Handicap Parking and My Invisible Illness

 

I have an invisible illness. To look at me you would see a short, fat, middle-aged grandmother. Sometimes I walk with a cane, but most of the times I don’t need it. I have a handicapped parking tag hanging on the mirror of my car. I park in handicapped spots. However, I get nasty looks when I get out of my car because I look normal.

I am not “normal”, I have Fibromyalgia. This is a connective tissue disorder. The health professionals’ don’t know what causes it, or how to cure it. There is no blood work that says, yes, you have it or, no, you don’t. It is diagnosed by a list of symptoms and a series of pressure points on the body.
They symptoms of Fibromyalgia are many and varied. What affects one sufferer may not affect another. In my case it is chronic fatigue and chronic pain. The fatigue can be overwhelming. Some days, just thinking about getting out of my bed or my chair is more than I can deal with. Doing everyday activities like washing my hair may not be possible because I can’t hold my arms up long enough to lather in the shampoo much less have any remaining strength to rinse it out.

Chronic pain is another major symptom of this disease. It is not like any pain I have ever had. My muscles hurt. My joints hurt. My skin hurts. It hurts to have the lightest touch. Being hugged can be torture. Shaking hands feels like a vise. This is where the pressure point diagnoses comes in. There are eighteen pressure points on your body. A doctor who is familiar with the illness knows how hard and where to press. If he gets a reaction on eleven of the eighteen, it is considered a diagnosis. The day I went in because of the pain, I had a response to all eighteen pressure points.

Other symptoms that go with the illness do not in and of themselves mean you have Fibro. They can be indicators of other illnesses or mean nothing at all. I have a tendency to drop small items such as keys. I have also dropped large items because I thought I had a good grip on them and didn’t. This is not always constant and some days are better than others.

It can also alter your vision. Some days it is hard to focus and other days I have clarity of vision I haven’t had in years. Some days I can walk as I did ten years ago, and some days it is all I can do to make my legs work. Some days I can eat whatever I want. Some days my stomach is in an uproar and getting any distance from a toilet is not an option.

How does this affect my everyday life? In some ways, it has been extremely negative. I have well-meaning friends and family tell me about the latest miracle cure. They also give me unsolicited advice such as if you would only . . . fill in the blank . . . you would feel better. On the other hand, there is this wonderful new doctor, treatment or vitamin that will surely cure me. They are offended when I don’t jump at the latest offering or advice, but what they don’t understand is that I have looked at all the suggestions they are offering me, and I found them lacking, quackery or just plain dangerous.
I can no longer work, even part-time. The fatigue and pain would put me to bed. I know, because I tried working part-time. At the end of the first two weeks, I was in tears. At the end of the second two weeks, I was in the bed for most of the next five months.

My love life is not what I want it to be. It is difficult for my husband to make love to me knowing that his slightest touch can be painful. This might work if you are married to a sadist, but most husbands don’t want to hurt their wives. The fatigue also plays havoc with my love life. I get tired quickly.
I have three beautiful grandchildren. I have not bonded with the youngest two as well as I have with the oldest. Because of the fatigue and tendency to drop objects I didn’t hold them as much as I did the first one.All of this led to a tremendous amount of guilt and anger. These have to be dealt with in order to move on with your life.
Grieve.
Grieve for the abilities you have lost.
Grieve for the uncontrollable changes in your life.
Grieve for the plans you had that will not come to pass.
Grieve for the you, you could have been.
Get angry.

Find someone who will listen without judging. Who will let you blow off steam. If cussing makes you feel better, use every foul word you ever heard and make up new ones. Get it out of your system. Dealing with the guilt and the anger are not going to happen overnight, and once you deal with it doesn’t mean it will be gone forever. You will have periods where they will come back. Don’t be alarmed or get depressed, well maybe for a little while you can be depressed, but deal with them in the way you know works for you. The only exception here is substance abuse. It is very tempting to drink, smoke pot, do pills or eat yourself into a stupor to make it all go away. However, this are only temporary fixes, and adds to your problems. It is not what you would tell your children or your friends to do. So, don’t you. (End of sermon)

All is not lost. I have been able to make positives out of the negatives. I now work from home as a freelance writer. It has been a slow journey, but I am making progress. I have written a few articles and been paid for them. I was a regular book reviewer for Romantic Times Bookclub Magazine, and had to stop as I had a short story published. I am developing an online reputation as a writer doing research columns, writing book reviews and teaching classes online.

