- Joined
- Mar 26, 2015
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I want to clarify, first off, that I am pro-psychiatry. I believe psychiatry can be used to provide relief from many different things. Chronic fatigue (a disorder of both the body and the brain), depression (although I think most ADs should be pulled off the market. Wellbutrin is an example of a good one), ADHD (neurological disorder or not, the medications help people. It's too bad it gets diverted/abused sometimes. I have seen people's quality of life greatly improved because of those meds. The benefit of rxing them far outweighs the risks), anxiety (which ruins many people's lives and leaves them in torment, despite what society thinks), PTSD (as long as neuroleptics are not used. I can not believe they are but they are.), and many other things. It is my belief that psychiatry should ONLY be used to provide relief. To make people feel better.
Certain neuroleptics such as Zyprexa can be used to stop a psychotic episode. I'm not arguing against short term (1-2 weeks) use of neuroleptics to stop psychotic episodes if other options fail. Regrettably, other options are never considered thanks to the influence of companies like Johnson & Johnson.
I am making a case for why neuroleptics should be used as a last resort and should never be coerced or forced. I do believe benzos should be tried to stop the episode first. If a patient shows no psychosis after being calmed down with benzos, they should not be leaving the hospital having been coerced or forced into taking neuroleptics.
Now, psychosis aside: neuroleptics should NEVER be used as a maintenance drug for children diagnosed bi-polar. They should never be used on autistic children either. In my opinion, this is not just bad medicine. It is pure evil.
But what about lack of insight?
Lack of insight is not a good reason to torture someone.
I am going to make a case for why AOT (assisted outpatient treatment) is legalized torture.
I am going to list some of the effects of a popular neuroleptic called invega sustenne, which in it's depot form does not leave the patient's system for 4-8 months due to an incredibly long half-life. I do not call these side-effects because they are main effects of blocking dopamine and seratonin. Akithisia and severe depression are not SIDE effects of neuroleptics just like a mood lift and more energy are not SIDE effects of Wellbutrin.
These same effects are present with all neuroleptics, with abilify being the least tormenting.
Most of these effects do not manifest until 2-4 weeks into "treatment." The neuroleptics do not reach their full potential to do harm until around 6 months into treatment if what I read is correct.
They are forcing children to take this stuff, and sometimes even forcing parents to give it to them. Even in cases where no psychosis is present, just a diagnoses of bi-polar or autism. I will never understand why they are giving this stuff to autistic kids. That is not TREATMENT.
These drugs will invariably ruin a child's life.
These drugs are used long-term based on the dopamine hypothesis in cases of psychosis.
http://en.wikipedia.org/wiki/Dopamine_hypothesis_of_schizophrenia
"The excitatory neurotransmitter glutamate is now also thought to be associated with schizophrenia. Phencyclidine (also known as PCP or "Angel Dust") and ketamine, both of which block glutamate (NMDA) receptors, are known to cause psychosis at least somewhat resembling schizophrenia, further suggesting that psychosis and perhaps schizophrenia cannot fully be explained in terms of dopamine function, but may also involve other neurotransmitters.[24]
Similarly, there is now evidence to suggest there may be a number of functional and structural anomalies in the brains of some people diagnosed with schizophrenia, such as changes in grey matter density in the frontal and temporal lobes.[8] It appears, therefore, that there are multiple causes for psychosis and schizophrenia, including gene mutations and anatomical lesions.
Psychiatrist David Healy has argued that drug companies have inappropriately promoted the dopamine hypothesis of schizophrenia as a deliberate and calculated simplification for the benefit of drug marketing."
I agree with David Healy.
"Further experiments, conducted as new methods were developed (particularly the ability to use PET scanning to examine drug action in the brain of living patients) challenged the view that the amount of dopamine blocking was correlated with clinical benefit. These studies showed that some patients had over 90% of their D2receptors blocked by antipsychotic drugs, but showed little reduction in their psychoses. This primarily occurs in patients who have had the psychosis for ten to thirty years. At least 90-95% of first-episode patients, however, respond to antipsychotics at low doses and do so with D2 occupancy of 60-70%. The antipsychoticaripiprazole occupies over 90% of D2 receptors, but this drug is both an agonist and an antagonist at D2 receptors."
So slowing a person down, which benzos also do, can stop a psychotic episode. I agree with that. The problem is maintenance.
But let's say they are effective for preventing SOME relapses in SOME patients SOME times. Is it worth making the person live in torment against their will?
