I grew up disabled in a third world country, which meant watching people celebrate my basic milestones instead of providing me with an equally inclusive space. Growing up as a disabled multipotentialite was somehow even more confusing. Those like me were not only cheered on for basic achievements like attending and succeeding at school, but were heralded as “geniuses” for doing these things.
In India, Inspiration porn—“the portrayal of people with disabilities as being inspirational to able-bodied people on the basis of their life circumstances”—is not only rampant but cherished. As a multipotentialite in the making, I was confused by being placed on a pedestal by everyone I encountered outside my family—Look at her, she goes to a school, plays the bass and writes! Being congratulated for wanting to do everything and having diverse interests may seem harmless at first, but for a disabled individual, it can be triggering. This excessive praise is a form of ableism. It’s never encouraging to be looked upon as doing well for myself despite a disability.
One of the worst things you can do to a disabled person is celebrate their basic right to life. If I pursued two hobbies, they were celebrated. If I made friends, I was encouraged to share my experience and inspire others like me. As a young multipotentialite, I was looked upon as someone compensating for her disability by overcompensating in the other fields. If I was interested in five different fandoms and four different disciplines at school, it was seen as a brave disabled person instead of a brave multipotentialite.
It took a lot of unlearning in therapy with a trained counselor to unpack my years of conditioning and to learn how to speak up against how I’m perceived as a disabled multipotentialite. At first, I felt an uncontrollable need to rage—until I learned coping mechanisms.
Here are a few things that helped me understand how to look past my rage and love and accept my two intersecting identities: multipotentialite and disabled person.
Nobody knows your journey better than you
Being born disabled meant that I came to consciousness knowing myself via the ways others saw me—as brave, bold and fearless. None of these virtues were acquired as skills. As far as my treatment journey was concerned, my fearlessness was fed to me. I was conditioned to believe that I was extremely brave and I did not need to cry, as crying spelled weakness. As a multipotentialite, I practiced these traits by shuttling between pursuits and ambitions. However, as I grew older, a fear of not being good enough started to gnaw at me. I began to have external outbursts—breakdowns, which were seen as “uncharacteristic” of my overall persona. As a disabled child, I hadn’t been allowed to develop that persona myself. It had been handed to me by peers, guardians and family, and it didn’t feel authentic to me.
As a multipotentialite, it is difficult to accept that I have to pause my life frequently to endure multiple hospital visits and treatments. I sometimes break down at the prospect that a personal project has failed due to my health and impending hospital visits. I was seeing my life’s journey through the eyes of others, who perceived me to be a certain way when I felt completely at odds with that role.
In therapy, I learned to understand that it was okay to fail and okay to embrace both fear and strength as time allowed. I began to understand the value of acknowledging my fear. I vocalized my insecurities about surviving the pandemic as someone who lives with chronic illness. This allowed me to grow as a multipotentialite, too. I had been constantly stressed about being the best in every project I undertook. In therapy, I learned that my progress doesn’t have to be linear. I started out wanting to be the best at everything, but my journey as a disabled multipotentialite meant embracing my failures and telling my story boldly. Whether that meant success or failure? That was secondary. My truth is mine alone, and it’s not written by someone who doesn’t know all the parts that make me who I am.
Today, I pursue my multipotentialite projects through the lens of enjoyment, and being a little silly wherever possible. I no longer allow others to write my narrative and control it. I own my strength and my vulnerability.
Asking for help isn’t a sign of weakness
One of the first things my parents instilled in me is that I am no less than anyone else I encounter in life. Thus, asking for help was never an option for me. While that may have fueled the feminist agenda, it was personally counterproductive. In the interest of me not seeking help, my parents provided me with absolute accessibility and inclusivity. This ought to exist in the wider world, but as a multipotentialite who is also disabled, I’ve rarely seen my needs met by the world at large. While my needs were addressed in a private capacity by my family, making my life easier, this never translated to my larger sociopolitical context. Asking for an inclusive environment was seen as a sign of weakness.
Since my disability is “invisible” and I “look” functional, I have never relied on asking for external help or taking advantage of any “perks” offered to those with disabilities. This meant that I steered clear of stating any of my special needs until recently. I believed that not seeking help would make me appear tougher and that people would then take me seriously. However, this attitude started affecting my life and my work. The internal pressure that I put on myself to always deliver 110% helped me perform as a multipotentialite. I could juggle hobbies, activities, ambitions and passions seemingly flawlessly! But all that pressure affected my life, when paired with living with my chronic illness.
