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"People with disabilities for the most part get what you mean when you talk about not having capacity..."

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“People with disabilities for the most part get what you mean when you talk about not having capacity for something, and thanks to the prevalence of the spoon theory, ‘spoons’ is pretty well understood, especially online. For nondisabled people, however, these concepts are both alien because they don’t get the underlying issue; it’s not that we are tired and don’t feel like doing something, or do not want to. It’s not that we are trying to get out of doing something or are interested in avoiding responsibility. It is that we either cannot do something, or can only do it at great personal cost, and we must weigh whether that thing is worth it.”

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s.e. smith @ Cuteifying Disability – this ain’t livin’ (via notemily) I might have linked this before? But it’s still awesome. (via criptheatrequeer)

I also want to add this quotation:

I have a hard time talking about these things in cute terms because these things are not cute. They are scary and frustrating and intimidating.

I like the language of ‘spoons’ because of the quantization, the idea that each task requires a discrete unit of energy. I also have a hard time with using it for myself because it doesn’t account for the importance of self-care in my life. It’s not so much that I have limited energy so much as that if I fail to perform adequate self-care, my energy will become limited. Then we get into issues of what constitutes self-care, because my self-care doesn’t necessarily look like your self-care, and oh, look, I suppose it’s time for me to write a blog post.

(via pastthestorm)

I’ve tried explaining my current situation using spoons but a lot of people don’t get it. So right now, I have sealed myself off from the world mostly and I’m letting that speak for me.


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