I win this time.

ellievsbear
Today's Document
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@thischroniclife
I win this time.
Flare days be like
make posts about disability accessible
[ID: collection of tweets from Amanda Hackwith @ajhackwith reading
âIf youâre fuzzy on why changes to the ADA is such a big deal, I get it. Iâm keenly aware of what being abled blinds you to. Iâm here to introduce you to the thing that dominates my husband and Iâs life: Logistics. Hey. Abled friends. This thread is for you. #HR620
Disclaimer: I am not physically disabled. My husband is. He has used a wheelchair since birth. Iâm using âweâ in here because thatâs how weâve experienced it, and this is shared with his permission. OK? Ok.
The reality of living with a disability is Logistics. We donât just do something. You figure out if we CAN do something. And then try to chase down the secret hidden puzzle of how WE do it. Because, I guarantee you, we are the exception. We are always the Exception.
So: join us. We leave home. We donât call for an accessible taxi because that will take an hour. We canât take a zipcar because thereâs no hand controls. Walking through the door is Logistics.
We take a bus, praying that no one else with a wheelchair, walker, baby carriage, grocery bag, or big-ass backpack has already taken up the two accessible spots on the entire bus. Two. If so, weâre out of luck.
Or we take a hip, tech-will-set-us-free rideshare. There is no accessible option in the app. We pray that the ride that comes wonât drive off when they see a chair. That the folding chair will fit.
Maybe we walk home. We fought city hall for neighborhood curb cuts last year! Only fancy condo construction has torn them out again. For months. So we walk in the gutter of a busy industrial street.
We see a show. We canât buy tickets online. We have to call to see if one of the five accessible seats in the theatre is available. Thereâs only one âcompanionâ seat. We arenât expected to have friends.
We book a hotel. We have to investigate how crappy the accessible room is. (Itâs usually a less desirable retrofitted room.) How a ânormalâ room is laid out. If we can âget awayâ with being treated as normal. For once.
We fly. We introduce ourselves to the attendants. We PROMISE we wonât be a bother. That we wonât need assistance. That we wonât need to rely on the rickety chair they want to strap him to, Hannibal-style. We make the attendants nervous.
We fly. We successfully board, but the bathroom is twenty feet to the back of the plane. We donât have our chair. We hope we donât need to pee for the next nine hours.
We want to do a fun tour of a new city/country/landmark. We spend hours calling tour companies, emphasizing how low fuss we are, how independent we are, how weâre one of the âcoolâ disableds, if only they have room to fold his chair with the luggage. We promise to be good.
We want to eat at a special restaurant. Itâs in a historical building. We crawl on our knees and throw the chair up the stairs to eat there anyway. There are stairs and there are stares. We are everyoneâs free entertainment.
We eat at a restaurant. Itâs accessible, sure! Just call ahead and Jimbob will throw a board across the steps for you to roll up. Or thereâs an accessible entrance! Itâs the loading ramp, out back. Through the pee-soaked alley and trash cans. Canât miss it.
We eat it a restaurant. Itâs totally accessible! Except for the bathroom upstairs. You can hold it until we get home, right honey?
Work has a social event. Itâs held at one of the above âtrendyâ restaurants. But HR totally apologizes, okay? Be cool. We can be cool.
We want to go home. We become invisible to taxis. He hangs back until I flag one down and glare the driver into submission.
W apartment hunt. All the cute ground floor dog-friendly units are lofts with stairs. All the accessible units have been rented out to able-bodied people because âno one wants themâ.
We apartment hunt. The âlargeâ bedroom doesnât leave enough room to either side of the bed for a wheelchair to sit. The glitzy new apartments have bathroom doors too small to get through.
We apartment hunt. The building is totally accessible! Except for that one tiny step. In the common room. To all the amenities youâre paying for.
And this is important: We are white, educated, financially secure, fairly young and healthy aside from the wheelchair. In other words: BEST CASE SCENARIO. We literally are operating and interacting with the ADA on every privilege we can manage.
If youâre surprised by what Iâve said, keep in mind the majority of the disabled community has it so much worse. With so much less resources. Even WITH the existing ADA. #HR620
No imagine how much worse, more hostile, the world will be if every target of discrimination had to ask each business, in writing, one at a time, to please not break the law. And they have 90 days to ignore them. And another 180 after that. Every restaurant. Every store. #HR620
Imagine you had to beg every business to allow you to exist. Imagine people complaining about ânuisance lawsuitsâ and âsupport peacocksâ to you. Your existence is a nuisance. Your existence is over legislated. Your existence is unnecessary. Now call your damn senators. #HR620 â
/end ID]
Social anxiety is basically Conspiracy Theories about yourself.
a wee doodle to remind myself that fresh starts are a good thing, everyone grows at their own pace đąđąđą
doctors: you need to be an active part of your care
Me: okay great, hereâs a list of symptoms and how they affect me on a daily basis. hereâs up to date info/ research on 2 things I suspect could help/ could be possible diagnosis and I was wondering if we could look into this
doctor: No, not like that.
