Friday, April 25, 2008

Girlcott of Seal Press

I've always intended to go back and review one of my favorite disability autobiographies, Connie Panzarino's The Me in The Mirror, which I read back when I was a teenager. But, you know what? It's published by Seal Press, a company that I cannot support or endorse at this time. Not even for Connie Panzarino, who was an amazing white, queer, disabled woman. I haven't found a good online reference on Connie that doesn't reference and quote the book, so I'm just not going to say that much more about her right now.

Someday I hope Seal Press sets this right and I can talk about an interesting book and an empowering woman. Connie Panzarino, that is.

Friday Music: Chavela Vargas

April 17, last week, was the 89th birthday of Chavela Vargas, the legendary Mexican-Costa Rican singer. My friend Penny Richards of Disability Studies, Temple U. moderates a mainly read-only Yahoo group, Born on this Date, that features one important woman in history each day. Here's what she wrote about Vargas:

"Una mujer tiene muchas vidas que vivir. Para hacer muchas cosas y romper parámetros como yo he hecho, hay que ser muy mujer. Después dirá."

[A woman has many lives to live. In order to do so many things and break so many limits, as I have done, one has to be very much a woman. At the end it will be told.]

--Chavela Vargas

Today on our homepage: Mexican-Costa Rican singer Chavela Vargas, born Isabel Vargas Lizano on this date in 1919, in San Joaquín de Flores, Costa Rica. She remembers having polio and being blind during her childhood, but says that she was cured by shamans. She left Costa Rica at age 14, and there she sang rancheras (folk songs) on the streets to earn her living for years. She wore a red poncho and smoked cigars, carried a gun and dressed as a man, to protect herself in such a visible and vulnerable life. She acquired a limp as a young woman--she says she jumped out of a window after disappointment in love.

In time, she became a popular cabaret singer in Mexico, touring the US and Europe, a favorite with the likes of Frida Kahlo (with whom she had an affair, she says) and Diego Rivera. Her stage shows were frank in their sexuality--she dressed in dashing men's clothing and sang songs of seduction to the women in the audience. In 1961, at the age of 42, the first recording of her music was released, Noche de Bohemia. She retired for health reasons in the 1970s, only to return to performing in 1991.

She released an autobiography, Y si quieres saber de mi pasado (And if you want to know my story...) in 2002. In it, she recounted a 15-year bout with alcoholism in the 1960s and 1970s. In 2003, she appeared at Carnegie Hall in New York, in a show introduced by Salma Hayek and promoted by Spanish film director Pedro Almodóvar, a friend. She has appeared in several of Almodóvar's films, and also in the recent biographical film Frida; she also appeared on the soundtrack of that film. She recently appeared in the film Babel, again as a singer.

She was awarded Spain's Great Cross of Isabela la Católica in 2000.

Today is Chavela Vargas's 89th birthday. She lives in Veracruz, Mexico.

She's on YouTube, here are just a few of the many clips there:

http://www.youtube.com/watch?v=duVaGM_JsME (a 2006 live performance)
http://www.youtube.com/watch?v=yQnNY8zMihs (a recent live performance)
http://www.youtube.com/watch?v=yuVjT2Rl7Bg (a 1998 performance for Spanish TV)
http://www.youtube.com/watch?v=0gQ31m4Yt0s (clip from "Frida")
http://www.youtube.com/watch?v=3bBRp-co68I (audio only)
http://www.youtube.com/watch?v=gqHh2U4TSJQ (audio only)
http://www.youtube.com/watch?v=XGESStAwS1k (slide show accompanies audio)
http://www.youtube.com/watch?v=cF6jEclOMcw (slide show accompanies audio)
http://www.youtube.com/watch?v=-mnZcErj-SA (slide show accompanies audio)
http://www.youtube.com/watch?v=6D2e8JMsTho (slide show accompanies audio)
http://www.youtube.com/watch?v=XAIF1IgiLeo (slide show accompanies audio of duet)

http://es.wikipedia.org/wiki/Chavela_Vargas
http://en.wikipedia.org/wiki/Chavela_Vargas
http://www.allmusic.com/cg/amg.dll?p=amg&sql=11:br63mps39f8o
http://www.afterellen.com/archive/ellen/People/2005/1/chavelavargas.html
http://www.afterellen.com/archive/ellen/People/2005/1/chavelavargas2.html

http://www.glbtq.com/arts/vargas_c.html

See also:

Yvonne Yarbo-Bejarano, "Crossing the Border with Chabela Vargas: Chicana Femme's Tribute," in Sex and Sexuality in Latin America (NYU Press 1997). A shortened version is online here:
http://www.lolapress.org/artenglish/chabe13.htm

Happy belated birthday, Chavela!

For another fan of Chavela's, Brownfemipower, whom I miss very much.

