Showing posts with label history. Show all posts
Showing posts with label history. Show all posts

Friday, March 14, 2008

Governor-designate Paterson

From the New York Times: 'David A. Paterson in his first news conference as governor-designate on Thursday, a day of busily preparing for the transition'

On Monday, March 17, 2008, David Paterson will be sworn in as governor of New York. He will be the first legally blind governor in U.S. history.

Fifty-three year old Mr. Paterson has been blind since childhood when he had an infection in his eyes. In a New York Times article, Mr. Paterson says, "I don't act the way I did when I was 17, like I can do everything myself, because I realized the minute I do that, no one helps me. So I learned to be a little more pragmatic about life." Mr. Paterson receives his briefings via lengthy voice mail messages from his staff, and so that he doesn't need to use notes, he memorizes all his speeches. He also says that he has felt more discrimination from his blindness than from his race.


Steve Kuusisto shares his thoughts on Paterson's governship in an op-ed piece in today's New York Times.
"New Yorkers will no doubt discover that Mr. Paterson will take great interest in the details of governance and that this will require him to take sincere interest in people. He'll ask more questions than your average politician. And those who work in his administration will find that they are important not simply for knowing things but because they can describe how they learned those things in the first place. That's perhaps the most important thing for the public to understand about professionals who are blind -- we are by nature tireless in acquiring information, and we remember virtually every detail of what we read or hear."

For further interesting information - Penny Richards offers a comprehensive list of blind elected officials through history over at Disability Studies.

Wednesday, August 08, 2007

“…not this separate category of human beings”

Fifty years ago, babies born with developmental disabilities were routinely placed in institutions by their families under the direction of their family doctors. Health care professionals often advised families to forget the child, to have other children, and move on with their lives. It’s an appalling time in our history – babies and young children routinely abandoned and forgotten.

I think it’s important that we recognize and remember this cruel part of our history. Kay Olson from the Gimp Parade says,


“My personal thought on what happened 40+ years ago is that it was a tragedy for whole families and has undoubtedly had a lasting impact on how we view developmentally disabled people today. That is, we're still living with the legacy of those folks being segregated, made invisible, and devalued. It has impacted how we view developmental disability and the way we think of difference - we have all been taught implicitly by this history that people who are intellectually or developmentally different do not belong among us because they're dangerous, completely incompetent and lack any ability to contribute to society.”

While I was away last week, CNN covered the story of one man’s search for his sister. Jeff Daly made a documentary, “Where’s Molly?” in which he talks candidly about what it was like to be a 6 year old and have his sister sent away, rarely spoken of and advised to be forgotten. CNN shows a clip of the documentary and has an excellent article on Jeff’s and Molly’s experiences.

Kay’s words above are in a CNN blog that she wrote on this topic. She writes about he challenges of accurate diagnosis and the even greater challenges of predicting potential.

More from Kay on how the line between “us” and “them” is not so solid and clear cut:

“I think the main thing that nondisabled people don't necessarily know or understand is that developmentally disabled people are not this separate category of human beings. People tend to think, "We can do things. They cannot." And there's no line like that dividing all of us. There are shades of ability, varying talents that surface in surprising places. This is true for physical disabilities as well. Most of us, in the course of our lives, discover we have abilities or affinities for some things and lack talent elsewhere, so this idea that a certain class of people lack value or the ability to contribute inevitably underestimates and wastes a lot of human potential.”

I think it’s important that Jeff and Molly Daly’s story be heard. We cannot move forward until we acknowledge where we have come from. Jeff Daly is now working to reunite families affected by this tragedy. There is a national registry, called The National Find Families Registry, to help families affected by institutionalization to find each other.

Thanks to Elizabeth Cohen and Jennifer Pifer of CNN for bringing this important issue to the public’s attention. So often, it feels like the media’s stories about disabilities are superficial and artificial, “feel good” stories that are designed to entertain or “inspire” those without disabilities; stories that maintain difference, segregation, and the status quo. This is a real story with important ramifications, things to contemplate and learn, and also with actions to be taken.

