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You are here: Home / Explore / Nikki's Notes / When Misinformation Spreads Faster Than the Coronavirus

When Misinformation Spreads Faster Than the Coronavirus

By Know-it-All Nikki Leave a Comment

The internet and ignorance have created the perfect vessel for its own version of the coronavirus (aka COVID-19) and we MUST FLATTEN THE CURVE.

The last couple of weeks has been full of inaccuracies and misinformation. As the COVID-19 pandemic continues on, I fear it will only get worse.

Why? It’s simple. We have turned into a “need to know now” society. If we have to wait any length of time for accurate information we get antsy. Being antsy leads to speculations and assumptions. We begin to seek out information from anywhere and anyone who has an opinion or knows someone who knows someone who maybe has a clue. At some point, we don’t even care who it comes from; if it sounds complicated and scientific-y enough then it must be true.

But let me be clear – not everything shared on social media is a fact.

 

If you’ve spent even five minutes on Twitter or Facebook (either in your own groups or the general newsfeed) in the last week or two, then you are probably brain-crampingly overwhelmed with thoughts, opinions, and conspiracy theories pertaining to COVID-19. Hell, even the news can’t get it right.

That’s because the information is changing at Ludacris speed. By the time we get the news, it’s old news.

We go to bed at night and when we wake up, the whole world has changed again. Every day in Alaska is a little like that for me.

By the time I wake up in the morning, y’all are on your third cup of coffee and you’ve shared eleventy billion things on Facebook. You’ve run marathons, had three meetings, and you’re halfway through your day.

But we, as a society, like misinformation, it’s possible that we relish in it. Misinformation has more holes in it than your favorite pair of underwear; you know you have no business wearing it anymore it but you simply can’t bring yourself to part with it. Rather than drag yourself to the store to shop for new underwear, the kind with only the required number of holes in it, you put that faded, stained, holier than Sunday morning underwear back on (are those supposed to be flowers on your panties or are they tiny coronaviruses, I can’t tell.)

The same goes for social media sharing; rather than track down a source or fact check, you send the post out into the public (or at the very least, your friends’ list). You do it quickly because like I said, we are a “need to know now” society and the faster you can get information out to your friends and family, the safer, more informed they will be. Right?

Wrong.

Consider for a minute that the misinformation you’re sharing IS the coronavirus. You know the symptoms, you have all of them and aside from being tested, you suspect you have it. Would you invite your grandma who has heart and lung conditions over for lunch? Hopefully not.

Yet, we keep on posting inaccurate and potentially harmful information and it needs to stop.

Last night, I was filling my tablet with ebooks (future post to come!) and I clicked back over to Facebook and read a post by a man in a local group I belong to. Obviously it was about the coronavirus. Right away, the information seemed… off. Just three days earlier, I watched a live webinar from the Adult Congenital Heart Association about COVID-19 and CHD patients (like myself). Between what I have read via the CDC, WHO, and the webinar, the information in the man’s post was not just contradictory but also missing information.

I did what any self-respecting know-it-all does, I called him out. I linked him to the ACHA webinar, which is now on YouTube and asked if he could tell us who his sources were or at the very least, can he link us to something he had read that supports what he was posting?

I moved on with my evening and as I was shutting down tabs (we will not discuss how many I had open, I had a lot of books, okay?!), I saw notifications on Facebook and I wanted to clear them. The gentleman I had called out had replied back to me but when I went to read his reply, the entire post was gone. Coincidence? I think not.

I then came across the same post, shared by one of my favorite people on the earth.

My suspicions had been confirmed: the post was making its rounds and people were sharing it like they were the experts.

I copied a bit of the text from the post and pasted it into Google. No surprise it showed up in search results on a few sites. One of which was a news station! (Remember what I said about even the news not being able to get the information correct?!)

Another search result brought up the post on Reddit. Both the news station and Reddit pointed back to a woman on Facebook.

Apparently inquiring minds wanted to know where she found her information and she was only too happy to share it!

I don’t really know what’s more concerning at this point, the fact that the post has had nearly 90,000 shares or that a news station picked it up and shared it too (scroll through the comments, those are always the best part).

