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Looking forward to going away on holiday on Friday!

I’m going to Devon with the church just for three days on Friday (my support worker will be coming with me just in case I have a seizure- I have live in care you see). It’s been a very difficult few years with brain damage and brain surgery and a skin graft and loosing loved ones so going away is just what the doctor ordered! So I bought a few new dresses! Looking forward to wearing them too! So should be a good time!
#Anxiety
#Depression
#Hallucinations
#Epilepsy

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Bipolar & Psychosis: The Voices in My Head #BipolarDisorder #Psychosis #Hallucinations #SchizoaffectiveDisorder

Good morning, I hope you’re doing well today and you have a wonderful week ahead.

I am diagnosed with Bipolar Disorder and Psychosis. Here is an account of an episode where I was hearing voices. I initially posted it on my blog so I’ve edited it to make sure it is compressible to read.

Looking back a few months ago now, I had two episodes were I was hearing the voices in my head once again. Nothing sinister or anything like that, nor a command to do anything detrimental. Literally the situation was that I walked up to the pub about 1pm each day to me a friend. I had my MP3 player (I know they went out of fashion years ago), and I just use the right earphone as I’m deaf in my left ear. So, I was beginning to hear chatter. Nothing clearly but it was like I was in a pub or restaurant or something like that and I could hear the conversations of the people around me. It doesn’t worry me, or scare me as I’ve experienced this before, I have had these voices from years and years ago and to me at least, I know they aren’t dangerous to me or sinister. So I even took my hearing aid out of my left ear to see if they were coming through that, but no, I was still hearing them. I got to the pub and then turned off MP3 player and then chatting with my friend and then it all stopped. I walked home afterwards though and then it started again.

A few days later I had to collect my prescription from Mountcroft (Mental Health Resource Centre) for extra Quetiapine. So I met a mate near my house and we walked up to the promenade by the sea front and then to the next town where the Resource Centre is, and I collected the script. No voices at all.

So at the time I was then on 750mg per day of Quetiapine! 250mg when I get up and 500mg before bed! (Update: The Quetiapine didn’t work and it was discontinued in favour of Olanzapine)

I’ve noticed that I think it is more prevalent when I was silent in my mind and the thoughts weren’t racing when it happens. Basically when I’m Bipolar Manic I have too much going on to hear the voices.
It’s crazy isn’t it that I have now experienced a new scenario. I would try to see if it would happen if I had both earphones in my ears, but as I said I cut the left earphone off as it was redundant. After spending a small fortune on earphones over the years I’m not spending any more money on another set! 🤣

I wish I could have a way to record my voices and then be able to put them together in a download or something like that so people can have a listen to my voices and then they can get a better understanding of what it is like to have mental illness.

#MightyTogether #MentalHealth

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The closed door #Incest #MajorDepressiveDisorder #GeneralizedAnxietyDisorder #PTSD / #dissociations #psyctoticfeatures

We have a ranch house with 2 bedrooms on the main floor. Whenever I have virtual therapy I tend to look at one of the bedrooms and I see a flashback of my abuser in the bedroom. It’s part of my psychotic features. I was crying in therapy cause he saw me #Hallucinations . I decided to close the bedroom door now I’m having #Flashbacks of him behind the door where I can see his shoes. This happened when my mom took me in her bedroom and asked if he was doing anything to me. I know he isn’t there but 8 yr old me says he is. The abuse never took place in this house. Welcome to #PTSD

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Well, another night with absolutely no sleep! 3rd night now and feeling exhausted to my core......

This is now my third night without sleep and my hallucinations are worsening every night - making it too scary to close my eyes.

I see him when I'm awake and when I'm asleep and am not sure how much more of this I can take!

Was due to start therapy sessions but Landlord has evicted me (as he wants to sell the property), so therapy has been withdrawn until I'm more settled.

Life just feels vicious at the moment!

#Insomnia #PTSD #Hallucinations #Depression #Anxiety #MentalHealth

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Bipolar 1 with hallucinations?

#BipolarDisorder #biploar1 #SchizoaffectiveDisorder #Hallucinations #CheckInWithMe
I am wondering if anyone else on the Mighty experiences auditory or visual hallucinations? Please tell me about your experience so I know I'm not alone. I hear music and have been seeing shadows that I know aren't really there. But it feels so real when it's happening. Thank you so much. 💕

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Confusion all the time.

My schizophrenia is not really scary like paraniod schizophrenia. Its just i see the world differently, too far away from reaity.

i don't have visual hallucinations only auditory. But I have visual hallucinations when I was first diagnosed.

It feels like my delusions mimics reality.

Like when it was still 1st December that I heard about pets at risk of dying during fireworks and intense noise during welcoming a new year. I felt worried and I believed that my dogs will definitely die. I saw it in my mind they are dropping dead.

Voices keep telling me to tell the people around you not do noisy things and force the if I have to. They tell me hurtful things like you are a worthless owner, that it will always be my fault if my dogs die.

But I have this feeling that this is something wrong.

You may say that I have the advantage because I am a bit aware during delusions.

