Mental Health Coming off Invega (paliperidone) injections, v 5.0

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@Mick04 please remember that even though nearly everyone in this thread has experience with anti-psychotics, NONE OF US ARE DOCTORS. If someone tells you all anti-psychotics are bad just because they had an adverse reaction to some of them, please take that with a grain of salt. Invega appears to be the extreme of anti-psychotics that have negative side effects but there are other anti-psychotics out there that have helped people live fruitful, meaningful lives.

For myself, 17 years ago I was on Risperdal injections and later pills for a almost a year. I experience extreme anhedonia and was numb to the world. I had mild sexual dysfunction where I could orgasm but not ejaculate. It wasn't until I got placed on Abilify that my life came back. On the max dose of Abilify (30mg) I was able to complete a master's degree with a 3.8 GPA and work full time for many years after that. In the last few years before covid I was active in jiu jitsu, training about 3 days a week. I would have never had the energy to train martial arts if I were still on Risperdal.

My point is that we are all different and medications have different affects on each of us. If you were on Invega and it didn't work for you or if the side effects were too great, that doesn't mean that ALL anti-psychotics are evil. It just means you haven't found one that works for you yet. I'm not even saying Abilify is a magic pill that works for everyone. I am saying that because it worked for me, I am living proof that some anti-psychotics do work. We just have to give them time to work.
Thank you so much 🥺
 
I got through another day of training today. Wasn't as good as yesterday but still good enough & proud of myself for getting through the day. Last night I had really bad insomnia I couldn't get to sleep until midnight even though I went to bed at 10pm. I couldn't shut my mind off even though there's not much that goes on in there. I was trying not to let myself feel frustrated. I was still able to get up at 7:30 this morning okay enough but had no energy or motivation. I'm devestated because the unit I had my heart set on has been taken off the market today. It's really hard to find a good enough place at the right price, in a good enough area especially since I have 3 cats. So I'm frustrated because it's probably going to be a while before I come across another place I like. I wanted to do an exercise dvd again yesterday after work & really was going to but then it got too late & decided not to. I even had a tiny bit of motivation to do it. I was going to do it today but don't feel like it at all really & it's gotten too late again. I'm feeling abit blah I'm trying to stay positive but I just want to start losing weight & look like myself again & I want to find my own place again. I also really want to start feeling things again & feel the effects of coffee again
 
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What do people do when they have extreme anhedonia plus can't walk. I stay all day in bed but since I don't sleep that's really hard. I'm just all day with my suicidal thoughts
 
What do people do when they have extreme anhedonia plus can't walk. I stay all day in bed but since I don't sleep that's really hard. I'm just all day with my suicidal thoughts
I know it’s hard the anhedonia it will get better for you I just don’t know when everyone is different. What do you mean you can’t walk? Weakness in the legs? Loss of strength? If you can’t walk definitely sounds like me which is “drug induced parkinson” but I could be wrong which was the worse for me I couldn’t even stand up in the shower complete nightmare which takes awhile to improve but the good news is anhedonia and sleep will improve first. I haven’t forgot about making a new YouTube video I had to delay my leave into today was meant to be last week but working in a online delivery hub for a supermarket and Covid been a problem still and people needing to isolate for 7 days has been a nightmare so later today I’ll make a video and upload it. :)

It’s funny about two or so years so I got offered to take levodopa and carbidopa to help when I seen a specialist but I declined that. but it would be interesting to see if it did improve the symptoms of drug induced Parkinson’s but mmmmm.
 
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I know it’s hard the anhedonia it will get better for you I just don’t know when everyone is different. What do you mean you can’t walk? Weakness in the legs? Loss of strength? If you can’t walk definitely sounds like me which is “drug induced parkinson” but I could be wrong which was the worse for me I couldn’t even stand up in the shower complete nightmare which takes awhile to improve but the good news is anhedonia and sleep will improve first. I haven’t forgot about making a new YouTube video I had to delay my leave into today was meant to be last week but working in a online delivery hub for a supermarket and Covid been a problem still and people needing to isolate for 7 days has been a nightmare so later today I’ll make a video and upload it. :)

It’s funny about two or so years so I got offered to take levodopa and carbidopa to help when I seen a specialist but I declined that. but it would be interesting to see if it did improve the symptoms of drug induced Parkinson’s but mmmmm.
Weakness in the legs. I have to walk at small steps.

But what to do when you have severe anhedonia?

