Fibromyalgia as a Dopamine Deficiency Condition
More Overlaps Between Chronic Stress and Chronic Illnesses
This follows on from my recent article:
in which I wrote, in reference to the overlaps between the symptoms of chronic stress and those of chronic diseases:
“…note also, that this is definitely not saying that everyone will get all of these symptoms… chronic stress manifests very differently in each of us, resulting in our own personalized basket of symptoms “picked” from these lists… the diagnosis we eventually get from the doctors then depends on how closely the contents of our unique basket matches to a specific collection of symptoms which has been given a disease label, almost via a flowchart…”,
Subsequently, a reader, Christine, sent me a link to an article reframing fibromyalgia as a dopamine deficient condition [just like Parkinson’s], which is a perfect illustration of the above sentiment. Here, we consider what this article about fibromyalgia has to say, and what we can learn from this connecting-of-the-dots. Not only does it re-iterate the point above that all these diagnosis labels are manifestations of the same thing, but it also highlights an important nuance I missed before.
The new lesson is that we can learn much more by considering the similarities and commonalities between various chronic disease diagnostic labels, rather than the emphasis on the differences. In my view, there is much to be gained by sharing the wisdoms and strategies gleaned across the different [artificially] siloed community boundaries. Indeed, I believe that this artificial silo-ing, mainly due to the ultra-specialized nature of our current medical systems, has done more harm than good. Thus, I advocate for knowledge synthesis and generalization above separation, specialization, and reductionism, and for much more cross-fertilization, and cross-pollination, between the different disease labels. Especially important is the co-sharing of solutions and wisdoms by members of the different communities themselves with each other.
The article we consider here is Central Role of Dopamine in Fibromyalgia, and the following quotes are taken from the article’s introduction.
“Fibromyalgia is a common disorder known chiefly for its association with chronic widespread pain and tenderness to light palpation. A diagnosis of fibromyalgia in the clinical setting is based on the classification criteria established by the American College of Rheumatology, published in 1990. While historically considered a disorder of the musculoskeletal system, included within the greater symptom complex that comprises the so-called ‘fibromyalgia syndrome’ are a striking number of neurological phenomena that include dysautonomia [disorder of the Autonomic Nervous System]… and restless legs syndrome. Patients also frequently complain of cognitive dysfunction (commonly referred to as ‘fibro fog’) characterized by impaired concentration and short-term memory consolidation, impaired speed of performance, inability to multi-task, and frequent cognitive overload.”
“Given the absence of readily demonstrable peripheral tissue pathology, fibromyalgia research in the last two decades has focused increasingly on the central nervous system as a potential source of symptoms. Indeed, among the more recent hypotheses regarding the pathophysiology of the disorder is that fibromyalgia represents a state of dopaminergic hypo-function [deficiency] that develops subsequent to changes in limbic function following exposure to chronic stress. This proposition was originally drawn from three key observations:
fibromyalgia has been characterized as a ‘stress-related’ disorder due to its frequent onset and apparent exacerbation of symptoms in the context of stressful events;
the experience of chronic stress results in the disruption of dopaminergic activity in otherwise healthy organisms; and
dopamine plays a dominant role in natural analgesia within multiple brain centers such as the basal ganglia, ventral striatum, thalamus, and limbic cortex.”
So here is a first example of cross-fertilization of ideas that can occur, by looking outside of our own particular “disease” silo: in all my research and studying of dopamine, in the context of dopamine deficit conditions such as Parkinson’s, I have never come across the concept that dopamine is explicitly a “natural analgesic” [pain reliever] before! Indeed, in their conclusions, the authors say:
“… dopamine is a catecholaminergic neurotransmitter that plays a prominent, albeit historically lesser known, role in natural analgesia within the central nervous system… indeed, it has been demonstrated that the analgesic capacity of classical analgesics (i.e., mu-opioid receptor agonists, such as morphine) is derived in large part from their capacity to activate dopaminergic neurons.”
