📄Bluelight Archive Navigation 30/303

Mental Health Coming off Invega/Xeplion (paliperidone) injections v 8.0

Status
Not open for further replies.
Hi everyone I may have found some hope. I've seen every neurologist in the book and they have constantly said they can't find anything. I was on a lyme disease forum and by freak chance somebody said they can help me. I said it's an impossibility. There is no way you can fix the damage that is going on. He said for me to send my mri from march which was two months after the injection. He was the only one pinpoint where the damage after seeing the top neurologists in my country,who keeps saying they found nothing. He looked at my pineal, pituitary and hypothalamus glands. He noticed that they were all flattened out or had been somewhat compromised. He's requesting me to get a second mri this week so he can compare the two. From there He is going to rebuild my dopamine and neurons with angiogenesis and neurogenesis techniques. I told him that i've spent almost four hundred thousand dollars in insurance and personal money to get better. He actually looked at my scans for free and gave me a free consultation, which I was very impressed with. I'm hoping and praying that he will help me.
 
why you say weed bad for pssd?
It desensitizes serotonin receptors and it makes my junk cold again, but only for a day. Gonna continue to lay off of it until I really feel better. I might smoke again at my sister's birthday party in a few days, but in moderation. It also makes my disassociation worse.

I think I'm getting sensation back! I don't feel horrible numbness when I walk. I can describe this as "greatly reduced sensation" rather than "genital anesthesia". I'm still having intense dreams and occasional nausea, so I'm still in the withdrawl period and there's still a chance this is withdrawls.

I had a nightmare that I had to go back to the mental hospital because I was obsessing over my PSSD so much. I was crying and trying to tell people antipsychotics and SSRIs will make my PSSD worse/permanent and a whole room of people laughed at me. :/ I woke up so confused and upset, I completely believed the dream as it was happening. It flowed more logically than my dreams usually do.
 
Last edited:
Have you been taking other antipsychotics like him after invega
she had 17 shots brodie

is it a good sign to have normal semen consistency and color

mental abilities are coming back a little just hard to notice bc i still feel dumb

sorry mods i was cussing out hospital staff i hate mental hospitals and hate the people who work there everyone here does we have the right to be angry i will try not to cuss them out more but its hard cause i hate them please dont ban me this place is the only thing that gives me hope
 
sorry mods i was cussing out hospital staff i hate mental hospitals and hate the people who work there everyone here does we have the right to be angry i will try not to cuss them out more but its hard cause i hate them please dont ban me this place is the only thing that gives me hope
No problem. It's all good because you recognize why they were deleted and that's good. No bans for cussing or ranting. Just deletions.

Appreciate that you will not go there though.

Have a good weekend. Or as good as you can anyway.
 
which has almost happened to me once when i was 14 right before i started smoking weed this girl at a mental hospital who was really my type who i had a huge crush on and couldnt leave her alone her boyfriend who was older than her and a gang member tried to cut my dick off when we were all out of the hospital luckily he couldnt reach me and she left him long time ago. sheesh god mf damn my fucked up life has had so many catastrophies
 
Omg I’m getting a dopamine hit from ciggies yay
i was getting one from vaping kind of not from weed or anything else i tried weed once it just amplified the invega poison feeling i vape every few days to every day now and it increased my tolerance so i feel it like 20-50 percent at first i could feel like 50 percent <please don't suggest illicit drugs use to other members - SMod>

if anyone needs positive uplifting posts just go to my profile and see what i liked
 
Last edited by a moderator:
Incoming mega reply post!!!!!! 😆😋

I really hope more recovered/recovering people start posting here again because this place is becoming a little scary with just newly injected people freaking out. Although that does go to show that most people probably do recover or start recovering after the first year, they just don’t post about it
The Invega thread always ebbs and flows with phases of good news, then a period of bad news, then it will become good and positive and uplifting again, and then bad and negative and scary again, and so on and so forth. It's just the nature of the thread. Stick with us and ride it out, if this thread is overall helpful for you ❤

