Mental Health Coming off Invega Sustenna (Paliperidone) v3

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You were just really lucky. A year after one shot and I haven't seen a single fractal
Can you explain what you mean by this? Are you able to feel high off of substances? The MDMA trip i had was quite amazing and I’ve been feeling less of a depression since then. Then again I was actually extremely schizophrenic before the shot. Like I could’ve literally gotten shot once from jumping onto some guys truck while he was at a red light at night. All he did was yell at me while i was in the middle of a breakdown. The Invega cured my psychosis fortunately.
 
Hello all! Again, I am excited to report good news. For some reason today waking up I feel like my normal self pre-psychosis and pre-Invega. It has been about 2 months exactly since my last shot (I’ve had 4 high dose shots; I needed them!). Anyway after supplementing with L-Dopa, Ashwaganda, and using nicotine and having an MDMA experience a few days ago, I literally am feeling great in this moment. It is a sunny day and I actually feel like socializing with people. ESPECIALLY you all who have been going through Hell. I’m not sure what is causing an early recovery for me. I am going to assume it is because I was a legitimate schizophrenic before the shots and now after 2 months my brain has finally stabilized itself. It feels great not having my life ruled by fucking psychosis. And when I tell you I had horrible psychosis it was HORRIBLE. I’m having self love and I looked in the mirror today and felt great about how I look. I want to tell you guys that it does get better; however! Not for everyone. During my worst times I was indulging in heavy Invega research. And to be honest not everyone recovers. With that being said I’d like to applause those who made it through this. I feel like I have maybe a month or so left until I’m back to how I need to be. Some people don’t want to hear this but the Invega helped me in the long run. I really could’ve gotten myself killed during my psychosis. I love you all and stay strong.
 
Nice to read thanks for sharing. 😃
I’ve felt like how your feeling for a while now almost 6 months off. Still have intense muscle stiffness, frequent urination, 2-3hr sleep increments tho. That’s what makes me moody/depressed sometimes. Hoping it will pass, hurts to stand for long periods of time, walking is uncomfortable.
 
Nice to read thanks for sharing. 😃
I’ve felt like how your feeling for a while now almost 6 months off. Still have intense muscle stiffness, frequent urination, 2-3hr sleep increments tho. That’s what makes me moody/depressed sometimes. Hoping it will pass, hurts to stand for long periods of time, walking is uncomfortable.
Thank you for the reply! Fortunately I’ve experienced none of these side effects. I am going to try a jog in a few moments. I’ve noticed that my body did feel lopsided and jogging was something I was unable to do properly just a few weeks ago and that annoyed me. As well as working out, it just didn’t feel natural. It could be muscle stiffness in my case too now that I think about it.
 
Thank you for the reply! Fortunately I’ve experienced none of these side effects. I am going to try a jog in a few moments. I’ve noticed that my body did feel lopsided and jogging was something I was unable to do properly just a few weeks ago and that annoyed me. As well as working out, it just didn’t feel natural. It could be muscle stiffness in my case too now that I think about it.

please share your developments, a day or two following the shot I developed a pinched back and became lopsided walking, really bad, like hobbling. That improved a couple days later but not fully, now my right leg feels or is short where before I was grounded what felt perfectly. This in combination with the back stiffness has been a death sentence to my athletic life. Would run/soccer/hike everyday. I think it all stems from the back stiffness. My analysis is basically my back was unique due to soccer and the invega has told it to behave differently in some capacity and it’s not liking it and stiff as a result.
 
Hello all. Today I am feeling a little better than yesterday, which is pretty good. I’ve been only 2 months off of the medication and I am seeing a speedy recovery fortunately. My emotions have finally returned as of a few days ago after my MDMA experience. I believe this has contributed a lot to my recovery as well as supplementing with Ashwaganda and L-Dopa. I still lack motivation in some areas as well as the inability to maintain proper sexual health. I am hoping that this will fade eventually. I have also noticed that I no longer have the will to work out as much as I used to, but these are minor issues compared to my behavior pre-Invega. I am grateful for my experience as it was rough and taught me a lot about my condition in return. I do believe that many times with other victims of Invega it depends on your initial frequency of dopamine and serotonin production that dictates recovery. I am not at my fullest, however I am recovering. A month ago I literally felt dead and wanted to off myself nearly everyday. Is there anything anyone can recommend for the recovery of sexual functions?
 