My husband and I are learning to adapt to the illness and have a mutually satisfying love life. My children and grandchildren are learning to cope and know that they are loved in spite of what I can no longer do. We are learning how to adapt the activities we love to do as a family so I can take part and everyone can have a good time.

My friends and family are learning to look carefully at treatments and doctors not just for me, but for themselves too.

Now, if I could just get people in parking lots to quit giving me dirty looks when a “normal” looking woman gets out of a car parked in a handicapped spot.

Submitted by guest writer Deborah Brent

©2024butyoudontlooksick.com
  • Sophie

    It has your driver’s license number onit, too. (Or state ID card number.)

  • Sophie

    What an arrogant a hole you are! Your audacity knows no bounds! You clearly have no idea as to anything about MS, yet you’re giving this woman medical advice and even suggesting she and her doctor aren’t properly treating her illness. Your gall is astonishing.

  • Sophie

    Yeah Samuel, her DOCTOR is in charge of her case, not you!

  • Sophie

    Please God, PLEASE BLESS Samuel here with an advanced case of Multiple Sclerosis. Secondary Progressive will do nicely. You’ll be doing him such a favor, increasing his understanding and maybe even empathy for another human’s suffering. Thank you, Lord.

  • Sophie

    Perhaps not, but our NEUROLOGIST certainly knows far better than you or anyone else.

  • Sophie

    Yeah, that’s because in the United States you’re INNOCENT until PROVEN guilty, doh! And there are rules of evidence; sadly, your own personal opinion isn’t admissible evidence. It therefore “proves” nothing.

  • Sophie

    Your statement is so filled with false statements I won’t live long enough to address them all. You’re not going to get a placard by fiiling out a form and forging nature’s a doctor’s signature. The DMV clerk is not issuing placards until you receive your card in the mail, just like the plates on your car. A doctor has to fill out his own SEPARATE form, complete with all the proper diagnosis codes, AND his medical license number. Then he sends it to the state office where it most certainly IS “validated.” You are making this up as you go along. Your claims are simply untrue.

  • Sophie

    That is correct. Unless you are a law enforcement officer, it is none of your business if – in your MISTAKEN OPINION – someone is “breaking the law.”

  • Sophie

    Thank you for your learned medical opinion, Dr. Options.

  • Sophie

    She was WORRIED ABOUT HER MOTHER who was SO ILL standing alone for 10 minutes while she wsited for Chris to park the car. Another jerk cherry-picking the posts to completely mischaracterize what the poster said.

  • Sophie

    @Parker Foster: The hatred here is palpable. I’ve seen this and other instances of vitriol directed towards people with all sorts of different afflictions, many of the posts far worse even than some of these. Incredibly, you’ve even got posters below declaring that prosthetic limbs don’t “count” as a disability.

    The cancer that’s been slowly eating at society has metastasized, and every system is now riddled with aggressive, malignant tumors – hatred, envy, greed, violence, indifference, selfishness, ignorance, and fear. We’re seeing those here, spreading the rot to anyone they can destroy. It’s disgusting.

    I have a special wish for all the haters here. I hope that each and every one of you will soon be blessed with a disease of your very own – but I get to choose, and I choose pancreatic cancer. A very, very, rapid, painful, case of pancreatic cancer that will ravage their bodies to match their already rotted hearts and shriveled souls. Bless them every one with no more than 6 months of life, but let it be the most agonizing 6 months they have ever lived. Let every day be a blur of hideous pain, nausea, and vertigo. Let them shrivel into cadaverous versions of their former selves; let children scream in fear when they see them in public. Let their families abandon them and their homes be foreclosed on, leaving them destitute and alone. It’s their own Karma, after all; you always get back what you put forth.

