Aaaand We're Back!

I've been on an extended blogging break since December 2, 2017.

The conventional explanation is that I ran out of things to write about. It's more accurate to say that I had lots of ideas that seemed good for 20 minutes or so, but then quickly became stale. Now I've got several topics to work on that have stayed interesting to me for at least several weeks. Hopefully they will all turn into posts worth writing and reading ... something a little more than the usual themes of disability rights in the late 2010s.

I will start back for real with a Disability Blogger Linkup this Friday, February 9, followed by a regular blog post on February 23, then a Monthly Reading List on the 28th. I'll probably stick with that basic monthly routine for awhile. I am also thinking of adding occasional very short "Disability Thought Of The Day" posts. We'll see about that.

However it pans out, it feels good to be back and thinking again about the Disability Thinking Blog. I have missed it.

Disability Blogger Linkup

It's time for the November, 2017 Disability Blogger Linkup! If you are new to this, click here to see previous Disability Blogger Link-Ups.

The idea is to share something you have written that's about disability in some way. Please be sure to link to a specific article or post, not just the main page of the website it's on. Also, to make the links easier for visitors to identify, in the “Your name” blank, type the title of the article you are posting. In the "Your URL" blank, paste the URL address of the item. Like this:

Name = Title of your article.
Your URL = Link to your article.

Then click the "Enter" button. That's it! If you have any trouble making it work, or have any questions, feel free to email me at: apulrang@icloud.com.

This Link-Up will close at Midnight Eastern on Sunday. The next Disability Blogger Link-Up will start Friday, December 8, 2017.

Monthly Reading List

Disability-related articles worth reading last month:

How to Get Disability Accommodations at School
s. e. smith, Teen Vogue - October 2, 2017

Why Sex Education for Disabled People Is So Important
Ariel Henley, Teen Vogue - October 5, 2017

Teen Vogue has been doing a lot more political reporting lately, most notably since last year's election. It's also publishing great and relevant writing on semi-political topics, including those related to disability ... like disability accommodations in school and sex education for disabled students. Whether it's a new practice or standard operating procedure for Teen Vogue, t's good to see sophisticated but at the same time accessible articles like this, by disabled writers, in a "mainstream" magazine.

The Conundrum of Consent, Care, and Disability
Emily Wolinsky, Medium - October 14, 2017

This Is Why Consent Doesn’t Exist For Disabled Folks
Mia Mingus, The Establishment - October 29, 2017

These two disabled writers do rather different things, in different but similar online publications, with the same topic ... the meaning of consent when you need other people to help you with basic self-care. It's one of those areas where disabled people have to assert contradictory things. We have to convince people that depending on other people to "wipe our butts" doesn't mean an inherent loss of dignity. Independence is possible, with the right help and tools, even for a quadriplegic. On the other hand, we sometimes need to remind ourselves and others that this reliance does imply a loss of autonomy that isn't always a fair trade. We have to admit that those able-bodied people who fear the loss of dignity that they see in disabled people are, in a way, onto something.

You Are Special! Now Stop Being Different
Jonathan Mooney, New York Times - October 12, 2017

Mr. Mooney starts out with a vivid, down-to-earth description of what it's like to be a kid with Attention Deficit / Hyperactivity Disorder, (A.D.H.D.). This in itself is valuable because A.D.H.D. is still a fuzzy concept in some peoples' minds, including my own sometimes. Much of my professional life was in the 1990s and 2000s, so there is still a little corner of my brain that thinks of A.D.H.D. as a former "disability du jour," a condition that suddenly everyone was talking about and every kid seemed to have. Today, that might be anxiety. But, these conditions emerge and become talked about because they need to be described, studied, and talked about. So even now, Mr. Mooney's testimony is important. At the same time, he gives a crystal clear explanation of the Social Model of all disabilities ... the fact that in addition to our disabilities themselves, we have to deal with the way society regards them, and usually those barriers are the hardest to deal with. That's not an especially new idea, but it keeps needing to be explained in fresh terms.

Upcoming Blog Topics

I was meant to put up a blog post this weekend, But, instead of writing a complete post on one topic, I ended up brainstorming at least four different topics I want to write about over the next few months:

Disability Communities: Contested Ideas and Non-Negotiable Principles

What principles are we mostly settled on, and which are still largely contested within the disability community?

Disability Communities: Radicals, Activists, and Everyone Else

In which I continue to try to sort out the different subdivisions and mindsets within the disability community.

