Chris Timothy
Bluelighter
Okay, I got the suspicion the pressure sensation has been because of not the greatest care in spacing and ratio, because looking at the affinities Naltrexone really should sufficiently block the k-opioid receptor. I can spare a little more Naltrexone upon taking stock, so let's test that hypothesis, shall we. The day is stained with Naltrexone's noise profile anyway.
2/3rds Naltrexone now taken an hour prior, with the other 1/3rd half an hour prior. Roughly doubled the supplements as well, one half half an hour prior, other half at lift-off.
12mg 3-HO-PCP rectally. Some minor noise during come-up, no ear pressure. Noise profile not readily distinguishable from NAC's hiss, somewhat more tolerable than presumed serotonergic dissociatives like MXPr and MXiPr. I'd guess though partially blocked it's noisier than O-PCE, but I'd have to look into whether d-opioid reception is relevant to ear function or whether other mechanisms are at play. The effect definitely still is sedating and pleasurable, and I reckon a little kratom cousin won't hurt.
Edit to follow up that the ear was indeed perfectly protected during this trial. Which is to say I did indeed redose 12mg on the tea.
The behaviour though was unacceptable, the kratom-ish hole made a mess of the place with objects almost lost and local social structures disrespected. Opioid dissociatives are not for me in case I didn't already gathered that from the ear terror it has already given me before, almost ruining my sanity with this crap.
2/3rds Naltrexone now taken an hour prior, with the other 1/3rd half an hour prior. Roughly doubled the supplements as well, one half half an hour prior, other half at lift-off.
12mg 3-HO-PCP rectally. Some minor noise during come-up, no ear pressure. Noise profile not readily distinguishable from NAC's hiss, somewhat more tolerable than presumed serotonergic dissociatives like MXPr and MXiPr. I'd guess though partially blocked it's noisier than O-PCE, but I'd have to look into whether d-opioid reception is relevant to ear function or whether other mechanisms are at play. The effect definitely still is sedating and pleasurable, and I reckon a little kratom cousin won't hurt.
Edit to follow up that the ear was indeed perfectly protected during this trial. Which is to say I did indeed redose 12mg on the tea.
The behaviour though was unacceptable, the kratom-ish hole made a mess of the place with objects almost lost and local social structures disrespected. Opioid dissociatives are not for me in case I didn't already gathered that from the ear terror it has already given me before, almost ruining my sanity with this crap.

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