#what is it when its not quite agoraphobia but its not really 'normal' social anxiety either
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talkorsomething · 3 months ago
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When the urge hits but you're literally just trying to sleep so you can't even do anything Productive about it
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leirathemartian · 3 years ago
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This is a really nice article about how the pandemic enforces and exacerbates anxiety, panic disorders, and especially agoraphobia.
I have a lot of different kinds of anxiety, and that includes panic attacks. They're painful, awful things... your body telling you to run from something you can't see. Unable to calm your racing heart or slow your breathing. The beginning of the pandemic hit at an awful time for me -- I had been home from a week-long stay in the hospital for about 2 weeks when we got the order to work from home. I was already struggling with panic from the trauma of being ill enough to stay at the hospital, and the pandemic just reinforced that I was so, so vulnerable.
I was thinking while I was reading this that I'm glad the pandemic didn't hit while I was in grad school. I went through a bout of quite bad agoraphobia in graduate school, where I couldn't go to my office without a panic attack. Going to the grocery store was an exhausting endeavor as I vainly struggled to control my anxiety (I ordered a lot of delivery). I had to prepare myself extensively for any and all social interactions. The reasons for this were complex and multi-faceted, but I think it was probably the worst my anxiety has ever been. And had the pandemic hit during then? I don't know. I think I wouldn't have been able to leave my house. I struggled enough with that last summer, and my anxiety was in a much better place then.
I don't get panic attacks as often as I used to. Or, well, I start to get them, but they don't blossom into the full thing. My heart just races, but it's in the background. (That's taken so much work, and I'm so grateful to my therapist, although I sadly don't see him anymore) But it still doesn't take that much to trigger them, and somedays I feel like, will I ever be normal? Will I ever be able to handle the prospect of going to the bank without deep, throbbing panic?
But I leave my apartment. If anything, sometimes it feels like a gift to have somewhere to go, as long as I'm with a "safe" person. I cling, a bit, to my safe people, knowing that their presence among others will be enough to keep my anxiety safely locked up.
I guess what I'm trying to say is this piece resonates a lot. I wouldn't call myself agoraphobic now, but I've been there. And the pandemic... it's exacerbated so many mental illnesses.
Be kind to yourselves. The last paragraph:
Thieving my own life back, piece by piece, from fear will take even longer than that year and a half in the comforting arms of isolation and confinement. Despair takes so little time to dig its pits, and it takes so long to climb out, hand over hand, hanging over the abyss. But somewhere up there is the bright warm light of a walk in the summer afternoon without fear, somewhere up there is the tinkle of glasses in casual fellowship, somewhere up there is Midtown and Lisbon. The long, slow work must be done, and when I emerge, the brilliantine world will be waiting.
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kirstielol · 5 years ago
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FMLS90
27/10 - Spend a little time reflecting on your current level of positivity. Is your current approach serving you well? What are some ways you could improve your outlook on things?
i’m pretty happy with my current level of positivity! it’s something i’ve worked hard on for the past ~4 years now. i’ve tried really hard to change the way i view myself.
depression and severe self loathing is something i’ve dealt with for most of my life. i used to wallow in it. in my early 20′s i had this horrible tumblr account where i reblogged nothing but self hating crap. i surrounded myself with that stuff. no surprise that my depression and self harming was at its worst around then.
when i made the decision to get healthy physically, i also made the decision to work on my mental health, instead of just letting it control me. i stopped using that old tumblr account and started treating myself better. it took years of being  mindful of my thoughts to stop the constant self deprecating thoughts.
there’s still room for improvement though. i have social anxiety, health anxiety, agoraphobia.. and i’m autistic. i have trouble doing things that “normal” people can do, and i often feel useless and like a burden because of it. so i need to work on not letting that happen. but i’ve come a long way in the past 4 years so i should be proud of that at least. i’m also 4 years self harm free, after almost 11 years of regular self harming.. i’m pretty proud of that! and that’s all thanks to me working on my positivity!
