THE_REAL_OBLIVION
Bluelight Crew
I'm seeing my psydoc soon. Off the bat I'll say I'm diagnosed with GAD, I told BL that since a long time, but I never really said I have Bipolar I, the most I could endure was the yellow 10mg of Paxil for 3 months and I think I tolerated this without going into mania like with all SSRI's/SNRI's I tried later on, was because I was prescribed 0.25mg xanax 4 times a day for a month and a half, I was a benzo virgin then, only having used some so me and some friends could drink less alcohol, and that was 2mg clonazepam pills from my weed/acid guy. I'm able to handle Manerix (moclobemide) a reversible MAOI that requires no diet restrictions, other than massive amounts of strong old cheese, amounts nobody would eat pretty much. It's not available in the US, but Canada, Australia and the UK have it. It works fast too and boosts benzos and opiates. But it made me feel stupid-happy, know what I mean? It made me dumb-happy like I could read very distressing news or a friend or family member being mad at me and I would shrug it off and was happy all the time, which annoyed me.
He understands I cannot take SSRI's/SNRI's (I'll spare you what happened to me when I got on 20mg paxil a day), failed experiments with Wellbutrin (made me more anxious and felt a bit like very cut meth pills (methbombs) and Effexor XR where a single 37.5mg starting dose had me get massive pupils like if I was on L, Shrooms, MDMA etc. + a strange all over body feeling and nausea I had to buy some benadryl to kill it.
So I've had myself thinking of bringing up Trimipramine, which could be a good idea, if I don't get any serious side effect. I've been prescribed nortryptiline and amytriptiline in the past for a type of neuralgia that fixes itself after some time, apparently, to take with 375mg naproxen 4 times a day and 30mg temazepam (15 a month) and the neurologist then also gave me a cortisone infiltration in the upper part of my neck. Tolerated them well, especially nortryptiline, it actually worked for the pain, the naproxen I should have asked for Ketoralac instead, but I didn't know better then. I only had one bad experience with TCA's or Tetracyclic? (not sure if it's the former or latter), Trazodone, this stuff gave me vivid nightmares and night terrors and the fact I was scripted Ritalin 10mg twice a day then did not help (as far as I remember, I read back in, well, likely 2002, the first time I went to a GP all of my own, I remember reading that there was some toxicity increase with ritalin when used with trazodone, should have given me a tiny dose of benzos like the other GP when I lived in Montreal, 0.25mg clonazepam 3-4 times a day and Ritalin might have worked, they blamed the seizure I got on the Ritalin alone, with the benefit that I was going to have a Dexedrine script instead, which was very beneficial at least for 5 years when almost done with college, never finished my Masters but at least I did 1 year..
Trimipramine seems ideal because of how it does not mess with REM sleep and is known to have analgesic effects. I'm sure the guy (psychiatrist) would have no problem prescribing me an anti-depressant, but I really just want something so I can reduce my benzo intake, where I would only need them through the day for the GAD and have something else than another benzo for sleep. The monograph from the generic maker, the only one who still makes trimipramine up here, has me hesitating, possible side effects are as numerous as methadone. I don't suffer from any cardiovascular disease, nor diabeetus, so that's a bonus to start with.
Any advice or experience with Surmontil (the brand name isn't marketed anymore here, I'm sure it's still there south in the land of the 2 horrible choices of presidents. Also, I called my pharmacy and the pharmacist told me they only had 12.5mg and 25mg pills, when the monograph says there is also 50mg pills, 75mg capsules and 100mg pills. I'm not sure what dose would work best for me, but in the monograph, they really push the 75mg gelcap for some reason, the studies in it all use those. She told me I'd be surprised if you are given more than 25mg at once when you start. I'd def start with 12.5mg, if going that route anyway, due to how sensitive my brain's neurotrasmitters are to any change in serotonin and norepinephrine in particular. I think it's all the LSD I've had (250-300 trips in my life, last trip was from ETH-LAD last summer, but I hadn't had any L other ergoloids since '08.
I need some rest during a certainly, uncertain time in my life where I could be, my endocrinologist will only dispense meds after 3 blood work indicating the same thing in intervals of 3 months, the final one I took last week; where I could end up needing hypothyroidism medication, prolactine lowering meds and restart a Testosterone treatment, but with something less drastic than SC/IM Delatestryl, we discussed me and her (the endocrino) using Androgel and if that gives me painful cysts like Delatestryl did on my chest which turned into gyno, which has receded since I stopped using Delatestryl and Anastrazole (anti-oestrogen med), and in case that doesn't work well either, the oral (pill) option, which doctors here even my ORT doc who started the whole low T caused by methadone and continuing into my bupe regimen, not as bad as when I was on methadone though, said that pills for low T either worked or didn't at all, it's literally a heads or tail situation, she told me she rarely ever scripted pills for low T, only when other things have failed/caused more issues.