    As for myself? I’m fine with saying this. I feel no remorse, no guilt. Why should I? Everybody dies; you, me, them – in their case, why not fast, and horribly? Nor am I afraid of Karma. There’s nothing more Karma can do to me than I’ve already got to deal with. Bring it on.

  • Sophie

    Ben, how could you possibly have missed the rest of that paragraph? Or are you deliberately ignoring it, cherry-picking only the phrase you believe “proves” your incorrect statement?

    The law states clearly “without the use of an assistive device OR THAT CAUSES THE PERSON TO BE UNABLE TO WALK MORE THAN 200 FEET, INCLUDING, BUT NOT NECESSARILY LIMITED TO: (list of SOME of the included diseases)

    You, sir, are dead WRONG.

  • walker

    I wouldn’t know what that’s like. My fibromyalgia makes it too hard for me to go out when most of the spots are taken. I can only really go out in public when there’s not very many people out and about, so there’s usually tons of handicap parking spots of both kinds left after I park.

  • walker

    That’s sort of part of the point, with an invisible illness sometimes we look and seem perfectly fine and healthy but we aren’t. Having a problem you don’t see doesn’t mean it’s any more or less valid then your mother’s condition.

    Now those idiots that don’t have a parking tag and take up a handicap parking spot, those are no good. Or people who just “borrow” one from someone who actually does need a handicap tag.

  • walker

    The people using it for convenience are the ones that don’t even have a handicap tag at all. Having an invisible illness doesn’t mean you aren’t sick. That’s sort of the point of this site Heather.

  • walker

    I would say some of the comments that I read are only further proof that this site needs to exist as a wonderful resource for us with invisible illnesses. Just because someone is in a wheelchair doesn’t mean they don’t see us take a few good steps and think that we can always do that. At least to me it really stings reading that because I wish I was that healthy. I would rather park in the very back of the parking lot and just walk up to the door, walk around the store for over an hour, and walk back to my car loaded down with purchases. It would certainly make my life a lot easier.

    But as I said it’s only further proof that the site needs to exist. I look fine. I can sometimes walk like a normal person. That doesn’t mean I am abusing the system and shouldn’t have a handicap tag use on the bad days.

    And part of me wishes I could better relate to their issue. Most of the time when I go shopping there are plenty of handicap spots, because I can’t go out when there’s too many people out and about. It’s way too draining and flare inducing. While they are out circling the parking lot wishing they had some orange traffic cones in the back of their van so they could just park and move on with having fun, I’m curled up in a heating blanket with a mug of tea watching Netflix.

  • walker

    If that were true then being able to take 1 good step would feel the same as the 1000th step (or 10,000th step) for everyone. Your eyes aren’t the best dianostic equipment known to man, and no one has made you judge, jury, and executioner over who has and who does not have a tag. Yes there are people who abuse the handicap tags, but you can’t know that just by glancing at someone. And being rude to anyone here won’t change that.

  • walker

    OK I know you made this comment three years ago, and I really hope school is going well for you, but I can so relate to that since I was born with fibro. Young doesn’t always mean healthy and normal, even if we wish it did. Gentle hugs.

  • walker

    Just because you see me walking ok between the door and my car doesn’t mean I can park in the back of the parking lot and make it to the door.

  • walker

    I knew the people might give me dirty looks when I got my handicap tag, since I’m under 30 and don’t look sick, so I have just been ignoring all looks since I got it. For example at the grocery store I pull into a handicap spot and walk right up to the door and sit my butt down in a power scooter cart and go about my business. Just because someone has eyes doesn’t mean that they are more qualified than my doctor to tell me what I can and cannot do without even talking to me.

