Chronic pain and medical marijuana

Posted by ladyjane85 @ladyjane85, Jul 16, 2016

A nurse friend tried me on marijuana oil smoked in an electronic pen since nothing works with my pain under everything pain management has tried. I did not respond - can one be immune to it as I am with all procedures on my back and all pain relievers

Interested in more discussions like this? Go to the Chronic Pain Support Group.

@cbrackle

That is correct. I’ve been in the medical cannabis program her in MN for almost a year. While trying to figure out what if anything helps I was spending between $600-$1200/ month (all out of pocket.
For me, it may take the edge off, but if I try to use enough to really cut the pain I get dizzy (equilibrium out of kilter) no high, just cannot function.
Unfortunately, the one thing that helped (specific opiod -extended release) is no longer covered by insurance. My out of pocket would be >$3000/month. Way more than my meager disability payment.
Considering looking outside the US for treatments.
Knee jerk reactions and sweeping restrictions by the lawmakers have put me back in pain treatment more than 8 years.

FYI, I also have and keep trying anything I can afford (or not) just to see if they help.
I have a surgically implanted Spinal Stimulator, a DRG (dorsal root ganglion) stimulator that took 7 surgeries to correctly place (still only 20-30% effective after healing in place.
Far infrared sauna, biomat, Gabapentin, sleep aids, CPAP, physical therapy, nerve injections and ablations, etc.
I know most of these treatments work on most people. Just not me.

I truly hope and pray that all of you out there find the right treatment to relive your suffering.
Carl

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Wow, reading that it took 7 surgeries to place the Spinal Nerve Stimulator properly indicated to me that you need to find a better medical team.
I don't know how a CPAP would influence any permanent pain.
My implant was put into the right position from the beginning, and I am on a CPAP for sleep apnea, and not for pain.

Talk to the Mayo doctors, and I am sure you will receive help!

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@cbrackle

That is correct. I’ve been in the medical cannabis program her in MN for almost a year. While trying to figure out what if anything helps I was spending between $600-$1200/ month (all out of pocket.
For me, it may take the edge off, but if I try to use enough to really cut the pain I get dizzy (equilibrium out of kilter) no high, just cannot function.
Unfortunately, the one thing that helped (specific opiod -extended release) is no longer covered by insurance. My out of pocket would be >$3000/month. Way more than my meager disability payment.
Considering looking outside the US for treatments.
Knee jerk reactions and sweeping restrictions by the lawmakers have put me back in pain treatment more than 8 years.

FYI, I also have and keep trying anything I can afford (or not) just to see if they help.
I have a surgically implanted Spinal Stimulator, a DRG (dorsal root ganglion) stimulator that took 7 surgeries to correctly place (still only 20-30% effective after healing in place.
Far infrared sauna, biomat, Gabapentin, sleep aids, CPAP, physical therapy, nerve injections and ablations, etc.
I know most of these treatments work on most people. Just not me.

I truly hope and pray that all of you out there find the right treatment to relive your suffering.
Carl

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We need to start hammering our legislatures for them to get off the bogus notion that, by restricting legal prescriptions of opioids for pain relief, reduces the number of people OD'ing on the medication. In stead what is happening, just like during the Prohibition on alcoholic beverages, illegal distribution and consumption in an uncontrolled environment is making criminals, pharma pushing ineffective medication for treatments to reduce pain, and perhaps some politicians wealthy.

REPLY
@cbrackle

That is correct. I’ve been in the medical cannabis program her in MN for almost a year. While trying to figure out what if anything helps I was spending between $600-$1200/ month (all out of pocket.
For me, it may take the edge off, but if I try to use enough to really cut the pain I get dizzy (equilibrium out of kilter) no high, just cannot function.
Unfortunately, the one thing that helped (specific opiod -extended release) is no longer covered by insurance. My out of pocket would be >$3000/month. Way more than my meager disability payment.
Considering looking outside the US for treatments.
Knee jerk reactions and sweeping restrictions by the lawmakers have put me back in pain treatment more than 8 years.

FYI, I also have and keep trying anything I can afford (or not) just to see if they help.
I have a surgically implanted Spinal Stimulator, a DRG (dorsal root ganglion) stimulator that took 7 surgeries to correctly place (still only 20-30% effective after healing in place.
Far infrared sauna, biomat, Gabapentin, sleep aids, CPAP, physical therapy, nerve injections and ablations, etc.
I know most of these treatments work on most people. Just not me.

