candidsurprise
Bluelighter
- Joined
- Oct 18, 2017
- Messages
- 134
So I've been dealing with treatment resistant depression for a long time now, and I've been through the ringer of therapy and medication to no avail. At this point the medical system has failed me, and there's nothing more that they can do besides ECT which I'm not willing to undergo. So I've taken to self-medicating, and I've been doing a lot of research on different compounds and combinations of compounds that I might use.
I've developed a weekly routine which successfully gives me relief from my severe depressive symptoms on the days on which I'm self medicating. The routine goes like this
Week 1:
Mon - 40mg oral Methamphetamine (Xanax + seroquel for comedown)
Tue - 5x GBL 1.7ml (throughout the day)
Wed - Tramadol 250mg
Thurs - Tramadol 250mg
Fri - Tramadol 250mg
Sat - 5x GBL 1.7ml (throughout the day)
Sun - Tianeptine sulfate 25mg + 5-HTP + L-Tyrosine
Week 2:
Mon - 5x GBL 1.7ml
Tue - Tianeptine sulfate 25mg + 5-HTP + L-Tyrosine
Wed - Tramadol 250mg
Thurs - Tramadol 250mg
Fri - 5x GBL 1.7ml
Sat - Tianeptine + 5-HTP + L-Tyrosine
Sun - 5x GBL 1.7ml
And I repeat this rotation every two weeks. The meth, Tramadol and gbl give me near total relief of all symptoms. The Tianeptine + 5 HTP is only slightly effective - these days are a struggle to get through but it's better than nothing.
Essentially I need one more medication/combo to both replace (or augment) the Tianeptine days, and to reduce my over-reliance on Tramadol and GBL. I'm treading a fine line with physical dependence with Tramadol in using it 5 times a fortnight. I've calculated my GBL usage to be quantitatively equivalent to the amount of Xyrem prescribed daily therapeutically - which was shown to exhibit no physical dependence. However it's still a risky game, so I want to reduce my Tramadol days to 4 days per fortnight, and likewise with GBL ideally.
A couple of other points: I have to schedule the Tramadol back to back which I know raises the risk of dependence. The reason being, I get a bit of a hangover after a single day of Tramadol, if I broke up my Tramadol usage id be dealing with multiple hangovers during the week. With this regimen I only deal with one, and it's mostly alleviated by the GBL. The other point is that I don't experience any cravings or compulsive dosing, and have been easily able to discontinue any of the medications at will. I recently took a 3 week break from Tramadol with 0 issues, despite having a huge supply in my cupboard.
So my question is mostly directed to the older users of this site that have experience with any of the older drugs that act on Gaba-A receptors. Or any of the newer users that have had the fortune of experiencing them. My reasoning is as follows: I'm underutilising my GABA-A receptors with my regimen, potentially missing out on a potent mechanism of relief. The consequence of this underutilisation is overutilisation of the mu-opioid receptor and the Gaba-B receptor (gbl). So I want to utilise my Gaba A receptor to take some of the burden from those other receptors. The problem is that benzodiazepines are the only current compounds that exclusively target Gaba A, and they do absolutely nothing for my depression, so they aren't an option. Barbiturates act on Gaba-A in a way distinct from benzos, and methaqualone/quaaludes act on Gaba-A in a way distinct from benzos and barbs. I understand that users of Quaaludes described it as conferring a strong sense of 'well-being'. Secobarbital and pentobarbital have similarly been described as creating such an effect. This reminds me of GBL descriptions, a compound that is nothing short of miraculous for my depression. So what I'm asking is whether moderate usage of these compounds could theoretically provide me with relief from my depression 3-4 days a fortnight (if redosed throughout the day)? Other Gaba-A compounds, most noteably alcohol and high dose phenibut, are not an option because they act on both Gaba A and Gaba B and thus would exhibit cross tolerance with GBL and downregulate Gaba-B to an excessive degree.
One issue that I've foreseen is excessive sedation induced by these compounds, which in my case would be an unacceptable side effect to their 'euphoric' or anti-depressant aspect. I've thought about using provigil (modafinil) concurrently if this becomes a real problem. Incidentally, provigil has some modest anti-depressant properties too so it could be a nice and effective combination. I am unable to take provigil by itself as it gives me horrible insomnia (and is only slightly effective) and I'm not willing to use my Gaba-A receptors for the sole purpose of fixing provigil related insomnia if I can use them to actually target the depression in the first place.
If this plan proves unfeasible (either through total lack of access to the relevant Gaba A compounds, or the lack of efficacy). I've thought about combining Tianeptine, 5-htp and provigil several days a fortnight and using a low dose of benzos to sleep; and make do with the limited relief that will provide me with.
Thanks guys, and feel free to comment on any aspect of my regimen/plan, this post isn't exclusively focused on the title question - I would love some feedback on the long term viability of this regimen. Also any thoughts on microdosing psychedelics for depression? I havent tried this approach and some have found it to be effective.
