I've entered the daytime treatment at the University Medical Centre of Groningen. I was very resistant at first, but now I'm getting the hang of it. The therapists are actually pretty good. The co-patients are nice. I like being part of a group; hanging out with people and having good conversations.
I've had an appointment with a p-doc and a doc-assistant. The p-doc was the guy in charge of the Anxiety & Compulsion department. He was a very friendly man. The doc-assistant was a sharp eyed woman whose look became more and more stern as I revealed the myriads of meds I've been trying, mostly on my lonely own.
I chose for complete honesty. It was a decision I made spontaneously in the beginning of our conversation, though several events had paved the way for it.
Indeed, their stance towards medications is that they prefer, ideally, to have a patient try cognitive behavioral therapy with exposure therapy first - without meds, and see how far he/she gets, and only then, if medication is still necessary, look at pharmacotherapy. The idea is that meds that help with anxiety undermine what exposure is all about: dealing with anxiety upfront, and learning to walk without crutches, so to speak. Nevertheless, they don't urge you to quit any medication right away; they are aware that quitting meds can cause withdrawal syndromes and that this should happen when someone is ready for it. So, in practice, they have people continue some of their meds, while urging them to taper off others.
Another stance that they have towards meds is that they think any med prescription should be 'evidence based', which means that they don't support off-label prescriptions. They only support prescribing a drug for the conditions for which it has been approved. They think this is the only truly scientific way of going about it.
I strongly disagree! The indications for which a med gets approved are often not based on sound science, but on the guesses of the pharmaceutical company that markets the med. A pharmaceutical company will try to market a drug for a certain condition and might not be interested to fund research after other applications. Moreover, at the time a drug gets approved, there is often very little known about its precise working mechanisms. In time, the knowledge about a drugs specific modes of action will grow, and these new discoveries may point to other applications than that for which the drug had first been approved. Then there are the many drugs who have run out of patent, and don't have million dollar companies behind them to further explore their possibilities.
The way I see it, only prescribing meds according to protocols means not looking at what a drug actually does, but only looking at what it has been approved for. This is not true science - this is submission to statistics! Submitting sound thinking to the power of the number - a power that has many stronger powers behind it and is influenced by these in very subjective ways.
I think one of the reasons why Dr. Stephen Stahl is such a brilliant psychiatrist is precisely because he doesn't just look at the numbers, but looks at what a drug actually does in the brain and in the body.
An example of the tension between true science and the subjective game of drug approvals is the fact that fluvoxamine, i.e. Luvox, has only been approved for OCD in the United States, but not for depression. Luvox though is an SSRI like any other, and can therefore be an effective antidepressant as well as an effective treatment for OCD. In most countries, Luvox is approved for both conditions. Would this mean that Luvox would help Dutch patients with depression, but can help Americans only with OCD? That is pure nonsense, of course.
Luvox can serve as a further illustration of my point. Years after Luvox had been approved for depression and(/or..) OCD, it has been discovered that the drug is a potent sigma-1 agonist. Sigma-1 receptors play a role in depression and anxiety, but also in delusions. One study explored the latter possibility and gave 300mg of Luvox to a group of patients with schizophrenia for an extended period of time. This high dose of Luvox appeared to be very effective for schizophrenia. But it's only one study; the drug is off patent, so there is no money to confirm these results with further research - Luvox' possible use as an antipsychotic med will probably never be exploited. And why not? Because people - meaning healthcare professionals! - don't look at what a drug actually does, but only look at the label.
The psychiatrist of the treatment centre wasn't too happy about most of the meds I take. The Zoloft (sertraline) was alright, since it has been approved for OCD.. I could continue taking it until I was ready to taper it down. The Buspar made them frown, since it has only been approved for General Anxiety Disorder, not for OCD.. The fact that it helps me is apparently not relevant! The Neurontin (gabapentine) puzzled them evn more. Is it the right med for the type of pain I have? The fact that even in small amounts it helps me tremendously with anxiety, is of no importance, since it hasn't been approved for anxiety disorders! Also, my TCA's didn't make them very merry. Later, when I thought about it, I figured I could have them support my amitriptyline (Elavil), since it has officially been approved for chronic pain.. Of course, amitriptyline would also help me with depression and anxiety. But that would be a counter-argument, since they don't want my meds to make my life too comfortable!