I'm almost 10 months in and feel no relief whatsoever ever.I dread getting up in the morning and the most devastating is the erectile dysfunction.The one thing that is really murdering me inside is looking at my 4 children, knowing I have no choice other than to go.I am suicidal 24/7.I read somewhere that people have lived like this for 10 years.If someone could tell me how that is done I will give my life to them and work for free. I do have someone from an alternative medicine company that is willing to work with me and very familiar with these symptoms.Its my only choice at this point.
Welcome to the thread, and I am so sorry you struggling so very badly. Others have already said a lot, but I want/NEED to say that you are a parent. You have 4 kids. Suicide is not an option. It's just not. You will completely destroy your children's lives forever if you kill yourself. So get that thought out of your head please ❤
I think my prostate is gone.They say your prolactin level render you castrated.I can get an erection While i'm sleeping but I cannot ejaculate. Also too the worst part is the hand tremors. I don't know what to do. My sleeping is horrendous. I'm constantly suicidal
It's actually not feasible for your prostate to disappear. Who is "they" when you say "they say"?? You can still get an erection, right?? Even though it's when you're sleeping, it's still an erection, which means your genitals are still working. They will recover with time, please have faith in that and continue to read other people's recovery stories ❤

Wow tbh your case seems the most rare out of most that I’ve seen .
I know that you mean well, but comments like this are not helpful. They just make the person feel even more weird, isolated, and less confident about recovering. Try to be a little more tactful, yeah?

I am 18 months off invega and doing much better I was hopeless for 12 months and started gradually improving since then it takes a long time I thought the anhedonia would never go away especially since it hadn’t let up once I hit a year I kept going and it went away at 13-14 months at that same time my libido returned

@ap_sucks hasn’t recovered he’s banned for some reason
He was banned for very good reasons. We don't need to discuss it publicly. And we do not take banning people lightly here on Bluelight. We have a strict banning protocol that we adhere to, that applies to every single member of the forum, which can be found here:
https://bluelight.org/xf/threads/🚫the-bluelight-warning-system🚫.611710/
And the Bluelight User Agreement, I.e. the Bluelight rules can be found here:
https://bluelight.org/xf/pages/BLUA/

I see so many success stories with larger dosages than I got. I'm in a really bad spot and I don't know what to do. It's been ten months and i'm stagnant. I don't think I can last for 2 more months.
Please stick with us and keep posting here for support ❤

My tremors have started to fade about 130 days out so I’m guessing this is the dopamine pathways starting to heal. Felt some joy when hitting a nice tennis shot but still low energy and feeling a bit disconnected. I’m hopefully things will continue to gradually improve
That sounds like great progress! Thanks for sharing that with us! I hope things continue to get better and better for you ❤

Neuropathways can’t heal themselves, once they’re destroyed they’re destroyed! Where do you people come up with this pychobable bullshit! dopamine receptors rekindled all this crap. Once you have brain damage the damage is done! You might be able to improve and get better but that damage doesn’t go away! Ever look at a drug addict that recovers, you can tell he’s done hard drugs before. Ever look at someone who’s been on antipsychotics they look like they’ve been on some shit…they aren’t normal looking anymore. Ban me if you want to. But I’m not here to give false hope! Damage is damage. Ppl say they “recover” I’m sure they don’t feel adrenaline from songs anymore and so on and so forth. Those things are damaged. ppl here sound dumb. Oh I felt good for a minute taking a walk. Like that’s good! Ppl actually feel good all the time in real life not medically fucked! They spring out of bed and tackle the day! “Oh I felt good for a moment, I can work so that’s good I shower and shave now” wow big victory! Like these things take ten mins out of a normal persons day!
I'm not sure what you're currently going through in your personal life right now but you were not this aggressive before. Has anything changed for you that might have triggered some anger responses in you?
To address your comment about someone taking hard drugs and always looking like they've been an addict: I was a severe, heavy alcoholic and drug addict for over 15 years. I've been clean and sober for nearly 2 years now and looking at me, you would never know my past 🙂 I even had a small patch of cirrhosis on my liver detected in January 2021, now it can't be detected on my liver ultrasounds. And I thought cirrhosis never went away 🤷‍♀️ People can and do heal from all sorts of damage, especially in the brain. Neuroplasticity is real, and very pertinent to the healing and recovery of people's brains after taking antipsychotics such as Invega. Please don't be so discouraging to people who are here for hope, support and advice.

