Activist movements, as in almost all things, can suck you dry—there is always more to be done, more people to reach out to, more actions to plan, more art to make, more reaching out. But at a certain point you have to be able to say, this is my limit. But we’re not socialized in a way to know what our limits are, to think thoughtfully about our capacity, and how to use self care in order to build our capacity. We’re not socialized to be able to say, “Enough, I can’t do this any longer.” I’ve seen it wear down on people until disease forces them to make big life changes.
Ever since Leslie Feinberg died from Lyme Disease, I’ve known we need to talk more about Lyme Disease in the queer community. I didn’t know how to have that conversation, so I just started to bone up and educate myself.
I watched the documentary Under Our Skin, free streaming on You Tube, which according to folks I know with Lyme, it is an accurate portrayal of what it’s like to seek treatment for Lyme Disease and it is shitty. It’s the kind of helpless I feel when I see really big world problems that need solutions. But I know what I do have control over and that’s learning more about it, asking questions and opening conversations.
Part of being camp counselors is participating in a lot of non-consensual woo. I totally didn’t identify it as woo at the time (and balked at all forms of religion and spirituality), but having been a lifelong Girl Scout, I really knew how to plan rituals and ceremonies chock full of meaning for our girls.
Spunky and I used our current spirituality and past Girl Scout training to design a ritual recently that I thought might help some of my blog readers who are interested in getting energy unstuck.