I hope you can see how debatable and far removed from real life their position is.
For now, they leave the pharmacotherapeutical responsiblity with my f-doc, with whom they want to discuss my medical regimen.
As for me, I know I am obsessed with meds, and I know my way of experimenting with meds is rather capricious. Still, I have great difficulty to submit to a professional view that is not mine and that I am very critical of.
I am still interested in 5HT2A/C-antagonism, of which I have talked here (and elsewhere) before. Servier's new drug agomelatine (Valdoxan) is a 5HT2C-antagonist, but only a rather weak one, it seems. Prozac is a pretty potent 5HT2C-antagonist, and I'm thinking of returning to low dose Prozac for this reason. Cyproheptadine, an old antihistaminergic drug, has my interest because it's a potent 5HT2A-antagonist and also a moderately strong 5HT2C-antagonist. Unlike amitriptyline, which is a much stronger antihistaminergic than a 5HT2A/C-antagonist, cyproheptadine's 5HT2A-antagonism is about as strong as its antihistaminergic properties.
I'm still taking amitriptyline (Elavil), and have upped my dose to 25mg, and more recently (yesterday) to 37.5mg. Amitriptyline offers both 5HT2A and -C antagonism (or -C partial agonism). It's too bad that it's such a strong antihistaminergic. I have noticed though that when I go up slowly, I quickly develop tolerance for the antihistaminergic sedation.
The Neurontin (gabapentin), as stated above, helps very well with anxiety. I have noticed no pain relief from it yet, though, and sometimes I even suspect it might paradoxically make my pain worse. I think I need to go to a higher dose to have a better idea of what it's doing.
I have now tried Valium (diazepam) three times, and boy, I love it. It's much less sedating than Ativan (lorazepam); it leaves my cognitive abilities mostly intact; it doesn't even seem to impair my memory (hardly any retrograde amnesia); and it gives me an antidepressant and anxiety-defeating boost. 'Mother's little helper' - indeed. Daddy likes it too.
But well, at the treatment centre - you may have guessed it - they're not too fond of benzo's.. No way they're gonna prescribe that, unless you're hooked already, in which case they're gonna make a plan for you to taper off. Hm, I've been honest, so I told them I have no physical dependence on benzo's..
Perhaps taking Valium daily for a prolonged period of time isn't a good idea anyway. Some people on some forums swear that long-term use of Valium will eventually make you more depressed. Anybody any comment on that? I should ask on the benzo board, I guess..
As for modafinil (Provigil), selegiline, amisulpride, piribedil.. I have only a couple of pills left. And I have no income at the moment. I'm parasitizing on my wife. Plus at the treatment centre, they want me to leave those drugs. Hm.
Well, that's all for now, folks. Feel free to ask any questions and give any feedback. Be gentle..
I've had an appointment with a p-doc and a doc-assistant. The p-doc was the guy in charge of the Anxiety & Compulsion department. He was a very friendly man. The doc-assistant was a sharp eyed woman whose look became more and more stern as I revealed the myriads of meds I've been trying, mostly on my lonely own.
I chose for complete honesty. It was a decision I made spontaneously in the beginning of our conversation, though several events had paved the way for it.
Indeed, their stance towards medications is that they prefer, ideally, to have a patient try cognitive behavioral therapy with exposure therapy first - without meds, and see how far he/she gets, and only then, if medication is still necessary, look at pharmacotherapy. The idea is that meds that help with anxiety undermine what exposure is all about: dealing with anxiety upfront, and learning to walk without crutches, so to speak. Nevertheless, they don't urge you to quit any medication right away; they are aware that quitting meds can cause withdrawal syndromes and that this should happen when someone is ready for it. So, in practice, they have people continue some of their meds, while urging them to taper off others.
Another stance that they have towards meds is that they think any med prescription should be 'evidence based', which means that they don't support off-label prescriptions. They only support prescribing a drug for the conditions for which it has been approved. They think this is the only truly scientific way of going about it.
