World Autism Awareness Day - Don’t “Light It Up Blue”

World Autism Awareness Day - Don’t “Light It Up Blue”

Instead of promoting “Light It Up Blue”, we should promote the awareness and acceptance of autistic individuals in our society instead of isolating them.
Adrian
Adrian
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April 2nd is noted as World Autism Awareness Day or W.A.A.D where people around the world recognize and encourage others to raise awareness for people with autism throughout the world. This resolution was passed in November of 2007, as an initiative to improve human rights. Since its start, the awareness and research has increased across the globe. World Autism Day is one of only four, health-specific United Nation Days that recognizes Autism in hopes of the world uniting to aid in research, diagnosis and treatment for those affected by the disorder.

“Light It Up Blue” is one of the many proposed initiatives proposed by Autism Speaks, observed on W.A.A.D. dedicated to Autism Awareness. However, there is controversy because the slogan “Light It Up Blue” is from the Autism Speaks foundation; instead of promoting people with the disorder, they promote “ending autism,” yet only a small portion of their large budget goes towards helping autistic people and their families. Their budget primarily goes towards researching for a “cure” and prenatal test for pregnant women. Aside from this, the rest of their money goes towards marketing, which paints autism as something bad. So instead of providing support, they are isolating the Autistic community.

The Light It Up Blue campaign ropes in a lot of media support from ignorant people who do not understand the complexity of autism. Social media is playing a huge role in increasing the stigma around ‘finding the cure’ for autism, instead of supporting their local families and autism organizations. Many people are left unaware that their posts on Facebook will not help anyone; they need to do something.

Like many other issues in this day and age, the Light it up Blue campaign is based on stereotypes. For example, the reason we light everything blue, is based on the gender stereotype that boys like blue, because Autism is more likely in males than females. The diagnosis Autism as well, is based on the typical behaviors of a male child, rather than the behavior of a child of either gender. This often leads to the misdiagnosis of Autistic females, because it is a “boys disorder.”

Ultimately, the W.A.A.D. does not promote the awareness of Autism all year long, rather only promoting awareness for one day. Like many issues, it doesn’t go away the following day when April 2nd ends. Instead of promoting “Light It Up Blue,” we should promote the awareness and acceptance of autistic individuals in our society instead of isolating them. The day of awareness is helpful to the cause, but lighting it up blue does not change things; to change things we need to make a difference. If you really want to help those apart of the Autistic community, you should join the fight for acceptance and opportunities for those affected. You can do more than “Light It Up Blue,” and join the fight for equality for the men and women suffering from Autism.

Cover Image Credit: The Autism News

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I'm The Girl Without A 'Friend Group'

And here's why I'm OK with it

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Little things remind me all the time.

For example, I'll be sitting in the lounge with the people on my floor, just talking about how everyone's days went. Someone will turn to someone else and ask something along the lines of, "When are we going to so-and-so's place tonight?" Sometimes it'll even be, "Are you ready to go to so-and-so's place now? Okay, we'll see you later, Taylor!"

It's little things like that, little things that remind me I don't have a "friend group." And it's been like that forever. I don't have the same people to keep me company 24 hours of the day, the same people to do absolutely everything with, and the same people to cling to like glue. I don't have a whole cast of characters to entertain me and care for me and support me. Sometimes, especially when it feels obvious to me, not having a "friend group" makes me feel like a waste of space. If I don't have more friends than I can count, what's the point in trying to make friends at all?

I can tell you that there is a point. As a matter of fact, just because I don't have a close-knit clique doesn't mean I don't have any friends. The friends I have come from all different walks of life, some are from my town back home and some are from across the country. I've known some of my friends for years, and others I've only known for a few months. It doesn't really matter where they come from, though. What matters is that the friends I have all entertain me, care for me, and support me. Just because I'm not in that "friend group" with all of them together doesn't mean that we can't be friends to each other.

Still, I hate avoiding sticking myself in a box, and I'm not afraid to seek out friendships. I've noticed that a lot of the people I see who consider themselves to be in a "friend group" don't really venture outside the pack very often. I've never had a pack to venture outside of, so I don't mind reaching out to new people whenever.

