Well, I deserved that

Sitting here feeling the medium-grade anxiety that is my normal, complete with hypervigilant perseveration, and thinking, y’know, I have Valium now. I’ve taken it once since being prescribed it, for a severe anxiety dream that woke me up in a panic, but I haven’t been taking it for the crap I deal with as a matter of course.

So I thought, well, I’ll draw a card first. See what it says.

I shuffled the heck out of my Wild Unknown and drew The Moon, reversed.
Which is basically the card form of saying, yeah, you have fear and anxiety, and you know they’re about illusions, not reality, BUT YOU HAVE TOOLS SPECIFICALLY FOR THIS, YOU INFANT.

So, I took a Valium.

What my decks lack in subtlety they make up for in smacking me upside the head, apparently.

Two things

Two amazing things happened yesterday

1) My replacement copy of the Wild Unknown Tarot arrived, and after checking every inch I can confirm it is P E R F E C T.

2) For the first time in my (almost) 36 years on earth, I have talked to a doctor who took my word for it that dinky breathing exercises, yoga, meditation, and talking therapy do fuck-all for my anxiety, and that I need help. So she listened, and without any drama, she gave me my first ever script for Valium. I haven’t cried yet, but every time I think about it, I feel like I’m going to. Now, next time I get a day like Saturday, I don’t have to grit my teeth and ride out the misery and hide in my house. I have something that is going to help me step back from that miasma of fear and panic and just get on with my fucking life. I’m so fucking thankful.

jabberwockypie:

PTSD is your brain trying to make sure you DON’T DIE.

Humans are really good at adapting so that we don’t die.  That’s kind of our whole *THING*.  We adapt.

If something BAD and SCARY and DANGEROUS happens, your brain tries to teach you to react better next time.  If the Bad Scary Dangerous thing happens a lot, that’s reinforcing it.  With CPTSD, the Bad Scary Dangerous thing happened often enough and frequently enough that your whole psyche developed around it.

You learn to notice the tiny things that signal the Bad Scary Dangerous Thing might happen – even if you don’t consciously know that you know that – so that you are braced to react and defend yourself.  They become triggers so that you are primed to respond.

Hypervigilance? Better to panic unnecessarily than to get dead because you didn’t recognize a threat in time, right?  It’s uncomfortable and a waste of energy but you’re not dead.

Nightmares about the Bad Thing?  Dreams are PRACTICE.  You are trying to learn how to react better or faster or more effectively next time.

Avoidance? Dissociating is better than just completely breaking and shutting down entirely.

The thing is, even if you are not in that situation anymore, your brain did not get the memo.  It is trying! But it takes a lot of work to convince it that “No really, it is safe now!”

I guess what I’m saying is cut yourself some slack.  You are doing your best and you’re not dead. ❤

Back atcha, sweetie. You said it better than me, and you need to hear it from someone besides yourself. (I know I do.)

ruffboijuliaburnsides:

a quick reminder, not that there are many people who’ll see this:

sometimes someone won’t reblog a post that says something like “reblog if X matters to you” or “if you won’t reblog this bc it doesn’t fit your blog, unfollow me” or similar posts because the post is guilt tripping and they know that sort of thing either a) sets off their own anxiety, or b) sets off the anxiety of people following them.  Or because it’s a social media post that they are actually under no obligation to share even if they agree with it.

obviously there are certain issues, like when someone reblogs a lot of social justice stuff from you but never anything about one particular topic (i see this a lot with posts about antisemitism, from a lot of the jumblr people i follow), but in general, don’t assume someone is taking some sort of stance just because they didn’t reblog one particular post.

this psa brought to you by i don’t mind when the blogs i follow reblog stuff like that, but i almost never will bc i know it sets off people’s anxiety and i disagree with the guilt tripping tone most of them take.

I wrote a meta post on this very topic HERE in February about why these kinds of guilt and shaming comments are harmful, and why I won’t reblog posts containing them.

iamshadow21:

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.

Also, I have Feelings about ‘forgiveness’ being the advised ‘good’ thing for betrayal. This anchors in heavily with the way people treat victims/survivors of abuse.

You don’t get to decide that someone else who’s been abused in any way should ‘forgive’.

You never have to ‘be the better person’ and forgive those who hurt you.

You never have to listen to those who tell you if you don’t forgive your abuser, you’ll be living with that abuse for the rest of your life.

You never have to look at your abuse and say, “Actually, I feel okay with my past and what you did to me and have love and acceptance in my heart for it all, and forgive what you did.”

It is absolutely fine for you to live your life without forgiving.