I strongly disagree! The indications for which a med gets approved are often not based on sound science, but on the guesses of the pharmaceutical company that markets the med. A pharmaceutical company will try to market a drug for a certain condition and might not be interested to fund research after other applications. Moreover, at the time a drug gets approved, there is often very little known about its precise working mechanisms. In time, the knowledge about a drugs specific modes of action will grow, and these new discoveries may point to other applications than that for which the drug had first been approved. Then there are the many drugs who have run out of patent, and don't have million dollar companies behind them to further explore their possibilities.
The way I see it, only prescribing meds according to protocols means not looking at what a drug actually does, but only looking at what it has been approved for. This is not true science - this is submission to statistics! Submitting sound thinking to the power of the number - a power that has many stronger powers behind it and is influenced by these in very subjective ways.
I think one of the reasons why Dr. Stephen Stahl is such a brilliant psychiatrist is precisely because he doesn't just look at the numbers, but looks at what a drug actually does in the brain and in the body.
An example of the tension between true science and the subjective game of drug approvals is the fact that fluvoxamine, i.e. Luvox, has only been approved for OCD in the United States, but not for depression. Luvox though is an SSRI like any other, and can therefore be an effective antidepressant as well as an effective treatment for OCD. In most countries, Luvox is approved for both conditions. Would this mean that Luvox would help Dutch patients with depression, but can help Americans only with OCD? That is pure nonsense, of course.
Luvox can serve as a further illustration of my point. Years after Luvox had been approved for depression and(/or..) OCD, it has been discovered that the drug is a potent sigma-1 agonist. Sigma-1 receptors play a role in depression and anxiety, but also in delusions. One study explored the latter possibility and gave 300mg of Luvox to a group of patients with schizophrenia for an extended period of time. This high dose of Luvox appeared to be very effective for schizophrenia. But it's only one study; the drug is off patent, so there is no money to confirm these results with further research - Luvox' possible use as an antipsychotic med will probably never be exploited. And why not? Because people - meaning healthcare professionals! - don't look at what a drug actually does, but only look at the label.
The psychiatrist of the treatment centre wasn't too happy about most of the meds I take. The Zoloft (sertraline) was alright, since it has been approved for OCD.. I could continue taking it until I was ready to taper it down. The Buspar made them frown, since it has only been approved for General Anxiety Disorder, not for OCD.. The fact that it helps me is apparently not relevant! The Neurontin (gabapentine) puzzled them evn more. Is it the right med for the type of pain I have? The fact that even in small amounts it helps me tremendously with anxiety, is of no importance, since it hasn't been approved for anxiety disorders! Also, my TCA's didn't make them very merry. Later, when I thought about it, I figured I could have them support my amitriptyline (Elavil), since it has officially been approved for chronic pain.. Of course, amitriptyline would also help me with depression and anxiety. But that would be a counter-argument, since they don't want my meds to make my life too comfortable!
I hope you can see how debatable and far removed from real life their position is.
For now, they leave the pharmacotherapeutical responsiblity with my f-doc, with whom they want to discuss my medical regimen.
As for me, I know I am obsessed with meds, and I know my way of experimenting with meds is rather capricious. Still, I have great difficulty to submit to a professional view that is not mine and that I am very critical of.
I am still interested in 5HT2A/C-antagonism, of which I have talked here (and elsewhere) before. Servier's new drug agomelatine (Valdoxan) is a 5HT2C-antagonist, but only a rather weak one, it seems. Prozac is a pretty potent 5HT2C-antagonist, and I'm thinking of returning to low dose Prozac for this reason. Cyproheptadine, an old antihistaminergic drug, has my interest because it's a potent 5HT2A-antagonist and also a moderately strong 5HT2C-antagonist. Unlike amitriptyline, which is a much stronger antihistaminergic than a 5HT2A/C-antagonist, cyproheptadine's 5HT2A-antagonism is about as strong as its antihistaminergic properties.
