19 Years of Story

This month, February 2018,  marks the 19th anniversary of my spinal injury. Way before I was forced into the life I have now, I was always a person who consciously observes the world around me. In these last 19 years, I have observed a lot about the life of living with a disability. Some good, some bad.

 I was never a person who was truly accepted by my peers. Growing up, I moved a lot. I was constantly the new kid. Always alone. Slowly, this led to me being an unintentional outsider. Back then I hated it. I wanted to have friends. I wanted people to like me. I wanted to hang out with all those people at the lunch table that were laughing and having a great time. The problem was they did not want to include me.

 As I grew older, I found my own footing. I began to not care about fitting in. I started to have confidence and pride in myself. I began to meet people who included me without question. Then I fell and had a spinal injury. I was disabled in a wheelchair. I woke up to paralysis and very quickly began to observe that I once again did not fit in.

 After I had my injury, I was fortunate to have the support of my family—a father who constantly told me how I could still do anything I wanted despite my disability and a mother who set an example of acceptance, patience, and resilience. She had been disabled all my life and she continued cook, clean, and travel the world!! She did the most she could do.

I also had a lot of friends and family who called. I was so grateful for this because after I became injured, I was literally air-lifted out of the life I once had. I was very active in my community. I played in a band, made art, supported and helped cultivate a scene. I went from this culturally rich life surrounded by people to living in my parent’s basement. Robert, my long-time partner and band mate had to work. I was alone quite often, so it was nice to have people to talk to.

 As the months went by, I slowly became comfortable as a person living with a disability. It wasn’t easy to re-learn how to brush my teeth, use the toilet, take a shower, put on clothes, get out of bed, get in bed, and manage having no bladder or bowel control. I had to learn how to live again. Despite the situation, I came out of it very calm, happy, and ready to conquer the world! When my relatives or old friends would see me, they would quite often share at how amazed they were at my positivity. The positivity came me naturally. It wasn’t something I had to struggle to acquire.

When I would go hang out with a group of people, I often found myself saying, “What’s going on? I’m the one that’s paralyzed and I’m the happiest person in the room!” It’s not necessarily true, I’m not always happy, but when I make an effort to go out into the world, and believe me it is an effort, I want to enjoy myself. I am so lucky that I can always get lost in the moment no matter what’s happening.

Having this positive attitude is great for me and my mental state, but there are some negatives to this blessing. Quite often, because of my natural positivity, people forget I am a person that lives with a disability. On a certain level that actually makes me happy but on another level, it deeply saddens me. Do I have to fit into the stereotype of what a person with a disability is—depressed, angry, helpless—for people to actually acknowledge my disability?

 I want to make it clear what I mean when I say acknowledge.

·       When you go to a show to watch a band and the space is completely inaccessible. Sitting in a corner alone watching all the people walk by you with their beer saying hi and not one them saying, “Hey, do you want to see the band? Let’s clear space for you to do that.”

·       When you are taking portraits to raise money to get a van so you can increase the independence of your life and, due to your disability, you cannot get the lighting right. Suddenly, you see a friend walk in and you are so happy because you think they can help. You ask them to take a test photo. You do it and that person looks at it and says, “Oh god! You made me look like Stephen Hawking’s mother! Haha!” and walks away instead of saying “Hey, it looks like you are having a hard time. The lighting is harsh. Can I help you set up your lights?”

·       When, after overcoming the obstacles of being disabled to play in a DIY band, you travel to a town where everyone knows you are in a wheelchair and there is no ramp for you to get in or out of the space you are playing. Not one person even thought of it. Then your band mate calls to complain how your partner upset some people because he was vocal about the lack of awareness or empathy towards your situation. In that moment it would have been really nice to hear, “I am so sorry there wasn’t a ramp there for you. That must have really been hard for you. Next time, we’ll make sure that doesn’t happen.”

·       Or when your family and friends know you suffer from great amounts of pain but because they do not what to say, they just don’t call, leaving you alone and isolated. Which when you are in pain, is especially heartbreaking.

 Pain. I have it every day of my life. But like my mother, I choose to do everything I can despite it. I wake up barely able to move my body, wishing that I only had paralysis. Paralysis, for me, was not something that was impossible to overcome. But pain? Pain is a completely different game. When there are no solutions, you have to make a choice. Will I let this pain completely smother everything I want to do, or do I want to enjoy everything I can? Unlike other types of pain, my pain is from nerve damage—specifically neuropathy and spasticity. There is no real cure for this. After wasting many years with the medical industrial complex to try to find a way manage this pain, I finally decided that I am not waiting for a cure. I will push past this pain and do whatever I can.