I'm not going to lie, when I hear people talking about all the fun they're going to have with their "friend group" over the weekend, part of me wishes I could be included in something like that. I do sometimes want to have the personality type that allows me to mesh perfectly into a clique. I couldn't tell you what it is about me, but there is some part of me that just happens to function better one-on-one with people.

I hated it all my life up until very recently, and that's because I've finally learned that not having a "friend group" is never going to be the same as not having friends.

SEE ALSO: To The Girls Who Float Between Friend Groups

Cover Image Credit: wordpress.com

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It's National Eosinophil Awareness Week And More People Should Be Talking About It

It's time to raise awareness about eosinophil-associated diseases and support those, including myself, who are affected.

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For anyone who is unaware, May 19 to May 25 is considered National Eosinophil Awareness Week as recognized by the American Partnership for Eosinophilic Disorders (Apfed) since 2007. The purpose of this week is to raise awareness and help educate individuals on the various eosinophil-associated diseases. Despite its existence being virtually unknown to many people, this week has become very significant in my life and I think more people should be having conversations about it.

If you had asked me about eosinophil-associated diseases two years ago, I wouldn't have been able to say a single thing besides maybe defining an eosinophil the way I learned to in my AP Biology class senior year of high school. But as of a few months ago, it has officially been one year since I was diagnosed with an eosinophil-associated disease — something I never imagined would happen in my life. While I won't share too much of my own experience because it's honestly quite personal and still a little sensitive to discuss, it's safe to say that eosinophils completely changed my life.

I was fracturing bones like it was my job — I think I had upwards of nine stress fractures in my legs and feet in a year and a half time period. I had to stop playing sports my senior year of high school and couldn't run at all. I was nauseous 24/7. I was rapidly losing weight to the point where I had lost close to 35 pounds and none of my clothes fit me. I couldn't swallow anything, including water. Eating was painful. I had no appetite.

I was sick and in pain ALL the time to the point where I would get emotional or even cry.

I missed school days, tests, exams, social events, and eventually had to quit my job for an entire summer because even getting out of bed was hard for me. Ultimately, even the decision about the college that I chose to attend was partially based on my health and the doctors I would need to visit frequently.

But the most significant thing was that I was experiencing severe depression and anxiety and was honestly just straight-up scared. Think about it: I was experiencing a wide range of life-altering symptoms yet no one could figure out why and even when they did, there was no cure and only limited options for treatment. Unfortunately, this is the reality for many patients and their families. The process of diagnosing an eosinophil-associated disease can take years and require pretty much every medical test you can even think of because these diseases are all classified as rare diseases.

I was experiencing symptoms for a year and the journey to an accurate diagnosis took about a year after that. The journey itself was not easy, as it involved numerous doctors and countless medical tests to eliminate other potential diagnoses like cancers, parasites or even celiac. Since then, I have been involved with treatment for a little over a year. For me, treatment involved several medications and steps, including gaining the weight I had lost.

But the main piece was cutting pretty much everything out of my diet, meaning no gluten, dairy, soy, eggs, seafood, or nuts. Gradually over time this treatment involves reintroducing the foods individually (each for a three-month period) to see what can be tolerated or which foods make my eosinophils act abnormally and then restricting my diet accordingly.

Since starting treatment my life has been gradually changing in a positive manner, which is something I couldn't have imagined when I initially became ill. Yes, I will still be sick for the rest of my life and experience the chronic waxing and waning of this disease, but hopefully years of experience and knowledge will make me better equipped to handle it. One day there may even be a cure. But until then I will continue to raise awareness and participate in National Eosinophil Awareness Week in solidarity with the few who are also sharing in my experience living with an eosinophil-associated disease.

While I wrote this article with the intention of participating in Eosinophil Awareness Week by raising awareness and educating (to some extent), it was about more than that. I wanted to give you a synopsis of my story and the challenges I face to make this week more understandable and more real. This was because I know that eosinophil is not only challenging to say (even I struggle) but also challenging to conceptualize.

If you're interested in learning more or you're still confused, I recommend doing some quick reading on Apfed's website because they are extremely helpful in the way they simplify the complex information.

If you would like to see what you can do during National Eosinophil Awareness Week, you can also click here to visit Apfed's day-by-day guide for the week, which included some fact sheets, information about wearing magenta to support the cause, and other information about individual participation.

Editor's note: The views expressed in this article are not intended to replace professional medical advice, diagnosis, or treatment.

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