I have no power here.

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See, that’s what the app is perfect for.

Sounds perfect Wahhhh, I don’t wanna
deaf-sakura
deaf-sakura

🌻Updated Classroom Wishlist!

Hello everyone! I am a first year teacher from the United States, just trying to beef up my classroom tools, toys, & resources. Some of these are absolute essentials, such as disinfectants and gloves, while others are fun things that can help my students work on their academic, movement, language, and social goals. I’ve tried to keep the price range super wide, so there are some cheap things as well as more pricey.

I work in what’s called an MD special education classroom. MD stands for Multiple Disabilities, meaning that all of my students have more than one major challenge that affects how they learn, as well as related health issues. All of my students are bright, powerful, and capable, and have shown me every day just how successful they can be. They thrive in environments that focus on social connection, exciting multisensory experiences, and valuing their unique contributions to our classroom community.

Please do not feel obligated to contribute, but if you do, then please know your gift will be so appreciated!

🌻🌻🌻🌻🌻🌻🌻🌻

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btrnojutsu
allfrogsarefriends

honestly even when the pandemic is over (whenever the fuck that happens), there are still gonna be thousands of people disabled bc of what covid did to their lungs, brains, kidneys, etc and we’ll probably see ourselves suffering another eugenics movement bc thats literally what happened after spanish flu, ppl were disabled and dipshits were like “these Unfit Unwell ppl are a drain on our resources”

the-home-kvetch

Hi I’m one of these people! Covid gave me ME/CFS and POTS, made my (probably pre-existing) EDS much worse, and caused part of my spine to fucking dislocate (because of the inflammation combined with the EDS).

Please hold people accountable for saying eugenics type shit, including “people need to work for money,” “disabled people are taking up resources,” and “disabled people shouldn’t have kids.”

Source: allfrogsarefriends
flavoracle
flavoracle

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My wife and I took our kids to the zoo yesterday, and thank so my awesome/sexy/amazing wife, I learned about something really cool. It turns out the Portland Oregon Zoo now offers “Sensory Inclusion Bags” that can be checked out for free from the front office.

These bags include things like noise-cancelling headphones, sunglasses, and fidget toys. We checked borrowed three bags for the kids, though at one point when my son wasn’t using his headphones anymore, I gave them a try too.

It’s hard to describe what the experience meant to me. When I was growing up with ADHD, adaptive equipment for sensory overload wasn’t really common or commonly available (at least not as a treatment for ADHD) and by the time I became an adult, I figured I pretty much knew all the coping skills I needed to get by.

And while, yes, I can get by, I realized that there may be far more adaptive techniques and equipment available these days than I’ve ever considered trying. And that even as an adult, I can explore new ways to improve my life with ADHD.

Once I put the headphones on, I didn’t want to take them off for the rest of the zoo trip. It made an experience that’s usually overwhelming and draining far more enjoyable for me, and I was amazed at how much more focus I could give to my family and the parts of the zoo that I actually do like.

I felt a bit self-conscious at first, mostly worrying that I would embarrass my wife as an adult wearing adaptive equipment, but she was FANTASTICALLY supportive, and didn’t even hesitate when I asked if it looked weird or made her uncomfortable. And I was pleased that I didn’t ever really get a sideways glance from the other people at the park either.

It was a wonderful experience, and I have my brilliant/gorgeous/visionary wife to thank for it.

chronic-ills-of-narnia
chronic-ills-of-narnia

When abled people write about us, they imagine how THEY would feel if they lost the ability to do the things they love. They write us hating our adaptive equipment and our disabled lives and bodies and desperately dreaming of being like them. Because if they suddenly became us, all they would want is their old lives and selves back. They don’t know how to write us as whole people exactly how we are. They can’t imagine us feeling pride or love for ourselves or for the things that help us live (mobility aids, sensory equipment, speech aids etc). They write us, but they don’t tell our stories. They tell their stories in our bodies.

talking to the disabled community and future special ed teachers in online spaces: *complicated social theory on the intersection between accessibility, pedagogy, and building up community-based school systems*

talking to my administration: So when the room is too HOT…it makes the kids sick. BUT the kids are already sick, so it makes them VERY sick! 😲  SO IF YOU DON’T COME INTO MY ROOM TO FIX THE AIR CONDITIONING IN THE NEXT HOUR WE’RE ALL GETTING SUED FOR CHILD ENDANGERMENT.

educhums i teach middle school i teach special education accessibility multiple disabilities lol im teaching ONE student for summer school but it happens to be the kid who can't regulate their own body temperature dont worry tho ill keep her safe! :) if it gets too hot we'll go play in the main office with all the admins! :)))))) this WILL be someone elses problem lol

Fun fact!!! You can actually get stipends for attending bigger professional development courses as a teacher! Meaning that I’m actually getting payed to attend some of these summer camps/courses.

I’ve already racked up $700 and am planning to use this money to build a sensory room at my school (which is such a relief because YES, my kids absolutely need this and NO, my district won’t give me any funding). So yes!!! I’m already off to a great start for next year!

i teach middle school i teach sped educhums sensory needs i teach special education sensory room
xxindiglow

Anonymous asked:

Do you have any triggers?

marauders4evr answered:

Jello, Popsicles, Soup Broth. 

marauders4evr

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Nah, I never joke about Jello, Popsicles, and Soup Broth…

marauders4evr

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Indeed, I am!