Special Needs Parents vs. Disabled Adults

An attempt to understand this very awkward, sometimes nasty and mutually traumatic relationship.

Three Trends In Disability Activism

Things have changed in thinking about disability, mostly for the good, but changes should at least be noted.

Anyone have any other ideas? What topics or questions aren't getting enough attention in disability blogging and journalism? Share your ideas in the comments section below.

Disability Blogger Linkup

It's time for the October, 2017 Disability Blogger Linkup! If you are new to this, click here to see previous Disability Blogger Link-Ups.

The idea is to share something you have written that's about disability in some way. Please be sure to link to the specific article or post, not just the main page of the website it's on. Also, to make the links easier for visitors to identify, in the “Your name” blank, type the title of the article you are posting. In the "Your URL" blank, paste the URL address of the item. Like this:

Name = Title of your article.
Your URL = Link to your article.

Then click the "Enter" button. That's it! If you have any trouble making it work, or have any questions, feel free to email me at: apulrang@icloud.com.

This Link-Up will close at Midnight Eastern on Sunday. The next Disability Blogger Link-Up will start Friday, November 10, 2017.

Monthly Reading List

My favorite articles from September, 2017:

My daughter doesn’t have ‘Special Needs,’ She’s disabled
James Davis Smith, Washington Post - September 28, 2017

There are a few lines here that made me raise my eyebrows, but overall it’s a welcomed endorsement by a parent of a disabled child of the idea that parents of disabled children should notice and listen to the broader disabled community. If nothing else, Mr. Smith capably explains why people are drawn to saying “Special Needs,” and why they should feel comfortable saying “disabled” in stead.

Arresting Disabled Bodies
Sarah Jones, New Republic - September 28, 2017

This is one of the most insightful mainstream magazine articles I have seen on the complex meanings involved when disabled activists like members of ADAPT protest and get arrested. On one level it's quite simple ... people who suffer the most from bad health care policy have good reason to make their protests as aggressive and dramatic as possible. But this writer also gets how ADAPT uses people's ableist assumptions ... especially their paternalism and pity reflex ... to draw attention to more substantive issues like health care, and at the same time contradict the assumption that disabled people are passive and weak.

6 Ways Your Social Justice Activism Might Be Ableist
Carolyn Zaikowski, Everyday Feminism - September 20, 2017

This goes well beyond Disability Prejudice 101. Every item here is a real and specific problem disabled people encounter within progressive culture. But for me, item 5 is the most welcomed observation ... that "policing and enforcing academic rhetoric" can be exclusionary and alienating to people we don't want to exclude or alienate. This is not a whiny, privileged attack on "political correctness." It is a real, internal critique of our excessive use of jargon. To me it also suggests a related problem, in which "academic rhetoric" ends up becoming more important than the ideas and issues it is meant to describe.

The ‘Madman’ Is Back in the Building
Zack McDermott, New York Times - September 20, 2017

This is one of the rare articles on any kind of disability that manages to be gritty and pessimistic, while at the same time somehow liberating and uplifting. It presents a pretty negative view of mental illness ... one that doesn't seem too compatible with the idea of "neurodiversity," or the Social Model of disability. Yet, it doesn’t evoke pity, and it doesn't seem to me to suggest that people who are mentally ill are either dangerous or useless. Mostly the impression is that they are just massively pressured and trying really hard.

I have chronic pain and nothing works for it. I'm afraid I'll be forgotten in the opioid crisis.
Julian Malinack, Vox.com - September 28, 2017

I have to admit that while I think my views about disability in general have improved in the last couple of years, my views on chronic pain have probably gotten worse, mostly because of the opioid crisis. I need to read more articles like this one.

Who's Disabled?

People sometimes ask, "Is it okay for me to say I'm disabled?" What do they mean? A variety of things, I think:

• They have some condition that's in the ballpark of disability, but they have struggled personally over whether they themselves want to identify as disabled.

• They view themselves as disabled in some way, but worry that other disabled people won't accept that, or that they will be accused of "appropriating" disability identity and culture.

• They think that if they refer to themselves as "disabled", their friends and families will be sad or disapprove, or worse ... believe they are faking in order to gain some kind of advantage or benefit.

• They are focused on one of the more narrow, specific definitions of "disabled," such as qualifying for Social Security Disability, being entitled to a "handicapped parking" permit, or being covered under the Americans with Disabilities Act.

