Coming off Invega/Xeplion (paliperidone) injections v 12

I did and no one ever stated if their old hobbies, ability to retain information, and way of thinking ever came back... its month 8 and not seeing tge signs so im worried.
my understanding is that EVERYTHING comes back, if it didn’t then there would be a lot of people complaining, my symptoms seem to have worsened recently, so indeed I am also worried but I saw two people who’s symptoms got worse and they recovered

if you are not seeing seeing signs by 8 months then it’s possible you could recover by the 1.5 month mark or 18 months, the person who’s symptoms have worsened recovered at like 1.5 month mark
 
my rimficin came today, hopefully how long do you plan on taking it?
Really? Where did you order it from?
Um, not sure today I didn't take any, i only have 30-40 tablets left i think, so i plan to lower the dosage, maybe take just 2 a day. I hope i will feel better by 6 month naturally.
 
Really? Where did you order it from?
Um, not sure today I didn't take any, i only have 30-40 tablets left i think, so i plan to lower the dosage, maybe take just 2 a day. I hope i will feel better by 6 month naturally.
I got it from India mart, took like a week and it looks legit, I got 360mg since I only took 2 doses and since it’s been 3 months, I think I am going to take it 3 times a day for 3 weeks because the enzyme inducer effects last for longer
 
I did and no one ever stated if their old hobbies, ability to retain information, and way of thinking ever came back... its month 8 and not seeing tge signs so im worried.

Re-read them then. People state everything comes back, but considering it being month 8 for you; You do deserve some opportunity to be a bit concerned about your well being.
 
Doctor from university:

My answer:

His reply:

My final answer:

I’am still waiting that this “Dr. Cecere” contact me via mail or phonecall since the last time you told me about him, maybe he forgot?

Anyways if he is still uneducated about the brain damage of AP’s injections like your team, not even him can help me.

Honestly i’am disappointed about the behaviour of a so called “university unit hospital” but it is what it is, some normal folks out there have more knowlede about the damage and alterations by these injections than your team.
Your doctors do not know about sometimes permanent Neuroleptic-Induced Deficit Syndrome (NIDS)? It is under-researched and under-recognized, i.e. not formally recognized in diagnostic manuals like the DSM-5 or ICD-11, but is a known condition.

According to AI search: "A. Rifkin's 1984 paper "Neuroleptic-induced deficit syndrome" is often cited as the foundational description of Neuroleptic-Induced Deficit Syndrome (NIDS). Rifkin described it as a state of apathy, lack of initiative, and emotional blunting directly caused by antipsychotics, distinguishable from depression and the primary illness.
Associated Researchers: Look for work from this era by John Kane, Stephen R. Marder, and Theo C. Manschreck. They often discussed "secondary negative symptoms" or "akinetic depression" induced by high-potency typical antipsychotics like haloperidol.
Search Terms: Use these in PubMed/Google Scholar: "neuroleptic induced deficit syndrome," "akinetic depression," "secondary negative symptoms antipsychotics," "drug-induced parkinsonism affective."


There is a new group "Iatrogenic Neuroimmune Disease Association" that put out a research document last year with a brief paragraph about NIDS:

Image-1-18-26-at-12-50-PM.png


Source: https://img1.wsimg.com/blobby/go/8c...l Findings 2.0 - F2705s.pdf?ver=1763662133954

It is hard to compile data/evidence with cognitive dysfunction, but we need to be prepared to defend our claims for when situations like this one arise, so we can't be gaslit, silenced or ignored.
I was skimming old threads and users have been suggesting we do this for years, e.g. @deficiT in 2024:

Fun fact: "It took psychiatry 20 years to recognize TD [tardive dyskinesia] as an iatrogenic illness, even as it afflicted half or more of hospitalized patients (Gelman, 1984)." - Peter Breggin from "Brain-Disabling Treatments in Psychiatry" (1997).
"In 1983, Dr Peter Breggin wrote about the risk of tardive dyskinesia in children and tardive dementia in children and adults in his book "Psychiatric Drugs". This book and his efforts resulted in the U.S. FDA requiring the 1985 expanded class label for tardive dyskinesia for all neuroleptics."
G9SO2sm-XUAEc5-x.jpg


Anyway, good on you for persevering @RisperdalConsta50mg
 
Your doctors do not know about sometimes permanent Neuroleptic-Induced Deficit Syndrome (NIDS)? It is under-researched and under-recognized, i.e. not formally recognized in diagnostic manuals like the DSM-5 or ICD-11, but is a known condition.

