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Prikvačeni tweet
#AutismParent - there is no such thing. Nobody parents#autism. You parent autistic children. Autism isn‘t its own bodily entity seperate from the autistic person. There‘s no#AutismMom. There‘s no#AutismDad. If you call yourself that you are dehumanizing your child. Don‘t.Prikaži ovu nitHvala. Twitter će to iskoristiti za poboljšanje vaše vremenske crte. PoništiPoništi -
Only took an hour for the acemisics to show up. I was waiting already, y‘all are really slacking... Always happy when bigots just come right out into the open like that - allows everyone to report, block, and create the inclusive safe community we want to be a part of.
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Asexuality is a lot more common among autistic people than among non-autistics. The same goes for other forms of being LGBTQA+. When we consider the differences in experiencing and processing, this is not surprising but rather a logical consequence. Please accept asexuality!
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Asexual people deserve the same rights to have their sexuality respected and protected as anyone else. Asexuality is a valid and complete sexuality, just like any other. Asexuality is not lesser than. Asexuality is not a lack of anything.
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Asexual people experience corrective therapy and treatments. Asexual people experience corrective rape. Asexual people are often not only marginalized by allocishet society, but also within the LGBTQA+ community because they are deemed „not really LGBTQA+“ (they are).
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Asexuality = not experiencing sexual attraction Asexuality ≠ not wanting/liking sex Asexuality ≠ unnatural/broken/sick/wrong/bad/etc. Asexual people are LGBTQA+ and marginalized. Asexual people can discover they‘re asexual at the same age others discover their sexuality.
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If you publish autistic peoples content, pay them. And pay a competitive rate. If you can‘t afford to pay us, make it a non-profit project...for EVERYONE involved. Profitting off us without paying us adequately is unacceptable.
#equality#DisabilityRights#ActuallyAutisticHvala. Twitter će to iskoristiti za poboljšanje vaše vremenske crte. PoništiPoništi -
Needing support to live an autonomous life, regardless of how substantial that support is, doesn‘t justify institutionalization. Please don‘t try to justify it with arguments about lack of resources. I know about the lack of resources. I live it. It doesn‘t erase our rights.
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When someone self injures, the solution isn‘t to lock them up in a padded cell, drug them, and restrain them. The solution is to find out what caused the injury, to eliminate that cause and prevent it in the future, to provide protective gear and support, to enable autonomy.
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I also wrote this thread with something else in mind: The fact that I sometimes injure myself during meltdowns doesn‘t justify institutionalizing me. I still have the right to an autonomous life. I deserve to get the support I need to be able to live with my husband.
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Luckily I rested appropriately even though I didn‘t always know I had a concussion, so I recovered well. I‘ve had several MRIs done in my life and for sure I don‘t have any brain damage. But not everyone is that lucky. So please learn the symptoms and better safe than sorry!
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So far, the symptoms I regularly get from my migraines are worse than the ones I got from my concussions. So because my concussions were mild, and I‘m used to symptoms most people aren‘t used to, I didn‘t even consider I was having a concussion until I got a more severe one.
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I didn’t know I had had a concussion until I got a more severe one and sought medical help. I grew up with severe migraines with aura, which means I am used to SEVERE headaches, nausea, vomiting, dizziness, vision disturbances etc. so I underestimated my concussion signs!
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During my concussion recovery I - took pain killers when necessary - rested a LOT..that was definitely the main treatment - avoided things that strained my eyes (less screen time, no reading) & in turn my brain - avoided sudden and harsh movements - drank a lot - ate mild foods
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It‘s important to note that not having any more discernible symptoms does not automatically mean your concussion is fully healed! If at all possible, please work with a medical professional to guide you through your healing process. Don‘t take concussions lightly.
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During my concussions I never lost consciousness. My main symptoms were - headache - nausea - dizziness - trouble concentrating - eye strain causing headache - feeling tired ranging in severity from mild to moderate, and duration from about an hour, to a couple of days.
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My severest concussion occurred when I fainted in the bathroom, fell, and hit my head on the floor. It took about two weeks to fully recover from. My other concussions occurred from headbanging and they were mild. They took a couple of days to a week to fully recover from.
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Recovery time for concussions depends on the individual case. If hospitalization is not required, rest is still absolute key. Avoid anything that stresses your recovering brain more. Pain medication that DOESN‘T increase bleeding risk may be taken (please ask a doctor).
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You may have a concussion even if you only experience one or some of these symptoms, and even if you only experience them briefly. Symptoms may only last a couple of minutes and you may still have a concussion. If you were unconscious, even a moment, PLEASE get a brain scan!
Prikaži ovu nitHvala. Twitter će to iskoristiti za poboljšanje vaše vremenske crte. PoništiPoništi -
Concussion symptoms: - headache - nausea - vomiting - memory problems - concentration problems - feeling dazed/confused/otherwise „off“ - dizziness - balance problems - blurry/double vision - mood/behavior/personality changes - sensory sensitivity changes - loss of consciousness
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Most people think of car accidents or football players when they hear the word „concussion“. What many don‘t know, is that a concussion can ocur from much less impactful blows/jolts/shakes. If you hurt your head in ANY way and get concussion symptoms after, please see a doctor!
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