But it is the opposite.

I was so confused. Is this real or not?

It is the worst battle ever.

It's so exhausting. I think this is not a delusion but suddenly I think it is a delusion.

My mind then started to be fragmented and during that anomaly my brain suddenly put another "story plot" that causes another rabbit holes of delusions then produce another confusion.

And then when I shared it with my mother suddenly I snapped back to reality.

I realized that my dogs will gonna be okay. I look back and saw how exaggerated that delusion is about my dogs death. I was too far away from reality.......

Then back to the rabbit hole of delusions and end up confused again.

#Schizophrenia #MentalIllness #Delusions #distortedreality #Hallucinations #OCD

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Update

Update: It hurts my heart and soul so much that I am not worth the help, trouble or time to my 'doctors'.

My Rheumatologist told me he couldn't help me. He suggested i find a new doctor. This after I spent a year trying to hold out like my parents wanted in hope that he was a good doctor in the long run-but my base instinct was correct in that he would only bring me harm.

He put me on this medicine that he didn't know would help but it did for two ish weeks and then it stopped working. I told him I could see the bad effects it brought, more pain like holes drilled all in me, significant hair loss-I now have half of the hair I use to( a whole new traumatic experience that I had never wanted to go through, and yes I am on vitamins to lessen those effects. I imagine I would be hairless without them), swelling even more than I already am, painfully in my hands and face. I have lost a Lot of my muscle strength and not just because I am bed-bound, even more exhausted beyond belief. If I walk around my room once I am exhausted and starting to blackout, a few other problems and the worst side effect of them all: SEVERE SCARY Hallucination!!

Needless to say I have not been helped and only added to by my MANY doctor visits here. The real concern is that they think I am just a bad patient when I just don't have doctors who want to stick it out and help me and that is the worst thing in the whole world that I can't really explain. It is like a vital part of life that everyone else gets lovely access and help with, you start off with the worst ones that add trouble and debt with their crazy costs and if they don't help you, they still get to keep your money while you are left with the severe hurt and pain.

I told this doctor a month and 2wks ago that I wanted OFF this medicine and I needed an appointment to get that but he refused and instead told me to increase the medicine 35%!

I decided that forget him I was going to try to go off it on my own. The only one who has gotten me off medicine safely with no side effects was me. I know best how to do it after all these years, how nuts is that to realize??
So I tried going off it and the pain was UNBELIEVABLE! My hands were without any use whatsoever. I couldn't move and my body wouldn't work at all.

My appointment with the Rheumatologist on Tuesday said he couldn't help anymore when the fact of the matter was a fellow doctor asked about my full body psoriasis and despite him telling me last time he didn't care to look at my full body rashes at their worst, he now cared when we finally had gotten things slightly calmed. He scoffed at our explanations and thanks to my severe horrible memory issues that no doctor will help me with, I had left my phone with pictures of my rashes at its worst, at home! So we couldn't prove the troubles not that he was in the mood to listen of course. *sigh* It hurts my heart and soul so much that I am not worth the help. They don't see me as worth the trouble and time.

The reality was that this doctor just didn't care enough to work hard to help me. And I wasted a whole year on him to prove to my parents that he was a bad doctor like I warned them after a first meeting with him. Now I am on this medication that he put me on. That is a weekly medicine so it will take me at LEAST a month and a half to safely go off this medicine and by then who knows what I will have had to go through. I am so scared and in pain too of course.

When he told me he wasn't going to be my doctor anymore he told me I could just go off this medicine cold turkey that caused me to lose half my hair, break out in full body painful itchy red rashes for the past few months, swelling body, SEVERE awful hallucinations 24/7 extra pain, blurry vision, so much more exhaustion that I can barely change clothes with help every three days and that is it. He has never listened to my side effects before and I of course knew he was wrong as he hasn't understood my meds even up til now(The pharmacist I talked to verified I was right in tapering off so score for me! ;) ), 🤦‍♀️

The beginning of going off these horrific meds starts today. I am SO SO SO not ready for more scary hallucinations. I am sure my parents aren't ready either.

oh my gosh I am just so tired and angry at all doctors here. none of them are helping me and just causing more issues I have to deal with on my own. I comfort myself that I called him out on his nonsense the last 3 appointments. lol that was so very satisfying. I may look young but I have been around the medical block all my life. I like to think I would make a semi decent doctor too! 😁😁😉 Heaven knows I would NEVER abandon my patients or make them take a drug that gave them horrible side effects. Effects that made them seek out a therapist and made others think they were crazy! I would actually listen to them and take note of each change they mentioned as I would recognize that they know their body better than I do.

Oh my heart. Dear friends I am so very lost and hurt and hurting. It has been such a horrific 6 months. But onward we must go because the more awful things get, the better they can become. Please let the good finally find me soon. I am SOOO Beyond ready!!!