Hey has anyone tried a dopamine receptor agonist?

It looks as to do the exact opposite of a dopamine antagonist like Invega.

Something like pramipexole? Any thoughts can anyone chime in? I’ve been reading the user reviews tho and there are a lot of stories of this drug causing major problems... the l-dopa seems more safe.
 
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Hello all. Today I am feeling a little better than yesterday, which is pretty good. I’ve been only 2 months off of the medication and I am seeing a speedy recovery fortunately. My emotions have finally returned as of a few days ago after my MDMA experience. I believe this has contributed a lot to my recovery as well as supplementing with Ashwaganda and L-Dopa. I still lack motivation in some areas as well as the inability to maintain proper sexual health. I am hoping that this will fade eventually. I have also noticed that I no longer have the will to work out as much as I used to, but these are minor issues compared to my behavior pre-Invega. I am grateful for my experience as it was rough and taught me a lot about my condition in return. I do believe that many times with other victims of Invega it depends on your initial frequency of dopamine and serotonin production that dictates recovery. I am not at my fullest, however I am recovering. A month ago I literally felt dead and wanted to off myself nearly everyday. Is there anything anyone can recommend for the recovery of sexual functions?

My body didn’t produce semen until about 4 months later. I produce about 1/10th of what I use to produce and besides that my fluid is mostly water. On the bright side it appears I still qualify to create a child. As a side note I don’t recommend masterbating I don’t think this will help only weaken you.

I have a feeling running may help with all things.

What brought you to Ashwaganda and L-Dopa and can you say you noticed a difference or was it mostly just a “why not” decision. What about a dopamine agonist? Thoughts?
 
Hey has anyone tried a dopamine receptor agonist?

It looks as to do the exact opposite of a dopamine antagonist like Invega.

Something like pramipexole? Any thoughts can anyone chime in? I’ve been reading the user reviews tho and there are a lot of stories of this drug causing major problems... the l-dopa seems more safe.

Yes. I tried many times. So did almost anybody else who knew something about invega being a dopamine antagonist and was desperate for an antidote.

I tried acid and plant based psychs. Acid didn't do anything at all, not even pupil dilation. Plant based psychs I tried gave me all the effects of plant based psychedelics like nausea, respiratory depression, but made me drowsy while I was on them. No visuals, no crazy thinking, no deep thinking, no euphoria.
Invega does increase blood pressure and affects heart rate, as do most dopamine agonists. Therefore, the combination is unsafe physically or at least unpredictable. For the record, when I did try pharmaceutical dopamine agonists, and not psychedelics, they only slightly energized me, and they only helped in canceling out the sexual side effects by a very small amount. However, I did feel a lot worse the following day, as my dopamine receptors were being overworked.

Let me tell you, the best way to deal with it is to just not touch the dopamine receptors at all. Slowly forge new connections. It'll be hard, but you have to recondition yourself physically.

Exercise as your body allows to help rid yourself of it faster. Drink lots of water. Water dilution helped me a lot. I went to a hospital and got IVs done to restore fluid, and the docs said it was the best safest thing they could do. Follow the rules of drug detox diets, because that's exactly what this is.
 
Yes. I tried many times. So did almost anybody else who knew something about invega being a dopamine antagonist and was desperate for an antidote.

I tried acid and plant based psychs. Acid didn't do anything at all, not even pupil dilation. Plant based psychs I tried gave me all the effects of plant based psychedelics like nausea, respiratory depression, but made me drowsy while I was on them. No visuals, no crazy thinking, no deep thinking, no euphoria.
Invega does increase blood pressure and affects heart rate, as do most dopamine agonists. Therefore, the combination is unsafe physically or at least unpredictable. For the record, when I did try pharmaceutical dopamine agonists, and not psychedelics, they only slightly energized me, and they only helped in canceling out the sexual side effects by a very small amount. However, I did feel a lot worse the following day, as my dopamine receptors were being overworked.

Let me tell you, the best way to deal with it is to just not touch the dopamine receptors at all. Slowly forge new connections. It'll be hard, but you have to recondition yourself physically.

Exercise as your body allows to help rid yourself of it faster. Drink lots of water. Water dilution helped me a lot. I went to a hospital and got IVs done to restore fluid, and the docs said it was the best safest thing they could do. Follow the rules of drug detox diets, because that's exactly what this is.