Looking forward watching your video
 
I know it’s hard the anhedonia it will get better for you I just don’t know when everyone is different. What do you mean you can’t walk? Weakness in the legs? Loss of strength? If you can’t walk definitely sounds like me which is “drug induced parkinson” but I could be wrong which was the worse for me I couldn’t even stand up in the shower complete nightmare which takes awhile to improve but the good news is anhedonia and sleep will improve first. I haven’t forgot about making a new YouTube video I had to delay my leave into today was meant to be last week but working in a online delivery hub for a supermarket and Covid been a problem still and people needing to isolate for 7 days has been a nightmare so later today I’ll make a video and upload it. :)

It’s funny about two or so years so I got offered to take levodopa and carbidopa to help when I seen a specialist but I declined that. but it would be interesting to see if it did improve the symptoms of drug induced Parkinson’s but mmmmm

I know it’s hard the anhedonia it will get better for you I just don’t know when everyone is different. What do you mean you can’t walk? Weakness in the legs? Loss of strength? If you can’t walk definitely sounds like me which is “drug induced parkinson” but I could be wrong which was the worse for me I couldn’t even stand up in the shower complete nightmare which takes awhile to improve but the good news is anhedonia and sleep will improve first. I haven’t forgot about making a new YouTube video I had to delay my leave into today was meant to be last week but working in a online delivery hub for a supermarket and Covid been a problem still and people needing to isolate for 7 days has been a nightmare so later today I’ll make a video and upload it. :)

It’s funny about two or so years so I got offered to take levodopa and carbidopa to help when I seen a specialist but I declined that. but it would be interesting to see if it did improve the symptoms of drug induced Parkinson’s but mmmmm.
Hi could you please tell me your youtube channel or link me your videos? I would love to see them. Cheers!
 
Sorry. Just i tried 4 antipsychotics now. Seroquel being the last one and it didnt work out well for me. My next plan is to try rexulti as i have heard good things about that. I honestly would rather live med free then be on meds but my parents are forcing me to take meds. I dont know many ppl like you who are on an antipsychotic and feel fine on them. Most people just feel terrible on them.
No worries. I apologize if it seemed like I was coming down too hard on you. And I did not intend to minimalize the harm Invega has done to you and others in this thread. I have also seen in this thread that there is hope for people coming off Invega albeit sometimes it can take a while.

I agree with you that a lot of people feel terrible on APs. However I would also add that many of them, if they stick it out, can experience a reduction in side effects after enough time has passed. Not all, but many. Like I said before, we are all different and what works for one person may not work for another and vice versa. Although I think we can all agree that Invega is an exception and is quite awful.
 
Pff I'm still gutted theyve put me on antypsychotics. Normal people shouldn't have their dopamine receptors reduced if they don't fit the schizophrenia,bipolair disorder,etc diagnosis. To put a normal person who has nothing wrong with him suddenly on ap's. I'm actually jealous of the people who still have their thoughts,cognition,planning abilities,intelligence,etc

Even if I might/must be recovered, have improvemts for a part (its difficult to measure as I don't even remember how I felt before the ap's). I mean you ask: did I feel like this even before ap's, is it just the exam stress? Idk its definetely out of my system but I'm still worried if the ap's left me some after effects.

Even if I know can read again,watch video's there's still that 'ocd' in me who still doubts/asks if I'm FULLY recovered (which what you finally expect/want after the discontinuation). I mean I learned to drive a car recently and I drive great (compared to where I felt on ap's, but driving a car isn't difficult). I mean I see tons of evidence which might suggest Ive recovered but there theres that guilt/doubt in me which still convinced its all fake or that surely things have improved (due enough evidence/proof: eh reading,etc) but not like it was fully before Invega. I actually feel guilty, because you normally don't ever take ap's (if you're healthy) and should not feel what I felt.

Really you ask: is it the exams Just? Is it because I'm lonely? I mean the ap's shouldn't be on my mind. Also because of covid everything was closer, so you couldn't cope as before the pandemic (you werent as free as before, so you we where isolated).

I mean I feel the need to go out, to shop,to buy clothes (things which interesses me before Invega), but there's that guilt I shouldn't do that (Because of the exams too). Its like you get that dopamine again and suddenly should experience as the Invega stripped it out of me. But yeah I'm kinda homeschooled, and isolation doesn't do you good sometimes (its temporary I know that's what I remind myself)
End of the rant. Idk maybe writing it out kinda seems theurapheutic.

But idk might be the exam stress as I'm homeschooled and its different than normal school where you het help from teachers,etc I have to do shit alone.
 
