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#so they could see how often the professionals dont even know what the disorders i AM diagnosed w are.
moodr1ng · 2 years
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twice recently ppl who work in mental health care have asked me about how having schizoaffective disorder affects my relationships and while there is a legit answer to that. the reason theyre asking is bc they think "schizoaffective" means something about affection or relationships. so i sit there and explain literally the diagnostic criteria of schizoaffective disorder. to ppl who are mental health providers. and to be clear i explain it bc they legit do not know what schizoaffective disorder means. so thats normal
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hi, i wanted to get any kind of input or opinion because i think theres something really wrong with me. ive always been obsessed with labels and terms to identify myself, always switching them around and finding a new one regularly to base myself off of. right now at least i have no actual sense of identity and its very possible i could just be reaching because i tend to do that a lot but i dont remember a time where i genuinely had a hold on who i was, aside from when i had a really unhealthy obsession with one singular person for about 2 years. my entire life and mental state revolved around them during that time and to be honest, even though we arent on speaking terms anymore, still seeing them on socials messes me up pretty often.
anyway, the main issue is that i dont really know who i am or who i even want to be. i cant even really keep a name/nickname to go buy for longer than a few months only because i know it inconveniences the people around me (however few there are now). and thats another thing! im really iffy about making connections with people now because a lot about it makes me uncomfortable, like the responsibility and having to deal with another person all the time. i know that sounds really shitty, but i feel like i spent all my love ill ever have on that one person for two years and now that its gone, its never coming back. im still very lonely now but the thought of trying to fix that is really uncomfortable to me. its not that im incapable of making friends, its that after a while ill kind of get tired of them? something about consistency makes me restless and i know its shitty because im a really up and down kind of friend, like recently ive only been talking to people when i feel like it, which is one big reason i dont want to make friends and put people through that.
back to the labels and identity thing. its always kind of been there, but recently the urge to cling to some sort of label or answer for my behavior and thoughts and feelings has been so strong that i almost wish i was genuinely delusional or something. or just that something was seriously wrong with me, just so that i have something new and big to cling to. i know thats bad and unhealthy but i dont know how else to function. ive been thinking recently that i have a lot of narcissistic traits, or at least self centered tendencies. i always operate like im the main character. i always do things with the thought in mind that there will be no negative outcomes for me, and if there so happens to be one, then ill somehow weasel my way out of it. i think that everything will always go well for me, which is weird because it very much has not in the past. a lot of bad things have happened to me, but in a weird fucked up kind of way im glad they did. because now i have some sort of trauma to cling to and roll into my identity. but the flaw in that is that i need a new one every so often. i cycle through different traumas and disorders and sexualities and genders and names and everything that i really, genuinely dont know who i am. and thats why i think somethings wrong with me. because what normal person thinks and operates like this? i dont know if i fully described the reality of my situation, or if im just saying that because i want it to seem worse, but thats about it. sorry for the long ask. i hope you can get around to answering
Hi anon,
I think to some degree its okay to like labels, as they can provide us a sense of structure and being able to name things can give a lot of people comfort. It's also okay to change your identity, as identities are fluid and naturally change over time. You're allowed to change your identity as many times as you want because it's literally yours to dictate, you know?
However, there are many different possibilities as to why you may be experiencing this frequent shift in identity. While I can help explain what these possibilites might be, it is crucial to consult with a mental health professional for an accurate assessment and diagnosis.
One of the possibilities is that you could have some narcissistic tendencies, as from my understanding of NPD, it's about basically trying to regain control of feeling worthless or helpless by constructing a reality of grandiosity that can be incredibly fragile (please correct me if I'm wrong).
Also in the realm of personality disorders, the idea of having "identity disturbance" and "unhealthy obsessions" with someone is characteristic of BPD. Identity disturbance, also sometimes called identity diffusion, is described as an "incoherence, or inconsistency in a person's sense of identity. This could mean that a person's goals, beliefs, and actions are constantly changing. It could also be that the person takes on personality traits of people around them, as they struggle to have and maintain their own identity." Of course, you can experience identity disturbance without BPD, but it's still a common experience among pwBPD.
Another possibility is tired to when you said "i cycle through different traumas and disorders and sexualities and genders and names and everything that i really, genuinely don't know who i am" as it reminded me of how a system might experience their identity, especially if they don't realize they're a system. This is not me saying you're definitely a system, but the possibility of plurality could be something to explore further as well.
Ultimately, this could be something to explore further with the guidance and mediation of a mental health professional such as a therapist, who can work with you to identify more concretely why you may be experiencing these things. They can also help you navigate these feelings and provide guidance tailored to your specific needs.
It's important to practice self-care and be gentle with yourself as you navigate your identity. Please know that it's okay to take your time and embrace the journey of self-discovery. If anyone has any additional insights or suggestions, feel free to add on. Otherwise, I hope I could help, and please let us know if you need anything.
-Bun
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scatterpatter · 1 year
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Mnnngh art vent under the cut
I really miss when art was easy for me. It used to come so, so easy, even though I'd say my art wasn't as good as it is now. Like I'd def say I've improved, but its so much harder to get art out now than it used to be
I look back at the art I used to make and I seriously lament how easy it was. Even if it was just doodles, I could get so many out, I remember back in like 2019 i could often get at least one doodle out a day and it felt great. It was my outlet, my way I connected with others, the way I shared ideas and made stories, and now I feel that outlet has been practically severed and it really, really hurts
Artfight def hurts the worst. I was so excited for this year, so ready to reconnect with a lot of my friends and bond over silly AF attacks, and it was genuine! I didnt have any big plans this month other than just doing my job so I was so happy to do this. July last year was awful, I was in a horrifically abusive situation and that abuse reached its peak last July, I was in a bad bad place. But I've completely cut that abuser from my life and I'm in a much better space, so I really thought this July would be me turning things around
But as soon as I got a lot of attacks, I just- fucking shut down. I kept thinking on how much "make up revenges" I'd have to do and it got to the point where I'd get overwhelmed every time I picked up my tablet. What became "Hehe can't wait to make art for my friends!" Quickly spiralled into "Oh god I need to do so many revenges I cant keep up", and it just made me catatonic and I hate that. And the worst is that I know no one's exepcting me of anything, I dont have to revenge everyone, its all for fun- I know its just this expectation im putting on myself and im the only one disappointed in myself but I just cant stop how catatonic its left me and its really tough to deal with because ive only done 1 attack so far. Ive spent the entirety of July going "shit i need to work on attacks. Its ok ill do it later." And now its July 31 and ive only done one. I set a goal of doing at least ten. I thought ten wouldve been manageable, but I just cant do what I used to do and it really really hurts
And I keep being told that Im having a hard month. That works been stressful and working 40hr a week leaves me with significantly less free time than I had back in college, so of course i have less time/energy for art, but it still hurts because I dont. Feel like work has been that bad. Yeah its been bad but ive dealt with horrific stress before and ive handled it fine. I feel like if I go "its been a rough month" ill be saying that every month. And i dont want that. Im really healing and im getting in better places, I feel like still struggling this much doesnt feel "right". Hell my therapist just told me that i might be in remission or partial remission for my major depressive disorder. Like I have a professional telling me im getting better but I still struggle to do something that came so easily and it hurts really really badly.
Im gonna see what i can do for last minute attacks. Might not be great attacks, but i want to see if i can get something, anything out. It just hurts because i had so many ideas for my friends and I dont know what Ill be able to do for them and I feel horrible. I feel severed from them and from my main outlet of connecting with others.
And i know its just a sign of burnout or art block or mental illness or what the fuck ever. But I feel like ive been making too much progress in myental health to be struggling this hard. I love making art and i love artfight and sharing art with my friends but as soon as I try, I go completely catatonic and its really really hard because i used to be able to do this so easily and i want it to be easy again but I dont know what im doing wrong to still be struggling this hard
Idk bottom text
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Tips for someone closeted abt their disabilities? Asking for a friend
hiiii !!! love you, i hope you are doing fine!
hmmm, THAT IS A COMPLICATED TOPIC YEAH... you can only mask so many of your struggles and a lot of it depends on the relationship you have with others and the enviroment you are in. i am not sure i can help, but i will ramble for a bit, okay!!
generally speaking:
1. keep in mind you do not need to tell someone. and if you can deal with it, especially if you are in a stressful risky enviroment where telling people could have repercussions on you, sometimes it can be beneficial to remain hidden. your identity really decides what you can and cant do in society 2. what also factors into this is whether you have a professional diagnosis. i am Very pro self diagnosis but unfortunately not everyone is and professional/school/uni enviroments just straight up dont really care. being taken seriously is always a huge struggle, no matter the disability/chronic illness. 3. seeing how your health is on the line, its usually good to be honest and upfront about it, since it can really help!!! its still definitely worth it, may that be to ask for accomodations, clear up confusion, or just to get it off your chest. its freeing!!
from my own experience, here is what i found:
i am always as upfront and unapologetic about it as possible. this is difficult and it takes practice but it is worth it. i feel like the more confident you appear, the more people are likely to instinctively take you seriously. + it always sets a sign to yourself and others to not treat the topic with any shame!!
people can be ignorant on accident, when they dont understand smth. so instead of describing what your disability does, i find it helpful to tell others how it affects your life and, if necessary, what they can do to help you/create a safer enviroment for you.
i think its generally good to start out by using easy terms and categories other people will instantly recognize before getting into the details. to be relatable, as the kids say and love to be. depends on the situation though. (like, for example, i have narcolepsy. no one knows what that is but if i tell people its a neurological disorder, that includes seizures and excessive exhaustion and tiredness, they instantly get a vague idea.)
be prepared to provide whatever the other end may accept as "proof". this is upsetting and it sucks. but you have to expect it unfortunately, even in casual enviroments. if you dont have anything official, a clear definition of how disability affects your life can help get the serious nature of the situation across.
you will find yourself explaining your disability over and over and over, so lay out a "battle plan" in your head that contains the most important information (symptoms, how it affects your daily life, which kinds of aid you need with it) it gets tedious but private people will often just.... forget. we all have our own lives and disability is usually unfortunately not a topic on peoples minds. (we can change that however >:))) )
this one sucks but. take care of yourself and be prepared to treat yourself better than the people who may push your away bc of this. i have ended many relationships with friends and family because they treated me terribly in relation to my disability. there are always people who will love and understand you.
if you know someone who already knows and supports you, it can help to have them be present. just as backup you know. and even if thats unnecessary, as emotional support.
as for any sort of school or work enviroment: gotta bite the bitter pill and just hand a docs diagnosis letter to people and ask for what you need. in relation to this, look up what sort of benefits/accomodations you can receive in your country and hand info on that in alongside the diagnosis. sometimes theres also local social services who can provide accessible info on this. you gotta be direct and demanding about it or no one will do anything, in my experience.
this got kind of lengthy, so i hope some of it is helpful somehow?!??! aaaaaaa
also, everything depends on the kind of disability ofc and the specific stigma related to it. my personal issue is people keep hitting me with the "wow i wish i could sleep as much as you do" (bruh,... my days are like 10h long. with maybe 4h i can "work" in. permanently) so i always try to lead the conversation in a way that wont give others a chance to attack me in predictable ways o|<
its genuinely super hard but necessary and sometimes extremely good for you to be open about your disability. the world wasnt made with us in mind but with more information and social acceptance, it can be. never let others get you down!!! youre strong as hell!!
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call-of-ishmael · 3 months
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Mental Illness and Fictional Characters
Id like to make a post of general discussion on canonical or interpreted mental illness in fictional characters and why, well, its complicated!
Im the Ishmeal OCD poster, so i clearly like analysis on that sorta stuff
But one thing i want to mention too is
The most perfect of writing, the most accurate and made by a person with that condition writing even, is never gonna be perfect
What do i mean by this?
Well going back to the character im very interested in, ive seen a fair share of people, even some with OCD say they dont think she has it, to them they do not see any manifestations of it. And you know? Thats not a wrong position to have, they arent incorrect.
Cause mental illness is a varied and complicated thing
When it comes to saying a character has or doesnt have a certain disorder you cant treat it the same you would a real person, cause you cant sit down a character and interview them and do psychometric testing on them
In my own experience having OCD while me and someone else with the condition can relate to a lot of what we struggle with in a lot of ways, we will differ often times pretty drastically on HOW it affects us. Its why often times a trained professional is needed for evaluation, theres a lot of factors
Also even if something is canon it doesnt really mean its accurate, Toko in Danganronpa is stated to be DID but... shes not as far as i know a very good example of it and has a lot of negative common stereotypes attached to her.
And sometimes, it could even be outright been stated for a character to NOT have a condition and it still fits eerily uncannily well into how they act
I can talk about endlessly on why i find Ishmaels experiences deeply uncomfortably real and relatable and how she behaves in a way i feel is OCD and fits with my own lived experiences
And someone else can say how they think she doesnt at all fit their own lived experiences with OCD and with the experiences of others theyve met who have it
And neither of us are really wrong. Cause mental illness is more varied than youd think! To the point theres talk in the field of psychiatry on if our current diagnostic apporach and labels are even sufficient enough for it!
