Say Something Random: psychological Conditions Version
Memories are funny because one minute you can barely remember something and then it's like getting hold of the end of a piece of string and you keep pulling it and pulling it and the more memory comes until you can see the whole big picture that you forgot about
It's nuts that
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We have existence
It's nuts that
Thats kind of a neat way of wording about that ,But when I think about it. that is most often how it has worked for me too.
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Diagnosed hfa
Loves velcro,
Sad to put a sad spin on it , but that process reconnected me. To a series of traumas that went all the way back to my crib time. It was a serious humdinger of a thing, to go back in time like that , And realize,side effects of early traumas.
Then Using what I have learned since then to try to forgive, So I could think about getting on with my life . But occassionally can do that with nice memories too.. . Connecting dots ...kinda .
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Diagnosed hfa
Loves velcro,
Yeah that's really sad that Jakki
thank you for sharing that
Each time I remember something it takes me a while to recover and then i start again going through the process of it
It's like my brain is protecting me so much that it only reveals so much at a time and it's taking years as well
It's not just something that happens within a few weeks
It really is a long process
I think it's incredible how it all works
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We have existence
I think it was about February this year that I had my last big reveal
It floored me and I told my therapist that I don't want it to happen again because that one nearly killed me off
But it feels like there's another one in the pipeline
I remember from the last one how there was like a build up of smaller memories that all came together to make the picture of the incident
So I'm thinking a similar thing is happening now except it's not exactly the same because it's a different memory
And I'm thinking it maybe from an earlier time as well, just because of the thoughts that I've been having lately
My T always tells me to never force it so I've just gotta trust in that and let it happen naturally
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We have existence
ASPartOfMe
Veteran

Joined: 25 Aug 2013
Age: 67
Gender: Male
Posts: 38,084
Location: Long Island, New York
I just felt my life has been too boring. I'm not invalidating other people's experiences here of not receiving a diagnosis in childhood, but what I'm saying is from personal experience only and that I was very unhappy and angry and confused about knowing I had a diagnosis as what I may have been if I hadn't known what was ''wrong'' with me.
The thing is, being diagnosed in childhood and getting statemented at school, it feels like your life is mapped out for you. You can't really do the normal teenage rebellion because you're more watched closely throughout school by your mentor, so if you didn't turn up to any classes your mentor will take a note and pass it to your form-tutor and your parents, and it's just harder to get away with such things. Also having a mentor in class with me marred my reputation to my peers, making them think I was ''ret*d'' and feeling embarrassed about being seen hanging out with me. So I became socially isolated and lonely and just relied on my mentor for friendship, further socially isolating me from my peers.
So I did feel like my diagnosis had become a hindrance and looking back I think that I probably would have engaged more in friendships with my peers had I not have got diagnosed. I might have ''went off the rails'' a bit, but in a way I sort of wanted to but had nobody to go off the rails with. My sister went off the rails by getting involved with boys and having to be grounded by our parents, causing lots of normal teenage arguments. I'm NOT saying that's good, but all I could do was watch all this drama unfold and be no part in it and just live like a 5-year-old kid; always kept safe indoors and leading a predictable innocent life where nothing happened to me and no boys liked me and no friends wanted me. I was probably the ideal teenager really, but not really, as I had a lot of outbursts of feeling sorry for myself because of my overwhelming social isolation and worthlessness, which caused a different set of problems for my parents.
It's difficult to explain. I'm probably just seeing the grass as greener but I just felt disconnected and out of touch when I was a teenager. I tried to rebel a bit in school but it didn't really work. I tried seeming cool, while blissfully unaware that having unshaved legs exposed is totally socially unacceptable when you're female, so while trying to be cool I just looked like a jackass in PE class wearing shorts with legs covered in hair, to which everyone seemed too polite to say in the first couple of years of having hairy legs but then some girls pointed and giggled at my legs just as we were coming to an end of our school lives. I wish they had pointed and giggled earlier on so that it could have been a wake-up call I needed to make more effort to fit in as a teenage girl. My mum often told me to shave my legs back then but being so she was my mum I never listened to her, and I didn't exactly look at the other girls' legs and I had no close friends to learn these things from. So I learnt the hard way instead.
