14 Truths Only People With Bad Vision Can See With 20/20 Clarity

14 Truths Only People With Bad Vision Can See With 20/20 Clarity

What is it like to have good vision? I honestly have no idea.

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You grew up wearing glasses or you got glasses when you were older. Either way, you know the struggles.

1. Trying to lie down while wearing your glasses is impossible.

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Even though you've had glasses for years you still have yet to figure out how to lay down with glasses and not break them or have them fall off your face.

2. You prefer contacts over glasses or glasses over contacts.

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They are two very different sensations, but everyone has their preference.

3. You have a distinct memory of trying contacts

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No matter if you got it quickly or absolutely hated them, you have definitely tried them at some point.

4. If you wear glasses, people are shocked to see you without them

Honestly, I don't even recognize myself sometimes.

5. If you wear contacts, people are shocked to see you in glasses

"yOu WeAr GlAsSeS?"

6. People always ask if they can try on your glasses.

And then they either immediately take them off and screeching from the blurriness or looking baffled and saying, "Wow you really do have bad vision."

7. Trying on your glasses when you wear contacts.

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And you don't even recognize yourself for a second.

8. If you're like me and HAVE AWFUL VISION, you get incredibly annoyed when people with -1.5 prescription complain about being unable to see

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I'm a -10 and -9 so please tell me how it's impossible for you to see. YOU CAN BUY GLASSES AT TARGET.

9. You wonder what it's like to actually be able to see.

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I've had glasses for 15 years and can't even imagine what it's like to be able to see with just your eyeballs.

10. You wonder if you could survive without glasses.

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My roommate and I have tried to see if I could walk to class without glasses. It didn't go so well.

11. You've been called "four-eyes" throughout your entire life.

Because it's SO funny to make a joke out of your pain.

12. You're always worried about reflections in your lenses in photos.

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It doesn't happen often but when it does, you don't even realize until you're trying to post the picture on Instagram.

13. Picking out glasses is the most fun you can possibly have.

It's like creating an entire new identity. You have to find the perfect frames that capture everything about you.

14. Losing your glasses is the worst. thing. ever.

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BECAUSE YOU NEED YOUR GLASSES TO FIND YOUR GLASSES. Velma understands your pain.

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What Having Type 1 Diabetes For 11 Years Has Taught Me

When I was diagnosed, the only thing that I could think about was that whatever this "diabetes thing" was — it must be really bad. Little did I know that, almost 11 years later, I could look back at this "diabetes thing" as something that has been really good for my life.

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In the middle of July in 2008, I started drinking an average of two or three gallons of water a day, going to the bathroom two or three times per hour, and losing a ton of weight. On July 21, 2008, after my parents pretty much self-diagnosed me at home with extra ketone strips, my doctor came into the room with tears streaming down her face and the news that I had Type 1 Diabetes. Everyone in the room, including the doctors, was crying. The only thing that I could think was that whatever this "diabetes thing" was- it must be really bad. Little did I know that, almost 11 years later, I could look back at this "diabetes things" as something that has been really good for my life.

Over the next couple days, I experienced a lot of new things- learning how do to seven to eight injections a day in my stomach, eight to fourteen finger pricks a day, a lot of big medical words, a lot of tears, and thankfully the knowledge that this all was not my fault. I found so much comfort knowing that I had diabetes because my immune system that killed all my beta cells, and knowing that there was nothing that I could have done to prevent it.

At that point, I knew God wanted this for me for some reason.

In the week following the diagnosis, I loved having diabetes. I felt special because I was different and my friends wanted me to talk about it all the time because they were fascinated by all things diabetes related. However, as I continued to have injection after injection and count carb after carb, I began to question why this had to happen to me and began to question why I should even take care of myself because, after all, this taxing disease would follow me for the rest of my life.

My perspective completely changed as I sat down to watch the 2011 Indy 500 with my dad. Watching the Indy 500 had been a tradition for my dad and me since he first showed me the sport in when I was nine. I loved the history, the loud engines, and the high speeds of it all and became a big fan of Danica Patrick, before she went to NASCAR.

The 2011 Indy 500 seemed like any other race, but little did I know that it would be the last Indy 500 I would watch on the couch.

As they introduced the drivers, we watched as Charlie Kimball, a rookie, waived to the crowd. By the time he had finished waiving, my dad was in tears. This was because as Charlie was waiving to the crowd, they announced him as Charlie Kimball, the first IndyCar driver to drive with Type 1 Diabetes. This was absolutely unheard of and it seemed literally impossible that he could race at more than 220 miles per hour while having diabetes, an extremely unpredictable disease. With tears in his eyes, my dad turned to me and said words I will never forget.

"You're going to meet that guy, Mary Clare. I want you to know that you can do anything with diabetes."

Meeting Charlie for the first time in the pit of the Iowa Speedway in Newton, Iowa. June 2011. Photo Credit: Mary Clare Halpin

Later that year, at a race in Newton, Iowa, my dad's promise was fulfilled as I met "the first IndyCar driver to drive with Type 1 Diabetes"- Charlie Kimball. Charlie took my sister, my dad, and me into the pits on race day to show us his race car and how he manages his diabetes inside and outside of the car. He told me "the diagnosis of diabetes has been a speed bump, not a roadblock." I decided in that moment to make diabetes my speed bump and that I wasn't going to let it slow me down; after all, Charlie can go 220+ miles an hour with diabetes.

In the days following the race, I wrote Charlie a four-page thank you note explaining all that he done for me. I did not hear anything back from Charlie until the next May, when my dad got a call from ESPN. They were calling him to asking him if I could be a part of the piece that they were doing to show how Charlie inspires kids with diabetes for the pre-show of the Indy 500. We obviously said "yes" and a few weeks later an ESPN crew came to Kansas City to interview my mom, my dad, and I and to film me at lacrosse practice and dance class.

After they finished, the producer told my family that they wanted to finish the piece, which aired before the start of the race, by filming me live in the pits talking to Charlie before the Indy 500. We made the trip out to Indianapolis that Memorial Day weekend, a tradition that will always be extremely special to our family because what Charlie has done for my life. Charlie brought us to dinner with his family and friends on Friday night, brought me with him to ride in the race parade the day before the race, inspired me through the way he helps those with diabetes, and introduced me to the all the traditions and the magic of the Indy 500, something that means the world to me.

Talking in the pits with Charlie at the Indianapolis Motor Speedway before the 2012 Indy 500. May 2012. Photo Credit: Mary Clare Halpin

Because of Charlie's living example and light he brought to my struggle, my life has been changed forever. I no longer look at diabetes as something that hurts me, but rather has helped me. I feel lucky that God chose me to have diabetes because I wouldn't have met Charlie and I wouldn't be the person I am today. I have not only been able to experience incredible things and a positive outlook on something difficult I have to deal with every day due to Charlie's impact on my life, but I have learned two extremely valuable lessons at a young age — bring light to others and find your "why."

I try everyday day to bring light to each person I come in contact with because I know it can change lives, just as Charlie has done for me. I try to bring light because we all have something that affects us every day and it just takes one person to change our "_____ thing" into something really good.

When the injections get to be too much, or I do not want to get up in the middle of the night to treat my low blood sugar, I think of my "why." Finding the deepest desire of my heart, to be a good wife and mom someday, and using it to motivate me to do the simple and the big things has made my life so fulfilling. I know that, as I am enjoying my life with my own family someday, I will be thanking the nineteen-year-old me someday that I did the work to make my dream possible.

However large your "roadblock" or struggle may seem, know that I am rooting for you. If you just change your perspective and use it instead as a speed bump, you can slow down and use improve your life. And you'll win your race.

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