All posts by Anna

Call to Action: Tell Parliament to Stop Discrimination against people with disabilities who immigrate to Canada

An awesome way to guarantee that you will not be allowed to immigrate to most countries – even if you otherwise completely qualify – is to have a disability, or have a disabled immediate family member.

Despite the Canadian Charter of Rights and Freedoms explicitly guaranteeing that laws in Canada cannot be written to discriminate against people with “mental or physical disabilities” (Section 15 of the Charter), Canada’s Immigration Act allows someone who otherwise passes all of Canada’s immigration requirements to be denied immigration because they “might reasonably be expected to cause excessive demand on health or social services”.

What has this meant in practice? Well, in 2009 Chris Mason, an immigrant from the UK who was injured on the job while working legally in Canada, was deported back to the UK because of his disability. In 2010, Ricardo Companioni was initially denied immigration to Canada from the US because of his HIV-positive status, but managed to argue in Federal court that he and his partner would pay for their drug treatments and thus not be part of Canada’s care system – a solution that is not available to many people. In May, the Barlagne family lost their appeal to be allowed to stay in Canada, as their youngest daughter has Cerebral Palsy. The reasoning was that the court did not believe the Barlagnes would be able to pay for their daughter’s care.

None of these stories are unique. Even when the Bill was being debated in Parliament, Members were bringing up concerns about how the “excessive demand clause” would affect people whose families had disabilities. In 2000, when Wendy Lill, a Member of Parliament, asked:

We have a charter of rights which talks about each Canadian being entitled to equality under the law. The Will to Act Task Force, which was established several years ago, talked about equality of citizenship for persons with disabilities.

Clause 34 talks about how a foreign national or other permanent resident would be inadmissible on health grounds if their health condition might reasonably be expected to cause excessive demand on health or social services. This is the only clause in the bill which seems to me would in any way relate to a person with a disability making an application to come to Canada.

I would like to know if a family with a child who has a disability such as Down syndrome or cerebral palsy would be accepted in this country. [emphasis added]

She was assured by the then-in-power Liberals that:

I think it is internationally accepted, in the Geneva convention and other statutes, that the best interests of the child can indeed be defined. In the case of a disabled child, I believe that the intent is to prevent abuse. The abuse might be that the only reason for someone wanting to come to Canada would be to seek free health care of some type.

However, in the case of family reunification, if we are talking about bringing a new family to Canada, if a child has a disability, frankly, I am absolutely confident, having met the men and women who work in citizenship and immigration, that we would take all of that into account and we would not allow it to stand in the way. [emphasis added]

I’m very happy for the no-longer-in-power Liberals that they were certain situations like the Barlagnes would never happen in Totally-Awesome-To-People-With-Disabilities Canada, but since we live in this Canada, I think their optimism was misguided. As has been amply demonstrated by reality.

The Council of Canadians with Disabilities has recently written yet-another-letter urging the Hon. Jason Kenney, Minister of Immigration, to review the “excessive demand clause”. You can read the letter in full at their website.

I have adapted their letter to send to Mr Kenney, as well as my MP, and provide that letter for my fellow Canadians to adapt or use in any way they see fit.

This is a discriminatory policy. People with disabilities and their families are not drains on the Canadian economy. We are people, and we should not be denied equal rights because of our disabilities.

My letter is below:
Continue reading Call to Action: Tell Parliament to Stop Discrimination against people with disabilities who immigrate to Canada

Recommended Reading for Wednesday, June 2, 2010

Discrimination is only discrimination if you end up being sacked

The study apparently says that many people with MS put off telling their bosses (and so receiving appropriate accommodations at work, which might help them to manage their MS) because they are afraid they will be discriminated against.

Dr Simmons says that fear is unfounded, because “only 15 per cent of people [left] their jobs because they were sacked”.