After my friendâs suicide, I realized something: We ask people to reach out. But we never explain how.
Hey ghosties, we really enjoyed this article and thought it raised some good points about asking for help, what do you think?
if I hadnât learned to say these things I wouldnât be here. This article is really important.
Please read and share this article. I know that if Iâd seen something like this several months ago, I couldâve gotten help before I made an attempt on my life.
Iâm one of the lucky ones. Not everyone gets the second chance I got, and learning how to reach out is vital to making sure we donât have to rely on second chances.
Bookmark this. Reblog it. Share it with someone you trust or know is struggling. Learning how to ask for help (and how to recognize when someone is in crisis) saves lives.
You are all to lovely to be lost to the world. Please always remember that.
Pre-nap me: gosh I'm just a lil bit sleepy I could use me a lil nappy nap
Post-nap me: why.... Why do I exist in this world.... How do I know what is real... What is the truth.... I'm so thirsty
[Image Description: A black color block with text that reads âsupport disabled queer peopleâ]
Life hack
Got something you need to do at a certain time every day (e.g., take meds)? Start giving your cat a treat right before you do it. You may have trouble remembering, but your cat absolutely will not. Â
This might be the most genius idea Iâve ever read.
Me, right after I get a new diagnosis: HA, I knew it! All those crappy doctors who told me I was faking it were WRONG! This is great news!
Me, several hours later when the news actually hits me: *sobs alone in my room*
HEY GUESS WHAT HAPPENED TODAY
The House of Representatives voted in favor of destroying key provisions of the ADA to allow businesses to continue, penalty free, to remain inaccessible, possibly indefinitely.
All yâall who like to talk about ableism on here and are eligible to vote in the US:
call your senators. Tell them no on 620. Tell them why accessibility and the ADA matter to you.Â
Washington Post: House passes changes to Americans With Disabilities Act over activistsâ objections
Newsweek: House Votes to Gut the Americans With Disabilities Act to Nip âAbusive Lawsuitsâ
Now with citation! (thank you!)
accessible background info + supports and alternatives for calling your senator (written before the house vote, with a new statement here)
find your senatorâs contact info here
When someone who doesnât have a chronic pain illness tells you that most chronic pain is in your head.
Some people can lift 200 pounds. But if they carried it everywhere they went for an entire day without ever putting it down, theyâd severely tear their muscles and cause permanent damage to their body.
Some people can enter a 140° car in the summer to get something out of the car. But if they stayed in the car, theyâd die from the heat.
Some people can hold their breath underwater for 30 seconds. But if they tried to go scuba diving without the necessary gear, theyâd drown.
Clearly, someone doing something for a short period of time does not automatically mean that they can do it indefinitely with no problem.
So why do people assume that if someone can walk for a few seconds, they donât need a wheelchair?
the two bad fatigue moods:
gets super emotional, cries over the smallest things, empatheticâ˘, canât handle anything, irritable, overstimulatedâ˘, anxious
canât feel anything, barely able to think, apathicâ˘, canât relate to anything, emptinessâ˘, canât cry, slowâ˘, dissociating
this post is abt chronic illness and chronic fatigue and I hope ppl who rb this knows that
I have a third, moment before I break mood:
ridiculously goofy, slap happy silly, uncontrollable giggling, especially at the most inappropriate times. Laugh at anything, gain many suspicious looks. Highly likely to break in to super emotional, highly sensitive mode without warning. Laugh til you cry. Cry until youâre sobbing.
Shout out to mentally ill people who dropped out of school
- shout out to the kids who were âso brightâ and âheading somewhereâ and had to drop out because school was too much to handle along with mental illness
- shout out to the kids who struggled to get where they got before they dropped out
- shout out to the kids who tried and tried and tried and still couldnât finish
you arenât unintelligent because you dropped out of school, you arenât a delinquent or a bad person because you dropped out of school, just because you did what you had to doesnât make you a bad person
What I think I sound like when Iâm talking to a new doctor about my chronic illnesses:
What the doctor hears: