how much do you smoke a week ??

A

aquastoner

Member
hey curious ive tried those vaps they worked for a minute then id get bored its just not the same.And i understand the coding im on my pc 10 out of 18 awake hours a day so i feelya brother lol
 
theexpress

theexpress

Well-Known Member
tumorhead said:
For years I smoked an 1/8 a week. Now I smoke like 4-7 joints a day after growing my own. Also I take a bunch of meds now and I have to smoke more to get stoned.
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an eight a week? lol.... i dont even recal a time in my life were i could make an 8th last a week...
 
tumorhead

tumorhead

Well-Known Member
aquastoner said:
Hey tumorhead let me ask you do you think the eatables and meds ruin for smoking ?
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Edibles work still but have to be really really strong. I buy butter at a dispensary and it's got 2 grams of hash settled in the bottom and is stronger than I've ever made even when I use a LOT of bud (more bud than oil).

Most meds are fine but one Im on interacts with pot, it's weird. At first it exaggerated every side effect of pot that I normally never had. It gave the worst drymouth, confusion, and tiredness. I read other people have interactions with the type of drug and have had delirium and other weird shit. The drug class is "tricyclic antidepressant" and isn't used for depression but for nerve pain.

And yeah at 1/8 a week, even when I worked construction I still got stoned off my ass with .5g a day.
 
A

aquastoner

Member
Well i dont like any pharmaceutical drugs even advil wont take it only flu meds will i take out off desperation .Thanks for answering back
 
tumorhead

tumorhead

Well-Known Member
aquastoner said:
Well i dont like any pharmaceutical drugs even advil wont take it only flu meds will i take out off desperation .Thanks for answering back
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I didn't either, didn't go to the doctor for 10 years. I'm still in my 20's and take chronic opiates, anti seizure, and 2 anti depressants for neuropathic pain. All my lab work is stellar otherwise.
 
A

aquastoner

Member
Just watch the antidepressants sometimes the accumulative affect can be worse than what your treating.That sucks in your 20s and have bad back good luck with that brother im in my 40s and its a bitch been dealing with it ten years but the trick is not to stop moving .
 
cannabineer

cannabineer

Ursus marijanus
tumorhead said:
Edibles work still but have to be really really strong. I buy butter at a dispensary and it's got 2 grams of hash settled in the bottom and is stronger than I've ever made even when I use a LOT of bud (more bud than oil).

Most meds are fine but one Im on interacts with pot, it's weird. At first it exaggerated every side effect of pot that I normally never had. It gave the worst drymouth, confusion, and tiredness. I read other people have interactions with the type of drug and have had delirium and other weird shit. The drug class is "tricyclic antidepressant" and isn't used for depression but for nerve pain.

And yeah at 1/8 a week, even when I worked construction I still got stoned off my ass with .5g a day.
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Have you tried Neurontin or any of the newer meds indicated for neuropathic pain? cn
 
tumorhead

tumorhead

Well-Known Member
cannabineer said:
Have you tried Neurontin or any of the newer meds indicated for neuropathic pain? cn
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Yeah I started with neurontin up to 2400mg/day and it didn't work nearly as good as the tricyclic antidepressant called Nortriptyline. Amitryptiline is similar. My pain is "atypical" which is harder to figure out than other neuralgias. Currently he's thinking it's thalamus pain syndrome. The previous neurologist diagnosed me with "tolosa-hunt syndrome" after an MRI and spinal tap, which is 1 per 1 mil population rate of occurrence.

Instead of tegretol which is carbazapine I take a newer one called oxcarbazapine and take 1200mg/day. Then I got to the max dose with the nortriptyline over the past year, so he added cymbalta which has a similar effect blocking nerve pain signals in the brain, I take the max dose of it, and before I backed off on nortriptyline from 150mg/day to 100mg I started getting seratonin syndrome causing my muscles to jerk randomly. They still do but less often.

Then I get oxycodone for short term flare ups. Basically all the meds take a week to kick in, and if I stop taking them you still feel good for a week but then it hits you and takes a week of agony to kick back in. Been seeing a neurologist every 3-4 weeks for a year now.

It feels like someone is tearing my face off or fileting it, then it feels like an ice pick shoved through my eye back to my tonsil, infected, and jerking it around. It's unreal. When I move my eye I get a stabbing ice pick pain behind the eye. It was disabling before I got on the current meds so they got me by the balls.

And it took 7 months for anyone to take me serious because all my lab work is flawless, I'm completely healthy by their test standards, but once I got the mri that showed the lesion on my trigeminal nerve they believed me.
 
cannabineer

cannabineer

Ursus marijanus
tumorhead said:
Yeah I started with neurontin up to 2400mg/day and it didn't work nearly as good as the tricyclic antidepressant called Nortriptyline. Amitryptiline is similar. My pain is "atypical" which is harder to figure out than other neuralgias. Currently he's thinking it's thalamus pain syndrome. The previous neurologist diagnosed me with "tolosa-hunt syndrome" after an MRI and spinal tap, which is 1 per 1 mil population rate of occurrence.

Instead of tegretol which is carbazapine I take a newer one called oxcarbazapine and take 1200mg/day. Then I got to the max dose with the nortriptyline over the past year, so he added cymbalta which has a similar effect blocking nerve pain signals in the brain, I take the max dose of it, and before I backed off on nortriptyline from 150mg/day to 100mg I started getting seratonin syndrome causing my muscles to jerk randomly. They still do but less often.

Then I get oxycodone for short term flare ups. Basically all the meds take a week to kick in, and if I stop taking them you still feel good for a week but then it hits you and takes a week of agony to kick back in. Been seeing a neurologist every 3-4 weeks for a year now.

It feels like someone is tearing my face off or fileting it, then it feels like an ice pick shoved through my eye back to my tonsil, infected, and jerking it around. It's unreal. When I move my eye I get a stabbing ice pick pain behind the eye. It was disabling before I got on the current meds so they got me by the balls.

And it took 7 months for anyone to take me serious because all my lab work is flawless, I'm completely healthy by their test standards, but once I got the mri that showed the lesion on my trigeminal nerve they believed me.
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Ypu've been through quite the wringer then. My sympathies. cn
 
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