I assume this means that that’s 15% of people leaving their jobs, and not 15% of people who told their bosses they had MS. If it’s the latter, that’s actually a significant amount of discrimination – about 1 in 6! But even if it’s the former, that seems to me to be fairly significant. It may be that not many people are getting sacked because of their MS, but it does tend to support the idea that it is a realistic possibility that you will be sacked if you tell your boss you have MS. In other words: the fear of discrimination (eventuating in unemployment) is hardly unfounded!

Screen Reader Access to SharePoint

As many screen reader users have found out the hard way; Microsoft’s SharePoint service is not very screen reader friendly. It can be navigated, but is clearly not understandable for your average user. Microsoft’s apparent lack of interest in adhering to w3c standards further complicates the situation. Despite this, many of us have to use SharePoint in our daily work. So with that said, I am writing this article to share with other screen reader users some tricks, tips and general information I’ve gathered over time while working on the “SharePoint issue”. I have primarily been working with the 2003 and 2007 editions of SharePoint, but most of these items hold true with 2010.

LINKAGE: Black Fashion Museum

Museums and other archival institutions typically display the extraordinary rather than the ordinary, the First Lady’s inauguration ball gown rather than her J.Crew shorts. But because of the implausible convergence of racial, gender, sexual, class, and language barriers that confront non-White and working women, their lives and their accomplishments were not deemed extraordinary in their time. The material evidence of these lives not considered important enough to save or to study. Museums and other archival institutions that privilege white middle and upper class women’s experiences collude in the ongoing marginalization and erasure of the material cultural histories of minoritized American women.

Call for submissions: /Slant/Sex/

This is a call for bold, honest investigations of the sexual female/trans self that polite society has yet to fully embrace.

We particularly encourage submissions from women of color, older women, queer women, women with disabilities, and transgender/two-spirit/intersex/gender nonconforming folks.

Experiences of Transgendered Profs a Case Study in Sexism

In an excerpt published in the Australian newspaper The Age, The Hidden Brain author Shankar Vedantam discusses the different post-transition experiences of transgendered Stanford professors Ben Barres and Joan Roughgarden. Unsurprisingly, they paint a depressing picture of the prevalence of sexism even in the supposedly egalitarian world of university research.

Where ever you are is where I want to be: Crip Solidarity

What does crip solidarity look like? Between crips?

We are traveling, trying to track down food. My chair can’t go into this restaurant, your dog isn’t allowed in that restaurant; so we will order in. You can’t fly to the meeting, so we will come to you—all of us. They won’t let you go to the bathroom because they say you’re “too slow”, so we will demand they do—and make them wait for you—together. Sometimes we are comrades, sometimes we are strangers, but we will stay together. We move together.

I know what it is like to be left behind, left out, forgotten about. I know you know as well. We vow to not do that together, to each other.

Canada: Council of Canadians with Disabilities Chairperson’s Update

The month of April is an important anniversary month for the disability community, and indeed all equality-seeking Canadians, because on 17 April 1985 Section 15, the Equality Section of the Charter of Rights and Freedoms, came into force. Governments had been given a grace period, where they had the opportunity to bring legislation and policies into conformity with the standard set by Section 15. As we all know, the Governments of the day had a very limited vision of what was required of them and few changes were made. When Section 15 came into force, Canada’s equality-seeking community began to make use of Section 15 as a new tool for eliminating barriers. CCD, and other groups in the disability community, began to undertake test case litigation, based on Section 15 and other articles of the Charter, to create equitable outcomes for Canadians with disabilities.

Headlines:

Discovery could help treat spinal injuries: U of A researchers uncover trigger that causes muscles to move without signal from brain

Canada: Schools lack access to mental-health professionals, report says

International Disabilities Alliance Disability Rights Bulletin May 2010

Global News

Spain first country to submit its initial report to the CRPD Committee

On May 3rd, 2010, Spain submitted its initial report, on the implementation of the Convention on the Rights of Persons with Disabilities, to the Committee on the Rights of Persons with Disabilities (the CRPD Committee). This means that Spain has become the first country to submit a report to the Committee on how the rights of persons with disabilities are being implemented. For the moment, the report is only available in Spanish. Please click the following links to have access to the report and its annex: Spanish report and Annex.

