Representation without Understanding – Vic Kelly
I really appreciate Vic Kelly talking about the difference between lack of representation and poor or lazy representation. As writers, research is important. It’s not enough to just decide a character is in a wheelchair without considering why, or how that affects their day-to-day life. As with so many of these essays, this post has given me a lot to think about as a writer.
Tomorrow, Morgan Dambergs will bring this whole series full circle, talking about non-binary gender and referencing the Alex Dally MacFarlane post that helped bring about this collection of guest posts.
Update, August 2022: Eight years have passed since writing this piece. Vic no longer views Jason Street (Friday Night Lights) as good representation, partially because the actor isn’t a wheelchair user, but mainly because of the leaning into the “my life is over” storyline. Vic is also no longer happy with their description of Joe Swanson as a breath of comedic fresh air. The pinnacle of disabled representation in sci-fi and fantasy is Rosie Lyons in Russell T. Davies’ Years and Years, played by Ruth Madeley, who is herself a wheelchair user and informed the character to a huge degree.
At a very basic level, wheelchair users are not an under-represented group in fiction. We’re just very misunderstood.
Take a moment and I’m sure you’ll easily come up with a dozen characters with wheelchairs: heroes and villains, lead protagonists and supporting characters. They might be from science-fiction or period drama or comedy. You might not be able to think of a character in fantasy—although they do exist—but I’m certain you can come up with a dozen.
I’m going to make a few predictions about your list. Most of the characters are white men. Over half are extremely intelligent. Most of them have vaguely defined injuries. Most of those with clearly defined injuries lost their legs rather than injuring their spine.
My final prediction is that the creative team will only have done some real research if the story is about the disability itself. Otherwise, the wheelchair is at best, descriptive color and at worst, so misunderstood that it might as well not be part of the story.
I’ve been using a wheelchair for almost 16 years, and while friends claim not to see that as one of my defining characteristics, it is. Wheelchair user goes on the list with Irish, gay, ex-pat, hearing impaired, and writer. We are the sum of our experiences and being a wheelchair user is a very different experience to not being one. I am not defined by my disability, but it is part of my daily life and it affects almost everything I do.
Becoming a wheelchair user later in life—or indeed acquiring any condition or disability that drastically changes our interactions with the world—provides a unique perspective on representation. There is a before and after. There is an acquired desire to connect to something that previously was just a plot point or some descriptive color.
In my case, I went from not really thinking about wheelchairs to seeing them everywhere—not to mention seeing the obstacles to their passage. I lost that inattentional blindness that we have about things that don’t affect us. I found myself wanting to know more about my new state, and even needing to find evidence that I hadn’t completely lost my old life, that I still had possibilities.
I gradually realized that very few of the characters I found meant something to me.
There have been some characters that work or at least come close to being good representations. Jason Street (Friday Night Lights) is one. As far as the writing went, Gail Simone’s Barbara Gordon (Birds of Prey) was another, although the art in those comics was rarely as well researched. The Open Hands Initiative’s Bashir Bari (Silver Scorpion) is a character I hope to see again as he was really well done. Finally, as absurd as his physical prowess is, Joe Swanson (Family Guy) is a breath of comedic fresh air.
Despite those few names, some fundamental issues remain. Unless the character’s sole purpose is to tell a story of emotional struggle and physiotherapy (Jason Street) or the disability makes a climactic scene more dramatic (Jake Sully in Avatar), there is a real disconnect between the reality of a wheelchair user and the fictional world.
Many of these issues are subtle but irritating. The wheelchair might not fit the character’s injury and lifestyle. Barbara Gordon has gone through a dozen heavy, thoroughly unsuitable wheelchairs thanks to poor research by artists. The chair might be an absurd contraption. Professor X’s floating metal box in the early 90s and his seated Segway in New X-Men spring to mind. Undefined spinal injuries often lead to inconsistent portrayals of what the character can physically do. Yes, quadriplegics can play sports like wheelchair rugby and go bobsledding, but that doesn’t mean they have full upper body control.
It could be argued that I’m nit-picking but if these characters were supposed to represent people like me, then they failed on some level. The research wasn’t done—or wasn’t complete—and the effect alienated me rather than making me feel understood or included. Some characters fail completely. Professor X, probably the most famous wheelchair-using character, has no traits that show him to have a disability except the wheelchair itself. Even his injury is vague. He’s a better representative for premature alopecia than for spinal cord injury.