But I'm not, repeat, NOT, implying that I wish anything that could cause trauma happened to me. I'm just saying that I wish I had a more active teenage sort of life, in experimenting and having fun. Instead I just felt behind, watching all of it but never being party to it.
You are not unusual about being resentful about being diagnosed at a young age. An autism diagnosis is both a permanent diagnosis and a diagnosis that is both misunderstood and comes with stigmas. Most young children and sometimes even young adults are not mature enough to handle that. On the other hand I read many accounts by members who are resentful they were not told. Because they did not know they were confused as to why they struggled or concluded their problems were a result of their character flaws.
There is no way for parents know when is the best time to tell their children as we are all individuals.
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Professionally Identified and joined WP August 26, 2013
DSM 5: Autism Spectrum Disorder, DSM IV: Aspergers Moderate Severity.
“My autism is not a superpower. It also isn’t some kind of god-forsaken, endless fountain of suffering inflicted on my family. It’s just part of who I am as a person”. - Sara Luterman
I just felt my life has been too boring. I'm not invalidating other people's experiences here of not receiving a diagnosis in childhood, but what I'm saying is from personal experience only and that I was very unhappy and angry and confused about knowing I had a diagnosis as what I may have been if I hadn't known what was ''wrong'' with me.
The thing is, being diagnosed in childhood and getting statemented at school, it feels like your life is mapped out for you. You can't really do the normal teenage rebellion because you're more watched closely throughout school by your mentor, so if you didn't turn up to any classes your mentor will take a note and pass it to your form-tutor and your parents, and it's just harder to get away with such things. Also having a mentor in class with me marred my reputation to my peers, making them think I was ''ret*d'' and feeling embarrassed about being seen hanging out with me. So I became socially isolated and lonely and just relied on my mentor for friendship, further socially isolating me from my peers.
So I did feel like my diagnosis had become a hindrance and looking back I think that I probably would have engaged more in friendships with my peers had I not have got diagnosed. I might have ''went off the rails'' a bit, but in a way I sort of wanted to but had nobody to go off the rails with. My sister went off the rails by getting involved with boys and having to be grounded by our parents, causing lots of normal teenage arguments. I'm NOT saying that's good, but all I could do was watch all this drama unfold and be no part in it and just live like a 5-year-old kid; always kept safe indoors and leading a predictable innocent life where nothing happened to me and no boys liked me and no friends wanted me. I was probably the ideal teenager really, but not really, as I had a lot of outbursts of feeling sorry for myself because of my overwhelming social isolation and worthlessness, which caused a different set of problems for my parents.
It's difficult to explain. I'm probably just seeing the grass as greener but I just felt disconnected and out of touch when I was a teenager. I tried to rebel a bit in school but it didn't really work. I tried seeming cool, while blissfully unaware that having unshaved legs exposed is totally socially unacceptable when you're female, so while trying to be cool I just looked like a jackass in PE class wearing shorts with legs covered in hair, to which everyone seemed too polite to say in the first couple of years of having hairy legs but then some girls pointed and giggled at my legs just as we were coming to an end of our school lives. I wish they had pointed and giggled earlier on so that it could have been a wake-up call I needed to make more effort to fit in as a teenage girl. My mum often told me to shave my legs back then but being so she was my mum I never listened to her, and I didn't exactly look at the other girls' legs and I had no close friends to learn these things from. So I learnt the hard way instead.
But I'm not, repeat, NOT, implying that I wish anything that could cause trauma happened to me. I'm just saying that I wish I had a more active teenage sort of life, in experimenting and having fun. Instead I just felt behind, watching all of it but never being party to it.