Elections for the CRPD Committee

The election of six Members of the CRPD Committee to replace those whose terms are due to expire on 31 December 2010, and to increase the membership of the Committee from twelve to eighteen persons as a result of the 80th ratification of the CRPD, will occur during the Third session of the Conference of the States Parties to the Convention. The Conference of States Parties will take place in New York from 1-3 September 2010.

On May 3, the Secretary-General of the UN sent a letter asking States Parties to nominate candidates to the Committee by July 1. The CRPD Committee has recently published a section in its website on these elections. For further information on the elections for the CRPD Committee, please click here.

IDA has prepared a number of documents explaining the process as well as a questionnaire to be filled in by candidates. Please click here to access these documents and to get more information on these elections.

IDA is including in its website, information on those nominations that have been decided at national level. To have access to the information on the candidates, please click here.

OHCHR

The OHCHR has recently published on its website on disability a new tool: “Monitoring the Convention on the Rights of Persons with Disabilities. Guidance for Human Rights Monitors.” Please click the following links to see this publication: pdf version of report or word version of report.

CRPD ratifications reach 86

The ratification of the CRPD by Nepal, on 7 May 2010, has increased to 86 the number of States Parties to the CRPD. Ratification by Nepal of the Optional Protocol (OP) increased to 53 the number of the States Parties to the OP. The number of signatures to the CRPD is 144, while the OP has 88 signatures.

Treaty Bodies

The CAT Committee, in its 44th session, considered from 26 April-14 May 2010 reports from Austria, Cameroon, France, Jordan, Liechtenstein, Switzerland, Syrian Arab Republic and Yemen. To have access to the disability analysis of the Concluding Observations adopted by the Committee during this session, please click here.

IDA prepared a number of documents (uploaded on the CAT Committee website) with suggested recommendations for the Concluding Observations, which were adopted by the Committee in this session. Some of these recommendations have influenced the Concluding Observations of the reviewed States such as Austria, to which the Committee recommended to cease immediately the use of net beds as it constitutes a violation of article 16 of the Convention.

Universal Periodic Review

The UPR Working Group has held its 8th session from 3-14 May 2010. In this session, the following countries were reviewed: Kyrgyzstan, Kiribati, Guinea, Lao People´s Democratic Republic, Spain, Lesotho, Kenya, Armenia, Guinea-Bissau, Sweden, Grenada, Turkey, Guyana, Kuwait, and Belarus. The review of Haiti was scheduled for this session but was postponed.

For an analysis of the refer ences to persons with disabili ties in the UPR Working Group reports, please click here.

Upcoming Meetings

The 54th session of the CRC Committee (25 May-11 June 2010) will consider reports from Argentina, Belgium, Grenada, Guatemala, Japan, Nigeria, The Former Yugoslav Republic of Macedonia, and Tunisia. OPSC: Argentina; Belgium; Colombia; The Former Yugoslav Republic of Macedonia; Japan and Serbia. OPAC: Argentina; Colombia; Japan; Serbia and The Former Yugoslav Republic of Macedonia.

Click here for the references to persons with disabilities in the States’ reports, lists of issues, and written replies.

Upcoming Session of the Human Rights Council

The 14th session of the Human Rights Council will take place from 31 May-18 June, 2010, in Geneva. Click here for further information on this session.

IDA has prepared a disability analysis of the following reports prepared for the 14th session of the Council.

Special Procedures

The following Special Procedures reports, which have been prepared for the 14th session of the Human Rights Council, include references to persons with disabilities: Independent Expert on cultural rights; Special Rapporteur on migrants; Special Rapporteur on education; Independent Expert on extreme poverty; Special Rapporteur on racism, and the Independent Expert on Haiti. For detailed information on the references to persons with disabilities in these reports, please click here.

UPR

All UPR Working Group reports, which were prepared at the 7th session of the UPR (February 8-19, 2010) and will be presented to the 14th session of the Council, include references to persons with disabilities. Click here for the disability analysis of these reports.