  • Bishop Small

    take it to one of the specialists to sign

  • Bishop Small

    bull, the law has not changed if you meet the requirements for your state then you have the right to get a placard. if your doctor is skimping on writing out the information for a placard either he doesnt believe you have enough need for one or he just doesnt want to fill out the paperwork. in either case he is skimping on your care because if he doesnt see you as having enough need then he is either not treating you properly for your current condition or your claiming more issues then are reality( i am not claiming you are but its the only two options there)or if he doesnt want to fill out the paperwork what other paperwork is he not filling out because he doesnt want to take the time. so consider your actual case is it laziness on the doctor’s part or over exaggeration on your part in some way. the reason i say this is not to be mean or question your actual needs. it is because i am still figting with the va doctors for an actual diagnosis for the ankle pain i get it was diagnosed as torn ligaments in both ankles originally but two surgeries have not fixed it in the right ankle and now 15 years later the new doctors are wanting to call it diabetic neurapathy since i was diagnosed diabetic in 2013 yet my complain dates to 1998. do not let your doctor skimp on doing the paperwork he is supposed to do unless eh can give a factual reason that you dont need it not that its just so common that the mva is not honoring it.

  • Bishop Small

    (1) is blind.

    (2) does not have full use of an arm or both arms.

    (3) cannot walk 200 feet without stopping to rest.

    (4) cannot walk without the use of, or assistance

    from, a brace, cane, crutch, another person,

    prosthetic device, wheelchair or other assistive

    device.

    (5) is restricted by lung disease to such an extent

    that the person’s forced (respiratory) expiratory

    volume for one second, when measured by

    spirometry, is less than one liter or the arterial

    oxygen tension is less than 60 MM/HG on room

    air at rest.

    (6) uses portable oxygen.

    (7) has a cardiac condition to the extent that the

    person’s functional limitations are classified in

    severity as Class III or Class IV according to the

    standards set by the American Heart

    Association.

    (8) is severely limited in his or her ability to walk due

    to an arthritic, neurological or orthopedic

    condition.

    (9) is a person in loco parentis of a person specified

    in paragraph (1), (2), (3), (4), (5), (6), (7) or (8)

    above.

  • Bishop Small

    or they could have any number of other issues as shown below which can be verified by looking up the pa dmv form i copied from
    (1) is blind.
    (2) does not have full use of an arm or both arms.
    (3) cannot walk 200 feet without stopping to rest.
    (4) cannot walk without the use of, or assistance
    from, a brace, cane, crutch, another person,
    prosthetic device, wheelchair or other assistive
    device.
    (5) is restricted by lung disease to such an extent
    that the person’s forced (respiratory) expiratory
    volume for one second, when measured by
    spirometry, is less than one liter or the arterial
    oxygen tension is less than 60 MM/HG on room
    air at rest.
    (6) uses portable oxygen.
    (7) has a cardiac condition to the extent that the
    person’s functional limitations are classified in
    severity as Class III or Class IV according to the
    standards set by the American Heart
    Association.
    (8) is severely limited in his or her ability to walk due
    to an arthritic, neurological or orthopedic
    condition.
    (9) is a person in loco parentis of a person specified
    in paragraph (1), (2), (3), (4), (5), (6), (7) or (8)
    above.

  • Bishop Small

    these days most placards are serialised. in maryland not only do you have to show the placard but have to carry a card in your wallet with your name on it and matching serial number. it also list the condition code for which the placard was issued. i had a cop attempt to write me a ticket for parking in a handicap spot becase i did not have my placard visable it was above the visor at the time. but the van i was driving was my mother’s and had handicap plates which the officer did not see. he ran the plates when i pointed them out to him and then wanted to get angry because the plates were registered to my mother not me. and again tried to write the ticket. i handed him the cards that showed i was also disabled and had the right to use a handicap parking spot. and in maryland you dont have to hang a personal placard if the vehicle is plated but you do have to show proof that you have a disability warranting use of the spot or that you are with someone who has the right to use the space.

  • Bishop Small

    if his mother wouldn’t allow them to have a placard what makes you think she would have allowed them to put her in a wheel chair or would have wanted to be seen in a walker? his statement was he dropped her off in front of the store because she would not get a placard so to save her some energy strength they dropped her off in front of the store and went to use a regular parking spot. he isn’t complaining that he could not use a handicap parking spot as a way to make his life easier he is saying her pride would not let him make her life easier by being able to be by her side from the time they arrived at the store and parked because he had to drop her off close enough that she could make it into the store then park. i know what he means because my grandmother was the same way it took two years a broken wrist and a broken hip from falls before she would be convinced to use a cane outside of the house and getting a placard or a plate ” not putting on of those thing on my car”

  • Bishop Small

    (1) is blind.

