How My Parents Helped Me Find My Disabled Identity

Photo of a young person playing drums. The person's face is not visible, but they are positioned behind the drum set.

I have always loved the way drums sound. During parades, my focus was always on the marchers with the snares; while at concerts my neck was perpetually craned as I struggled to see over the taller members of the crowd who was pumping the rhythm into my usually-tired body. I loved the drums so much that in my early teens my parents purchased me a drum set. They did so even after I had (sometimes with tears in my eyes) shown that playing pained me.

I gripped the sticks too tightly. The single bass drum in the set, rather than relying on the fluid movements of my feet, was powered (very inefficiently) by my hyper-tense legs. The act of playing the drums, no matter how ineptly or for how short a time, was virtually always exhausting and rarely fruitful. Despite these realities, my mother would smile after every impromptu jam session. “Sounds great, honey,” she would say, as my father rubbed my tense shoulders.

My parents provided a safe environment for me to come into my own, yet they never kept me too sheltered. When my mother says I’m doing good work, I believe her. This is in no small part due to the fact that she is among the first to tell me when I’m being foolhardy; to remind me when I’m getting a bit too big for my britches. “You are a smart man, but that does not mean other people have nothing to teach you,” she reminds me frequently enough to quash the worst of my arrogance. I don’t have to read between the lines. I don’t have to consider that my parents may be keeping me ignorant of some reality, or sparing me some perceived pain by coddling me.

“It hurts me to play,” I finally confessed as we sat on a hotel porch together watching the sun set, “but I want to play. I want to prove to everyone that I can do it! I want to inspire! I want to be somebody!”

I felt a lump growing in my throat as my father turned to me and said bluntly, “You probably won’t be a great drummer, but the way you communicate is amazing…what you make people feel is remarkable. Not because of how you walk, or fall or overcome, but because of how you connect with them.”

In that moment, it became clear: I didn’t have to play the drums to love them. I didn’t have to prove anything. I was more than good enough just as I was, with all the gifts I have. Around the same time, my interest in the drums had found its way into my writing. I had composed a poem about my experiences trying to learn to play: a poem that won first prize in a school-wide contest. When my mother read it, she was genuinely moved. My father, equally impressed, gave me a hug and said, “You really do have a talent for writing.”

There is a crucial lesson here that every parent of a disabled child can learn from my amazing mother and father.

It’s important to understand the difference between parenting without pity and expecting normalcy.

This is a trap that I have seen many parents fall into. Disability can be quite unexpected. As parents scramble to navigate the landscape it creates, most rely (understandably, sometimes) on the following dichotomy:

  1. My child can be “normal.” (good)
  2. My child will live on the margins as an outcast with no opportunities. (bad)

Parents are right to not wish the second option on their children. However, expecting a child to be “normal” is seldom the answer. This is because being “normal” and “accepted” are often conflated. Every person deserves the respect and acceptance that comes with being human, but making a child behave “normally” often strips them of a potential connection with disability identity and culture. This connection often creates our most fierce and respected advocates and thought leaders. In my case, this connection is what makes me feel whole.

I don’t play the drums anymore, but I still love them. I write now, and I love that too.

My parents didn’t just buy me a drum set that day. They gave me permission to try. They let me learn who I was and who I wasn’t, instead of telling me. They treated me with love and respect whether I was flailing around on the drums or penning my next masterpiece.

I love you, Mom and Dad.

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Rooted in Rights exists to amplify the perspectives of the disability community. Blog posts and storyteller videos that we publish and content we re-share on social media do not necessarily reflect the opinions or values of Rooted in Rights nor indicate an endorsement of a program or service by Rooted in Rights. We respect and aim to reflect the diversity of opinions and experiences of the disability community. Rooted in Rights seeks to highlight discussions, not direct them. Learn more about Rooted In Rights

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Why Do I #CripTheVote? Because the Disability Vote is Power.

A bright blue sign mounted in grass that has an accessible icon and an arrow that says vote on it.

This post is part of a partnership between #CripTheVote and Rooted in Rights. 


As a child, I didn’t think being disabled had anything to do with voting, or vice versa. I saw that my parents always voted, but I didn’t see it as an important part of my life as an American. Experience taught me just how wrong I was.

When I was 18 and first tried to vote, I almost didn’t succeed. There were many hurdles, including obtaining transportation, filling in my ballot, and proving my identity.

I had no driver’s license and didn’t yet have a government identification card. My disability didn’t completely destroy my capacity to vote, though. I didn’t have to worry. I had my brother to vouch that I was who I said I was.

“Can you vouch for him?” The volunteer asked my brother, flitting his hand toward me. I was already stressed, and now I felt my identity being doubted. I felt small.

I remember that I had “spoiled” a few ballots. My spatial reasoning is impaired, and the ballots were cluttered to the point that I struggled to fill them in properly. The third ballot was the charm. I remember being both ashamed at the looks I got from the voters and volunteer staff, and also proud that I was finally voting, my hands trembling as I slid the ballot into the slot of the voting machine.

From my place in the passenger’s seat, after I had cast my vote, I thought to myself: what if I didn’t have my brother? If there was no champion to vouch for me, would my voice go unheard? How many people are turned away because they don’t have a license? How many people go unrecognized because they don’t have reliable transportation?

Plagued by these thoughts, I asked my brother: “what will I do next time, when you aren’t here?”

“You’ll be able to drive by then” he insisted as we turned down the quarter-mile-long dirt road to our childhood home.

It’s been six years. I still don’t drive.

But I’m fortunate. I now have a government Identification card. My brothers don’t drive me, but my parents do. And yet, my disability leaves me in a precarious position — moving from one chauffeur to another.

“What will I do when you aren’t here?” I ask that question to my parents now. In a rural area where public transit is non-existent, the answer isn’t a good one.

If I lose the support of my aging parents, I too will go unrecognized. I vote while I can. I vote, even when it’s difficult, because voting might be stressful, but it’s important.

I vote for myself. Living with a disability makes it difficult to get and keep a sense of belonging. I frequently feel that disability is my personal struggle — that I don’t have a voice. When I vote, I get the feeling that I’m part of the fabric of America, not just as a voter or a disabled person, but as both at once. When I vote, I not only reclaim some of the political power lost to my disability, I become someone empowered and emboldened.

I vote for others. I still ask myself those questions from the passenger’s seat, my father beside me; the combines standing sentry on the way to the small building that houses a single voting machine for the town’s 74 residents.

I wonder how many people walk like me, talk like me, think like me, live in places like this, and are locked out of the political process.

I vote because there is power, agency, and dignity in voting.

When I cast my ballot in November, I will be claiming this power for myself, and showing that others deserve and demand it as well. That’s why I #CripTheVote.


Rooted in Rights exists to amplify the perspectives of the disability community. Blog posts and storyteller videos that we publish and content we re-share on social media do not necessarily reflect the opinions or values of Rooted in Rights nor indicate an endorsement of a program or service by Rooted in Rights. We respect and aim to reflect the diversity of opinions and experiences of the disability community. Rooted in Rights seeks to highlight discussions, not direct them. Learn more about Rooted In Rights

Click here to pitch a blog post to Rooted in Rights.