Other reports

IDA has undertaken an analysis of other reports that have also been prepared for the 14th session of the Human Rights Council. Click here to access this analysis.

About the IDA Disability Rights Bulletin

This bulletin is intended for experts advocating for the rights of persons with disabilities, in particular within the Geneva-based human rights framework. It is prepared by the IDA Secretariat, which also provides support to the Group of States Friends of the CRPD.

For more information about IDA, its CRPD Forum and its member organisations, please visit: www.internationaldisabilityalliance.org.

Contact us via email at: stromel@fundaciononce.es.

Signal Boost: Online Web Study on How People Give Route Instructions

The DiaSpace project in Bremen is running a brand new quick (5 minute) online web study into how people give route instructions in dialogue. This will be our final call for participation so we hope you can take this study!

The goal is that our findings will help us develop more responsive wayfinding systems so that people who can’t manually control their wheelchairs can interact via dialogue instead. Another application which we’re working on is about helping elderly people find objects in their home by describing where they are in an understandable way. So it’s all in a good cause!

Please participate, and just as important, please forward this email on to your friends! We’re really having a hard time getting enough participants who are native English speakers, as DiaSpace is based in Germany. The only conditions for participation are that participants be native or very fluent speakers of English and 18 years old or older, and not visually or cognitively disabled.

Here’s the link to the experiment.

The experiment only takes 5 minutes, and if you’re using Windows Vista, you’ll need to run it on Firefox, as it won’t work on Internet Explorer for Vista. (It works on Internet Explorer for other operating systems than Vista though.)

[I completed it and I assume it worked fine in Google Chrome.]

It also really is a very short experiment.

Recommended Reading for Monday, May 31

A Canadian quarter (25 cents) showing a woman using a wheelchair for curling
Description: A Canadian quarter (25 cents) showing a woman wheelchair curling. Photo by flickr user zzd, used under a creative commons license.

Comics and disability: XKCD and dyslexia, Natalie Dee and Tourette’s syndrome [I strongly recommend checking the comments on this one]

I’m not an expert in either of these disabilities. But I know enough about ableist jokes to recognize it when I see it: jokes that appropriate experiences and conditions without thought, without care, without any kind of redeeming value beyond a short laugh from a likely mostly able-privileged audience. And that is what both of the above instances look like to me.

I like both of these comics, and I’ll continue reading them. But this synchronicity of ableism was pretty disappointing.

No, I’m not okay: How I found help for anxiety

The pressure to be a “Strong Black Woman” plays a huge role in the way many of us were taught to deal with stress. Related to the concept of a “Superwoman”, the “Strong Black Woman” appears to hold everything in her life together seamlessly. Yet, there is often nothing further from the truth.

Faithful Fools Street Retreat, Gender Identity Disorder, and Disability As Class

Disabilities that directly rule out paid work** involve not only medical identity questions, but material consequences, too. Under capitalism, for example, everyone in the working class who is “able” to work — able to try to sell their labor power — is forced to do so in order to survive. People who are unable to work may or may not be sufficiently supported by governments and families, but regardless are often seen as burdens (unlike non-working owning-class people, whose mere existence and proprietorship are supposedly essential to a functioning economy). And so “disability” becomes its own system of distribution and class organization under capitalism. Welfare services help keep permanently unemployed disabled people alive (at least the ones deemed “worthy”), while both stigma and artificial scarcity of benefits help ensure that everybody else keeps working.

When is Gala Darling going to quit with the racist cultural appropriation bullshit?

Well, I am not internet famous, and I don’t particularly aspire to be internet popular. So I am just going to say this, and I hope you will say it with me: not seriously considering your white privilege when you are repeatedly called on it, and calculatedly using cultural appropriation to make yourself seem marketable and “glamourous” is racism. And deleting comments that call you out on this behaviour is unsurprising, but equally shitty behaviour.