Thanks for sharing. Thoughts on Ashwaganda and L-Dopa specifically?

How did you manage the IVs at the hospital? How often and what did you figure they did? Were you having muscle tightness?

What drug detox do you recommend? What I’ve read is high in protein is good for dopamine problems. I’ve also noticed that my shits are so small compared to how they used to be it’s like my body is utilizing everything I eat intensively.. however I’m not as hungry as I used to be. Perhaps due mostly to my inability to excercise as often. This drug reminds me of one of those computer viruses that locks up your computer and stops you from doing anything except reinstalling windows.
 
Hey I have found an interesting but tough to read article regarding Paliperidone, how long it takes to release from the injection site and how long it can last in the system. It does seem to suggest levodopa helped. I think it’s worth a read and I have some questions if someone can please answer.



QUOTE:
Moreover, in our case, EPSs persisted for more than 6 months since the last injection, although the serum concentration of paliperidone was expected to gradually subside. PP is an insoluble ester of paliperidone and dissolves very slowly in the interstitial fluids at the site of injection; paliperidone enters the systemic circulation over an extended period of time (125–245 days).18 In addition, the serum half-life is relatively long, roughly 25–49 days.9 In the case of such extended-release medications, it is necessary to consider that they can persist in the body for approximately 4–5 times longer than their half-life, even after discontinuation. Therefore, considering previously reported data and our case report collectively, paliperidone could remain in the body after cessation of treatment, and this could cause persistent EPSs.

QUESTION 1: When it reads that the medication could persist 4-5 times longer than it’s half life is this suggesting that the medication is likely to be active for up to 4-5 times longer than the half life or that the half life estimate could be 4-5 times longer?

QUESTION 2: Considering the medication takes up to 125-245 days to release into the system might it be a good idea to have blood drawn via Chinese cupping on the injection site? Thoughts?


ARTICLE QUOTE: He exhibited hand tremors, lead-pipe rigidity, gait instability, sialorrhea, and oral dyskinesia, in addition to his severe hallucinatory delusions (PANSS score of 125, DIEPSS score of 22). Despite receiving no antipsychotics over the 6 weeks after admission, we observed no improvement in his EPSs (DIEPSS score of 21) and no improvement in his psychotic symptoms (PANSS score of 138). Therefore, we started levodopa at a dose that increased to 400 mg/d. After 1 month, the EPSs gradually improved (DIEPSS score of 13), so aripiprazole was started at 6 mg/d, and then increased to 18 mg/d, while actively monitoring EPSs for signs of deterioration. His psychotic symptoms gradually improved and EPSs did not worsen after 2 months (PANSS score of 88, DIEPSS score of 5). Finally, neither his EPSs nor symptoms had deteriorated over the following 6 months. His prognosis is demonstrated in Figure 1. Importantly, he had no the other side effects including liver/renal dysfunction.

QUESTION: Who has tried levodopa or L-dopa? Did it help with any side effects? How long did take? Side effects? Withdrawal?

My current reflection on all this...

My stance on this medicine is that it should not be injectable, enforced or extended release. If the individual commits a crime in psychosis prosecute him. If he recommits the same offence due to psychosis and not taking his medication prosecute him accordingly as a repeat offender. This idea that people should be in prisoned and forced to take medication that could significantly impact and reduce the quality of their life for any amount of time because they are acting bizarre or socially incoherent in my opinion is wrong and evil. Offer options and counselling and besides that leave people alone regardless of their clinically observed “mental illness”. I feel this way strongly because I believe there are non-pharma ways to combat mental illness and even without combatting I think in time it will resolve itself after the individual faces social fallout and personal difficulty and reflects. After medication I was still unstable it wasn’t until I literally sat in my bed in my own room alone and thought deeply about everything that I realized I was paranoid and unwell. No doctor helped me with that. In fact the doctors made me more stubborn and more resistant in general. I observed this same stubbornness and bitterness in others as well. You can’t force the truth. It doesn’t work that way.
 
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Can anyone speak to...

- Mucuna pruriens: Mucuna pruriens contains high levels of naturally occurring L-dopa, which is the precursor to dopamine.

- Rhodiola: exerts multiple effects on the central nervous system, including improving dopamine's stability and inhibiting dopamine reuptake
 
Thanks for sharing. Thoughts on Ashwaganda and L-Dopa specifically?