I'm sick of this shit and the remnants of the gyno, non painful to the touch lumps (they were painful back when the showed when only using Delatestryl before I was put on an anti-oestrogen medication) close to my nipple on the left side, which is apparently 20 fucking centimeter, but nope, no biopsy has been made, she says the blood tests would have said if I had any sort of cancer going on, which I find hard to believe, but sure. Reminds me of the Dead Kennedys song "Trust Your Mechanic", it's literally fix something, another falls apart, back to the doc, where they are paid by visit from our taxes. I'd really love for all this to end at once
He understands I cannot take SSRI's/SNRI's (I'll spare you what happened to me when I got on 20mg paxil a day), failed experiments with Wellbutrin (made me more anxious and felt a bit like very cut meth pills (methbombs) and Effexor XR where a single 37.5mg starting dose had me get massive pupils like if I was on L, Shrooms, MDMA etc. + a strange all over body feeling and nausea I had to buy some benadryl to kill it.
So I've had myself thinking of bringing up Trimipramine, which could be a good idea, if I don't get any serious side effect. I've been prescribed nortryptiline and amytriptiline in the past for a type of neuralgia that fixes itself after some time, apparently, to take with 375mg naproxen 4 times a day and 30mg temazepam (15 a month) and the neurologist then also gave me a cortisone infiltration in the upper part of my neck. Tolerated them well, especially nortryptiline, it actually worked for the pain, the naproxen I should have asked for Ketoralac instead, but I didn't know better then. I only had one bad experience with TCA's or Tetracyclic? (not sure if it's the former or latter), Trazodone, this stuff gave me vivid nightmares and night terrors and the fact I was scripted Ritalin 10mg twice a day then did not help (as far as I remember, I read back in, well, likely 2002, the first time I went to a GP all of my own, I remember reading that there was some toxicity increase with ritalin when used with trazodone, should have given me a tiny dose of benzos like the other GP when I lived in Montreal, 0.25mg clonazepam 3-4 times a day and Ritalin might have worked, they blamed the seizure I got on the Ritalin alone, with the benefit that I was going to have a Dexedrine script instead, which was very beneficial at least for 5 years when almost done with college, never finished my Masters but at least I did 1 year..
Trimipramine seems ideal because of how it does not mess with REM sleep and is known to have analgesic effects. I'm sure the guy (psychiatrist) would have no problem prescribing me an anti-depressant, but I really just want something so I can reduce my benzo intake, where I would only need them through the day for the GAD and have something else than another benzo for sleep. The monograph from the generic maker, the only one who still makes trimipramine up here, has me hesitating, possible side effects are as numerous as methadone. I don't suffer from any cardiovascular disease, nor diabeetus, so that's a bonus to start with.
Any advice or experience with Surmontil (the brand name isn't marketed anymore here, I'm sure it's still there south in the land of the 2 horrible choices of presidents. Also, I called my pharmacy and the pharmacist told me they only had 12.5mg and 25mg pills, when the monograph says there is also 50mg pills, 75mg capsules and 100mg pills. I'm not sure what dose would work best for me, but in the monograph, they really push the 75mg gelcap for some reason, the studies in it all use those. She told me I'd be surprised if you are given more than 25mg at once when you start. I'd def start with 12.5mg, if going that route anyway, due to how sensitive my brain's neurotrasmitters are to any change in serotonin and norepinephrine in particular. I think it's all the LSD I've had (250-300 trips in my life, last trip was from ETH-LAD last summer, but I hadn't had any L other ergoloids since '08.
I need some rest during a certainly, uncertain time in my life where I could be, my endocrinologist will only dispense meds after 3 blood work indicating the same thing in intervals of 3 months, the final one I took last week; where I could end up needing hypothyroidism medication, prolactine lowering meds and restart a Testosterone treatment, but with something less drastic than SC/IM Delatestryl, we discussed me and her (the endocrino) using Androgel and if that gives me painful cysts like Delatestryl did on my chest which turned into gyno, which has receded since I stopped using Delatestryl and Anastrazole (anti-oestrogen med), and in case that doesn't work well either, the oral (pill) option, which doctors here even my ORT doc who started the whole low T caused by methadone and continuing into my bupe regimen, not as bad as when I was on methadone though, said that pills for low T either worked or didn't at all, it's literally a heads or tail situation, she told me she rarely ever scripted pills for low T, only when other things have failed/caused more issues.
I'm sick of this shit and the remnants of the gyno, non painful to the touch lumps (they were painful back when the showed when only using Delatestryl before I was put on an anti-oestrogen medication) close to my nipple on the left side, which is apparently 20 fucking centimeter, but nope, no biopsy has been made, she says the blood tests would have said if I had any sort of cancer going on, which I find hard to believe, but sure. Reminds me of the Dead Kennedys song "Trust Your Mechanic", it's literally fix something, another falls apart, back to the doc, where they are paid by visit from our taxes. I'd really love for all this to end at once

Last edited: