Disability Blogger Linkup

It's time for the February, 2017 Disability Blogger Linkup!

If you are new to linkups, 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 the main page of the website it's on.

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 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, March 10, 2017.

Throwback Thursday

Three years ago in Disability Thinking ...

Two Down, One To Go
February 9, 2014

Three years ago, it looked like we might be seeing a boom in disability on TV. Three shows premiered in the same season with important disabled characters ... two half-hour comedies and one hour-long police procedural, which was also a remake of a classic series from the '60s and '70s that featured an iconic disabled character. One of the shows, The Michael J. Fox Show, even had a disabled character played by an actor with the actual disability. Growing Up Fischer had an exceptionally talented and well-liked cast, plus some innovative storytelling techniques. The shows all looked promising.

All three series failed though, and they were all so "meh" that I don't remember any anger or mourning in the disability community.

The next big news for disability on TV came a year later. It was American Horror Story, with the season titled Freak Show, about an ensemble of literal early 20th century "freaks"... that is, disabled, physically deformed people ... in a traveling show. "Freak Show" was divisive just within the disability community, even before the first episode aired. Proponents pointed out that some of the disabled characters were played by actors with the actual disabilities, and argued that depicting the real-life historical abuses of "freak shows" could provide a platform for promoting more progressive messages about disability. Detractors countered that no positive "messages" imaginable could overcome the ugly stigma and visceral trauma of watching a show about the cruel exploitation of "freaks."

As it turned out, "Freak Show" was something of a dud, too. It was neither as exploitative as feared, nor as revolutionary as hoped. It had moments of both horror and insight, but the show itself was too flawed in other ways to boost any really positive or even interesting ideas about disability.

I guess that's one of the key things about disability on TV. No matter how "good" the disabled characters and disability stories are, if the show itself is weak, it won't work, and it won't matter.

Today, we have Speechless, a character-driven, family-based comedy that is largely, though not exclusively focused on a nonverbal teenage boy who uses a wheelchair. The show has done a lot to get the disability details right ... including casting a disabled actor to portray the disabled teen ... and the disability community mostly loves the show. But the reason that even matters is that the show is good in general, and it is broadly popular.

I wonder if the creators of Speechless studied the failed disability shows of 2013/14 to identify what worked, and be alerted to what didn't. If so, those disappointments appear to have been worth it.

Weekly Reading List

Since I took a couple of weeks off from blogging, this week's reading list is playing catch-up.

Will Disability Rights Have a Permanent Place in the White House?
David M. Perry, Pacific Standard Magazine - January 26, 2017

The title question never really comes up in the article, but it's the question you want to ask after reading it. The article is actually a lovely talk with Maria Town, who had a job in the Obama White House specifically dedicated to the disability community. I'm feeling very nostalgic about the Obama Administration right now, but I think even if you didn't like him, if you're a disabled American, you almost have to have felt good that there was a smart disabled person working in the White House on disability issues. I think there should always be someone in that job in the White House, even though I can't at present begin to imagine who that might be or how it would work out in the Trump Administration.

Watch the Appointments
Ari Ne'eman, Sometimes a Lion - January 22, 2017

I'll make this short. If you want some expert analysis of the actual political landscape facing the disability community right now ... and you want it to be sober and non-panicky, but also realistic ... read this. Every time Ari writes or speaks about disability issues, he covers lots of familiar territory, but adding an extra layer of depth that doesn't usually make it through into disability activism Tweets and Facebook posts.

Why I've Given Up On Being Healthy
Jody Allard, BuzzFeed News - January 24, 2017

If I include an article on this list it usually means I like it, but this really is one of the best articles on disability I have ever seen in a mainstream publication. It's an account of one person's journey with disability, but almost by accident it ends up being

I Don't Speak for Laura
George Estreich, New York Times - January 27, 2017

There's so much standard smarm and sentimentality from parents writing about their disabled kids ... so when a parent shows a modicum of self-reflection and humility on the subject, it's gold to me. That sounds like I'm minimizing this piece, but actually I think it's really good. This belongs on the list of Essential Reading for "Special Needs Parents."