Thursday, April 24, 2008

Check out Disability Blog Carnival #36

The latest Disability Blog Carnival is now up at Abnormal Diversity where the theme is Abuse. I submitted a post on something that happened to me about two years ago, and there's much more to read on the topic. Check it out.

Disability Blog Carnival icon of Frida KahloThe next Disability Blog Carnival will be on May 8 at CripChick's. The theme will be Disability Identity and Culture. From CripChick:

Here are some topic ideas!:
• What is disability identity? If you are disabled, do you feel disability is a part of you and your experience?
• What is disability culture to you? How do you put it out there or live it every day?
• Does disability intersect with your other identities (i.e. queer person, person of color, person of faith, etc.)?
• Is pride, community, or the Disability Rights Movement important to you? Why or why not?
• How do you feel about the word disabled? Is it a political term with power to you or do you despise it?
• Do you see disability outside of a rights framework (i.e. is disability something that is more than advocacy to you?)
• If you identify with the autistic acceptance movement, the deaf community, or other groups, how do you feel about disability? Many people do not want to associate with the disability community— how do you feel about this?
• Have you felt alienated [left out] from the disability community because of racism, exclusion because of your disability, the media or other factors? How has this affected your identity as a disabled person?

And some topic ideas for allies:
• Why is disability important to your work or politics?
• How do you feel about the Disability Rights Movement and what would you say to activists who downplay this movement or even disability as an important social justice issue?
• How do you see disability intersecting with feminism, reproductive justice [movement that focuses on ALL people having ALL control of their bodies], and other movements that work to end oppression?
• What do you see in your role as an ally?

CripChick also provides a list of resources for anyone wanting to bone up on the topic before participating. Deadline for submissions is May 4. The carnival submission form is available here, or leave a comment with your submission's link at CripChick's, or email her with the info at consciouslycrip [at] gmail [dot] com.

Other recent Disability Blog Carnivals have been at Reimer Reason on the theme of The Hardest Part, Andrea's Buzzing About on Breaking Out, Wheelie Catholic on Appreciating Allies, and Sunny Dreamer on Standing Outside the Fire.

Image description: The icon above, provided by CripChick for the upcoming carnival at her place is a color image of a self-portrait by Frida Kahlo with the words "DISABILITY BLOG CARNIVAL" in bold black type across the painting. The image is a close-up of Frida in her wheelchair from the 1951 painting "Self-Portrait with Portrait of Dr. Farill" described in detail in both English and Spanish here.

Cross-posted at Alas, A Blog

Tuesday, April 22, 2008

Participate in the 3rd Annual Blogging Against Disablism Day, May 1, 2008

Blogging Against Disablism Day, May 1st 2008

It's time to be BADD!

Once again, the amazing Goldfish is sponsoring Blogging Against Disablism Day on May 1st. BADD is an annual event where disabled and non-disabled bloggers everywhere write about ableism, disablism and disability prejudice and discrimination.

Last year over 170 bloggers contributed. I've been proud to be a part of this the past two years and I can't wait to see what everyone has to say this year.

Details on how to participate are at Diary of a Goldfish, including a notice of Language Amnesty. Goldfish explains:

You can write on any subject, specific or general, personal, social or political. In the previous two BADDs, folks have written about all manner of subjects, from discrimination in education and employment, through health care, parenting, family life and relationships, as well as the interaction of disablism with racism and sexism.
It's a good chance for allies to get their feet wet on a topic they might be hesitant to address, I think. Hope to see you there.

(Image description: The above logo for Blogging Against Disablism Day is one of several available --easy copy-and-paste code -- at Goldfish's. This one is a square divided into a headline naming the event and a grid of 20 colorful boxes, each featuring the simple shadow of a person, with one box showing a person using a wheelchair and one other person holding a cane.)

Monday, April 21, 2008

The Russian

On my first night at the rehab hospital, I was about as vulnerable as a person can be. I'd been in the ICU at a different hospital for a month. I had a new tracheostomy and was using it to breathe with a ventilator -- a new and frightening experience for me. I also had a new feeding tube, a PICC line, a catheter for urinating, and I'd barely been out of bed for that whole month.

I was weak and unable to speak. I communicated by writing on paper, which required the absolute cooperation of whomever I was communicating with. Basically, they had to consent to let me "speak" by handing me paper and pen, then waiting for me to write my message. (BTW, this procedure is the reason I am kinder to spelling errors -- my own and everyone else's. Spelling used to be a pet peeve. Ah, the luxury.)

Leaving the ICU, I chose between two rehab hospitals that I knew nothing about. My parents visited each and each sent representatives to meet me, "assess" me and lobby hard for me to choose their institution. I made a wild guess, choosing the hospital farthest from my home and requiring almost an hour's more commute each way for my parents as they came to see me most every day for the next three months.

