Showing posts with label communication. Show all posts
Showing posts with label communication. Show all posts

Friday, November 02, 2007

Call for submissions on wealth, redistribution, and class, and a few other things

1) I wanted to do "NaBloPoMo," or National Blog Posting Month. I'll admit the initial temptation was due to the great lolcats-themed badges. I am easy, anything related to that website wins me over immediately. But I do think it would be a great chance for me to learn to write shorter (and more frequent) posts, connect more with other diabetes bloggers doing it, and to force me to finish up all the half-written or outlined posts (there are lots) on stuff I've been wanting to write about, and generally get more comfortable writing and enjoy getting stuff out. However, I am really behind with the class I'm taking and at work, and kinda stressed, so I need to be looking for ways to limit, not increase, my internet time.

2) I went to my diabetes doctor this week - a few thoughts, I will write more later. There wasn't much in the way of surprises or even guilt because I know I've been struggling with my blood sugars a lot the last few months, and part of it is this weird absorption issue, among other things.

3) There's a new project that I heard about at Aid & Abet that looks great. It's a website called Enough, looking for submissions on wealth, redistribution, and class by November 15th-ish (loose deadline). I think it would be cool to get some stuff from you folks out there that involves health/illness, disability, and how that both affects and is affected by wealth, class, our economic system, and ideas for change, etc. I'm hoping to submit something.

One of the coordinators describes what they're looking for:

Call for Submissions: Enough

What is the difference between financial security and hoarding wealth?
What are some ways we can share resources to support community and movement-building?
How can we talk to each other about personal money issues and politics without guilt, shame, and judgment?
What does a politics of wealth redistribution look like in the day-to-day, and what are the obstacles to developing conversations about this in political communities we belong to?

These are some questions we’ve been thinking about, and we’re interested in jumpstarting conversations about how we conceive of and live a politics of wealth redistribution. We’d like to invite you to contribute some writing to a website we’re creating to explore this topic, called Enough.

The ubiquity of capitalism in the U.S. can limit our ability, even in radical communities, to conceptualize creative responses to oppression and injustice. This can manifest both in how we build movements (reproducing bureaucratic, hierarchical, business-type models; packaging and “selling” social justice work to foundations in exchange for grants), and in how we deal with personal finances in our own lives (defaulting to patterns like hoarding, excessive consumerism, and individualism in how we conceptualize our lives and futures and economic security).

We’d like to address some of the ways that class privilege and capitalist dynamics function even within communities and within the lives of individuals working to fight oppression and economic injustice. It can feel taboo to share details about things like income, inheritance, class background, debt, and spending. Silence and secrecy about money make it difficult for us to challenge ourselves and each other when classist dynamics arise. Social conditioning trains us to hoard money rather than share it and build community. We want to get people talking about building shared values and practices around wealth redistribution, because we think figuring out how much is enough, and when to give away money, are key under-discussed questions in anti-capitalist politics.

Some examples of the kinds of things we’re looking for:

-Pieces about how your class position has changed over the course of your life, and how that has affected feelings of responsibility about wealth redistribution.
-Stories about cool methods of figuring out what is “enough” when it comes to making/saving money. How do class background, class conditioning, fear, guilt, and other factors influence how you think about this question? How do you figure out what you need versus what you want when it comes to consuming?
-Examples of (or ideas for) community-based support systems that serve as alternatives to individualistic models of taking care of ourselves.
-Strategies for redistributing wealth in your community, or to support social justice work.
-Discussion of how ideas about wealth, security, scarcity get reproduced in families.
-Diatribes on the politics of inheritance.
-Discussions of professionalism and salaries.
-Exciting models of people dealing with money ethically in activist spaces and organizations.
-Strategies for overcoming immobilizing guilt about class or money.
-Anti-capitalist/anti-racist/anti-imperialist analysis of personal choices about saving for retirement, buying real estate, taking certain jobs, supporting our community, etc.
-Diagnostic worksheets to help people figure out any of the following:
My place in the economy (local, domestic, global)
Am I rich?
What sources of security do I have that I may not be aware of?
How do I know if I need something or just want it?
What are my resources besides money?