28/10 - How does social media impact your mental state? Do you find the people you follow here help put you n a positive or negative mental place?
the people i follow here DEFINITELY put me in a positive mental place! i love the fitblr community! my feed is full of nothing but positivity. it really helps keep me in a positive mental state.
as for other social media.. i only use instagram aside from tumblr. i completely stopped using facebook a couple years ago, and it was because of the sheer amount of negativity i saw every time i scrolled through the app.
idk if it counts as social media but i also use reddit quite a lot. but the only “subreddits” that i follow are about mycology, cats, and bullet journalling lol. so no negativity there!
and about a year ago i went through all the accounts i was following on instagram, and unfollowed a whoooole bunch of people. old acquaintances from high school, ~influencers~, basically anything that wasn’t putting me in a positive mental place. and i followed a bunch of new accounts.. mostly artists, and cat foster accounts.. because nothing’s better than a feed full of art and kittens 🥰
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maximuswolf · 4 years ago
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Social anxiety, working 100% remote, got an offer for double the salary... but will need to go to the office eventually. Thoughts? via /r/Anxiety
Social anxiety, working 100% remote, got an offer for double the salary... but will need to go to the office eventually. Thoughts?
So about a year and a half ago I had a panic attack in the office of my previous job, which lasted a full day, and I ended with heavy anxiety (non-stop palpitations, some shaking and sweating...) for the best part of the following month. Things never got quite back to normal tho, and ever since I've developed some form of anxiety disorder. I very recently started talking to a therapist (please don't roast me on this :( ), he says it's most likely social anxiety (which makes sense to me) with some agoraphobia sprinkled; but we are still navigating it.
That old job was very stressful and I believe that + me being generally anxious and unresty all my life piled up and triggered this thing for good. Can give more details if it's relevant.
Today tho, I live mostly by myself (one housemate) and work as a software dev for a company that's 100% remote. Pay is good (around 60k), I like my coworkers, manager is chill, I've got my office setup here and no real pressure to leave. I'm kind of indifferent about the job ngl, it's a "pay the bills" thing, I could do it for some years but don't love it. I'm not super bothered about that, I have my own hobbies and I appreciate keeping my job separated from the rest of my life (tho I'll admit, this whole thing made me discover and got me interested on VR-assisted therapy...).
I recently got a contractor offer from a big company in the same field as the current one I'm working on, the job is more or less the same thing (btw don't mind the "legal implications", it's cool), except this second company is offering nearly double of my already decent pay (around 110k). The catch is that it's on their policy that I'm expected to go to the office about 3-4 times a week on normal circumstances (I can do 1-2 days remote).
Of course, right now that does not apply because of covid - all work is remote, and tbh, it probably won't apply for the next 6 months or so at least. But once things get "back to normal" is when it can get hairy - it's a big company and the people from the company that I've talked with about this can't make any guarantees that down the line they could make an exception for me. They still tell me I should accept the offer because "don't worry about it, this covid thing will take a big while and even after it's done, they won't ask everyone to start going straight away". They also tell me it's a chill place to work on.
Right now I have anxiety even on zoom calls, I keep my camera off anytime I can and when it's facetime I'm very uncomfortable, I start having palpitations and my palms get sweaty and shit - I can still manage to finish them and I can present/do pair programming. However, I can totally see myself having panic attacks in the office because that's exactly how this blew up for me.
So here's the thing: I'm just starting therapy now, so it's possible that I could learn to manage anxiety to the point that, when the time arrives, I can start going to the office - but it's possible I can't (I'm still at the point where I struggle to go get my groceries :|). It's possible that they will, when the time comes, like my work enough that they'll just let me continue remote - but no guarantee.
I'm of 2 minds on this - one part of me thinks its an irresponsible risk and that I'm fortunate to be doing good in a very accomodating position right now, also I do enjoy being remote now; on the other, I've gotten to where I am right now by job hopping, it's a very substantial amount, I'll still have some time to get better, and what if it's actually better for me to force myself into a position where I must be more social?
And about he money, is not really that I need more money, I live way below my means, but I value my time a lot and in this regard, I'd make my years worth twice as much. I'm in my mid 20s and I like to invest, so for me big amounts today translate into early retirement tomorrow.
I'm yet to talk to my therapist about this, so this is me in part writting down my thoughts to clear my mind up a bit before that. Also, I'd love to hear from someone that went through something similar as I think it's a bit of a counterintuitive situation.
Thank you all!