According to AI search: "A. Rifkin's 1984 paper "Neuroleptic-induced deficit syndrome" is often cited as the foundational description of Neuroleptic-Induced Deficit Syndrome (NIDS). Rifkin described it as a state of apathy, lack of initiative, and emotional blunting directly caused by antipsychotics, distinguishable from depression and the primary illness.
Associated Researchers: Look for work from this era by John Kane, Stephen R. Marder, and Theo C. Manschreck. They often discussed "secondary negative symptoms" or "akinetic depression" induced by high-potency typical antipsychotics like haloperidol.
Search Terms: Use these in PubMed/Google Scholar: "neuroleptic induced deficit syndrome," "akinetic depression," "secondary negative symptoms antipsychotics," "drug-induced parkinsonism affective."


There is a new group "Iatrogenic Neuroimmune Disease Association" that put out a research document last year with a brief paragraph about NIDS:

Image-1-18-26-at-12-50-PM.png


Source: https://img1.wsimg.com/blobby/go/8c970a38-146a-4f63-a408-d45f62d06b4b/downloads/c4249329-78d0-4acd-9c36-778a0248909e/PSSD Clinical Findings 2.0 - F2705s.pdf?ver=1763662133954

It is hard to compile data/evidence with cognitive dysfunction, but we need to be prepared to defend our claims for when situations like this one arise, so we can't be gaslit, silenced or ignored.
I was skimming old threads and users have been suggesting we do this for years, e.g. @deficiT in 2024:

Fun fact: "It took psychiatry 20 years to recognize TD [tardive dyskinesia] as an iatrogenic illness, even as it afflicted half or more of hospitalized patients (Gelman, 1984)." - Peter Breggin from "Brain-Disabling Treatments in Psychiatry" (1997).
"In 1983, Dr Peter Breggin wrote about the risk of tardive dyskinesia in children and tardive dementia in children and adults in his book "Psychiatric Drugs". This book and his efforts resulted in the U.S. FDA requiring the 1985 expanded class label for tardive dyskinesia for all neuroleptics."
G9SO2sm-XUAEc5-x.jpg


Anyway, good on you for persevering @RisperdalConsta50mg
I cannot imagine how smart you were before these shots. A tough rebel you are.
 
I found a positive recovery story, i am posting it below. This is not me, this is someone on another forum who recovered;

"I am happy to report that I am at twenty-two months and 100% recovered. I am back in the gym hitting the weights, and I have never felt better. I am more creative and productive than I have ever been at any point in my life.

There was so much negative talk on here when I first joined nearly two years ago, that I really believed that I would never heal. Don’t believe all of the negative crap. While it is rough the first year, you will be as creatively manic as me at the fourteen-month mark, and fully recovered in 18 to 24 months. Exercise and proper nutrition are the most crucial components. Hang in there, you got this."

I believe this person got 2 loading injections. Dont know the dosage.
 
I found a positive recovery story, i am posting it below. This is not me, this is someone on another forum who recovered;

"I am happy to report that I am at twenty-two months and 100% recovered. I am back in the gym hitting the weights, and I have never felt better. I am more creative and productive than I have ever been at any point in my life.

There was so much negative talk on here when I first joined nearly two years ago, that I really believed that I would never heal. Don’t believe all of the negative crap. While it is rough the first year, you will be as creatively manic as me at the fourteen-month mark, and fully recovered in 18 to 24 months. Exercise and proper nutrition are the most crucial components. Hang in there, you got this."

I believe this person got 2 loading injections. Dont know the dosage.

Loading dosage is always 234 + 156.
 