But gosh, you think, won’t it make me a toxic, bitter ball of hatred, unable to process trauma and move on? That’s what all those well-meaning people tell me.

No.

Actually, what happens is you work out that your abuser is irrelevant. Gradually, you won’t think about them every minute, or every hour, or every day. Eventually, you’ll go longer and longer, until you barely think of them at all, and your life will be as full as anyone else’s of things that are not the abuse or abuser.

That’s where I’m at. And I never had to forgive my abuser to get there.

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.

beepboopbipolar:

Sometimes being chronically and mentally ill is like having a newborn baby that can’t tell you what’s wrong, you know you feel horrible and you can’t lie down and you can’t sit up but you don’t know why. You go down the list- are you hungry? thirsty? sleepy? too hot? depressed? just lazy? a terrible person? And then it dawns on you- you’re in horrible pain, all over. And it’s always been there in the background, it’s just worse right now than usual, for no apparent reason. And there’s nothing you can do about it.

wrangletangle:

When we say “executive dysfunction”, I think it’s important to acknowledge to ourselves (and make clear to those who don’t struggle with it) that we’re talking about a basket of different struggles that we’re labeling with one name for convenience. One person’s executive dysfunction may not look like another person’s, even though the outcome (not being able to complete a task) may look similar from the outside.

Some people with executive dysfunction struggle to break down tasks into their component steps. Others struggle to connect cause and effect (’if I do this, this other thing will likely happen’), which makes daily life a confusing and sometimes terrifying black box. Still others can break down steps and parse out cause and effect, but they can’t start the first task (hello anxiety my old friend), or they get partway through and get distracted by a tangent or forget what the next step was because there were more than three (ah add i never miss you because you never leave), or they run out of energy before they can finish (tons of situations can cause this, both physical and mental). Sometimes people have a poor sense of how long it will take to do tasks, never seeming to budget enough because they don’t track time internally well. Others can only complete a task when they have sufficient adrenaline to spike their brain into focus, which usually means working in panic mode, which associates those tasks with Bad Feelings and further reinforces any anxiety the person may have.

And this isn’t just a few people. This is large-scale, across many groups struggling with different issues, from heavy metal poisoning to autism to add to chronic illness to anxiety to schizophrenia to mood disorders to traumatic brain injury, and more.

What we need, as a society, is to build better structures for supporting those with executive dysfunction, structures that acknowledge the multiple different types and causes. Because we cannot keep throwing the baby out with the bathwater here. We throw away incredible human potential that could help all of us because our society is set up to require a single skill which a large percentage of our teen and adult society doesn’t have and can’t easily develop (or they would have, trust me), or previously had by has temporarily lost due to injury or illness.

Instead of treating executive function as something that some people have developed and others haven’t, like artistic skills or a talent in maths or the ability to visualize systems or managing people, we treat it as a default that some people haven’t mastered because they’re [insert wrongheaded judgment here].

What if we treated the visual arts that way? If you can’t draw skillfully, you must be deficient in some way. How can you not draw? Anyone can draw. You start as a young child with crayons, what do you mean you can’t do this basic task?

Never mind that it’s a really complex skill by the time you’re expected to do the adult version, rather than the crayon version. Never mind that not everyone has been able to devote energy to developing that skill, and never mind that not everyone can visualize what they want to produce or has the hand-eye coordination necessary to accomplish it.

Now, I have friends who say that anyone can draw, and maybe they’re right on some level. But it’s hard to deny that it helps that drawing is optional. That you can opt out and no one thinks any less of you as a person. Executive function is treated as non-optional, and to some extent, since it’s involved in feeding and clothing and cleaning and educating oneself, it’s not entirely optional. But we make all of those tasks much harder by assuming by default that everyone can do them to an equal degree, and that no one needs or should need help.

If we built a society where it was expected that I might need timed reminders to eat, I would probably remember to do it more often. I certainly did as a child, when the adults around me were responsible for that task. Now that I’m an adult, the assumption is that I somehow magically developed a better internal barometer for hunger. Many people do. But I and many others did not. Recognizing that there are many of us who need help and treating that need as normal would go a long way toward building support into the basic fabric of our society.

But then, I guess that’s been the cry of disability advocates for decades; just assume this is a thing people need help with and build the entire structure with that assumption in mind.

How to Live Better With Executive Dysfunction

strangerdarkerbetter:

How to Live Better With Executive Dysfunction

Yesterday we talked about what executive dysfunction is and today we’re going to talk about some ways to live a better life with executive dysfunction. If you’ve ever tried to look for resources on how to cope with executive dysfunction, I’m sure you’ve had the same desire I did to bang your head against a wall in frustration as basically all of the resources out there are for how parents can…

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