Submitted February 01, 2021 at 11:49AM by throaway203478029374 via reddit https://ift.tt/3j74pzm
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myectjourney · 7 years ago
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ECT Evaluation & current my medication list (2/28/2018)
This post will go over the questions asked during my evaluation and parts of the discussion.
Duration of appointment: 1 hour 30 minutes (hour and a half)
*** TW suicide/self harm mention/questions regarding suicide/self harm. TW for detailed medical procdures and sezuires***
Current Medication List:
Lithium (For depression. 2nd time around with no results. After this evaluation, I quit.)
Clonazepam (For anxiety and panic attacks)
Propranolol  (For anxiety)
Zolpidem (For insomnia)
Evaluation (first appointment):
Doctor introduces herself.
We go over my intake form (which I filled out 2 weeks before my appointment. It included an extensive questionnaire.)
I was upfront about my diagnoses and that I was interested in ECT not TMS because ECT has a history of being more effective despite of there being more side effects. She did listen to this and didn’t bring up TMS at all during the evaluation.
She asked about my prior history with therapy. How long have I been in therapy and what for?
“Tell me about your life. How do you spend your days?”
I talked about how my illnesses have been getting progressively worse and how different drugs I’ve taken have effected this because of bad reactions.
I explained that I have had a lot of breakdowns. I classify them as “psychotic breakdowns” not panic attacks because I felt they were different from when I have panic attacks. She asked me to clarify my word choices, just so she could get a better understanding of what I meant by that.
She asked “How often are these kinds of breakdowns are happening?”, “How long do they last?”, “Explain what your episodes are like.”, “What causes these episodes?”.
Talked about personality disorders. We talked about how I am suicidal and how long I’ve been this way.
Talked about how many times I’ve tried to commit suicide. “How did you try to commit suicide?”
Talked about past history with self harm. “When you cut yourself, were you intending to harm yourself for some relief or to bleed out and die?”, “What stopped you from dying?” I explained that people came to my aid or there were times where I stopped myself because of my own fear of death. Even though I longed for it, I also fear it. “How many times have you stopped yourself versus someone stopping you?”. Some point between asking about suicide and self harm, I was asked “Have you ever been hospitalized?”.
“How often do you have panic attacks?”, “What does a panic attack look like?”
“Have you ever heard voices that weren’t there or seen things that aren’t there?”
“How often do you see your therapist?”, “How long are your therapy sessions?” “In your current situation you are having disregulation episodes which you are calling ‘psychotic breaks’ that are happening sometimes daily, or at least one a week in which you are pulling your hair, screaming, being disassociate and during these episodes are you trying to kill yourself or saying you want to kill yourself?”
To my partner who was in the room with me (my request): “How often does she talk about suicide?”
“How many of your suicidal attempts or gestures are caused by social stressers or fear of rejection?”
“Do you get into conflicts often in your relationships with people?”
“Do you have a bit of a temper?”, “Do you lash out at people you love?”, “How often do you find yourself making suicidal statements to others?”
She asked about a situation that my therapist wrote in her notes regarding a past experience that set me off.
“Have you done additional therapy for your agoraphobia?” I explained that my therapist and I have tried to get me into DBT but my insurance won’t cover it so it was no dice. We talked about how my social anxiety has gotten worse and the agoraphobia has been more of a recent development with the progression of my social anxiety and traumatic experiences. I also talked about how I think I have Selective Mutism which is brought on primarily through PTSD attacks (when I am triggered) or under immense amounts of stress.
“How is your thinking and memory?”
“Have you held a job at any point?”
Talked about my family and abuse I suffered through them and my lack of contact with them.
Asked about my medical diagnosis. I informed her I was diagnosed with Fibromyalgia.
“Have you ever had a head injury, concussion, or seizure of any kind?” Nope.
“Any retinal detachments or metal implants in your face?” Nope.
“Any brain aneurysm, vascular clips in your head or neck, metal in your eyes, or pacemaker?” Nope.
“Any heart problems?” Not that I know of.
Confirmed where I was born and raised and who raised me (all questions answered on the intake form).
“Do you have any siblings?”
“How did you do in school?”, “What led to me not continuing my education?”
“Any religion?”, “Any military service?”, “Any legal problems?”
