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

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I got a good vibrator with the help of my friends. I hope it will help me recover from PSSD.
 
Hi everyone, my name is All, I was forced to take Invega for (bruuh šŸ˜ž) 16 months..., While in the end I had no reason to take it, I have the same symptoms as you , total chemical lobotomy, apathy , anhedonia , it's been 9 months since I stopped them and for 5 weeks I have had some positive periods of a few minutes to sometimes a few hours of feeling pleasure, libido, love or sensation but it's still too little for my taste,I don't know if it's a sign of remission because I wonder if its bursts of positive feeling reach those who have not yet recovered, here I am starting to take amisulpride very low dose because it seems that it increases the levels and the quality of dopamine, I don't know if it's a good idea for me to take it, thank you for reading my experience and I hope we all get our lives back !
It's highly unlikely a low dose of amisulpride will increase dopamine. I don't see a low dose of amisulpride having any benefits if you're trying to recover from anti-psychotic neurotoxicity
 
Most people here show signs of reversible damage. I don't care what psychiatrist say they are not real doctors and are teached nonsense and practice lazy medicine. There are many thousands of people worldwide complaining about the same things, side effects from meds. These meds are neurotoxic.
Whilst I agree that there are a lot of psychiatrists who are lazy and over-prescribe medications, psychiatrists are in fact real doctors. It's just very unfortunate that so many are so quick to hand out scripts when they should be looking for alternative solutions for their patients. It is uncommon to find a good psychiatrist who will do a thorough job, but they do exist.

Signs of severe braindamage would be ; anhedonia, complete loss of smell, long term akathesia, severe brainfog, severe memory impairment, complete loss of emotions, long term movement disorders including dyskinesia, blurry vision/ loss of vision, loss of hearing, reduced coordination and reduced nerve sensitivity in limbs or hand(measurable). If you have zero improvement or abysmal improvement in a few years time you probably have long term damage, chances are you get a slight recovery anywhere in 10 years and regaining some function through neuroplasticity where other brain areas take over/compensate the loss of function. Another sign of severe damage is burning brain syndrom where you get encephalitis and brain swelling

Another dramatic symptom of severe braindamage is not able to distinguish between the mental/physical state before the accident and after (wether be kinetic trauma or chemical). People will go around claiming they are cured while having severe symptoms. These people usually have severe behavioural problems you can also notice their grammar is really off, they also can make erratic statements and out of the ordinary religious statements.
If you have copy/pasted some of this from a website, please desist from doing so in the future.

However people who don't fully recover but claim to have recovered can also suffer from certain personality disorders such as narcistic personality disorder or avoidant personality disorder. I've seen many people on here that aren't mentally ill but do have personality disorders of any kind. You simply don't know their situation they can have full recovery but are attention seeking and claim they never recovered.
Please be VERY CAREFUL about "diagnosing" people with personality disorders. You simply have absolutely no way of being able to do this. Sure, you can speculate, but that's about it.
Similarly, be VERY careful about insinuating that someone who claims to have not yet recovered is just attention seeking. That is medical gaslighting and will not be tolerated on here. All accounts of someone claiming that they have not recovered are to be taken seriously.

Anyway if you lost emotions and they don't come back after years you definitely got damage. I've seen user invegasucks and AP sucks about burning brain. That's definitely encephalitis.
The symptom of the sensation of burning brain is NOT definitely encephalitis. There are other reasons why one might have this symptom. Please do not make claims such as this, you cannot diagnose people over the internet.

Lately i don't have the energy or motivation to check all kinds of forums because there's so much negativity on them it's not fun reading about problems. Maybe i'm insensitive or simply unable to know because i never experienced what you guys experienced. Most of you are in total panic about not ever getting better. Most of you are just a few months off medication and you're already in total panic you haven't even crossed the 2 or 3 year threshold yet. I've even seen some people improving 7 years off meds.

I know it sucks having these symptoms for such a long time but its nothing compared to trauma induced by severe kinetic accidents where people have such brain damage they are anhedonic for decades. They have such bad anhedonia they cannot even get the newspaper out of the mailbox. If breathing wasn't regulated by the parasympethic system they would've stopped breathing a long time ago.
Please do not belittle the struggles that the people in this thread are experiencing every day. This is a support group for people who are recovering from Invega and other related antipsychotics. You have not experienced this, so comments such as "it's nothing compared to xyz" are unhelpful, insensitive, and quite frankly, unasked for.