I'm still taking amitriptyline (Elavil), and have upped my dose to 25mg, and more recently (yesterday) to 37.5mg. Amitriptyline offers both 5HT2A and -C antagonism (or -C partial agonism). It's too bad that it's such a strong antihistaminergic. I have noticed though that when I go up slowly, I quickly develop tolerance for the antihistaminergic sedation.
The Neurontin (gabapentin), as stated above, helps very well with anxiety. I have noticed no pain relief from it yet, though, and sometimes I even suspect it might paradoxically make my pain worse. I think I need to go to a higher dose to have a better idea of what it's doing.
I have now tried Valium (diazepam) three times, and boy, I love it. It's much less sedating than Ativan (lorazepam); it leaves my cognitive abilities mostly intact; it doesn't even seem to impair my memory (hardly any retrograde amnesia); and it gives me an antidepressant and anxiety-defeating boost. 'Mother's little helper' - indeed. Daddy likes it too.
But well, at the treatment centre - you may have guessed it - they're not too fond of benzo's.. No way they're gonna prescribe that, unless you're hooked already, in which case they're gonna make a plan for you to taper off. Hm, I've been honest, so I told them I have no physical dependence on benzo's..
Perhaps taking Valium daily for a prolonged period of time isn't a good idea anyway. Some people on some forums swear that long-term use of Valium will eventually make you more depressed. Anybody any comment on that? I should ask on the benzo board, I guess..
As for modafinil (Provigil), selegiline, amisulpride, piribedil.. I have only a couple of pills left. And I have no income at the moment. I'm parasitizing on my wife. Plus at the treatment centre, they want me to leave those drugs. Hm.
Well, that's all for now, folks. Feel free to ask any questions and give any feedback. Be gentle..
18 Comments On This Entry
Page 1 of 1
therapeuticbrigg84
02 October 2009 - 11:20 AM
I def agree with you on disagreeing with their offlabel drug position. many drugs have been used on me, that have been used offlabel, that were successful, and many drugs that have been made used specifically for the diagnosis I have, but tended not to work.
I'm still looking for a drug that can help with my med related akathesia, or restlessness. I never was really that restless until I started medication. and now i have dropped many a drug because of this restlessness, it started when i was on zyprexa combined with lexapro. and continued on to seroquel, and eventually abilify, which made me go crazy restless for about 3 weeks. the only med that seems to help with it is the gabapentin-which has given me side effects(weight gain) from which i discontinued the drug for. and the other drug artane has helped but it also has weird side effects, especially when i discontinue the drug after using it successfully for a few days.
yeah my aunt frowns upon my buspar and gabapentin taking too. sometimes i think wouldnt it be better to not be on an SSRI, and be dependent on benzos for my anxiety, since ssris numb you for a longer period of time anyways.
dont they realize that anxiety is tied into depression, so that you should be able to use the buspar-even though many deem the drug ineffective. but since it is deemed ineffective they should probably let you use it for anxiety, since if it doesnt work, youll still have anxiety.
yeah i would like the answer to the valium question too, since whenever i take it, i liked it, and ativan sucks, so does klonopin.
I'm still looking for a drug that can help with my med related akathesia, or restlessness. I never was really that restless until I started medication. and now i have dropped many a drug because of this restlessness, it started when i was on zyprexa combined with lexapro. and continued on to seroquel, and eventually abilify, which made me go crazy restless for about 3 weeks. the only med that seems to help with it is the gabapentin-which has given me side effects(weight gain) from which i discontinued the drug for. and the other drug artane has helped but it also has weird side effects, especially when i discontinue the drug after using it successfully for a few days.
yeah my aunt frowns upon my buspar and gabapentin taking too. sometimes i think wouldnt it be better to not be on an SSRI, and be dependent on benzos for my anxiety, since ssris numb you for a longer period of time anyways.
dont they realize that anxiety is tied into depression, so that you should be able to use the buspar-even though many deem the drug ineffective. but since it is deemed ineffective they should probably let you use it for anxiety, since if it doesnt work, youll still have anxiety.
yeah i would like the answer to the valium question too, since whenever i take it, i liked it, and ativan sucks, so does klonopin.
bengaltiger
02 October 2009 - 12:30 PM
Hey, good to see you. I would not be able to tolerate those types of rules/restrictions. Sort of counterproductive of them to be so rigid, imho. It would be difficult for me to put up with what you're going through there.