Not sure how to close this other than remember to be nice to other people, headcanons and character analysis are at the end of the day a thing we do for fun
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bi-dazai · 3 years
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okay while we're on the subject of eating healthy and exercising, I want to vent/talk about weight loss. This is gonna be a rly controversial, very personal and extremely long post but I do want to make a point. I'm not going to discuss every fucking nuance of haes or my EDs. But for clarity, know that my eds are complicated and were mostly osfeds - minor anorexia osfed in high school and bed osfed when I was 18-19. after i realised how fat i was the minor anorexia came back and over the pandemic it became full scale anorexia nervosa.
I'm 5'3. The healthy weight range I should be in is in the high 40s-low 50s. I went up to TWICE that by the time I was just nineteen years old. It wasn't fun being fat. I consumed as much fat acceptance, fat activism content as I could, I pretended I was confident and happy even when I was fat. But I wasn't. Because people don't just get obese accidentally. A little overweight, yes. But obese? No. You get obese from depression, from giving up. You don't want to move so you don't. You're sad all the time, and the body positivity circles say eat comfort food, whatever and as much as it makes you feel better!! Do you know what that is? That's encouragement of BED. Do not say that. Because I did that. I ate sugar and junk food, I was still depressed.
I was reading these posts that were claiming fat people shouldn't be weighed at the doctor, that your weight shouldn't count, that BMI is incorrect and doesn't matter, etc etc. There were posts saying that they got "perfect bloodwork" (what even is that? I knew that was wrong, I've had chronic iron deficiency for a decade!) even though they were fat, so they had to be healthy, right? I got shown pictures of obese ballerinas and obese weightlifters blah blah blah. And I grew and grew, and I got to almost 85kg on the fast track to 100kg before reality smacked me in the face and I realised I was shortening my lifespan by decades.
Here's what it was like being obese!
- joint pain, constantly
- could barely walk anywhere without feeling out of breath
- couldn't find any fashionable, good quality clothes (plus size stores either carry unfashionable clothing, or fashionable but cheap quality clothing. I don't like to waste money on cheap clothes)
- more acne than I'd had in years
- oily skin
- more difficulty feeling "full"
- JOINT FUCKING PAIN
- rashes from skin rubbing against skin!
- even larger chest, making me MORE dysphoric
- back pain!!
- snoring - this is not just embarrassing. This is potentially deadly.
- DYSPHORIA
- KNEES. JOINT PAIN.
- DYSPHORIA
this was just things I felt physically, noticeably! The things that my fat was doing on the inside was even worse. Fat isn't just this layer of packing peanuts that appears on top of you. It coats your organs. It gets everywhere. It makes your entire body run worse.
Fat also makes it much more likely for you to not just GET cancer, but it it also makes it harder to FIGHT cancer. Being obese makes almost every single goddamn sickness on the planet worse because when you have THAT MUCH fat tissue the hormones and shit it secretes fucks EVERYTHING up.
Yes there are obese bodybuilders. Yes there are obese ballerinas. Let's talk about those two.
There are plenty of drs and dieticians who have pointed out the obvious - if an obese person was really, actually eating healthily and exercising every day, they would not stay obese forever. Its not magic, it's thermodynamics. CICO done right works for everyone. If you are eating healthy, appropriate portions for weight loss at your TDEE and exercising it would literally be IMPOSSIBLE for you not to lose weight!! Even more the heavier you are because when you exercise you carry around a lot more weight.
Obese weightlifters are still obese. They are not proof you can be obese and healthy. They are still going to die younger if they do not lose weight.
Let's talk about fat ballerinas. The only ones I've seen are trainee ballerinas, not professional ones. And their performance looks impressive at first, until you look closer. You notice their balance is never quite perfect, their control can be amazing and the best ever but they'll still be off. Why? Because fat moves around with your movement, and it displaces your balance and your line of movement. It's simply not possible to do something like ballet dancing as a fat person without risking major injury as well. En pointe is already stupid dangerous for the skinniest ballerina. Going en pointe at anything above 60kg is going to get progressively suckier the heavier you go. And god help your ankles because falling down will always end in a major injury.
I'm so fucking done with "fat acceptance". I'm tired of "body positivity" being a movement about obese middle-upper class white women and not about scars and disabilities etc like it was focused on in the start. I have no problems with Health at Every Size - every person should feel happy to workout, to eat healthy. I have no problem raising issue with people bullying others for their weight as well. That's wrong. But pretending that it's Healthy at Every Size is a fucking lie, and it's one that could've sentenced me to an early death. Healthy at Every Size said I was condemned to joint pain and oily skin and depression and exhaustion for the rest of my life based on cherrypicked sentences from studies that didn't agree with them. That "95% of diets fail" sentence in particular drives me up the wall. You don't need a diet to lose weight, you need healthy CICO, you need to eat below your TDEE, you need to eat healthy, and you need to exercise. All you have to do at first is go on a 10-20 minute walk, whatever pace you like, a few times a week.
You can BE fit, you CAN lose weight! You are not sentenced to having joint pain and an increased risk for cancer and a less effective COVID vaccine for life. You can change your body in incredibly ways. You have no idea what you are capable of.
There's this myth that weight loss takes keto and shakes and diet pills and crash diets etc. It doesn't. All it is is making sure you eat less than your TDEE, eating HEALTHY calories, and getting your heartrate up by exercising at least 175 minutes a week.
The human body is not meant to be obese. There's no such thing as a set point weight. There's CICO, there's nutrition, there's making sure your muscles dont atrophy. Weight loss and fitness isn't some magic thing that youre just born able to do. I was lazy throughout my entire teens. I thought fitness was something the popular girls did. It's not. It's for everyone. and everyone, especially in places with an obesity epidemic such as the US, UK, and Australia, should make use of it. It's a good thing. Walking is one of the best things you can do for your body, and it's incredibly rewarding in every way. Eating healthy and not eating until you feel like you're going to burst is rewarding in every way. And it's not like you can't ever have junk food again, you just have to limit it to a treat, a once or twice per week thing. And honestly, it makes it much more enjoyable that way.
Now I want to talk a little about my anorexia. My weight loss journey came to anorexia. This is because it was an eating disorder I'd had for a long time. I did not see a trainer or dietician, and I consciously decided to push myself too far. I consciously decide to eat less and exercise more when I am starving. This is not something that just happens because someone is eating at 1200cals. It happens because you have an eating disorder which you are born with. Saying people who eat 1200cals of healthy food a day and exercise right are "anorexic" is so fucking insulting to everyone involved. It's ableist and ignorant. 1200cals is also a pretty generous amount for anorexic ppl to eat. That's close to a binge in ED standards, so that should give you a reference for how offbase saying 1200cals is "anorexic" is.
My anorexia is healthy habits pushed into eating disorder territory. I eat healthy, yes, but I don't eat enough. I exercise, yes, but I often push myself too far when I'm already lacking energy. The advice I give people for health is correct, and I'm never going to go around saying "eat less than 1200cals" as weightloss advice. Eat less, sure, but there's a limit. Calorie counting is a good thing to do, tracking your macros and nutrients is good. But I do it too much.
I know what's healthy, a lot of ppl with restrictive and purgative EDs do. People with EDs can give some awesome health advice, we just can't follow it because we have a mental disorder. Believe it or not people with EDs discussing their EDs are not "pro-ana", pointing out that anorexia and people with anorexia are real and not some boogeyman you use to justify not losing weight and eating healthy is not pro-ana. Anorexia existing is not pro-ana and anorexics being anorexic has nothing to do with fatphobia.
this post is a rambling mess but i rly had to get some stuff clear on how I feel abt this stuff because it's getting concerning how much unhealthy shit, and then straight up ableist shit, that the fat acceptance crowd spews out.
A little exercise won't kill you, eating healthy won't kill you. You are not sentenced to ugly plus size fashion and joint pain and being out of breath for the rest of your life. Leave the Healthy at Every Size death cult and join the Health at Every Size movement. Let the doctor take your weight (it IS medically necessary). acknowledge that you are obese and it is affecting your health. It's scary but it can be the start of a new, healthy beginning. It was for me.
Losing 15kg has been the best thing in my life. Sure, the anorexia is there enjoying it for one reason. But the reason I truly enjoy it is because I've discovered what a healthier body feels like. I've discovered the joys of exercise, I've discovered the joys of eating healthy. I can fit nice clothes now. And I'm still overweight! I'm 66kg, that's 4kg away from the barest minimum acceptable healthy bmi. But I feel so so much better. I look better. I have a jawline! Good skin! Energy! It didn't fix me but it sure made me a hell of a lot better.
Please please try and eat healthy, eat an appropriate amount, go for walks. It's so so good, and if you do it right you WILL lose weight. You'll live past 50. You'll get to explore the world in a way you couldn't when going up stairs had you out of breath. You'll fit into that nice skirt you've been looking at. Your skin will clear up. You'll have energy and your mental health will improve.
It's so so fucking worth it to put effort into your health, like I cannot emphasise this enough. Please do it, I wish I could tell myself this when I was binging on junk because the FA crowd told me it was valid to comfort eat until I hurt.
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sleepy-shutin · 2 years
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hi! i think im going thru a self doubt stage rn. im in my 20s and after a traumatic event happened last year around may/june i started to hear voices and dissociate a lot. i already had issues recognizing myself in mirrors and i have no memory of my childhood. i had an instance of two significant voices speaking to me in hs when i also had a mental breakdown but then silence. i dont remember my hs years either except for that part. around may/june a lot of my friends started figuring out they were systems and since i shared so many symptoms like them i figured i am a system. i had a lot of activity a lot of people i interacted in my head until now. its been so quiet and now im doubting. i fear i may have hyperfixated on did/osdd to cope with the traumatic experience in may/june. my bpd is making things worse bc i bonded with the systems and now my doubt and my bpd are making me believe ill lose them all bc now i cant hear anything. im trying to see if there are any mental illnesses that could explain this. bc i have memories of stuff "i" did but i have no connection to. ik you are a rational person and can call out bs and i just want someone elses perspective on this that doesnt know me personally -p
i'll start by saying i'm not a professional and can't diagnose or un-diagnose someone with DID, so i'll give my advice for your situation and what helps me during periods like this, but i can't tell you if you have DID or not.
it's normal for quiet periods to happen even in DID. i've certainly had them, times where i was stable to the point that i haven't switched very often if at all, for days, weeks. one of those periods actually just ended for me as of a couple of days ago, where i started switching more again.
however, one of the best pieces of advice i can give to someone in a situation like yours is to take a step back from system spaces for a while. don't think about the possibility of having a system too much. keep a journal and try to journal as much as possible, but don't focus on who might be fronting or if you're experiencing passive influence, just exist. this is something that ends up showing me that i definitely still have DID in the end, and may help you figure out if you do or don't. take this time to not focus on DID and whether or not you have it, but just to focus on living your life instead, while keeping this journal to talk about your day. if you struggle with dissociative symptoms that make you feel numb or disconnected, or struggle with describing your emotions, you can always journal through the day instead of just once a day, and instead say something like "i went to the mall and i felt good". one thing we also like to do in our private discord server is use reaction images, custom emojis, memes, cursed images, whatever, as well as drawings, to show how we feel if we have trouble describing it in words.
having memories of stuff "you" did with no connection to it is a very normal thing for dissociation as a whole, not just DID. there's a whole category of dissociative disorders that could very well explain your symptoms if it's not DID. there's also the fact that BPD itself contains many similar dissociative symptoms to DID already.
i don't know what (you think) caused these voices to suddenly stop and quiet down, or what you've started/stopped doing that may be causing it, so i'll run through a few options.
if you're having a period that's not very stressful, it's normal to switch less or to have less activity from your system.
if you've experienced a huge stressful period and are calming down from that, this may also cause your system to be less active as one part may need to be in front while the others stay back and dissociative barriers increase.
if you're "frontstuck" it's normal to experience less of your system, or so i've heard.
if you've stopped interacting with system spaces as much and your system went quiet as a result, this may point to your system being socio/psychogenic in some form; i.e. you thought you had DID but it ended up not being that, but as a result of hanging out with a lot of systems/in a lot of system spaces as well as due to misinformation and misunderstanding of DID, you could have mistook normal symptoms of another dissociative disorder or BPD for DID instead.
it's also quite possible you're experiencing symptoms of DID and not noticing them because your perceptions of how DID works causes you to believe it's consistently more overt and hard-cut than it actually is. this is something i've done before as well, so if that's your case, it's likely the result of misinformation and misunderstanding of DID.
in short, it could be a lot of things; stress induced psychotic symptoms causing the hearing of voices that aren't there, a dissociative disorder, BPD, etc. i can't tell you what disorder you may have, but i hope these things can point you in the right direction here.
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flowerslightning · 4 years
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Have you heard about PFA and MFA?
or the full name is ‘Psychological First Aid’ (PFA) and ‘Mental Health First Aid’ (MFA)
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Can we relate it with Cloud Strife? As we all know, Cloud had mental illness and was struggling alone. Let’s take a quick look on this topic then and see if characters in FF7 ever give PFA/MFA to Cloud or to each other. This is going to be a looooong post although I tried to simplified it, so, yeah. Good luck reading this !