Despite the inaccuracies of the post, there are still things to take away from it, as someone I love and respect very much pointed out:

… the bottom line is this is something to not take lightly especially when you live in a state where everything is shut down. I have a job where I have to go to work because no one there is certified to do the tests I do every day. Even though I am supposedly in the at-risk group, over 65…  As with everything you read and hear you have to gleam the facts from the BS. So, go with whatever expert you believe the bottom line is that this is nothing to mess with or take lightly.

Look, folks, I’m not trying to tell you to stop informing or helping your fellow Facebook friend or family members, but I am telling you to please be sure you have the real deal before you post because what might look good on the surface, could turn out to be horribly wrong.

Case in point. YIKES!!

Instead of sharing things you can’t verify, try sharing and reiterating the things we know to be true:

  • The coronavirus can live on surfaces for a number of days.
  • Sing your ABCs while washing your hands.
  • Social distancing and self-isolating is the way to go.
  • Stay home if you are sick. That means no movie theaters, no restaurants, no parks.
  • Even if you don’t have the symptoms, you could still take the coronavirus home to someone who is more susceptible to the virus: the elderly, people with compromised or weak immune systems, those with underlying respiratory or health conditions. <– Those are the reasons why we practice social distancing.
  • The CDC and WHO are the best places for accurate and up to the minute information on the coronavirus.

And for the love of toast, STOP HOARDING THE TOILET PAPER.

In the coming days, and let’s be honest, weeks, I will share GOOD INFORMATION that you can put to use. You’ll laugh, you’ll make notes, maybe even bookmark the posts but you will hopefully stop cleaning out the grocery store shelves and draw on good instincts and common sense.

Who knows, maybe we’ll even turn into the kind of society that looks out for one another. I know, CRAZY, right?!

In the meantime, get cozy with the people in your household, reinstitute family game night, take the time to do some homeschooling (and thank your stars for the awesome job teachers do), start a new hobby, and learn how to be an introvert like the rest of us.

 

If you’re interested, here is the webinar from the ACHA. I suggest packing a lunch and taking notes. The first 25 minutes or so are the best for educating yourself on viruses and transmission in general and if you want to deep dive, the rest is how it pertains to CHD patients.

 

 

I know what you’re thinking…

Yes, I’m sure we will.

Filed Under: Nikki's Notes Tagged With: CDC, coronavirus, COVID-19, pandemic, Spaceballs, WHO

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Hi there!

I’m Nikki and I’m thrilled to have you here. I’m powered by a good chai latte, loads of chocolate, and humor. Here at Know-it-all Nikki, I dish up honest conversations about life with adult congenital heart disease and mental health. I also share my love of books, knitting, midlife, and life after divorce. So, pull up a seat and grab a beverage. Let’s spill some tea, have a lot of laughs, and a few good cries. To learn more about what makes me tick, CLICK HERE

knowitallnikki

#writer 📲 #Binder #bookblogger #Knitter 🐑 💙 #chd #ACHD #TGA📧 hello@knowitallnikki.com 📸 ©️ @knowitallnikki

Ok, okay, I won't go anywhere. Promise. . . . . #c Ok, okay, I won't go anywhere. Promise.
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#charliesworld #catstagram #instacats #catsofig #housecatlife
Technically, he's not ON my planner, thus preventi Technically, he's not ON my planner, thus preventing me from filling it out, but he IS laying on the stickers I need to fill in the days and dates.
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#charliesworld #instacats #catsofinstagram #catsofig #housecatlife catstagram
The world is falling apart. The world is falling apart.
Head to the blog (link in bio) and read the latest Head to the blog (link in bio) and read the latest. I've been trying to figure out how to write this for 2 months now and I still don't know if I got it right.
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.
#knowitallnikkimovestoohio #dtga #heartmonth #ACHD #adultchdsurvivor
Well poop, I missed day 4 (Early Answers, Lasting Well poop, I missed day 4 (Early Answers, Lasting Impact) and day 5 (How We Monitorthe Heart)! But it's fine! Because they both fit nicely for today's adventures which consisted of a carotid artery ultrasound (day 5) and a series of messages between myself and @nationwidekids to discuss how best to approach the weight loss struggle (day 4). 🤨😠

