So, state of me

Mental health – still blows, but is somewhat more bearable than three months ago

Talking therapy – is still useless for me, so I’ve finished my six sessions I get for free and am going back to reading books. Currently reading You Mean I’m Not Lazy, Crazy, or Stupid?, and have The Body Keeps The Score waiting in the wings.

Exercise – is something I should be doing, again, but I’ve been struggling to leave the house, so, ugh.

As for more mental health stuff, I’m trying to get back into drawing and colouring, and man, it is so hard after not doing it for about ten years.

Also, I found my old deck of tarot cards in the one of the boxes of belongings I’d left at home when I moved out and mum totally neglected, and it was utterly destroyed.

Yeah.

So I’ve ordered a replacement of the old deck I had, and ordered a new one too, both on Mum’s dime, since it was her fault my stuff was trashed, and she offered to replace things. There’s a lot I’m not going to bother with, and a lot I flat out CAN’T replace, but I wanted my damn deck.

I don’t tend to use decks like a lot of people do. I don’t think they’re magic or sentient or anything (no problem if you do), but I do think you can find answers by using a draw to look at your question sideways, if that makes sense, and using a card to make you think of a solution or look at a situation differently. So that’s what I’ll be trying to do with them. The replacement deck will take at least three weeks to get here, the new one will probably take over a month, so I’ve got some time to think about how to use them before they arrive.

I bought some remnant fabric from Spotlight in dark grey panne velvet, black satin and poly chiffon that’s patterned in grey, green and purple. They’re so I can make a cloth to lay out readings on and make some storage bags for the cards when I’m not using them. The bags at least will have to wait until I’ve got the decks so I know the dimensions and can make them the right size.

Anyone out there interested in tarot who has anything to suggest that might be helpful for me getting started, bearing in mind I tend to be an instinctive reader, not a rule follower, and my decks are going to be fairly gender neutral ones open to intepretation outside conventional cis/het/neurotypical norms?

autistic trait point system

neurowonderful:

taptrial2:

  • toe walking: +5 balance
  • flappy hands: +5 happiness, -2 stealth
  • jumping: +1 athleticism, -4 stealth
  • pacing: +7 athleticism
  • spinning: -60% from usual hp drain while dizzy
  • echolalia: +5 happy, +7 neurotypical patronization
  • sensory processing disorder: -30 total hp, +100 hp healed per 5 seconds in sensory heaven
  • need to chew: +30 jaw strength, +30 drool strength
  • the autistic artist: +50 self-expression, -200 self esteem
  • picky eater: -50 total hp, -80% hp healed from bad foods, +80% hp healed on favorite foods
  • special interests: -10 focus
  • sarcasm detection machine broke: -100 stealth, +10 neurotypical patronization
  • eye contact machine broke: -70 stealth, +100 eyebrow staring capacity
  • nonverbal: -200 stealth, +20 neurotypical patronization
  • stim toy collection: +50 happiness, -40% wallet

I love this. Nothing else has ever been as perfect.

meimagino:

bpdkageyamatobio:

I hate how asking “am I annoying you” becomes a self-fulfilling prophecy

literal actual pro tip, because i used to do this, along with “are you mad at me?” (which, as you know, results in people getting mad at you.)

try asking instead “how are you feeling?” or “i know you’re probably not [x emotion], but i’m having a rough day, could you reassure me that we’re cool?” that way, the focus is on either finding out how they actually feel in that moment, or on the fact that you need reassurance. they shouldn’t get upset that you’ve “assumed” (i know we don’t have control over it!) how they are feeling, because you haven’t said anything of the sort! you’ve only asked how they are feeling or if they can reassure you.

the trick here is making sure you’re surrounding yourself with people who are willing to be honest about how they feel + provide reassurance. (people who are not willing/able to do this should probably not be your close friends, though. idk about you all, but friendships like that are full of doubt and anxiety for me.)

