I would really appreciate it if people would spread this around! What YouTube is doing to LGBT+ videos and content creators is affecting intersex people, and, between the lack of intersex voices on the internet as a whole and the lack of people talking about intersex issues at all, this has a huge impact on what little we’ve been able to put out there.
One of the reasons we’ve been unable to create as much as other LGBT+ groups on the internet is because the stigma against us and how strong it is. What YouTube is doing is revoking the visibility we are getting and reinforcing the stigma that keeps us hiding.
The solution here is not as simple as turning off restricted mode. This sends a message to people that who they are is unfit to be seen, especially when done by such a huge, popular company whose tagline used to be “Broadcast Yourself”. And this still affects kids whoee parents won’t let them turn off restricted mode.
Please don’t just let this get 10 notes and disappear, please reblog this and make people aware. And, if you can, I encourage you to support intersex content creators on YouTube, including Emily Quinn (Intersexperiences), Pidgeon Pagonis, and Jenn Levine. You can find plenty of other good videos if you search “intersex” on YouTube.
god damn it
Diabetes Patients Are Losing Limbs And Sight Because They Can’t Afford Insulin
Diabetes Patients Are Losing Limbs And Sight Because They Can’t Afford Insulin
More on skyrocketing drug costs in the United States
“A medical professor who has tracked the cost of insulin over the
years says that a one-month supply of a popular version that cost $45
wholesale in 2001 cost $1,447 14 years later, an increase of almost
3,000%. That’s the wholesale price, not the retail price that an
uninsured patient would pay.“Yeah, that’s messed up.
Wow, it’s really rare I see something cross my dash that’s actually directly tied to my life on a personal level, but yea, I’m Diabetic Type 1 and this is a problem.
I’ve been off insurance for the last three or so years and have been working around through channel I can to continue to obtain insulin and supplies for my insulin pump (of which is currently a problem, fun) for free or at reduced costs.
The Lilly Cares program is one I heavily endorse if your insulin is a Lilly product. They’ve been incredibly helpful to me.
Please spread the word on this. There are a lot of young Diabetics like myself that do not have a support system, do not have insurance, and do not have jobs. Insulin is literally a life-sustaining medication for T1 Diabetics. Please do not just ignore this.