cameoamalthea:

greenjudy:

pyrrhicgoddess:

thgchoir:

no offense but this is literally the most neurotypical thing i have ever seen

Uhhhh… no.
This is what they teach you in therapy to deal with BPD and general depression.
When I got out of the hospital after hurting myself a second time, I got put into intensive outpatient program for people being released from mental hospitals as a way to monitor and help transition them into getting them efficient long-term care.
This is something they stressed, especially for people with general depression. When you want to stay at home and hide in your bed, forcing yourself to do the opposite is what is helpful. For me, who struggles with self harm- “I want to really slice my arm up. The opposite would be to put lotion on my skin (or whatever would be better, like drawing on my skin) the opposite is the better decision.” It doesn’t always work because of course mental health isn’t that easy, but this is part of what’s called mindfulness (they say this all the time in therapy)

Being mindful of these is what puts you on the path to recovery. If you’re mindful, you are able to live in that moment and try your best to remember these better options.

I swear to god, I don’t get why some people on this website straight up reject good recovery help like this because either they a)have never been in therapy so don’t understand in context how to use these coping tactics. Or b)want to insist that all therapists and psych doctors are neurotypical and have zero idea what they are talking about. (Just so ya know, they teach this in DBT, the therapy used to help BPD. The psychologist who came up with DBT actually had BPD, so….a neurotypical women didn’t come up with this.)

I have clinical OCD and for me, exposure therapy–a version of “do the opposite”–has been fundamental. I’ve had huge improvement in the last year, but I’m 100% clear that if I hadn’t done my best to follow this protocol I’d be fucked. I have a lot of empathy for that moment when you’re just too tired to fight and you check the stove or you wash your hands or go back to the office at midnight to make sure the door is locked. But the kind of therapeutic approach outlined above has been crucial for me. 

It’s hard to do. I’ve weathered panic attacks trying to follow this protocol. But I’ve gotten remarkable results. I was afraid to touch the surfaces in my house, okay? I was afraid to touch my own feet, afraid to touch my parrot–deliberately exposing myself to “contamination” has helped me heal. I can’t speak for people with other issues, but this has helped my anxiety and OCD. 

I feel that tumblr, in an effort to be accepting of mental illness, has become anti-recovery. Having a mental illness does not make you a bad person. There is nothing morally wrong with having a mental illness anymore than more than there’s something morally wrong with having the flu. However, if you’re “ill” physically or mentally, something is wrong in the sense that you are unwell and to alleviate that you should try to get better. While there is not “cure” for mental illness, there are ways to get better.

There was a post on tumblr where someone with ADHD posted about how much you can get done when you focus and was attacked for posting about being “nuerotypical” – when she was posting about the relief she got from being on an medication to treat her illness. 

I saw another post going around tumblr that said something along the line of “you control your thoughts, why not choose to have happy thoughts” which again was shot down as “nuerotypical” but while you don’t have control over what thoughts come into your mind, you absolutely can and should choose to have happy thoughts. In DBT we call this “positive self talk”.

I’m in DBT to help treat PTSD stemming from child abuse. The abuse and abandonment I experienced destroyed my self esteem and created a lot of anxiety over upsetting other people. DBT has taught me to recognize when my thoughts are distorting realty ‘no one likes you’ and answer back ‘plenty of people like you, you don’t need everyone to like you, especially if the relationship doesn’t make you happy’, to respond to the thought ‘I’m so worthless’ with ‘you’re really great and have accomplished something’ 

And it’s not easy to challenge your thoughts, it’s a skill that’s learned and it’s hard to force yourself to think something that doesn’t seem authentic or even seems wrong to think – it’s hard to be encouraging towards yourself when you hate yourself – but you force yourself to be aware of your thoughts and push back when you fall into unhealthy patterns 

That isn’t “so neurotypical” that’s recovery. 

Not shaming mental illness doesn’t mean shaming RECOVERY.

Pro-Recovery isn’t anti-disability. 

Do not shame healthy behaviors as “neurotypical”.

Learning healthy behaviors and taking steps to treat mental illness and disorders including taking medication if that’s what works for you is important. You shouldn’t be ashamed if you have mental illness, but you shouldn’t say ‘well I’m not neurotypical therefor I can’t do anything to get better’ – while there is no cure for mental illness, there is a lot you can do to get better, to function better, to manage your mental illness and be safer, happier, and healthier for it. 

I’m sort of on the fence here, because sure, there are things I can do as someone with depression/anxiety/PTSD to get myself out of negative patterns of behaviour and thought. These things are hard, almost always harder than just defaulting to how I feel and think without challenging them, but that doesn’t mean I shouldn’t try.

BUT.

