I imagine that my response to learning that I am chronically disabled was not how people expected it to be. However, the way I was told wasn’t average either. A text message, from my neurologist, stating my symptoms matched up with a disease called “Juvenile Myoclonic Epilepsy”. I texted him back a “thank you,” and everything went on. I did not cry, nor was I shocked or worried. I went to my bedroom and called my friend to laugh about it.
It might’ve been slow processing, as there were nights when I sobbed about my inability to do all I’ve ever wanted. Though, the thought process that I always circled back to was either thinking about it in a logical manner or the phrase “Life goes on”. I researched epilepsy after I had my first seizure, it is a frightening disease, yet I understood it. Abnormal brain energy created in the brain that can block neuron communication. I couldn’t look at it too hard before I felt silly over my own worry. In fact, I found the entire thing unimaginably intriguing. Checking what my EEG’s might’ve looked like, how many people Sudden Unexpected Death Due To Epilepsy killed in a year, what kinds of seizures existed, and their abundance. I prided myself on my own compartmentalization by using logic. It made me feel better that my love for research and science could improve my life quality.
I did mention another tactic I use. One I find marginally more embarrassing. “Life goes on”. I am not surprised that it is calming to me, as said, I try to find logic in my problems. The greatest known fact to those who have struggled in life is that: nothing stops the world. A majority of the time it feels like the world has stopped rotating. Whatever issue I am facing at the moment takes over my entire mind. I have to study, or I have to take out the trash, or I have to apologize to my friend, or I have to stop thinking. Life goes on. There is more after this. Just because the moment I am in is paused, does not mean that there is no solution to it. It took me a long, and medicated, process to grasp that. A sedentary second is an outlier in the vast years you spend going forward.
My reaction may not have been normal, but I believe it helped me grow more than sobbing would’ve. Forcing myself to look into the future made me want it more. Life goes on, and I will go with it.
I would be unbelievably grateful for this scholarship. I have never had the luxury of having a college savings account or a backup plan if college "didn't work out". The major I want to go into is not known for its cheap textbooks, STEM careers aren't praised for the minimum amount of money spent during college. Without the burden of financial worries, studying and trying my hardest to bring about change in the world would be easier. The money either going to textbooks, tuition, housing, or other important expenses that colleges give out, it would be a great help.
I would love to honor Arlin's memory with this scholarship, as a Latina woman going into STEM, I understand how important it is to strive in these fields. To make it known that we are enough, that just because we are a different ethnicity, gender, or ability range our contributions to science are still relevant. I have spent many days wondering how it would go as an epileptic in a lab, and knowing that there are women out there, in STEM fields, proving that it is possible is beautiful. I would be delighted to be one of those women to show young girls that it is a reality, that we are taken seriously, and that our memories, ideas, and research will live on.