Tramadol Does More Than Relieve Pain

Discussion in 'General' started by Cort, Aug 22, 2018.

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  1. Cort

    Cort Founder of Health Rising and Phoenix Rising Staff Member

    I took Tramadol for the first time last week. I was really surprised at the result; it did more than relieve my pain - my fatigue diminished dramatically and my cognition improved significantly - I was definitely thinking much clearer.

    Issie believes tramadol has all sorts of other effects including effects on the autonomic nervous system. I'm a believer.

    I'm just going to use it sporadically and I look forward to using it again.
     
    ritasheart, Zapped, Remy and 2 others like this.
  2. Paw

    Paw Well-Known Member

    Similarly, I've recently been experimenting with kratom -- not daily -- and was surprised to find it significantly energizing and clarifying. Issie may be on to something, or it could simple be that when you ease overall gnawing symptoms you free up the brain and other resources to function more normally.

    I do find with kratom, which lasts a good eight hours or so, there's a moderate price to pay the next day -- so I have to plan for it. If kratom lifts me from, say, a 5 to an 7 one day, I'll probably be a 3 the following day (ranking fatigue, malaise, and pain).
     
  3. frederic83

    frederic83 New Member

    Who is Issie ?
     
  4. Hip

    Hip Well-Known Member

    There's a thread here on how some ME/CFS patients find opioid pain medications substantially improve brain fog, fatigue and neurological symptoms like tinnitus.
     
    Last edited: Aug 26, 2018
  5. Remy

    Remy Administrator

    Nasty, nasty withdrawal from it though, if used regularly, probably due to the serotonergic aspects of the drug that are not found in regular opiates.

    I was given it as a "safe" alternative to hydrocodone after a serious accident, but it turned out to be a nightmare. It makes my list of potentially life-ruining drugs, along with Cymbalta and Valium.
     
    Paw likes this.
  6. Paw

    Paw Well-Known Member

    I don't disagree necessarily, but this points to the varied natures of our diseases. Cymbalta -- not to be toyed with -- has been a lifesaver for me, but my disease seems to have neurological roots.

    It's a tough dilemma to navigate -- when one's untreated symptoms (or bad "flu" days) are very similar to withdrawal from the strong drugs affecting opioid or serotonergic systems that can bring relief.
     
  7. Zapped

    Zapped Well-Known Member

    I use Tramadol periodically. Earlier, I had used it for years but wanted to ‘clean out.’ I titrated down for a week and stopped. My withdrawal was minimal - nothing more than a few sniffles. I suppose this is another example of different reactions for different
    Systems. OTOH, I was also taking OxyContin on occasion, e.g. about .5 pill maybe twice a week, which I also quit w/o incidence.

    I still use Tramadol ~ 3 pills a week and get similar reactions to Cort’s (post above). Go figure.:confused: ...and even more complete remission feelings with a small dose of OxyC. Also, dental Nitrous Oxide causes absolute clarity of mind in addition to its pacifying effects.

    FWIW, another drug which prevents or minimizes PEM for me is Methyl Prednisolone, a steroid.
     
    Last edited: Aug 28, 2018
  8. Zapped

    Zapped Well-Known Member

    See my post re @Remy... .
    I have evolved an observational premise that CFS is an intangible, like a feeling which is biochemical, i.e. in the brain. It’s causes may be close to the psychiatric field, but more tangibly, neurological mechanisms.

    I think we all have this dynamic which is so far undiscovered in its piecemeal constituency. It’s like the reaction of a chameleon changing colors. It’s cause, though unknown as yet suggests a psychoactive place in the mind, triggered by stress of some sort, likely inputted through the eyes, whether triggers are physical or mental.

    This is a neurological rabbit hole. It is difficult to explore because the science is so esoteric and complicated and neuroscientists have more pressing agendas. I wonder how many of them even take time to consider the nature of CFS relative to their specialized fields. Or, are they even aware of the problem, much of which has neurological correlations?