people fucking fully recover and say music comes back 100 percent with adrenaline idk wtf your talking about yea you should be fucking banned for spreading hopelessness buddy😀
People don't get banned for speaking their mind here on Bluelight. We have a very strict protocol that we follow for banning people, as I posted above.

I'm sorry I have to agree with him. This drug is pure poison. I've yet to see somebody recover. You should see the message board i'm on. Everybody is suicidal. In fact I think two members killed themselves with the last week or so. This drug was designed to make people vegetables. I'm almost ten months in and I haven't seen any improvement. There is one guy that is hopefully gonna help me. I cry every single day knowing I am not the person I used to be. I used to smile, laugh, high sexual, motivated and loved life. I am completely the opposite of that now. I hope you're are right, because people wouldn't be coming on this message board if they were feeling good. It's a struggle for me to survive every day. That's criminal. Not trying to be a jerk, just have to kind of agree with the guy above.
I have moderated THIS Invega thread for many many years and I have seen countless full recovery stories. Sure, I have seem some people who have not recovered as well, I'm not gonna lie. BUT the majority that I have seen post here have eventually recovered. I suggest that you now avoid whatever other message board you're on (Reddit, perhaps? Or a psych forum?), as it is clearly just instilling you with unnecessary fear and hopelessness. That is not going to help you recover, my friend ❤

stop calling people drug addicts when you are one yourself!
Please refrain from posting comments such as this. She is not a drug addict, there is nothing that she has said to make you assume that. Please do not whimsically throw around antagonistic accusations like that in this forum. Thank you.

Thank you SO MUCH for posting this! Stories like yours are so very much appreciated in this thread, as you know. I am so happy for you and your ongoing recovery journey ❤

Street drugs can really wreak havoc on people prone to psychotic disorders. Even just eating weed edibles (yes, even the indica ones) played a part in both my psychotic episodes.

The key here is fighting for people's right to advocate for themselves and get on the best regimen for their personal wants and needs. For some people, that's no medication, while others prefer to be on it. It helps that a lot of schizophrenic people aren't laid out on the massive doses most of us got in the ER.
I 100% agree, well said 👌❤

I can get high from weed but not enjoyable
So....don't use weed, if it's not enjoyable...?? It's very likely to be hindering and slowing down your recovery, so it's best to avoid it if you're not even enjoying the high 🤷‍♀️

I did get my mri results back. Apparently my pineal and pituitary glands are depressed. You can see that there is no connection whatsoever to the frontal lobes and the hypothalamus.
Now, this, I find extremely interesting....is it at all feasible that the physical changes in your brain anatomy shown on the MRI could be attributed to something other than Invega damage?? Have any of the neurologists spoken about that? Perhaps a rare form of early onset dementia, such as the type that my mother has?? She has a very rare type of fronto-temporal lobe early onset dementia, it's extremely slow progressing, she lives a fully functional daily life, but there are obvious anatomical changes in her brain on MRI scans, and she has various very gradually progressing symptoms such as personality change, forgetting names of things, saying the wrong word for something even though she is thinking the correct word, stuff like that. None of that is applicable to you, I'm merely illustrating that there are all types of other things that could be the reason for the significant physical changes in your brain...I will be VERY interested to read your updates and I wish you all the very best with the new practitioner.