Your dr. bob post/thread was excellent. I like that website, but it is not the easiest to navigate. You made mention of not being too fond of cymbalta. May i ask why? Was it simply the cymbalta/geodon combo, or is there another reason for your dislike? I know the price is obscene.
How are you faring on the zoloft? Is it keeping the depression/ocd at bay at your dose? You talk quite a bit about prozac in dr. bob's post also; having some interesting pharmacodynamics. Do you prefer one med over the other? Does one need to get to the higher doses of zoloft to get any dopamine reuptake inhibition or does that begin at the low doses too?
May i ask why you stopped the risperdal .5 mg if it was giving you a pro-dopamine boost? I hope you are doing well, my friend......in spite of the shackles you now are forced to wear...
P.S.... is the nortriptyline giving you a good night sleep?
Can you believe that guy who had his pdoc give him geodon for adhd????.........is it me or is that a bit out of the ordinary?
Your dr. bob post/thread was excellent. I like that website, but it is not the easiest to navigate. You made mention of not being too fond of cymbalta. May i ask why? Was it simply the cymbalta/geodon combo, or is there another reason for your dislike? I know the price is obscene.
How are you faring on the zoloft? Is it keeping the depression/ocd at bay at your dose? You talk quite a bit about prozac in dr. bob's post also; having some interesting pharmacodynamics. Do you prefer one med over the other? Does one need to get to the higher doses of zoloft to get any dopamine reuptake inhibition or does that begin at the low doses too?
May i ask why you stopped the risperdal .5 mg if it was giving you a pro-dopamine boost? I hope you are doing well, my friend......in spite of the shackles you now are forced to wear...
P.S.... is the nortriptyline giving you a good night sleep?
Can you believe that guy who had his pdoc give him geodon for adhd????.........is it me or is that a bit out of the ordinary?
therapeuticbrigg84
02 October 2009 - 05:43 PM
who the hell is dr bob? i dont know dr bob.
my name is bob but not doctor bob
my name is bob but not doctor bob
bunnyrabbit
03 October 2009 - 07:51 AM
I think the only explination for Luvox and Schizophrenia is the Sigma receptor it hits. There is a line of trial medications aimed at hitting that receptor to reduce psychosis. I noticed a difference actually, but it made me crazy. The only other SSRI to hit that receptor, though more lightly, is Zoloft. I took that for a number of years.
therapeuticbrigg84
03 October 2009 - 02:33 PMBrainbeard, on Sat 3 October 2009 6:13:05 GMT +0000, said:
Right now I'm not taking any nortriptyline directly. I take its mother drug, amitriptyline, and yes, the amitriptyline sure helps with sleep.
Geodon for ADHD... It might work. Anything might work, anything might fail. I looked at the side-effects of Neurontin yesterday with my f-doc, and we saw that it can cause depression and anxiety. He made the sobering remark that most psychotropic meds can cause precisely the symptoms that people are taking them for.
Cheers,
BB
Geodon for ADHD... It might work. Anything might work, anything might fail. I looked at the side-effects of Neurontin yesterday with my f-doc, and we saw that it can cause depression and anxiety. He made the sobering remark that most psychotropic meds can cause precisely the symptoms that people are taking them for.
Cheers,
BB
yeah i thought he was talking to me when talking about nortriptyline, cause i mentioned i was taking it, but maybe he got confused.
and also i was hoping someone would answer my restlessness(akathesia) problem. i suppose i could order some piribedil for that, as it's a dopamine type drug, but not too sure.
bengaltiger
04 October 2009 - 10:58 AM
Hi BB,
I understand what you mean when speaking of the comraderie you have developed with the other patients at the treatment center. The understanding of others in the same boat is a powerful boost.
When you mentioned possibly returning to prozac at low dose, just how low did you mean? For me, I can live with a little of the ocd/anxiety....but the depression is a bear. That is not something so easily tolerated.