It was the right choice. I ended up at place filled with amazing, dedicated people. But that first night was terrifying. And not just because of my own uncertainties.

I've got a knobby little tailbone that sticks out. I've never ever had a pressure ulcer (also called a "bedsore" or decubitus ulcer) anywhere on my body, including my tailbone, in part because I've spent quite a bit of time lobbying on it's behalf every time I put my body into strangers' hands, lay on a hard x-ray table, or require other people's assistance in keeping it healthy. For my four months in the ICU and rehab that meant an inflatable mattress on my hospital bed and frequent repositioning.

Sometime during my first night at the rehab hospital, I woke up needing help to roll over, a rather complicated process when I was so weak and had so very many tubes to avoid yanking. I rang the bell for help and a nurses' assistant showed up. I forget her name, but she had an accent so I'll call her "The Russian" as I did at the time to family and friends.

She understood I needed to be repositioned and she told me she needed to go get another person to help. It is commonly a two-person job in acute care settings and may even be required procedure, but when she didn't return and my butt began to ache badly from laying in one position too long, I rang the bell again.

The Russian returned alone to tell me she was trying to get help, then left again. I don't know exactly how much time passed, though it was easily 30 minutes since my first call for assistance, and it may have been as long as an hour. My butt was throbbing painfully now, sparks of nerve pain shooting down my leg. In desperation, I spent significant energy wrestling the pillow wedged behind my back away enough that I could shift slightly and ease the sharpest of pain to buy some time.

Shortly after, The Russian returned. Again alone. She saw the pillow had been moved and began berating me: "Why you bother me? You don't need help! You did this yourself after bothering me? If I catch you ever moving by yourself again don't expect me to do anything for you!"

I had no opportunity to tell her what I was thinking: "You will too frakking help me! That's your job! $ & % #*&!"

In order to reply, she would have had to agree to handing me my paper and pen, and she either didn't understand that's what I wanted or she purposely refused. It was a long fearful first night after that, not knowing if help would come if I needed it (for repositioning or breathing or whatever), and for the next many nights until I learned that her behavior was not typical of the institution or people working there.

In the morning when my parents arrived, I told them all about The Russian, writing the incident out for them in detail. I didn't take it further than that and neither did my parents.

Why? Because I didn't yet know if she ran the night shift, if others held her view and I was stuck somewhere where being the squeaky wheel might further endanger me. Because I was immersed in trying to get my primary doctor to hand me the paper and pen instead of telling me about my care and walking out the door. Because the speech therapy folks were busy giving me cognitive tests and asking things like if I knew where the window in the room was. Because in addition to my serious health issues I had one giant communication problem with getting people to treat me as an aware, active participant in my own recovery. Because the principle and all-consuming job in being an inmate in any institution is self-defense, just keeping well-meaning professionals from accidentally making you sicker.

My parents were equally immersed and could certainly have reported the incident, but when the abuse didn't recur, we all ended up focusing on the next most emergent issue. And there were dozens of them.

Was The Russian just having a bad night? Maybe. But I think she was hazing me. Three long months later, on the night before I came home, she stepped into my room to tell me what a pleasure of a patient I'd been. "No trouble." Compliant, she meant, of course. Less needy than other folks. There hadn't been a night for those whole three months that I hadn't been acutely aware of whether or not she was on duty.

The most disturbing part of this story is that I didn't tell her supervisors, right? I was conscious, had by wits about me (more-or-less), had caring family visiting daily, and knew at the time it happened that she was being abusive of her power over me. But this is how institutional abuse starts, why there is space for it to lurk even at excellent institutions. I was busy surviving and her behavior was only one of the many scary things I was subject to.

What would have happened if I had told her supervisors? Would I have been believed? Would I still have been subject to her care after essentially threatening her job? Were there a dozen other employees like her I just hadn't met yet who would hear I was "troublesome"?

What if I hadn't had any visitors to tell, providing, as my parents did, psychological assurance that further abuse could be responded to? What if I had been unable to communicate any of this to anyone, as was true for many of the people in rooms adjacent to mine?

Abuse doesn't really need much space to thrive, and it needs even less to occur only once. Probably not everyone would consider this abuse. But it was a verbal threat to deny me assistance while lying helpless in a bed from someone charged to show up if, say, my ventilator quit giving me air. Like any sort of intimate violence (domestic violence, date rape, etc.), violence against disabled people is contextual and opportunistic and can happen to anyone.

Sunday, April 20, 2008

Spring: w00t!

This winter has been longer than I could stand, but spring seems to finally have taken over. The subzero weather and endless snow has kept me indoors much more than I expected, and I stopped blogging for a while there as a way of spending less time in my own head while cooped up indoors.

Thanks to the people who emailed me with concern for my absence here. I'm good, and I promise to not go missing again without noting I'm on hiatus.