Hey guys.. I was wondering.. Are people who got Invega over psyhosis in better situation to recover then the ones that didnt got it for that?
That is a really really good and interesting question.....we'd have to go back through all the threads and tally up the ones who got Invega for genuine psychosis vs those who got Invega without psychosis, and then look at their success rates. Other than doing that, off the top of my head I honestly can't recall...it would be VERY interesting to see, though. Good question.

Weed definitely causes psychosis, I've known loads of people to get psychosis from continually using it. The ones who are fine use it once in a while, like monthly at a party...

Too high a proportion of people get psychosis from it, if you are one who has experienced it, just stop using it. You would be an unbelievable fool to do otherwise.

Some people are just stupid though so this falls on all types of ears.
This is true. Anyone who has ever even had ONE episode of psychosis, no matter what caused it, should avoid weed completely. THC is very likely to trigger psychosis in people who have experienced psychosis before.

is it a good sign that i did above average on a math test and hadnt done math in 3 years
Yes. You know it is.

This is so awesome to read!! Thank you so much for sharing your story with us!! Everyone here really needs to read uplifting success stories like yours. I hope you continue to improve every single day. Keep us updated! ❤

Also guys I’m gonna start smoking cigarettes again and tomorrow I’m planning to try ketamine… 3 months out will I feel anything?
Please do NOT do ketamine. Why would you do that? It's way too risky.

Hi everyone I may have found some hope. I've seen every neurologist in the book and they have constantly said they can't find anything. I was on a lyme disease forum and by freak chance somebody said they can help me. I said it's an impossibility. There is no way you can fix the damage that is going on. He said for me to send my mri from march which was two months after the injection. He was the only one pinpoint where the damage after seeing the top neurologists in my country,who keeps saying they found nothing. He looked at my pineal, pituitary and hypothalamus glands. He noticed that they were all flattened out or had been somewhat compromised. He's requesting me to get a second mri this week so he can compare the two. From there He is going to rebuild my dopamine and neurons with angiogenesis and neurogenesis techniques. I told him that i've spent almost four hundred thousand dollars in insurance and personal money to get better. He actually looked at my scans for free and gave me a free consultation, which I was very impressed with. I'm hoping and praying that he will help me.
Please keep us updated. Like I said above, I am really interested in your recovery and I want you to know that I am really rooting for you man. I really hope you can get some good help. Let us know how you go ❤
 
I only had one injection and it has wreaked havoc on my brain.Invega is known as a torment drug and there are numerous people who have had one shot and never recovered like me. I am 10 months in and see no relief whatsoever. If you go on Google it will clearly have numerous stories like mine.Look up on Drugs.com "Invega Sustenna Ruined my life".It gives a clear cut picture of what this drug does.My mri damage has nothing to do with dementia as the damage is in the center of my brain.
 
I only had one injection and it has wreaked havoc on my brain.Invega is known as a torment drug and there are numerous people who have had one shot and never recovered like me. I am 10 months in and see no relief whatsoever. If you go on Google it will clearly have numerous stories like mine.Look up on Drugs.com "Invega Sustenna Ruined my life".It gives a clear cut picture of what this drug does.My mri damage has nothing to do with dementia as the damage is in the center of my brain.
You checked on MRI, so how severe is the damage? Did you have dementia before invega and how old are you?
 
I don't have peace. I can't relax and feel good anymore.
I realized that the opposite of peace is suffering and agony, and invega primarily causes that, to the worst extremes that can't be grasped by imagination. It must be experienced to be truly understood how terrible it is.

Some of the heroin addicts beg for death during withdrawals, but invega puts this on an even greater extreme. It's much worse than heroin withdrawal and lasts much longer. People were through heroin withdrawals and who also went on invega confirmed that.

When I was around 1 year off, I was running outside and my head sometimes produced a sticky sound at the left top side of my skull. It went away in few months

Recently, I got the strongest goosebumps since going off invega.
 
most people who dont recover are older and have a weaker system and they had a shit ton of injections even people who have shit ton of injections are proved to recover too usually around a year and a half but its rare to never recover from a few injections
 
Six complete months update. Here goes nothing.

