Best 312 quotes in «disability quotes» category

I lost all I had known and gained a life I was yet to know.

I look down, worried something is showing after all, but if it wasn't for the incongruous absence of sensation on my left side, I wouldn't know. I look back up at her, taking a step closer because I kind of want to take a step back, and you can’t let that show. "What?" She tenses, even though I’m not even remotely close enough to, say, hit her. "I... I thought you were white." I snort, too relieved to take offense. "I'm adopted. Not my biggest problem at the moment." She smiles at me, looking a little relieved herself. "It just... it seemed a bit too... British, I guess." And it's then that I notice the slight twinge of her accent. “I am British. I was born here.” Her own skin is a light chocolate brown, light enough that it’s perfectly visible when she blushes. She looks so adorable that I almost resist, but not quite. “You have anything against Britishness?” I ask, coming to lean against the doorway on my good side, relieving the weight I have to put on the leg. “No!” she assures me. “No, it’s…” Her hands flutter nervously in front of her, like she hopes to pluck the words out of the air. “I just worry. Some people are weird about it. About me. Especially with the tutoring.

In fact, his travelogues spend amazingly little time discussing his blindness. Only one passage stands out for its frank discussion of his handicap and how it changed his worldview. In it, Holman was reminiscing about a few rendezvous from his past. Disarmingly, he admitted that he had no idea what his paramours looked like, or even whether they were homely. Moreover, he didn't care: by abandoning the standards of the sighted world, he argues, he could tap into a more divine and more authentic beauty. Hearing a woman's voice and feeling her caresses -- and then filling in what was missing with his own fancy -- gave him more pleasure than the mere sight of a women ever had, he said, a pleasure beyond reality. "Are there any who imagine," Holman asked, "that my loss of eyesight must necessarily deny me the enjoyment of such contemplation? How much more do I pity the mental darkness which could give rise to such an error.

I’m determined not to be any less than someone with two working legs." "If only people didn’t all have to rub that crippled leg in my face as if it were a sin. That’s the part that bothers me the most. I didn’t do anything wrong – something wrong happened to me.

In retrospect, it seems obvious that my research about parenting was also a means to subdue my anxieties about becoming a parent.... I grew up afraid of illness and disability, inclined to avert my gaze from anyone who was too different – despite all the ways I knew myself to be different. This book helped me kill that bigoted impulse, which I had always known to be ugly. The obvious melancholy in the stories I heard should, perhaps, have made me shy away from paternity, but it had the opposite effect.

I need to do something about college, but I’m not sure what.” “Where have you decided to apply?” “Nowhere yet. Any time I think about the schools I’ve visited, I feel overwhelmed. The campuses are so big that I know I’ll get lost. I dread making new friends. And the professors acted too busy to deal with someone like me. My parents will be wasting a huge amount of money.” “Your fears are no different than most high school seniors.” He studied me thoughtfully. “Must you go to college?” I opened my mouth to say Of course, I must—and then shut it again. The concept didn’t bother me nearly as much as it should have. Skipping college would be crazy. Right? It was hard enough for a disabled person to find a job, but being disabled with no degree would make it hopeless. “I don’t have a choice.” “Perhaps you have more choices than you realize.

In the areas of police complaints, health and safety, disability, and corporate regulations, the government is absolutely scandalous.

In the context of the autism world (and my outlook in general) this is were I stand equality is for everyone, everybody in the world - I look at both sides of the the coin and take into account peoples realities (that makes me neutral/moderate/in the middle). That means that you look in a more three dimensional perspective of peoples diverse realities you cannot speak for all but one can learn from EACH OTHER through listening and experiencing. I also try my best to live with the good cards I was given not over-investing in my autism being the defining factor of my being (but having a healthy acknowledgement of it) that it's there but also thinking about other qualities I have such as being a writer, poet and artist. I do have disability, I do have autism and I have a "mild" learning disability that is true but I a human being first and foremost. And for someone to be seen as person equal to everyone else is a basic human right.

I pulled on the restraints, frustrated, hurting, and completely devastated. I could feel tears sliding down my skin, into my ears, and back over my scalp. Which told me that they’d cut off my hair, too. For some reason, that little bit of vanity was what it took to undo me completely.

I saw a documentary about prostitution in Holland a few years ago, that said over there health insurance actually pays for monthly visits to a prostitute for the disabled, because they feel that sex is part of a healthy life, so unmarried disabled men have a right to have sex, even if it's with a paid prostitute. Pretty bizarre, huh? Can you imagine a US health insurance company picking up the bill for your romp in the hay with a hooker?