“How would you describe your mood today?”
We went over the meds I am currently on and my dosages. I told her that I won’t be on Lithium by the time we do the procedure. She said the lithium is less of a problem, I just need to be sure I don’t take it 2 days before we start the procedure. She was mostly concerned about the fact that almost all the meds I’m currently on are considered anti-seizure meds and a lot of them are highly addictive, especially the clonazepam and zolpidem. This is important because basically what ECT does is they induce seizures in the brain. This helps basically rewire your brain.
She informed me that LUCKILY they can reverse the effects of those 2 drugs with an antidote (pretty nifty) so they can get around that but she expressed concern that I might be “a little doped up”. I told her I was on a very low dose.
Talked about family history with mental illness. “Any one in your family commit suicide?” No. At least not that I’m aware of.
This is when we finally talked about diagnosis and treatment.
She said “Your diagnosis is relevant here because certain diagnosies respond better to ECT as compared to others. Based on your history, it seems like you have an expanding list of diagnosies and that can happen in psychiatry because they are checklist based and can be presented differently at different times. I think the over all picture is best captured by a personality disorder based on what you are telling me and that doesn’t mean you cant have ECT by any means but it does mean that there is a little more risk for you in a couple of ways. So people with a history with disassociation and a history of trauma, which very much goes with a personality disorder, have a harder time being put under repeatedly and hopelessness of ECT. It can be kind of re-traumatizing.”
She goes on to explain that there are cognitive side effects for people who have personality disorders (specifically similar to my symptoms), which can include something she called “Soap Opera” Amnesia where a patient will complete forget everything for a few days. It only has happened one in her experience but it was very scary for the person going through it and that patient did end up going to the hospital at some point. This wasn’t caused by the ECT though. Seizures do not cause this. This was basically psychosomatic; something this person developed as a result of the panic of being put under and having to go through that over and over again, hence why she disclosed this to me as someone with a personality disorder specifically issues with disassociation.  
She also explain that statistically, the effectiveness of ECT is a little lower for people with personality disorders versus those with just depression. It’s around 55% likely to be effective for people with personality disorders and around 87% likely to be effective for people who just have depression.
She said about a 3rd of people with just major depressive disorder that get ECT feel almost completely cured by it but with people with personality disorders, they might feel less suicidal and may be able to function better in day to day life but its way less likely to feel “cured” to that intensity.
We also talked about how she thinks I fit the description for BPD very much and that it looks different for different people. My favorite thing she said is that it doesn’t always look like “Girl Interrupted”. Luckily I already knew that and agreed with her on this matter. She talked about the stigma around it. Honestly, she was very understanding and knowledgeable (I mean, of course) but it was really nice to talk to someone who wasn’t bias about personality disorders.
Then we talked about the upsides and down sides of ECT in the most specific way we could.
Downsides being cognitive side effects, even if they are just doing the right side of my brain with pulses being as small as you can get and the dose being as low as possible, you can have cognitive slowing, feeling a little more spacey, attention is not “up to snuff”, and also short term memory problems. The most recent memories put in your brain are usually the ones that are effected first.
This can include the past couple week or months before the procedure.
During the course of ECT, 7-15 sometime 18 treatments, when youre having it 3-4 times a week, you might have trouble forming new memories.  It’s not that you won’t form any, just a little fuzzy.
All of things add up to a DRIVING RESTRICTION. They will not let you drive during the course of treatment. She said it doesn’t matter how you GET to the appointment but afterwards they will not allow you to take a cab/taxi, uber, lyft or by bus and you cannot drive yourself. You absolutely NEED SOMEONE TRUSTED/CLOSE TO YOU TO DRIVE YOU HOME.
ALSO, if you have a history of any heart problems, you are at risk of sudden death because when they induce the seizures, your blood pressure and heart rates goes up. For young healthy people, there is almost no risk of this happening.
There are the normal/common risk of anesthesia (Like waking up). They usually give you Brevital (which puts you to sleep) and Succinylcholine (to relax your muscles before the procedure). The muscle relaxant will stop your breathing but she said it’s nothing to worry about since they will be pumping air into your lungs manually via bag mask and will be closely monitoring you which luckily means no invasive breathing tube.Then they deliver the stimulus, which induces the seizure and then you slowly wake up after that. If the timing is wrong or the dosing is wrong, there is a SMALL but serious risk that you can wake up but still feel paralyzed. They monitor your heart rate and they try to make sure you are completely out beforehand but it’s still a risk.