The worst insult for me is the sudden cure. The cure negates the character as a representation. Most male comic book characters get cured: they’re cloned into a new body (Professor X); they have costumes that grow new legs for them (Flash Thompson in Venom; Soldier Zero); they get prosthetics that are indistinguishable in function from the real thing (Flash Thompson in Superior Spider-man); or they turn out to have been faking (I won’t spoil that one). Female characters get retconned out of existence (Wendy Harris from Batgirl) or retconned back to health (Barbara Gordon).
That last one particularly stung. While the art had often let the character down, it merely downgraded her from a great representative character to a good one. Gail Simone did some great work, showing in subtle ways that while Barbara Gordon had built a fulfilling life, she faced and overcame daily challenges. Those ranged from keeping her father from worrying about her to being immobilized—but far from helpless—when she was captured and had her wheelchair taken away. She was great. And then she was gone and we were back to pseudo-representatives like Flash Thompson.
Representation is important. When you’re a kid, it’s about having a positive role model with your defining characteristics. When you’re an adult, it’s about being reminded that you fit in somewhere and escaping into that character. And when you’re going through a major life change, it’s about finding solace in stories that show you that someone understands and that maybe you can overcome the challenges you face.
And that’s why representation without understanding hurts as much as not being represented at all.
Vic Kelly (pronouns: they/them) is a nonbinary, white settled Irish, hard-of-hearing, wheelchair-using, panromantic writer and scientist with OCD and cPTSD. They live with their spouse and a bunch of animals in rural Ireland. Vic divides their time between writing fiction, doing scientific communications work, and engaging in LGBTQIA+, disability and mental health activism. They can be found on TikTok, Instagram and Twitter as vic_or_vikki and on the Partner and Ally blog.
mg
February 27, 2014 @ 10:00 am
Thank you for a very illuminating essay. One question – what does “retcon” mean?
Jim C. Hines
February 27, 2014 @ 10:05 am
“Retroactive continuity” – http://en.wikipedia.org/wiki/Retroactive_continuity
EB
February 27, 2014 @ 10:08 am
Thank you for the phrase inattentional blindness. It sums up a concept that I have been much more wordy in expressing and expands it in illuminating ways.
betsy dornbusch
February 27, 2014 @ 10:10 am
I love this so hard. I worked for Quickie Wheelchairs for a number of years and had several friends who use chairs in those days. It stripped away all the illusion and fear for me, for sure. (I’m sure strangers in chairs think I’m staring for the wrong reasons but I love the technological/mechanical aspect of wheelchairs. I still find it fascinating.) I have to confess, I’ve never considered writing a character who uses a chair but now you’ve got me thinking…
M. Fenn
February 27, 2014 @ 10:38 am
Thank you for writing this. A character in a story I’m working on is in a wheelchair and I really want to get him right. You’ve reminded me how important that is.
Joie
February 27, 2014 @ 10:45 am
“… [R]epresentation without understanding hurts as much as not being represented at all.” This is it exactly. We hear “not all representation is good,” but I think yours is a far more accurate and descriptive phrase. Thank you for this.
LJ Cohen
February 27, 2014 @ 10:59 am
Before my writing life, I spent 25 years as a physical therapist in major rehab centers in 4 states. It infuriates me when characters with disabilities are plunked into a story with little purpose, save being an object acted upon by others, as the victim, as the savant, or with no actual research as to how the disability affects the character’s day to day life. One other trope that makes me want to scream is the disability-makes-character-a-saint story line. I used to teach a course on disability awareness for physical therapy students and my required books were a series of comics by an artist who became quadruplegic in a car crash. One of his titles was “Don’t worry, he won’t get far in foot” and the cartoon that went with it was an overturned wheelchair in the desert being studied by a sheriff and his posse. (It’s been about 10 years since I last taught so I don’t remember the man’s name)
Anyway, thank you for your excellent post.
Joel Zakem
February 27, 2014 @ 11:09 am
John Michael Callahan, whose drawings were often signed with only his last name. “Don’t Worry, He Won’t Get Far on Foot” is also the title of his autobiography. Callahan died in 2010.
