Look. Listen. I was there, saw Pete IRL and left partway through his speech drenched in that greasy kind of sweat that precedes keeling over and embarrassing oneself. For me the best parts of the event were the new best friends I made in line outside, and the second group of new best indoor friends crammed into a corner with me for the second hour of waiting.
Both groups were of my favorite demographic; women 10-15+ years older than me. Among us there was genuine enthusiasm for Pete and shared dismay at what we’ve let things come to. We wondered what it will take to get “young people” behind Pete the way they were with Bernie last time around. We ranked our favorites, we compared notes on the various campaign events we’ve been too, we admired one another’s fantastic taste in shoes and eyeglasses. In each group ladies leaned near me and asked in a confessional tone of voice if I thought Pete was “electable.” I reminded them that Donald and Barack weren’t electable either and urged them to not try to second guess their true affections. We talked about Roe v Wade and our embarrassment when we catch ourselves feeling critical of female candidate’s gestures or tone of voice because, WTH, that’s so sexist. In two hours we had time to cover a lot, including our favorite parts of his book, The Shortest Way Home, and how Pete inspires a kind of maternal protectiveness and pride in us. I think we were pretty unanimously all in for Pete.
I heard that the venue officially holds 500 people, but that was a handful of hundreds short of the crowd that showed up. I was in physical squish contact with everyone around me and I think that was a nearly universal condition. The HVAC was inadequate. Pete came onstage once they had packed everyone in and gave us one of the best ever renditions of his stump speech (according to someone I know who has watched A LOT of them on Youtube). But by then things had gotten hazy for yrmama. A woman reached through the crowd and tapped me on the shoulder. “Hi yrmama!” I mirrored her enthusiasm, “Hi!” but had no idea who she was. She wore a name tag but the only person I know with that name lives in rural Ontario. I was so confused.
*Late Breaking Edit: I’ve been thinking about the bit that follows the last couple days because I’m not happy with it. But I’m leaving it. ——–> The conclusion is wrong. ———-> This is right: Power-crazed volunteers will always exist and that’s okay. Victimhood though is useless and not at all yrmama’s brand. She wants to be more ready to stand up for herself. There’s no shame in pain or autonomic “dys”function. There’s no shame in anything because we are just little organized blobs of energy making things up as we go along. Electrons have a moral charge of zero.
Haziness postscript: I left while Pete was speaking and almost embarrassed myself even more by crying in public from disappointment. I’ve been feeling pretty good lately but had significant back pain that day. Indeed, during the hour we waited outside, my new best friends and I, I was happy to stand. A friendly volunteer patrolled the line offering folding chairs to the gimpy. After about 45 minutes I took her up on the chair not knowing how much longer we’d be waiting. She repeatedly assured the gimpy that there was ADA seating right inside so not to worry.
But the ADA pen was guarded this time. (Give a volunteer a nametag and a job and the power just goes to his head.) The guard looked me up and down, the cane, yes, but also yrmama’s tanned and muscular limbs. He said, “Well, can you stand?” yrmama said, “not the whole time.” “Can you climb up those stairs? There’s seats up there and I’d rather you went up there.” The “seats” were barstools which aren’t so great for bad backs but he’d successfully shamed me up the steps so I decided to stay and see how it went. How it went was it got more and more painful.
So that’s the lesson for today. Invisible disabilities, like those caused by Ehlers Danlos, are real. Ehlers Danlos, in fact, often gives one super-soft skin not prone to wrinkles hence my perpetually youthful appearance. I look strong because I exercise, and yes, people with chronic pain can exercise. I look good, but not looking as raggedy as I feel sometimes is one of my superpowers. People generally don’t fake chronic illness for the immense social benefits it affords them. They generally fake being okay so they don’t have to deal with explaining themselves all the time.