Best 312 quotes in «disability quotes» category

After my three year journey through the corporate government disability system, I came to the conclusion that it is blatantly rigged to deny eligible sickened people their earned benefits.

Although stigmatizing attitudes are not limited to mental illness, the public seems to disapprove persons with psychiatric disabilities significantly more than persons with related conditions such as physical illness (34-36). Severe mental illness has been likened to drug addiction, prostitution, and criminality (37,38). Unlike physical disabilities, persons with mental illness are perceived by the public to be in control of their disabilities and responsible for causing them (34,36). Furthermore, research respondents are less likely to pity persons with mental illness, instead reacting to psychiatric disability with anger and believing that help is not deserved (35,36,39)." World Psychiatry. 2002 Feb; 1(1): 16–20. PMCID: PMC1489832 Understanding the impact of stigma on people with mental illness PATRICK W CORRIGAN and AMY C WATSON

Another myth that is firmly upheld is that disabled people are dependent and non-disabled people are independent. No one is actually independent. This is a myth perpetuated by disablism and driven by capitalism - we are all actually interdependent. Chances are, disabled or not, you don’t grow all of your food. Chances are, you didn’t build the car, bike, wheelchair, subway, shoes, or bus that transports you. Chances are you didn’t construct your home. Chances are you didn’t sew your clothing (or make the fabric and thread used to sew it). The difference between the needs that many disabled people have and the needs of people who are not labelled as disabled is that non-disabled people have had their dependencies normalized. The world has been built to accommodate certain needs and call the people who need those things independent, while other needs are considered exceptional. Each of us relies on others every day. We all rely on one another for support, resources, and to meet our needs. We are all interdependent. This interdependence is not weakness; rather, it is a part of our humanity.

An exhausted parent can’t provide the best care, although occasionally, we have all had to do so.

An upbeat song played over the loudspeaker, and everyone's attention focused on the Jumbotron above the basketball court. "It's time for the Bulls' Kiss Cam. So, pucker up for your sweetie and kiss them." The camera found an older couple in their fifties. The man pulled his wife, I assumed, in for a quick peck on the lips. "Aww. That is so sweet," Trina said. She proceeded to yank poor Owen to his seat in case the spotlight landed on them. She'd do just about anything to get on television, even if it meant not kissing Owen tonight to do so. "That is so staged," I said and sneaked a quick peek at my phone, seeing if he messaged me back. He didn’t. "Really?" she countered and slapped my arm. Once I glanced her way, she pointed towards the large screen looming above. On the screen was Sebastian and me as the camera had just so happened to find us. It stayed there zooming closer. And closer. And closer. "Come on," the announcer called out, prodding us. "Just one kiss won't hurt." He had no idea what he was asking. A kiss would initiate feelings I couldn't avoid any longer. I momentarily forgot how to breathe as the song, “Kiss the Girl” from the Little Mermaid hummed at my lips. Not the best choice, but still. Everything became much worse once my giant moved into view, smiling my favorite smile. Sebastian inched closer; eyebrow cocked to dare me."No pressure or anything." I was quiet for a moment before whispering, "Game on, buddy." My eyes closed a few heartbeats shy of Sebastian's lips meeting mine. His hands rose, cupping my cheeks to keep me from pulling away. Like that was going to happen. Sebastian’s mouth moved against mine, and I conceded, kissing him in return. He tasted sweet and minty, like the home I’d been missing. The kiss turned from soft and tame to fierce and wantingas if neither of us could get enough. And already, I considered myself a goner. Everything became a haze. My heart thumped so wildly against my chest, I swore Sebastian could hear. The crowd surrounding us was whistling and cheering us on, and it only kept gaining momentum as the moments passed. The noise quickly faded until it was as if we were the only two people in the room. We could have been the only two people on earth. "Okay, guys." Trina tapped my shoulder, garnering my attention. "Camera has moved on now." That was our cue to separate, and I slowly drew away from Sebastian. He, in turn, slipped his hand to the back of my neck, holding me here. "Don't," he sighed against my lips. I didn't budge another inch. I didn't want to. Sebastian rewarded me by deepening the kiss. Dear God. There were sparks. My stomach flipped. My toes curled. My body warmed. Every single inch of me only wanted one thing and one thing only. If this continued for too much longer, it was easy to guess my new favorite hobby: Kissing Sebastian Freaking Birch. Needing some air, I pressed my palm flat against his chest. This time he released me as we both were breathless. Sebastian's eyes carefully studied me. He kept staring as if he could read my heart, my mind. And for those brief few seconds, I honestly didn't believe there were any secrets between us. His gaze shifted as he gauged what to do next, and I had no freaking idea where we went from here. We'd done it now. We crossed that line, and there was no way of ever going back.