LJ Cohen
February 27, 2014 @ 11:16 am
Thanks, Joel. You beat me too it. Just searched for him – curses to my sleep deprived brain for not rembering. http://en.m.wikipedia.org/wiki/John_Callahan_(cartoonist)
His cartoons made my students profoundly uncfortable and we spent a lot of time discussing why.
superbwg
February 27, 2014 @ 11:22 am
My brother was in a wheelchair for over a year after a spinal cord injury, and even after his “miracle cure” (drs. gave him a 1% chance of walking again) there is so much residual weakness and therapy that you never see when a character in a story get’s a miracle cure. At least in my brothers case there is so much more then just not being able to walk as part of his injury and healing process, there is still fatigue issues, pain issues, mobility issues and he has probably had the best case scenario as far as recovery goes. It always amazes me how little of the day to day stuff actually makes it into stories with people who have disabilities, and the miracle cure that has them going from wheelchair bound to cartwheels in a day is just argh! Your post was extremely well articulated, easy to understand and put into simple terms what I am sure is frustrating for some people to try and explain to those of us without disabilities. Thanks!
Derek Handley
February 27, 2014 @ 11:34 am
I actually looked that one up some time ago. I thought there must be a term for it – I was thinking something along the lines of cognitive blindness or cognitive ignore-something.
Whenever I get to know someone new who’s never known a wheelchair user, they always comment on how many wheelchairs are visible to them over the following weeks. That’s what made me realize it’s a real phenomenon.
Derek Handley
February 27, 2014 @ 11:35 am
Feel free to ask me questions if you decide to write a story with such a character!
Derek Handley
February 27, 2014 @ 11:36 am
Feel free to ask me questions if you have any. I’m happy to help out. I’ll be making a sort of “FAQ” over the next few months as a resource for writers so you’d actually be helping me out as well.
Derek Handley
February 27, 2014 @ 11:41 am
The wheelchair user as genius, the wheelchair user as saint, and the wheelchair user as heart-and-soul of the group are three common cliches.
I certainly can’t complain on one level, because all of those cliches are at least positive ones that don’t have the potential to cause any negative shift in the public perception of wheelchair users. See Nalini Haynes’ post from Tuesday, February 25 for the other side of that story.
However, they are cliches that can make it difficult for people who are newly disabled to find solace or escape or knowledge in fiction.
M. Fenn
February 27, 2014 @ 11:43 am
Thank you! I haven’t looked at the story in a little while, so I’ll take a look and see what questions pop up.
Derek Handley
February 27, 2014 @ 11:48 am
Thank you. And tell your brother I said hi.
While I wouldn’t want every story to focus on the whole recovery process, the miracle rate of recovery is always irksome.
I remember when Professor X got the use of his legs back in “Uncanny X-Men” in the 1980s, Chris Claremont did actually give some ‘screen time’ to his recovery process and physiotherapy. However, it was a bit of a tricky one for a friend of mine who was going through physio. Professor X could walk again because his body was cloned and the new body wasn’t injured. Then he kept having issues that were essentially psychosomatic – the body wasn’t injured but his brain couldn’t get used to being able to walk. It was handled well, but my friend had a real issue with that ‘it’s all in his mind’ idea.
lkeke35
February 27, 2014 @ 12:14 pm
The first time I ever met a woman in a chair was at my grandmother’s church. She’d lost one of her legs to diabetes complications. Sometimes I saw her in the chair and other times I saw her on crutches and in my twelve yr. old mind wondered why she just didn’t use the chair all the time as the crutches seemed harder to use. Later on after my grandmother lost her feet to diabetes she had to have a chair and I was her primary caregiver. And now my Mother has intermittent need for a chair because of gout.
That said, whenever I see any film, TV or book characters with prosthetics or in chairs I always wonder about the exact nature of their disability, how did they go to the bathroom -if at all, how did they reach things in stores or anywhere else, what’s their morning routine,etc.? And yes, why are all of them White, straight and male?
Now that I have intimate knowledge of those routines I can’t NOT think any of this.
browneyedgirl65
February 27, 2014 @ 12:16 pm
This is interesting. I note that the commentary also inadvertantly exposes another aspect of disability that is often overlooked — there is disability “before and after” as described here, but there is also born disability. And what a lot of people don’t realize, including the before/after folks is that there can be worlds of difference between these two groups of disability. Deafness is a prime example of this. Almost everyone regards deafness as a loss disability, that is, as a before/after person would view it. But being born deaf is an entirely different thing.
