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Mental Health Coming off Invega/Xeplion (paliperidone) injections v. 10

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RisperdalConsta50mg said:
Because protocol with risperidone is this:

21 days of oral phills, first injection MAX dosage 25mg. Next injection only after 14 days.

With me they did like that:

50mg injection “Cold blood”, 1ml everyday for the next 11 days, second injection 50mg at 12th day.

I got a overdose of risperidone, they don’t respect safety protocol and probably i was not psychotic, this is why it affected me in this way.

It’s basically like doing a chemio Therapy to someone without cancer by overdosing him with radiations ☢️
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I am not psychotic either, was given 2 injections of invega. Do you think it will affect anyone whos not psychotic negatively?

I want to know what is it about such a low dose of risperdal that made you like this? I thought risperidone is less risky than invega.
 
I was literally walkig really fast in circles for hours, when i was sitting i cannot keep my legs not moving and after 1-2 minutes of being sit down i felt this urge to stand up and keep walking and walking, so i feel you..
 
anonymoususer777 said:
I am not psychotic either, was given 2 injections of invega. Do you think it will affect anyone whos not psychotic negatively?

I want to know what is it about such a low dose of risperdal that made you like this? I thought risperidone is less risky than invega.
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Risperidone Injections came in these dosage: 7.5mg - 25mg - 37.5mg - 50mg.

I got the maximal dose,twice, without being psychotic at all. From what I can think, psychosis mean you have too many D2 receptors, they block 80% of them so you don’t have psychosis anymore but still can feel other signal like hunger,tiredness,thirst, etc..

Since we were not psychotic, we dint have too many D2 receptors, but they still block 80% of them and this result in all the sympthoms we have. The proof we don’t need this shit is the sympthoms that came out, someone that need this shit is just fine with it, no more psychosis,normal life, maybe just a sexual disfunction.
 
Sleep has improved. 5 hours is better than sleeping 30 minutes at a time.

As I'm doing energy work on myself throughout the days, piezoelectric shocks sometimes generate uncontrollable bodily movements (kriyas)--when stagnant chi is released--the sudden jolts being so powerful that I experience cracks and pops of my bones, sometimes even in my skull in places that would otherwise be very difficult for those pops to occur. Energy work at this point is a matter of precision; drawing my focus to blockages takes time and releasing the blockages is often difficult because more often than not the areas that were affected seem "twisted", as if the tissues themselves have been tangled.
 
RisperdalConsta50mg said:
This is a good question, i don’t have the answer for that
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From what I understood, people with psychosis usally recover fully, then after a while they fall again into psychosis, this is because their brain produces way more D2 dopamine receptors.

Since we were not psychotics, our brain don’t produce too many D2 receptors, so maybe this is not good for our recovery, idk, I’m trying to use logic
 
If you dont know maybe you are mistaken, i dont think recovery is impossible for misdiagnosed people. Maybe you are assuming a lot of things.

What is it about risperdal that makes it harder to recover from than invega?
 
Until we do a blood panel we cannot know if our sympthoms are there because we still have this poison in our blood or it’s just receptors desensibilization or up-down regulation.

Step 1: blood panel, at least you know if you still have this shit inside you

Step 2: If your body is fully detox but you still have sympthoms is because receptors are not the way they were before, so there you have to do a PET scan in order to know what is going on

3: With the result of the PET scan you know what is the problem and you can know exactly what treatment you need in order to recovery.

But Guess what? Is more easy to tell you are delusional, and to cover up the side effects/lasting effects of this poison in order to protect psychiatry and the big pharma behind.
 
anonymoususer777 said:
If you dont know maybe you are mistaken, i dont think recovery is impossible for misdiagnosed people. Maybe you are assuming a lot of things.

What is it about risperdal that makes it harder to recover from than invega?
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I know that after 14 months I’m only 10% recovered, maybe in 2 months i Wii tell “yo, recovery started his peak, 50% recovered now” or maybe i can tell “only 10% recovered after 20’months” I don’t know, i will be there and you will know how it goes
 
RisperdalConsta50mg said:
I know that after 14 months I’m only 10% recovered, maybe in 2 months i Wii tell “yo, recovery started his peak, 50% recovered now” or maybe i can tell “only 10% recovered after 20’months” I don’t know, i will be there and you will know how it goes
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I spoke to many people who were misdiagnosed and recovered so i doubt if not being in psychosis would be a reason to not recover. Be careful what you say based on personal experience as others might get severe anxiety.

Again i have to know why risperdal is so much worse than invega.

Have you tried adderal? Someone told me that it brings your emotions and sex drive back momentarily.
 
iridescentblack said:
Sleep has improved. 5 hours is better than sleeping 30 minutes at a time.

As I'm doing energy work on myself throughout the days, piezoelectric shocks sometimes generate uncontrollable bodily movements (kriyas)--when stagnant chi is released--the sudden jolts being so powerful that I experience cracks and pops of my bones, sometimes even in my skull in places that would otherwise be very difficult for those pops to occur. Energy work at this point is a matter of precision; drawing my focus to blockages takes time and releasing the blockages is often difficult because more often than not the areas that were affected seem "twisted", as if the tissues themselves have been tangled.
Click to expand...

RisperdalConsta50mg said:
I was literally walkig really fast in circles for hours, when i was sitting i cannot keep my legs not moving and after 1-2 minutes of being sit down i felt this urge to stand up and keep walking and walking, so i feel you..
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Thanks I sincerely hope it goes away in time. I’m hoping by when I’m at the three month mark that it’s gone. I’m currently at 32 days since my last injection.
 
iridescentblack said:
Sleep has improved. 5 hours is better than sleeping 30 minutes at a time.

As I'm doing energy work on myself throughout the days, piezoelectric shocks sometimes generate uncontrollable bodily movements (kriyas)--when stagnant chi is released--the sudden jolts being so powerful that I experience cracks and pops of my bones, sometimes even in my skull in places that would otherwise be very difficult for those pops to occur. Energy work at this point is a matter of precision; drawing my focus to blockages takes time and releasing the blockages is often difficult because more often than not the areas that were affected seem "twisted", as if the tissues themselves have been tangled.
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I’ve been sleeping 10 mins or so a time how did you fix it
 
anonymoususer777 said:
Risperdal consta, risperidone is not even a dopamine blocker, its abalancer so i wonder why your reaction to it was this.
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Am I doing myself harm in taking a paliperodone tablet, I stopped the invega injections,

But I haven’t slept since and that’s what I’m looking for,
 
lukeflowz said:
Anyone have Akathisia while on/coming off invega. I’m not sure how long this will last. It’s absolute torture.
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Hey yeah I had akathisia when I first got injected, it was absolute hell. I got prescribed benzotropine for it and it helped. You don’t have to suffer, ask to see a psych doc or possibly any doctor and tell them you have akathisia and need help
 
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