What about children who throw temper tantrums and the MANY other reasons neuroleptics are used, including autism of all things. Can the medical community at least agree that chemically inducing akathisia and severe depression is doing harm? Can the medical community agree that there are other options for how to deal with these problems?
I want you to be reminded that there are children in foster care who are receiving NO relief 24/7 from sever akathisia and severe chemically induced depression.
Then there are the side-effects. Those are really bad. You are probably aware of them. TD, heart problems, death, diabetes etc... But every drug has side-effects. That's why I chose to stick to the main effects.
Now, the UN did call for a ban on forced neuroleptics based on the fact that it is torture:
I would like to explain. I am not thinking that I will change the accepted norm within the profession. What I am hoping to do is get psychiatrists to personally reconsider prescribing or even forcing someone to take neuroleptics.
I have seen what these drugs do. They turn people into non-functional zombies with severe akathisia and severe depression - 24/7 with no relief. I hope some of you can at least agree that they should only be tried in the most extreme of circumstances, that they should not be forced on anyone (or at least on anyone who is not a danger), and that pharmaceutical companies are responsible for the slanted studies and extremely wide-spread use. They are giving kids with autism this stuff (risperadol for example). That is just evil. I don't donate anything to autism speaks anymore. They actually support this. They are torturing those children.
I hope I can at least get you to agree that they should never be used on CHILDREN, especially children who have no psychosis. Those poor kids, right now, are on drugs that chemically induce akathisia and severe depression. They will not get to have a childhood and their adult life will be ruined.
So please, reconsider before prescribing neuroleptics. Explain to the patient that it is not just "for clarity of thought" (that is an outright lie). Explain that the drug blocks dopamine and seratonin and explain to them what those things do in the brain.
Please, reconsider before going to get a court-order for a non-compliant patient. If that patient is not a danger to self or others (AS IN - NEVER ATTACKED ANYONE), please don't do it. Even if they are I am against it but please reconsider if they are not.
Neuroleptics are by far the most harmful psychiatric drugs on the market. They are serious business. They destroy lives and families. The benefits RARELY outweigh the risks, very rarely. Sometimes, maybe neuroleptics could truly be the only option. A complete and total last resort. But someone who has had a few non-violent delusions should not be tortured. Please reconsider.
Certain neuroleptics such as Zyprexa can be used to stop a psychotic episode. I'm not arguing against short term (1-2 weeks) use of neuroleptics to stop psychotic episodes if other options fail. Regrettably, other options are never considered thanks to the influence of companies like Johnson & Johnson.
I am making a case for why neuroleptics should be used as a last resort and should never be coerced or forced. I do believe benzos should be tried to stop the episode first. If a patient shows no psychosis after being calmed down with benzos, they should not be leaving the hospital having been coerced or forced into taking neuroleptics.
Now, psychosis aside: neuroleptics should NEVER be used as a maintenance drug for children diagnosed bi-polar. They should never be used on autistic children either. In my opinion, this is not just bad medicine. It is pure evil.
But what about lack of insight?
Lack of insight is not a good reason to torture someone.
I am going to make a case for why AOT (assisted outpatient treatment) is legalized torture.
I am going to list some of the effects of a popular neuroleptic called invega sustenne, which in it's depot form does not leave the patient's system for 4-8 months due to an incredibly long half-life. I do not call these side-effects because they are main effects of blocking dopamine and seratonin. Akithisia and severe depression are not SIDE effects of neuroleptics just like a mood lift and more energy are not SIDE effects of Wellbutrin.
- A Feeling of Restlessness with Inability to Sit Still -(Akitishia http://en.wikipedia.org/wiki/Akathisia#Drug-induced) This is so bad it leads to suicide in many cases.
- Severe depression - This is not like a normal depression. It is a chemically induced depression. http://en.wikipedia.org/wiki/Anhedonia Anhedonia is often called a negative symptom post-psychosis, but blocking dopamine and seratonin will chemically induce it. Many people report this to be so bad that they would rather die than continue to take neuroleptics. Many people on AOT orders HAVE committed suicide.
- Impaired thinking
- Extreme fatigue
- Sluggishness
These same effects are present with all neuroleptics, with abilify being the least tormenting.
Most of these effects do not manifest until 2-4 weeks into "treatment." The neuroleptics do not reach their full potential to do harm until around 6 months into treatment if what I read is correct.