This is news to me! However, it makes so much sense of what I experience every day: when a dose of the dopamine supplementing drugs kicks in, all my chronic pains and aches just melt away, and then just as suddenly come back in force when the dose wears off. I had in mind this was due to dopamine fluidizing the fascia and connective tissues, thus temporarily easing restrictions, but the direct pain relieving effects in the brain intuitively feels closer to the right answer.
As an aside, this natural analgesic effect of dopamine also explains why we are all so prone to addictions in the modern world, because, at least initially, our addictions quite literally take away our pain through generating dopamine. Of course, this eventually backfires as our bodies and brains become acclimatized, requiring more and more dopamine to have any pain relieving effect, requiring in turn more extreme “hits” from our addictions, and then just making the pain worse as we have larger and larger dopamine crashes on the other side.
The other part of the author’s conclusion is:
“… an increasing body of evidence suggests that fibromyalgia is associated with dysfunctional dopaminergic neurotransmission as demonstrated by neuroimaging studies that have revealed both a reduction in dopamine synthesis at baseline and a disruption of dopamine release in response to tonic painful stimulation…”!
So, in the view of the authors of the article, the pain of fibromyalgia is due to low baseline dopamine levels, meaning sufferers are more prone to chronic pain, but also that they cannot produce their own natural analgesic effects, as they cannot generate enough of their own dopamine for this purpose. The same will therefore be true [is true in my experience] of folks with a Parkinson’s diagnosis, who also have problems generating enough of their own dopamine supplies.
“Many of the symptoms that comprise the greater ‘fibromyalgia syndrome’ may also be related to a disruption of normal dopaminergic activity, including Restless Leg Syndrome, dysautonomia, dysphoria and cognitive dysfunction. Strategies aimed at enhancing dopaminergic activity, therefore, represent a rational approach to the treatment of fibromyalgia.”
The authors back this up by mentioning the success of some trials of low doses of the dopamine agonist class of drugs developed for Parkinson’s on folks with a fibromyalgia diagnosis.
I wonder, though, why they went straight for the dopamine agonists and don’t mention trials of the mainstay drug therapy for PD, namely straightforward l-dopa supplementation, either via natural sources [velvet bean extract] or pharmaceutical grade [Madopar, Sinemet, etc.]? I would be very interested if anyone with a fibromyalgia diagnosis was willing to self-experiment, at their own risk and of course provided they are not on counter-indicated drugs, and in consultation with medical professionals, by taking velvet bean [Mucuna Pruriens] extract to see if this helps? I would recommend taking one capsule of Biovea’s “Mucuna Dopa” supplement brand for this experiment, as I can vouch for the quality of this product, and that one capsule of this is exactly equivalent to a standard capsule of Madopar [pharmaceutical grade]. If it does work, this would switch off the pain symptoms for a while, like it does for Parkinson’s.
Indeed, this would be a test of how far the analogies between the two diagnoses go, with the caveat if this does work for folks with fibromyalgia diagnoses, this is still not the long term solution, because of the same trap that folks with a Parkinson’s diagnosis get stuck in: needing ever increasing amounts of exogenous dopamine, and hence getting ever increasing side-effects.
Instead, the goal is to start self-generating enough of our own endogenous supplies of dopamine again. So we now turn the arrow of cross-pollination the other way, and see what sufferers with fibromyalgia might have to gain from the lessons learned and wisdom gleaned by the more archetypal dopamine deficient Parkinson’s community.
First and foremost, we now know that folks with fibromyalgia would greatly benefit from reducing stress, and keeping as calm as possible for as much of the time as possible. This is because adrenaline, which is generated by stress, is made from endogenous dopamine supplies - that is, stress gobbles up natural dopamine. This not only means that acute stress will, in the moment, make the symptoms worse, but also when we are chronically stressed, we are constantly using up our dopamine as quickly as we are generating it by converting it to adrenaline, and hence there is never enough left to play an analgesic role. This is also another reason that exogenous dopamine supplementation is not the answer, because it just feeds into adrenaline, and hence helps to fuel chronic stress.