I’m a disability advocate whose triggers are Jello, Popsicles, and Soup Broth. 

marauders4evr

I legit just lost a follower over this. 

They must be really big fans of Jello and/or Popsicles and/or Soup Broth. 

marauders4evr

For those who have trouble detecting sarcasm - the last sentence about them being fans of said foods was sarcastic. But a few people have really unfollowed me over this. 

The other three replies, including the original, are serious. 

Jello, Popsicles, and Soup Broth are my legit triggers. I would never joke about that. 

I know it sounds bizarre. But trust me, I’m serious. 

(I’m also not a big fan of fluorescent lights.)

marauders4evr

It should be noted that I haven’t received this many death threats since the Great Snape War of 2013. 

marauders4evr

This is by far my favorite reply:

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marauders4evr

All right, folks, take your seats, because class is now in session! Let’s have a little talk…

Yeah, yeah, I know it’s Saturday, but learning is fun.

I’ve had seven surgeries in my lifetime and will probably have many more in the future. And one such surgery, which happened about nine years ago, involved really fun (*sarcasm*) things like tubes that are shoved up your nose and end up in your stomach (I know, I didn’t think it was possible either until they did it), eight gallons of really disgusting fluid, pain, lots of pain, and the direct order that I had to evacuate every single bit of food that was inside me.

And that was before the surgery even began!

After the surgery, I had to stay in the hospital for about a month.

And I was on what’s called a clear-liquid diet.

What’s a clear-liquid diet?

For this particular hospital:

Water, Jello, Popsicles, and Soup Broth.

A meal that was delivered to my hospital room three times a day.

That’s all I was allowed to eat.

For those of you who enjoy doing math: I was in the hospital for a month, which is roughly 30 days. I had to eat this meal three times a day. That’s 90 bowls of soup broth, 90 containers of Jello, and 90 Popsicles. Ninety times I had to eat these things. In the span of a month. 90.

Which means that nine years later, I am actually physically unable to eat these three items without vomiting. It’s a sensory trigger.

So why didn’t I talk about this from the beginning instead of enduring four death-threats, six unfollows, and nineteen messages/comments (not including the death threats and the ones that just said ‘Popsicles, Jello, Soup Broth’ over and over again)?

Well, there’s two reasons.

A.) I don’t have to. People don’t ever have to explain why something is triggering to them. Once they say that it is, it should just be a given.

And

B.) The above comment is right. I am a disability advocate. And part of that advocacy includes advocating on behalf of people with triggers. And so, you’ve all been part of a social experiment for the past few hours - an experiment to see how people react when they see that someone has really bizarre triggers (out-of-context).

And I’m a bit sad to say that many of you have failed. Even other people with triggers and/or other advocates. 

So listen because this is really important:

I know that triggers are a sensitive subject and I know that there are people out there who do joke about them.

But there are even more people out there who have triggers that seem really bizarre and even silly.

And you know what?

You cannot invalidate those triggers.

You cannot assume that someone is joking, you cannot assume that they’re mocking other people with triggers that are more commonplace or ‘sensible’, you cannot assume that they are anything less than genuine.

If someone tells you that they have a trigger, you need to believe them, no matter how bizarre it might seem.

Class Dismissed.

toughaqua777

Louder for those in the back.

If someone tells you that they have a trigger, you need to believe them, no matter how bizarre it might seem.

Source: marauders4evr
teacher-wangji

Interesting PD Session Today

teacher-wangji

So this week I’m attending a virtual “camp” (professional development) for new SPED teachers, and this morning the camp started off with a fantastic presenter. He is LeDerick Horne, a poet, writer, and advocate for students with disabilities, who also has a learning disability himself. One thing he said that really stuck with me was that disabled and neurodivergent teachers need to start “coming out of the closet;” he explicitly encouraged us all to be authentically and openly ourselves, not just for our sakes, but for our students. So they get to grow up seeing what a successful autistic person looks like, or a successful person with a chronic illness. And so that when major decisions are being made for them in districts and governments, they get someone sitting at the table who knows just how to represent them.

So today as our sessions continued, I brought up my own perspective as an autistic/ADHD teacher. I mentioned how I have to put a lot of effort into masking and being approachable so my students don’t miss out on opportunities in school, and how normalizing neurodivergency in young people through inclusion is going to positively effect all peers. And the best part?! I wasn’t even the only neurodivergent teacher! There was someone there with epilepsy, and another with the exact same diagnoses as me!

My afternoon session was a little more awkward when I mentioned it though. The coach didn’t know what to say about it and quickly wanted to move on. But I still think it’s just REALLY FREAKING NEAT how many disabled and neurodivergent people are finally able to become major stakeholders in special education, beyond being students. We’re like…double stakeholders, and we deserve to be listened to and respected for all the experience and education we’ve undergone.

…That being said that coach really did squirm when I mentioned my autism, so I’m DEFINITELY bringing it up even more now to get it through her head that the students we teach today have been and will always be her fucking equals.

teacher-wangji

Update: For today’s session, I changed my profile picture to this to politely remind everyone why we’re all even here:

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