I’m really tired”, you come to understand, is meaningless, giving the impression all will be well with a good rest and that if you’ve ever been tired, you know what it is to be exhausted.

It’d be easy to get lost here, in the spaces where I feel like a ghost. A spirit who couldn’t touch, or be touched. It’d be easy, so easy, to drown. But I keep swimming back towards the shore.

It [feminism] needs to recognise that disabled people aren’t inherently defective, but rather that non-disabled people have failed at creating a physical world that serves all.

I thought having a chronic illness would make my life detour in ways I didn't want to accept, but I've learnt that have a chronic illness made the only detours that are worth the growth.

It is disappointing to witness the corporate government disability system letting massive numbers of sickened people down during their greatest time of need.

I thought of the many people who had said to me, 'You're young; you've got plenty of time to recover.' This seemed the coldest comfort, the grimmest fact of all.

It appears that workers compensation lawyers only get paid if they win their case. If your case lies outside of mainstream cases with a history of winning, they are unlikely to take it.

It is hard to be charitable when you have been denied your disability benefits and your workers compensation for occupational disease.

It takes a lot of confidence, and self-love and self-worth to realize that you are capable. And that you have every right to leave your lane, and to do things in the same way that other people do.

It seemed unfair that despite the fact he could not use them, or feel them, his extremities should cause him so much discomfort.

I want to sharpen my pride on what strengthens me, my witness on what haunts me. Whatever we name ourselves, however we end up shattering our self-hatred, shame, silence, and isolation, the goal is the same: to end our daily material oppression.

I was sickened by what I witnessed when I went through the corporate government disability system.

Losing some faculties is worse than losing your life.

Most people do not realize how corrupt the corporate government disability system is until they become so sick that they try to use it.

Most people do not realize that the corporate controlled government has built a wall of deceit between them and their earned disability payments.

Most USA citizens never realize that the systems of public protection are essentially useless until they try to use them. At that point they learn the hard way that government agencies like OSHA, FCC, FDA, police internal affairs, disability, and the like do not work for them.

My ability is greater than my disability.

My disability lawyer warned me prior to the hearing that one of the worst judges had been assigned to my case.

My mother was determined that I should be able to walk two miles. If you could walk two miles, she said, you could get to most places you needed to get to. Actually, this is a fallacy. The fact that you can, with great difficulty, and taking an unconscionably time about it, walk two miles, will not get you anywhere you need, or at any rate want, to go. There were times when a wheelchair would have added another dimension to my life, but that was a forbidden subject; and it was not until many, many years later, long after my father and I were alone, that I took the law into my own hands and bought one; and instantly, dazzled with the new freedom that it brought me, swept my father off to his old haunts on an Hellenic cruise.

Never trust a corrupt corporate government judge.

It's not that there are no challenges to becoming a vegetarian or vegan, but in the media, including authors of popular books on food and food politics, contribute to the 'enfreakment' of what is so often patronizingly referred to as the vegan or vegetarian 'lifestyle.' But again, the marginalization of those who care about animals is nothing new. Diane Beers writes in her book For the Prevention of Cruelty: The History and Legacy of Animal Rights Activism in the United States that 'several late nineteenth-century physicians concocted a diagnosable for of mental illness to explain such bizarre behavior. Sadly, they pronounced these misguided souls suffered from "zoophilpsychosis."' As Beers describes, zoophilpsychosis (an excessive concern for animals) was more likely to be diagnosed in women, who were understood to be 'particularly susceptible to the malady.' As the early animal advocacy movement in Britain and the United States was largely made up of women, such charges worked to uphold the subjugation both of women and of nonhuman animals.

I've met so many parents of the kids who are on the low end of the autism spectrum, kids who are diametrically opposed to Jacob, with his Asperger's. They tell me I'm lucky to have a son who's verbal, who is blisteringly intelligent, who can take apart the broken microwave and have it working again an hour later. They think there is no greater hell than having a son who is locked in his own world, unaware that there's a wider one to explore. But try having a son who is locked in his own world and still wants to make a connection. A son who tries to be like everyone else but truly doesn't know how.

I was surprised at the great lengths that the government goes to in order to deny eligible disability claims.

I went to the doctors to get better, instead they made me sicker.

Memory loss is strange. It’s like showing up for a movie after it’s started. I’m sure I’ve missed something. I don’t know if it’s important or not. So I do the best I can to lose myself in the story and hope the gaps don’t matter. Later, I can look it up, or someone will remind me, or maybe it’s perfectly fine to not know.

Mistreatment of disabled people by the corporate controlled government is the root cause of a huge number of suicides.

My lawyer informed me after my disability hearing that she believed she had won my case because it was so strong.

Nobody can see pain. They have no frame of reference for pain that's happening to someone else. They can only see inactivity - which they interpret as laziness.

Now, Woolf calls her fictional bastion of male privilege Oxbridge, so I'll call mine Yarvard. Even though she cannot attend Yarvard because she is a woman, Judith cheerfully applies for admission at, let's call it, Smithcliff, a prestigious women's college. She is denied admission on the grounds that the dorms and classrooms can't accommodate wheelchairs, that her speech pattern would interfere with her elocution lessons, and that her presence would upset the other students. There is also the suggestion that she is not good marriage material for the men at the elite college to which Smithcliff is a bride-supplying "sister school." The letter inquires as to why she hasn't been institutionalized. When she goes to the administration building to protest the decision, she can't get up the flight of marble steps on the Greek Revival building. This edifice was designed to evoke a connection to the Classical world, which practiced infanticide of disabled newborns.

Not being able to talk sucks. There's no doubt about that. There's a lot of times when I almost feel like I'm trapped inside of myself. Like if I don't talk or yell or scream or laugh I'm going to explode. A lot of the time it almost feels like I'm suffocating.

One of the most dangerous things in life is a sickened person that has lost all hope for the future.

Our family was starting. We kept on moving with our young lives, shortly afterward and took Ben Young with us everywhere. But pretty soon Pegi started noticing that Ben was not doing the things some other babies were doing. Pegi was wondering if something was wrong. She was young, and nothing had ever gone wrong in her life. People told us kids grow at different rates and do things at different times. But as Ben reached six months old, we found ourselves sitting in a doctor's office. He glanced at us and offhandedly said, "Of course. Ben has cerebral palsy." I was in shock. I walked around in a for for weeks. I couldn't fathom how I had fathered two children with a rare condition that was not supposed to be hereditary, with tow different mothers. I was so angry and confused inside, projecting scenarios in my mind where people said something bad about Ben or Zeke and I would just attack them, going wild. Luckily that never did happen, but there was a root of instability inside me for a while. Although it mellowed with time, I carried that feeling around for years. Eventually Pegi and I, wanting to have another child after Ben, went to se an expert of the subject. That was Pegi's idea. Always organized and methodical in her approach to problems, Pegi planned an approach to our dilemma with her very high intelligence. We both loved children but were a little gun-shy about having another, to say the least. After evaluating our situation and our children, the doctor told us that probably Zeke dis not actually have CP-he likely had suffered a stroke in utero. The symptoms are very similar. Pegi and I weighed this information. To know someone like her and to make a decision about a subject as important as this with her was a gift beyond anything I have ever experienced. It was her idea, and she had guided us to this point. We made a decision together to go forward and have another child.

Parents of medically fragile children find themselves becoming experts in lots of different areas, including laws and regulations, research and treatments, and the various specialists that support the health of their children.

Physically, mentally, emotionally -- it seems like every part of me is broken in one way or another.

Next to God, Family is the best thing.

Occupational Safety & Health Administration (OSHA) is rigged to allow your employer to willfully damage your health and disability is rigged to deny you your earned benefits when you have become too sick to work because your toxic employer damaged your health.

Often times, celebrated disability is a excuse to cover up real abilities.

Our culture teaches that sex is for the sexy, and the only way to be sexy is to be pretty. No wait--that's still too weak. Sex should properly arise from sexiness. For unsexy people--fat people, old people, funny-looking people, disabled people--to even feel sexual desire is inappropriate, perverse, disgusting. For them to engage in sexual display is offensive. For them to have sex...well, there oughta be a law.

People often said to me what I couldn't do things when I was younger such as sports, writing, mathematics, geography, science etc - I pathway can always be tailored can change and that change itself is possible what did I excel in well art was one of those things of have gone BACK to to move FORWARD and have taken up poetry and creativity something that occupies my mind in way that creates happy thoughts, happy feelings, and happiness all round really. To invest in your strengths and understand but not over-define yourself by your deficits is something that has worked for me over the years and this year in particular (the ethos was always there instilled that I am human being first like anyone else by my parents and family but it has been tenderly and quite rightly reaffirmed by a friend also) it has made me a more balanced person whom has healthy acknowledgment of my autism who but also wants to be known as a person first - see me first, see that I have a personality first. I say this not in anger or bitterness but as a healthy optimistic realisation and as a message of hope for people out there.

People with disabilities are sometimes very humble and approachable, if you want a seasoned reputation, then behave like one of the handicaps.