• The Dark Side 💕 Welcome Guest 💕
    Posting Rules Bluelight Rules
    Notable Threads Urgent Hotlines
    Bereavement Mindfulness
    Suicide Support Anger Management
  • TDS Moderators: AlphaMethylPhenyl | paranoid android

Coming off Invega/Xeplion (paliperidone) injections v11

Status
Not open for further replies.
Trueart2 said:
It's a supplement, it pushes Invega out the body. Please read previous threads for more answers.

Take it and exponentially increase the rate in which invega leaves your body. Don't take it and continue on as currently.
Click to expand...
doesn’t it mess with other medicines like adhd?
 
Trueart2 said:
It's a supplement, it pushes Invega out the body. Please read previous threads for more answers.

Take it and exponentially increase the rate in which invega leaves your body. Don't take it and continue on as currently.
Click to expand...
Which brand is good?

I searched on my search engine, and while the price is cheap, there are more than just one or two types.

And I heard they aren't medically verified either.

Still, I plan to try taking them for now.

Could you possibly recommend a brand?
 
Hey everyone, have you ever felt an overwhelming surge of dopamine only in your dreams after getting an Invega Sustenna injection?

The strange thing is, that heightened dopamine state was exactly how I felt right before getting the shot.

I'm sure everyone remembers that heightened sensory awareness from childhood.

Everyone's senses—seeing, feeling, hearing, smelling—and memories from childhood are extraordinary.

But now, I can only feel it before falling asleep or in the middle of sleep.

Among those who recovered after taking the Invega Sustenna injection, has anyone experienced their senses returning or becoming heightened?
 
nom. said:
Hey everyone, have you ever felt an overwhelming surge of dopamine only in your dreams after getting an Invega Sustenna injection?

The strange thing is, that heightened dopamine state was exactly how I felt right before getting the shot.

I'm sure everyone remembers that heightened sensory awareness from childhood.

Everyone's senses—seeing, feeling, hearing, smelling—and memories from childhood are extraordinary.

But now, I can only feel it before falling asleep or in the middle of sleep.

Among those who recovered after taking the Invega Sustenna injection, has anyone experienced their senses returning or becoming heightened?
Click to expand...
Yeah, I dream like that- hence why sleep is my most important time of the day. Living day to day is painful - hopefully as this injection wears, ill feel better and can feel dopamine again during the day.
 
Trueart2 said:
1. To my understanding D2 agonists have been the perpetrator of making situations worse when it comes to antipsychotic damage, and I do not recommend. However you’ve gone far past the threshold of your half life(6 days), and 5 of those half lives(30 days.) The medicine at this point is completely out of your system but the damage still runs amock, I doubt it will help but at this point who knows.

2. The lady isn’t offering anything extremely beneficial to you. She’s going to give you a summary of what you already know and then forward you to someone else, who you have no idea about and aren’t guaranteed a successful interaction with. Granted at this point if you’re considering medical suicide, it really doesn’t matter what the financial costs are as your life will soon come to an end if you don’t get help. Nevertheless it’s still extremely important to consider the way spending 900$ will affect your life while living.

I don’t think she’ll tell you anything revealing, and if she does I doubt it’ll be anything truly helpful. For example we can get all these AI information about our receptors, but if there’s no active way we can apply this information it’s generally meaningless. Even if she does recommend you to someone this doesn’t mean they’re bound to helping you, and if they are bound to by medical code they can always just dismiss you by calling you crazy due to your psychiatric history. They’ll also have to research deeply about your condition. While doctors by profession are scientists this does not mean they’re willing to research your case for no monetary benefit nor recognition
Click to expand...
Well, so i May spent 660$ just to have nothing in return? But what if this time something happen? I want to try, we are talking about my life and potentially lifes of other people here if something useful came out..
 
this is what chatgpt said “

✅​

No — not meaningfully.

