GUEST BLOGGER: Can People with Invisible Illness Park in the Blue Spots Without Others Seeing RED?
This is an Op-Ed piece I wrote last year, which caused quite a stir at one particular web site. I’d love to hear your feedback too!
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“Do you know the fine for using someone else’s handicapped parking permit is $300?” “That parking spot is saved for the disabled! You should be ashamed of yourself!” Nearly everyone with an invisible illness has been told, “You don’t look disabled to me!” One of my friends replied, “Well, you don’t look stupid to me.” I just bite my lip to try to prevent the tears from forming, broken-hearted that I appear to be deceptive, when I would do anything to give back this parking perk that I use on a rare occasion.
As I circle the parking lot a fourth time on this day I hope for a spot to open up within two-hundred yards of the store, but there is nothing remotely close at this bustling superstore where I need to buy my prescriptions and milk for my toddler. My rheumatoid arthritis is flaring badly, causing extra fluid in my knees to dislocate pieces of loose bones. Every step is painful and unpredictable.
Finally I sigh in resignation and pull into the farthest “blue parking spot.” I reach for the placard–the one that has a bold white symbol of a wheelchair–and no, I don’t have a wheelchair–yet. So after fifteen years of having this “privilege” at my disposal I still warily scan the area before reluctantly dangling the placard from the rear view mirror. Is there anyone watching, wondering, or waiting, ready to confront me?
I’ve had scathing notes left on my windshield and many people, empowered by television exposés, have approached me with their opinions. Judgmental expressions and whispers sting just as much. My husband and I adopted a baby and when I would get my child of the car I would avoid eye contact with onlookers because I could hear their whispers of, “She’s not disabled! Or–if she is–she has no right to have a child!”
Nearly 1 in 2 Americans (133 million) live with a chronic illness. It could be diabetes, cancer, cystic fibrosis, fibromyalgia or even chronic back pain. Many illnesses make walking long distances impossible because of limited lung capacity, physical pain, or unpredictable numbness in the legs. According to statistics provided by the U.S. Census Bureau, about 96% of these illnesses are invisible. There is no sign of the illness existing, nor the use of an assistive device like a cane or a wheelchair.
I began National Invisible Chronic Illness Awareness Week in 2002, which is held this year [Sept 8-14, 2008], after witnessing thousands of people who had frustrations, fears, loneliness, and bitterness, about feeling invalidated. One’s illness, age, diagnosis, or level of disease degeneration, doesn’t change the emotional pain.
Strangers and loved ones alike doubt the severity of our illness or even the diagnosis. We’ve heard, “You look so good! You must be feeling better.” But we don’t feel better. We just bought some fake tan in a bottle and pasted on a smile.
National Invisible Chronic Illness Awareness Week is a time to acknowledge that invisible illness is more prevalent than we’d imagine and everyone–both those who are healthy and ill–can make a difference by encouraging someone with an invisible illness, rather than tearing someone down.
Are those parking spots painted blue because they give so many people the blues? That small area of square footage is a breeding ground for many frustrations as we are forced to defend our illness and character to total strangers. I’d gladly trade in my placard indefinitely for just a week of having my old body back when I could run, sit on the floor, or even hold a fork without tendons popping out of place.
I anticipate the day when a nationally designated system is formed. Texas law states that blue placards are for those who use assistive devices; red permits are for people with a “condition that impairs mobility.” In other states, red symbolizes six months of disability and blue is permanent. It’s confusing! And for one with invisible illness, the wheelchair symbol discredits both our physical pain and–in the eyes of others–our reputation. Until then, we rely on Invisible Illness Week bumper stickers.
The next time you see a healthy looking man loading groceries into his car–parked in the “blue spot”–don’t glare. Stop and offer to help him, or just smile nicely, giving him the benefit of the doubt. Seventy percent of suicides have uncontrollable physical pain as a factor. Your smile may save his life. At the least, it will astonish him, perhaps providing him with genuine encouragement he hasn’t felt for months.