Disclaimer : I’m not a psychologist. I’m still a student and psych is not my major field. During my intern, other than we got exposed a lot about psychiatric disorders and ways to deal with them, we also got trained psychological first aid in emergency department. If it wasnt because of this quarantine, i would have finished my training in emergency field. There might be false interpretation here or there, forgive me for that and pls correct any mistake in this post
This will probably trigger LTD. Sorry, but I had to, Pls read this post with open mind. Keep in mind I like both Tifa and Aerith, i have no grudges agaisnt Barret, Vincent, Nanaki or Cid so I am not being bias with any of them. I forgot a lot of stuff in OG (I played it when I was really really small), so I will be using lots FF7R and AC references here (and a bit from OG, depends whatever I remember)
Good to go? Allow me to rant. Read it slowly and if u skip some of it, u’ll probably mislead my actual words, and u’ll be triggered af. Don’t come at me with madness if u dont read the whole post properly
What is PFA and MFA? Generally speaking, if Basic First Aid is about covering the wound to prevent further bleeding, then PFA (Psychological First Aid) and MFA (Mental Health First Aid) is like applying a bandage on ur mental to avoid u continue being distress. 
Usually, PFA is often associated with disaster event or terrorism, where large number of people got affected. Meanwhile, MFA focus in one person who is developing mental health prob or already in mental crisis due to certain traumas, such as vehicle accident, house burned and etc
 Pls note that, certain people NEED MFA while the others may NOT NEED it. It is important to respect their needs/wants. Some victims may refuse verbally but they ACTUALLY NEED it (CLOUD STRIFE) and maybe some victims look like they dont need it, but they want it, and its super fine to give it
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PFA/MFA not only done by the professionals and it is not a professional counselling, although necessarily training is needed if u want to approach deeper in this field. PFA/MFA is also not a psychological ‘debriefing’ - in which MFA/PFA doesnt need to involve a detailed discussion of the trauma event with the victim, but instead, it is an alternative way to psychological debriefing that helps for long-term recovery. (unless if ure a pscyhiatrist, then u have to forget about MFA and ask detailed questions regarding the events to help the patient to recover)
MFA and PFA both almost the same, but I will mention more about MFA here.
MFA (Mental Health First Aid) is not just about comforting “Oh, are u alright. I’m sorry for what u’ve been through”, but it is also about assessing their needs and concerns, protecting them from harm, provide practical support and support them feeling able to help themselves and others.
The main key for these two term is RESPECT - respect victim’s dignity, respect both parties safety and respect victim’s rights to make decision. Even without the PFA, we should respect these three in whatever circumstance we are in. 
A lot of us honestly were born with natural skill of MFA bcause of our own empathy, instinct or experiences and some got trained professionally. Some of them already had MFA due to high common senses they have.  
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Some of the Do’s and Dont’s when giving MFA include;
Do’s : 1. Be trustworthy | 2. Respect their decision | 3. Be aware of and set aside ur bias | 4. Make it clear to them u are available for help even they push u away | 5. Respect their privacy and personal space | 6. Do remain calm and soft when the person in distress | 7. Listen and don’t interrupt their talking | 8. Help in terms of basic needs | 9. Create connection the person with others | 10. Give hope to them | 11. Provide private place to talk about the event | 12. Respect their strenght | 13. Advice small necessary matters or give simple words of encouragement | 14. Acknowledge positive features of what victims have done
Dont’s : 1. Rush in whatever the thing theyre doing with u | 2. Be dismissive | 3. Make promises u know can’t keep | 3. Ask anything in return for helping them | 4. Exaggerate ur skills | 5. Force help on people, being pushy | 6. Pressure them to tell their story | 7. Judge that person | 8. Put the person in risk of harm as result of ur actions | 8. Force them to accept ur idea/Listening to ur rant | 9. Talk rough | 10. Being bias with the people | 11. Touching that person too much | 12. Talk with the person in negative terms | 13. Abandon the person’s feeling
To simplify, there are 3 ways for MFA to begin, and I will only talk about one of them, the one that is the hardest to do, that is when u notice someone looks distressed and ure concern about them, and leading u to approach them first without them noticing ur concern. [Am I putting the right words here?]
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In Cloud’s case, who do u think the first noticed Cloud behaved oddly and went to help him first ? - yeah Tifa. U probably would say “OFC she went to help him, she met him first at the train station. That guy looked sick af, who wouldnt ask if he was alright. If Aerith/Yuffie/Jessie met him first, they would do the same”. Okay guys, that was not my point. 
Let’s focus one by one characters and see what Do’s and Dont’s MFA (Mental Health First Aid) they’ve done to Cloud and other charas. Keep in mind, none of them know what Cloud had gone through, but Cloud had showed some obvious sign he was unwell and only a few of them noticed that and took action for it. 
The symbol [X] means the Dont’s in MFA and ( ✔) means the Do’s in MFA.
Biggs Jessie Wedge -
I know there’s a thing about man helping man’s psychology and Jessie being flirty with a guy.They [X] thought Cloud was like how they saw Cloud. and they considered it as normal. They didnt see Cloud under distress so they dont have the need to concern his mental status. The good thing about them was, the three of them (✔) respect Cloud’s strenght, giving Cloud the confident to be in action. But, Jessie [X] had zero respect on Cloud’s personal space
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I wanna highlight about Biggs. Biggs had an attitude of overthinking stuff, but it wasnt so bad that would cause him harm, he just cared too much about his friends. So I believe Biggs was the type that would notice immediately when his friend being strange and would give MFA (Mental Health First Aid) with his own instinct even without the person asking it.
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During the Sector 7 Plate attack, where Biggs was severely injured, when Cloud said he was not a fan of kids and Biggs said Cloud had so much in common (in common of what? Cloud with the kids or Cloud with him?), Cloud gave him ‘a sad look’ and Biggs reached out his hand to Cloud’s head. Biggs (✔) remain calm and soft when dealing with Cloud’s feeling (who faced traumatic event but Biggs didnt know about it) on that moment despite his current physical status. And also he (✔) wished goodluck to Cloud, leading to prevention distress on Cloud
Marle -
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Marle [X] judged Cloud for someone who had no skills, but she entrusted Cloud to take care of Tifa’s well being. Not knowing who Cloud was, Marle noticed Cloud looked glum, she (✔) offered her ear for Cloud to rant and knew right away he was not having enough sleep, then (✔) advising him to sleep more . Lol, she was [X] biased with Cloud and Tifa. Not her fault, she only knew Tifa’s story, not Cloud’s. After the Sector 7 plate fall, we saw her being the most active member to help with the remaining citizens there. Marle without a doubt had given the citizens there PFA (Psychological First Aid) , by helping them with their (✔) basic needs, (✔) create connections, (✔) put away bias, (✔) remain calm and soft. 
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Barret Wallace -
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Barret was the same like Biggs Jessie Wedge. I’m sure Barret thought Cloud was just fine. Barret saw Cloud as a mercenary with stinky attitude,[X] judging him like that causing Barret to gave him the same attitude too. But overall, he (✔) respected Cloud’s strength a lot
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However, after the Sector 7 plate fall, Tifa and Barret were the one that hurt (mentally) the most, Tifa as usual locking her emotions, there we could see how Barret comforting Tifa by (✔) giving words of encouragement and proceed on (✔) hugging her to show his empathy. Barret also (✔) remain calm and soft spoken when talking to the survival victims of Sector 7 citizens. He also (✔) acknowledged what the citizens had done to survive
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Vincent Valentine - 
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Don’t be surprise Vincent was listed here. This guy here was like another version of Cloud but more mature. In addiction, they both kinda share the same pain. So, I personally think Vincent understands Cloud pretty well. In AC, where Cloud was mentally ill, Vincent saved Cloud from Kadaj and brothers and (✔) took him to safer place. That was a common thing to do. But let’s go deeper, Cloud never told him about himself, but Vincent already  (✔) aware of Cloud’s trouble with the geostigma stuff and Cloud’s current mental status. Vincent, (✔) calm and soft like always (✔) didnt hesitate to asked if all of these were just about ‘fighting’ and it made Cloud to ‘re-think’ further about his problem. He (✔) didnt pressure Cloud here, instead he was (✔) helping Cloud to understand the condition he was facing, and this lead Cloud to avoid distress.
Aerith Gainsborough -
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I know Aerith was special. She was an important character and devs created her to be ‘loved’ by the fans so that her death would be tragic. Aerith did almost all the things that shouldnt be done when giving MFA to mentally ill person. Some of u may say “Duh, Aerith didnt know anything about Cloud thus she had no intentions of giving him MFA”. Yup, ure right. Aerith didnt know about Cloud’s mental status but so as all the other characters in the series. 
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Aerith was [X] being pushy with Cloud, in lots of ways, from making him as a bodyguard for free to forcing him to wear a dress. She [X] forced Cloud to accept her idea about meeting Andrea, dance and gown. She also [X] forced Cloud to help picking the flowers. Aerith [X] didn’t let Cloud to have his own decision [X] neither giving him a chance to talk,  and [X] abandon his feelings (cough..uhm, Aerith resolution). She also had [X] no respect on Cloud’s personal space and [X] too much touching and leaning to him. Aerith also [X] put herself in danger and that worried Cloud.  She [X] looked down on Cloud in someways too
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However, at the Sector 5 slum, where the hooded man appeared, Aerith noticed Cloud was having trouble with himself, she (✔) encouraged Cloud to keep himself together. Also, throughout the entire game, Aerith always remind the team to (✔) have hope in everything. Her positive vibrant attitude was what (✔) made everyone able to believe in themselves. She also (✔) ensure Marlene’s safety and protected her. She was able to (✔) remain soft and calm when approaching Marlene. Remember Betty? Aerith took her time to helped her out and she even (✔) respected the little girl’s strength, (✔)slow and steady when saving her and (✔)soft spoken
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Tifa Lockhart -
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Tifa met Cloud at the train station, saw him being ‘not-so-fine’ state despite Cloud claiming he was completely okay. Tifa didn’t know what Cloud had gone through and  she (✔) didn’t pressure him to talk about it. She even helped him to (✔) find a place to sleep even when Cloud never asked for it. Tifa unconsciously was the first person to give Cloud MFA without knowing what Cloud had faced previously. And Cloud, on that moment, he really needed a help. Tifa also (✔) stated that if Cloud need anything, she would help him with it
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Tifa (✔) remain calm everytime Cloud had sudden headache, she didn’t leave him alone and (✔) didnt put any pressure on him by asking question. During the (✔) Alone At Last, they had privacy Tifa asked about what happened after he left Nibelheim. She (✔) listened and didnt interrupt him, (✔) neither pushing him to talk more. Moreover, Tifa (✔) put a distance with Cloud, dunno if she was the one who was being uncomfortable or she actually (✔) respect Cloud’s personal space and privacy. Tifa (✔) didn’t force him to stay at Midgar, she asked him and was glad Cloud would stay for a while. Tifa was no doubt (✔) respect all Cloud’s decisions too. Also, don’t forget, Tifa also helped Cloud to help (✔) make ‘close connection’ with the Avalanche members and people in Sector 7 slums. She also (✔) didn’t do much touching with Cloud (Well, I mean, she didnt touch him in clingy way)
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In AC, Tifa (✔) encouraged Cloud to have hope for Geostigma and the family
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Tifa did [X] put herself in danger by becoming Corneos bride participant and that gave Cloud trouble (but Tifa ensured him she would be fine on her own previously) And btw, in OG, I read about the fans questioning why Tifa [X] didnt tell Cloud the truth. I would like to argue this matter. TIFA IS A CHARACTER WITH REAL HUMAN FLAWS, she too had her own traumatic event and was not really sure of herself on what to do. However, considering what Tifa had done for him, Tifa had helped with Cloud’s psychology the most.
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I know Cloud was putting up a font, and that made him to have condescending attitude, and people couldnt see what Cloud was hiding behind the the bravery face. However, all of us as fans acknowledged the pain Cloud was suffering in the entire FF7 story. Some of the characters like Tifa, Marle, Vincent, Biggs noticed it and they took actions for it, while others, I do personally thing, they were hurting the Real Cloud’s mentality more. 
Long story short, Tifa was the one who gave mental health support the most to Cloud, followed by Vincent (AC), Biggs and Marle. Aerith did the worst with Real Cloud's mentality + she then died, mking Cloud be more miserable,
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However, Aerith actually had the best way to give MFA/PFA to children, but maybe the worst to Cloud. While Tifa gave the best MFA to Cloud which helped him to get himself together through out the entire time
Alright thats the end of my talk. Thank you for being with meee
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Hi… I wanted to ask this on anon so I didn’t ask on your personal, idk if this is too personal or anything to ask but
Do you have a problem with people saying they have a mental disorder if they don’t have a diagnosis? Like for me so… I have been diagnosed with anxiety but I am like 99% sure I have bipolar disorder. And like I know you can’t diagnose me so I’m not going to go into depth with my symptoms but ever since I was like, 11, I used to get very depressed to the point where I contemplated ending it but then i would snap out of it and I think for me my manic phase are hypomanic bc ive never experienced like the full range of those symptoms but my depressive phases get very rough esp if I have external stressors but it will go through what I assume to be these phases like sometimes within the day esp if I have a stressor.
