You see this map here??? This is from the battle for the net website.
Well our net neutriality is coming to a close and it seems we now have to march in order to get our voices heard! If our senators and congressmen aren’t going to read our letters, or listen to our calls then we’re going to march!
There are two marches going on!
Red Dots: May 2nd
Stars: May 10th
Mark BOTH of these on your calenders!
If your state doesn’t have a red dot or a star organize one now!
CALL YOUR SENATORS! MAKE THIS HAPPEN! SAVE NET NEUTRALITY!
!!!!!!!!!
I also drew this
I was watching Jack play The BOSS and it made me realise how important he is to me. Without him, I wouldn’t have gotten into most of the stuff I’m into now. He’s such a kind person and I’m so glad he exists
(Also I’ve wanted to draw him for ages now and just haven’t gotten around to it whoops)
When I saw this post on my dash, it kept disappearing every time the site finished loading. It had nothing to do with my blacklist extension, all evidence of this post on my dash vanished. I had to go to the blog of the person I’m reblogging it from DIRECTLY.
If you can see this post at all, even if it’s for a split second, try and like it and reblog it! Don’t let this post be hidden!
THE RULES DON’T GO INTO EFFECT UNTIL THE 23RD! YOU STILL HAVE TIME TO CONTACT CONGRESS AND TELL THEM TO S T O P the FUCKING FCC.
THIS IS GOING AROUND AGAIN.
IT DISAPPEARS BECAUSE PEOPLE LOOK INTO THE NOTES AND SEE THAT IT’S AN OLD POST AND DELETE IT.
DO NOT REBLOG THIS WITHOUT CORRECTED INFORMATION, IT MAKES PEOPLE HOPELESS BECAUSE THEY THINK IT’S OVER. IT IS NOT OVER.
@fightfortheftr (April 19, 2018): There have been a lot of inaccurate reports that the FCC’s repeal of #NetNeutrality will officially go into effect next week on April 23rd. That’s not true. It’s a bit more complicated than that. Ready? Here we go:
Its understandable many journos are confused by this. It’s legitimately confusing. The FCC order said it would go into effect 60 days after publication in the Federal Register, which would have been April 23rd. But, it still has to be approved by the Office of Management & Budget.
There was another FCC filing in the Federal Register that would imply the earliest the OMB could approve this (and its worth noting that approval is basically just a technicality) is actually April 27th, but its likely to happen some time after that, possibly even weeks after.
The most important thing for EVERYONE to understand is that nothing catastrophic or dramatic is going to happen immediately when the FCC rules go into effect. Telecom shills will immediately start saying “See? The sky didn’t fall, we never needed #NetNeutrality.“
They’re lying.
The ISPs aren’t going to immediately start blocking content or rolling out paid prioritization scams. They know Congress and the public are watching them. Rather, the death of #NetNeutrality will be slow and insidious. You might not even notice it at first.
And that’s the worst part. What will happen is over time ISP scams and abuses will become more commonplace and more accepted. They’ll roll out new schemes that appear good on their face but undermine the free market of ideas by allowing ISPs to pick winners and losers.
Over time we’ll see less awesome startups. Less awesome videos. Less diverse online content. And we’ll see more content that our ISPs want us to see. The Internet will be watered down and manipulated. It will change forever in ways that harm our democracy.
But it will take time.
So: don’t fall for ISP lobbyists talking points. They’re ALREADY claiming that #NetNeutrality was never needed since the sky hasn’t fallen, and the rules haven’t even gone into effect. But also don’t panic. The Internet is not going to die next week. Keep calm and keep fighting.
The Senate will vote in a matter of weeks on a Congressional Review Act (CRA) resolution to block the FCC’s repeal. Now is the moment to get engaged.
Her mental age is about three years old. She loves Winnie the Pooh, Beauty & the Beast, and Sesame Street. Even though the below picture is unconvincing.
