I have managed to drop from 2mgs klonopin to 1.5mgs. I took my time, took me a month to get there. I have stayed at 1.5mgs for a few weeks to give my body time to settle. I had been on 2mgs for about 15 years. After dealing with some withdrawls like insomnia and increased anxiety, I now seem to feel better than I did on the 2mg dose. It really feels like a huge success for me. Tonight I begin the next phase to get to 1mg. I have it mapped out to be another 1 month process dropping down in 3 phases about a 10% reduction each 10 days, then ending at 1mg and leveling for a few weeks. I hope that I will have the same success when I get to 1mg and my original anxiety from years past doesn't rebound. If not, I'll keep doing the same thing until I'm off it. At the very least I want to take the smallest effective dose and this is the only way I know to accomplish that. Anyway, I emailed Dr. Eskapa and received additional feedback including info on benzo's. I told him I dropped my dose to 1.5mgs, asked some other questions and this was his response. I found it very interesting and encouraging and thought I'd share. Here's what he wrote:
"I will attach a reply by David Sinclair specifically for another reader but may be of relevance (end of this email to you). I also recommend
http://www.benzo.org.uk/manual/ as a responsible way of coming off BDZs. However, I appreciate how tough it is to get off benzodiazepines (BDZs) and one should proceed as you are - with respect, caution and discipline. Discipline refers to sticking to the 1.5 mg dose and not raising it back "just for a day" ... bear with it.
Having said that, given your style of drinking I would aim to take the full dose 50 mg naltrexone before drinking (30 mins to an hour). You may try 25 mg on the first drinking occasion. I have tried naltrexone with and without alcohol just to see what the side-effects some folks (less than 8 %) report - generally nausea I had none ... and I am relatively 'med sensitive myself ... Do not expect side-effects. If they occur they are usually nausea associated and pass. You could try 25 mg but note David Sinclair on dosing in an email today: I underlined what he said about the dose of 25 mg. Point is that if you binge once a week the duration of your binge may not be covered by opioid blockade with only 25 mg. In this case take the 25 mg soon before drinking (30 mins) then drink then if you are continuing after say 4 to 5 hrs take the rest 25 mg) and that should take care of things. Here is David's quote for a forum reader:
"I don't think the final answer is in yet concerning dose. Theoretically, it should not matter. There should not be a normal dose-response curve for doses of naltrexone above 25 mg. A dose of 25 mg should be sufficient to produce 100% blockade of mu receptors for several hours. 50 mg should also produce 100 % blockade for about 24 hours. 100 mg should produce 100% blockade for 48 hours. If patients are being careful to comply in taking naltrexone an hour before drinking always, all of the doses should have the same results. If patients are frequently not taking naltrexone before drinking, the larger doses should be producing better effects, but also more side effects and more extinction of healthy opioidergic behaviors. If patients are being told to abstain and at the same time take naltrexone, the larger doses are likely to be more useful because they will be still active when the people relapse to heavy drinking.
We have not found significant differences between men and women in the effectiveness of naltrexone in either our clinical trial or in the Finnish clinics. Of course, a failure to find significant differences does not mean there are no differences. We did find that the liking for strong sweets was higher in men than women, and higher in alcoholics with a family history of alcoholism than in alcoholics without the family history. From this, one would expect better responsiveness to naltrexone in alcoholics with a family history of alcoholism - which has been found repeatedly including in our studies. One also would expect to find more responsiveness to naltrexone in men than in women, which as I said was not found to be significant in our results - but maybe just because we needed more subjects in order to get significance.
Many many people are benefiting from the Sinclair Method - using naltrexone properly - no reason why you should not be one of them."