I am in nursing school and I work at a psych hospital so like this isn’t coming out of nowhere, I am very familiar with all mental disorders and it was actually during my psych nursing class and learning about bipolar disorder that I was like… hm… why does this feel like a mirror right now. I am aware I should get to a therapist and get an actual diagnosis (if I had money I would lol) but like idk. Idk if it’s worth going to my doctor at my physical and being like “hey I think I have this” I am lucky enough now that I am in a good place and can manage my symptoms but I am terrified I will go through a stressor again and lose it so idk. I mean I feel like I already know the answer but I wanted to ask anyway to see your take :/
Anyway idk as a future medical professional I think self diagnosis got a bad rep and it’s like idk I think for mental disorders esp you can tell if you have anxiety and it’s a persistent problem. You can tell if you have depression. I know bipolar disorder is harder to diagnose but idk I think since I’m in the field it’s easier? Idk I felt like a sense of relief with learning about it and finding similarities and being like “well maybe that’s why I’m like that”. But idk now I’m feeling uneasy bc I don’t have a diagnosis and I don’t want to be like, stepping over people who were diagnosed. Thank you in advance if you read all this and yeah I’m sorry I know it’s a lot and this is controversial
ok this is a long post so im putting it under a cut but tldr, no i dont have a problem with it. it doesnt matter if you actually have an illness, it matters if you find a solution to your problem. if treating yourself like you have a certain condition makes it easier to go through life, then keep doing what works for you, you are doing nothing wrong. this all goes for physical and mental illnesses.
im a firm proponent of self diagnosis. i wouldnt be here if i didnt have the confidence to research mental illnesses and advocate for myself. as someone who is extremely familiar with the medical profession on account of being the daughter of a doctor and a nurse and spending my childhood running around a hospital, im extremely privileged to even have the knowledge and ability to do so, and i try to bear in mind the understandable hesitancy of people without this advantage. i know that you are well within your right to refuse medication that makes you sick, i know that you can complain about a doctor that isnt listening to you, i know that you are allowed and encouraged to be adamant about things you are told dont matter, and in addition to that, i have a VERY well known doctor and a nurse in my corner, and i am STILL treated as though i do not understand my own experiences enough to have any authority more often than i am not.
the reason self diagnosis gets a bad rep imo is because people have constructed this boogeyman of the worst case scenario, people collecting mental illnesses they dont have for attention as opposed to what it is, people doing research into their experiences and making theories on what they have so they can manage it. youll often see the take of "i dont hate self dxd i just hate people who do it for attention" and i think thats very irresponsible considering a symptom of many mental illnesses is thinking youre faking it and doing it for attention, nevermind the fact that attention seeking behaviour is literally a symptom of many mental illnesses people often dont want to empathize with. gatekeeping whos illness is real just keeps people who need help out. i could go into an anarchist screed about democratizing health, but basically, as someone whos life has been saved by my insistence on self diagnosis, and whos life has been made significantly easier by treating myself as though i have the conditions that i theorize i have, self diagnosis saves lives, and i, as an advocate for disabled people of all kinds on my island, will never put any conditionals on self diagnosis. it doesnt matter if you find the right name for your problem, it matters if you find a solution that works. i have yet to meet any of these fabled people who never try to receive a professional opinion, only people who literally cant.
as for feeling guilty, ill repeat how i opened this answer: it does not matter what exactly your problem is, it matters that you find a solution that works. in medicine generally, there will be a wide spectrum of problems with overlapping treatments, things which are similar but distinct, things which look identical but are completely different and at different levels of concern. it doesnt really matter which grab bag of bullshit your brain is reaching from, it matters that you know how to deal with what it throws at you, whatever that may be. dont worry about getting it right, worry about getting it working. okay?
for advice on how to deal with doctors, its helpful to pose it as a hypothetical as opposed to an absolute. when i bring up things im dealing with that i have a theory about i say "i think i have x" or "i think i might have x" or "i have a lot of symptoms of x". doctors are often egotistical and are easily challenged so it helps to pose it at a problem they can solve as opposed to one youve solved for them otherwise they get spooked. in my experience posing it this way leads them to actually interrogate this line of symptoms, and theyll ask you why you think that, and you can bring up symptoms that led you to that conclusion, and ones that give you trouble especially. for example, ive said "i think i may have autism or adhd? or both" to several doctors, and they either agree with me (i believe its been put in my file as a possibility now although i cant get an official test done due to financial and resource restrictions) or they ask why i think so, and i detail what i believe is due to my autism. its small, but this reframing helps a lot.
i think this covers all you said but my head is empty as hell.
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vavuska · 4 years
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AUGUST 9, 2020
Body positivity and false myths about health.
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Introduction
Today, the revered ideal body consists of a tall, slender physique known as the thin-ideal. This idealized image that has been constructed by the media via magazines, movies and advertising campaigns is having adverse effects on the lives of many women, such that more than half of the women are troubled by certain aspects of their appearance and are not accepting of their bodies as a whole. The preoccupation or obsession with their physical appearance has trapped Western women into subscribing to unhealthy narratives such as "I must be thin to be accepted and loved", "A thin body will make me happy", "Dieting will help me lose weight" or "Thinness equals beauty". These nagging voices often overrun women's lives and are linked to various psychological disturbances such as depression, eating disorders, anxieties, countless addictions, BDD, as well as low self-esteem (Rieves & Cash, 1996), relationship difficulties, and sexual dysfunctions (Dworkin & Kerr, 1987).
In addition to noting that people with perceived obesity (again, not medically diagnosed, just perceived) will experience microaggression, bullying, discrimination in housing, employment, education, and healthcare, Phelan notes that their interactions with healthcare professionals is directly affected by size bias.
In these studies by the Mayo Clinic, primary care physicians reported spending less time with obese patients, less communication, and open belief in stereotypes: this patient is lazy, undisciplined, and less likely to adhere to medical advice.
These negative interactions statistically raise a patient’s chances to: delay cancer screenings and routine care, avoid routine check ups, and are more likely to have unreported diagnostic errors.
This isn’t healthy. This isn’t saving or changing any lives. This is having the opposite effect, and it is happening precisely in the places where we are suppose to be receiving “help.”
What is body positivity?
Body Positivity is a social movement rooted in the belief that all human beings should have a positive body image, in doing so it challenges the ways in which society presents and views the physical body. The movement advocates the acceptance of all bodies no matter the form, size, or appearance.
I personally like the 4 Principles of Body Positivity conceptualized by Body Positivity Activist:
ACCEPTANCE OF WHAT IS: Our bodies as is (healthy, sick, skinny, fat, missing a leg, cancer survivors, and black, white, purple, blue and everything else,) deserve respect, visibility, acceptance and have intrinsic value.
REJECTION OF “BEAUTY” STANDARDS: Body-shaming of all types has been shown to yield detrimental long-term psychological effects such as negative body image, depression, anxiety, and a multitude of eating disorders. It serves no benefits, so we reject it entirely.
ACCEPTANCE OF CHANGE: Changes to our bodies—sickness, ailments, aging, pregnancy, surgery, accidents/trauma, putting on weight, losing weight, ALL of it—should be accepted, and should not diminish the value, respect, visibility of our bodies.
TOTAL INCLUSIVITY: Body positivity is inclusive of all bodies, not just those considered to be “fat” or obese,considering most humans are socialized to have negative perceptions of their bodies.
In short, body positivity and its principles are about acceptance, inclusivity, and respect. First aspect to notice: these are all social ideas, not medical ones. Why naysayers of body positivity consistently bring up the promotion of obesity when fat bodies are displayed is a mystery to me.
The second aspect of its definition one must notice: body positivity does not “promote” any body type. It is simply stating that all body types have intrinsic value. We certainly agree with this as a society. If you intentionally hurt someone’s body--again, regardless of the look, age, or state of that body--we consider that a crime. Body positivity simply concurs with this logic.
Lastly, body positivity by definition does not purport that evolution, change, and/or a healthy lifestyle is unacceptable. You can be body positive and be healthy. In fact, body positivity promotes taking care of yourself.
1 - “Your weight is entirely within your control, you are just being lazy”
As a random guy wrote on Facebook: “Body positivity is appreciating things that are beyond your control, like the colour of your eyes, skin colour, hair texture, height, etc. Weight is entirely within your control...if you eat a lot, you will get fat. Body positivity enables gluttony which is a slap to the face for underprivileged people everywhere in the world.”
That's not entirely true: gaing wight could be caused by hormones (pregnancy, menopause, ecc), genetics (for e.g. Peter Will syndrome) other medical condition linked to endocrines such as Cushing's syndrome or a malfunction of thyroid (hypothyroidism).
The involvement of genetic factors in the development of obesity is estimated to be 40–70%. Some of these obesogenic or leptogenic genes may influence obese individuals response to weight loss or weight management.
To date, more than 400 different genes have been implicated in the causes of overweight or obesity, although only a handful appear to be major players. Genes contribute to the causes of obesity in many ways, by affecting appetite, satiety (the sense of fullness), metabolism, food cravings, body-fat distribution, and the tendency to use eating as a way to cope with stress.
The strength of the genetic influence on weight disorders varies quite a bit from person to person. Research suggests that for some people, genes account for just 25% of the predisposition to be overweight, while for others the genetic influence is as high as 70% to 80%.
Obesity or overweight is not concerned about gluttony. It could depend on a lot of factors: physical and psychological. It is proved that people with depression or anxiety may experience weight gain or weight loss due to their condition or the medications that treat them. Depression and anxiety can both be associated with overeating, poor food choices, and a more sedentary lifestyle. Over time, weight gain may eventually lead to obesity.
Body positivity is about being conformable in our skins. Appreciating what we are and what we have. Body positivity does not promote any form of body, differently of what our media do.
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2 — “You cold loose some weight, if you put in some dedication”
This one deleted the previous comment in which he used abused, starving people in Auschwitz to promote a diet, but I have his second one: “I meant that the problem with losing weight is just calories you eat vs calories you burn, of course the amount of calories you burn depend on hormones and a lot of other things. However, everyone can burn more calories by exercising. The Auschwitz prisoners were just an example that it is possible to lose weight, no matter the circumstances, if you REALLY put your mind to it. How you go about increasing the gap between the calories you consume and the ones you burn is up to you. Also, long term, even a 100kcal deficit per day can help you lose weight. You dont have to starve yourself to lose weight.”
Loosing weight is not always a good thing and it is not as easy like those people think.
Muscle does weigh more than fat because it is a denser product. On average, the density of fat is 0.9g/ml. The density of muscle is 1.1 g/ml. Using the averages, 1 liter of muscle weights 1.06 kg or 2.3 lbs., while 1 liter of fat weights .9 kg, or 1.98 lbs. An easier way to think of it might be: if you have an equal volumn of fat and muscle, fat is going to weigh about 80% of what the muscle weighs. This can vary due to numerous factors including race, being extremely lean or being extremely obese according to “Exercise Physiology” by William D. McArdle, et al.
The ‘take away’ points are:
Yes, muscle weighs more than fat. But….. do not assume because you started working out and you are not losing weight it is because you are increasing muscle.
The higher percent muscle you have on your body the smaller your clothing size because muscle takes up less space than fat.
On the other hand, if you are loosing weight, don't presume you are necessarly loosing fat, you could also lost muscles and this is not a good thing.
For that guy, don't eat is the solution to every weight problem. This leads to a thing called anorexia (which is one of the most painful consequences of the idealization of a “perfect body shape” myth portrayed by media). And, again, this guy really thinks that abused starving people are a good example to promote a diet. He seems to doesn't know how work human body and that if you don't eat as much to sustain your body, you will begin to feel always tired, weak and such because your body doesn't have enaugh energy to consume. We will see this in the next point.
3 — “You better have a diet”
I use the word "diet" in this context to refer to any set of restrictive food rules (barring true medical and ethical concerns). If you are feeling guilt and shame about your food choices, it is likely that you are approaching the experience of eating from a "diet mentality."
The word "diet" often has a negative connotation, so many people prefer to say they are making a “lifestyle change.” But if your lifestyle change entails rigid food rules that invoke guilt when broken, you are probably on a diet, even if in disguise. And the truth is, the diet industry wants us to "fail" so that we will continue to purchase their products. When you jump on the latest fad bandwagon, you support a multi-billion dollar industry that profits by convincing us we are inherently flawed.
Diets do not help you maintain weight loss long-term. The idea that people fail at diets because of a lack of willpower is a myth perpetuated by the diet industry. Powerful biological factors essentially ensure that your attempt at dieting will fail. Researcher Traci Mann, who has studied dieting for more than 20 years, found that there are metabolic, hormonal, and neurological changes that contribute to "diet failure."
According to Mann, "When you are dieting, you actually become more likely to notice food. . . But you don't just notice it—it actually begins to look more appetizing and tempting." Mann also stated that as you begin to lose weight, "the hormones that make you feel hungry increase" and "the hormones that help you feel full, or the level of those rather, decreases."
For the average adult in a resting state, the brain consumes about 20 percent of the body’s energy. The brain’s primary function — processing and transmitting information through electrical signals — is very, very expensive in terms of energy use.