Lisa Copen is the founder of National Invisible Chronic Illness Awareness Week, www.invisibleillness.com, and author of “Beyond Casseroles: 505 Ways to Encourage a Chronically Ill Friend.” She is the founder of Rest Ministries which has served the chronically ill with spiritual support for ten years.






I think it is sad that people would be so cruel to yell at someone. But as you implied, many are ignorant of the truth. I have been very fortunate but then I guess as I stumble out of my car and stagger to get a cart or pull out my cane, I look like I belong there.
By the way, I love the film for II2007 and would like to see some variations on that in the future to add to my car instead of bumper stickers. We need to make people think.
Keep up the great work.
Nancy
Nancy Henson
August 23, 2008
Hi
I can totally understand you. I’ve had issues with getting a electric wheelchair in a store. An older woman who was working at this store refused to give me a wheelchair, she then implied that I did not need one. Okay try walking a mile in my foot steps then ask me I told her.
chronic chick
August 23, 2008
Well said! It is sad, that we are treated this way. I have responded kindly, when asked why I am using the spot, that legally, I’m not required to answer. I did have one person threaten to “call the police on me and turn me in.” I asked them if they wanted to use my cell phone to do so. I told that person that not all disabled people are in wheel chairs, and just because I am able to walk doesn’t mean it’s easy for me! Usually my service dog is with me, and when he is, no one says a word!
It would be great if they would unify the signs so that they were not confusing from state to state; and came up with a symbol that had more than a wheel chair on it to help designate the parking spots, or other disabled services.
One of my pet peeves is going to a dressing room with my service dog, or a restroom, and trying to squeeze into a regular sized one with him because a Mom with a stroller is in there with all of her kids. I am ambulatory, and am sure there are some who may think my dog can wait out side the room, but he carries my meds. and other needs in a back pack, so how exactly is that supposed to work?
Thank you Lisa, for another well written blog!
Maribeth
August 23, 2008
you can obtain a handicap sign, but you need to speak to your dr. your dr knows your condition and can fill the paperwork out for you. i know that this sign has helped me out a great deal, i hate it when people stare or say gee you look good.
i would gladly let them trade a day of pain for looking so good. keep the faith that is all you can do and just practice kindness when these idiots want to be combative. it is your body, you know it better than anyone else. also, see if you have lawyers you can consult with for free who are disablity lawyers to help you.
if you do not like your dr. get another one. you are paying their wage, not the other way around.
raven
August 23, 2008
I’ve had mostly positive interactions with store personnel when I’ve needed an electric cart. Only a few times have I had to get a temporary handicapped tag. Truthfully I should’ve done it more often, but it is such a pain to have to climb the steps to the police station to get the permit. I wish there were an easier way!
I have used such circumstances to educate people about my illness (lupus) and it’s intricacies and challenges. It is not always easy, but I have found that those who listen seem genuinely sympathetic and compassionate when they realize what I have to deal with on a regular basis.
Joyce Meyers
August 23, 2008
Thank you! You said this very well and described to a “T” how I feel about using the Blue Parking spots.
Like you I have heard, “But you look too healthy to be so sick!” more times than I can count. And on those days when I have to use a Blue spot, I avoid eye contact as much as possible so I don’t see the nasty looks.
Gail E aka the Stitcn 'n Frog
August 23, 2008
Dear Lisa,
I am a roll call of illnesses that impair mobility, but all invisible. They include degenerative disc disease, pulmonary hypertension, congestive heart failure, FMS, CFDS/ME and I’m probably forgetting a couple. I use handicapped parking, for which I have a plate, all the time. Fortunately, there is enough invisible illness disability in my Maine paper mill town that people tend to mind their own business.
The Rev. Daniel Beegan
Rev. Daniel Beegan
August 23, 2008
I too get embarrassed when I pull into a handicap spot, however, if I am hurting, or starting to show signs of pain, I will park in a blue. I refuse to drive around searching for something else – most of the time the driving alone has just flared me up. I found a website called handicapfraud.org and I left them a message about: “What if you can’t see my pain.” “What about when I walk into the store feeling okay, and walk out hunched over walking like a granny from the pain?” I never went back to see the response.