Folks with a Parkinson’s diagnosis have found that dealing with, and healing our traumas is a massive part of this necessary stress reduction, and the same will be true for fibromyalgia according to the above findings.
Secondly, folks with a fibromyalgia diagnosis will need to avoid disappointment, and cultivate a mindset in which we learn to take pleasure in the motivating part, in the effort, the seeking and striving, because celebrating the win (a big, quick peak in dopamine) more than enjoying the pursuit, rebounds into the pain side of the pleasure-pain balance system, and too much of this will lower baseline levels of dopamine.
Thirdly, folks with fibromyalgia diagnosis will benefit by avoiding and overcoming addictions, as these also result in much lower baseline dopamine levels (see my review of the Dopamine Nation book cited above).
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I have ordered the Mucuna Pruriens that you recommended for an experiment to see if this supplement decreases my so called fibro pain. I understand this is not a long term fix, that it is an experiment that gives me the basis for the next decision. You can contact me at my email address if you are interested in hearing how it goes. buddah.mama@yahoo.com
I am doing the first two, of the three things you mentioned at the end of your article. 1. reducing stress, and keeping as calm as possible for as much of the time as possible. 2. avoid disappointment, and cultivate a mindset in which we learn to take pleasure in the motivating part, in the effort, the seeking and striving, because celebrating the win (a big, quick peak in dopamine) more than enjoying the pursuit, rebounds into the pain side of the pleasure-pain balance system, and too much of this will lower baseline levels of dopamine. I have some work to do on number 3. folks with fibromyalgia diagnosis will benefit by avoiding and overcoming addictions.
Thanks for taking this idea further Gary. One problem we have is with the "diagnosis" in the first place. The diseases we are diagnosed with, you with Parkinson's, me with Fibromyalgia and now "long covid" and type 2 diabetes, are NOT what is actually wrong with us. These diagnoses are, at best, sets of symptoms that might lead us to the true cause of our "malaise" if we follow them deeply enough - which medicine never does.
OUR INTERFACE WITH THE OUTSIDE WORLD AS THE CAUSE OF HEALTH OR DISEASE
I am building a thesis at the moment that ALL health is related to the interactions of our core metabolism, with the outside world. The body requires the right interactions with the outside world, which are, to some extent, determined by genetics. This goes from the obvious food, hydration and air, to light, perception of beauty, smell, grounding, toxins, EMFs, social relationships etc. And when we manage any of those interfaces badly, our entire body has to tweak all the systems in the body to redress the balance and find a new balance. Eventually our "balance" is so far away from true North, that we start to experience symptoms, but those symptoms are not what is wrong with us. They are telling us which part of our body systems is taking up the slack for the systems directly impacted by our faulty interface with the outside world.
Sorry, this is hard to explain without it seeming messy and complex because we have multiple interfacing ideas, that all work together.
Providing we are born fully functional, we all have a core metabolism we need for life, but we also have genetic limitations that might make us more vulnerable to particular physical breakdowns. The reason we get any disease is some breakdown in the interface between the body and the outside world. It is that interface that we have to manage better, and any intervention that does not address the faulty interface may work initially but the issue, whatever it is, will recur.
EXAMPLE OF CORE GENETICS REQUIRING INTERFACE ADAPTATIONS
As a simple example, my physiology is designed for low sun, northern climates. If I go out in the sun, my genetics mean I WILL burn. And if I stay in the sun I will continue to burn because I do not tan. Of course, I cannot recover if I continue to expose my melanin free skin to the sun. And it is not possible to "cure me" of being melanin deficient - that's down to genetics. In that context, my skin will recover from being burnt once or twice, but eventually will become damaged and even potentially cancerous. This is my interface with the outside world that I have not managed well. If I get skin cancer, I can possibly use black salve to cure this instance of the skin cancer, but if I am stupid enough to go back out in the sun, then I will get the same disease again because I am not correctly managing my interface with the outside world, based on my personal genetics.