But it also ties in beautifully with day 6 of #heartmonth, #choosingjoy because despite all of the crap that goes along with being an adult with CHD, I am genuinely joyful. Some of comes out in sarcasm but I've told people if I'm not cracking jokes or inserting some token sarcasm into the day, then something is truly wrong. The last 2 years have been hard, but believe me when I say, I AM HAPPY and I'm wearing red today!
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#ACHD #congenitalheartdefectsurvivor #WearRedforHeartMonth
I almost missed it, day 3 prompt for #heartmonth i I almost missed it, day 3 prompt for #heartmonth is #lifebetweenappointments 

Yeesh, where do I start? Right now my life between appointments is a little chaotic. The number of appointments has increased a thousand fold than what I was used to growing up.  There are more appointments now than I had when I was pregnant with all four kids!

I struggle to keep them straight or where they're going to be. I write them down in a paper planner, my wall calendar, and my phone's calendar. And I still wind up looking them up multiple times because I don't trust my brain's ability to recall.

I'm expected to write down detailed symptoms. I don't recognize symptoms as symptoms. It just feels like a Tuesday to me. But do try to have a normal life, the docs encourage: eat right, be active, get sleep. How do I do that and not wonder if what I'm feeling while I'm trying to be normal is a symptom?
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.
#heartfailure #congestiveheartfailure #congenitalheartdefect
Waiting. . . . #catsofinstagram #charliesworld #in Waiting.
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#catsofinstagram #charliesworld #instacats #catsofig #catstagram
Day 2 of #heartmonth is #motivationmonday. All I c Day 2 of #heartmonth is #motivationmonday. All I can say, is sometimes motivation feels like the end of a very long tunnel; a pinprick of light in an otherwise black abyss. Motivation eludes me more than I care to admit. When it feels unattainable I feel like the little girl I used to be, opening my eyes in a pitch black room, are my eyes actually open? Making my way across the room, arms outstretched, hoping I don't run into anything, or worse, fall. 
And then other times, like on this Monday, motivation arrives and it feels easy, like a special occasion you'vebeen waiting for. So you wear the anatomical heart earrings your daughter bought you and you don the gifted knit heart cowl your knitty BFF made for you and for a day you feel normal.
.
.
.
.
#congenitalheartdefectsurvivor #congestiveheartfailure #dtga
Today kicks off the first day of #heartmonth. I st Today kicks off the first day of #heartmonth. I still think it's silly to only give one day, one month, or even one week to talk about heart disease. Alas, here we are. 

I'm going to do my best to follow the 28 daily prompts for #heartdisease and #chdawareness but I make no promises.

Today's prompt is #BeyondtheDiagnosis. To me, looking beyond being born with a CHD means a few things:

It's the invisible things that can't be measured on a chart, like the fatigue, sadness for the health I wasn't born with, and the mental math of asking myself if I have enough energy for all I want to get accomplished in a week, or even a day.

It's being seen as a whole person; not the condition the doctors are treating. This a part of me, not all of me. I'm still a parent, friend, writer, a hopeless romantic. Yes, I'm a heart patient, I ALWAYS will be, but I'm also opinionated, stubborn, funny, and a person with real feelings. 

But most of all it's refusing to be reduced to number in the healthcare system, or someone else's discomfort.
.
.
.
#chdawareness
Follow on Instagram

knowitallnikki

#writer 📲 #Binder #bookblogger #Knitter 🐑 💙 #chd #ACHD #TGA📧 hello@knowitallnikki.com 📸 ©️ @knowitallnikki