American Able: Why Does Fashion Have To Give Us Complexes?

Almost a month ago, Worn Journal posted a condensed version of this interview on their website. It caused quite a stir, being linked everywhere from Jezebel, to Bitch Magazine, to Sociological Images. Today, if you haven’t already seen American Able somewhere in the blogosphere, you can catch it on the TTC in Toronto. And you can read the entire extended interview and article here!

Of interest:
70 books on feminism – note for ableist language throughout the piece. *sigh* And, of course, no books about disability & feminism. However, there are a long list of books there, and I know “what books should I read to get a taste of feminism” is a common question.

Saturday Poetry

While I can never deny loving YouTube vids of singing in Sign, I’d like to post some examples of other art created by people with disabilities. Today, I thought I’d link to some poetry.

I’m only going to quote a line or two from each poem, as I think it’s important to read the whole poem.

Until the Day by Laura Hershey

(Inspired by, and dedicated to, Constance McMillan)

Until the day
the two girls in tuxedos

Fallen by Elizabeth Switaj [In Black Market Review]

I am watching the angels break their skulls

They are not the angels

Above the Cafe, by Elizabeth Switaj

darken night with coffee

April Poetry by cripchick

if i had time to make a zine, i’d put all these poems together. april is national poetry month so a bunch of radical women of color poets and i attempted to write a poem a day. this is what came about for me (ones on the top are the most recent):

[There are 8 poems, I don’t want to quote just one.]

I would give…. by blackamazon [Trigger warning for description of self-harm]

I would give….
up

all hope

of ever being seen as beautiful

It’s Always More Complicated: The “Justified” Abortion

[Trigger warning for “disabled child = burden” narrative.]

Last night I was reading several pro-choice tumblrs, one of which had linked to “The Choice“.

What makes us human? When is a life worth living? Worth ending? How much suffering is bearable? Is avoiding suffering brave or is it cowardice? When is abortion justified?

Should Fred be born, my wife would never return to work. My daughters would always come second. Some basic research online and asking friends in health roles showed a high chance of divorce before my son was a teenager, the stress of care literally tearing our family apart. Every news article we read showed little or no government support, with charities closing their doors. The doctors were encouraging about support; the real life carers we spoke to, not so much.

I’d never support killing a born child on any grounds. Yet here I was, suggesting death for a child almost born. I may not be a good man, but I’m a husband and a father. Had we not known, I’d be living with Fred’s condition today; but we take the tests so we can act on the information received.

So, let a bad man say the words that will condemn me: Fred’s life would have been less than human. It would have been filled with love, yes, but mostly loneliness, confusion, pain and frustration. The risk to my marriage and the welfare of my daughters was too much. I chose to minimise suffering. For my wife, for my daughters, for myself and most of all for Fred, I chose abortion. It was a choice of love.

I have complex reactions to this that are not really easy to talk about, but the one thing I do want to make clear:

Abortions do not need to be justified.

I know there are strong political and advocacy reasons why stories like these – the so-called “justified” abortion – are told whenever people talk about abortion and the law. They are “good” abortion stories, with the happy family, the desperately wanted child, the “horrors” for everyone had the abortion not been performed.

I struggle with these sorts of stories because I don’t know a way to talk about them. I want to talk about the way that disability is discussed in them – always, always, as horrible, as tearing families apart. And yet, these are people’s lives. I don’t think in any way they made a “wrong” or “bad” choice, or a “brave” one, either. They made the “right” choice, in that it was the “right” choice for their family, and I fear that talking about the language used is abusive. You’ve shared your painful story, your very personal story, and I want to now talk about disability and how it’s used to score points in the so-called abortion debate.

And yet, I desperately do.

I deeply resent the way anti-choice advocates point at people with disabilities and talk about how they’ll all be eliminated if we allow abortion-on-demand. The sheer amount of hate directed at Don when he goes to pro-choice rallies by the anti-choice contingent, because they see him as a traitor to their cause, is amazing to me.[1. Of course, they direct more at any pregnant pro-choice women – there’s a video clip from Toronto last year with someone telling a pregnant woman “I hope your child kills you”.]