All too often, I see disabilities set down as “loss scenarios” which is another way to distort and badly represent such a character.
Jessica Strider
February 27, 2014 @ 12:18 pm
Fantastic post and definitely some things to think about. I’d like to see more representations of different ways of living in fiction, but only if they’re accurate representations.
Orson Scott Card gets slammed a lot (and rightly so) for his views, but he’s also written one of the best characters in a wheelchair I’ve ever read. I’m not sure how accurate the character is, though I do know he was based on Card’s son, who was also in a wheelchair, so I’m assuming it’s pretty good. The character’s name is Issib, from the Homecoming Series. I remember that in book 2 there’s a scene where he’s in a tent with his prospective wife and she asks what he can do, in terms of sex and – by extension – everything else. And he replies that he can undo buttons with his mouth.
The scene stuck with me, and reminds me that necessity is the mother of invention. People find ways of doing things. Sometimes simple, sometimes remarkable. And to not underestimate people for any reason.
Great post, thanks for sharing your perspective.
sasha_feather
February 27, 2014 @ 12:24 pm
Hi, I’ve included this post at Access Fandom. Thanks!
Lenora Rose
February 27, 2014 @ 12:46 pm
This would be fabulous. (In addition to the friend whose book i mentioned on LJ. I have a story with a character with MS, who’s sometimes in a wheelchair, sometimes has crutches, and sometimes just a cane or nothing. I know someone with MS though I haven’t had a chance to ask her about the manuscript, and I’ve done research, but the more resources out there *specifically for writers and their common pitfalls* the better.)
Lenora Rose
February 27, 2014 @ 12:57 pm
i think it can be a problem to have an overly positive stereotype, too. (See also “The noble savage”). Some people act as if personally betrayed if they then see someone in that group who isn’t the “perfect patient”, or the person who’s a bit bitchy, or you know, people being people.
Derek Handley
February 27, 2014 @ 2:47 pm
Looking back, I see exactly what you mean. At the time of writing, I decided to focus on acquired disability because, in the context of representation, I felt that shift in perspective was very interesting. However, I haven’t even given a line of space to disabilities that exist from birth. I’ve focused on injury – which is my perspective, but as you point out, not the only perspective.
Before responding to your comment, I tried to think of a character who has used a wheelchair from birth on. I couldn’t think of a single one.
Thank you for the comment and for giving me food for thought.
B. Durbin
February 27, 2014 @ 3:13 pm
One thing you may want to do is walk carefully around a typical day and see how many obstacles you have to deal with. I’m able-bodied, but I’ve had enough friends with limited mobility that certain standard design elements scream out to me. For instance, my home—which was built in 1980—has a completely purposeless step up into the entryway. It’s useless because the first thing you do when you enter the house proper is step right back down—it’s almost as though it’s a deliberate wheelchair screen. (And if I had the money to redo the front wall, it would be gone SO quickly.) Then there are things such as hallway width, turning radius, and countertop height, and that’s just in a standard household. We won’t even talk about the completely unaccessible upper cabinets. And I live in a fairly level area—what would it be like to be somewhere with hills everywhere, or cracked sidewalks, or NO sidewalks?
Ken Marable
February 27, 2014 @ 4:03 pm
Very good example with those being born deaf. If you look at the debates surrounding Deaf culture and cochlear implants, it very quickly shows you that society’s common sense notions of disability are extremely limited. We try to lump so much together under a single label that it’s pretty much meaningless (and also naturally gives the able-bodied the impression that “those people” must be broken and worse off). It’s one of the main topics I discuss in the medical ethics courses I teach. There is a large amount of great scholarship on these issues including the medical model vs. social model of disability (not surprisingly, most of it from philosophers with disabilities) which opened my eyes even more to how poorly most of us understand disability.
Sally
February 27, 2014 @ 5:12 pm
As a friend of mine once said “Wheelchairs are a super-power. They make you invisible.”
For various health reasons, I have occasionally used a chair, and I know this is true. And I know the fear of lit cigarettes right at eye level.
Not everyone who’s in a wheelchair is unable to walk. And people who you do see walking aren’t faking it when they use a chair.
Great essay, Derek.
Derek Handley
February 27, 2014 @ 5:18 pm
Thank you, Sally.