Ok, okay, I won't go anywhere. Promise. . . . . #c Ok, okay, I won't go anywhere. Promise.
.
.
.
.
#charliesworld #catstagram #instacats #catsofig #housecatlife
Technically, he's not ON my planner, thus preventi Technically, he's not ON my planner, thus preventing me from filling it out, but he IS laying on the stickers I need to fill in the days and dates.
.
.
.
.
#charliesworld #instacats #catsofinstagram #catsofig #housecatlife catstagram
The world is falling apart. The world is falling apart.
Head to the blog (link in bio) and read the latest Head to the blog (link in bio) and read the latest. I've been trying to figure out how to write this for 2 months now and I still don't know if I got it right.
.
.
.
#knowitallnikkimovestoohio #dtga #heartmonth #ACHD #adultchdsurvivor
Well poop, I missed day 4 (Early Answers, Lasting Well poop, I missed day 4 (Early Answers, Lasting Impact) and day 5 (How We Monitorthe Heart)! But it's fine! Because they both fit nicely for today's adventures which consisted of a carotid artery ultrasound (day 5) and a series of messages between myself and @nationwidekids to discuss how best to approach the weight loss struggle (day 4). 🤨😠

But it also ties in beautifully with day 6 of #heartmonth, #choosingjoy because despite all of the crap that goes along with being an adult with CHD, I am genuinely joyful. Some of comes out in sarcasm but I've told people if I'm not cracking jokes or inserting some token sarcasm into the day, then something is truly wrong. The last 2 years have been hard, but believe me when I say, I AM HAPPY and I'm wearing red today!
.
.
.
.
#ACHD #congenitalheartdefectsurvivor #WearRedforHeartMonth
I almost missed it, day 3 prompt for #heartmonth i I almost missed it, day 3 prompt for #heartmonth is #lifebetweenappointments 

Yeesh, where do I start? Right now my life between appointments is a little chaotic. The number of appointments has increased a thousand fold than what I was used to growing up.  There are more appointments now than I had when I was pregnant with all four kids!

I struggle to keep them straight or where they're going to be. I write them down in a paper planner, my wall calendar, and my phone's calendar. And I still wind up looking them up multiple times because I don't trust my brain's ability to recall.

I'm expected to write down detailed symptoms. I don't recognize symptoms as symptoms. It just feels like a Tuesday to me. But do try to have a normal life, the docs encourage: eat right, be active, get sleep. How do I do that and not wonder if what I'm feeling while I'm trying to be normal is a symptom?
.
.
.
.
#heartfailure #congestiveheartfailure #congenitalheartdefect
Waiting. . . . #catsofinstagram #charliesworld #in Waiting.
.
.
.
#catsofinstagram #charliesworld #instacats #catsofig #catstagram
Day 2 of #heartmonth is #motivationmonday. All I c Day 2 of #heartmonth is #motivationmonday. All I can say, is sometimes motivation feels like the end of a very long tunnel; a pinprick of light in an otherwise black abyss. Motivation eludes me more than I care to admit. When it feels unattainable I feel like the little girl I used to be, opening my eyes in a pitch black room, are my eyes actually open? Making my way across the room, arms outstretched, hoping I don't run into anything, or worse, fall. 
And then other times, like on this Monday, motivation arrives and it feels easy, like a special occasion you'vebeen waiting for. So you wear the anatomical heart earrings your daughter bought you and you don the gifted knit heart cowl your knitty BFF made for you and for a day you feel normal.
.
.
.
.
#congenitalheartdefectsurvivor #congestiveheartfailure #dtga
Today kicks off the first day of #heartmonth. I st Today kicks off the first day of #heartmonth. I still think it's silly to only give one day, one month, or even one week to talk about heart disease. Alas, here we are. 

I'm going to do my best to follow the 28 daily prompts for #heartdisease and #chdawareness but I make no promises.

Today's prompt is #BeyondtheDiagnosis. To me, looking beyond being born with a CHD means a few things:

It's the invisible things that can't be measured on a chart, like the fatigue, sadness for the health I wasn't born with, and the mental math of asking myself if I have enough energy for all I want to get accomplished in a week, or even a day.

It's being seen as a whole person; not the condition the doctors are treating. This a part of me, not all of me. I'm still a parent, friend, writer, a hopeless romantic. Yes, I'm a heart patient, I ALWAYS will be, but I'm also opinionated, stubborn, funny, and a person with real feelings. 

But most of all it's refusing to be reduced to number in the healthcare system, or someone else's discomfort.
.
.
.
#chdawareness
Follow on Instagram

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