#AmplifiedMusculoskeletalPainSyndrome #Arthritis #Asthma #Anxiety #ChronicFatigueSyndrome #CheckInWithMe #ChronicPain #bedbound #ComplexRegionalPainSyndrome #CheerMeOn #ChronicIllness #Depression #Disability #DistractMe #EhlersDanlosSyndrome #Endometriosis #Fibromyalgia #GastroesophagealRefluxDisease #Grief #HypothyroidismUnderactiveThyroidDisease #Insomnia #Lupus #Lymphedema #PosturalOrthostaticTachycardiaSyndrome #PTSD #Psoriasis #MightyTogether #MentalHealth #Migraine #MemoryLoss #Hallucinations #HairLoss

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Advice on Hallucinations to Sufferers

Part 1 of 2 One can experience hallucinations for many reasons. From PTSD, to #Schizophrenia, to taking hallucinogens, or even just randomly throughout the day, one can hear unwanted and unreal voices and sounds, have tastes of food not eaten, smell odd odors, feel others touching them when no one is there, see things, or even feel presences around them.

For the first thing, it helps to note down characteristics and details of a hallucination, even naming them under what class of hallucination they are. Give them human names or give them silly names, and write down how they bother you, what their characteristics are, and how you have found relief against them.

For #Hallucinations, in my case most common is hearing detailed voices, one thing I’ve found that helps me is finding out what each voice wants, because they’re not all the same. I found the voice of “John” wants to command me, to quote, “ruin my life.” He’s very manipulative, but I’ve got a good handle on him. To use John as an example, he’s very narcissistic and likes to be talked about. So to note his details, he’s commanding and narcissistic, and to make him talk less I don’t give him what he wants. I disobey his commands, in whatever roundabout way he tries to command me.

For those very audible hallucinations, like someone calling your name, they want to be noticed. They want you to specifically go somewhere and look for them. They’re kind of like willowisps. Use reason to differentiate if they’re real, like the voice of that person can’t be there because I know they’re somewhere else, and if you have to, just ignore them. You don’t have to answer every beck and call. The best way to get rid of auditory hallucinations is to hear actual sound, like talking to someone or listening to music.

Tactile, or bodily, hallucinations are very unpleasant to me. I hate that someone is touching me that I can’t push away. This hallucination could be suggestive, like, BLINK. You might have noticed yourself blinking, or are doing so now. This is slightly like a tactile hallucination, like other hallucinations or even beliefs making you think you are being touched, then you notice a feeling in your body of being touched. Other times this is completely hallucination, like someone tapping your shoulder. The best relief to this is to move your body, and completely take over all feelings in your body by being mindful of how your body is situated. Notice every little thing about it, to your very breathing, and you will regain control.

Olfactory and gustatory hallucinations, smell and taste hallucinations, can be lumped up together. Ever eat a spoonful of salt thinking it’s sugar? The salt will taste sweet, for only a second. This in fact is a hallucination of taste. I have had these sorts of hallucinations even when I was not eating or drinking, taste of something sweet on my tongue, or something rancid in the air. What I do for this is drink water, something neutral. Taste the water, because it doesn’t have much of a taste. Smell the air. Breathe in and out. The hallucinations of these types will go away eventually if overpowered by real sensory stimuli.

Visual hallucinations, or hallucinations of sight, are the worst for me, my least favorite of all. Seeing something so vivid, sometimes almost imagined, other times flashes, or in the dark and just… there, can be terrifying. It instantly roots most of the other hallucinations to the person, creature, or object seen. I usually never have visual hallucinations thankfully, but every time I have it has scared the shit out of me. Monsters in the dark telling me, “Thanks for letting me in your room.” or hallucinated dicks floating around me, or even strange sexual patterns moving and changing around me, can all be absolute hell. The best way to get out of this hallucination is be in the light. You will notice you hallucinate, like dream, more in the dark, so turn on a light and calm down if this happens to you.

Feeling presences around you can be very scary, and I’m not sure what to categorize this hallucination as. Sometimes the other hallucinations will be coming from a specific spot, and that spot will move of its own free will. Sometimes it just feels like someone is there, right behind you, or in the closet. This is a hallucination, because when you check you will definitely notice nothing there. This sort of hallucination, as most hallucinations do, plays on fear and paranoia. Distract yourself from the monsters under your bed, and grow accustomed to what is normal to be there. If you need to, leave the presence somewhere and just go outside for a second. Most of the time it will not have

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Advice on Hallucinations to Sufferers

Part 2 of 2 followed you.

I have certain pleasant hallucinations too. My fictional characters jumping into my body and “being” me, and it feels like they’re very close to me and around me, which can be enjoyable. When certain other characters, like malicious villains, do this it is very annoying and intrusive. Think of it like this, imagine what are you doing right now, then someone else is doing the same thing and looking out of your eyes. I found it helps to visualize myself again and also split the characters up. Like good and bad traited qualities of them and then discarding the unwanted. I prefer having no hallucinations, but just note that some hallucinations can be pleasant.

I am a sufferer of #Schizophrenia and have hallucinated in many, many ways. My medication keeps a handle on most #Hallucinations, and I love that I can be one with reality again. Please ask if you have any questions at all about hallucinations, my illness, or even just my books or myself.