Cigarettes at eye level – the reason why I rarely go to large outdoor events where there’s alcohol…
Sally
February 27, 2014 @ 5:20 pm
It would have achieved the same end if it was that his brain had forgotten muscle memory and proprioception and such. Real physical stuff (as superbwg’s brother had) as opposed to having some sort of neurosis about it.
Derek Handley
February 27, 2014 @ 5:20 pm
I think you should definitely try to talk to your friend about the character. She will be able to shed some light on the intricacies of the condition. Even if you don’t directly use the research in dialog or narration, it will inform your story direction.
Sally
February 27, 2014 @ 5:24 pm
TABs are usually completely gobsmacked by the concept of the social model of disability, I’ve found.
(TAB = what most people call normal. It stands for “temporarily able-bodied”. An accident, a disease, or just getting old can make you no longer a TAB.)
Derek Handley
February 27, 2014 @ 5:26 pm
I lived in San Francisco for 18 months… that was an experience! Talk about hills. That’s the only time I ever considered getting a power chair.
I’ve seen some great accessible design but the one element that seems to be most frequently ‘off’ is the main door of accessible buildings. I’ve often found doors that are so heavy that I can hardly open them without help; and the automatic door openers aren’t always installed.
Sally
February 27, 2014 @ 5:41 pm
I only go to those on foot nowadays, or if they’re in a non-smoking place. I have never been so glad to wear coke-bottle glasses, let me tell you. Still doesn’t help the terror of realizing “FIRE COMING AT MY EYEBALL!”
Marie
February 27, 2014 @ 6:16 pm
Thank you for posting on this subject, Derek.
One of my favourite manga is called “Real” (by basketball nut Takehiko Inoue). It follows three young men, two of them in a wheelchair, and is about wheelchair basket ball (among other things).
I’m not qualified to judge if they are good representations or not so I was wondering if you’d heard of the series, or read it, and if yes, what is your take on it ? If not, I’d recommend it and would be very interested in having your opinion on the subject.
Lenora Rose
February 27, 2014 @ 6:58 pm
Walking with a heavy stroller gives an idea. It’s nto the same at all, but it raises a lot f the same issues. I live in a house with steps up in back and front, whcih would need serious renovations to add a lift to the second floor (There is NO WAY the lathe-and-plaster would support one, and it makes it really hard to find the studs that would). My neighbourhood is old, with a popular and slightly quirky commercial stretch (Think cafes, restaurants, and cute unique little shops) – and a LOT of it is grandfathered in for accessibility and other codes. Many of the buildings were built with a sunken first floor, meaning my favourite Chinese food place AND the best artisanal coffee house are both down stairs, and many shops and other restaurants are up stairs. Even a few of the ground floor places have a step. The next best coffee shop has a flat entry but the door opens *inward* into the tiny entryway (Which would be a fire hazard, but opening outward would put the door right int he flow of pedestrian traffic), and so you have to hold it pried open while fumbling with the next. Worse on exiting, and also makes it harder for others to reach out and offer their help.
It’s really annoying thinking I can’t pick up a take-out lunch or grab a coffee after my grocery shopping because I have a toddler. But that’s a temporary nuisance. How much worse when the barrier is one’s own self?
chordatesrock
February 27, 2014 @ 9:56 pm
Yes. This.
There are two failure modes for representation: lack of it, and bad representation. The former seems to be the better failure mode, but only because the latter is so horrible.
As a writer, and as someone who knows writers, I try to create good representation of various disabilities. I try. I had an interesting if uncordial conversation a while back with someone who (I think) would vastly rather default to nonrepresentation, about portraying disabilities you don’t yourself have. (Or rather about facilitating research for that in general– whether questions are okay, whether to encourage people to talk about their experiences, etc.) I suppose it’s my view that if you care about disability rights and media and the intersection thereof, that, ability and energy permitting, you ought to be trying to do something about it. (But then, I also think it’s useful to kiss ass and flatter people, and that’s not a popular opinion among any marginalized group.) Some people just want to be left alone, though, and it’s not really fair to say that it’s PWDs’ responsibility to fix this.