The worst symptoms after the procedure is headaches and nausea, which they will usually give you medication for and usually is the worst after the first treatment.
You will have an IV in your hand, before you go in, the nurse will make sure you have not eaten or drank anything in 8 hours.
They will talk to you for a few minutes to make sure you are okay and know whats going on. During this time they will put the IV in and inform you if there is any changes they need to make with anesthesia, then they administer the anesthesia. They will then induce the seizure (they usually start with a right unilateral which means they just do the right side of your brain and can change it to a bilateral procedure which is both sides of the brain later in treatment if needed) and the way they tell if you have seizured is by:
1.) putting EEG leads on your head so they can see your brain waves and
2.) They use a blood pressure cuff as a tourniquet around your ankle to stop the muscle relaxant from going into your foot so they can see that foot have a seizure.
Afterwards, they roll you out to the recovery room where you come down from the anesthesia which takes about 20 minutes.
The medical work-up and requirements before you schedule the procedure is a signed document from your PCP (Primary Care Physician) which they fax over, bloodwork, pregnancy test, and an EKG test (they will need a physical copy of the EKG tracings).
-END OF APPOINTMENT-
I hope this is useful info for someone out there!
If anyone has any questions, feel free to ask.
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meanwhileinoz · 7 years ago
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10+ Misconceptions About Mental Illness Need To Be Cleared Up Right Now
Mental illness is a myriad of conditions that appear in different ways. Moreover, because of the constant misinterpretation of mental illness on social media. Mental illness is often misunderstood.
Therefore, to inspire a more positive discussion on mental illness, here are a few anecdotes to clarify the confusion:
Depression comes with a mask.
I have depression. People don’t believe me because I appear outgoing and gregarious in social situations, but it’s just a large coping mechanism and something I need to do in many cases for client meetings and gatherings and such.
It’s exhausting. I’m drained and many times feel horrible afterward. I wish people knew that just because you appear happy or content on the outside, you can still be the opposite on the inside. Many people with depression go to great lengths to disguise or mask it, which makes it all the more difficult for others to see that there’s something wrong.
– ldn6
The intricacies of Mental health.
Mental Health is a spectrum. It’s extremely unlikely that any one person is 100% Mentally Healthy, and it’s unlikely that they’re the opposite. The  U.S. Department of Health and Human Services estimates only about 17% of adults are in a state of “optimal” mental health.
Just because you may have an issue though, doesn’t mean that you’re spiraling and unhealthy. Much like a physical health issue, a single episode isn’t the end of the world. – (Source)
Dispelling the ADHD myth.
ADHD; it DOES exist, and it’s not just about looking at squirrels outside the window.
And we’re not just seeking stimulants. Many of us hate taking medication because it makes us into zombies that can barely function and choose to deal with the symptoms of the condition rather than take Adderall or any other pills. – willflungpoo & Ketrel
Bipolar disorder needs to be understood better.
Usually when you say ‘I’m bipolar’, you get odd responses from either a) the people that think you are this rabid psycho bouncing off the walls one second and is dangerously suicidal literally the next second or b) the people who think “bipolar” is a normal, quirky personality trait. You know the kind: “you’re bipolar? me too! I’m so damn emotional all the time.”
I simply try to explain it to people as best as I can with a metaphor I came up with once: It’s not a balanced, steady rollercoaster of emotions, that most people experience and enjoy. It’s also not a rollercoaster that does 60 loops in a row, derails and explodes onto the ground below. it’s more of a rollercoaster that goes too high up with a bit too much energy and then gives everybody really bad whiplash when they drop to the bottom of the ride over and over until it’s too much.
The metaphor is kinda dumb at not completely accurate, but it just helps people understand better.
– zapsquad
Mental health and crime do not correlate.
Some people have an inherit fear of others who suffer from a Mental Illness. The media over-sensationalizes the effects of Mental Illness to a point where it seems that crimes are only committed by people who suffer from it.