Your doctors do not know about sometimes permanent Neuroleptic-Induced Deficit Syndrome (NIDS)? It is under-researched and under-recognized, i.e. not formally recognized in diagnostic manuals like the DSM-5 or ICD-11, but is a known condition.

According to AI search: "A. Rifkin's 1984 paper "Neuroleptic-induced deficit syndrome" is often cited as the foundational description of Neuroleptic-Induced Deficit Syndrome (NIDS). Rifkin described it as a state of apathy, lack of initiative, and emotional blunting directly caused by antipsychotics, distinguishable from depression and the primary illness.
Associated Researchers: Look for work from this era by John Kane, Stephen R. Marder, and Theo C. Manschreck. They often discussed "secondary negative symptoms" or "akinetic depression" induced by high-potency typical antipsychotics like haloperidol.
Search Terms: Use these in PubMed/Google Scholar: "neuroleptic induced deficit syndrome," "akinetic depression," "secondary negative symptoms antipsychotics," "drug-induced parkinsonism affective."


There is a new group "Iatrogenic Neuroimmune Disease Association" that put out a research document last year with a brief paragraph about NIDS:

Image-1-18-26-at-12-50-PM.png


Source: https://img1.wsimg.com/blobby/go/8c970a38-146a-4f63-a408-d45f62d06b4b/downloads/c4249329-78d0-4acd-9c36-778a0248909e/PSSD Clinical Findings 2.0 - F2705s.pdf?ver=1763662133954

It is hard to compile data/evidence with cognitive dysfunction, but we need to be prepared to defend our claims for when situations like this one arise, so we can't be gaslit, silenced or ignored.
I was skimming old threads and users have been suggesting we do this for years, e.g. @deficiT in 2024:

Fun fact: "It took psychiatry 20 years to recognize TD [tardive dyskinesia] as an iatrogenic illness, even as it afflicted half or more of hospitalized patients (Gelman, 1984)." - Peter Breggin from "Brain-Disabling Treatments in Psychiatry" (1997).
"In 1983, Dr Peter Breggin wrote about the risk of tardive dyskinesia in children and tardive dementia in children and adults in his book "Psychiatric Drugs". This book and his efforts resulted in the U.S. FDA requiring the 1985 expanded class label for tardive dyskinesia for all neuroleptics."
G9SO2sm-XUAEc5-x.jpg


Anyway, good on you for persevering @RisperdalConsta50mg
So, the whole damage is into the D2 Dopamine receptor? Not into the alfa1, alfa2, norandrenaline, GABA, 5HT2A Serotonin?
 
I found a positive recovery story, i am posting it below. This is not me, this is someone on another forum who recovered;

"I am happy to report that I am at twenty-two months and 100% recovered. I am back in the gym hitting the weights, and I have never felt better. I am more creative and productive than I have ever been at any point in my life.

There was so much negative talk on here when I first joined nearly two years ago, that I really believed that I would never heal. Don’t believe all of the negative crap. While it is rough the first year, you will be as creatively manic as me at the fourteen-month mark, and fully recovered in 18 to 24 months. Exercise and proper nutrition are the most crucial components. Hang in there, you got this."

I believe this person got 2 loading injections. Dont know the dosage.
Well, i’am at 18 months and 3 days, not recovered at all, the only thing that changed it’s tinnitus that came out at 13 months mark.
 
hi all just updating that im more or less the same no major improvements i guess thats what happens when you take 10 invega injections , its permanent for me but if u had less theres a good chance u will recover. I'm content though idc about anhedonia or anything i just live life . PS FUCK @YogirisingKundalini PIECE OF SHIT POLISH SCAMMER, HE BEGGED ME FOR MONEY AND THEN DIDNT PAY ME BACK SINCE JUNE OF LAST YEAR . DO NOT MESSAGE HIM OR HE WILL SCAM U . Fck polish people they are all scammers .
 
Your doctors do not know about sometimes permanent Neuroleptic-Induced Deficit Syndrome (NIDS)? It is under-researched and under-recognized, i.e. not formally recognized in diagnostic manuals like the DSM-5 or ICD-11, but is a known condition.