IDENTIFYING THE FAULTY INTERFACE
So our problem is in how to identify and then fix our faulty relationship with the outside world. And for the syndromes this can be fairly invisible. We have to trace back from the visible symptoms such as pain and stiffness, to potential interface issues. And to date, both medicine and natural healing don't trace back far enough. They still believe the symptoms are the core of what is wrong, rather than being the body's valiant attempt to find a new balance to accommodate what is really wrong.
Weight issues are a good way of illustrating how we do do this already to some extent but how we get it terribly wrong. The symptom of our faulty interface with the outside world is apparently inappropriate weight gain. We start from the weight gain and we assume the interface that is not well managed is food intake, so we adjust our food intake, often with little effect. So what if the faulty interface is something else entirely - nothing to do with our food intake? We now know that a lot of metabolic issues are related to some form of autonomic nervous system glitch that is causing us to live in fight and flight mode, which in turn, causes our body to do the right thing and stack on weight to see us through the next emergency. Once we change our question from "what are we doing wrong" to "what is our body doing right", we can see the same symptoms quite differently.
This is harder to do with all the much less obvious syndromes but we can do it. I discovered, many years ago, when I met up with a lady while we were walking our dogs, who also had fibromyalgia. We conversed very easily and I spotted something. We were both outraged at various things happening in the world, and we were both utterly unable to find any way of intervening. I coined the term "impotent outrage" and started to see the pain of FMS reflecting my outrage of what I see in the world and the stiffness (and so reduction of mobility) as reflecting the impotence. I decided I did not want to become less outraged, so instead I had to work out how to be less impotent. But in reality, as the global conditions have worsened, and my ability to intervene has lessened, so my FMS+ symptoms have worsened. This is my faulty relationship with the outside world. I have to either reduce my outrage, or become more effective. I am still struggling to do the latter.
FINDING INTERVENTION POINTS TO FIX FAULTY INTERFACES
The difference for me now is Andrew Huberman, who has taken me on a journey to understanding body systems rather than body parts or symptoms. From watching/listening to a lot of his material I have become much more aware of the body systems that are responding to my interfaces with the outside world and doing the best they can to achieve balance and keep me alive despite my faulty interfaces. My body has adapted from it's "native balance" to a new balance, to accommodate my "impotent outrage" (and maybe other faulty interfaces). Our symptoms are no more than a signal that our body is striving valiantly to make up for our faulty interfaces with the outside world.
The greatest issue with this approach is its complexity. We have to determine which is the key interface that is not being well managed, identify the downstream results of that mismanagement, and then work out how to intervene to set a new relationship with the outside world at the appropriate intervention point. At the moment I am working on my obvious shortfall of dopamine. Will increasing my dopamine levels trigger a re-balancing of my bodily systems - well it has to, to some degree, but will that lead to a healing throughout my body, who knows? Only time will tell - depending on which part of my dopamine system has gone walkabout and whether the interventions I use cause it to re-balance.
THE BODY SYSTEMS AND THE INTERACTIONS BETWEEN THEM
Potentially we can intervene via a range of bodily systems. The autonomic nervous system (electrical messaging) interfacing with the endocrine system (hormonal messaging) and the enzymatic system (chemical messaging) - are the new frontiers, particularly for the sports medicine types but potentially also for the invisible diseases that are besetting us. I wonder if there is even a word and a medical category that deals with all three "messengers" in unison (hormones, nerves and enzymes). And are there more messaging systems? And does an intervention in any of them trigger a response in all of them? I am guessing yes to the last question, although would have no idea how to trace that from intervention to resolution.
In looking at the interventions I am currently taking:
I am doing a vagus nerve exercise to intervene in the parasympathetic nervous system.
I am doing a Huberman breathing exercise that is supposed to reduce the production of stress hormones and so intervene in the sympathetic nervous system.
I am taking a dopamine precursor and working on behaviours to stimulate the dopamine cycle.
I am taking herbs to ensure a healthy balance of gut enzymes.
I am trying to get early morning sun to improve my sleep cycles.
I am protecting myself as best I can from 5G EMFs to protect my nervous system generally.
So intuitively I have ended up with indirect interventions in all three systems.
Whether any of them work to turn around my health decline, only time will tell.