I have read also that st johns wort helps break down invega faster. Although I don't know if that's true or not, a lot of people said it helped them.
There is a case report where they tryed that on a woman with paliperidone inside her body 2.5 years after last injection.
At first help reduce his paliperidone but when they stopped giving this, the paliperidone raised even more how it was before.
Is your fear based on data on how most people recover or just a fear inside you? Based on your experience, do most people fully recover?
We have to look aviable data: people complain for 1-2 years then they disappear, but, why?
Do they just give up and keep going with their damaged life? Do they fully recover and only the memories of what they go trough is traumatizing so they turn that page and never look back? Do they give up ending with suicide?
We don’t know what happen, we know that people who got only some injections just complain for 12-18 months then disappear.
I read a lots of posts where people saying creepy things like “you won’t never recover, but you can have a normal life” or “yes you will heal but you can have lifelong depression because your brain has permanentely damaged”
I also read a lots of topic where people say they recovered after 1 year, or after 14 months, or even after 17 months, one that I remember very well recovered after 22 months.
The fact that not a single health care professionel is telling us “yes you will recover, it just take 2 years” is creepy and we are almost panicking because of that and we fear it is permanent brain damage.
But if it’s permanent brain damage, where are all the people injected before us? Like those who got injected 3,4 or 5 years ago? They are no more complaining, why? They recovered? They suicide? They just accept the fact they had a damaged brain life and it’s ok for them?