According to AI search: "A. Rifkin's 1984 paper "Neuroleptic-induced deficit syndrome" is often cited as the foundational description of Neuroleptic-Induced Deficit Syndrome (NIDS). Rifkin described it as a state of apathy, lack of initiative, and emotional blunting directly caused by antipsychotics, distinguishable from depression and the primary illness.
Associated Researchers: Look for work from this era by John Kane, Stephen R. Marder, and Theo C. Manschreck. They often discussed "secondary negative symptoms" or "akinetic depression" induced by high-potency typical antipsychotics like haloperidol.
Search Terms: Use these in PubMed/Google Scholar: "neuroleptic induced deficit syndrome," "akinetic depression," "secondary negative symptoms antipsychotics," "drug-induced parkinsonism affective."


There is a new group "Iatrogenic Neuroimmune Disease Association" that put out a research document last year with a brief paragraph about NIDS:

Image-1-18-26-at-12-50-PM.png


Source: https://img1.wsimg.com/blobby/go/8c970a38-146a-4f63-a408-d45f62d06b4b/downloads/c4249329-78d0-4acd-9c36-778a0248909e/PSSD Clinical Findings 2.0 - F2705s.pdf?ver=1763662133954

It is hard to compile data/evidence with cognitive dysfunction, but we need to be prepared to defend our claims for when situations like this one arise, so we can't be gaslit, silenced or ignored.
I was skimming old threads and users have been suggesting we do this for years, e.g. @deficiT in 2024:

Fun fact: "It took psychiatry 20 years to recognize TD [tardive dyskinesia] as an iatrogenic illness, even as it afflicted half or more of hospitalized patients (Gelman, 1984)." - Peter Breggin from "Brain-Disabling Treatments in Psychiatry" (1997).
"In 1983, Dr Peter Breggin wrote about the risk of tardive dyskinesia in children and tardive dementia in children and adults in his book "Psychiatric Drugs". This book and his efforts resulted in the U.S. FDA requiring the 1985 expanded class label for tardive dyskinesia for all neuroleptics."
G9SO2sm-XUAEc5-x.jpg


Anyway, good on you for persevering @RisperdalConsta50mg
@ixi what are the effects of Neuroleptic-Induced Deficit Syndrome (NIDS)? It is apathy, lack of initivative, and emotional blunting and permanent for long term users or for any one randomly?
 
This is something called Neuroleptic-Induced Deficit Syndrome (NIDS)? It is apathy, lack of initivative, and emotional blunting and sometimes permanent. I have the energy to go exercise but no motivation (lack of initiative), i want to work on my hobbies but no interest (apathy), i feel pain for my loved ones but i dont cry for them like i used to (emotional blunting). For people who recovered, Did you have this and did it go away? @Invegatorture @silenthill @paranoid android and others Please answer.
 
Feeling a bit better, i took a bit of rimficin a bit of weed and a bit, of Vyvanse and my brain kind of connect to a livable vibe.

I got a mouse for my pc, new pen and paper.
I can feel my brain rebooting after 5 months and 9 soon 10ish days but it's, so fucking slow.
 
Feeling a bit better, i took a bit of rimficin a bit of weed and a bit, of Vyvanse and my brain kind of connect to a livable vibe.

I got a mouse for my pc, new pen and paper.
I can feel my brain rebooting after 5 months and 9 soon 10ish days but it's, so fucking slow.
I think it’s because you haven’t been taking it for long, i think you need to wait like 1 month or so to see changes then your dopamine has to regulate
 
I think it’s because you haven’t been taking it for long, i think you need to wait like 1 month or so to see changes then your dopamine has to regulate
The rimficin? I already took it for 3 weeks now i think, you can't take it forever it's not good for your body.

Nobody even knows how long invega still realesing after last injection.
Gemini think no more injection's after 6-6.5 months, and chatgpt think there's small amount of invega realesing after 7.5 months last time.
 
The rimficin? I already took it for 3 weeks now i think, you can't take it forever it's not good for your body.

Nobody even knows how long invega still realesing after last injection.
Gemini think no more injection's after 6-6.5 months, and chatgpt think there's small amount of invega realesing after 7.5 months last time.
how long are you planning on taking it?
 
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