The two of us come from very different class backgrounds (Tyrone grew up in a first- generation owning-class family, and Dean grew up on welfare) and we’re hoping for a specifically cross-class conversation about these issues. We think that the anxiety that can arise when talking about these things among folks with different experiences of class can be useful and productive, and we hope to create a space where we can learn by sharing our experiences and challenging each other.

Please send us an email if you have an idea you’d like to write about, a resource you think we should know about, existing writing you think we should post in this conversation. Your piece can be short or long, written in any style.

Please send submissions to: tyronius.samson(at)gmail.com and/or deanspade(at)gmail.com.

Monday, October 29, 2007

Newsflash!

Did you know that breastfeeding could abolish all diabetes? No, you didn't? That's because it can't!!

Last week, a nurse (possibly a nurse practitioner) said at a health care activism meeting, well, if everyone breastfed, there would be no diabetes.

Um... I say, I am diabetic and I was definitely breastfed for a long time.

Instead of owning up to the stupidity and insensitivity of her comment, or at least backing off a little, this woman says, "Really?!! Wow, you must be the outlier, the one exception! It's an inflammatory process!"

Hell no. This woman did not only just talk about me and my mother, but then she tried to defend her statement and act all surprised.

I thought about not even telling my mom (a nurse practitioner) about it because even though we both know it's bullshit, I don't want her to even think for a second about blaming herself or that I might blame her. But, I decided to, and she articulated another thing about it that bothered me. She said, "Doesn't sound like politics to me, sounds like blaming the victim." Yes, the blaming the victim thing. Stupid and fucked up. But I think it was politics, or "blaming the victim" masquerading as a political statement/rebellion, which bothers me even more. And blaming mothers is a recurring theme in our culture.
EDIT: As I was writing this post, I found this great discussion going over on Scott's blog about diabetes, breastfeeding, and blame/guilt.

I am actually all about breastfeeding for mothers that are able to, but this comment was just ridiculous for a couple reasons. Even though I do think traditional medicine can be harmful sometimes and natural methods have a lot to offer, the "natural medicine" pusher people piss me off a lot because they take it to an extreme that is able-ist and/or just dumb. Also, not all mothers are able to breastfeed for various health and other reasons.

In general, people that think they have a cure-all "natural" solution for my diabetes, or whatever else, are pretty arrogant to think that they have the fix to something that I devote endless time and energy to on a daily basis. If it was that simple and complete a solution, don't you think I would have found it? Or am I just stupid for muddling through with my traditional medicine? Do you want to see what happens to my body for even 4 hours without any insulin?

Now, that nurse wasn't suggesting she had a cure for me now. This is just an example of where that kind of statment takes you. It's a way of invalidating my very real experience. That's the problem with universalizing especially when you havent had that experience (and especially when you're working out of this ableist framework).

Also, even if it really was true that breastfeeding can prevent all diabetes, that's a pretty serious, loaded thing to say in such a cavalier way to someone you met 15 minutes ago.

I need to learn to write shorter posts. If you're getting bored, you can consider yourself done here! More ramblings of mine follow...


There are studies that show breastfeeding does significantly reduce the chances of a kid developing type 1 diabetes. And inadequate nutrition as a fetus, infant, or child can be linked to higher risks for stuff like type 2 diabetes and other health issues as an adult (one reason why I think we need to look at environmental stresses like poverty, etc. before anyone chalks up racial health disparities to genetics, which can often end up being just a new sophisticated incarnation of scientific racism). But for her to talk about this one single cause is really inaccurate. And her justification that it's an "inflammatory process" doesn't help her case, because there are so many different triggers that contribute to inflammation.

Also - speaking of ableism - this nurse also made a bunch of comments about well, if something ever happens to me, that's it. pull the plug. She was trying to make a point about the excess money we spend in the U.S. on heroic measures like ventilators at the end of life. I actually agreed with some of what she was saying, that we need to reexamine what life is and how we're spending our healthcare dollars, and if we really want, from a financial
and quality of life standpoint, to be living hooked up to tons of stuff instead of letting ourselves die peacefully when life is ending. But I don't think needing outside assistance from other people, machines, or drugs are the definition of when life is worth living or not, and her statements went too far into ableism and almost even eugenics.