In the last few years, I have had to come to terms with asking for help and seeking time to adjust my life according to my “special” needs. It took a while to accept this, and even now I struggle to make my needs heard. It helps when I am in an environment that anticipates some of those needs for me. Today, I find it convenient to tell potential dates and employers about my condition, so they know what to expect from me. This also allows time for them to be able to provide me an inclusive space.
Juggling ambitions while living with chronic health condition is a challenge
Perhaps the only time I feel like I’m letting myself down is when my physical state does not allow me to pursue my goals and passions at the pace and in the ways I would like. I can’t take a leap of faith and leave town to travel and explore the world, even if I wanted to. There are certain physical activities that I cannot pursue when my health is deteriorating. Honestly, sometimes even functioning at my day job becomes a challenge. As a multipotentialite, this is a bitter pill to swallow. On one hand, I can and want to pursue everything. On the other, my chronic disease and I are completely tied, and my whole life must play out within the limitations of that bond. This might sound familiar to those who struggle with motor disability or identify as neurodivergent, too. While we can be as ambitious as an able-bodied person, our pursuits will always be bounded by our condition and how we are coping through it.
While living with a disability can restrict your options for pursuing many things, it does not mean that you allow the disability to get the best of you in all situations. What helps me find my center is taking creative liberties to turn difficult situations around. I make sure to reserve sedentary hobbies and passion projects for times when I have to spend a day in a hospital bed. I know I’ll be all alone and will have the time to follow through on what I’m working on. There are always hardships, but the silver lining in being a disabled multipotentialite is the frugality and innovation you learn around keeping yourself occupied and happy through your journey. You have to accept the whole package—the good, the bad, the ugly and the easygoing, chronically ill self.
Your turn
If you are an able-bodied multipotentialite, do you ever feel restricted or limited by the conditions of your life? If you are living with chronic disease(s), do you ever feel exhausted by trying to cope with them along with being true to your multipotentialite self? I would love to hear from you on the states and conditions that are out of your control and limit your passion projects.
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Cristina S Ryan says
I have lived with an invisible disability since I was 15. It comes in pulses, similar to how you describe. Keeping pace in the areas I choose is always a challenge, even when I am at my best. But when I am down, everything goes down with me. In those moments I have times when I rail against my multipotentialism. Why can’t I be satisfied with a simple life?! Rebuilding my life from the bottom involves years, years to increase my capacity to a point where I feel like I am juggling my interests and hobbies like ya’ll- struggling with the “how do I fit it all in my busy calendar” instead of “how do I work consistently enough to not end up homeless again?”
I enjoyed reading this, but I don’t share the experience of being celebrated for normal milestones. I have had to work against the opposite problem: people seeing me as sick and “what a shame”, expecting nothing of me, expecting me to fail but not caring when I succeed because that is normal. Maybe its an American thing. I was suffocated by people telling me “you can’t do that” “aim lower” “do less”. I learned to hide my disability as best I can to try to remain free from people thinking I am any different, even though the truth is I am working twice as hard as my peers on a swords edge. Whenever I go through a flare, and it becomes apparent that I have to drop my projects, possibly my job, and ask for help, it is always a traumatic and terrible experience of shame for me. I still rail against being “a shame” when I am sick. I internalized the denial of my illness and found ingenious coping mechanisms and wellness practices and biohacking to fit in, but it always comes back around. It was always denial.
We have both internalized the stories created about us and our illness, with different cultural narratives. And we have both worked hard to unlearn those and find what is true. For me, my edge has been telling people I have a disability (first coming to terms with it myself) and wanting to become more of an activist. My experience of being barred from participating in the world of science because I cannot work 60 hours a week is not my failure, its is the systems. But it still scares the shit out of me to tell my science peers I am disabled and can’t work. That is a culture that highly celebrates workaholism and judges anything less as laziness.
But for me, the internal work is always about de-coupling what I DO from who I AM and my WORTH. My accomplishments and projects don’t define me. It is one thing to say that, and another to learn it deeply.
Eshana Anand says
Hi Cristina,
Thank you for reading my piece and honouring us by sharing your experience to be a part of your journey. In my experience of interacting with others like us, I have observed that those who ‘acquired’ a disability/chronic illness later in life (as opposed to being born with it) share the same experience as you—where the society expects you to settle for an easy way out and ‘go easy’ with your goals and ambitions.
I wholeheartedly resonate with your thought about the institutional failure of being more inclusive, especially for disabled and chronically ill. Regardless of how corporates (as I work in one myself) can claim to be ‘inclusive’, we are passed over for leadership roles because we are told we cannot deliver the ‘hustle’ the way someone who is able bodied can, making the work-force a brutally limiting space. Even in India, the opportunities for the disabled are few between associate roles and they are often looked at with the gaze of pity and not considered ‘equal’ to anyone else. While people like us may not necessarily be equal in physicality, the opportunities that don’t come our way also do not harbour an equal and inclusive space. I fully understand and share the frustration of a work culture globally that celebrates being a workaholic and any excuse to not be it is labelled as ‘lazy’ and people are passed over.