Lastly, I have to say how much I admire Kay Olson’s style of advocacy. Her approach is thoughtful, reflective and encourages open dialogue. She is thought provoking and assertive without being hurtful or condescending. Kay is the quintessential advocate. I learn a lot from you, Kay - Thanks!

Wednesday, July 25, 2007

Illinois Youth with Disabilities Leadership Summit

I just returned this evening from a disability conference in Springfield, Illinois. The Illinois Youth with Disabilities Leadership Summit is a great chance for young people from Illinois to learn about disability history, disability law, and disability advocacy, and a chance to meet and get to know other young people.
This was my first year going as a mentor, and I had a wonderful time.

This is an annual event - if you are a young person in Illinois who has a disability, check it out and consider it for next year!

Thursday, May 03, 2007

Thoughts on Blogging Against Disablism Day

Tuesday’s Blogging Against Disablism Day was a rousing success. I have read posts that were thought provoking, sad, insightful, funny, and informative - all exploring the many varied aspects and perspectives on disablism. Thanks to everybody who read and commented on my post.

I feel enriched, encouraged and invigorated.

I didn’t really have favorites from the day. Each post was unique - it's worth reading every single one.

Here’s a sampling of quotes from the day:

"Bullies and teachers had made it very clear to me which of my traits were desirable and which were not. Every time I saw myself I saw all those undesirable traits to my disgust and shame."

"He was my grandpa who had gone blind but that was somehow different from him being a blind person to me at that time."

"In fact, the U.S. Supreme Court has been so hostile to disability rights that Congress has started to consider legislation that's aimed at restoring the employment discrimination oversight powers to the ADA."

"So how did anyone get the idea that it's abnormal to need services?"

"Maybe labor and delivery rooms would sound like this,
'It's a boy! No hair, dark eyes, 46 chromosomes! Congratulations'
or
'It's a girl! Blond curly hair, blue eyes, and 47 chromosomes! Congratulations!'"


"OK, then. Where are you all? Where are the hordes and hordes of disabled bloggers of colour? Huh? What? Where are you?”

"Your finally getting married to the love of your life. Do you:-
(a) Hold your wedding at a restaurant without an elevator, with multiple stairs over many different levels so that your nephew, who is a power chair user, can’t attend.
(b) Invite your neice to be your bridesmaid, knowing that her brother won’t be there to watch her.
(c) Tell your nephew’s family, when they offer to pay the difference it would cost you to change the venue to a more powerchair friendly place, that the day is not about your nephew - it’s about you.
(d) Consider your family and hold the reception in an accessible restaurant/venue so that the whole family can enjoy the day and watch you get married."

Having chronic, invisible & controversial diagnoses also makes you aware that there’s a hierarchy of ‘acceptable’ illnesses.”

“Note that, discrimination against disabled people (at Ellis Island)wasn't a benign oversight, nor an unforeseen consequence of broader policy--disability discrimination was the policy.”

“So where are the self-reflective posts by nondisabled folks about ability, bodily privilege, fear of people with cognitive disabilities, or even angst about becoming impaired? Where is the recognition of participating in and privileging from an ableist culture?”

"We have a couple of people in our lives that have that "deer in the headlights" look whenever they're around us."

"So, there I am, in my wheelchair, waiting to cross the road. The total stranger next to me, having had a good, long, sideways stare, eventually says, “So what’s wrong with you then?”
My options would appear to be:
tell them what my disability is - which is no secret, but really none of their sodding business
say 'You first - what’s wrong with you?' - which will confirm them in their opinion that all disabled people are peculiar and embittered - after all, they were just trying to be nice!"



“. . . what if there was ableist discrimination, if the able-bodied encountered whispers, inaccessible buildings and transport, stares, intrusive and rude comments, and more?”(great 3 minute video demonstrating this point)

Thursday, January 25, 2007

Carnival!

Another carnival is here!

Check out the fabulous three act carnival on disability history and disability in the arts over at Disability Studies Temple U. Penny has put together a bunch of great posts and even some food!