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Coming off Invega/Xeplion (paliperidone) injections v11

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twinpeaks123 said:
this sounds cringe but before invega, I had plans to improve my appearance and just look amazing in general, invega has now put these plans on hold

I could have done so much in 9 months-12 months, fuck invega and fuck psychiatry
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I had plans to transition to ultramarathon running, working more,finishing my book ..invega put me on the bed
 
lukeflowz said:
Guys is it normal for me to not feel much difference in just a little over 3.5 months. My akathisia is gone, but I still have the mental agony and anhedonia. I feel pretty much the same as when I was on the injections. Is there any hope for me ?
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I have been told by three people that month 2 to 6 is the worst for people who recover. I have seen some say they start to feel better after month 6, some after month 8 and later. I myself feel like its getting worse but hope to feel better by month 8. Make sure you stay as active as possible, drink lots of water and fluids, stay as busy as you can.
 
RisperdalConsta50mg said:
I came to read a Reddit post where someone says that if you don’t recover in 2 years (24 months) and you report that here into bluelight, then the moderators just ban you, is that true?
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Ask a moderator like @paranoid android . I thought it was a good thing that there are barely any members here over 2 years old, unless they are kind enough to come back to share their recovery stories. I myself am curious to know what happened to the members who used to be active here over 2 or 3 years ago. If they left because they recovered and moved on in their lives, that is good news, but if they just commited suicide or gave up coming here, i would like to know that too. Although i have spoken to several members who didnt fully recover even after 2 years. I really hope everyone i have spoken to here is recovered before 2 years.
 
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anonymoususer777 said:
Ask a moderator like @paranoid android . I thought it was a good thing that there are barely any members here over 2 years old, unless they are kind enough to come back to share their recovery stories. I myself am curious to know what happened to the members who used to be active here over 2 or 3 years ago. If they left because they recovered and moved on in their lives, that is good news, but if they just commited suicide or gave up coming here, i would like to know that too. Although i have spoken to several members who didnt fully recover even after 2 years. I really hope everyone i have spoken to here is recovered before 2 years.
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I don’t think someone who is not recovered just give up and stop to post about and just “take it”.. I don’t think everybody just suicide or learn to live with the disfunction without complaining.. But I can’t process how someone (like me) can have sympthoms for like 17 months or more but then out of nowhere start to recovering.. Idk, i don’t think biology work like that
 
RisperdalConsta50mg said:
I don’t think someone who is not recovered just give up and stop to post about and just “take it”.. I don’t think everybody just suicide or learn to live with the disfunction without complaining.. But I can’t process how someone (like me) can have sympthoms for like 17 months or more but then out of nowhere start to recovering.. Idk, i don’t think biology work like that
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Maybe just like most people who cant process how they can have symptoms for 6 to 8 months than feel better. Right now myself and many others do not think recovery is possible. I dont know where the person who used to exist before invega has disappeared. I am feeling worse daily only hoping that i will recover.

In your case, sleep is important for recovery so get some sleep aids.
 
7 months no sign of recovery,I'm in constant pain. Brain is constantly blank. Why this unnecessary suffering? Why? I need a solution
 
anonymoususer777 said:
Ask a moderator like @paranoid android . I thought it was a good thing that there are barely any members here over 2 years old, unless they are kind enough to come back to share their recovery stories. I myself am curious to know what happened to the members who used to be active here over 2 or 3 years ago. If they left because they recovered and moved on in their lives, that is good news, but if they just commited suicide or gave up coming here, i would like to know that too. Although i have spoken to several members who didnt fully recover even after 2 years. I really hope everyone i have spoken to here is recovered before 2 years.
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How many of those people took 1 injection. Did they recover after a single one?
 
anonymoususer777 said:
Maybe just like most people who cant process how they can have symptoms for 6 to 8 months than feel better. Right now myself and many others do not think recovery is possible. I dont know where the person who used to exist before invega has disappeared. I am feeling worse daily only hoping that i will recover.

In your case, sleep is important for recovery so get some sleep aids.
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I already had sleep issues and insomnia before tinnitus came out, now it’s basically impossible to sleep due to tinnitus
 
RisperdalConsta50mg said:
I already had sleep issues and insomnia before tinnitus came out, now it’s basically impossible to sleep due to tinnitus
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Was the tinnitus in both ears, or just one? In the case of the latter, you should have sought steroid treatment as that can sometimes be effective, but there's no guarantee. Ask me how I know. Menieres since early 2020, hearing changes since late 2020, and getting worse. Slowly.

Do you think the tinnitus was caused by the invega or by something else like a virus or loud noise exposure?
 
Finally my hellish Invega symptoms seem to be coming to a close. A lot of these were triggered by Vraylar, but still... *in addition to.

As I've learned though, it seems healing from Invega is a lifelong process and as I've said before, recovery is something you decide yourself.
 
Flynnal said:
Was the tinnitus in both ears, or just one? In the case of the latter, you should have sought steroid treatment as that can sometimes be effective, but there's no guarantee. Ask me how I know. Menieres since early 2020, hearing changes since late 2020, and getting worse. Slowly.

Do you think the tinnitus was caused by the invega or by something else like a virus or loud noise exposure?
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My tinnitus is caused by receptors upregulation or downregulation or hypersensivity or sensivity deficit, never had tinnitus in my whole life
 
iridescentblack said:
Finally my hellish Invega symptoms seem to be coming to a close. A lot of these were triggered by Vraylar, but still... *in addition to.

As I've learned though, it seems healing from Invega is a lifelong process and as I've said before, recovery is something you decide yourself.
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Be more clear and explicit, what do you mean?
 
RisperdalConsta50mg said:
I came to read a Reddit post where someone says that if you don’t recover in 2 years (24 months) and you report that here into bluelight, then the moderators just ban you, is that true?
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Probably not. There was one dude named Believeingod123 who got banned for excessively pushing the idea we’re all permanently damaged + consistently starting disagreements with others. Aside from him, I don’t know of anyone who got banned from this thread.
 
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