Poverty in America

Poverty and Disablism

Published May 01, 2009 @ 11:35AM PT

Hey all, it's BADD! Click the logo on the left to visit the BADD homepage at Diary of a Goldfish and read all the BADD posts as they come rolling in.

I'm attempting to be an ally to my Autism colleague Dora Raymaker and other blog friends by participating in Blogging Against Disablism Day.

Disablism, or ablism, as it's known in the US, is prejudice towards people with disabilities.  Like racism or sexism, it can be individual or institutional (why isn't every single place we traverse handicap-accessible??).  In the US and worldwide, people living with disabilities are overrepresented among the poor.

One only need read the regular comments of our fabulous reader Danetta to understand how closely being disabled - or differently abled - is to falling into poverty and getting stuck there.  To that end, our fabled notion of "bootstraps" can be unintentionally discriminatory.  I don't know about you, but what comes to mind for me with that phrase is an able-bodied man tugging on his boots and then heading outside to earn a day's wages!  So hearty!  So feisty!  So independent!

We make it extremely difficult for those living with mental illness or developmental or physical differences to be as independent as that notion conjures.  I personally feel particularly passionate about the issue of mental health.  My mom is a mental health practitioner for 2 decades now, and is often repeating that we need to think of mental illness like we would diabetes, absent stigma and shame and meager resources (though this assumes we don't highlight diabetes in our attempts to shame overweight people for their size).  She's worked in public and private hospital settings, of late focusing on getting people out of institutional environments and into homes and/or community settings.  In my neighborhood, a group home often comes under fire from homeowners who dislike its presence on our blocks.  I seconded a participant on a neighborhood listserv who pushed back, saying that it's not up to us to restrict the rights of others to live in our neighborhood and that the diversity is welcome.  No surprise, this is the same homeowner's association who rails against affordable housing plans, fullstop, without consideration for its overall necessity and potential to benefit the neighborhood with tenants who are not local college students.  (We live in the shadows of Boston College, and a stone's throw from Harvard and BU.)

Finally, I come from what my aunt describes, herself include, as a "long line of drunks and nuts."  There's something comforting in that, an empathetic ear when I need one, and an accompanying lack of judgment.  Poverty and disability are present here, but mostly what I find when I'm with my relatives is a lot of love, warmth, togetherness, irreverent perseverence - and a hell of a lot of intimate knowledge of the modest strengths and major limitations of our social safety net.

Share this Post

Related Posts

Comments (4)

  1. Mark Romoser

    Have you run across any disability initiatives in your travels to New Orleans and the Gulf Coast? One of the many ideas I generated in the months after the Federal Flood was that all that new construction down there would have to be ADA-compliant, giving the "World's Most Interesting City" a chance to become the "World's Most Accessible City" as well.

    Posted by Mark Romoser on 05/01/2009 @ 04:54PM PT

  2. Leigh Graham

    Mark - that's a smart idea, and you know, I have not!

    Posted by Leigh Graham on 05/01/2009 @ 07:28PM PT

  3. Kate Scott

    Mark- my organization- the Greater New Orleans Fair Housing Action Center- is currently investigating whether or not newly constructed multi-family developments in post-Katrina New Orleans are compliant with the accessibility requirements specified in the Fair Housing Act.  Look for the results of our investigation on this within the next few weeks.

    Posted by Kate Scott on 05/06/2009 @ 10:07AM PT

  4. Reply to thread
  5. Danetta Amschler

    That's a good point about boots and boot straps.  First off, one has to be able to afford boots to even have the possibility of having boot straps by which to "pull oneself up".   Secondly, even if one has boots - with boot straps - one must be able to put on said boots before one can use them to pull one self up.  Among my disabilities is arthritis of the Facet joints of my lumbar spine - odds are, if I got the boot on (which would be a rare day), I wouldn't be able to pull myself up by any boot straps or get the boot off by myself at the end of the day.  The docs would prefer I quit walking stairs - so I keep asking when they're going to fund my move and the difference in my rent.  See, between the arthritis and some hip and knee problems, I'm doing good to keep my dog walked.  Never mind athletic feats like putting on boots and pulling myself up by boot straps.

    But I swear, if (here in real life) I hear one more person going on about how the disabled "don't want to work" and "choose" to be disabled to receive health care I'm going to scream.  I'd love to work if only I could find something that didn't annoy my disabilities (and sitting very long is a problem, so are florescent lights due to neuro problems that are triggered by light).  Then again, any remote chance at work that I even MIGHT have would be totally dependent upon my ability to get timely access to appropriate medical care, so unless our health care system is fixed it looks like I'm stuck here on SSDI until I'm either magically cured of some incurable conditions (or at least treated with stuff not invented yet) or the system is finally fixed - so I'm not holding my breath to return to work anytime soon, as much as I'd LOVE to do so.

    Then too, even if I did get to work, I'd need an awfully understanding employer.  Between the arthritis, light triggered neuro stuff, gastroparesis, and using a service dog for the neuro stuff and PTSD (another of my disabilities - and one few are willing to accept as based on how so many seem to think mental illness is contagious or it means I'm just waiting to be predatorially violent) - I suspect I'd be pushing the limits of the ADA.

    Come to think of it, I could probably come up with ideas for snarky (but not necessarily post appropriate) responses to "pull yourself up by your boot straps". 

    Posted by Danetta Amschler on 05/02/2009 @ 07:32AM PT

Add a Comment

For your comment to be published, you will need to confirm your email address after submitting your comment.

If you already have an account, click here to log in.

Comments on Change.org are meant for further exploration and evaluation of the ideas covered in the posts. To that end, we welcome constructive comments. However, we reserve the right to delete comments that are offensive, abusive, or off-topic; that contain ad hominem attacks; or that are designed to subvert or hijack comment threads rather than contribute to them. Repeat offenders may be permanently removed from the site at our discretion.

Author

Twitter Feed

Leigh Graham

Leigh is a PhD candidate in urban planning at MIT, and a consultant on U.S. Gulf Coast recovery. She sits on the Board of the Allston-Brighton Community Development Corporation in Boston, and has worked with non-profits, foundations and local governments on policies and programs aimed at reducing urban poverty and inequality.

close

This user's Profile page is not public. They have restricted it to only their friends.

Already a Member?

Create an Account

You must create a Change.org account to complete this action.
If you already have an account click here.