Hold That Head!

Lately I have been endeavoring to send letters of recommendation to colleges and universities across the U.S. on behalf of students who are applying to graduate schools.

I only write letters for those students whose work and preparation will make them successful graduate students and accordingly the process of writing these letters is fairly pleasant. (It feels good to say that Casper Hauser will be a credit to the profession, whatever that profession might be. He has, after all, come a long way from the feral state that characterized his former days.)

The "thing" that does not feel good is the relative inaccessibility of the various online recommendation websites that some of these colleges and universities are now using.

If you use screenreading software for the blind you will be able to access some of these sites, but others are largely inaccessible.

Well that’s no big deal. After all, stores like Target have resisted making their websites accessible for years. Even when there isn’t some kind of organized hostility to electronic or digital accessibility, there’s a cluelessness and systemic inattention to accessibility in all kinds of areas that intersect with higher education. I could go on and on about this topic but I need to maintain my equilibrium today.

Two of these online recommendation sites have form fields that screenreading software can’t engage and when you write the "help" line you actually get an e-mail that asks you to enter your problem in another inaccessible place.

I hold my head. I spit gently into my hanky and proceed.

S.K.

The Easy Things

There’s a poem I particularly like by Robert Bly entitled “Eleven O’clock at Night” in which the poet lies down in his bed and wonders about the usefulness of his day. Bly asks the all important question: “What did I accomplish today?”

Some years ago I found a sermon, written by my paternal grandfather—it was in Finnish but the title in translation was: “What Does God Ask of You Now?”

I was only 19 or so when I found that sermon and after translating the title I scoffed. “What a silly, old fashioned and entirely dark sensibility,” I thought. I was “hip” after all, and accordingly I was filled with adolescent despair and a lot of bad ideas from the sixties including “don’t trust anyone over thirty.”

My Finnish grandfather was an immigrant to the United States. He was a Lutheran minister and he offered church services in rural Minnesota, Wisconsin, Michigan, and in his later years to the Finns who worked in the leather tanning factories and quarries in Massachusetts.

I have recently heard civic officials in more than one American city say in public that providing basic services to people who have disabilities is too difficult. I won’t name the towns and I won’t disclose the identities of the Babbit-like city council types—at least not for now. There are plenty of blockheads on the planet’s surface and I’ll risk carpal tunnel if I start typing their names.

My point in this instance is that providing special education to kids in our public schools, or putting in accessible curb cuts are no longer “choices” in the old-fashioned sense—at least the Americans with Disabilities Act says so.

Yet all over America (and even in relatively prosperous towns) one sees and hears a kind of adopted scarcity rhetoric when it comes to the provision of basic civil rights.

Here’s how the thinking that I’m alluding to actually works:

Continue reading “The Easy Things”

Congratulations Simi Linton, author of "My Body Politic"

As mentioned previously on this blog, Simi Linton has a blog called Disability Culture Watch, which she categorizes as "A disability-focused commentary on the arts".  Here is an excerpt from her "About" page:

"There is an emerging cadre of dancers, actors, writers, performance
artists, and painters who are actively engaging with both the fact and
idea of disability. The most exciting work explores what disability
provides the artist, rather than what feats someone can perform despite
disability. When disabled artists use their unique bodies and voices,
something innovative happens.  My job is to follow these turns and
twists on the cultural map, selectively reporting and critiquing this
vital phenomena."

Simi is the author of My Body Politic (University of Michigan Press, 2006) and recently she has been awarded grants, one from the Puffin Foundation and one from the Lower Manhattan Cultural Council, to develop a stage adaptation for the book.  Congratulations, Simi!  We can’t wait!

With permission from Simi, the summary of her book, as found on her web site, is copied below for our review.  Follow this link to learn more, as well as to hear two selections from the book, read by the author herself. 

Continue reading “Congratulations Simi Linton, author of "My Body Politic"”

New Article: Women's Access to Health Care

Congratulations to Kara B. Sheridan, of If the World had Wheels, for the recent publication of her article titled Women’s Access to Health Care in New Mobility, The magazine for active wheelchair users.

"Considering the mountain of barriers blocking access to health care
services for women with disabilities, it’s easy to become overwhelmed…"

And Kara, a big CONGRATS for earning that Masters Degree as well!


Ya Gotta Love These Gimpy Girls

The Gimpy Girls.  They are "Clearly, Frankly, Unabashedly Gimpy" and in their words

“Gimp” in two definitions in Webster’s Dictionary, means “vigor” or
“fighting spirit” and a “person who walks with a halting, lame walk.”

And sooner or later every last damned one of us finds ourselves
Gimpy and in need of all the vigor and fighting spirit we can muster.

Presently, 51 million people – that’s 18 percent of all Americans –
have a disability, says the U.S. Census Bureau. And the nation’s 78
million baby boomers are just entering their 60s – making for more
Gimpy people than ever before.

The Gimpy Girls’ passion is to make life easier for Gimpy people
everywhere – regardless of their personal architecture – and have some
tongue-in-cheek fun doing it.

Check out their growing list of "Gimpliments".  Ya gotta love these girls – and their attitudes!

~ Connie

The transition

Nowadays its customary to hear people talking all the
time about “transitioning” much in the way they used to talk about “flossing” or
“dating”—you can hear people say, “I’m transitioning right now,” as if they’re
actually undergoing a metamorphosis. The reformation of transition into a verb
carries with it the implicit assumption that transitioning is a good thing. One
doesn’t say, “I’m transitioning from the Titanic to a lifeboat,” or, “I’m
transitioning from heroin to methadone.” Transitioning implies
forethoughtfulness and purpose.