They are forcing children to take this stuff, and sometimes even forcing parents to give it to them. Even in cases where no psychosis is present, just a diagnoses of bi-polar or autism. I will never understand why they are giving this stuff to autistic kids. That is not TREATMENT.
These drugs will invariably ruin a child's life.
These drugs are used long-term based on the dopamine hypothesis in cases of psychosis.
http://en.wikipedia.org/wiki/Dopamine_hypothesis_of_schizophrenia
"The excitatory neurotransmitter glutamate is now also thought to be associated with schizophrenia. Phencyclidine (also known as PCP or "Angel Dust") and ketamine, both of which block glutamate (NMDA) receptors, are known to cause psychosis at least somewhat resembling schizophrenia, further suggesting that psychosis and perhaps schizophrenia cannot fully be explained in terms of dopamine function, but may also involve other neurotransmitters.[24]
Similarly, there is now evidence to suggest there may be a number of functional and structural anomalies in the brains of some people diagnosed with schizophrenia, such as changes in grey matter density in the frontal and temporal lobes.[8] It appears, therefore, that there are multiple causes for psychosis and schizophrenia, including gene mutations and anatomical lesions.
Psychiatrist David Healy has argued that drug companies have inappropriately promoted the dopamine hypothesis of schizophrenia as a deliberate and calculated simplification for the benefit of drug marketing."
I agree with David Healy.
"Further experiments, conducted as new methods were developed (particularly the ability to use PET scanning to examine drug action in the brain of living patients) challenged the view that the amount of dopamine blocking was correlated with clinical benefit. These studies showed that some patients had over 90% of their D2receptors blocked by antipsychotic drugs, but showed little reduction in their psychoses. This primarily occurs in patients who have had the psychosis for ten to thirty years. At least 90-95% of first-episode patients, however, respond to antipsychotics at low doses and do so with D2 occupancy of 60-70%. The antipsychoticaripiprazole occupies over 90% of D2 receptors, but this drug is both an agonist and an antagonist at D2 receptors."
So slowing a person down, which benzos also do, can stop a psychotic episode. I agree with that. The problem is maintenance.
But let's say they are effective for preventing SOME relapses in SOME patients SOME times. Is it worth making the person live in torment against their will?
What about children who throw temper tantrums and the MANY other reasons neuroleptics are used, including autism of all things. Can the medical community at least agree that chemically inducing akathisia and severe depression is doing harm? Can the medical community agree that there are other options for how to deal with these problems?
I want you to be reminded that there are children in foster care who are receiving NO relief 24/7 from sever akathisia and severe chemically induced depression.
Then there are the side-effects. Those are really bad. You are probably aware of them. TD, heart problems, death, diabetes etc... But every drug has side-effects. That's why I chose to stick to the main effects.
Now, the UN did call for a ban on forced neuroleptics based on the fact that it is torture:
I would like to explain. I am not thinking that I will change the accepted norm within the profession. What I am hoping to do is get psychiatrists to personally reconsider prescribing or even forcing someone to take neuroleptics.
I have seen what these drugs do. They turn people into non-functional zombies with severe akathisia and severe depression - 24/7 with no relief. I hope some of you can at least agree that they should only be tried in the most extreme of circumstances, that they should not be forced on anyone (or at least on anyone who is not a danger), and that pharmaceutical companies are responsible for the slanted studies and extremely wide-spread use. They are giving kids with autism this stuff (risperadol for example). That is just evil. I don't donate anything to autism speaks anymore. They actually support this. They are torturing those children.
I hope I can at least get you to agree that they should never be used on CHILDREN, especially children who have no psychosis. Those poor kids, right now, are on drugs that chemically induce akathisia and severe depression. They will not get to have a childhood and their adult life will be ruined.
So please, reconsider before prescribing neuroleptics. Explain to the patient that it is not just "for clarity of thought" (that is an outright lie). Explain that the drug blocks dopamine and seratonin and explain to them what those things do in the brain.
Please, reconsider before going to get a court-order for a non-compliant patient. If that patient is not a danger to self or others (AS IN - NEVER ATTACKED ANYONE), please don't do it. Even if they are I am against it but please reconsider if they are not.
Neuroleptics are by far the most harmful psychiatric drugs on the market. They are serious business. They destroy lives and families. The benefits RARELY outweigh the risks, very rarely. Sometimes, maybe neuroleptics could truly be the only option. A complete and total last resort. But someone who has had a few non-violent delusions should not be tortured. Please reconsider.