This is completely untrue, as the American Psychological Association found that only 7.5% of crimes are directly related to Mental Illness.
– (Source)
Depression is not an illusion.
Depression.
“But you don’t have anything to be depressed about, sweetie.”
That’s like saying, ‘But you can’t have asthma! This room is full of air!’
– kernunnos77 & eeyore102
The importance of decreasing stigma.
Mental Health affects everyone. Research estimates that 1 in 5 people experience mental illness in their lives. So even if you aren’t suffering from it, someone you know might be suffering.
This is why it’s so important to decrease a stigma about Mental Health and open up a conversation about it. Everyone will experience the effects of it and the more we are able to understand and communicate about it, the more positive our relationships can be.
– (Source)
Psychologists are really trained professionals.
On the heels of that, it’s important to talk to a medical professional about your mental health instead of just your close family and friends.
Treating Mental Health takes more than just ‘Talking and Listening’ and the techniques that Psychologists use are developed through years of education and training to positively impact their patients.
– (Source)
I think you deserve that rest.
I have severe anxiety. So much so it’s developed into agoraphobia. I stay in my apartment most days, and only really go outside in public accompanied by my safe person. The common misconception is that I’m lazy. I don’t have a life. Because I stay inside all day, most days, and I’m content not leaving. But I do a lot. I draw, I’m learning how to sew, and I try to get out a little more every day but it’s baby steps.
People also think I’m lazy because I sleep a lot. I have regular panic attacks. At least 3 times a day. It’s rather exhausting. My brain feels like it needs rest after having one.
– MetalMaiden420
Misconceptions about Anorexia.
I have anorexia. I think the most common misconception is that it is about being thin. I have honestly never met a person who developed an eating disorder because they wanted to look like some photoshopped model. For us, it’s about perfection and control, it just so happens that thinness is a trait that our society admires, which is why we strive to achieve it. At a certain point, you are intellectually aware that you are not attractive and dying, but this irrational little part of your brain won’t let you eat because you’re still too big. There is no such thing as “small enough”, once the disease takes hold no amount of weight loss can satisfy.
– purpleelephant77
Seeking help isn’t a sign of weakness.
For some reason, even with this debilitating stigma that people dealing with Mental Illness face, it’s still seen as weak to look that in the face and say: “I’m going to go to a therapist anyways”. That doesn’t make sense at all.
But for people with Mental Health issues, opening up emotionally is a very trying experience. That’s exactly what happens in therapy, you open up your emotions and face your mind at its worst.
How could that be seen as weak? – (Source)
Yeah, just stop thinking like that.
OCD isn’t about being organized and anal. It can be overwhelming and paralyzing at it’s worst and telling us to “just not have those thoughts” isn’t helpful.
– mycatisawh***
Another great analogy for anxiety.
Anxiety is that unwelcome, creepy stranger at a party that won’t leave you alone.
One thing people don’t get is how debilitating mental illness can be. With anxiety, it isn’t simply just worrying too much about a deadline…that’s stress. Stress is good. Anxiety is bad. Anxiety starts with automatic thoughts that ruminate into something bigger. It’s worrying about things out of your control. I’ve been told more times than I can count to “just quit worrying so much.” I don’t think people realize how much effort I have to put in to getting myself into healthy thought patterns. It is a daily battle to fight off thoughts like “everyone hates me” and “you’ll never amount to anything”, and not let them ruminate to the point where I cancel my day and crawl back into bed. – frazzled_wumbologist
When people think your illness doesn’t even exist.
I have Dissociative Identity Disorder.
Easiest way to explain it is that I’m so good at compartmentalizing, the compartments can’t all access each other (work-me can’t access school-me can’t access home-me). And since people are kind of the sum of their experiences, my different ‘mes’ seem different from one another.
Did you know DID affects from 1-5% of the population? That’s the same as depression, schizophrenia, and a host of better know physical illnesses. Did you know that doctors trained in trauma only find the CATALYST for DID to be controversial? In other words, they know it exists, they just don’t know why only some child abuse survivors end up with it. Most people think the existence of DID is controversial when it really isn’t anymore.