    (2) does not have full use of an arm or both arms.

    (3) cannot walk 200 feet without stopping to rest.

    (4) cannot walk without the use of, or assistance

    from, a brace, cane, crutch, another person,

    prosthetic device, wheelchair or other assistive

    device.

    (5) is restricted by lung disease to such an extent

    that the person’s forced (respiratory) expiratory

    volume for one second, when measured by

    spirometry, is less than one liter or the arterial

    oxygen tension is less than 60 MM/HG on room

    air at rest.

    (6) uses portable oxygen.

    (7) has a cardiac condition to the extent that the

    person’s functional limitations are classified in

    severity as Class III or Class IV according to the

    standards set by the American Heart

    Association.

    (8) is severely limited in his or her ability to walk due

    to an arthritic, neurological or orthopedic

    condition.

    (9) is a person in loco parentis of a person specified

    in paragraph (1), (2), (3), (4), (5), (6), (7) or (8)

    above.

  • Bishop Small

    acces to a disability placcard and the right to park in a handicap desinated space is not limited to only not able to walk 200 feet. that is the least restrictive of the choices but that doesnt make it the minimum.
    (1) is blind.
    (2) does not have full use of an arm or both arms.
    (3) cannot walk 200 feet without stopping to rest.
    (4) cannot walk without the use of, or assistance
    from, a brace, cane, crutch, another person,
    prosthetic device, wheelchair or other assistive
    device.
    (5) is restricted by lung disease to such an extent
    that the person’s forced (respiratory) expiratory
    volume for one second, when measured by
    spirometry, is less than one liter or the arterial
    oxygen tension is less than 60 MM/HG on room
    air at rest.
    (6) uses portable oxygen.
    (7) has a cardiac condition to the extent that the
    person’s functional limitations are classified in
    severity as Class III or Class IV according to the
    standards set by the American Heart
    Association.
    (8) is severely limited in his or her ability to walk due
    to an arthritic, neurological or orthopedic
    condition.
    (9) is a person in loco parentis of a person specified
    in paragraph (1), (2), (3), (4), (5), (6), (7) or (8)
    above.

  • Bishop Small

    or you can do like my mother does on my bad days pull up to the store front drop the chair and me off then go find a parking spot handicapped or not. requiring a chair does not mean your brother is extra special then those of us who also have disabilities that allow us to park in a handicap spot. the only point in your statement that i even remotely agree with is the issue of van accessible parking spots and them being used by legitimate handicapped persons because there are no other spots available. of course by the time you get there after i have parked and made it in the store some one else has come out and opened a non van accessible handicap spot so all you see is my mom’s car unnecessarily in a van accessible spot

  • Bishop Small

    ok ill give you one, i have perefeal neurapathy in both feet. it is not constant, so when i get out of the car it may be possible for me to walk into the store, however the longer i stand or walk the worse i get. it starts with a tingling in my toes then proceeds to a burning feeling like a molten metal band around my ankle joint, if i continue to stand or walk my feet will eventually go completely numb to the point that i have stepped on a nail and driven it through my shoe and into my foot till it was pushing the skin on top of my foot up. i didnt realise it i thought i had a piece of something stuck on my shoe and kept scraping my foot to try to dislodge it. so going into the store i may appear perfectly fine and by the end of the trip if i have been on my feet long enough i may appear fine then as well as it is so much easier to walk when every step is not in constant pain only issue is i cant actualy feel my feet hitting the groundi feel it in my knees. on some days i have to have my cane just to get into the store but since on those days i know i am going to need a mobility cart im not bringing the cane as it doesnt fold down enough to fir in the cart so i have to try to grip it between my knees or bend over and pick it up when i dont or set it aside when i have to stand to get somethign off a higher shelf. on my worst days when i know its going to be a long trip i bring my own wheel chair that is why there is a wheel chair ramp on the back of the car. so ask yourself again would you be able to tell that when i entered the store i would need not only the mobility chair in the store or that i needed anything to get into the store on my good days. and to clarify what im saying some days it only takes from the car to the store for my feet to start tingling but other days i can get all the way to the back of the store before they do, and some days i cant get out of the store with out the mobility cart to take me to the car to the point that my mother who drives me has actually gone and gotten my wheel chair from the car because i didnt use a cart and got stuck somewhere in the store with no mobility carts available