The exact percentages are difficult to ascertain, but we have pretty good estimates of where that energy is going, though it varies by the area of the brain. In the cerebral cortex of mice, about a quarter of the brain’s energy goes to maintaining the neurons and glial cells themselves — the processes that all cells go through to remain alive. The remaining 75 percent is used for signaling — sending and processing electrical signals across the brain’s circuits. These numbers seem to be very similar in humans.
The brain is an energy-hungry organ. Despite comprising only 2 percent of the body’s weight, the brain gobbles up more than 20 percent of daily energy intake. Because the brain demands such high amounts of energy, the foods we consume greatly affect brain function, including everything from learning and memory to emotions.
Just like other cells in the body, brain cells use a form of sugar called glucose to fuel cellular activities. This energy comes from the foods we consume daily and is regularly delivered to brain cells (called neurons) through the blood.
As Mann explains, when you diet, "Your metabolism slows down. Your body uses calories in the most efficient way possible... When your body finds a way to run itself on fewer calories there tends to be more left over, and those get stored as fat."
Thus, it is no surprise that studies show that 95 percent of people will "fail" at diets. Most people can lose weight in the short-term; however, over time the majority will regain the weight they lost—and potentially gain even more. Working to suppress your weight below your natural body weight is ultimately a fruitless effort—in fact, it's an utter waste of time.
4 — “Being overweight or obese means being unhealthy”
Studies have found that anywhere from one-third to three-quarters of people classified as obese are metabolically healthy. They show no signs of elevated blood pressure, insulin resistance or high cholesterol. Meanwhile, about a quarter of non-overweight people are what epidemiologists call “the lean unhealthy.” A 2016 study that followed participants for an average of 19 years found that unfit skinny people were twice as likely to get diabetes as fit fat people. Habits, no matter your size, are what really matter. Dozens of indicators, from vegetable consumption to regular exercise to grip strength, provide a better snapshot of someone’s health than looking at them from across a room.
According to an article in The Nutrition Journal by Dr. Linda Bacon and Lucy Aphramor, "Most epidemiological studies find that people who are overweight or moderately obese live at least as long as normal weight people, and often longer."
So, you can be under or normal weight, but that's doesn't make necessarly much more healthy than a overweight people. You can't say that a person is not "healthy" by judging on their physical appearance.
Some feminist points of view
Now, aks yourselves why so many cisgender etherosexual men are so upset from seeing plus size models in media? Do they really care about stranger's women heath?
NOPE!
Oh. Maybe is because they are the ones who lose something in seeing women considered not attractive for their physical appearance being accepted and admired?
YES.
Female beauty standard in media are designed for heterosexual male consumption.
As women gain economic and political power, their beauty should matter less.
Feminist scholars have contended that cultural norms and expectations encourage girls and women to be attentive to and psychologically invested in their physical appearance, which can undermine their well-being and contribute to eating dysregulation, depression, and other psychological difficulties (Cash, Ancis, & Strachan, 1997). Mary Wollstonecraft (1792), who is considered to be the founder of feminism, asserted that women's preoccupation with appearance was due to impoverished education, domestic subjugation, and vain pursuits toward which women were directed by their culture. The feminist perspective reaffirms the declaration that a woman's self-worth, ability, and livelihood are not centred on her physical appearance.
Wayne Dyer (1976/1995) elaborated on this: “many women have accepted the cultural dispatches and behave in ways that they are supposed to when it comes to their bodies. Shave your legs and underarms, deodorize yourself everywhere, perfume your body with foreign odours, sterilize your mouth, make up your eyes, lips, cheeks, pad your bra, spray your genitals with the appropriate bouquet, and falsify your fingernails. The implication is that there is something unpleasant about the natural you, the essentially human you, and only by becoming artificial can you become attractive.”
Peterson et al. (2008) posit that feelings of powerlessness may lead a woman to rely on external evaluations of her body as well as to control her eating behaviours. In contrast, feelings of empowerment may decrease the likelihood that a woman will internalize society's messages regarding attractiveness and hence develop schemas that highlight the importance of appearance. Overall, what is suggested is that feeling empowered in one's life may translate to reduced self-objectification and, in turn, to a decrease in negative evaluations of body image.
As this gross guy said:
“Those women aren't thin they look healthy, your problem with them is that their not grossly obese, I've got news for you, most men don't find grossly obese women attractive. Women decide what they want to look like and that happens to be appealing to men, the media has nothing to do with it, women have been beautifying themselves in order to attract men for millennia.”
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Young-Eisendrath (1999) elaborates on the psychological damage done by this: “the belief that we must be thin in order to be successful results in feelings of insecurity about ourselves and our abilities. Obsessive control of the female body leads not to power but to shame, self-consciousness, confusion, illness, even death by eating disorders. Longing to be reassured of our worth and validity, we submit to humiliating advice from experts who tell us what and when to eat, and how to exercise, as if we were children.”
In summary, the obsession with physical appearance often distorts reality, making individuals vulnerable to a host of psychological difficulties, including depression and anxiety, and even abuse (Hooks, 1995). Seeking the ideal body type, which is thinner genetically than 95% of women, is also harmful, as the anxiety it creates about weight is focused upon unnatural thinness rather than health (Williams, 1998).
Body positivity protects women from negative feelings about their bodies: women are encouraged to refute the message of the importance of thinness and develop more empowering self-definitions based on other attributes such as their intelligence or creativity. Feminist ideology thus emphasizes that a woman's self-worth should not be determined by her physical appearance.
This male obsession about our weight, saying that we are not "healthy", is just another way to cotrol our bodies, girls!
Lisa Turner, a food writer and nutrition consultant, summed it up best: “Losing weight is not your life's work, and counting calories is not the call of your soul. You surely are destined for something much greater, much bigger, than shedding 20 pounds or tallying calories. What would happen if, instead of worrying about what you had for breakfast, you focused instead on becoming exquisitely comfortable with who you are as a person?”
Some final conclusions
So telling to every people "you are fat, lazy, ugly and need to exercise for your own health" is not only harmful but not even ever correct for all the reason above.
The person you are insulting online could be “overweight” because has a condition, is highly depressed for past suffering experience (I know girls with past of sexual abuse who used to eat to find comfort for a pain that her cannot express in other ways). Or maybe not. To make it easier for you to understand, you must stop to judge people we don't know on their physical appearance, body shape or weight and we must try to be polite, so you will not get yourselves into embarrassing situations saying stupid things like "oh, sorry... I didn't know you had this thing...", after giving unrequested health suggestion to strangers or insulting them?
Have you ever consider how harm can do on others your “caring about strangers” health? What YOU are doing is causing eating disorders and low self-esteem on others. Body positivity helps to accept ourselves and not to spend our time into stupid considerations about our bodies.
THAT'S WHY WE NEED BODY POSITIVITY!
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A little list to summarize:
Don't give unrequested health suggestion: they don't ask and you are not their doctor;
Every person need to be accepted and respected as they are;
Obesity bias adversely affects a person’s likelihood to get help;
Your body works better when you thinking happy thoughts about yourself;
Negative body image DOES promote obesity. And anorexia. And a lot of other bad stuff.
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credulouscanidae · 4 years
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i feel so endlessly frustrated at myself because i can see the patterns of my thoughts, know the logical and practical steps i need to take in order to fix them, and i just...cant do it. i acknowledge that these feelings cycle; im a sucker for nostalgia. i look at all of these things ive shared with my friends, all these memories and selfies and fun times, and i know i can have that again. and i know that i just look at these things and think that “things were better then”, because its so easy to trick yourself into thinking that when all youre seeing is a condensed collection of happy times. i think 2016. that was easily one of the worst years of my life, or at least the ones with the most changes. it was the 180 flip from child to adult, the year i lost so much of my identity, and gained a new one. i was mentally and physically a completely different person by the end of that year. and yet, i look through these photos tonight and see just how many jokes and fond memories i shared with my friends. maybe because i was 19/20, i still had that immaturity about me so i was able to let loose. maybe being isolated inside for 2+ months has made these selfies sting more. maybe i miss when we were all in school and not at work, when we could all plan get-togethers a little easier. idk.
but this wasnt meant to be a nostalgia rant, but its definitely triggered those thoughts.
because in all these group selfies i saw tonight i saw how insanely different i looked within a year. it was when i developed my starving-orientated disordered eating, it was when i came out as trans and so changed my hair and wardrobe. 2016 was fucking wild. and i saw glimpses of how i used to be, and how despite being in so much pain, that was the year i took a leap and finally did something for myself that would set me up for success, rather than failure. and i dont do that for myself often. and im prouod of younger me for doing that.
because it shows that, no matter how much pain i have continuously been in for almost my entire llife, that i can take steps to improving my life. even though coming out as trans is not the same as confronting trauma, i think living as a truer reflection of who i am has definitely helped me feel more comfortable and confident.
and i want to lose weight again, because the confidence i radiated at my peak ED/lowest weight was unmatched to antyhing ive ever felt before. Ive gained a bit of the weight back (which funny enough since being on hrt i still look different/different weight distribution), but i want to lose it again in a healthy way. and i know i have to get out of my feedback loops and actualy work for it, as hard as fuck as it may be.
i dunno man. im nearly 24. i know thats still 6 years left of my 20s, but if ive learned anything from the past few years, its that they go by fast and i will be pushing 30 before i know it. and i dont want to be fucking 30 years old and still not have worked myself out. i mean, its ok if me or others havent, but i just. i dont know. i dont want to turn 30 and say “aha cool thats 20 years i have been extremely suicidal and self harming and full of trauma and brain rot”
which is why, as hard as it is, im really trrying to get the ball rolling on geting diagnosed with whatever-the-fuck-i-have. getting the ball rolling for me has taken ...well...ive received it, convinced myself its not worth it, and stop it. i cant keep running away from help. its discouraging when your professional is a bit shit so. idk. i know ya gotta keep trying. 
i need to start an exercise routine, just doing my daily walks again would help so much, because my body is in so much pain from a sedentary lifestyle. 
the most ive done is actually start drawing daily, which was previously really hard for me to do. im proud of myself for that. i want to release my webcomic, i want to consistently do commissions, and i cant do any of my artistic goals with my previous workflow i only have just managed to improve on.
and thats the hardest thing about being mentally ill. you have to put more effort in to survive, the odds are stacked against you, and you have to set up and stick to methods that’ll help, even though that means fighting against symptoms that discourage and impact u so severely. and it also means some days you cant fight it, and you have to give up. relapse happens. im just tired OF it happening.
though, i thankfully feel different. as a teen, i felt there was no way out besides suicide, as a fresh adult i realized there is hope, and i have ambitions and something to give to this world, but i was still very suicidal, and still lived wallowing and unable to get out. but as a young adult, i know i have to set up my life now to pave the path for the future. ive always been screaming for a release,and that release used to be suicide. now? my release is mental wellness. and fuck, its the much harder path to take. bpd, cptsd, whatever, it rots my brain and drags me down and makes me act on bad habits and behaviours, but dammit. one day im going to get that release.
maybe not all of it, maybe not till im 40.
but one day.
im going to look back and see how i am now as how i used to be, not what i still am.
maybe one day i’ll experience that release..
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ellas-cottage · 6 years
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FLOP POST AHEAD!!!!!!!!! --- If you want a 968 word essay on where i stand on fat acceptance as an aspiring health professional, you’ve come to the right place.
edit as of 2022-06-08: L post + L positions + no longer want to be in the medical field + gained the weight back + wrote this when i struggled with disordered eating
If you dont then i have a little rant on self care at the end, so thats crunchy.
Okay. So listen, I don't often make my own posts. And when I do, they get like one note, so it doesn't matter. I mostly just reblog random shitposts from people or memes, or their opinions, that vaguely line up with mine.
 But a few days ago, I had a very interesting encounter with someone that I shan't name-drop, because I'm a very decent person, you know, but that person has a very, very warped image, I would say, of what I think. So, since I am a dumbass, and I do not know privacy from my own ass, I basically have my future job in my bio (which is trauma surgeon or paramedic, depending on what I choose), but, I also have “anti-fat acceptance” or “anti-Health at every size”, or both, I don't know: I'm not in Tumblr right now. And, that person seemed to have a problem with that with the fact these two things do not align (in their opinion).
 And let me tell you why they absolutely fucking align.
 I am anti fat acceptance. I'm not anti fat people. Which is very different. Fat people are literally just fucking people. Now, I don't like people, but that's completely unrelated to their weights, to their sex, or their fucking gender, whatever the fuck they decide to identify as; you can be fucking plantkin and I'll still love you if you have a good personality. I could not care less especially about your weight. What I care about, on the other hand, are people who make the dumbest. Fucking. Excuses. to justify their bad lifestyle choices. Now these are the people that I have a problem with. If you make excuses to your grandmother at Christmas because she tells you that you've put on a few fucking pounds that's none of my business. What is my business, however, is when a person uses their public platform to spew bullshit facts about health, to impressionable people, especially impressionable young people such as fucking 12 year olds on this goddamn hellsite; that is what I have a problem with.
 These people should not have to suffer the consequences of your misinformation.
 Just because you're 25, and 250 fucking pounds, and you haven't had a heart attack yet doesn't mean you'll live to see 50. You have to understand that at some point, you'll become old, like everyone does, and that if never tried to be even remotely healthy, you will die at an age under your expected life span.