As an autistic/adhder who struggles with reading vocal tone and expression, I rely on ‘am I annoying you’ and ‘are you angry’ on a regular basis because I genuinely need to know this information. ‘How are you feeling’ is useful if I actually want to know the other person’s general state of mind but the former are NEEDED because they are specific and to me, bored, thinking about something, tired, in pain and annoyed ALL LOOK THE SAME. Unless I ask, I am uncertain, and I might make my partner annoyed by misreading a situation. ASKING COSTS NOTHING and she answers me honestly. It saves time and stress on both our parts. I need specifics. Generalities might work for others, but for a lot of ND people, brutal, truthful nonambigious honesty is so, so much better. YMMV, but that’s my personal preference. I understand puns and idioms, but NT doublespeak? Why don’t NT people just say what they meeeeean? Seriously.

geekysciencemom:

What is Autistic Burnout?
a guide from Autism Women’s Network

Signs:
• Lack of motivation (hard to care about goals when everyday life is overwhelming)
• Loss of executive functioning abilities (decision-making, organization, etc.)
• Difficulty with self-care
• Easier to reach overload or meltdown
• Loss of speech, selective mutism
• Lethargy, exhaustion
• Illness, digestive issues
• Memory loss
• Inability to maintain masks or use social skills
• Overall seeming “more autistic” or stereotypical
• May have period of high energy before collapse

Causes:
• Passing as neurotypical / suppressing autistic traits
• Doing ‘too much’, too much stress
• Aging: needing more downtime, having less energy
• Changes, good or bad (relationships, jobs, living arrangements, belongings, environment, routines…)
• Sleep deprivation, poor nutrition, dehydration
• Illness
• Sensory or emotional overload

Strategies:
• Time
• Scheduling breaks, managing spoons
• Leave of absence
• Stimming, sensory diet
• Exercise
• Massage
• Reminders and supports
• Routines
• Better environment/job/etc.
• Boundaries, saying ‘no’
• Dropping the mask/façade
• Solitude
• Absolute quiet
• Creative projects, passions, special interests
• Paying attention to reactions and your body

Sources:
“Autistic Burnout – Are You Going Through Burnout?” Anonymously Autistic.
Endow, Judy. “Autistic Burnout and Aging.” Ollibean.
“Help! I seem to be getting more autistic!” American Asperger’s Association.
Kim, Cynthia. “Autistic Regression and Fluid Adaptation.” Musings of an Aspie.
Schaber, Amythest. “Ask an Autistic #3 – What is Autistic Burnout?”
Thanks to Lindsey Allen, AWN Nebraska, for compiling this guide ©Autism Women’s Network 2017

autisticwomen:

Happy Autistic Pride Day (today, June 18)! 

[image descriptions: 

Image one has a pride flag and AWN logo, with black text on a gold block: “When we chose acceptance and love over fear, we teach our children that they can make this world a better place.” – Lei Wiley-Mydske, What Every Autistic Girl Wishes Her Parents Knew

Image two is the AWN logo with pride rainbow stripes.

Image three reads Happy Autistic Pride Day from Autism Women’s Network with pride stripes, and has the AWN logo.]

adhighdefinition:

BBC Horizon 2017: ADHD and Me with Rory Bremner

“For as long as I can remember, I had a really active brain. The problem is, when it gets too active… it jumps around all over the place, gets distracted by a million and one things when it’s supposed to be concentrating. I used to think that was just what it was like to be me. But recently, I’ve come to suspect that it’s what it’s like to have ADHD.

lexrhetoricae:

adhighdefinition:

Things You Should Never Say to People with ADHD and Why!

People with sensory processing disorders like fibromyalgia and other chronic pain diseases have the same experience. Until I started talking to people with ADHD, I didn’t realize it wasn’t normal to spend every waking minute feeling your clothes against your skin or cataloging the changes in sound and light and smell. It wasn’t until I watched Elementary and saw the characters around Sherlock not noticing sensory details around them that he picks up that I realized it’s not normal for brains to do this. 

Unlike folk with ADHD, though, I never had this experience full blown until I was in my twenties. It build gradually over about a decade, and I thought I’m just getting older.  I didn’t have these issues as a young child, so my lack of focus in my mid-20s  had to be age-related, not ADHD, right? 

And that’s how you trick yourself into thinking you’re normal for years. It’s easier than admitting difference, even as you carefully pick out only silk and pure cotton clothes, wash everything (including yourself) in unscented soap, and eat only a handful of foods (mostly sugar, because it’s boring and you don’t have to think about it much). 

Spoonies, pay attention: if you can’t focus, it may not just be the pain. What else is your brain, primed for pain signals, now also processing without end? 

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.