Come on guys, keep pushing this!!
This is so important!
Come on guys, keep pushing this!!
This is so important!
BOND is a tiny touch module. It can be a pendant or a bracelet but it comes in pairs. You keep one and you give one to a friend. When you touch it, your friend feels it. No matter where they are on the planet. We don’t do tweets, we do tickles.
we need this
gonna put it on my dick
THAT IS NOT THE INTENDED USE SIR
This is actually so cool because some people wear bracelets and necklaces and things as comfort items. I used to wear a necklace from my grandma to remind me of her and I would touch the pendant on it when I was feeling down or stressed. So imagine (if she were still alive), every time I did that she would know I was thinking of her, drawing strength from her.
And then imagine poking it and the other person feels it and pokes back and you end up in a real life facebook poke war.
I would send messages in morse code
magine you and your best friend have one. When the friend dies, he/she is buried with the bracelet. A couple weeks later, you feel someone touch your wrist.
Well this escalated from cool tech to perverted hilarity to something heartfelt then finally something out a creepypasta
Fun fact about American health care: if I ever need an organ transplant, I’ll somehow have to hide my autism, depression, and anxiety from the doctors, or else I’ll be disqualified under ideas about quality of life. It’s really great to know how valued disabled and neurodivergent lives are.
So here’s a thing many people don’t know about me: I used to be a medical data analyst. (I still do it occasionally, but not as a full-time job.) It’s a pretty self-explanatory job: I took data - often in enormous datasets - and analyzed it to find patterns. (Obviously, we couldn’t associate these with individual patients; this was just after HIPAA had come into effect, and so this data was very heavily scrubbed to remove any identifiable information.)
One of the patterns I looked for was quality of life and quality of care for people with severe and persistent mental illness (SPMI). For our purposes, that meant major depression, bipolar disorder, general anxiety disorder, schizophrenia, borderline personality disorder, and “other SPMI” (I encourage you to not send me messages telling me how those categories are terrible, because a) it was ten years ago and b) I wasn’t in charge of the categories.) In particular, we looked at injury, illness, and death in people with SPMI, compared with the general population, while they were in the hospital and at certain intervals after they were released (30 days, 60 days, 90 days, 180 days, and 1 year).
People with severe and persistent illness were much more likely to become ill and/or die in the hospital or shortly after discharge than the “general population”. People with schizophrenia had nearly ten times the deaths while in the hospital, and twelve times the injuries and illnesses.
Just as telling were the notes associated with the patient records. There was a significant pattern in the terminology used. In patients in the “general population”, doctors tended to use the word “is”: for example, “patient is suffering from abdominal cramping”. In patients with SPMI, doctors tended to use the phrase “claims to be”: for example, “patient claims to be suffering from abdominal cramping”.
It was clear to us that medical professionals - in general, I know for a fact that there are doctors out there who don’t do this - were assuming that patients with severe and persistent mental illness were inventing some, if not all, of their symptoms - that the symptoms were not real, and therefore did not need to be treated.
And because of that, these patients were falling ill and dying at alarming rates.
This isn’t personal anecdotes. I spent more than a year analyzing this data - which came from actual hospitals in the United States - and finding these patterns. There’s a problem here.
(I would prefer not to give out the name I was using then in public here, but if you’re interested, message me privately and I’ll see if I can get you links to the articles.)
This is a culture war. The right side is winning, at great cost. At great personal costs to people like Anita Sarkeesian, Leigh Alexander, Zoe Quinn and even Jennifer Lawrence, and countless others who are on the frontlines of creating new worlds for women, for girls, for everyone who believes that stories matter and there are too many still untold. We are winning. We are winning because we are more resourceful, more compassionate, more culturally aware. We’re winning because we know what it’s like to fight through adversity, through shame and pain and constant reminders of our own worthlessness, and come up punching. We know we’re winning because the terrified rage of a million mouthbreathing manchild misogynists is thick as nerve gas in the air right now.
Us Social Justice Warriors – this is me, stealing that word in order to use it against my enemies- are winning the culture war by tearing up the rulebook, and there’s nothing the sad, mad little boys who hate women and queers and people of colour can do about it. Nothing, at least, that doesn’t sabotage their strategy, because they can win their game from day to day, but they’re losing the war. They can punish me for writing this, and I’m sure they will, but that will only prove my point. I’m not afraid anymore.
Every time they make an example of one of us, ten more stand up in outrage to hold her up or take her place.
We are stronger, smarter and more numerous than anyone imagined, and we are not to be fucked with."
Excerpt from WHY WE’RE WINNING: SOCIAL JUSTICE WARRIORS AND THE NEW CULTURE WAR by Laurie Penny (via femfreq)
"From 2006 to 2012, a white police officer killed a black person at least twice a week in this country." - MHP