I am very very uncomfortable with Stone claiming that when someone is finally diagnosed with a known organic disorder, they were not misdiagnosed, but had "functional" symptoms before they developed this disorder.
where did he make this point?
I am very very uncomfortable with Stone claiming that when someone is finally diagnosed with a known organic disorder, they were not misdiagnosed, but had "functional" symptoms before they developed this disorder.
I do think stress plays a larger role in FND than many other disorders as the Limbic System is disregulated, arguably leading to a more severe response to stress, or cues are more readily perceived as stressful. The Limbic system is also involved with many other processes, which it will interfere with when disregulated.
It could be that there is a clear organic cause, that hopefully then can be targeted effectively. I think that for better or worse, FND is the best 'working title' for those diagnosed as such, as further tests yield no further evidence for other known diseases. Many FND sufferers that get a swift diagnosis and have good access to interdisciplinary care improve, and some may recover completely. In the meantime research keeps ticking over, and will give new insights.
See this post by @Woolie where she gives some references.where did he make this point?
I don't really understand your second point. They have framed it in a simplistic and kind of reductive, meaningless way--thoughts/emotions cause symptoms. That framing concerns me.
I'm not sure that challenges in avoiding misunderstandings means that these difficult topics should be avoided. But I make no claims to really know what the best way to handle all these things is.
I think FND is really difficult to write about concisely because i) it's complicated, uncertain and touches on areas where old and inaccurate assumptions can be embedded within our language and ii) there seem to have been deliberate attempts to use language in a manipulative way to 'help' patients by managing their beliefs without their fully informed consent (some patients seem unconcerned by this - we all have different preferences and desires... some are just better than others). And other reasons too.
Or FND is hard to write about because it's an incorrect explanation.
It is equivalent to conversion disorder, which comes from Freud who used what today would be considered "recovered memory therapy" to unmask the emotional trauma he believed was causing unexplained illness. Recovered memory therapy is now considered a method to implant false memories in patients. Freud also told stories about successfully treating patients with his methods but these were later exposed as fabrications.
But what is the alternative then for patients diagnosed with FND? Is there a more specific, alternative diagnosis that would be a better description of their medical condition?
Yes but are they aware of the official classification?
"In ICD-10, functional neurologic disorders are classified exclusively in the psychiatry section as dissociative (conversion) motor/seizure/sensory disorders (F44. 4)."
(as far as I can see in ICD11 they are 'Dissociative neurological symptom disorder')
see also:
Dissociation and functional neurologic disorders.
https://www.ncbi.nlm.nih.gov/pubmed/27719880
Once the patients have twigged to what the term really means.Because this field is so highly controversial, there is a euphemism treadmill whereby every few years or decades they come up with a new term with which to fob off these patients from neurology clinics, once the old term has become too offensive.
takes people to post #7 in the S4ME thread you refer to rather than the beginning of the thread. Was that intentional?
MSAC recognizes that the symptoms presented as a part of this disorder are by definition not due to a disease of the nervous system, but they mimic neurological symptoms and patients with these presentations are commonly referred to neurologists for evaluation.
This is an eyeopening publication from Johns Hopkins which gives a picture of diseases and medicine which has moved into the 21st century in a way which has not been happening with ME and CFS research. This reveals the sophistication of understanding of multiple complex subgroups within a disease, or group of associated diseases, to be able to find appropriate treatments for individuals.
Quoted from LEAP “A rheumatic disease is big, and its effect can be devastating. However, a disease such as rheumatoid arthritis, scleroderma, or Sjögren’s is, in fact, multiple diseases, each slightly different. Each subgroup has a different trajectory of illness, and may respond better or worse to various forms of treatment. But it gets smaller still. One of our Greene Scholars, Sergi Regot, is studying individual cells that are molecularly and genetically identical; they should all behave in the exact same way, but they don’t. This is because of countless tiny factors that we are now beginning to explore. …….
In other work led by Thomas Grader-Beck, we are using new approaches – collecting data from patients and their lives as their disease evolves over time – to build a framework to discover ever-more precise patient subgroups, at scale, and help us refine our care even further. This is precision medicine at its finest: now we can analyze thousands of points of data to find patterns and tailor our diagnosis and treatment for each subgroup – instead of unsuccessfully treating a very heterogenous group of people as if they were all the same.”
This is why I think we need research like this new GWAS proposal, which is now being run by researchers of the highest calibre.
HOPKINSRHEUMATOLOGY.ORG
www.hopkinsrheumatology.org
It is difficult to talk about FND because it is a mess.
That is exactly what it is.I feel that in Neurology the label psychogenic is the 'God of the Gaps'