And the really bad part is, abuse is always denied, always minimized. To come out from that scarred, with a mental disorder that was, in essence, thrust upon you by others when you were too young to resist, and to then be denied or minimized….there is a reason only my spouse and my therapist know I have this disorder.
– ThrowawayDIDhardenuf
Maybe people are actually sick?
People who really are suffering from a Mental Illness aren’t faking it for the medication. I can’t understand why this is such a permeating thought. Mental Illness is such a debilitating condition and the stigma is so overbearing that it would be completely undesirable to fake it.
These are real medical conditions that are treated by real medicine and real doctors. Ignoring a broken foot and continuing to walk on it won’t let it heal
– (Source)
Misconceptions about Borderline Personality Disorder.
Borderline personality disorder does not mean I am an axe-wielding homicidal bunny boiling stalker. Never have been.
Therapy helped massively with my emotion regulation and crisis management skills. Also suffer from depression, so life is a constant juggling act and some days are better than others. I’ve been mean, manipulative and suicidal and I self-harmed. The guilt of the way I acted is what usually drives the depression. Many people make the assumption that all borderliners are evil, usually because of bad experiences.
There are bad people with BPD. But there are also good people who want to change their lives for the better.
– Welshgirlie2
Clearing up more misconceptions about OCD.
I have autism & OCD and as soon as people find out, they start making Sheldon Cooper jokes and asking if my pencils not being aligned perfectly on my desk makes me freak out. OCD does not universally equal being a neat-freak, and autism does not universally equal being a socially stunted outcast.
My desk is a disaster and I can function fine in most social settings, but I can’t drink out of a cup without rinsing it out first(even if it just came out of the dishwasher), I pick my bottom lip till it bleeds, I can’t look people in the eye, I add up number sequences(like totals on receipts) till I’m left with a single digit number and if the number isn’t “good” I get uneasy, and I have horrifying intrusive thoughts that replay in my head for sometimes weeks at a time.
The autism isn’t so bad, but the OCD is really bad. It sucks and I wish I didn’t have it.
– Lydious
No one is immune.
Children can suffer from Mental Health problems too. It’s also not just a product of a bad childhood experience or a bad parent. These things just happen to everyday people.
In the UK, 1 in 5 children have been diagnosed with a Mental Health problem, and 1 in 20 teenagers suffer from depression specifically.
– (Source)
A personal account of the stigma people face.
High Functioning schizophrenic. Being close to 40, I’ve lived with the stigma of not being able to be trusted, that it’s just an overactive imagination & that I have more than one person living inside of me since I was a teenager. But mostly it’s the overactive imagination one that really bothers me.
– iwsnvrhr
Stop saying this please.
Having suffered from both Anxiety and Depression, many times I’ve been told to just “snap out of it”, which obviously isn’t possible. I’m not sure people always realize how debilitating these illnesses can be for people.
– Anonymous
Maybe don’t judge people by their medical history?
People with Mental Health concerns can absolutely hold a job. Like we mentioned before, these people aren’t violent or constantly having manic episodes.
In fact, studies have shown that employees with Mental Health issues are just as punctual, motivated, and work at a level on par with or greater than other employees.
Misconceptions about Tourettes.
It really drives me nuts when I say I have Tourettes to someone and they immediately let out a string of swear words.
Yeah no. If you told me you had alcoholism, my immediate reaction wouldn’t be swaying back and forth and slurring my words. Thanks for belittling my issues.
I wish there was more awareness about Tourette’s outside of the Hollywood version of it. It sucks living with constantly twitching, but it sucks telling someone you have it and having them think you have a hilarious malady and making a joke about it. I’m easy going, but for some reason, that really gets under my skin.
– my_Favorite_post
Although, there are some terrible people out there.
PTSD is something that stole certain joys away from me (shooting guns, fireworks, etc.) And it really sucks. To see people fake it and use it to get notoriety and discounts makes me sick to my stomach. I can only trust therapists or doctors with my issues. Not complete strangers.
– nessn12
We’ve been talking a lot about the debilitating effects of Mental Illness, but the truth is it’s not a life sentence. People can recover completely from their Mental Illness with the right help and medication.
Some issues aren’t curable, but they are treatable. Again, with proper medication, it’s entirely possible to live a happy and positive life.
– (Source)
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