How did you manage the IVs at the hospital? How often and what did you figure they did? Were you having muscle tightness?

What drug detox do you recommend? What I’ve read is high in protein is good for dopamine problems. I’ve also noticed that my shits are so small compared to how they used to be it’s like my body is utilizing everything I eat intensively.. however I’m not as hungry as I used to be. Perhaps due mostly to my inability to excercise as often. This drug reminds me of one of those computer viruses that locks up your computer and stops you from doing anything except reinstalling windows.

I've tried ashwaganda. It helped reduce sexual sides, but on no other area.

I went to the ER because the invega shots gave me dystonia, restlessness, akathisia, etc. They question you on whether you're suicidal or hallucinating. They gave me iv fluids to dilute the invega from my system with water. It was just water really. They also gave me benadryl and lorazepam to cope. You never wanna take too much of either, they're just there when it gets too unbearable. Drink lots of water to dilute it tbh. I felt a huge difference for a few days after they rehydrated me. Force your brain to think by focusing on what you love to think about. Don't let your mind surrender. Also, a lot of nasty sides come from high blood pressure so hydration helps with that as well.

Careful with protein diets, it's super easy to put on weight with invega. I gained 40 pounds relatively quickly. It's harder to lose. Try high fiber diets so you poop a lot. Any low fat diet that makes you excrete and urinate should be good tbh.

Also, if it's killing your appetite instead of upping it like it should, that means you might have either a blood pressure thing, or an akathisia thing, or an anxiety thing on your hands. If it makes you feel like crawling out of your skin and agitated, you're getting akathisia, which is the worst. If you don't feel like eating because it's bringing you down then it's just anhedonia. I agree, it is like a virus, it usually makes you eat a lot, and fat tissue is what it binds itself to. Dangerous

For the ivs I made it clear to the docs that it was a physical issue, so they didn't bring out the psychiatrists,whixh would have sucked. Avoid telling them that the invega makes you wanna do things that will harm yourself or others, no matter how understandable it may seem, they'll tie it to your illness and shoot you up some more. Instead I kept a cool mindset. It cost me a lot though. Healthcare is expensive in America. Only had it done once.
 
I've tried ashwaganda. It helped reduce sexual sides, but on no other area.

I went to the ER because the invega shots gave me dystonia, restlessness, akathisia, etc. They question you on whether you're suicidal or hallucinating. They gave me iv fluids to dilute the invega from my system with water. It was just water really. They also gave me benadryl and lorazepam to cope. You never wanna take too much of either, they're just there when it gets too unbearable. Drink lots of water to dilute it tbh. I felt a huge difference for a few days after they rehydrated me. Force your brain to think by focusing on what you love to think about. Don't let your mind surrender. Also, a lot of nasty sides come from high blood pressure so hydration helps with that as well.

Careful with protein diets, it's super easy to put on weight with invega. I gained 40 pounds relatively quickly. It's harder to lose. Try high fiber diets so you poop a lot. Any low fat diet that makes you excrete and urinate should be good tbh.

Also, if it's killing your appetite instead of upping it like it should, that means you might have either a blood pressure thing, or an akathisia thing, or an anxiety thing on your hands. If it makes you feel like crawling out of your skin and agitated, you're getting akathisia, which is the worst. If you don't feel like eating because it's bringing you down then it's just anhedonia. I agree, it is like a virus, it usually makes you eat a lot, and fat tissue is what it binds itself to. Dangerous

For the ivs I made it clear to the docs that it was a physical issue, so they didn't bring out the psychiatrists,whixh would have sucked. Avoid telling them that the invega makes you wanna do things that will harm yourself or others, no matter how understandable it may seem, they'll tie it to your illness and shoot you up some more. Instead I kept a cool mindset. It cost me a lot though. Healthcare is expensive in America. Only had it done once.

Iinitially after the first shot I was barely walking like a crawl walk followed by drooling and tightness and pain in my neck. As well a pinch in my lower back. I felt like I had to pee so bad but it took my 10 minutes of trying before I could and sometimes I couldn’t and had to come back. Then walking improved to a lopsided shuffle which is where I’m at currently. It’s like an efficient shuffle, most people would probably just think that’s my normal gait before invega. Then I had akathisia bad, could not sit still had to constantly move, do push-ups, stretch, run, pace etc. That went away after 3 weeks but the pacing didn’t leave until 1 month after I missed my monthly injection.