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Does anyone else here struggle with showering? Before invega I always showered everyday sometimes twice a day I couldn't imagine going a day without showering. Now I can only shower every second day. Washing my hair is such a chore. When I was at my worst sometimes I went up to a week without washing my hair now I wash it every 4 days
 
Does anyone else here struggle with showering? Before invega I always showered everyday sometimes twice a day I couldn't imagine going a day without showering. Now I can only shower every second day. Washing my hair is such a chore. When I was at my worst sometimes I went up to a week without washing my hair now I wash it every 4 days
I had the same issue as you've described. I still struggle but at least I feel the motivation to do it. What I also felt was lack of caring in hair,looks,etc it was way less than before. I couldn't care if Ive showered or not, or did my Hair,etc
 
Today a sleep specialist told me I might not recover my sleep. I'm very depressed. Plus all my family think to blame xeplion for my state is psychosis.
I spend another day in bed. I want to die
 
What is going on with invenga effects after is off. All psychiatrists I know except one deny the possibility of those effects
Well, I suspect it’s because those psychiatrists aren’t educated in the severity of the possible side effects of antipsychotic withdrawal. You can google the side effects and there are several informative resources that show it is indeed from the Invega. This website here has a whole list of possible withdrawal symptoms you can show your psychiatrist if you need to.
https://psychscenehub.com/psychinsights/antipsychotic-withdrawal-syndrome-tapering/
If you scroll a ways down the page, you will find a helpful picture describing the withdrawal symptoms.
 
I'm 4 months off in 3 days. I know how hard it is. It's like a living nightmare. It's ruined everything it's also ruined my pyshical appearance so badly which makes everything else so much harder to deal with. I'd be able to deal with the side effects the not feeling hunger or tiredness & anhedonia so much better if it hadn't made me look like such a freak physically. I'm hiding away from the world because I look so horrible
I can relate to how you feel, Invega really distributed fat in disproportionate places. Around 13 months off is when I started doing 1 hour light walks and then 14 months I started doing the rowing machine 6 days a week. I know it sucks but you’ll get there eventually. It just is a very slow recovery process. I remember being worried it would last forever but it’s slowly recovering now and will keep getting better. You have hope, you will make progress. Sending you healing vibes and positivity.
 
Hi @Kaatrina Thank you so much for posting an update! It's great to hear from you, and so good to hear you're doing so well! There are a few people in this thread who are really struggling at the moment so I really hope they can find hope from your experiences <3
I’d like to be a beacon of light and hope for those of you struggling through this…keep going it is hard it is brutal but you will make progress and you will recover. I cannot guarantee you a specific timeframe but for myself I’m approaching 15 months off the Invega Injection and am still making slow but sure recovery. It will happen for you too…sending healing love and positive vibes to everyone in here. Keep fighting…each day that passes is one more day closer to the victory. Not if, but when. You are all champions.
 
Well, I suspect it’s because those psychiatrists aren’t educated in the severity of the possible side effects of antipsychotic withdrawal. You can google the side effects and there are several informative resources that show it is indeed from the Invega. This website here has a whole list of possible withdrawal symptoms you can show your psychiatrist if you need to.
https://psychscenehub.com/psychinsights/antipsychotic-withdrawal-syndrome-tapering/
If you scroll a ways down the page, you will find a helpful picture describing the withdrawal symptoms.
It is not the withdrawal, I had the effects while being under the medication. I was forced by my family to get injections and now they think I am psychotic for blaming a good medicine
 
Did you see the post I found of a list of people who have recovered it says how many shots they had & how long it took to recover? It's got links to their profiles so you can look at all their previous posts. There's people on the list who have had 6 shots
I’ve had 7 shots and still recovering slowly at month 15 of no injections.
 
It is not the withdrawal, I had the effects while being under the medication. I was forced by my family to get injections and now they think I am psychotic for blaming a good medicine
Yes the effects while under the medication are very similar to when coming off the medication. The medication can also cause something called tardive psychosis which you may want to google. Are you still on the medication?
 
I had the same issue as you've described. I still struggle but at least I feel the motivation to do it. What I also felt was lack of caring in hair,looks,etc it was way less than before. I couldn't care if Ive showered or not, or did my Hair,etc
Yeah I can relate…it has to do with the blockage of dopamine in the brain. Sometimes I would take hot baths and it took every ounce of my strength and willpower just to be able to get out. It will improve just is a very slow process.
 
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