Take Me As I Am: Dating and Disability Etiquette
Vilissa Thompson, Easterseals Thrive

Vilissa is one of the best disability bloggers / writers out there, but she usually writes about somewhat heavier social justice topics. So it's great to read her thoughts on dating and disability. I wish someone had given me something like this when I was a teenager, wondering whether dating and relationship topics were even applicable to "someone like me." Add this to the "Essential Reading for Youth with Disabilities" list.

Affordable Care Act Repeal

There are two aspects of the disability community’s discussion about possible repeal of the Affordable Care Act that I think need more clarity. First is the enormous variety of reasons, good and bad, that people have for opposing the ACA. The second is what the actual consequences of repeal would be, (with or without replacement), for people with disabilities.

Over the weekend I did some brainstorming on these questions, which I want to share. I’m not going to go into depth on each item or observation. I just want these ideas out there.

First question: Why do people oppose the Affordable Care Act?

1. Philosophically & morally opposed to government involvement in another major industry -  healthcare.

2. Philosophically & morally opposed to the individual mandate to buy health insurance.

3. Believe good health insurance is a reward for hard work, not a universal right.

4. Want better health insurance, but don’t trust the government to handle it right.

5. Believe the ACA is too much of a gift to private insurance & pharma industries.

6. Want a single payer national health insurance program.

7. Unwilling to sacrifice any (more) of their own wealth to make things better for others.

8. Wealthier people who resent paying higher taxes on their excellent private health insurance plans.

9. Marginally poor / working class people who resent paying premiums on the ACA markets while others get Medicaid.

10. Blame rate increases on the ACA, even though rates almost always went up each year BEFORE the ACA.

11. Still associate the ACA with the website rollout debacle.

12. Unaware of how crucial the ACA has already become to tens of millions of people.

13. Don’t understand how popular parts of the ACA, like covering pre-existing conditions, depend on unpopular parts, like the individual mandate.

14. Some younger, healthier people would rather pay extra-low premiums for very bare-bones insurance plans that the ACA prohibited.

15. Confusion … some honest, some willful … between repealing the ACA and fixing its flaws.

16. Not clear on what the ACA is, what Obamacare is, or how health insurance even works. It’s all confusing and yuck!

17. Believe the ACA is a disaster because “everyone” says so.

18. Instinctively don’t believe that Trump or like-minded Republicans would really do anything truly harmful.

19. Believe that some are just panicking, while others stoke the panic for partisan political reasons.

20. Compelled to undo Obama’s signature accomplishment because … well … OBAMA.

Note that you don’t have to think all of these things at once to oppose the ACA. In fact, some of these reasons come from polar opposite ends of the usual political spectrum. And, it should go without saying that I, personally, do not subscribe to all or most of these reasons. It should go without saying, but I feel like I should say it anyway. I love "Obamacare." It enrages me that a few slightly different election outcomes in the Midwest and we would be discussing serious plans to make the ACA better. But, things are as they are, and instead we're on the defensive. So ...

Second question: What are the likely consequences for disabled people if the Affordable Care Act is repealed?

First of all, let’s talk about people dying. Saying "disabled people will die" probably sounds like politically motivated exaggeration to a lot of people who aren't familiar with disability issues. Disabled people WILL die of course, if the ACA is repealed. Even if is replaced, if it is replaced with any of the models Republicans in Congress are batting around now, people will die who wouldn't have died otherwise.

However, premature death isn't the only consequence of ACA repeal for disabled people. To mention just a few others:

1. Ending Medicaid expansion in states that opted to implement it would cause many medium-income disabled people to lose Medicaid eligibility.

2. Losing Medicaid means losing home care, which many disabled people absolutely must have in order to live independently and productively.

3. More disabled adults would have to continue living with parents, or go back to living with parents, curtailing their life development and exhausting families physically, emotionally, and financially. 

4. Many disabled people, deprived of work, unable to function independently due to loss of home care and other supports, would wind up in the care system of last resort: nursing homes ... paid for by Medicaid once every penny the person has is spent.

5. Most disabled people need and use health insurance all the time, not "just in case." We can’t shop around or risk going without in order to economize.

6. Chronic and delicate medical conditions would go untreated, or inadequately treated, resulting in more illness and disability, which is both traumatic and costly.

7. Lack of health insurance, and insecure health insurance, makes it much harder for disabled people to get and keep secure employment.