Edna and “Cookie.” I think she was trying to play it cool.
My name is Jeanie. I’m Edna’s younger sister. I’m also her guardian and caregiver.
That’s me on the left. (Hey, you never know. After a year of writing a blog about online dating – Jeanie Does the Internet – I’ve come to learn that there are A LOT of fools on the internet.)
ANYWAY, I’m not “doing the internet” anymore. I’m taking care of Edna full-time, after completing my MFA in Writing for Screen & Television at USC.
May 16, 2014. I wanted a picture. Edna wanted breakfast.
In case you’re wondering where our parents are, they’re dead. Our mom died of breast cancer when she was just 33.
Us with mom before she died. (Obviously.)
As for our dad, he peaced-out around the time my mom got sick. His loss – we’re awesome.
Here we are being awesome at the beach. Pushing a wheelchair in the sand? Not so awesome.
In case you’re wondering “What’s wrong?” with my sister – as a stranger once asked me on the street – NOTHING. Yes, Edna has a rare form of epilepsy – Lennox-Gastaut syndrome – but I don’t know if that’s anymore “wrong” than people who don’t have manners.
Basically, Edna was born “normal,” and started having seizures as a baby. They eventually got so bad that they cut off the oxygen to her brain, causing her to be mentally disabled. Or impaired. Or intellectually disabled. Or whatever you want to call it – except “retarded,” because in 2010, President Obama signed Rosa’s Law into effect, replacing that word with “intellectually impaired.”
Which is cool and all, but services for the disabled and the people who care for them are SEVERELY LACKING. Also, there’s a bunch of people working in taxpayer-funded positions who are supposed to help families like us, but don’t. (Big surprise, I know.) They just fill out paperwork (whenever they feel like it) with asinine statements like this:
YUP. I transport my sister down the stairs in her wheelchair, because that is not only safe, but TOTALLY PRACTICAL. Why doesn’t everyone in a wheelchair just take the stairs, for God’s sake? Stop being so lazy, PEOPLE WITHOUT WORKING LEGS!
But, as it says above, Edna’s legs do work. Whether or not she wants them to, is another story.
Edna refusing to go inside.
These are the stairs that I have to carry her up – by myself – on a daily basis. That is, until one of my legs break and both of us are just sitting at the bottom of the stairs, helpless.
For six months, I have begged – BEGGED – the State of California to help my sister, which they are required by law – The Lanterman Act specifically – to do so. But they’ve told me “these things take time” and that I “need to amend my expectations.” (That was said to me when I refused to place Edna at AN ALL-MALE CARE FACILITY. Because yes, that was an “option” that was offered to me.)
Prior to Edna moving in with me in my one-bedroom apartment, she was living with her amazing caregiver, Gaby, back in Tucson, where we went to high school and I did my undergrad. Edna’s reppin’ the Wildcats below.
But back in November, Gaby also died from breast cancer. (FUCK YOU, BREAST CANCER!) This picture was taken a month before she died. She never even told me she was sick because she didn’t want me to worry.
By the way, we were raised by our grandma. Edna and her were very close.
She’s dead, too. Surprise.
She died when I was 20 and Edna was 21. That’s when I became Edna’s legal guardian and Gaby stepped into the picture to help me out with Edna.
So, six months ago, after Gaby died, I moved Edna to California, where I tried to get the folks over at The Frank D. Lanterman Regional Center to help me. I’ve told them I’m worried about our safety – that one of us could get hurt on the stairs – I’ve told them I can’t afford to pay the private babysitters $15/hour because the ones social services sent me who make $9/hour were unreliable (they didn’t show up on time or at all so I could get to school and work), untrustworthy (one of them let Edna go to the bathroom in the kitchen and then took her into the bathroom because “that what I thought I was supposed to do.”)
But the people over at the FLRC don’t return my calls, they don’t file the paperwork on time – and the first caseworker that was assigned to us actually LAUGHED AT my sister when he came to our home to evaluate her. When I reported him to his supervisor, she told me, “That’s just [insert name of said jackass].”