I’m glad to hear that you are on the path to de-coupling your identity from what you do—it is indeed a tough one and I hope you learn and imbibe it over time to empower many others like you in disability activism space.
Vanessa says
Thank you for sharing, I could relate to so much of this. I find that appearing able bodied but not actually being able bodied seems to confuse so many people and make accommodations and inclusiveness harder.
Eshana Anand says
Hi Vanessa,
Thank you so much for reading my story and taking the time out to reply. I personally feel sensitivity is the first step to making the world a level playing field for those of us who live with visible and invisible health conditions. It’s an interesting scenario when you don’t visibly look sick and ‘blend’ with the world but the way people behave in front of someone who is visibly sick/disabled vs someone who isn’t is a telling sign of how we are so far away from becoming an inclusive world at large.
Mapalo Chibwe says
Indeed. Thanks for sharing. As someone who lives with an invisible disability. This hit home.
Himdeep Singh says
Thanks for sharing, Eshana. I appreciate your journey and your struggles as a disabled multipotentialite. It’s tough for me when I start comparing my life to others. And also when I feel afraid that I may be alone because of my disability in romantic relationships. However, I am learning and seeing that its all about loving the totality of my being rather than striving to be a certain way. If a person really loves me, they will accept the good, the bad, and the ugly, as I am willing to do so as well. So, keep it up and cheers to continuing our journeys wherever they lead into love, laughter, and tears.
Eshana Anand says
Hi Himdeep,
Thank you for reading the piece and sharing your thoughts. I relate to your fears of acceptance in romantic relationships to a large degree. We’re on the same path; especially when you say that finding someone who values the totality of your being is the sight of hope. I claim this vibe in my interpersonal relationships—whether platonic or romantic. Here’s to being fearless in our journeys forward, cheers!
Barbara says
Well I am able bodied except I ocassionally drop stuff for no appearent reason (but it doesn’t concern me much). On top of it, I am highly sensitive person that can get overstimulated by trying too hard to finish one project as fast as possible. I do get myself often to the point I can’t focus cause I haven’t ate anything in a while, am too tired to look for any other way of solving the issue so I stubborn up and keep trying and trying. It’s not good. So yea, I can partially relate as if I had not enough sleep I am useless. But I wanna do something. But can’t…
I developed two ways of working on projects: active and passive. Passive means I am developing idea and means to do it, or have reached checkpoint where I can pick it up later and active is just doing it right now. My unfinished hat, shirts decoration and lamp are looking at me right now as I’m typing 😀 .
Anyway, thank you for sharing this with us. I can’t imagine how hard it is spending days in hospitals or depending on it… Respect for finding strenght to get help and finding ways to deal with it 🙂
Katy says
Thank you for sharing! My chronic conditions are both visible and non-visible, and as I’ve gotten older not only do people still assign character values to me, they now also assign medical conditions. Those also come along with assumptions about what I’m doing wrong with my life to even have the medical condition they’ve diagnosed me with. So when I read what you wrote about traits being assigned to you by others I really appreciated. You have articulated that experience, and what is actually happening; where I couldn’t connect the words to do so myself
Celine Francis says
Hi Eshana, thanks for your article!
I was able-bodied until the day I fell sick. A huge (second) burn-out which has lasting consequences on my health. I used to juggle with tons of projects at the same time, working 7/7 – I crashed on my sofa and couldn’t do anything more. Not even able to read for months – sentences didn’t make any sense. That was 5 years ago.
Since then, I regained some of my strength and energy, but not everything. I have cognitive issues, too. I had to come to terms with that. But it’s not once and for all, gosh no. I have to consent to it regularly. I know it, so I feel better about it.
What helped me is to see that we are all limited – in a way or another. Or we all will be, one day or another, when being sick, older, etc. We usually don’t want to see it, that’s all. So I tell people about my limits. I wrote a book about it. And I secretly hope that it will allow them to recognize their own vulnerability and limits.
I still juggle between projects, but at my own rhythm (which is asap – as slow as possible). Because I have less energy, I have to be more careful about what I put in priority. So I learned to prioritize better. Energy is a scare resource, so I have to pay attention how I will spend it. My present is more focused (and, in a way, more interesting) than my past. Knowing something is precious and rare – that makes it valuable.
Good luck with all your endeavours!