I gained 30 lbs. I water fasted for 4 days and lost 10lb but then I got tinnitus as a result.

Considering all this were they still professionally allowed to continue to inject me?

Do you think the invega only affects the brain which then affects the body? Or do you think it also directly affects the body soft tissue?
 
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A 2 month recovery is possible. I feel totally normal now in every area. I woke up with the hardest boner just now and all I wanted to do was screw my girlfriend lol. I would say that as of now I’m completely recovered in my opinion. I also went through bouts of extreme motivation yesterday while working. I ran last night as well as my body felt normal. I’ve lost all the weight and the appetite. The only thing that is really different is that I no longer feel like doing drugs like I used to. I tried weed last night as well with some hash, I definitely got high but it really was just uninteresting. I’m funny and like talking to people again, my emotions are back. But also my horrible anxiety. I have an appointment in two days so I’m not tripping. Hoping for some buspar. I believe the supplements and the MDMA fixed me. I’m going to rinse wash and repeat today and I’ll let you guys know.
 
Iinitially after the first shot I was barely walking like a crawl walk followed by drooling and tightness and pain in my neck. As well a pinch in my lower back. I felt like I had to pee so bad but it took my 10 minutes of trying before I could and sometimes I couldn’t and had to come back. Then walking improved to a lopsided shuffle which is where I’m at currently. It’s like an efficient shuffle, most people would probably just think that’s my normal gait before invega. Then I had akathisia bad, could not sit still had to constantly move, do push-ups, stretch, run, pace etc. That went away after 3 weeks but the pacing didn’t leave until 1 month after I missed my monthly injection.

I gained 30 lbs. I water fasted for 4 days and lost 10lb but then I got tinnitus as a result.

Considering all this were they still professionally allowed to continue to inject me?

Do you think the invega only affects the brain which then affects the body? Or do you think it also directly affects the body soft tissue?

If you're on a court order they're legally permitted to keep injecting you in the United States. If not, they can still inject you if you signed a consent form. Never sign away your rights. Moreover, it becomes easier to sue your doctor for concealing side effects if you didn't sign what they made you sign.

Your medical team won't care if you gain weight or akathisia. They know it happens so frequently, but some are brainwashed into thinking they're doing you a favor. Others fear authority too much to question drugging you, some even know what they're doing but enjoy the money too much. Just pray for better times brother. Or have faith if you don't believe in prayer.

The body works by getting signals from the brain. Invega fries your dopamine receptors, which you need for a lot of activities, like smooth motor functions. It will diminish your ability to feel pleasure from orgasms, drugs, etc. You won't be able to learn if your brain doesn't reward you dopamine if you learn something new. In essence it retards you. But please don't let that drag you down. You have to remember it's not you. It's your meds that are doing that to you. It does get better.

Drooling, muscle stiffness, shuffling legs etc is all common with neuroleptics. You have to keep yourself distracted. Try to think, but don't be dragged down if you find yourself unable to think. Once you start getting better (usually a few months in, depending on how badly you were dosed) you should stop coming to this thread because it might trigger you into a negative spiral, unless you got a serious issue of course.

Above all, remember you're not alone. The shrinks are making a killing off forced drugging. I know that voluntary use of neuroleptics can have positive applications, but Invega literally lobbies to promote their drug, so people can have their lives ruined.
 
A 2 month recovery is possible. I feel totally normal now in every area. I woke up with the hardest boner just now and all I wanted to do was screw my girlfriend lol. I would say that as of now I’m completely recovered in my opinion. I also went through bouts of extreme motivation yesterday while working. I ran last night as well as my body felt normal. I’ve lost all the weight and the appetite. The only thing that is really different is that I no longer feel like doing drugs like I used to. I tried weed last night as well with some hash, I definitely got high but it really was just uninteresting. I’m funny and like talking to people again, my emotions are back. But also my horrible anxiety. I have an appointment in two days so I’m not tripping. Hoping for some buspar. I believe the supplements and the MDMA fixed me. I’m going to rinse wash and repeat today and I’ll let you guys know.

How much Ashwaganda and L-Dopa are you taking per day? What product?
 
Two articles worth reading...

First concerning Mucuna pruriens in great depth


Second concerning dopamine supplements...

 
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