Four Strategies I’m Using to Move Forward in the Wake of the Election
I am remembering the legacy of resistance I come from. Before every event and performance I produce I do a circle prayer/offering of good intentions where I honor our queer ancestors. (If you’re curious what that looks like skip ahead to minute 9 of this video.) I don’t take for granted my ability to be a fat queer flamboyant femme, I know that just thirty years ago I wouldn’t have this access to express my authentic self. The ease I have being a weirdo in this world is because of the blood, sweat, and resistance of those people that came before.
It looks like it might get harder to be a weirdo for awhile. And at least I know that we have communities and we can create some really beautiful shit. And grass roots works a lot faster than government, the glacial pace of regression under Drumpf won’t be able to move as fast as we will. We can support each other and we can continue to make change.
Four Great Queer Art Presales and Kickstarters Happening Now! (A Couple Ending Soon!)
There are FOUR amazing queer artists doing crowd funding to develop capital to finish their amazing projects! A couple are ending in just a few days so act soon!
I believe that supporting queer art is vital to survival. In a world where we don’t see ourselves represented in mainstream culture, where even if we do see an LGBT person probably they aren’t fat, a person of color, disabled, older and/or working class. And speaking of class, it can be really hard to fund your projects as an artist with limited means and without parents or relatives who can patron, or the skills and resources to write grants.
We Need to Be Talking About Lyme Disease in the Queer Community
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.