 So the reason why I am anti fat acceptance is basically the same reason why I want to go into medicine: it's because I want to help people. It’s because I care about health. I want people to be the best they can be. I want them to be as healthy as they can be. Being obese, or even overweight is not healthy (use your logic here. Being 2 pounds overweight is not the same as being 10 pounds overweight. Genetics and shit. You seem to like that argument, this is where you’re supposed to use it), it's putting a strain on your heart, it's putting a strain on your joints, and if you’re severely overweight, it's fucking around with your internal organs. Never in the world will I ever believe that someone who is extremely extremely overweight or obese is healthy, because, in like 97% of cases (I just pulled that out of my ass, don’t quote me on that), they're not.
 You can be beautiful. This has nothing to do with beauty or aesthetic of whatever. I’m saving that for later. Beauty comes from inside you, and not just from what you look like, it comes from how you act.
 This is why I find that a lot of people in your fucking movement (the fat acceptance movement) are not beautiful. Because to me making excuses for your poor choices is not beautiful. It's cowardly.
 Now I am one of those people that thinks that everybody should have body positivity. Everybody should love themselves, regardless of their weight, of their race, of their gender or whatever the fuck else. Everyone should love themselves.
 But, yes, there is a but, loving yourself is not just treating yourself. (And even then, treating yourself is not sitting on the couch all day eating 6 fucking pizzas and calling it self care). Self-care is taking care of yourself, in all of the spheres of the self. So, for your mental, your spiritual and your physical spheres. So you see, taking care of your mental health would be to relax for a day, you know, and to eat what you like without feeling guilty about it and to drink a nice cup of tea and to smell flowers and shit. Something good for your spiritual health would be to meditate to go to whatever church or synagogue or mosque or whatever other place of worship for your particular religion. It could be anything, like listening to TED Talks that you like. And finally, for your physical self, would be to eat fruit, to go to the gym, go for a little walk in the park, drink water… not eat three bags of fucking Cheetos!
 We've all done this. We've all eaten way too much junk. We all probably felt guilty about it at some point. What I want for you is not to feel shitty about what you eat, or don't eat. I want for you to be the best you can be, and not even for me (obviously, I’m just some asshole on the internet), for you, for your kids (if you have kids, if you want kids), for your significant other (if you want one), for your family and for yourself.
 Because trust me, physical health greatly improves mental health.
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my-autistic-things · 5 years
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hi um, i don't know if you give advice or anything like that, but i think i'm on the autism spectrum. i was diagnosed with adhd, but given a lot of my triggers and stuff i dont know how to phrase i think i was misdiagnosed, and i have no idea what to do ?? idk sorry if you're not comfortable answering this but im just confused and you dont have to answer
Hi there! I'm happy to answer asks like these don't worry :) I'll make a longer post about this (as I do often) to make sure I can fully answer.
If you feel as though you were misdiagnosed, it is definitely a possibility! ADHD and autism are quite similar, and even the testing is similar as well. Depending on your age, how well you do in school, the way you dress and present to the psychiatrist, and even how much you know about ADHD/autism all affect how the psychiatrist diagnosed you (not even mention if you're afab). Given that youve gotten an ADHD dx, I wouldn't be surprised if you are actually ADHD and also are autistic. If you feel as though you are more autistic than ADHD, you can still have both and "feel more autistic". But, if you don't match the key ADHD symptoms, then you're not likely to be ADHD. ADHD and autism are similar enough to be mistaken for each other by someone not considering one or the other, but I think it's a good idea to take into consideration that you have a pro-dx of ADHD nonetheless. I'd also like the point out, if your a minor, the psychiatrist reports to your parents primarily. If your school/parents suspected ADHD and went for an ADHD test, they don't test for ASD at the same time unless specifed to do a full testing for every possible learning disorder/disability/psychiatric disorder. Just from an ADHD test, you can't be diagnosed with ASD. The psychiatrist could suspect ASD, and could have even mentioned it to your parents, but they could have waived it away or even the doctor could have felt it wasn't important. It all depends on the situation. So maybe bringing it up with your parents in a casual way would be a good idea. Like "hey I was doing some research into ADHD and I found that autism is actually kinda similar! I wonder if it's a possibility I have autism as well! It seems as though I have sensory issues and I really need routine moreso than people with ADHD....did the psychiatrist ever mention anything like that?"
Can you talk to the psychiatrist that diagnosed you? Email? Phone? Make an appointment to see them in person? They probably would be able to tell you if they can suspect ASD as well as ADHD and you "don't have enough symptoms to be formally diagnosed". This can be taken in two ways: either you really don't (and you should listen to a professional's reasoning), or they just don't know you well enough to know all of your symptoms (very good possibility, only you know yourself best).
My primary advice: Get a checklist (there's the DSM-IV online as well as explained versions for both ASD and ADHD). Copy paste that into two documents. The first, edit it into a literal check list (so you can put a check next to each symptom). The second, under each symptom write out how it applies to you. This will take a lot of work, but try at least getting the key defining symptoms of both written out. If you don't have the key traits of autism, then you don't have autism. If you do, even if you're wondering if you *actually* fully qualify as that trait or just slightly, then it's worth bringing it up to your psychiatrist and make a whole deal of it.
When you go to see them (or a different psychiatrist), bring all of your notes/checklist/symptoms with examples or situations that'd happened, and make sure you voice everything important. I would even recommend giving them a copy to look at in case you forget a point or think one isn't worth mentioning but it actually is.
I would also recommend following autism and ADHD blogs and submitting a few asks to blogs asking "is this and autism thing or an ADHD thing?" though, it probably is both since they are similar.
Above all, I'd like to say that it really doesn't matter the label you receive as long as you're able to be happy living your life. If a label is what you need to identify your traits with, then definitely pursue a formal diagnosis to clear everything up. If you're fine without a formal diagnosis, that's great too. A diagnosis isn't going to change your personality, your traits, or how you live your life. It's different if you need specific accommodations and such, but take a bit to think how an ADHD vs an autism dx is really going to affect your life. It all comes down to what you want, but I say this because I know a few people who really don't think it's worth the hassle so don't worry to much you need a pro-dx to have your traits valid.
Good luck!!! (You can message me if you want to too!)
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neopronouns · 6 years
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hi! i was just wondering if you could suggest a better category name for my gender? i identify as truscum, but i feel like the "scum" part is completely wrong, since scientifically proven facts arent really scum. i dont want to basically go around saying im scum, but i cant find a better title for the life of me! i was thinking maybe something that surrounded "correct" or "not ignoring and denying obvious evidence." thanks! uwu
awwwww, i can totally help you out nonnie!! although, i think you’re headed in the wrong direction with this new label.
considering that truscum are scientifically inaccurate about most things*, i’d go with something more akin to...hmmmmm... how about ‘parading disproven ideas around as facts and ignoring when you’re proven wrong’, ‘disregarding what both medical professionals and leading trans rights groups say is fact’, and ‘harassing people who don’t fit your mold of transness’.
well, ‘scum’ DOES fit the bill pretty well, but if you want an alternative, might i suggest ‘asshole’, ‘science denier’, or ‘historically inept’? those sound pretty accurate to me!!
*sources for some shit y’all get wrong or ignore under the cut uwu!!
first off, here is a good explanation of how one can have dysphoria and not even realize it. a person could believe they simply are experiencing symptoms of depression and are nondysphoric, but they’re actually dysphoric and not able to recognize it due to how it’s often insisted that dysphoria is simply bodily distress. someone who says they’re nondysphoric could very well BE dysphoric, and you wouldn’t know, and you’d drive them out of a community that you believe they need.
there is no definitive difference between male and female brains currently recognized (additionally, a source i see many truscum throw around had a sample size of roughly 80-90 people. sources with sample sizes as large as 2500 have disproved that one).
there aren’t only two sexes and, in fact, our bodies are often made up of ‘patchworks’ of sex characteristics, meaning that almost nobody experiences their sex the same as someone else, which can affect gender identity.
peruse through this wikipedia page of historical third-gender identities - this is a indicator of how humans have never experienced gender as simply male and female, as we’ve always found words for those who fit into both or neither.
this is a very good explanation as to why people coin xenogenders and other labels that seem nonsensical.
this page not only has some wonderfully informative and helpful information (for both cis and trans people alike), but it sums up the ‘tucute’ point of view (cough the correct view cough) very well: “Not all transgender people have gender dysphoria. On its own, being transgender is not considered a medical condition. Many transgender people do not experience serious anxiety or stress associated with the difference between their gender identity and their gender of birth, and so may not have gender dysphoria.”
here is a lovely video with lots of informational sources in the description that i definitely recommend you read! they’re mostly about nonbinary genders. the video also has a wonderful quote somewhere near the end that i feel sums up my feelings very well: “...it doesn’t hurt you or inconvenience you in any way to respect someone else’s self-identification."
sex and gender are social constructs!
more sources on this post!
this lists some of the many reasons why medicalization of transness is a horrible thing for trans people, and how societal treatment is far more distressing to trans people than their actual trans identity
yet another article about how societal pressure causes dysphoria rather than a person’s transness itself
demedicalizing transness does not demedicalize dysphoria, because dysphoria is a diagnosable mental disorder and being transgender is simply an identity.
“Apparently, distress and impairment are the two essential characteristics of a mental disorder, and they found transgender people can experience some distress but not because they are transgender, but because of social rejection and violence.”
“Not all transgender people suffer from gender dysphoria and that distinction is important to keep in mind. Gender dysphoria and/or coming out as transgender can occur at any age.”
this is a great article about how the term ‘transtrender’ is harmful and how policing the gender identities of those you don’t think are really trans is transphobic
gnc trans people face more discrimination than gender conforming trans people
annnnnnd that’s only a few! you see, if you take the time to listen to others’ experiences, search through some scholarly articles, and otherwise just look through lgbt+ history, you’ll find that your pov only serves to harm our community and the young trans people who need the community to live and thrive.
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scripttorture · 6 years
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So I’ve seen a few organized crime asks and wanted to ask something for a book I’ve been working on. How do I show characters living with things like chronic pain and depression and anxiety after being exposed to violence, without adding to stigma that mentally ill people are violent? I don’t want readers to think committing violence will not affect people in any way, but I also don’t want readers with mental illness to think their own disorder is a punishment for something they haven’t done.
That’sa good question.
Anda bloody difficult one.
I’vebeen pretty open about having mental health problems, intrusivethoughts about violence and how these stereotypes have effected me.
Butthat experience only really allows me to speak for myself. I can’treally speak for the  millions, of other people in the same position.Some of them are likely to feel differently. I’ve seen peoplerespond to @scriptshrink’s blog by saying they don’t thinknon-mentally ill people should write about mental health at all.Personally- I don’t agree, but we’re not a monolithic group.There are huge differences of opinion here.
So-other people may disagree. This is a subjective issue rather thansomething I can fall back on research papers and statistics for. Keepthat, and my biases, in mind.
Whenit comes to writing my philosophy is ‘balance’. Which in thisparticular case means that I’d try to add in more mentally illcharacters who are not violent criminals.
Oneof the easiest ways to do that in this scenario is to include thefamilies of these criminals.
Let’spause for a moment for a tangent into a real life case. Take a lookat the appendices of thisbook (freely available online here),we’re looking at Case Group B, Case No 3, page 168 out of 196.
Theyoung woman of ‘Case No 3’ was the daughter of a torturer and thecases are Fanon’s notes taken as a mental health professionalduring and after the Franco-Algerian war.
WhatI’m trying to highlight here is the way violence can impact themental health of witnesses and people who are only peripherallyinvolved as well as attackers and victims. I think including peoplefrom these groups could help because it gets to the root of whatyou’re driving at: that violence causes mental health problemsrather than the other way round.
I'dalways encourage people to include victims in their stories, if itcan be done in a way that allows them to be fully rounded individualsrather than objects.
Howeverthat’s not always possible if the story focuses on the ‘badguys’.
Otherwitnesses and public officials can also be used to show the effectsof violence. I suppose police officers are the obvious group to leapto but in places where the levels of violence are high there oftenseems to be a huge pressure on health care professionals. They’reexposed to much of the violence of organised crime and they’resometimes deliberately targetted (as in Mexico and Pakistan).
Ifyour story involves any of the criminal characters being injured andin need of emergency treatment- well @scriptmedic always used tosuggest trying to give medics more personality even if they’re onlyin the story for a short amount of time. A connection with thepatient over shared mental health problems could be a good way to dothat. Especially since a doctor could plausibly voice the obviousconnection: they feel this way because they’re exposed to violenceevery day.
Ithink if you can it’s also important to take the time to show thesemental health problems developing in your abusive characters.Establish that they were violent long before they were mentally ill.
Youmight not have space in the story to show that development from thebeginning of the character’s time in a gang. But if you don’tthere are other ways to work that in.
Havinga character reflect on their past is a possibility, or having someonewho knows them well point it out to them.
‘Youknow you never had to take those pain pills until you started doingx’
‘Youdidn’t have these days before you joined the gang-’
‘Youwere so much calmer when-’
Andso forth.