I don’t see these same people at protests and demonstrations about making Halifax an accessible city. I don’t see them at demonstrations about improving health care options. I don’t see them doing anything for people with disabilities except using them as pawns, and I loathe them for it.

And yet, many pro-choice advocates also use people with disabilities as pawns in these so-called debates. They hold up stories of fetal abnormalities as “justified abortion”, as the acceptable test-case, the one they know the general public is likely to agree with. I see no analysis, no discussion, of the ableist nature of this narrative. It’s an acceptable justified abortion because the fetus was abnormal, and who wants a broken child that’s going to ruin everyone’s life?

All abortions are justified.

It troubles me so much that it’s only the “abnormal” fetuses that are okay to use as abortion stories.

[Originally published on my tumblr]

[Note: Things we are not going to do in this thread: Debate whether or not abortion is “okay”. Publish shaming comments towards women who have abortions. Talk about people with disabilities as burdens. Discuss individual actions as though they occur in a complete vacuum and are not influenced by societal attitudes and pressures.]

Signal Boost: Canadian Post-Secondary Institutions & Liberated Learning Youth Iniative

Since February our project team has been creating awareness of the Liberated Learning Youth Initiative, which strives to empower students with disabilities through access to a new Speech Recognition transcription system. During the project, participants will be given special user accounts where they will be able to upload recorded lectures and receive speech recognition generated, multimedia transcripts.

The call to participate is now available. Brief application forms for Students, Faculty, and Support Professionals are posted at www.transcribeyourclass.ca. This fall 2010 academic year, there will be 75 user accounts available. Given the project focus, applications from students with disabilities directly will have priority. Applications from Faculty and Support Professionals provide institutions with the opportunity to reserve an account, given that many prospective students are not accessible over the summer/not yet registered for fall courses.

We encourage you to review the participation criteria on the website, share this message within your institution and various networks, and apply to participate. Please contact any of our project team for assistance with the application or for more information.

We look forward to working with you.

Liberated Learning

Why History?

The committee approved my thesis proposal (and I passed my French Proficiency Exam – necessary for Canadianists) and thus I’m now at the stage of my MA where I’m researching, reading secondary sources, and writing stuff up.

[When I lay it out like that it looks so sad and boring. This is the bit where I get to do what I want, in the archives! Looking at letters and school records! I get to apply theories and see if they work, and maybe even develop my own! This is totally my idea of how to have a fun summer! Also, the archives are air-conditioned, which helps.]

My particular project is focusing on the development of residential schools for blind and deaf children and youths. I’m looking at how and why they were founded, what their teaching methods were, and who they hired to work there. I’m also looking at the types of jobs that these children were trained for, and what that says about the way disabled children were perceived by society at large in Nineteenth Century Canada.

I’m also wondering exactly how many blind piano tuners and deaf printing-press operators the province of Nova Scotia thought it could support.

I’ve written before that the history I do is explicitly political. It’s partly about a part of our past that is highly neglected, and partly about arguing, simply by doing it, that this history is important, that it has long-term consequences that we’re still feeling.

But I also write it because people with disabilities have a past, a present, and a future. Because we’re important enough that having a history that’s not just focused on a few Great Examples – Helen Keller, Louise Braille, Beethoven, Terry Fox – isn’t enough. Because knowing how things turned out in the past might give us some insight into how things might be in the future.

Another reason I’m doing this is because it challenges people, and asks them to think.

Every time I tell people I’m doing disability history, “centering the experiences of people with disabilities in the historic narrative”, they are taken aback. They’re surprised. Just by doing history in my department, and telling people how awesome my research is, I’m making more of them think about disability, and about people with disabilities. Without ever having a conversation about language, people in my department have stopped referring to people doing unthinkable things as “mentally insane”. Without my ever leading a classroom discussion about theory and frameworks, my classmates discussed the assumptions about disability presented in several of the readings we did.