The way I look at it is this: If someone wants to come up to me and “discuss” my placard, they are more than welcome to. My doctor knows my condition. My doctor signed off on my placard (cause in California you can only get one through them) and darnit, I have the paperwork in the glove box to prove I am allowed to be there. Oh, and while you are standing there asking me questions, why don’t you help me get my grocery’s into the car, cause most likely I am having a bad day.
Christine
August 23, 2008
Very true! Thanks for sharing! I’m twittering this!
Christi
August 23, 2008
ON THE PARKING PLACARDS FOR THE DISBLED;I KNOW EXACTLY WHAT YOU ARE TALKING ABOUT.I AM LABELED BY TWO STATE AGENCIES AS PERM DISABLED AND PERM TOTALLY DISABLED.BUT I HAVEN`T WENT AFTER MY PLACARD YET.IT STATES “YOU MUST SHOW DIFICULTY IN WALKING AND NEED ASSISTANCE OF SOME TYPE”. WHEN MY RSD IS FLAIRED UP I COULD USE A CANE.BUT I DONT ALWAYS NEED A CANE SO I HAVE DONE W/O A PLACARED.. I ALSO CAN IMAGINE THE LOOKS,BUT THAT I DONT CARE AS THEY DONT HAVE MY PAIN.TK
TOM KANE
August 23, 2008
I have rheumatoid arthritis and my mom is severely disabled due to her rheumatoid arthritis. One close look at her hands or her gait would tell you she is not healthy, but I have been with her when she used her parking sticker and received glares. Like you, she only uses hers when necessary but people do not just look for the sticker, they look for the wheelchair and they are very quick to judge.
Thank you for writing this. One day perhaps people will just look for the sticker and when they see it, assume it was given for a good reason.
Jennie
August 24, 2008
I am so on the same page!!!! I hate it when people have the nerve to think they know what is happeningin your body!!!!
It amazes me how ignorant people are!!! I am so happy you have posted this. I can’t remember how many times family members have said, “you look better, now you can stop all those drugs!” I just want to scream!!!! It takes you to a place where you think no one will ever understand you!
If you do not mind I am going to put up a link to your site…this needs to be read!!!! I am at migraine community on blogspot.
People just do not get it! I say you use that placker with pride!!!
No your illness should not define you, it is a small part of you. How you treat others and yourself makes you who you are. If others don’t understand that…than o’well it is there loss.
GREAT JOB ON THIS
Hope you all have a pain free day!
Liz Bratcher Carley
Liz Bratcher Carley
August 24, 2008
I have a temp blue placard (3 yrs) in the state of Florida and whenever I park in one of these spaces, I also get those looks and am embarrassed even though there are days when I hurt so badly and if I can’t park closer, I turn around and drive back home. I constantly have people tell me I don’t look “sick? My most recent illness was lung surgery a month ago where they found cancer. thank God they got it all but I have breathing problems now and can’t walk far from that and this does not include the “other” illnesses that I must deal with. I definately fit the part with this Invisible Illness image. It would be wonderful if people could be more accepting and loving instead of judging by what someone looks like.
Patty Hartman
August 26, 2008
I actually carry my cane, even if I don’t need it that day, just so I “appear” disabled. No one can see Fibromyalgia or Interstitial Cystitis, but they are real.
I have even gotten the remark “if you feel that bad, you shouldn’t be shopping!” Well, my groceries do not get delivered by ELVES!! Very few people realize that we don’t “go shopping” for fun anymore. That is a luxury we can’t afford. If we are out, it’s because we need something at the store.
I wish people would just keep their opinions to themselves.
Kim
August 26, 2008
I have to tell you I agree 100% that disability parking should be a federal law. The same in every state. I wonder sometimes if my Michigan disability permit would even count in other states.
Marsha
September 6, 2008