Youcould also approach this by looking at the way older more establishedmembers see younger members. If your older mentally ill character whohas seen a lot of violence now has this ‘kid’ trying to tagalong, wanting to learn the ropes, wanting to be ‘tougher’ and‘stronger’- It would probably be naturally for the character tolook back and think ‘I thought like that too, before the painstarted, before I needed the pills, before I spent weeks at a time inbed. This dumb kid has no idea what they’re asking.’
Bothof these tactics are… attacking the idea at the joints. The firstone is establishing that mental illness exists outside of violentaction and the second is establishing that the character was violentbefore being mentally ill.
Thereare probably other ways to approach doing this. These are just theways that stood out to me and that I thought would fit the scenariobest.
Ithink you’d probably also benefit from finding a beta reader orjoining a writing group.
Becausethis sounds like the sort of scenario where the execution is going tobe incredibly important to how this comes across. It’s not justabout picking a few strategies it’s about making sure they acrosseffectively on the page. And the best way to find out is to getpeople to read it. Ask them about the story. Ask them how theportrayal of mental health problems comes across. Ask for theirsuggestions for more elements or improvements.
Honestlythis helps so much. I can’t count the number of times my writinggroup have picked up on inconsistencies, unclear passages or justplaces where re-writing things a little could improve the emotionalimpact of the scene. Clarity, consistency and good use of atmospherewill go a long way to achieving what you want in this story.
AndI’ve found that it’s very easy to assume we’ve got all thosethings the way we want them as we write. Because we know what wemean. Showing other people our work and getting their feedbackreassures us when we havegot it right and helps us figure out what to do when we haven’t.
Ihope that helps. :)
Availableon Wordpress.
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aceyanaheim · 5 years
Text
Okay let’s try this one more time.
Questions from this thingy that I saw a friendo do last year.
Introduction: Acey. That’s it that’s the introduction.
Diagnosis: I’m working on getting a Diagnosis but Autism and some form of attachment disorder.
As of 2019:
Neurocognitive and Cognitive Disorder due to Seizures
Major Depressive Disorder
General Anxiety Disorder
Social Anxiety Disorder
Personality Change Due to Seizure Disorder ( later confirmed by a second psychiatrist to be Borderline Personality Disorder)
C-PTSD symptoms ( still waiting on final diagnosis but symptons have been confirmed and disorder is very likely.) 
Autism more or less confirmed by multiple professionals  but still waiting to be able to afford testing.
Symptoms: 
Autism/ASD : Can’t read tone. Hard time with social interaction. Sensory issues. Adherence to routine. Stimming. Scripting. Childish behaviour.  Meltdowns. Hyperfixation.
Attachment Issues: I tend to attach/get attached to people really fast. At the same time I push them away or tell myself I don’t matter to them. I also have a hard time getting attached to people. It’s either super quick or like pulling teeth. I want to be with people all the time. Codependence I guess is the word I’m looking for.  
Social Anxiety: I’m...basically always scared when I’m talking to people? I’m scared I’ll say the wrong thing. I have my answers and messages rehearsed and proofread and sometimes vetted by someone else ( unless it’s sensitive info)  and I still feel like something comes across in a negative way. ( like This is too cheerful, That’s too morbid, does that sound dismissive? If I say This I fuck up in this way but if I say THAT I fuck up in another) It couples with my autism since that...actually makes me say awkward/wrong shit all the time. 
Has come down since starting Lexapro but still present.
Emotional Flashbacks: Feelings that were there while you were experiencing the traumatic event. Happen at random triggers. Incredibly strong. To the point that they don’t correspond to the stimuli and feel freshly felt. ( tied to C-PTSD) 
Hyper-vigilance ( tied to C-PTSD)
Anxiety attacks
Panic Attacks
Don’t act as mature as other people my age/more at home with younger people.
Hypersensitive to any perceived rejection. 
Brain fixates on bad memories and repeats them : C-PTSD
Constant fear of it happening again: C-PTSD
Black or White thinking: I’ll think someone’s sick of me or can’t stand me at stuff like being left on read while also deciding I love them and they’re the best person ever when they do something nice to me. Intense but have some modicum of self awareness. ( i know on some level people dont dislike or hate me, i still spiral though)
“Duckling Syndrome” ( is what i call it) : I’ll see someone be nice to me and all I can think of is how much I want them to adopt me, to take me home, to make me part of their family. It’s too strong to be anything but disordered. It hurts. ( possibly part of bpd) 
Has in the past put self in bad situations to not be alone ( connected to bpd/attachment disorder) 
Other Stuff I either need to mention to my shrink and/or hasn’t been tied down to any of my dx disorders:
I want things to be Just So. Like I want a certain kinda paper for certain kinds of mediums in art. I want my food in a certain order. I eat it in A Certain Order I get really uncomfortable otherwise.
I think I’ve depersonalized or dissociated at least five times..but..only when things get REALLY bad...like when I spiral. I still get those two confused even after reading the definitions but it’s like….I don’t feel anything? But I’m weirdly aware that I’m supposed to? Like I flipped a switch. Also mixed with this weird its not real feeling. I hasn’t happened in roughly a year tho so I dunno if it counts? Its been happening again this year. Still unsure if disordered or stress reaction.
I tend to struggle with depressive episodes from time to time. Like I’ll just lay on the bed and not wanna do anything. I have games to play, I have hobbies I could indulge in but I just..don’t want to. Don’t see the point.
Have thought that I’d be better off not existing. ( AKA suicidal ideation) Currently under control.
I’ve developed these like...weird paranoia spells? Like this one time a cop yelled at me ( to mess with me) and I was suddenly terrified of him following me and hurting me and my dad ( which yes can be attributed to the amount of police brutality you hear about, especially to people who don’t speak english fluently but like I saw it in my mind’s eye and it would not stop and the dude left and I was still seeing in my head him like following me home and hurting us) or like just recently some man asked about my dog and how much she was worth and this weird ass alarm went off in my head to get the hell away from him and what if he follows me home? What if he takes my dog? What if he follows me home AND takes my dog? They’re pretty sporadic ( though not as much as I want them to be)  but they’re also really intense. Have stopped since I started Lexapro.
Physical Self Harm in the past to ground, to punish myself, in times of high emotion. All of the above. ( has stopped as of last year. Even intrusive thoughts about it are at a minimum.)
Obsession with being “good”: If I ever do something I think is a mistake I all but turn on myself. I beat myself up. I think of myself as a bad person ( there’s only Good and Bad for me..but only in regards to myself) I have to be nice. I have to be kind. I have to be good in a way that’s disordered. ( this compounds with my social anxiety and bpd to bind me into being a “good person” ( someone who never gets mad never talks back never does anything but niceness irregardless of the fact that..it’s impossible) I tend to think if I’m “bad” that people need to punish me, yell at me, or hurt me. That I need to Atone) ( could be part of CPTSD due to past abuse. Answer pending) 
Intrusive thoughts: mostly about self harm but also about “learning my place” and...calling myself things I’d rather not say. I’ve so far at least managed to recognize they’re intrusive ( might be related to any of the disorders listed above but also with past abuse but unsure at the moment. Shrink thinks its tied to bpd. Could be tied to past abuse I haven’t discussed in therapy yet.)
Disordered Eating of sorts: due to my mother being paranoid about unhealthy food I’ve gone days where I can’t bring myself to eat something because I’m scared it’ll hurt me. There’s times where I’ve needed my friend to tell me to eat. There’s times where I feel like if I eat I have to exercise it off. It’s about control, it’s about fear, it’s….about everything but weight. Hella strong last year. More or less brought under control as of this year. But remain as intrusive thoughts and pop up as intrusive thoughts from time to time.
React badly to being alone, especially at home and not getting social interaction. Depression kicks up, sometimes depersonalization ( might have ties to childhood epilepsy -having to be on lock-down  and kept indoors a lot due to my own risk of being hurt via seizure- but combines with bpd/attachment disorders) 
Have Shown Signs/Moments of Age Regression ( more often than not with the emotional flashbacks but not always)
Literally all the symptoms act up at night/around bedtime. Mostly anxiety but some others that have now been associated with bpd. Causes sleeping problems ( I hesitate to call it insomnia because I do sleep but it can get as bad as 3 hours a night until i just conk out at the end of the week -or 2 weeks- out of sheer exhaustion. Has been present since I was a teenager.) 
In The Past: Recklessness and disregard for personal safety and care.
Sometimes get this  physical feeling like my brain is overloaded. Often with hypervigilance or spirals where my mind races.
Stigma:
“I’m autistic” “I’m so sorry”
“I’m autistic” “And you’re sure you wanna go for that major?”
“I’m autistic” “But not that kind of autistic right?”
“I mean if you need accommodations to take a test then are you really cut out to have that kinda job?”
I consider myself a very patient person.
“She doesn’t know any better. You know she’s special” ( I was standing right there)
“I guess you don’t love anyone huh?” ( I was uh..I was nine years old)
“You’re codependent as fuck” ( that one my abuser said to me...after...making me codependent on her..yeah) 
“You talk like a robot. It’s like you don’t feel anything.” ( eeemotianl detachment due to CPTSD in my teenage years) 
“You’re choosing not to grow up” ( when expressing fears of develomental problems/disordered behaviour that could cause lack of maturity. I was asking for help) 
“You’re a lot”
“People with your disorder tend to be a problem for other people”
“You need therapy” “I am in therapy” “Then why are you still acting like this.”
“You’re just making excuses.”
“It’s like you like to cause trouble.” ( circa 2013)
“You just wanna hurt people that’s why you’re doing this.” ( circa...most of the 2000s) 
Multiple people in my family constantly make it a point ( or have in the past like..for most of my life) to tell me no one’s wanna live with someone like me ( I’m forgetful and before I figured out some ways to help it and the depression was bad uber messy)
Multiple people in my family try to discourage me from trying things because “you know you have that...thing”
And I mean..the usual constant bombardment of Autism being something you have to Fix. Of it causing people you love pain, and them never being happy because of it, of it being a defect.
People around me use autistic as an insult.
General comments about how horrible living with my mentally ill family must be ( ignoring that I’m mentally ill as well) and how my parents probably wish we weren’t disordered ( ignoring that they are also disordered) and how basically there’s no way for us to be happy.
I think at one point someone actually said to me something along the lines of “I bet your parents wish you and your siblings were born differently”
“I’m so proud you can do this incredibly easy thing that I think is all you can really do and I’m gonna talk to you in the most condescending tone about it like who’s a good lil autistic person look at you, talkin and solving basic problems and everything.” ( obvs paraphrased but thats...usually the gist) 
Define Your Disorders
Autism: a developmental disorder that affects communication and behavior.
Attachment Disorder: the condition in which individuals have difficulty forming lasting relationships ( it was the only one I can find that doesn’t talk about RAD as I don’t have the criteria for that. This one’s tricky cause I don’t have the proper diagnosis for it yet, for all I know it could be part of a bigger disorder)
BPD:a mental health disorder that impacts the way you think and feel about yourself and others, causing problems functioning in everyday life. It includes a pattern of unstable intense relationships, distorted self-image, extreme emotions and impulsiveness. Symptoms include emotional instability, feelings of worthlessness, insecurity, impulsivity, and impaired social relationships.
Major Depression Disorder: Depression is a mood disorder that causes a persistent feeling of sadness and loss of interest. Also called major depressive disorder or clinical depression, it affects how you feel, think and behave and can lead to a variety of emotional and physical problems. You may have trouble doing normal day-to-day activities, and sometimes you may feel as if life isn't worth living.
General Anxiety Disorder.:  Excessive anxiety and worry (apprehensive expectation), occurring more days than not for at least 6 months, about a number of events or activities (such as work or school performance).
Amnesic Disorder Due To Epilepsy :Inability to remember events for a period of time.
Myth about your disorders and the truth
Autistic people are dangerous
Autistic people are unfeeling
Autistic people are uncaring
Autistic people are all nonverbal
Autistic people are all mentally challenged. ( I ??)
Autistic people ar a burden on their families/a parent who abuse or even  kills their autistic child ( which happens so much it’s an acknowledged problem)  deserves sympathy.
Autistic people are brainy and mostly male.
Autism is a spectrum disorder. People exhibit different traits and while some hyperfocus on things that help them academically some hyperfocus on things that don’t or that even make their grades suffer like other interest tend to. ( my hyperfocus was fanfiction and I failed like five classes because of it) I have a friend who’s autistic and likes to party and drink and hang out with people. I have another friend who’s autistic who likes to skate and science. I’m autistic and I like neither of those things. We’re all over the place in every way even when we do share some common traits
Literally we all have people and things we care about.
Literally all of us have affectionate moments. I’m fairly physically affectionate if I’m close to/feel safe with someone.
Nonverbal and autism aren’t always correlated. Further, some autistic people go nonverbal for a bit but can speak other times.
Autism looks different in girls/afab people because we’ve been socialized differently.
Parents who kill their autistic kids are just straight up horrible people and I resent having to be told to have sympathy for them while simultaneously wishing I had “autistic” written on my forehead so I could be angry without a guilt trip and also simultaneously hoping to god I never stop passing for neurotypical because apparently the moment you show too many traits no one cares if someone hurts you or worse.