Being denied disability payments shatters your faith in corporate government.

Annie looks dreamy, but she always does because she can’t see farther than three feet away. Elizabeth looks vaguely angry, but she always does because she can see farther than three feet away.

As an experienced electrical engineer in the USA, I was earning in excess of $100,000 annual salary plus benefits. There was no incentive whatsoever to be disabled and in poverty on a corporate government disability program.

A seemingly simple task like taking a bath or wearing a condom feels like multitasking to someone who suffers from hemiplegia or has only one hand.

Based on what I saw in my disability hearing, my lawyer won my case. It was very surprising to receive the disability denial letter several months later.

Blatantly deny me my disability benefits and we will have a problem.

Blatantly lie to me and we will have a problem.

Boredom is probably more frequent and more tormenting if you do not have sight or hands.

But nobody writes fairy tales about the ugly and poems are not there for the broken and I will never find myself in the words of a hymn nor will any whispered prayer ever say my name (which name, which me am I looking for?) because I am shouting at a cross splintered into pieces by my angry fists, and crying at the stained glass falling like killing rain around me.

But I live here, in this place. And I don’t know how to tell you that. I don’t want you to squirm, or take my hand and say it’s tragic. I don’t want you to roll your eyes as though I’m playing a macho game of one-upmanship: My pain can beat up everyone else’s adolescent pain, so I’ll just be over here in the corner, savoring the depths of my stoic suffering and shedding no more than a single tear when I listen to every single cover of “Hurt” and “Hallelujah” on repeat. No, you can’t help me. Don’t try to help me. Please try to help me.

But the thing is that it has provided Mrs Scorrier with a pretext for saying what, I own, has quite sunk my spirits. She told me that Charlotte has a horror of *deformity*, which makes her wish that just now, when she is in a delicate situation, it might have been possible for Aubrey to visit friends.

But in today’s world, being seen as intellectually, cognitively, or developmentally disabled is dangerous because intelligence and verbal communication are entrenched markers of personhood.

Calamity with us, is made an excuse for doing wrong. With them, it is erected into a reason for their doing right. This is really the justice of rich to poor, and I protest against it because it is so.

Can the child who is Dell; be the outer emoodiment of man's quest to save himself? To cure himself?...Or, to "be" himself?

Corporate government social security left me sickened, unable to work, and without any disability income for the rest of my life.

Compassion, acceptance and LOVE is the cure to MOST of the issues that plague this world.

Choosing to accept yourself is a political act. An act of liberation.

Cosmopolitanism seeks a _we_ that does not rely on the exclusion of _others_ but, instead, recognizes and confirms each other as part of the planetary _we_. The cosmopolitan _we_ is not grounded in a monolithic sameness but in a constant alterity and _ethical singularity_ of each individual human person regardless of one's national origin and belonging, religious affiliation, gender, race and ethnicity, class ability, or sexuality.

Corrupt corporate governments employ corrupt bureaucrats that enact corrupt policies.

Deny me my workers compensation benefits and we will have a problem.

Death. Starvation. Blindness. Another grim day in our village.

Dad would call it my Sisyphus toll. Push a boulder up a hill, pretending it’s okay, and come nightfall it - and I - come crashing down. But he forgets the view each time I make it to the top.

Did you have to understand life to plunge in? Even kindness, when he encountered it, was a riddle half the time. If you walked into a door and bloodied your nose, it was one thing, but empathy for handicaps had never been his thing when he himself had none. Empathy had been for people of good cheer.

Disabled in the USA? Congratulations, you have now obtained the secret corporate government status of ‘Garbage’.

Disability Justice allowed me to understand that me writing from my sickbed wasn't me being week or uncool or not a real writer but a time-honoured crip creative practice. And that understanding allowed me to finally write from a disabled space, for and about sick and disabled people, including myself, without feeling like I was writing about boring, private things that no one would understand.