I am also an autistic person who probably also has inattentive type ADHD, and ignoring my body and mind telling me “okay, I need to leave now, I need to shut down for a while, I need to recharge, I need to get out of this environment” and pushing into areas of sensory and social discomfort CONSTANTLY is a great way for me to end up in meltdown, shutdown, and maybe even end up with a “hangover” for days where all I can do is sleep and watch TV. I was constantly told, as an undiagnosed autistic person, that these sensory and social limits didn’t exist, that “everyone else” was just fine, so these messages were fake and that I was just “shy” and “high strung” and needed to push myself. Scared in social situations? Do public speaking! and so on, and so forth. Neurotypical standards of what was resonable to “push through” resulted in periods of being housebound, temporarily nonverbal, and so anxious and depressed I couldn’t do anything. It absolutely tanked my self-worth. It made me disregard these warning signals my autistic brain gave me that could have helped me avoid burnout. Learning how to notice and respect these warning signals has been an incredibly difficult process, because ignoring them was reinforced so often, for the first twenty-five years of my life.

So, lists like this have their place, but for neurodiverse people, they are only useful if they have the self-knowledge about what is useful and what is going to be harmful. This is something I didn’t have until very recently, and something I still struggle with. It’s lists and advice like this that made me continuously force myself into situations that harmed me, and made me ruthlessly repress stimming and selfcare that may have helped me. Those stimming and selfcare behaviours didn’t conform with the list/advice, you see. They were particular to my neurotype, and were things I had to discover/rediscover for myself, because no professional or well-meaning non-professional ever knew they were needed, BECAUSE NONE OF THEM WERE MY NEUROTYPE.

So, yes, challenge negative behaviour and thought patterns.

And yes, it’s the most neurotypical thing I’ve ever seen.

Listen to your body and your mind and take care of your SELF. Because there is no ‘one size fits all’ for mental health.

asanvan:

Check out the trailer for DEEJ, a film made by an non-speaking autistic advocate!

“A nonspeaking young man dreams of autistic civil rights. The
documentary film DEEJ with its insider view of autism, challenges us all
to live inclusion.”

https://www.deejmovie.com/

Genuinely sitting here with tears in my eyes. I read Reasonable People some years ago now, and it remains one of my favourite autism books, period. Since I found out there might be a film, I’ve been waiting, patiently, hopefully, and this looks like it’s going to be just as amazing as I hoped. So excited for the full movie. So happy.

drakonera:

Image description:

If you believe this person can pay attention without seeing your face, [image of a woman on the phone]

why can’t you believe they can too? [images of children looking down/away]

Eye contact makes comprehension harder for many autistics.

tigerator:

before you ever even consider having a child you should be ready to handle a disabled child, you should be ready to handle twins, you should be ready to handle a gay child or a trans child

because if you’re not ready for your child to be anything other than one straight, cis, able bodied and able minded child, you’re going to end up neglecting and abusing somebody for years to come

and even if your child is all that, you might have a feminine boy or a masculine girl on your hands. so be fucking ready for your child to be a human being and not YOUR PRODUCT or PROPERTY or CREATION

fucking sort your shit out, i am so tired of shitty parental sob stories about how “hard” it is to “raise” (read: beat the divergency out of) an autistic child or whatever. do you know what’s harder? being the divergent child of parents who you’ve already let down by virtue of existing in a way they didn’t ask for. putting up with years of neglect and abuse because you’re just not good enough for them, you weren’t what they were planning for or expecting.

Giveaway A Day in April

stimtastic:

The “Giveaway A Day” is back by popular demand!

image

April is Autism Acceptance and Autism Awareness month. It’s also a month
that can be really hard for autistic people. So we’re hoping to making things a
little less hard by creating a fun new giveaway each day.

Most giveaways will be stim toys, jewelry and items made by autistic and
neurodivergent artists, but we’ve also got a few big days planned,
including iPad Airs, weighted vests, premium AAC apps, and noise
cancelling headphones. We’ll also be doing second-chance giveaways–one
more chance to win a giveaway you entered during the preceding week. That means
each giveaway you enter gives you two chances to win! 

April 1st Giveaway – how to enter: 

  • The first giveaway is easy to enter – just reblog this post to help spread the word! 
  • We’ll draw 1 winner for every 100 reblogs and each winner will receive the chewable jewelry item of their choice.
  • Deadline to enter: 1 PM (EST) April 2nd 


Executive Function tip: Bookmark the master post on Stimtastic.co and check back regularly for updates. We’ll post details
on each days’ giveaway, including how and where to enter, who won and
what’s coming up next. 

Please check the general rules on the master post before submitting questions. Spoons are in short supply in April! 🙂

***A note about deadlines: Doing a giveaway every day is a lot of work so some drawings might not happen right at the announced time. Some drawings might happen later than announced, but we will never draw a winner before the stated deadline. 

Thank you to 

Half Crazy, Completely Brilliant for the wonderful graphic!

Autism Acceptance Month Resources

k-pagination:

View full page for all details.

Things to do that support the Autistic community

General

Support the Autistic Self Advocacy Network (ASAN), an autistic-run nonprofit that does a lot of policy work

Support Autism Women’s Network (AWN), an autistic-run nonprofit dedicated to providing community and resources to Autistic women and girls.

