Skip to content

The unexpected benefits of being disabled

Three people are outside at a barm having fun. One is a masc-looking person sitting in a manual wheelchair holding a beer, one is a masc-looking person standing with a prosthetic leg, and the third is a femme-looking person holding a drink, smiling and standing.

Being disabled is hard. It’s different for every person with a disability. But for me, it’s exhausting juggling pain, fatigue, medical appointments, societal attitudes and barriers, and all the other normal things adults must deal with on a daily basis.

But I’m not always upset about living with a disability. Most of the time, I feel gratitude for the experiences I have had in life due to being disabled. These experiences have made me a more empathetic, inclusive, and fulfilled person.

Living with disability changes the way you think about the world and the way you interact with the world. These are some unexpected benefits of being disabled that I didn’t anticipate over a decade ago when I first started identifying as a person with a disability.

Understanding priorities and living in line with my values

I don’t have a lot of spare time and energy, so I must be careful and considerate with the time and energy I do have.

In another life, I think I’d probably spend a lot of time doing things I don’t care about because I wouldn’t be thinking about how I need to budget my spoons. I like that my disability has made me understand what I care about and leads me to make sure I am always spending my time and energy wisely.

I feel like when I look back on my life in five, ten, or twenty years, I won’t have regrets because I have been intentional with the way I live in line with my values.

Empathy, compassion, and connection with other people

I have had a lot of bad experiences interacting with people who don’t understand my access needs or judge me for my disability because I don’t “look disabled”. I have faced discrimination and barriers in the workplace and during my study.

These things are awful to experience, but I feel proud knowing that my experiences make me an empathetic person who can make people feel safe and included. I feel good knowing that in a world of many people who don’t “get it”, I can help other people with disability feel seen and included.

Being forced to have work-life balance

In another life, I’m pretty sure I would have pursued a career that would embody stereotypical success – maybe a lawyer, politician, or dentist. I would have chased achievement and wealth.

As a young child, all I cared about was achievement and how I could pile up more extracurricular activities. Living with pain and limited energy has required me to slow down from a full-time job to working four days a week. It’s been frustrating not to have a choice in the matter, but I get to experience more living.

Having friendships with depth and feeling truly known

I met most of my friends doing work in disability advocacy. They know about all my health issues and the things that can make me feel unwell. I never worry about being judged and I don’t have to navigate any worries that my friends will get annoyed if I must reschedule or can’t do certain activities because I know they care about spending time with me, not about what we are doing. The friendships I have are based on who we are as people, not about the activities we do together. I know a lot of people who go through life never really feeling seen by their friends or family, but because of my disability, I have made connections with people that I treasure.

Living with a disability will probably never get easier, but the rich experience I have in life because of my disability make it easier to accept the challenges that I’ll likely continue to face.

Article written by anonymous.
Interested in writing for the Belong Blog? Reach out to zoe@drc.org.au with your ideas.

Looking for a disability community where you feel understood and connected? Join Belong, our free disability network, with both in-person and online events.

 

A picture of Emma, a woman with light skin and short dark brown hair with light brown strands. She's wearing a purple dress and smiling in front of a wall of flowers.

“Your blood work is normal” An all too familiar tale of medical misogyny

For decades, disabled writer and campaigner Emma Robinson has experience chronic pain and chronic illness. But for decades, she experienced medical gaslighting and mysogyny.
A light-coloured wall with a closet of clothes peeking out at the side, with the shadow of a person across the image, their hand outstretched.

Should we be calling disabilities “invisible” and “hidden”?

The terms "hidden" and "invisible" disabilities are used a lot. But in the medical system, could they be causing more harm than good?
Saffron has tanned skin and long brwn hair, wearing a red dress with white polka dots, posed with her walker. She's standing in a street smiling.

Being disabled changed my life for the better – here’s why

Saffron Canny-Smith didn't always call herself disabled and chronically ill. But now she's embraced her disabled identity, everything has changed. She is disabled, and she is proud.