  • Bishop Small

    that is not the only reason to be issued a placard as per the pa dmv website and the placard form itself :
    (1) is blind.
    (2) does not have full use of an arm or both arms.
    (3) cannot walk 200 feet without stopping to rest.
    (4) cannot walk without the use of, or assistance
    from, a brace, cane, crutch, another person,
    prosthetic device, wheelchair or other assistive
    device.
    (5) is restricted by lung disease to such an extent
    that the person’s forced (respiratory) expiratory
    volume for one second, when measured by
    spirometry, is less than one liter or the arterial
    oxygen tension is less than 60 MM/HG on room
    air at rest.
    (6) uses portable oxygen.
    (7) has a cardiac condition to the extent that the
    person’s functional limitations are classified in
    severity as Class III or Class IV according to the
    standards set by the American Heart
    Association.
    (8) is severely limited in his or her ability to walk due
    to an arthritic, neurological or orthopedic
    condition.
    (9) is a person in loco parentis of a person specified
    in paragraph (1), (2), (3), (4), (5), (6), (7) or (8)
    above.
    now it may be different in your state but in mine those are the rules and if you can tell im wearing an ankle brace, or that i have a heart condition or that my right arm doesn’t have full mobility with my hand in my coat pocket. then i would like to know how.

  • Bishop Small

    and actually the doctor’s do know this it is on the form they have to fill out and certify as to what conditions the patient meets to qualify for the placard or tag. they have to sign their name saying that the patient meets those guidelines if the patient doesnt actually meet those guidelines and some one proves it then they can get in trouble with the medical board and be banned from signing any further such forms. i know this because my primary care provider at the va would not sign the form based on my request she had to have a signed report from my otho doctor and my podiatrist that the fact that i wear braces on both knees as well as on my left ankle and on good day use a cane and bad days need a wheel chair qualified me for the placard, now maybe that is just the va being its normal asinine self but the info is on the form front and back. and the doctor has to read the form to decide which category the patient falls under.

  • Lynne Blanks Adcock

    You know if we can’t have empathy for each other on here then why would you expect anyone who does not have a chronic illness to understand??? We are all in some form of pain and need to be respectful of each other.

  • Michelle

    I actually have turned people in who I KNEW were abusing the system or parked in handicap parking w/o a permit. I suppose if it hit closer to home I would be more proactive, but as it is I’m pretty passionate about a few other things at the moment. 🙂

  • Ben

    Well all I can ask is for you to pay a little more attention to what you see in your own state. If you see the vast majority of disabled parkers walking over 200 feet unassisted you can be fairly certain most are abusing the system.

  • Heather

    The ADA doesn’t have anything to do with who qualifies for disabled parking. The ADA regulations address the physical attributes of disabled parking. Things like how many their need to be, the signage, the width of the spaces and access aisles, the slop/grade of the spaces, the surface material, etc.

    The federal government only has recommendations of who should qualify for disabled parking spaces. It’s the states that actually define the qualifications.

    I’m not attacking anyone, I’m simply pointing out what the rules and qualifications are. The only people that should feel attacked or bullied by that are ones that don’t meet the criteria.

  • Heather

    I’m encouraged that you seem to be understanding the issues better Michelle, which is all I’m asking. No need to police the handicap spaces. Understanding the issues and spreading that understanding will be very helpful.

  • Heather

    What you are finding in this thread are people who truly need disabled parking are speaking out on their own behalf. That they are fed up with the lack of understanding of their needs. That too many people use disabled parking for convenience which blocks someone in a wheelchair or using a walker.

    If you believe misinformation about laws is being spread then link your state disabled parking permit application and correct the misinformation.