I think that people with disabilities are so busy making
a “go” of their situation that they seldom have time to say they’re
transitioning. As a blind person I don’t say that I’m transitioning down the
street, though I probably could. The trouble is, I’m too busy trying to get
somewhere and get there in one piece and avoid walking into street lamps or
dumpsters to feel that I’m transitioning my way down the sidewalk.

But I want to be one of those transitioning people. So here’s my plan:

I’m transitioning from being a young blind person to being an older blind person. I don’t care so much anymore what other people think about my physical difference. I’m just me.

S.K.

Superfest International Disability Film Festival

Guess whose book was made into a film that won an award?!  Yep!  Keep reading! 

Thank you to Day Al-Mohamed at Day in Washington for bringing this to our attention.  Congratulations to Sven Werner of Luxemberg for winning the Pamela K. Walker Award.  Our congratulations to ALL actually…

The following is taken from the Superfest 2007 Awards page:

SUPERFEST XXVII WINNERS 

Congratulations to this year’s award winners!
   
The following contains a list and descriptions of the
    award-winners for SUPERFEST XXVII (2007).
To browse through photos from the award-winning films, click here.

Superfest XXVII Award Winners’ List 
   

Best of Festival   

  • The Epidemic [51 min.] Producer: Niels Frandsen, Denmark

Excellence Awards   

  • No Bigger Than a Minute [52:30 min.] Producer: Steven Delano, U.S.
  • Outsider: The Life and Art of Judith Scott[26 min.] Producer: Betsy Bayha, U.S. 

Achievement Awards
   

  • Headstrong: Inside the Hidden World of Dyslexia and ADHD [26:41 min.]                         Producers: Chloe Sladden, Ben Foss, Steve Schecter, U.S.
  • Stroke [58 min.] Producer: Katarina Peters, Germany
  • The Rest of My Life: Stories of Trauma Survivors [25 min.]                                            Producer: Gabriel Ledger, M.D., U.S.   

Merit Awards   

  • Carmela [30 min.] Producer: Guillermo Lopez Perez, Mexico
  • Darius Goes West: The Roll of His Life[92 min.] Producer: Roll With Me Productions, U.S.
  • Mercury Stole My Fire [12:12 min.] Producer: Anitra Nelson, Australia
  • Seeing Is Believing [13 min.] Producer: Tofik Shakhverdiev, Russia
  • Symphony of Silence [22 min.] Producer: Yves J. Ma, Canada

Spirit Award

  • No Bigger Than a Minute [50:15 min.] Producer: Steven Delano, U.S.
       

Pamela K. Walker Award   

  • Planet of the Blind [20 min.] Producer: Sven Werner, Luxemburg

Emerging Artist Award   

  • Let Us Spell It Out for You [2:36 min.]  Producer: Joseph Santini, US.

Monica Moshenko Interviews Howard Renensland, Founder & CEO, [with]tv

Monica Moshenko, host of Disability News & Views Radio Show has interviewed [with]tv Founder and CEO, Howard Renensland.  On her website she introduced Howard by writing this:

Howard Renensland, Father, Advocate, Actor and CEO & Founder, [with]tv

[with]tv
is a start-up corporation devoted to providing television and Internet
programming of, by, and for people with disabilities. Driven by his own
experiences the past 22 years advocating for his own daughter Victoria,
Howard found the single most debilitating factor limiting people with
disabilities is not their disability, but their image in mainstream
media. There is no mainstream television channel in the world
addressing the needs of and targeting people with disabilities as
viewers, consumers and participants. Howard resolved to change that by
creating , an inclusive media outlet that defines all people by their
talents and the quality of their stories, rather than by disability; a
place where his daughter Victoria and everyone else can work in a
universally designed workplace with a welcoming, inclusive workforce –
with-tv is born. Listen to this compelling interview with Mr.
Renensland to learn more about with-tv and how you can get involved
now! http://www.with-tv.com Television of, by and for people with
disabilities…..and everyone else.

Mr.
Renensland, President and Founder of [with]tv, has been a professional
actor, writer, director, and teacher for thirty years. He is a member
of Screen Actors Guild, American Federation of Television and Radio
Artists, and Actors Equity Association. Mr. Renensland has appeared in
over 400 television commercials, numerous radio ads, and hundreds of
print ads as well.

LISTEN TO THIS!

Thank you, Monica!

Cross-posted on [with]tv 

"Big Al" Makes a Name for Himself

Alex Moshenko is the son of disability advocate Monica Moshenko, Parent, Advocate and Host of Disability News Radio and friend and volunteer of [with]tv.  This is her son’s story:

"My name is Alex Moshenko. I am 14 years old now. I was diagnosed with a form of autism, Asperger syndrome, when I was six. I never cared about it too much. I actually made someone laugh when I was first told about it, which is always a good start – better to laugh than cry."

The above is Alex’s introduction to an article he wrote for TAP Magazine: The Autism Perspective titled “Who is Big Al of Al’s Wrestling Talk?"

"Ever since then, I have had sensory issues and social skills problems, but I am able to stick to something and learn all I can from it. I have been on TV multiple times and in the newspaper a few times too. I have been an advocate for autism since I was about eight years old. It was then that I first found out about wrestling."

Like his mother, Alex is now the host of his own radio program: Al’s Wrestling Talk

Meet Alex and read his story, in his own words, at:

Living with ASD / UNDERSTANDING AUTISM By Alex Moshenko :
Download  tap_2007_3_who_is_big_al_21.pdf

And keep an eye out for this young man.  I think this is a "you ain’t seen nothin’ yet" kind of situation!

Continue reading “"Big Al" Makes a Name for Himself”