You are not unusual about being resentful about being diagnosed at a young age. An autism diagnosis is both a permanent diagnosis and a diagnosis that is both misunderstood and comes with stigmas. Most young children and sometimes even young adults are not mature enough to handle that. On the other hand I read many accounts by members who are resentful they were not told. Because they did not know they were confused as to why they struggled or concluded their problems were a result of their character flaws.
There is no way for parents know when is the best time to tell their children as we are all individuals.
Yes, I mean I don't blame my parents how they handled it. My mum probably thought it was the right thing to do at the time to tell me and everyone we met. My dad chose to keep it quieter, which I prefer. But at least it means my mum wasn't ashamed of me or my diagnosis, but at the same time it often felt like she hated my diagnosis and wished I didn't have it, probably because I was impacted negatively by it so it felt more like a problem than an identity. My mum lacked confidence and also had anxiety and RSD, so often worried of what other people thought all the time and she also compared me to other people's kids, which is never a good thing to do. She'd often get angry and upset because she felt her kids weren't normal (my brother had emotional problems and my sister had learning difficulties), and she'd looked at her sister's (my aunt's) kids and see the contrast. They were confident, popular, sporty, and bright, and got all A's at school and were in the school sports teams and were very popular and outgoing, with no emotional or learning issues. Even now as adults they're confident; both in good jobs, both own their own homes, and have just landed on their feet really because they were just born with that confidence. Me and my sister and brother aren't doing so well. Well, my sister seems okay, but she has a baby that she and her partner can barely afford to keep, and I think they are in debt, so maybe that's not so good. My brother has never moved out and is living on benefits because he's too depressed to work, and has mental health issues. He's also anorexic. And while I'm living with a partner and working, I struggle bad with anxiety, believing that I'm going to be homeless in the future and feeling extremely anxious and upset about it. Also I got bullied at work, which caused me a lot of stress, and I'm also worried about my job as there is a chance the place I work could shut down, and I find looking for new jobs really daunting and we'd be living in poverty if I were to claim benefits, especially when Farage gets in and takes our human rights away. I just live in fear and it isn't fair.
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My diagnosis story and why it was a traumatic experience for me:
viewtopic.php?f=35&t=416910&start=1056#p9695026
Autism is the part where your senses and processes are not giving you a full picture and context of the matter due to your own cognitive profile and countless environmental or sensory interferences.
The mind is the part where one would register this into a reaction on uncertainty because of not having the full picture and context.
This is also where one would judge the quantity and complexity of something.
Along with the awareness or lack of thereof.
The human is the part where anxiety stirs because of that uncertainty.
This is also where being stressed is signalled because of quantity or complexity, loop it back to the mind and say "this is overwhelming".
This is also where if said complexity and quantity and overwhelm be transformed into more anxiety or something else.
Then between the latter two, it can loop, it can spiral.
Whether or not autism is the starting point of distortion or not, my priority is the human.
This is how I slice them thin.
This is the 'in-between'.
I just stop at the human part of the equation, interfere from within and react differently from there.
No, this is not as easy as it sounded. Most humans don't actually do this. NTs generally just don't go further than the registration bit.
In fact, many practices stops at the mind part, not at the human part.
But that's because most people are mind first, emotions second -- I was forced to do the opposite.
As someone forced to live with an emotions first system, stuff like CBT won't ever work for me.
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Brian0787
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Joined: 19 Aug 2024
Age: 37
Gender: Male
Posts: 1,482
Location: Pennsylvania, United States
I went to the ER this morning after a severe panic attack. The worst one I've had since I called an ambulance to the house. Luckily my Dad took me to the ER. I'm very grateful for him. The ER Doctor was very blunt that I need to be on antidepressant medication and take it consistently. I've been using Ativan a good bit and he made a good point that it's just a band-aid. I was taken aback by his bluntness and his tone which came across as condescending but realize he is right and am grateful for his candidness. I haven't been taking my medicine as consistently as I should.
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