Another thread filled with the rather predictable criticisms of ME/CFS patients. I really think that a lot of patients do not understand their own disease all that well at the neuropsychological level.
Emotional symptoms are a major component of ME/CFS, and in my view are under-investigated. If you read the Canadian Consensus Criteria, you will see that there are three different areas of emotional dysfunction in ME/CFS (though a patient may not suffer from all three):
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Emotional lability (unstable or random emotional responses).
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Emotional overload may be unduly stressful (many patients report that they find emotional discord or social disharmony very stressful and unpleasant).
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Emotional flattening (also known as blunted affect; this is where your emotions have largely dried up, and so your mind only responds weakly to emotional stimuli such as films that would normally create a robust emotional response).
These emotional dysfunctions of ME/CFS can be quite debilitating (I find the emotional overload and sensitivity to social disharmony particularly problematic), and deserve to be better investigated and better understood biomedically (with the emphasis on understanding via
biomedical investigation, not via the mumbo-jumbo "all in the mind" psychogenic ideas of ME/CFS).
I suffer from both emotional overload (sensitivity to social disharmony), and also the emotional flattening. I personally think that the emotional flattening is one of the contributing factors to why ME/CFS patients don't tend to find themselves in relationships. I used to be quite romantic, but I find the ME/CFS emotional flattening kills off all romantic thought, such that in my present state, I don't feel that I even want a relationship (low libido I think also plays a role in this).
I have found some supplements and drugs (see
this post) that
temporarily bring back some emotional responses, but unfortunately their effects are only transient. I also notice that
vitamin B2 seems to reduce my sensitivity to social disharmony a little bit.
Interestingly enough, as the suspected enterovirus that triggered my ME/CFS spread to over 30 friends and family, after a few years with this virus, quite a few infected people reported that their emotions felt weakened — and this was also something I observed myself in these people (ie, independent to their comments, I noticed myself how many of them had dried up somewhat emotionally).
I think there should be more research into how enteroviruses such as coxsackievirus B and echovirus can affect emotional processing and emotional health in the general population, not just in ME/CFS.