Quotes of All Topics . Occasions . Authors
I didn't know anything was wrong with me when I was growing up. I thought everyone went to occupational and speech therapy, I thought these were common things. I thought I was quite normal until I went to school and someone told me it wasn't normal to have a disability.
Once you're retired and are no longer counting on earned income to live on and supplement your nest egg, you're done with disability insurance. At that point, though, the need for long-term care insurance - which protects you from spending that nest egg too fast - takes over.
I'm not here to impose Sharia law, and I'm not here to have a message about disability being inspirational - I'm here to make people laugh. But when I can layer things and make people not only laugh but question, make people not only laugh but be offended... I have to do that.
It became very clear to me that Yooralla was not as interested in media coverage that explored issues faced by people with disability as it was in giving a pat on the back to journalists who maintained the status quo by giving readers the warm and fuzzies over their morning paper.
My Dad doesn't see limitations; he either sees hard workers or people who are lazy. As a result, despite any disability or obstacle, my siblings and I all lead relatively happy and successful lives. I believe a good deal of this is due to the fact that excuses were rarely tolerated.
'CSI's been a great blessing for me. It's been a platform that's allowed me to go around the country and the world, really, and speak on issues of disability, but I've never - I'm a professional actor, so I studied for years; I do theater. I never want to disrespect what got me here.
Do you really think that Social Security disability insurance is part of what people think of when they think of Social Security? I don't think so. It's the fastest-growing program. It grew tremendously under President Obama. It's a very wasteful program, and we want to try and fix that.
My siblings, along with my parents Chris and Kath, are the reason that I am successful. Whether I wanted to become an elementary school teacher, enter and win Alternative Miss Ireland, enroll to do a Ph.D., or visit the White House to speak about fashion and disability, they supported me.
I've spent a great deal of time over the past decade as a caregiver for various family members. It gives me a perspective on the struggles that many New Yorkers face with illness, disability, health care, insurance difficulties, and trying to work with and also take care of family members.
The last thing you ever want to do is extend the period of frailty and disability and make people unhealthy for a longer time period. So lifespan extension in and of itself should not be the goal of medicine, nor should it be the goal of public health, nor should it be the goal of aging science.
There is no doubt that the participation of women in the workforce is a serious productivity boost, but to enable this ambition, there must be investment in care - child care, aged care, disability care, health, and education - which are essential social support structures to enable women to work.
I didn't learn to read until I was almost 14 years old. Reading out loud for me was a nightmare because I would mispronounce words or reconstruct things that weren't even there. That's when one of my teachers discovered I had a learning disability called dyslexia. Once I got help, I read very well!
We fill our lives with all sorts of things that make it easier for us to get along in the world: wheelchairs, crutches, grabber sticks, hearing aids, canes, guide dogs, modified vehicles, ramps, as well as other kinds of services and supports. Disability does not necessarily mean dependence on other people.
We've overmedicated kids. Quite frankly, some of the overmedication of kids are because welfare moms want to get additional benefits, and if they can put them on SSI through maintenance drugs, they can also put them on Social Security disability and get a separate check. That is wrong on every single level.
The workers who harvest our food have been systematically denied the basic rights that are granted to all other American workers. They can be fired for trying to form a union or for attempting to improve their working conditions. They are not eligible for overtime pay, disability, or even unemployment insurance.
There are 58 million people with some kind of disability in America, so it's the largest minority, really, in America, and it lags behind in education and economics and jobs, so outside of 'CSI' and outside of my music, I serve on a couple of boards, and I'm trying to be a part of the movement that changes this.
I've had tons of bullies who would call me retarded, even on my Facebook page. It's sad and it really hurts. I want to tell people not to use the word. Don't say your friend's retarded when they do something foolish. If you have a disability, keep working hard. Whatever it takes, do it, and don't be mean to people.
It's the thing I struggle with every day: the mental diligence and stamina needed to sit in front of the computer, open the file, start writing and to keep doing so, word after word, until I've created the next story. A combination of learning disability and chronic health issues make that the hardest thing for me.
The Southbank Centre Unlimited Festival was a distinct moment in time, an amazing counterpoint to the London 2012 Paralympics. There is no question that a major shift in perspective is taking place, that the world is waking up and greeting - as if for the first time - the extraordinary community of people with disability.
Growing up in a group home, and with an undiagnosed learning disability to boot, the odds of success were not on my side. But when I joined the high school football team, I learned the value of discipline, focus, persistence, and teamwork - all skills that have proven vital to my career as a C.E.O. and social entrepreneur.
I seem to be thinking rationally again in the style that is characteristic of scientists. However, this is not entirely a matter of joy, as if someone returned from physical disability to good physical health. One aspect of this is that rationality of thought imposes a limit on a person's concept of his relation to the cosmos.
If Republicans are aiming for the heart, for compassion, the last thing they should do is abandon the sanctity of life. Instead, they should tell Americans that they believe in the dignity and value of every human being, from the defenseless unborn child, to the newborn with a disability, to the 90-year-old dealing with dementia.
There are a lot of people who are moving from unemployment to disability rolls, and there are a lot of people who have been out of work for a long time who are unable to get jobs. And I think that from a long-term perspective, this is not just a human tragedy, but it's going to be a potentially big hit on the economy in the future.
As a caregiver, I always thought I had empathy for Chris's situation, and certainly one family member's disability affects the whole family dynamic in myriad ways. But as I go through various tests and discomforts and uncertainty about the future that cancer can bring, I feel a strong, visceral connection to what Chris went through.
Union members not only earn higher median wages; they are more likely to have paid sick leave, short-term disability, and employer-provided child care. Giving people a voice at work - the ability to organize and negotiate for their fair share of the value they helped create - is absolutely essential to a growing, vibrant middle class.
Barring extreme physical and mental disabilities, each and every one of us is where we are today -- be it poor or wealthy, happy or sad, on the streets or in a condo, in a Mercedes or a rusted-out Pinto -- because of the choices we have made during our lives. It's the choices we have made that put us where we are, not the choices others have made for us.
I just remember when my first child was born I called the personnel office and I asked them about their leave policies. And they said, "Leave policies? Women just leave and they don't come back." And I said, "But I want to come back." They said, "We have no leave policy." And then they said, "Why don't you apply for disability?" Well, having a child is not a disability.
There are millions of people out there ignoring disabilities and accomplishing incredible feats. I learned you can learn to do things differently, but do them just as well. I've learned that it's not the disability that defines you, it's how you deal with the challenges the disability presents you with. And I've learned that we have an obligation to the abilities we DO have, not the disability.
There are things that I really find important, and that we need to remind ourselves of. When you think about disability, do you really think about it? Someone who's a full-time trainer or a boxer, someone who's got a major disability, but who doesn't let that get in his way, that's a really good message for someone who is able-bodied. It can make them think, 'Wow, I suppose I could be doing better for myself.'