These are small things. If I’m lucky, I’ve made 30 to 40 people reconsider their ideas of disability and think about people with disabilities in the past.

And yet, these small things are so satisfying.

Recommended Reading for Wednesday, May 26, 2010

T-shirt with GOMPERS showing a tree and several children and an adult walking.  Some of the children are using crutches or wheelchairs.
Description: T-shirt with GOMPERS showing a tree and several children and an adult walking. Some of the children are using crutches or wheelchairs.

By Flickr user Cobalt123, used under a Creative Commons License
Disability Blog Carnival: Tell the Story!

Another awesome collection of posts in this month’s carnival!

Well, at long last here is the Disability Blog Carnival on Story. I am adding posts and such as I go… so visit often, there may be new rides!

Details on the next Carnival.

Rolling Around in My Head will host the June Carnival – June is ‘pride month’ wherein people celebrate LGBT pride – So I thought we’d have a pride carnival, I want people to submit the blog (or even two) that they wrote that they are most proud of. Not the one that got the most comments, but the one that you felt said what you wanted to say, how you wanted to say it and you are proud of it.

Also, Penny is looking for hosts for upcoming Carnivals. Doing Carnivals can be a bit time-consuming, I admit, and can take up energy that you may want to put someplace else, but you can get a lot of help with it, too. When we did the Carnival, lots of folks emailed in links, and Penny was really generous with link-sending as well.

Also in Carnivals: The Eleventh Carnival of Feminist Parenting!

Welcome to the eleventh edition of the newly two-monthly Carnival of Feminist Parenting. It looks like my decision to make it two-monthly – and the hard work of readers plugging it in their own blogs – has paid off, because I’ve had lots of submissions for this edition!

Executive Functioning Blues

Uh-oh. This is not good. A local autism society is requesting that my workplace participate in some sort of autism walk. There is a puzzle piece on the page. There is a breezy suggestion about who should head up the efforts, and the person named is a friend of mine. I check the autism society’s website to see how they have described the event. Although it has been publicized as a Missing Piece March, it seems that it will be more of a festival, with games for kids and information booths. I click through the site, and find no mentions of devastating diseases or burdens on society. Hmmm…the event itself is described as a place where autistic kids can be themselves without being judged. Barely a mention of the existence of adults, and of course no questioning of why autistics can’t be themselves everywhere, but I’ve certainly seen worse. On to the links page.

So Now What?

During my phone call with GDA yesterday, I was ensured that they are always discussing me and which dog(s) would be best. So, they will definitely keep looking for the right dog for me. However, I was also told that they would totally understand if I opted to go to another school, since I’ve been waiting so long. She said they really just want me to have a good guide dog, no matter where it comes from. So, she assured me that it’s okay to re-weigh my options (especially since nobody has any poodle cross breeds right now, which factored into my original decision last summer). And this is actually something that I have been thinking about more and more lately.

Autistic Man Tasered for Unknown Reason

The state of Georgia is getting a bad name with me for its treatment of autistic people. Last Friday, an autistic man was tasered, taken to the ground, and charged with disorderly conduct for a reason that remains unclear.

Academic Conferences: Who Can Afford to Attend?

The money I have spent is on my mind since I heard one scholar at the last conference I attended implore people with a disability to attend conferences. Great advice I thought which was quickly followed by a second thought: who can afford to attend these conferences without institutional backing? When I attend a conference all expenses come out of my pocket including registration. All academic conference are expensive and I draw the line at $200. This line eliminates many conferences I would like to attend and I will admit I make exceptions and spend more once in a while. Am I being cheap as my son would suggest? I think not when one adds in the cost to register, hotel or motel accommodations, food and transportation. For instance the conference I attended last weekend at Union College cost me almost $500. To me, that is an expensive weekend–a work weekend no less.

Headlines:

Canada: Disability group honours Tim Horton’s owners

US: Continuing education with disabilities

Australia: Disability Tax Reform Introduced into Parliament