    Many psychoactive drugs already yield dramatic palliative results for the various stages of CFS, e,g. dealing with cognitive issues, crashes and PEM. They, the various rxs can change the course of CFS, maybe not cure it but make it tolerable, doable?

    In conclusion, I would raise research appeals around the various neurological camps. This calls for the classic paradigm shift in focus - to research and funding in neuroscience. It seems reasonable that the time is right. Infectious disease stalwarts have for decades beat the same old drums looking for viruses, immune dysfunctions, mitochondrial disorders, and dietary experiments with little to no real effective results, like looking for the lost keys under the lamp posts. Why not work backwards from palliative psychoactive drugs and explore how the mechanisms in the brain are affected by them? IMO, they will then find CFS and PEM are neurological events triggered by ‘X’.
     
  9. Paw

    Paw Well-Known Member

    Zapped, your theory rings true enough -- although I wouldn't be surprised if it's not universally true.

    Meanwhile, as we continue down the rabbit hole, new research is suggesting opioid activation might be a more fruitful approach to depression than glutamate reduction.
     
  10. Issie

    Issie Well-Known Member

    Tramadol works on all the neurotransmitters. Originally they werent sure how it worked. But a few years ago it was listed in the opiate catagory as a class 4. Makes it frowned on by doctors and others who aren't familiar with its range of properties .

    That being said, it can be addictive and I've heard can have some bad withdrawal issues. It also can stop working and most people increase their dosages and then you could have a problem. I have found it along with Bentyl to be my best POTS moderator. I take a very low dose and cycle on and off it. (In an off cycle now. ) I don't seem to have issues with withdrawal other than my POTS and FM get worse. Also have issues not sleeping as well. I take such a small amount, may be why I don't have much trouble just stopping it.

    There is a lot of info out there about it. It does work on seratonin, dopamine, NMDA and calcium channels. It calms my hyper response down when I get surges with POTS or Mast cell. I'm super sensitive to medicines though. 1/2 of a 50 mg. pill can be enough to do that. I don't really take enough to help with my pain. Yet I'm sure it does help. I usually take it at night. (Unlike other SSRI or SNRI it doesn't affect sexual function or feeling.) It has been used off label for those who didn't respond to those drugs.

    I hypothesize (if) there is a connection with POTS and the sympathetic nervous system hyper response due to high glutamate. I seem to have conversion issues with the channels between GABA and glutamate. (GABA paradoxes and keys me up. Every medicine that is supposed to up GABA and cause a parasympathetic response - does the opposite. Also supplements do the same. I don't have that trouble with Tramadol.) Though some of us with the subset of higher blood pressure and HYPERPOTS, many of us, have very high standing NE (norepinephrine) levels. This increases tachycardia and aids in heart pumping for blood flow and oxygen - (probably a compensation - yet very uncomfortable ). Tramadol works on NMDA (glutamate channels).

    It also has mild calcium channel blocking properties possibly helping with mast cell issues. GastroCrom is also a mast cell stabilizing drug and is also a mild calcium channel blocker. It has helped me with my mast cell issues. Along with Allegra and 1/2 of a Zantac. I really didn't see much improvement until I added mast cell moderators.

    I sent Cort lots of research papers. Maybe he will share some of those. He has the knack to summarize better than me.

    For some of us maybe it's the opiate receptor that needs a little tweak. Not sure why it's frowned on when it may be needed. As long as someone is being careful and using it wisely with doctor supervision. It's another neurotransmitter that our body naturally has. It could get out of balance too - same as seratonin, dopamine etc.

    I plan to try some other things on this off cycle. See if they may work as well. But so far, this has been my best help. I've had POTS friends that this was horrible for. We are all so different.
    Issie
     
  11. Issie

    Issie Well-Known Member

  12. Issie

    Issie Well-Known Member

  13. ritasheart

    ritasheart Member

    I use a pain reliever sporadically when I must rise to an occasion and not crash from it. I feel if I used it all the time, it would stop working. My mother and sister took Tramadol daily for FM. I take what I take to get clarity and energy for outings (medical mostly).
     
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