We Need Power to Live

by Stacey Milbern: For More Info, Go Here…

Remarks by Stacey Milbern at Light up the Blackouts: A Vigil and Community Gathering -Oakland

Whether it is fascism or environmental climate crisis created by greed, disabled people — especially disabled people of color — are, as disability justice activist Patricia Berne says, the canary in the coal mine. How we are treated is often an indicator that there is a big problem. We saw that with nazi extermination. We saw that with the current administration cutting food stamps, housing, and health services.

Right now when there is a climate emergency, people who live in nursing homes and institutions get left behind. Often times staff, families and community members want to rescue them, even physically fighting nursing home administrators, but are barred because of policy. It is not uncommon for people in institutions to die because they were not rescued. Many advocates are fighting for what we call the right to be rescued. The. right. to. be. rescued.

This week in the Bay Area disabled people and elders without power are having difficulty breathing, moving, eating, and staying alive. A friend is going without her nebulizer treatments. A neighbor didn’t have a way to store his insulin. Another community member is home bound because she needs power to open and close their garage. Countless number of people are being forced to throw out groceries without knowing where the money will come to replace them. Blind people are crossing the street without there being traffic lights or audible signals that tell them when to cross. Lack of street lights makes people even more vulnerable. Community members are going without medications they need. Have you tried communicating in American Sign Language in the dark? Not easy. I myself use life sustaining medical equipment, my ventilator, 16 hours a day. My doctor completed extensive paperwork telling pg&e why I need power to live. (Let me say that again — My doctor completed extensive paperwork telling pg&e why I need power to live. There are so many more disabled people impacted by the powerapocalypse than the medical baseline program — the eligibility requirements for the program are significant and require a disabled person to have a healthcare provider. ) On Tuesday I called pg&e to ask for protocol for medical baseline users. I was on hold for two hours and twenty minutes. I hadn’t received any notice from pg&e but saw my house on every map as about to lose power. When I was finally connected, the representative confirmed there was nothing really in place. He literally told me “this is why we let the public know so you would have time to prepare.” To PG&E, my life is not important.

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