• They take the word "disabled" very literally, to mean unable to do anything. From this point of view it can seem both inaccurate, (everybody can do SOMETHING), and discouraging ... as if calling yourself disabled is not only descriptive, but predictive.

I've thought about it a lot, and here is the definition of disability that makes the most sense to me. It's a personal definition, not a legal or bureaucratic one:

If you have a physical or mental condition that you have to think about and plan around every day, then you are disabled.

This definition encompasses any physical, mental, cognitive, and sensory impairments. I personally don't include temporary impairments, impairments that are seamlessly adapted, (like glasses for nearsightedness), or ordinary variations in personality, talent, and physical makeup.

Any thoughts?

Disability Blogger Linkup

It's time for the September, 2017 Disability Blogger Linkup! If you are new to this, click here to see previous Disability Blogger Link-Ups.

The idea is to share something you have written that's about disability in some way. Please be sure to link to the specific article or post, not just the main page of the website it's on. Also, to make the links easier for visitors to identify, in the “Your name” blank, type the title of the article you are posting. In the "Your URL" blank, paste the URL address of the item. Like this:

Name = Title of your article.
Your URL = Link to your article.

Then click the "Enter" button. That's it! If you have any trouble making it work, or have any questions, feel free to email me at: apulrang@icloud.com.

This Link-Up will close at Midnight Eastern on Sunday. The next Disability Blogger Link-Up will start Friday, October 13, 2017.

Monthly Reading List

It has been a pretty good month for disability reading ...

‘I am a hard worker’
Terrence McCoy, Washington Post - August 27, 2017

The Washington Post has done a series of articles about "disability" recently ... focused on disability as it relates to employment and Social Security benefits. Most of the articles have been awful, full of vile stereotypes about disabled people, low income people, and people in certain regions of the U.S. They have also perpetuated politicized and easily debunked myths about SSDI and similar benefits. However, this latest article at least, and at last, tries to convey the web of barriers many disabled people encounter when they try to get jobs ... from the classic "work disincentives" built into benefits systems, to intersecting factors like poverty, poor education, and simply the way today's economy and job markets are structured. More pieces like this would be ... better.

Florida Demands Parents Call Their Kids 'Limited' or Lose Health Care
David Perry, Pacific Standard - August 28, 2017

This article highlights some pretty profound contraditions in thinking about disability ... so many and so hard to discuss that I will probably have to blog about it separately. On one level, it is about straight up dishonesty and corruption in Florida disability services. On another level, it's about the unnecessary insensitivity and cruelty that creeps into disability service bureaucracies. On a third level though, I think it also calls on all of us to revisit our fundamental understanding of disability, maybe for a third or even fourth time. I'll try to explain what I mean at some future date.

My IEP Gave Me PTSD: A Student's Perspective
Mandy Ree, Ravishly - August 18, 2017

This piece gave me some of the same feelings as the first one. There is a straightforward story about services that are supposed to help disabled kids being dispiriting and traumatic for them. At the same time, there is probably a deeper story to be picked apart about how Special Education got to this point. My take is that the increasingly pedantic coldness of IEPs is at least partly a result of two praiseworthy efforts: 1. Expecting Special Education to include more 'education,' as traditionally understood, and 2. holding Special Education accountable for educating disabled kids. But we haven't figured out how to get tough in these good ways without making the whole process mean and scarring for actual disabled kids.

What Is Identity-First Language, & Should You Use It?
J.R. Thorpe, Bustle - August 9, 2017

This goes into my growing collection of especially good explanations about the differences between Person-First and Identity-First language. This one does three things I always look for in this kind of discussion. 1. It gives a fair hearing to Person-First langauge, and doesn't simply label it as an ableist plot of non-disabled meanies. 2. It addresses head on the idea that even having these discussions about language might be a bit trivial. And 3. It reinforces the call to let disabled people ... meaning each disabled individual ... choose the language they prefer at any given moment in their lives.

'You don't break a promise you give to yourself'
Cara Chapman, Plattsburgh Press-Republican - August 9, 2017

I added this article from my hometown paper because it both is and isn't a "disability story." On the surface, it's about a police officer's perseverance and grit in the face of a bit of bureaucratic absurdity. It's also about a good boss, the Police Chief, who does seemingly all he can to help someone return to work after a period of medical leave. He's even willing to go on record saying he objects to the barriers the officer faced. At the same time, underneath the surface, it could and maybe should have been a story about employment and people with disabilities, the ADA and reasonable accommodation, and about how disability discrimination often hides in fine print and procedures rarely questioned.