But if it’s not, then whose responsibility is it? That of CND (currently nondisabled) writers? They likey don’t know enough to create good representation; where should they learn? It isn’t PWDs’ responsibility to educate anyone, but the other option is going to other CNDs, and how would they know? By clinical research? Seriously, when have professionals ever demonstrated an understanding of the actual experience of disability or any condition greater than could be expected from a member of the general population? The only thing distinguishing them from John Q. Public is their certainty that they know what they’re talking about.
So it’s not PWDs’ responsibility to fix it– that wouldn’t be in the least bit fair– but it is up to PWDs to fix it anyway, and doesn’t that just figure.
chordatesrock
February 28, 2014 @ 2:48 am
When you post your FAQ, may I link it at accessportrayal?
Sally
February 28, 2014 @ 7:12 pm
And that’s also a barrier for many of the rest of us. I have the upper body strength of a newborn (heh) and can’t open heavy doors. Neither can someone who’s pushing a stroller, or has severe arthritis, or just has their arms full of stuff. Automatic door openers are the best.
Jim C Hines series on Equity
March 1, 2014 @ 3:16 am
[…] Representation without Understanding – Derek Handley […]
Links: Saturday, March 1st | Love in the Margins
March 1, 2014 @ 11:23 am
[…] Representation without Understanding – Derek Handley – This post highlights some of the problems I had with the previous link. If you don’t understand the marginalized experience you’re writing about, you run the risk of perpetuating harmful stereotypes. Not all representation is good. […]
Karen Bertke
March 3, 2014 @ 12:05 pm
Derek, you hit the nail on the head with this one. I was helping a cancer patient out of her wheelchair when a woman tried pushing past me. When I asked her to stand back she snidely said, “I’ve been waiting just as long as they have”. I replied, “Can’t you see she’s in pain?” The woman FINALLY looked over to see the girl (for the first time, apparently) with no hair, hunched over with tears in her eyes, with her wheelchair behind her. “Oh, you should have told me” was all she said. People seem to be BLIND when it comes to wheelchairs. They are simply an obstacle to go around, over or through. Sally makes a great point about irregular wheelchair users. I would love to see a story where the hero is wheelchair bound, especially in the case of cancer, or severe respiratory problems, where they can have good days when they can walk a short distance on their own. I’ve heard people complaining about “obviously healthy” people using handicapped parking spaces. I took them aside and told them about people with breathing problems, who are okay one moment and on oxygen, stored in their trunk, the next; and of cardiac patients who are okay until they aren’t… Invisible handicaps are not even represented in literature it seems. If anyone knows of an author who depicts Severe Airborne Allergies, Food Allergies, Cancer where the patient isn’t dead, and Hidden Cardiac Conditions that don’t immediately end in death, please let me know.
I sympathize with you for the cigarettes at eye level. I have a scar on arch of my foot from a cigarette I stepped on when it had been tossed into our yard still lit. My dad was burned on the arm by a man seated next to him. I think cigarette use and awareness of those around you is much the same as the “invisible wheelchair”. Smoking is their right and they take no care of those around them. They don’t want to trash up their cars so they throw the butt out the window to trash up your yard instead…
I know we can’t install lifts into older buildings, but a buzzer that sounds to let them know someone with a physical handicap or stroller needs assistance would be nice.
I, unfortunately, have an invisible handicap. I am severely allergic to many things that people take for granted… How often have you sprayed an air freshener, used scented lotions or body wash or shampoo, worn perfume or cologne, used hair spray in public, lit a scented candle, used an e-cigarette (I’m allergic to the nicotine you breathe out, not just the smoke), or smoked in public? Any one of these can send me into a coughing fit that causes my lungs to close up and leaves me drowning in my own mucus. It can end with me using my inhaler or vomiting (gag reflex from the enormous amounts of mucus my body is producing, trying to wash away the irritant). Forget about going into “Bed, Bath and Beyond” unless I’m wearing a mask… I’ve been fortunate not to end up in the hospital as so many other do (you should look up the statistics for trips to the hospital – about 774,000 cases in 2009 were for asthma alone, not counting infections, food allergies, etc.). I had coworker who complained about my incessant coughing. I finally explained to her that SHE was the problem. Scented hand lotions, perfumes, hair spray and heavily perfumed body washes she used were killing me. It was no wonder to me why her daughter was always sick and coughing soon after she came into her mother’s workspace when she was fine only minutes before… I gave her a card from my allergist, along with a survey to see if your child suffered from allergies. Hopefully her daughter is now being treated.
