keeps dragging on so it's understandable that some on the front lines are fed up with those who keep it going.

Conservative pundit Candace Owens has been very vocal about her opposition to the COVID-19 vaccine and mask-wearing. She often tweets that she's proud to be unvaccinated, even saying that no one in her family will "ever touch the COVID-19 vaccine."

If that decision only affected her, then this wouldn't be much of a problem. But, unfortunately, there are many people who cherish her opinion.

Owens needed to get a COVID-19 test earlier this week but was denied by Suzanna Lee, co-founder of Aspen COVID Testing because she's actively encouraged the spread of the virus.

"I've just learned of this testing request and as the owner of this business am going to refuse this booking and deny service," Lee wrote.

"We cannot support anyone who has proactively worked to make this pandemic worse by spreading misinformation, politicizing and DISCOURAGING the wearing of masks and actively dissuading people from receiving life-saving vaccinations," the email continued. Lee then directed her to a free testing facility at city hall.

Owens shared the letter on Twitter calling Lee a "danger to the Aspen community."

Owens responded to Lee by saying it was the most "hilarious email" she's ever received in her life and criticized her for politicizing the virus. This is pretty hypocritical from someone who has repeatedly politicized the virus.

It's debatable whether it's ethical for a healthcare provider to deny Owens a test but there were no real consequences for her actions because there are other places to get tested.

But what about doctors who are the last line of care and only have a limited number of beds. Is it fair for them to prioritize someone who got the vaccine over someone who didn't? All things being equal, doesn't the person who got the shot to protect themself and others deserve care more than the person who did not?

A doctor in Alabama recently said he would no longer treat unvaccinated patients.

"We do not yet have any great treatments for severe disease, but we do have great prevention with vaccines. Unfortunately, many have declined to take the vaccine, and some end up severely ill or dead. I cannot and will not force anyone to take the vaccine, but I also cannot continue to watch my patients suffer and die from an eminently preventable disease," Dr. Jason Valentine, a physician at Diagnostic and Medical Clinic Infirmary Health in Mobile, wrote in an open letter.

Last month, Dr. Chavi Eve Karkowsky wrote a piece in The Atlantic saying that unvaccinated people are beginning to run up against "compassion fatigue" in America's hospitals.

"To many medical providers working today, the rejection of lifesaving COVID-19 vaccines feels like a giant 'Fuck you' from 29 percent of American adults. We will keep providing the best care possible, but they are making our job much harder," she wrote.

"Doing the work of curing human bodies is harder when some of one's faith in humanity is lost," she added.

The COVID-19 pandemic has been an awful time to live through because millions of people have suffered and our lives have been completely upended.

Even if the virus does go away there will be one thing that will never change. It's left many of us with a diminished view of humanity. It's disheartening to realize that at a time when lives were on the line there were opportunists who knowingly promoted the spread of the deadly disease through misinformation.

We'll also never forget that at a time when a virus was raging, millions of people had the opportunity to do what they can to stop the spread and did nothing.

What are the consequences? For Owens, the annoyance of having to find another testing place. But for many others, their lives.

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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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A sad-looking Labrador Retriever

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