Showing posts with label talking about O.I.. Show all posts

Dear O.I.,

I know all the trash they talk about you, and believe you me, I know FAR too well what you do -- but despite all of that I'm glad we're together. Our relationship has had its fair share of bumps and fractures (hah, see what I did there?) but I've come to appreciate your quirks and learned to manage your more annoying habits.

Let's think about the first time when I, through my own self-realization, truly appreciated you. I was very young at the time, and we were still getting to know each other so it was pretty rough going between you and me. But I was sitting on the medical table in the cast room at Children's Hospital, twiddling my thumbs while I waited for my doctor to saw off yet another cast... that you were responsible for. I had spent the past couple of months relying on my parents to carry me everywhere, had spent weeks getting sponge-bathed, and was starting to get sores from having to be on my back in one place for so long. Needless to say I was more than ready to be rid of your baggage.
As with many other times I have been in the cast room, this time I was not the only patient. There was a little boy seated, or should I say squirming and wailing, on the table next to me. His parents were trying to shush him, his face was a violently furious red, and he screamed for all he was worth - twisting his face away from his broken arm. I wanted to tell him that closing his eyes wasn't going to take the pain away. I wanted to tell him that no matter how much he screamed and thrashed, it wouldn't work either, in fact moving more would just make the pain bolder. I wanted to tell him that soon it'll be all over. I wanted to tell him about patience, about healing, about getting stronger, about how in the bigger scheme of things -- his broken arm was nothing. I was probably no older than 10 but I knew these things because you had taught me all about them. In fact, these were your gifts to me and at 10 I knew that these were the things that made me different from my friends.

About that, you taught me how being different is something you adapt to instead of fighting against. You know, there are often days and nights when I think to myself that if political leaders and iron-fist world rulers could understand the things you have taught me, perhaps there wouldn't be as much struggle, hardship, strife, or anger in the world. Maybe people would want to work harder to mend, to converge, to be patient, to be stronger together, to adapt. You've taught me how to survive by adapting. Whether that's by adapting to other people's expectations of me, to the tall shelf that I can't reach, to the bank teller who never seems me, or to my friend's house that I can't get into -- you've showed me how everything is possible.
I wanted to thank you for that possibility that you continually reveal. In times like these I see so many people who have lost sight of possibility, hope, and clarity for themselves. It is a frightening and incredibly sad sight, and although I have so many amazingly supportive people in my life who help make my own possibility happen -- I believe that it all begins with you. Sure, I have to fumble and wrangle your neck a few times before you'll show me the way but it is ALWAYS so worth it!

Sometimes though, I'm not sure if you realize your scarier influences on people. Sometimes you bring a lot of fear and unknown into people's lives and I resent you for that. Aren't there better ways to prove your point? Less dark? Less of a hassle? Ways that aren't as much of a struggle for folks? Do you have any idea the fear you put into a mother who has her O.I. baby taken away because she's being investigated for child abuse? Or what about the fear of a child who isn't sure he'll be safe at school that day? Or what about the unknown for the twenty-something who isn't sure she'll ever have a 'normal' independent life outside of her parents' home? Or what about the family who isn't sure their O.I. child will live past the next day? I have seen so many of these instances play out and what makes one situation find success is strength and determination. You drag us screaming and kicking to prove what we are made of. You are unrelenting in your instructions. You give us no option but to prove the best of ourselves, but in order to do that, I understand that you must first put us in the worst case scenario. I just wish you wouldn't do that... all the time. Like, sometimes, can't you just let ME handle the remote control to life? Why does it always have to be YOU who gets to choose which channel we watch?

We can't get rid of each other. This relationship is made up of a promise more sacred than that of a vow, it'll last longer than the rust of a wedding band, and no amount of money could pay divorce lawyers to end it. So I have resolved to make the most of this -- whatever this is, whatever you are, and whatever it is you do. But after all, making the most of things is the first lesson you taught me 20 years ago when we first met, right? And just look at where it has taken us now!

With love and admiration,
Sandy




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Disabilities: It Doesn't Need to be Awkward

Everyone knew she was brilliant, everyone knew she was a difficult professor, everyone knew she had all the 'right' and prestigious degrees after her name, and everyone was a little intimidated by her. While other professors on the small college campus were okay with students calling them by their first names, it was always Dr. E---- with her. No one ever asked if it would be okay to call her by her first name, like an unwritten law that's just the way it was. Not only was she the Chair of the Humanities department, head of the Honors Program, my Honors English Comp professor, and my academic adviser. But on top of all of that the first thing everyone saw was that she used a power wheelchair and also walked with crutches.


"Sandy do you know why Dr. E---- is in a wheelchair?" My friend asked while we were eating in the dining hall.
"Uhh no, not really. I mean there are all kinds of rumors but I dunnno the real reason." 
"So what do you guys talk about? Do you talk to her about disability stuff?" 
"Umm no, not at all. She helps me pick classes, makes sure I'm finishing my major on time, signs all the forms, and then I leave her office. Honestly I only ever see her once or twice a semester, just to choose classes and check-in." 
I don't know how many times I had the above conversation with friends and other students on campus. Whenever they asked me if I talked with her about "disability stuff" I always got confused. I mean, should I have been talking to her about 'disability stuff'? And what exactly is disability "stuff" anyway? In my mind she was my academic adviser sooo... I only talked to her about academic advising stuff! 

