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Well Being

Someone wrote a coronavirus parody of the Bare Naked Ladies' hit 'One Week' and it's perfect

Someone wrote a coronavirus parody of the Bare Naked Ladies' hit 'One Week' and it's perfect

Well-written parodies are gold, but they can be hard to come by. Everyone and their at-risk-for-coronavirus grandma thinks they're a great parody writer, but only a chosen few can pull it off successfully.


Enter Twitter user @daniAWESOME. She wrote a near-perfect coronavirus parody of Bare Naked Ladies' "One Week," and posted it on Twitter. (Of note: She doesn't have a huge Twitter following, but she IS being followed by President Barack Obama—for real—so well done, sister. ALLL the high fives.)

She generously invited whoever felt inclined to put the lyrics to music, and someone named Pepper Coyote took her up on it. Ah, the beauty of social media. Twitter can be a cesspool, but then incredible gems like this come out of it.

Here are the full lyrics so you can sing it on your own, followed by the video rendition. (A few of the verses have been changed a bit in the recorded version, but it's great.)

It's Been

One week since we quarantined
Said we'd all stay inside
And eat our groceries

Five days since you FaceTimed me

Saying
Be symptom free or don't come and see me

Three days since the living room
Became my office
and work moved onto all Zoom

Yesterday you'd abandoned me
But it'll still be two months till we get to be free

Wash your hands in the kitchen sink
Don't wanna be the link
That gives Corona to your fellow man

I don't have snacks but I wish
I had stocked up on tuna fish
I cleared my pantry
Well before the worst had yet began

Don't run your errands during peak times
Use Amazon Prime
As long as postal service comes through

Good thing we still have Netflix
Barnett's a dipshit
Love may be Blind but it is dumb too

Gonna be a flake and skip spring break
Because Miami's an outbreak
Full of sick college kids whose conduct could be safer

Gotta stop the shows
Cause if they go
Then the Pandemic's gonna grow
Cause they are dangerous
By order of the mayor

I cannot help it if I got Corona from my dad
Trying hard not to cough and I feel bad

I'm just trying to avoid my own funeral
Can't even go out to eat
Or I'll get ill

I called my senator for universal sick leave
I have a growing need to keep paying my bills

It's been
One week since COVID 19
Threw our plans in the air and killed our parties

Five days since emergency
We flatten the curve or be Italy

Three days since we all cocooned
We realized we can't beat this and no one's immune

Yesterday, someone coughed on me
And now it's eighteen months till we can all be free

Over in China, when some got stricken
They all got locked in and COVID stopped tickin'

Walking the dog with a mask on
When everyone's gone
And if I see somebody I run

At grocery stores I'm feeling panic
At home I'm manic
At doctor's offices I'm terrified

Like Idris Elba I'm feeling ill
Kay I don't feel ill
That's hypochondria all magnified

Gonna shut down all the fitness clubs
And shutter all the social hubs
And tell deBlasio stay home to work your hamstrings

Gotta make a joke but its too soon
Cases balloon between the Boomers and the sick
Until we get some vaccines

How can I stop watching news because it makes me sad
Need to know but all signs pointing to bad

We help our fellow man, and friends, that is beautiful
Drop off some food like a queen
For good will

We need the science and we need the people to believe
We need the tests before more people get hurt

It's Been

One week since the distancing
Dropped our lives to the side for our wellbeing

Five days since the testing grew and yet
Still not as much as all the other nations do

Three days since the briefing room
He said he's not the one to blame, and what can we do?

Yesterday, you just texted me
Cause it'll still be two weeks till we break quarantine

It'll still be two months till we break quarantine

It'll still be two years till we break quarantine

Close the stadium, sports are on deep freeze

Well done @daniAWESOME and @peppercoyote. Thanks for keeping us all entertained while we hole up in our homes.

One Week of COVID 19 - Barenaked Ladies parody - Lyrics by @daniAWESOMEyoutu.be



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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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