The whole “autistic people are dangerous” thing is mostly people showing videos of meltdowns which only happen under high stress and is something people use to demonize us and make us seem like burdens...and is actually why the whole “sympathy for an abusive/murderer parent of a neuroatypical” thing is fucked ten ways from Sunday. We aren’t dangerous.
I don’t...have a lot for the attachment disorder since I’m still waiting to figure out what that one’s really about and I haven’t really….met anyone else who has anything like it or shares symptoms with me.
I think off the top of my head it’s when people think it’s “cute” that you’re super clingy or go the other way and say people with attachment issues are uncaring. The first one romanticizes a behaviour that you’re trying to work on fixing/curbing and that is honestly hell. The second one is...is just as untrue as saying an autistic person is inherently uncaring ( or any mentally ill person for that matter)
I’ve also seen people say that people with any kind of attachment disorder are broken and that I feel confident enough in saying that they’re not...and I’m not.
I’ve been told people with BPD can’t be aware of their own disorder and have been denied testing due to this. 
I’ve seen people say people with BPD are a problem to others.
Anxiety: I’ve seen a lot of people who think it’s fake. And also that the only way you can have anxiety if you’re rocking back and forth gasping for breath.
There’s actually multiple ways to have anxiety attacks.
Tips for those who know/love someone with same disorders/symptoms
Well, starting off with, and keeping in mind that I’m not a proffesional or expert in...literally anything ever like ever ever....
A very dear friend of mine once said “it’s a whole lot easier to be supportive than it is not to be” Let people with disorders tell you what they need, and then respect it. Open communication and making them feel safe is key...to everything. Being informed is important but at the end of the day, different people will experience things differently and what they need is really down to them. Don’t assume that reading about their disorder means you know what they need better than them. Don’t talk about how their disorder affects you. Even if you have good intentions, you’re going to make them feel bad. If you’re a parent, don’t talk to others about your child’s disorder in front of them. And if they don’t like a therapist, listen to them as to why. Don’t assume it’s just because “they’re disordered” that’s lazy parenting.
Take triggers seriously, talk to them about what symptoms they need help with, and which they’d rather process or deal with  on their own. Just..show that you have that initiative, that you’re there for them. Listen. Be patient. Establish boundaries gently but firmly. If someone with my attachment disorder is ringing you a lot and you need time to yourself, let them know. Explain. Don’t go radio silent. People with autism can be bad at reading you. Again explain, be patient, but don’t just....leave them there to guess what they did wrong. C-PTSD is traumagenic in nature so I’d add to taking triggers seriously, be ready for Tragic Backstory drop behind disclosing some triggers ( and understand how much they have to trust you to disclose that.) but also be ready for “I just don’t want this in my field of vision and I don’t feel comfortable talking about it just yet.” Don’t push for details. Don’t push period.
And also just....treat em like people you know. Disordered people are still people, let them exist outside their disorders and do the things that people in that relationship that you have with them. ( whatever relationship that is) do. 
How your disorder/s affect your relationships 
In the past -and before I was a bit more self aware- it’s made me uber clingy. I would call friends constantly, message them a lot. Think someone was my best friend or even closer than they really were because they were nice to me. It scared people off.
On the flip side I would also convince myself people didn’t like me or I was nothing to them the moment I caught myself having strong feelings. ( which as said before would happen mcquicklike)
As one can imagine this would put a lot of pressure on new friendships. Often it would sour them, sometimes it would make people dislike me. Sometimes it’d make them unconfortable. Which as my disorder also affects how I receive rejection...was..really bad.
On the flip side of the flip side I was also incredibly ride or die and it left me open to a lot of manipulation and abuse from friends. I couldn’t be mad at them if they hurt me. I couldn’t say no to anything they said. I needed them.
My anxiety also contributes to this as I would constantly go through a checklist of how many good interactions vs “bad” or awkward interactions I had with people before I let myself feel like I was safe to call people my friends. Or even say I did okay interacting.
I had a lot of nights while I was making friends in college where I just felt like I was nothing to anyone. Like I was messing up. Looking back, it was just standard new friend interactions.
The more people mean to me, the more I’d freak out-I didn’t want to lose them. So it made it hard to even enjoy the friendship milestones I did achieve.
I’m using past tense because it’s gotten a lot better as situations that were making this 10 times worse have alleviated somewhat but there’s still seeds of it and sometimes it flares up. I’m just aware enough I can sometimes if not stop it identify it as my disorder talking. I don’t keep lists anymore but sometimes the thought pops up.
Facts About Your Disorder You Wish People Knew
I wish people knew what scripting and autistic burnout was. And that adults can have autism. And that vaccines don’t cause autism so stupid ass people didn’t risk their kid getting sick because they’re scared of my neurology.
I wish the only thing when I search about
I wish people took triggers seriously.
I wish more people knew about attachment disorders period.
I wish people knew how hard it all is sometimes.
 Favorite healthy coping techniques
Plushies, pillows. Physical grounding techniques that include physical stimming. I’m very tactile when it comes to my autism and stimming so grounding techniques were Good Textures are involved help double.
For attachment disorder spirals: Watching YT animators or vloggers. Like a lot. It recently chased off my sleeping problems. 
Playing with my dog.
Walking outside.
Going to the beach.
Looking at buildings. ( I don’t..I don’t know why?? It’s like a visual stim I guess? Like buildings that stand out to me due to their shape or being different than I usually see)
Basically going outside. ( to look at buildings, to look at nature, to the dog park, out in the grass in front of my building just..Outside Good, Inside Bad) 
Sending fun stuff to friends/doing things for them.
I tend to get a good happy chemical surge from helping people/doing nice things for people so that’s something I really like using to my advantage. I’m looking at volunteer options.
Also cartoons and Disney Channel shows I watch a lot of those.
Cooking. I can’t understand this one either but cooking and baking sometimes even gives me more energy.
Current biggest struggles with your disorder/s
Being at home tanks my mental health. I don’t drive. So I’m home a lot.
Seeing families be happy hurts sometimes. And that’s my main confort narrative.
Seeing my friends with their families hurts sometimes.  All I can think of is how much I wish I was a part of that. So I have to...not spend time with my friends.
I’m afraid to live alone.
I can’t get anything done sometimes. My train of thought has been crashing to the point that I completely lose it and I miss goals and deadlines almost every month. I need to get assignments done, build a portfolio, at least keep shrink dates, its all a hurdle lately. Even before that it’s hard for me to get stuff done when I’m home on  my own ( aka when I’m supposed to be doing things) because all my brain can think is “we’re alone we’re alone we’re alone. It’s too quiet. We need to talk to someone.” According to my shrink DBT will help with this. I can’t wait.
It’s hard to see a myself having a good future sometimes. Because of how many hangups I have and how late I am in addressing them ( I’m 28) and how much there is to do.
 What not to say to a person with similar/same disorder/s
“You’re making it all up”
“You should just get over it, it happened so long ago”
“You’re bringing me down stop talking about this”
“Its all in your head”
“Every one feels that way really”
Anything dismissive.
Anything from the stigma answer.
Literally any kind of pity (granted thats more a me thing due to childhood epilepsy meaning i had to deal with a lot of that. But honestly I’ll stand by it bc I’m not sure anyone really ...likes pity. )  
Ways in which your disorder/s affect your daily life
I deal with executive dysfunction which makes it hard to get anything done. I feel like I’m starting over constantly. I feel like my age doesn’t match my brain. All of this augments my depression.  I have to take days off in the middle of the week to just do nothing or catch up to all the stuff I haven’t done. I miss deadlines or just barely make them. I’m also a budding workaholic which I used to do to avoid dwelling on all these feelings so having to take breaks isn’t….something I’m used to or really like. I at one point handled school, work, and 2 editing jobs. I used to do martial arts, I like running, I like swimming. I’m the kind of person that needs to be on the move and lately that’s hard because spoons and energy.
Also a lot of basic self care is hard to get done because of the dysfunction mentioned above.
Things that give you hope
The fact that I’m finally getting therapy.
I guess having people I can talk to about it.
My family isn’t as bad as it was back in 2014.
I guess I know that even if I feel like I’m at a dead end, I’ll figure something out. That’s what I do. I mean that’s life, you think things are never getting better or that something’s the end of the world but really time marches onwards and so do you and you figure it out. Things fall into place. I believe life has a funny way of working out. If anything because it kinda has to, it can’t stand still yknow. I have moments of clarity where I just kinda remember that ( its not my first rodeo.in regards to hard times or Things That Happen..its not even my hardest rodeo so..if I got through that..you kinda figure you can muddle through this and see what comes next yknow) I’m oddly hopeful for the first time in a long time so, it’s p cool.
Treatment types and personal choices
I spent most of my childhood, and teenage years...and early 20s dodging therapy and help due to it being controlled by my mother and having really bad experiences with it in the past.I do regret it sometimes but I comfort myself with the fact that it was what seemed like the best decision and i didn’t have the information I now have about keeping her out of things. 
After finding better insurance and getting into university I found a way to get myself a psychiatrist and am working on finding talk therapy. For the most part I tended to patch myself up a lot by finding ways to quiet the thoughts I had ( saving text messages to remind myself people dont hate me. Talking myself down. Joining social activities. That sorta home brew stuff. I’ve been soloing a lot of shit I probably shouldn’t have been until recently but hey live and learn. Also I didn’t have insurance.) As of recently I’m on an antidepresant and  hopefully going into DBT. That reminds me I have to call them.
Your support system
I’ve found some really nice friends like they’ve kinda just collectively adopted me and when your disorder stems from losing family that..that’s been incredibly helpful. All my close friends are long distance but they help me. My younger sister is also there although i try to limit how much she’s privy to as she just turned 18. My brother and I tend to spend limited time together due to him having his own stuff goin on but I’d also put him there. My parents sorta count as....one supportive unit? ( they try with the best of intentions but it uh..thats..thats really all I can say about them)
Reactions from those who learn about your disorder/s
I get told I can’t possibly have them because i “look too successful” or whatever ableist rethoric they got going. When I talk about C-PTSD symptons I get side eye for “trivializing” it as they don’t believe I can have it and think I’m exaggerating anxiety symptons. When I talk about Attachment Disorders…..I often don’t because people always say something along the lines of “people with that are often too damaged and you don’t fit the bill” which..ouch.
Mostly it goes from “you don’t look like a damaged and/or psychopath crazy person” to “oh...I guess you are one” with a bit of “okay thats fine” but still anger and impatience when I show symptoms.
I don’t talk about my disorders a lot.
 Future hopes and dreams
I’d like to get my attachment disorder under control as it’s the main life wrecking thing I have. After that or along with that I’d like to live somewhere where I get the social interaction I kinda need.
I wanna be happy with whatever profession I have and just..my life in general.
I hope DBT helps. Whatever it is It’s my first time even trying it.
I have a couple of personal creative goals but I don’t wanna jinx them by disclosing them ( I did mention I had anxiety)
Interactions with other people with the same disorders
I follow some peeps with BPD and also folks on the spectrum on tumblr. I don’t really have a lot of  analog interaction. ( again no driving + suburbia = being cooped up A Lot)  My sister and I share some disordered traits so we talk about them often and that helps a lot.
Things you want to work on/improve
The whole black and white thinking and maybe getting things done on time. I’d like to get the spirals under control too.
 Work/school experience with disorder/s
Shit’s hard.
Often I don’t get the help I need and have learned to overcompensate/regulate so I can still get things done. I pretty much need to work since i don’t believe I’d qualify for disability. I get in trouble a lot for spacing out ( dissociating) and forgetting things at work. Work friendships are also slow burn if not just nonexistent due to my autism and people..not really knowing what to make of it. I’ll probably have to quit working while I study since I can’t really split focus enough to do both lately. Further, a lot of my energy needs to go into school things staying afloat and that tends to mean I can’t do things that contribute to my mental health ( i.e spending time with friends, going out, sometimes even therapy, taking breaks) as I’ve found out that sends me way back in recovery.
Free space!
Here’s a picture of my cat. She’s a demon. What it said Free Space.
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Family history of mental disorders?
Mother has Bipolar disorder and depression. Sister has bipolar disorder, anxiety, depression, and eating disorders, Brother has anxiety and shows signs of ADHD, Dad has what we suspect is ADHD and possibly some disorder traits from past trauma. Used to have anger issues.
I uh..I used to call us “The Madhouse” for most of my late teens and early 20s.
Media representation of disorder/s
Attachment disorders: characters who are stalkers and so desperate for love family and acceptance they’ll do anything, even hurt people to feel it. Also often don’t have depression and can do things like learn villain skills.
Autistic traits are often cherry picked and portrayed in an unfavorable light. I think I’ve seen some rare cases of actual representation though.
How do you feel about talking about your mental health?
I don’t...like it as much as talking about mental health in general. Most of my life is...me running away from trauma and trying to  reclaim a life outside of it. It’s what I did with my epilepsy of course that one was easier because the seizures went away. 
Talking about it feels like going back. I wanna just move on with it. But I’ve reluctantly come around to see that talking about it is a way to move on. And I mean its not like dodging it’s worked out that well for me so.
 The true face of mental illness (Selfie if you’re comfortable with it)
Aww yiiss. Selfies.
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