To be honest towards the end of my college career I did wish that I talked to Dr. E about "disability stuff." I was about to go off into the 'real world,' and felt like though I had gotten an excellent education and made incredible friends - some part of me still felt extremely underdeveloped. But she never pressed me about anything and I was too awkward to know how to bring anything up. Questions like "how do you go about finding an accessible apartment in the city?" Or "how did you get your license and afford that car?" And "Is it hard for someone who is disabled to find a job in the private sector while still keeping disability benefits?" Or "How did you go about having the school put that huge ramp right outside your office?" And "Is that a pet dog that you have or does your dog help you with things?" These and other questions lingered on my mind towards the end of my  senior year, but no matter how many times we met for coffee, or met so she could write my letters of recommendations, or to talk about how my last semester was going - I just couldn't seem to get the words out of my mouth. I loved college! I loved the life, independence, the academics, my friends, and the clubs I was involved in. I don't regret any of it, except... maybe not having been as close to my academic adviser as I could have been. 

I had always been like that: Forever awkward and uncertain around others with disabilities, regardless if the other person had O.I. or not. Maybe it's because my parents mainstreamed me right after preschool? Or because they raised me exactly the same as my two unaffected brothers? Or because I had just never associated with anyone with a physical disability, never mind O.I., outside of a hospital waiting room? (And even then it was usually forced by my mother...)
"Hey, she has O.I. too and she's probably also waiting for Dr. Shapiro. Why don't you go talk to her?"
"Why? That's stupid. What am I going to say to her?" 
Do I say "hi, uhhh.... we have O.I. Let's be friends?" I have rehearsed that phrase so many times in my head and it just sounds dumb. 

It occurred to me that up until fairly recently I didn't even SEE myself as someone who has a disability, or is disabled, or is anything other than normal. And while I still view myself as 'normal' I am beginning to understand that there is a part of me that has a different identity than the majority of society. There's an aspect of me that belongs to this whole other community that is unbelievably awe inspiring and tremendously strong. As much as my parents tried to raise me otherwise, there is something about me that is fundamentally and genetically different from my brothers. They won't ever get it, and I understand that. And while I am now proud to just begin to become a part of the O.I. / disability community, the transition is still awkward. It's like a muscle that hasn't been stretched because it has been in a cast for the past five months; except in this case I think it's a muscle that hasn't been stretched for the past two decades or so. 

It's starting to feel a little less odd to use that muscle: 

Last week at the mall I was weaving in and out of a crowd of tourists, a huge throng of people had sought refuge inside the mall from the heat wave. That's when I saw the wheels. They weren't just wheels, I quickly recognized their thickness and the same pale gray rubber color; then I recognized the oddly jutting shape of her Permobil C300 wheelchair. Immediately I knew she also had O.I.! Since I have the symptoms when I recognize O.I. in someone else it's like finding a matching puzzle piece: she had a large head, a tiny torso, and almost no neck to speak of. Her wheelchair was almost identical to mine except she didn't have footrests - she had no need for them as her legs didn't go past the edge of her seat. Just as she had caught my eye I had caught hers. We were on opposite sides of the kiosks selling over priced tourist gadgets; from the corner of my eye and between the spaces of legs and bodies I saw that she was unsure if she would be able to talk to me. 
I went ahead a bit and thought to myself oh cool, another O.I.'er that's neat. But then remembering my experiences with Dr. E and my readers here, I slowed down and decided to pull over, seconds later she had zoomed up next to me. That's how I met F and we had a normal conversation! I didn't feel awkward and I wasn't fumbling for things to say; and while we did talk about "disability stuff" I didn't feel pressured to bring it up, and nor did I feel vulnerable talking about it in the brief conversation that we had. 

Talking with others:
  • If you're like me and have never met (or only met a few) people with O.I. you probably understand the bit of awkwardness that I wrote about. From what I hear, it's supposed to be a little awkward and overwhelming at first!
  • Just be polite. In the situation above, F was nice enough to bring up the O.I. first. She asked "do you mind if I ask you what your disability is?" And even though, I think, we both knew that we had O.I. I thought it was considerate of her to ask anyway - it can be embarrassing to just assume
  • Along those same lines you can always say "I'm not really comfortable talking about it with people I don't know really well" if you'd rather not get into everything
  • Be genuine. This is just my opinion but if someone is going to talk to me or be my friend because we have the same disease, that is going to strike me as a little weird. I understand that people want to connect with others who are going through similar situations but I think that the connections can be more meaningful if you also get to know the person!
  • Ultimately I have found that everyone that I have associated and communicated with (either in person or virtually) have been really understanding about where I come from, my experience with other people with O.I., and my own life experiences. So don't be afraid to say "hi" or "what's up" because if you think about it (given how rare the condition is)... it's really cool when there's someone else with O.I. in the same place at the same time as you! 

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