  • Michelle

    Most may be, but not necessarily unassisted which means they still qualify – at least in my state. I’m sure there are those who abuse the system and it’s great that you’re working to stop that.

  • Michelle

    No, I don’t believe everyone is using a hidden prosthetic or brace and I’m sure there are some people who are using the permit illegally and I don’t condone that. However, I’m not going to police everyone’s use of handicapped spaces just like I’m not going to police everyone who smokes (which is more dangerous to public health, btw) to make sure they are the designated number of feet away from public buildings.
    If there are a lot of fraudulent handicap parking permits being issued, it needs to be stopped for sure. If you think someone is using a hpp illegally, call the police and turn them in.
    Take care.

  • Heather

    Are you seriously claiming that someone who cannot walk 10 feet would have no visual indication that their walking ability is severely limited?

  • Heather

    If they are fraudulently using disabled parking than it is our business.

    Yes, someone could be wearing a hidden prosthetic or brace. Are you claiming everyone you see walking farther than 200 feet has a prosthetic? Also, keep in mind that some states, like Florida, don’t allow people with prosthesis to qualify for handicap parking if the prosthesis significantly restores their ability to walk i.e. (there no longer severely limited – they can easily walk more than 200 feet with a prosthesis).

    Lastly, It’s not obvious at all that their doctor signed the form. It’s not even obvious if the placard is theirs or someone else’s. Not to mention, just like prescription drugs, even if a doctor has signed the form, that doesn’t necessarily mean they actually need or qualify for a handicap parking permit.

  • Ben

    Oh believe me I’m advocating. I’ve been working with local, state, and federal level political representatives/senators and city engineers. It’s not so much a government corruption issue, it’s more of an entitled society issue. Disabled parking is mostly an honor system, unfortunately many people put their own convenience ahead of honoring the system. They all know the rules, they know they are either bending them or just plain breaking them.

    Lastly, I take it your answer to the question would be most people you see using handicap parking is walking more than 200 feet. And I would agree, most are.

  • Michelle

    I don’t watch every single person walk from the handicap parking and those I do, I don’t stare at them to see if they are wearing leg braces or something else -unless it’s blatantly apparent. If you think someone is breaking the law, call the cops. Otherwise, all you’re doing is spinning your wheels and wasting time complaining. Get out and lobby for harsher restrictions, if you think that’s the problem. If you think government corruption is the problem, do something about that – or, at least try.

  • Michelle

    I don’t actually watch everyone who parks in a handicapped parking spot and I imagine some people wear braces under their pants, so it’s not plain to see they aren’t walking on their OWN – UNASSISTED. If someone has a handicap parking permit, it’s not my business to ask why they got it. Obviously, their doctor signed the form. It’s not my business & not yours, either.

  • Heather

    Correct, which means they on their own power without aid cannot walk 200 feet. So I’ll ask you the same question Ben asked you in an above post. What percent of people do you see parking in handicap parking that get out of their car and walk UNASSISTED over 200 feet?

  • Michelle

    “Cannot walk 200 feet UNASSISTED”. That’s what it says here in Oregon, anyway.

  • tamsets

    If you have such an issue with those using handicapped parking who don’t appear disabled, then perhaps you should consider addressing those concerns to the federal government and the American’s With Disabilities Act. Attacking or bullying those that YOU feel don’t qualify is wrong.

  • tamsets

    Initially, I joined this sight and this specific discussion believing that others with invisible illness would be encouraging one another. What I have learned through this thread is that there are far too many judgmental people out there that make assumptions about people they believe to be “faking” their illness and giving their opinions and spreading misinformation about the laws regarding handicapped parking. I DO NOT have to share my medical information with someone wanting to be parking enforcer judging and yelling at me if I do not use an assistive devise when I get out of my car. Some days are better than others and if I don’t need it I don’t take a handicapped spot, but I certainly do not deserve to be shamed or bullied when I do.

  • Heather

    Some people do have a high pain tolerance, perhaps you are one. If the pain does not limit you, why would you need to park closer? If it does limit you, in what way does it?