Discrimination is the most polite word for abuse aka denying equal opportunity by anyone in power based on age, ancestry, color, disability (mental and physical), exercising the right to family care and medical leave, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, political affiliation, race, religious creed, sex (includes pregnancy, childbirth, breastfeeding and related medical conditions), and sexual orientation.

Do not take the world too seriously, nor let too many social conventions oppress you.

Do not rely on a corporate government for anything.

Dreams are like living things; they can grow, they can suffer disabilities, they can have deficiency diseases and they can also die off when they meet unfavourable and favourable conditions respectively.

Don't grab people. Would you like it if I grabbed you? If you would like to offer assistance, ask if the person needs it.

Disability is not an inability, nor is it an ability to be lazy but an ability to do something.

Disabled people are now having to beg for small payments that once were held up as entitlements, and a way of making society fairer.

During the nine months I carried Cerian, God came close to me again unexpectedly, wild and beautiful, good and gracious. I touched his presence as I carried Cerian and as a result I realized that underneath all my other longings lay an aching desire for God himself and for his love. Cerian shamed my strength, and in her weakness and vulnerability, she showed me a way of intimacy. The beauty and completeness of her personhood nullified the value system to which I had subscribed for so long.

During the time I went through the corporate government disability system, I was aware that I had a strange sickness that would eventually kill me if not properly diagnosed and treated.

Eligibility for government disability payments for many sickened people only exists on paper, it does not exist in reality.

Even though our journey as parents of a medically fragile child began with emotional turmoil, it has since become a purposeful odyssey that brings meaning and depth to our lives. This is the road we were born to travel.

Finally, especially in the case of medical-response canines and those that serve handlers with invisible disabilities, it's not merely the necessity of the dog that's questioned but also the existance of the disability itself. And for these partnerships, some of the greatest problems arise.

Every time I can’t tell where someone’s calling me from in a room and every time I accidentally start to put my earbuds in both ears I think about you.

For lots of us, disabled people are not our teachers or our doctors or our manicurists. We're not real people. We are there to inspire. And in fact, I am sitting on this stage looking like I do in this wheelchair, and you are probably kind of expecting me to inspire you.

For those that have recognized that suicide is a better option than a lifetime of sickness, disability, extreme poverty, and never ending treatments from an incompetent corporate controlled medical profession, you are to be congratulated on your good judgment.

Given that the corporate government disability system is denying sickened Mauna Kea workers their earned disability benefits, it falls back onto their very high altitude past employer to compensate them for their loss of earnings, pain and suffering.

Had getting rid of his uneven limp, leg braces, and most of the crookedness in his back made that much difference? Or was the difference in the Barrayarans?

Healing severe or chronic pain, I believe, includes transforming our relationship to the pain, and, ultimately, it is about transforming our relationship to who we are and to life.

Here is the voice of my main Character in my Talon book series, I’ll let her introduce herself to you: My name is Matica and I am a special needs child with a growth disability. I am stuck in the body of a two year old, even though I am ten years old when my story begins in the first book of the Talon series, TALON, COME FLY WITH ME. Because of that disability, (I am saying ‘that’ disability, not ‘my’ disability because it’s a thing that happens to me, nothing more and because I am not accepting it as something bad. I can say that now after I learned to cope with it.) I was rejected by the local Indians as they couldn’t understand that that condition is not a sickness and so it can’t be really cured. It’s just a disorder of my body. But I never gave up on life and so I had lots of adventures roaming around the plateau where we live in Peru, South America, with my mother’s blessings. But after I made friends with my condors I named Tamo and Tima, everything changed. It changed for the good. I was finally loved. And I am the hero and I embrace my problem. In better words: I had embraced my problem before I made friends with my condors Tamo and Tima. I held onto it and I felt sorry for myself and cried a lot, wanting to run away or something worse. But did it help me? Did it become better? Did I grow taller? No, nothing of that helped me. I didn’t have those questions when I was still in my sorrow, but all these questions came to me later, after I was loved and was cherished. One day I looked up into the sky and saw the majestic condors flying in the air. Here and now, I made up my mind. I wanted to become friends with them. I believed if I could achieve that, all my sorrow and rejection would be over. And true enough, it was over. I was loved. I even became famous. And so, if you are in a situation, with whatever your problem is, find something you could rely on and stick to it, love that and do with that what you were meant to do. And I never run from conflicts.

He's just like the rest of us - amazing in his own right, and no better or worse than anyone else.