 I do not waste time on the idea of trying to remain “positive about it all” because my pain is not positive. The intensity of it keeps me from doing everything to my complete and fullest potential. This makes me both really sad and it pisses me off, and that is ok. Nobody will ever find the complete package. That package being a world where sadness, anger, and all the emotions in between does not exist. The modern thought of fixing a person because they are not happy for an actual reason with drugs is wrong and unhealthy. The “remaining positive” dilemma does not only affect People Living with Disabilties (PLD), it has become ingrained as part of the modern human condition.

 The human condition. We, like all animals, instinctively look at people that are different from us and form opinions based not only on the color of your skin, your gender, your religion, your sexual preference or identity, and your ability but also on things like financial status, fashion, and even the food you choose to eat. In the United States, we are seemingly very lucky to live in a country that has laws like the Right to Vote Act and the ADA to protect the Civil Rights of our citizens. The ADA specifically protects the rights of any PLD so they can have the independence and opportunities they need. These are opportunities available to the able-bodied on a regular basis so that the luxury of having that ability is actually taken for granted. How would an able-bodied person feel if they were physically stopped from participating? This happens to the PLD everyday. When all you are greeted by are broken curb cuts, inaccessible businesses, or people parking in the accessible spot to pick up their pizza or get a cup of coffee, it makes you realize how much society does not include you or truly acknowledge your disability. Having the laws is one thing. Abiding by them and expressing concern for your fellow humans is another.

 I do not want to give the impression that I do not have friends and family that have gone way beyond my expectations for me in these years but from my experiences living life as a person with a disability, I start thinking about humans. We’re the only species that are born a certain way and then try to correct their behaviors or actions. Throughout our history we have protected women and children, spoke up when one human is oppressed to another. Most importantly, we have found ways to save lives, achieve longevity, and conquer fatal diseases. If this was 50 years ago, I certainly would have not lived. It is because of this drive for us to live longer and have stronger lives, we have essentially created a larger community of People Living with Disabilities. We pat ourselves on the back at what a great job we do saving these lives but really, what good is it to save people’s lives and not support them to be able to live? People Living with Disabilities, like every person that is oppressed, are constantly accepting the bad with the good and asking, “How do I fit in the world? What is my place here?”  At some point you have to make a decision: “Do I want to fight for the rights of all humans?” Yes!! Then that fight becomes your life purpose. This how the fight for everyone’s equality is achieved.

 I certainly understand the isolation that can occur because you do not have the right color skin or are not the correct gender.  I have never felt so unwanted as I have as a person living with a disability.  I think that needs to change but my question is how? 

9 thoughts on “19 Years of Story”

  1. Have you ever considered about including a little bit more than just your articles? I mean, what you say is important and everything. But think about if you added some great visuals or videos to give your posts more, “pop”! Your content is excellent but with images and video clips, this site could definitely be one of the very best in its niche. Amazing blog!
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  2. Rabin Chatterjee says:

    While reading your Blog, I had many ideas in my mind that I wanted to write about. But, when I came to the last part of your Blog, only one thing remained paramount in my mind, the question that you have raised “needs to change, but how?” Do I have the answer ? No. But I believe raising this question is a necessary and essential first step. I read your subsequent Blogs and I learnt one term from there that I would try to include in my vocabulary “able-centric world”. I don’t know the answer, but I congratulate you for raising the question.

    1. Thank you Rabin Uncle. I also do not have the answers but if we do not ask them then we will never find solutions to them.

  3. Jayanta Banerjee says:

    Hi Priya:
    After reading your article I was very impressed about your expressive quality in writing. I’m a friend of your dad since our primary school days in India. Also your parents visited me a few years back in Puerto Rico. I saw you once many moons ago when I visited your parents in Florida.
    There is a Spanish saying, “En los caminos duros sólo los duros caminan”. You are one of them! Jayanta Banerjee

    1. Hi ! It’s so nice to hear from a person that knew Baba. He was a great man and I hope to live up to everything he has done and taught me in life. Thanks so much for your kind words. xoxo

  4. I’ve never read anything that I have related to so much. Thank you. I’m here to fight the good fight with you.

    1. Thank you Jewel. We should talk soon ! 🙂

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