8. Disabled people who have jobs that include health insurance would be trapped by their jobs, unable to pursue better, more suitable employment opportunities.

9. Not being able to stay on parents' health insurance in the early 20s would make independence and starting strong careers much harder for disabled youth.

10. Disabled people who have managed to cultivate fulfilling life goals and dreams would be thrown back into sheer survival mode, to nobody’s benefit.

These consequences are serious enough, without even considering an actual death toll.

So, what does all of this suggest about how to confront ACA repeal? I don’t know. Maybe just that while we hammer away at the broad, blunt concept of ACA repeal, we also need to pick apart the opposition and take time to explain in detail what it all means specifically for disabled people.

Yes, it's annoying and offensive that we keep having to explain ourselves. But if ever there was a time to repeat the obvious to people who should already know, this is probably it.

Disability Blogger Linkup

I'm shifting to a monthly schedule of weekend-long Disability Blogger Linkups instead of bi-weekly. This is January's linkup, all ready to be packed with disability writing goodness.

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 the main page of the website it's on.

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 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, February 10, 2017.

Weekly Reading List: Children & Youth Edition

A lot of my disability reading this week had to do with kids ...

Beating of Disabled Teenager Highlights a Crime That Often Goes Unpunished
By Mitch Smith and Richard Pérez-Pena, New York Times - January 6, 2017

Whenever another case of horrific individual cruelty against a disabled person comes to light, my first instinct is to want to put it into context. And I don't mean mitigating context. In cases like this, I mean remembering that these situations and acts aren't super-rare, and the youths who did it aren't evil unicorns. They reflect fairly common ableism that's usually muffled by layers of social norms that these kids apparently lacked or rejected, on that day, for a hundred reasons we'll probably never really know. Like many other disabled people whose comments I've read, I am just as upset that this case got so much attention mainly because white supremacy apologists and racism deniers hyped it for their own purposes. It's all a fucking mess.

The Life of a Disabled Child, From Taunts to Hate Crimes
Margaret Carlson, New York Times - January 6, 2017

This is hard to read because there's a lot of disability thinking in it that is just past expiration date. Veteran NYT columnist Margaret Carlson is on the right side of things here, and she's sincere. But once again the actual disabled person, in this case her brother, appears as an abstraction, and her concept of systemic progress is a decade or two old. Still, I'm glad she chose to add her thoughts and experiences to the conversation.

What About Dignity and Respect? When Our Disability Attitudes Fail Us
Ellen Stumbo - January 6, 2017

I keep meaning to go back and try to say something useful about the conflict, (maybe disconnect is a better word for it), between "Special Needs Parents" and disabled adults. Ellen Stumbo makes an incredibly moving and helpful contribution here. Her courage to be self-critical suggests that maybe it's time for a disabled adult to write something that endorses what she says here, but also questions some of the stridency and self-righteousness we often convey when we write about the tone and practices of disabled kids' parents.

Schools Get Guidance On Restraint, Seclusion
Michelle Diament, Disability Scoop - January 6, 2017

I only hope that all this effort by the Education Department doesn't get flushed in the first 100 days of the Trump Administration, during some kind of "clean sweep" of "regulations and mandates." On the bright side, you can reverse laws and eliminate regulations, but you can't as easily suppress good ideas. Once spoken and documented, continue to exist regardless.

Three Tips to Make Classrooms Mobility Device Friendly
Zachary Fenell, Think Inclusive - July 9, 2016

What I love about this article from last summer is that the advice in it comes from disabled adults who were asked to suggest ways to make school better for disabled kids. While we obviously don't have all the answers ... and our perspectives can become skewed by either nostalgia or trauma ... we have been there, and as adults we have the tools to interpret our experiences the way many kids can't yet for themselves. It is truly surprising how seldom disabled adults are asked to weigh in on how best to raise, nurture, and educate disabled kids.

Disability Podcasts ... Updated

It’s been awhile since I posted about disability podcasting. That’s partially because there is still surprisingly little of it out there. What I mean by “little of it out there” is that there are few podcasts by disabled people posting episodes regularly. My own podcast’s checkered, inconsistent history is a good example. I also get the feeling that the same creative impulse that prompts people to do audio podcasts is being channeled more into making YouTube videos. Still, there are a couple of newish disability-themed podcasts I listen to that are worth your time.