I truly hope and pray that all of you out there find the right treatment to relive your suffering.
Carl

Jump to this post

I’m not certain of what mmj you’re using that is causing these symptoms but if you provide me more detail I may be able to help or seek assistance from your dispensary to find a pharmacist who is knowledgeable on cannabis. I recently changed what I use which was too much THC. Didn’t make me too high as I no longer get buzzed, but didn’t give me the desired effect. I increased my CBD intake with tinctures 3x day, in between hitting high CBD low THC oil. I was able to decrease my oxycodone to 2x day and I’m sleeping better too. Only downside is my increased snoring causing my wife to complain. It took me about a month to feel the gradual effects change. If you depend on your health being regulated by your insurance good luck. You need to control your health improvement on your own before you run out of time.

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@collins1979

Yes pain in the legs i started having whrn i was in highscho aleady. In feb 2021 he also draw blood i will also see if i can srnd that results also. It was a pain that come and goes. I was tested pos for covid on 16 july. I went back to dr on 18 aug 2021 that is when he draw blood to check my full blood counting. Because i waz not getting better. My legs bame worse. Numbess feeling, pins and needles. Shortness of breath, headaches . Difficulty stepping on my feet. Cant walk nor stand on my feed for long

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I’m sorry for you’re in such distress but your symptoms sound like long hauler symptoms. Have you been vaccinated? Hope your doctor appointment provides you with results.

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@kenc

We need to start hammering our legislatures for them to get off the bogus notion that, by restricting legal prescriptions of opioids for pain relief, reduces the number of people OD'ing on the medication. In stead what is happening, just like during the Prohibition on alcoholic beverages, illegal distribution and consumption in an uncontrolled environment is making criminals, pharma pushing ineffective medication for treatments to reduce pain, and perhaps some politicians wealthy.

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Here in PA our county AG is hammering on opiate prescriptions and making chronic pain patients and prescribers jump through hoops just as more docs obtain their ‘x’ waver to initiate addiction treatment medications for needy patients.

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@jenatsky

Here in PA our county AG is hammering on opiate prescriptions and making chronic pain patients and prescribers jump through hoops just as more docs obtain their ‘x’ waver to initiate addiction treatment medications for needy patients.

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More people become addicted and over dose, when not under a doctor's care/oversight.

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@jenatsky

I’m not certain of what mmj you’re using that is causing these symptoms but if you provide me more detail I may be able to help or seek assistance from your dispensary to find a pharmacist who is knowledgeable on cannabis. I recently changed what I use which was too much THC. Didn’t make me too high as I no longer get buzzed, but didn’t give me the desired effect. I increased my CBD intake with tinctures 3x day, in between hitting high CBD low THC oil. I was able to decrease my oxycodone to 2x day and I’m sleeping better too. Only downside is my increased snoring causing my wife to complain. It took me about a month to feel the gradual effects change. If you depend on your health being regulated by your insurance good luck. You need to control your health improvement on your own before you run out of time.

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Hmmmm, I have a similar experience. I am using more of less......in a way. I find that two droppers of mj with more CBD is better than one dropper with more THC. This came to me after my recent surgery. So far so good. I still like the higher THC if I have to be social and "charming" for a period of time. Thanks for the offer to help find out from the pharmacist. Sometimes I find the manufacturer's support teams very helpful.

May you be content and at ease.
Chris

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@kenc

We need to start hammering our legislatures for them to get off the bogus notion that, by restricting legal prescriptions of opioids for pain relief, reduces the number of people OD'ing on the medication. In stead what is happening, just like during the Prohibition on alcoholic beverages, illegal distribution and consumption in an uncontrolled environment is making criminals, pharma pushing ineffective medication for treatments to reduce pain, and perhaps some politicians wealthy.

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@kenc. Thank you for your strength in posting this

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@jenatsky

I’m not certain of what mmj you’re using that is causing these symptoms but if you provide me more detail I may be able to help or seek assistance from your dispensary to find a pharmacist who is knowledgeable on cannabis. I recently changed what I use which was too much THC. Didn’t make me too high as I no longer get buzzed, but didn’t give me the desired effect. I increased my CBD intake with tinctures 3x day, in between hitting high CBD low THC oil. I was able to decrease my oxycodone to 2x day and I’m sleeping better too. Only downside is my increased snoring causing my wife to complain. It took me about a month to feel the gradual effects change. If you depend on your health being regulated by your insurance good luck. You need to control your health improvement on your own before you run out of time.

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After 9 years of using prescribed morphine sulfate when needed for nerve pain caused by myofascial pain syndrome, I was needing 60 mg. to control the pain. Recently I began using CBD cream, and I now can take only 45 mg. of morphine sulfate to get the same result. I'd love to know a doctor in my locale who is knowledgeable about cannabis use. I hate using morphine, but I cannot tolerate the pain when it occurs.

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What area do you live in? I was on MS ER too but switched to Buprenorphine Patch about 5 years ago and have much better results than with MS. And the increased CBD has permitted me to decrease my PRN oxycodone down to 2x day from 6x day.

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