Do you really think life with illness isn't worth living? And do you want to say that to me and the woman sitting next to me that looks like she might have cancer? Besides being a messed up way of thinking, MOST people live with illness or disability in some form at some point (especially people that are not upper-class white people like she and I). And I think to not recognize that is both inaccurate and ableist in that it reinforces this idea that healthy and perfect (and requiring no outside help from other people/medicines/therapies/etc) is the "normal" state for everyone, and a fall from that is remarkable or abnormal.

Saturday, October 20, 2007

follow-up on my fat runner soapbox

I got a response to my letter to the guy who wrote the stupid column about fat marathon runners = unprepared marathon runners:

When you note that you limit yourself to shorter races, you underline my point. You have wisely decided that the marathon is a challenge that requires intense preparation and may at this point be too much for you.

Many years ago, I trained my butt off to run a marathon: 12 weeks at 60 miles per week average, with some 7-day stretches over 100 miles. That is how I viewed the challenge of the event - something to be respected and taken very seriously.

The result? A 3:33 marathon for someone who had been 40 pounds overweight - 12 years earlier. I got myself in shape well before I tackled 26.2 miles. The training was a diet by itself.

For a variety of reasons, I never was able to put in that training time again. That is why my marathon career ended at 1.

Thanks for writing / PH
What irritates me the most about this most is the patronizing and wrong assumption that I have "wisely decided" a marathon is too much for me at this point, presumably related to my fatness.
As if:
a) He knew why i wasn't running a marathon. He doesn't - my reasons include being busy with school/work, diabetes struggles right now (which aren't caused by my fatness, thankyouverymuch), and not really wanting to. My knee pain is about #4 or 5 on that list, and if I lost weight I may or may not still have it.
b) I must be on this path (or at least be trying to be on it) of fat to skinny - I'm not.
c) The destination of the fat to skinny path is a marathon, you can't just do one while you're fat.

Also note his use of "in shape" to not only mean in shape, but also skinny as if they mean the same thing (my whole beef with his original column).

Thursday, March 15, 2007

discomfort with anger, civility, and diabetes

I have been meaning to write something about diabetes and class. And then I was going to write something just about diabetes and things I've been thinking about my experiences since I've had to life more within them (and more constantly) lately with the problems I've been having. But then I got lazy. And then I got into an argument with my dad, so this is what I wrote instead. There's a lot of other things I want to bring out eventually, but too tired now.
PS I don't hate my dad, and this isn't meant to be a personal attack. I'm just frustrated and it illustrates really well what I think happens in a lot of situations.

my dad is so into civility and doesn't like anger. so frustrating to communicate with. since he can't deal with anger, frustration, or conflict, he can only discuss things on his terms or not at all. I asked him (i worked so so hard to be nice and "rational" and articulate cuz i knew this would be an issue) to stop 2nd-guessing me when I say i know what the problem is and my pump isn't working after another incidence of him continuing to second and third-guess me even after i spend a lot of time/energy laying everything out. and i said my anger was healthy and necessary and part of life.

now he says he won't discuss my diabetes with me anymore if that's what i want. it's not, i just want to discuss it without being constantly 2nd guessed. or if i "all i want do to is express my anger" (cuz clearly that's incompatible with conversation or intelligent exchange, of course). i was trying to stay understanding and communicate well with him, but it didn't work. he legitimately has some emotional issues with avoiding conflict i think, but still not fair and a cop-out. he got just what he wanted - this conversation about my diabetes doesn't occur unless it is on his terms, unchallenged. and it's so about upholding a fucked up civility - keeping me from getting angry or us from getting in a conflict under the guise of trying to avoid somethign that upsets me (which is there no matter what, by the way, and it's his reaction, not my diabetes itself that i was upset about in that moment), rather than actually addressing my concerns and engaging with me.