The Accessible Stall

Emily Ladau and Kyle Khachadurian are friends who have different disabilities, and subtly different ways of thinking about disability and disability issues. Actually, sometimes the difference isn’t subtle, though their disagreements never become unfriendly. Basically, this is the podcast to listen to if you want to explore the pros and cons of different schools of thought on disability. It sounds serious, and it is in intent, but the dialog itself is fun and surprisingly light. This is a great podcast for anyone in the disability community, but maybe especially for people just beginning to think about disability issues in a deeper way.

In Sickness + Health

I have only just started digging into this podcast’s back catalog, but I’m pretty sure I’m going to learn at lot from it. In Sickness + Health explores what you might call the chronic illness sector of the broader disability community, focusing on how we actually think about and relate to our bodies when they don’t work as designed … or when they actively rebel against us. I tend to gravitate more towards the social, political, and practical aspects of disability culture, yet my own disabilities very much fit into the more medically involved chronic illness zone. So this podcast is probably perfect for me. At the same time, it also seems to do a good job of connecting the very personal physical and emotional aspects of disability with the social and political dimension. Basically, I am very intrigued. I’ll be listening more in the near future.

Note: I am also adding this as an update to a post I did back in August, 2014: Disability Podcasts.

Weekly Reading List

Welcome to the first Weekly Reading List of 2017.

2016 People of the Year: The Resisters
Josie Byzek, New Mobility - January 1, 2016

This is an interesting format for a disability rights news article ... a series of profiles of key individuals involved in a specific issue. Besides that, the public relations fight against the "Me Before You" film was definitely one of the bright spots of 2016, even if the film itself was one of the year's darkest moments for disabled people. And tying it in with other aspects of "better dead than disabled" trends is astute and important.

Defending Health Care in 2017: What Is At Stake in New York State
Families USA Fact Sheet - December, 2016

Whatever happens to health care programs on the federal level, people are probably first going to notice real-life changes in each state, and it's going to play out differently in each one. The sooner we come to grips with that layer of the issue, the better.

Disabled Community Weighs In On Ride Sharing
Dave Lucas, WAMC Northeast Public Radio - December 29, 2016

I have to admit that I'm not sure myself how feasible it is for services like Uber and Lyft to provide equal service to wheelchair users. Guide dogs and providing reasonable personal assistance, absolutely. That should be no problem at all. But a certain segment of the wheelchair using population needs adapted vehicles, and that's a tough thing for a loosely organized group of contractors bound by an iPhone app to provide. What I can't stand though is lawmakers saying that accessibility and equal service are detailed to be worked out later. We know from experience that details are never worked out later. They have to be worked out from the start, no matter how hard it seems.

I had a lump in my breast. So why did the radiologist focus on my disability?
Susan S. Turner, Washington Post - January 1, 2017

I don't mind doctors, nurses, and medical technicians being curious about my disability. Within reason, I am happy to "educate" them. I think what we're all looking for is a modicum of courtesy and self-awareness, along with a recognition that our disabilities aren't always at the center of our medical problems. Sometimes, disabled people are just plain sick.

Tips for Creating a Home for Aging Owners
Kaya Laterman, New York Times - December 30, 2016

It's good to see a high-quality article in the New York Times on making homes accessible, and the aging connection is obvious. I just wish there wasn't still such a divide between articles on "aging in place" and articles on "accessibility for the disabled." They call for the same steps, even if they aren't exactly the same topic.

Top Ten Posts of 2016

Inspired by a New Year’s Eve Top Ten post by fellow disability blogger Vilissa Thompson, here are the Top Ten posts of 2016 here at Disability Thinking:

10. Three Threats To Disabled People Today
July 6, 2016

9. Independence Day
July 4, 2016

8. What's The Problem?
September 27, 2016

7. I Used To Think ...
August 16, 2016

6. Looking Ahead To The 2016 Paralympics
July 5, 2016

5. Growth Attenuation
March 25, 2016

4. Disputing "Ableism"
January 22, 2016

3. #CripTheVote: Notes On "Crip"
March 29, 2016

2. Weekly Reading List, March 28
March 28, 2016

1. Disability Etiquette In 3 Questions
August 6, 2016