If anything those SSRI, anti-psychotics and COVID vaccines are far more dangerous than weed or CBD ever will be. People who have health problems should not get COVID vaccines that includes people who have impaired immune system caused by anti-psychotics. 1 out of 20 who take vaccines have severe side effects. People who take COVID mRNA vaccines have dramatic increase in contracting other COVID strains, 1 in 35 suffer from myocarditis. Neurologist already establish that vaccines can cause neurological damage. Effects of the COVID-19 vaccine include weakness, numbness, headache, dizziness, imbalance, fatigue, muscle spasms, joint pain, and restless leg syndrome are more common. Severe neurological complications included Bell's palsy, Guillain–Barre syndrome (GBS), stroke, seizures, anaphylaxis, and demyelinating syndromes such as transverse myelitis and acute encephalomyelitis. As cherry on top most people who took the vaccine have a higher degree of contracting long COVID

I remember some time ago you were anxious about people who wrote about not recovering, you said you needed to stop visiting the forum and how this forum makes you feel yet you believe big pharma lies and walk blindly without any negative emotions into getting a COVID-19 mRNA vaccine thinking it will help you. You don't have to get side effects immediately these neurological side effects can developed many years later
This thread is for the discussion of Invega and people's recovery after having Invega. Discussion of COVID-19 and COVID-19 vaccines is irrelevant and will be deleted. Here is a COVID-19 thread if you wish to discuss anything related to COVID-19:
https://bluelight.org/xf/threads/the-dives-covid-thread.920426/

Hi everyone, my name is All, I was forced to take Invega for (bruuh šŸ˜ž) 16 months..., While in the end I had no reason to take it, I have the same symptoms as you , total chemical lobotomy, apathy , anhedonia , it's been 9 months since I stopped them and for 5 weeks I have had some positive periods of a few minutes to sometimes a few hours of feeling pleasure, libido, love or sensation but it's still too little for my taste,I don't know if it's a sign of remission because I wonder if its bursts of positive feeling reach those who have not yet recovered, here I am starting to take amisulpride very low dose because it seems that it increases the levels and the quality of dopamine, I don't know if it's a good idea for me to take it, thank you for reading my experience and I hope we all get our lives back !
Hi and welcome to the thread ā¤ I'm so glad you're finally starting to notice some good signs of recovery! I actually don't know much about using amisulpride post-Invega so I will do some reading and get back to you...

I got a good vibrator with the help of my friends. I hope it will help me recover from PSSD.
This is great, and you've got some lovely friends ā¤ But be a little bit cautious about trying too hard or too frequently with the vibrator to get your normal function back. I'm speaking from experience as someone who also has a clit lol. And you may have already noticed this from your current experiences, that extended attempts at stimulating it can actually end up numbing it, like the nerve endings get overloaded/exhausted and just get tired and give up, kinda thing? Then you end up just really (REALLY!!) frustrated and upset. So maybe just try it oh I dunno, once a day, whenever your libido would normally peak (everyone is different, I'm actually a mid-afternoon person which is ummmm not convenient hahaha). But yeah, don't overload your clit.

2 months off and I’ve got my period back finally… yesterday I cried too. I hope this is a sign for recovery
This is great news on both counts!! Definitely signs of recovery ā¤
 
Hi and welcome to the thread ā¤ I'm so glad you're finally starting to notice some good signs of recovery! I actually don't know much about using amisulpride post-Invega so I will do some reading and get back to you...
oh great, that would be a great help to me because as my periods of feeling are too random, fluctuating and as I want to resume my life with my wife and feel my love for her again, I don't dare to wait any longer without doing anything, I just took amisulpride very low dose which according to my new psychiatrist (who is very dedicated to healing me without taking any risk)said it regulates dopamine in a way to regenerate potential emotional responses however I have still having trouble trusting psychiatrists and i dont know its is true and this medication suppresses the libido and so I can't know if it's worth continuing or if I try a natural cure, if you find something it would be a big help to me. valuable help thank you very much šŸ™šŸ˜Š
 
It's highly unlikely a low dose of amisulpride will increase dopamine. I don't see a low dose of amisulpride having any benefits if you're trying to recover from anti-psychotic neurotoxicity
indeed fortunately that you told me, you are probably right my doctor told me that it would increase transmission in certain areas but it seems more to be a type of dopaminergic modulator, which makes me think if I continue to use it take or not, thank you !
 
I don't think i'll heal. The way i just can't cry feels weird to me, like it's some kind of brain damage. I find it hard to believe i'll just wake up one day and regain my ability to cry out of nowhere. I can feel it in my skin that the damage is permanent.
 
I don't think i'll heal. The way i just can't cry feels weird to me, like it's some kind of brain damage. I find it hard to believe i'll just wake up one day and regain my ability to cry out of nowhere. I can feel it in my skin that the damage is permanent.

It’s painstakingly slow recovery , but you will recover.
 
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