In this spoken-word, disability-dance video, I will speak on my experiences with chronic pain as a person who is queer, racialized, and nonbinary. It will detail the judgemental critiques and biases I have experienced with doctors, paramedical professionals, psychiatrists and psychologists, nurses, and social workers in my seven years living with chronic pain. The video will specifically confront the idea that people with chronic pain are lazy, overexaggerating, or unwilling to help themselves and looking to be rescued. The video will depict me using various pain-management strategies such as self-massage, adaptive devices, heating pads, and others in a disability dance. This dance video will be paired with my original spoken-word poetry. Healthcare providers will be confronted face to face with a slice-of-life experience of a person's constant battle to manage and cope with living with chronic pain, a struggle that is nothing less than valiant and exhaustive. It will specifically tackle issues of isolation, loss, and grief that many people with chronic pain experience under the loss of the welfare state and an increase in neoliberal individualism. The end of the poem will contain a text with themes of disability justice, offering real-life strategies that healthcare providers can incorporate into their practice to support better relationships with patients living at the intersection of disability, racialization, queerness, and transness.
RECOMMENDED FORMAT: Self-directed, Small Group, Classroom Course
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CURRICULUM DETAILS:
Lessons: 1
Est. Lesson Length: 30-45 minutes
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