Long Covid has dramatically changed my life, causing debilitating fatigue, depression, dysautonomia, and brain fog, which I called a cute little name for brain damage.
I hesitated to speak publicly about my health due to fear of career discrimination and assumptions about my abilities. It's a personal and professional risk.
Having to still think about Covid fucking sucks. Trust me, I get it. But empathy alone is not enough without actions of solidarity.
I want able people to learn from disabled people. Books like Disability Intimacy and Care Work are essential resources to understand these issues.
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