Other Groups and Stuff to Support

Check out the Autism Acceptance Month Website (run by ASAN)

The #RedInstead Campaign instead of Light it up Blue

Follow the Autism Acceptance Day page started by Paula Durbin-Westby

Things to avoid 

Avoid Autism Speaks and Lighting it Up Blue, and organizations with a focus on cure, prevention, etc.

Avoid Posting Personal Details about your Autistic Relatives Online (links are explanations)

Click here to view more details on the page.

Autism Acceptance Month Resources

sleepy-hylian:

queen-val:

mrs-transmuter:

elaxisfae:

lolhooplacatz:

crazyeddieme:

just-a-penis-with-a-dream:

kibblesundbitches:

unaspi:

bluechirri:

fishyinspace:

supervengers:

cishetsnotinvited:

transheadcold:

nauticus:

friendly reminder not to support lindt this easter season, or apparently ever again, because they support autism speaks.

Wowwwwwwww

SIGH.

can someone please explain why autism speaks is so bad?

because they’re adamant that autism is a disease that can be “cured”. They don’t have a single autistic person on their board. Autism Speaks produces advertisements, small films, ect. about what a burden autistic people are to a society. They only spend about 4% of their money on “family services.” They create a stereotype that makes it hard for actual autistic people, like myself, be heard and recognized as actually autistic. I was diagnosed with Bipolar Disorder before they realized that I actually showed signs of Asperger’s. They don’t actually help us. 

That’s the problem with Autism Speaks. 

(tw for violence, ableism, abuse, murder, and death)

It goes deeper than not having any autistic board members. Many of the allistics running the organization promote the horrific notion that you’re better off dead than autistic, and their influence and “activism” only supports the ideology resulting in the continued murder of autistic children and adults by their parents and caregivers.

Former Autism Speaks board member Harry Slatkin, whose wife, Laura, continues to serve on the Board of Directors, stated in an interview with Town and Country while still a board member that sometimes he hoped their autistic son David would drown in the backyard pond rather than “suffer like this all his life.” Evidencing a pattern of similarly violent rhetoric, Autism Speaks is also responsible for the 2006 PSA “Autism Every Day“ in which their then Vice President states on camera that she considered putting her autistic daughter in the car and driving off a bridge, and that the only reason she refrained from doing so was because her other, non-autistic daughter would have been waiting for her at home—her autistic daughter was in the room as she made these statements. Furthermore, the producer of this PSA explicitly admitted that the film was intentionally staged to portray negative images of autistic people and their families.

Only four days following the release of “Autism Every Day,” pathologist Karen McCarron smothered her autistic daughter with a garbage bag. McCarron stated that she murdered Katie because her “autism had not been improving,” had thought about killing Katie, that made an earlier brief attempt at suffocation, wanted to cure Katie, thought killing Katie would make her “complete” in heaven, and wanted to live without autism and thus had to kill Katie. Investigators found that McCarron was obsessed with different treatments for Katie. (See People v. FRANK-McCARRON, 934 NE 2d 76 – Ill: Appellate Court, 3rd Dist. 2010.) Though it is not presently possible to draw a direct connection between Autism Speaks’ PSA and Katie’s murder, this crime and dozens like it only underscore how the kind of rhetoric that Autism Speaks favors only serves to recklessly endanger the lives of autistic people.

(source article)

Autism Speaks also publicly supports the Judge Rotenberg Center, a group home for autistic and neurodivergent students that uses “treatments” like food and sleep deprivation and electric shock to try and train the residents into acting neurotypical. The center has changed states three times in an attempt to bypass regulation against abusive treatment, and their practices have resulted in the deaths of more than one student.

It’s not just an issue of Autism Speaks making it harder for us to get proper diagnoses and treatment. Autism Speaks is actively killing us.

Well shit.

I was eyeing up their strawberries and cream lindor the other day but this is more important than delicious chocolate.

you all need to know this. You really do. Please do not support Lindt or anything that supports autism speaks. Please.

Seriously Lindt makes my favourite chocolate ever?? but My boyfriend is my favourite person ever so looks like I’m gonna go find a better candy maker, one that doesn’t support murder.

ghirardelli > lindt, and not just because of the autism speaks thing.

I have autism and IM NOT JOKING THIS IS IMPORTANT

Exactly. The autism “research” that autism speaks does, reeks very heavily of eugenics.

Okay, but it’s not enough to just not buy this brand of chocolate. It has to be made known exactly what kind if org Autism Speaks is. The reason they spend so much on PR is so that the general public never funds out how reprehensible they are. No non-autistic person I speak to is ever aware of these things.

If you find out an company is partnered with Autism Speaks, contact them. Call, email, write letters. Offer alternative charities. It may not work every time, but the more people you tell, the fewer people will be likely to donate to them in the future.

this post is from 2014, anyone know if lindt still support autism speaks?

https://www.autismspeaks.org/site-wide/lindt

Unfortunately this is an ongoing thing every year.