Glad you are having success with the elavil. So now at 37.5 mg, you are having almost no problems with the antihistaminergic se's? Excellent. My only issue with that med is the side effects. I am due to begin desipramine, and i am concerned with the tca side effects. My pdoc is sharp, and believes that it is a potent, effective med. If it had some type of dopamine action, that would be even better...
. Do you have any thoughts regarding desipramine?
Speaking of valium, i use it, and have no problems. I take it as directed; less if possible to keep my tolerance low...therefore making it more effective when i need it.
About the risperdal 5mg, if not for the hyperprolactenamia, would you be inclined to take it? My pdoc says it also serves very well in keeping the ruminations at bay. Have you actually tried it? My only drawback would be any emotional flattening/dulling that would occur. Is that likely at only .5mg dose?
Take care, my friend. Hope you continue to be well....
Bengaltiger...
I understand what you mean when speaking of the comraderie you have developed with the other patients at the treatment center. The understanding of others in the same boat is a powerful boost.
When you mentioned possibly returning to prozac at low dose, just how low did you mean? For me, I can live with a little of the ocd/anxiety....but the depression is a bear. That is not something so easily tolerated.
Glad you are having success with the elavil. So now at 37.5 mg, you are having almost no problems with the antihistaminergic se's? Excellent. My only issue with that med is the side effects. I am due to begin desipramine, and i am concerned with the tca side effects. My pdoc is sharp, and believes that it is a potent, effective med. If it had some type of dopamine action, that would be even better...
Speaking of valium, i use it, and have no problems. I take it as directed; less if possible to keep my tolerance low...therefore making it more effective when i need it.
About the risperdal 5mg, if not for the hyperprolactenamia, would you be inclined to take it? My pdoc says it also serves very well in keeping the ruminations at bay. Have you actually tried it? My only drawback would be any emotional flattening/dulling that would occur. Is that likely at only .5mg dose?
Take care, my friend. Hope you continue to be well....
Bengaltiger...
therapeuticbrigg84
04 October 2009 - 03:02 PM
one note:
lexapro 10 mg = prozac 20 mg.
and i also heard that the lowest available dose of prozac is like 10 mg. and 20 mg prozac is the therapeutic dosage. so sure you can try 5 mg supposedly, but it may not do much just like 5 mg of lexapro, doesnt really do much either.
lexapro 10 mg = prozac 20 mg.
and i also heard that the lowest available dose of prozac is like 10 mg. and 20 mg prozac is the therapeutic dosage. so sure you can try 5 mg supposedly, but it may not do much just like 5 mg of lexapro, doesnt really do much either.
therapeuticbrigg84
05 October 2009 - 10:54 AM
ok, well ill admit, i had been on lexapro for a few months at 10mg before i said 5 mg is nothing.
but you're really pushing it with that 5HT2c antagonist stuff about prozac, it's main and only significant action is serotonin reuptake. everything else is secondary. Now, i can see with the Geodon talking about the 5HT2 antagonism, but with prozac no.
but you're really pushing it with that 5HT2c antagonist stuff about prozac, it's main and only significant action is serotonin reuptake. everything else is secondary. Now, i can see with the Geodon talking about the 5HT2 antagonism, but with prozac no.
therapeuticbrigg84
08 October 2009 - 03:26 PM
fine, now i agree with you, i guess i didnt know as much as i thought i knew about prozac. i just assumed that it was a standard issue SSRI.
therapeuticbrigg84
09 October 2009 - 10:27 AM
right, no u didnt seem too pissed off except at the beginning. but i mean when you write shit online you can kind of not take it the wrong way, cuz its just written words. so u basically take it with a grain of salt most times... unless u start capitalizing shit, but otherwise no.
now that i think of it, i do kind of tend to shout things, lol. like "hey guy there, im right!" lol, sometimes i can get things right.
wait a second, let me go look prozac up on wikipedia-lol jk!!
now that i think of it, i do kind of tend to shout things, lol. like "hey guy there, im right!" lol, sometimes i can get things right.
wait a second, let me go look prozac up on wikipedia-lol jk!!
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