I don't really have much to say. It's hard to disentangle my PSSD symptoms from the aftereffects of invega. I can say that taking Prozac made me worse, I also smoked weed while I was on it and I have a condition that probably stopped me from metabolizing it correctly. Every day I wake up with regret from not choosing an SSRI I had used before with no problems other than weight gain, something I wanted to avoid because I have NAFLD.

My PSSD symptoms have improved, which is intersting and good since a lot of people don't improve in the first few months. It gives me hope that it's just withdrawl or it's going to be short term. I observed that before people start getting sensation back and such, their genitals return to their normal size and texture and mine have improved in that area. I got windows from coffee and weed where I had acceptable orgasms. My genitals aren't completely numb and I get flashes of pleasure, but the sensation is greatly reduced. If I can find a way to consistently and safely induce windows, I could continue living like this for years, but it's really sad that I lost my perfect sexual functioning and most of my pleasure. I only got to have sex once.

My cognition is mostly pre-invega, but sometimes I still have a hard time thinking creatively. I feel more empty and blank. My brain used to be a rainforest, now it's like the Mojave. But there are still a lot of living things in the Mojave desert. I look at things and I know how to draw them again at least.

I never thought I would be wiped out by psychiatric drugs like this. I never knew it was possible. I had such a strong personality and strong feelings, I didn't know emptiness or anhedonia before all this shit. Life has never been so dull for me, except directly after taking invega.

The constant dysphoria hasn't stopped, I want to crawl out of my own skin a lot of the time. Speaking of skin, the paresthesia I got from Prozac is also gradually getting better.

I'm laughing at stuff, I can cry, a little bit of fear is coming back. I don't have zero emotions, but I still feel a void that was once so full. I wish I cared about things again. I was a passionate person who cared a lot about political causes like trans rights and lots of intersectional liberation stuff. I love humanity and I believe we can be better. I just wish I could find it in my heart again to try to bring about utopia.

Everything I was, was beautiful. I always felt dirty because of my intrusive thoughts, hated myself over embarrassments in my past. But I was still this deeply moral, loving human being. Now I feel like I don't react to anything like I should.

I'm finding more pleasure in food, I snack because snacking good now. But I don't get the tingle in my lips from eating anything, I'm missing so many physiological responses.

I'm in a better place than the constant panic and pain and regret, but it's not that much better. I kinda want to die, but I still want to see if I'll get better or if it just becomes more bearable.

Some lyrics are stuck in my head and they help me feel better. "There will come a day when you feel better//And you'll rise up free and easy on that day// and float from branch to branch, lighter than the air// just when that day is coming, who can say, who can say?" It's from Up the Wolves by the Mountain Goats. It's a song about recovering from child abuse, but I'm clinging to that part.

Here's another song for y'all.

 
Last edited:
doubt there is a difference in success rates with people who were psychotic vs those who werent if anything severe psychosis might decrease chance of full recovery
 
You checked on MRI, so how severe is the damage? Did you have dementia before invega and how old are

From what it shows, my pineal gland is flattened out it's definitely damaged.Im going for my second mri on Monday to see what the damage is further.Im hoping this person can help me... but as they say the damage is permanent.I hope they can help me.Im also not letting this doctor get away with what they did to me.Im moving forward with litigation and they will not ever do this to someone again.
 
From what it shows, my pineal gland is flattened out it's definitely damaged.Im going for my second mri on Monday to see what the damage is further.Im hoping this person can help me... but as they say the damage is permanent.I hope they can help me.Im also not letting this doctor get away with what they did to me.Im moving forward with litigation and they will not ever do this to someone again.
I would like to know how many % of it is damaged or shrunk and also your age. For sake of research on this, it will be very beneficial for you to answer.
 
Status
Not open for further replies.
Top