*Sigh...post title altered to bring more in line with the rules. The bottom line is that we can't tell you what to take, period. We don't tell people what to take, but if they're absolutely going to take something, we can help make usage as safe as it can be*
I've developed a weekly routine which successfully gives me relief from my severe depressive symptoms on the days on which I'm self medicating. The routine goes like this
Week 1:
Mon - 40mg oral Methamphetamine (Xanax + seroquel for comedown)
Tue - 5x GBL 1.7ml (throughout the day)
Wed - Tramadol 250mg
Thurs - Tramadol 250mg
Fri - Tramadol 250mg
Sat - 5x GBL 1.7ml (throughout the day)
Sun - Tianeptine sulfate 25mg + 5-HTP + L-Tyrosine
Week 2:
Mon - 5x GBL 1.7ml
Tue - Tianeptine sulfate 25mg + 5-HTP + L-Tyrosine
Wed - Tramadol 250mg
Thurs - Tramadol 250mg
Fri - 5x GBL 1.7ml
Sat - Tianeptine + 5-HTP + L-Tyrosine
Sun - 5x GBL 1.7ml
And I repeat this rotation every two weeks. The meth, Tramadol and gbl give me near total relief of all symptoms. The Tianeptine + 5 HTP is only slightly effective - these days are a struggle to get through but it's better than nothing.
Essentially I need one more medication/combo to both replace (or augment) the Tianeptine days, and to reduce my over-reliance on Tramadol and GBL. I'm treading a fine line with physical dependence with Tramadol in using it 5 times a fortnight. I've calculated my GBL usage to be quantitatively equivalent to the amount of Xyrem prescribed daily therapeutically - which was shown to exhibit no physical dependence. However it's still a risky game, so I want to reduce my Tramadol days to 4 days per fortnight, and likewise with GBL ideally.
A couple of other points: I have to schedule the Tramadol back to back which I know raises the risk of dependence. The reason being, I get a bit of a hangover after a single day of Tramadol, if I broke up my Tramadol usage id be dealing with multiple hangovers during the week. With this regimen I only deal with one, and it's mostly alleviated by the GBL. The other point is that I don't experience any cravings or compulsive dosing, and have been easily able to discontinue any of the medications at will. I recently took a 3 week break from Tramadol with 0 issues, despite having a huge supply in my cupboard.
So my question is mostly directed to the older users of this site that have experience with any of the older drugs that act on Gaba-A receptors. Or any of the newer users that have had the fortune of experiencing them. My reasoning is as follows: I'm underutilising my GABA-A receptors with my regimen, potentially missing out on a potent mechanism of relief. The consequence of this underutilisation is overutilisation of the mu-opioid receptor and the Gaba-B receptor (gbl). So I want to utilise my Gaba A receptor to take some of the burden from those other receptors. The problem is that benzodiazepines are the only current compounds that exclusively target Gaba A, and they do absolutely nothing for my depression, so they aren't an option. Barbiturates act on Gaba-A in a way distinct from benzos, and methaqualone/quaaludes act on Gaba-A in a way distinct from benzos and barbs. I understand that users of Quaaludes described it as conferring a strong sense of 'well-being'. Secobarbital and pentobarbital have similarly been described as creating such an effect. This reminds me of GBL descriptions, a compound that is nothing short of miraculous for my depression. So what I'm asking is whether moderate usage of these compounds could theoretically provide me with relief from my depression 3-4 days a fortnight (if redosed throughout the day)? Other Gaba-A compounds, most noteably alcohol and high dose phenibut, are not an option because they act on both Gaba A and Gaba B and thus would exhibit cross tolerance with GBL and downregulate Gaba-B to an excessive degree.
One issue that I've foreseen is excessive sedation induced by these compounds, which in my case would be an unacceptable side effect to their 'euphoric' or anti-depressant aspect. I've thought about using provigil (modafinil) concurrently if this becomes a real problem. Incidentally, provigil has some modest anti-depressant properties too so it could be a nice and effective combination. I am unable to take provigil by itself as it gives me horrible insomnia (and is only slightly effective) and I'm not willing to use my Gaba-A receptors for the sole purpose of fixing provigil related insomnia if I can use them to actually target the depression in the first place.
If this plan proves unfeasible (either through total lack of access to the relevant Gaba A compounds, or the lack of efficacy). I've thought about combining Tianeptine, 5-htp and provigil several days a fortnight and using a low dose of benzos to sleep; and make do with the limited relief that will provide me with.
Thanks guys, and feel free to comment on any aspect of my regimen/plan, this post isn't exclusively focused on the title question - I would love some feedback on the long term viability of this regimen. Also any thoughts on microdosing psychedelics for depression? I havent tried this approach and some have found it to be effective.
*Sigh...post title altered to bring more in line with the rules. The bottom line is that we can't tell you what to take, period. We don't tell people what to take, but if they're absolutely going to take something, we can help make usage as safe as it can be*
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