I think both the advertising industry and well-meaning authors do a disservice to the handicapped when they don’t do their research. It confuses the perceptions of the public as to how they should behave, what they need to do to help, and even how to identify the people as handicapped.
Hope authors take note of this and start thinking about how they can portray these hidden handicaps and invisible wheelchairs in something other than a supporting role. (Not the wheelchair bound tech support or the sickly research assistant for the superheroes at large…)
Sally
March 3, 2014 @ 4:49 pm
I used to go to meetings of a disability rights/arts group, and I LOVED that they always had requirements for no perfume or scented body wash or any of that crap. Even people who aren’t sensitive to scents don’t want to smell your cologne or candles from 10 yards away! I’m so glad they have unscented detergents and soaps nowadays, though I still have to hold my breath in that aisle.
And even mild food allergies suck. There’s the kid who will need the ER if they get peanuts, and then there’s someone else who will “only” projectile-vomit from them.
The joy of linkspam (8 April 2014) | Geek Feminism Blog
April 8, 2014 @ 10:55 am
[…] […]
Karen Bertke
May 14, 2014 @ 9:09 pm
Hey Sally, Today I went to my allergist’s office and a woman there reeked of perfume, despite the large sign on the outer door that clearly reads “For the safety of our patients, please do not wear perfumes or colognes in this office”. My niece and nephew are the ones who carry epi-pens in case of exposure to shrimp or tree nuts (Tylenol makes me throw up- we have both types in my family!). As for going into the detergent aisle at the local grocery… Hah! I grab an employee and send them into the aisle for me. The manager knows me by name now after my last attack. You’d think I was dying from the way people kept trying to call 911. (Okay, so I couldn’t breathe… What’s new about that?)
My friend with epilepsy says he’s faced the same problem. He can have a seizure in safety as long as there’s someone there who knows what to do. Bystanders always want to call 911.
1. When the seizure begins, the patient sometimes has what is known as an “aura”, where they see lights, hear tones, experience enhanced sense of smell or feel pain. If they do, they can give warning to someone who knows what to do.
2. Get them to a safe place (off stairs, away from sharp objects or steep drops, steer to the side of the road if driving) and lay them down on their side.
3. Do NOT try to hold them of stick anything into their mouth. My friend (90lb weakling) broke the principal’s arm (200lb football type) when he tried to hold him down. People in seizure are insanely strong and have NO control over their bodies (they’re as dangerous as someone on a bad drug trip). Putting something in their mouth only breaks teeth and puts you in range to get hurt. Loosen ties or remove any clothing that might choke or injure them. Remember, you only have about 20 seconds to do it in. Prioritize!
4. Don’t call the life squad if they have warned you that they are seizure prone and have asked you not to. (There is one exception to that rule.) If you don’t know them well, call 911 immediately for help. Here’s what you need to do: Mark the time that the seizure begins and TIME it (this may sound weird, but it is VERY important – read on…): a. The Tonic phase. Loss of consciousness occurs, and the muscles suddenly contract and cause the person to fall down. This phase tends to last about 10 to 20 seconds. b. The Clonic phase. The muscles go into rhythmic contractions, alternately flexing and relaxing. Convulsions usually last for less than two minutes. (The exception: If they go on for more than five minutes or the cycle starts again- CALL the life squad, even if they told you not to previously.)
5. When they come out of seizure they’ll be exhausted and hurting (think “Charlie Horse” on a grand scale). Get them home to rest. IF THEY HAVE NEVER HAD A SEIZURE BEFORE, call the life squad immediately! They must be checked by a doctor to determine the cause of the seizure (some are life threatening). Whatever you do, don’t act like they’re a freak show. I hate when people act that way when I have an allergy attack or a nose bleed (chronic rhinitis) so I can well imagine how they feel after a seizure (VERY SELF CONSCIOUS!). Don’t act like they are diseased or contagious. Don’t mother hen them. They are used to seizures happening. Ask what help they need and follow instructions.
Gee… Amazing how the discussion of wheelchairs can get you off topic onto other “invisible” handicaps. By the way, my sister is overweight and uses the motorized wheelchair at the grocery because she’s broken her back three times, not because she’s lazy. Just for the jerks out there who made LOUD COMMENTS about how she might lose some weight if she’d get out of that chair and walk a little! So many assume they know better than the doctors…