St. John’s wort induces liver enzymes (CYP3A4, CYP2C9, P-gp).
But paliperidone is NOT primarily broken down by the liver — it is mostly excreted unchanged through the kidneys.

So:

  • St. John’s wort is unlikely to increase the breakdown or clearance of paliperidone.
  • Taking it on November 30 would not make paliperidone wear off faster.”
 
bing says “

✅ Estimated Clearance​

  • Major levels gone: By March 2026
  • Effectively cleared: By April–May 2026 (with St. John’s wort possibly nudging this earlier by a few weeks)

So in short: even with St. John’s wort, paliperidone from those October injections would still be present well into early spring 2026, but by April–May it should be effectively out of your system.”

so it doesn’t even clear it by that much, what’s the point in taking it?
 
I'm feeling more positive about recovery right now. My restlessness has definitely eased up abit because I don't complain about it as much. It's just happening so slowly I barely noticed. It's still there, but not as bad. 68 days since last injection.
 
they told me you can take the injection for convenience and I obliged, why did they never warn me on the harms it could cause?
 
Last edited:
twinpeaks123 said:
they me you can take the injection for convenience and I obliged, why did they never warn me on the harms it could cause?
Click to expand...
Because if they did then you newer would take it in the first place, and they know that, so they dont tell a single thing about.

Like how they did to me, they just told me “it’s risperidone injection so you don’t have to take oral pills everyday” and that’s all.
 
RisperdalConsta50mg said:
Because if they did then you newer would take it in the first place, and they know that, so they dont tell a single thing about.

Like how they did to me, they just told me “it’s risperidone injection so you don’t have to take oral pills everyday” and that’s all.
Click to expand...
They don’t even told me that risperidone it’s an antiosychotic because if they did i would ask them “why are you giving me antipsychotic injection if i never had psychosis?”

They acted like i had a master on pharmaceutical and i already know what that was, in fact it happen very frequently that they act like that: hiding what the medication is, and his side effects.
 
RisperdalConsta50mg said:
Because if they did then you newer would take it in the first place, and they know that, so they dont tell a single thing about.

Like how they did to me, they just told me “it’s risperidone injection so you don’t have to take oral pills everyday” and that’s all.
Click to expand...
they told me they give me pills to test if I would experience side affects but that is also risky, they should have just warned me straight up on what the side effects would be

now my life is potentially ruined, i really really really don’t want to die, there’s so much to life I wanna experience
 
RisperdalConsta50mg said:
Because if they did then you newer would take it in the first place, and they know that, so they dont tell a single thing about.

Like how they did to me, they just told me “it’s risperidone injection so you don’t have to take oral pills everyday” and that’s all.
Click to expand...
Sadly I was told the same thing about the invega injection. They even said it was more beneficial than the tablets because the injection supposedly bypasses the liver. They handed me an information sheet on invega, showing only the benefits of the injection- which all turned out to be horseshit. I went back 5 times to get injected again and its been pure hell since then.
 
lukeflowz said:
Sadly I was told the same thing about the invega injection. They even said it was more beneficial than the tablets because the injection supposedly bypasses the liver. They handed me an information sheet on invega, showing only the benefits of the injection- which all turned out to be horseshit. I went back 5 times to get injected again and its been pure hell since then.
Click to expand...
is this uk?
 
lukeflowz said:
Sadly I was told the same thing about the invega injection. They even said it was more beneficial than the tablets because the injection supposedly bypasses the liver. They handed me an information sheet on invega, showing only the benefits of the injection- which all turned out to be horseshit. I went back 5 times to get injected again and its been pure hell since then.
Click to expand...
They told me “we have to look at the benefits even if there are some risk” but they never told me any of these risk like i would develop neuroleptic malignant syndrome that can lead to DEATH.

You know, hidding information like that one it’s very concerning and this is a very bad violation of the rights of the patient here in my country. Yeah i sued them because of that and all the others shitty thing they did to me.
 
Status
Not open for further replies.
Top