He was one of the two caseworkers that contributed to the report I mentioned above, which also included this:
So let me get this straight – I have to feed, bathe, dress and help Edna in the bathroom and you can’t deduce whether or not she is able to vote? What in the fuck?!
Now I realize I seem angry. And you can bet your balls I am. I’m also sad. Sad for those who don’t have family to stick up from them and who waste away God knows where, monitored by no one. Or monitored by people who physically and sexually assault them.
I’m also sad for the caregivers who are SO EXHAUSTED – trying to take care of their loved ones – while also trying to take care of themselves and battling a system that is supposed to help, but does nothing of the sort. And I know a lot of people give up. They let their dreams, their marriages, their friendships slide. All while trying not to resent the very person you’re doing it all for.
Edna wanted to sit next to me the other day while I was writing. Clearly, she’s not impressed.
Here’s the thing: I REFUSE TO GIVE UP. I’M NOT GIVING UP ON HER OR MYSELF. I’m going to pursue my dreams while taking care of her, AND while ensuring that the people paid to do their jobs ACTUALLY do them.
That’s where you come in. I need you to help me get my story out there. Because I know I’m not alone in this. I want to connect with families who are in similar situations and also show people who have no idea what it’s like to care for someone with a disability (or even a loved one who is sick) that it can be rewarding. Super fucking hard. Exhausting. Painful. Isolating. But, rewarding.
I’m going to get help for my sister – and others. My hope is that by sharing our story, I can bring awareness to the lack of services and help for the disabled.
STOP SCROLLING. THIS PERSON ISN’T ASKING FOR MONEY AND THIS POST WON’T MAKE YOU SAD.
This is a really uplifting and inspirational story of a family sticking by each other and making things work despite a whole lot of shit
They just want to find other people in the same position they are, for a sense of community and to feel like they aren’t alone.
I know out of all of you, some of you have followers who are living with and taking care of intellectually or emotionally disabled family members, and this lovely and unbreakable pair of sisters need to find them.
SIGNAL BOOOOOOOOOST
I sincerely hope these girls receive the help they need. Godspeed, ladies!!
theres a new product by verzion called “hum” that allows your parents to track your car and places you go, if your parents are controlling like mine please check under your steering wheel to make sure that they havent installed this
here is what it looks like installed:
you can read more about it here, and here– this excerpt sums up what information Hum will send:
“a car’s owner will be able to get notified on their phone when the vehicle leaves a pre-determined area or drives faster than a set speed… [Hum] will enable location tracking and a driving log, which measures travel times, engine idle times, and average speeds.”
People in abusive relationships, please check your cars.
DO NOT TRY TO UNPLUG IT BY YOURSELF!
To add to this nightmare, I’ve just heard of a thing called ForceField where people get to monitor and block internet sites that you’re going on if they don’t approve.
It tells the user what sites/apps you’re going on, for how long you’re on them, and WHERE YOU ARE ON AN UPDATING MAP.
So you know if you’re in an abusive household and use sites like tumblr to escape and talk to friends, you could be cut off from that.
They say “it’s not spyware” but it sure sounds controlling and creepy to me.
signalboost
God. Fuck. That’s scary.
Life 360 is another tracker. My parents have used it on me, not allowing me to delete it from my phone, and sometimes even demanding selfies to prove I was where the map said. (As if I’d go anywhere without my phone)
SpectorPro is another one. Afaik it can’t track location, but it takes screenshots roughly every 20sec to allow the installer to watch a video of your computer activity. It also tracks all keystrokes, so passwords aren’t safe, and records any website you visit + the duration. It’s incredibly creepy and a huge violation of privacy, and was one of the cornerstones of my abuse as a kid.
even if you’re not in an abusive relationship/family, please spread this because you might have just saved someone’s life
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