As a linguist, I want to find the words to measure chronic illness
11–20 of 26 posts
Re: As a linguist, I want to find the words to measure chronic illness
#12Funcap maps fairly well to the mild,moderate, severe and very severe descriptions that have been historically used and its fairly precise and improvements of 0.5 are very measurable. Its not popular yet but it should be its probably the best functionality questionnaire.
In regards to linguistics there is a real issue with people who have never had a sensation understanding someone else describing it. ME/CFS is 4 symptoms and a few other groupings of them under the Canadian Consensus criteria but a lot of focus is put on fatigue and PEM. But the fatigue is not something someone who doesn't have the disease could understand. Its not tiredness like not sleeping enough, its somewhat more like the worst flu you ever had and made you want to stay in bed (which most people have not experienced) but its still underplaying the muscle weakness and lack of stamina and general feel of unwellness that encompasses this fatigue, its like all the cells in the body have no energy. There is simply no way to express this and have someone understand how debilitating that is and the consequences for breaching capacity, which make ME sufferers worse sometimes permanently. We just don't have the words or really the understanding because while many biological issues have been found nothing has yet been accepted as a biomarker of the condition.
Re: As a linguist, I want to find the words to measure chronic illness
#13Words are virtual. At the same, experiences are real. Also, real is their impact of our lives. "A headache" can be anything for from a slight discomfort, to something crushing, putting in a blank stare. It can be of various lengths, various frequencies, impacting us in various ways. Both matter.
> I want practitioners and researchers to help us name things so that they can measure them, and so that those measurements can be accurate reflections of our internal realities.
I think it is one of things where LLMs can shine - by translating one's own notes, ones own recordings of everyday life, into a summary.
This used to be a bottleneck - so people HAD to resort to some questionaries (binary or Likert scale), to make it quantitative. Now we can automatically process actual text. (It was possible before, to some extend, with simpler models like word2vec or Latent Dirichlet Allocation), but with LLMs we can actually get the full context, not only look for keywords, their groupings and associations.
Re: As a linguist, I want to find the words to measure chronic illness
#14I think words are less the problem so much as evidence. The symptoms of chronic conditions kind of are what they do. Maybe you could say something like: I planned to complete five items on this list today and only completed one, because I was too fatigued to continue and could not complete another item despite telling myself to do so or attempting to engage in the activity. This creates a goal-outcome gap in language…
Re: As a linguist, I want to find the words to measure chronic illness
#15Wittgenstein is a difficult read, Pragmatism is not difficult, but I feel like many people wouldn't understand what is being said.
The goal of this would be to teach how language is the basis for all science, and as a result cannot explain what is realistically happening, but rather a useful estimation.
But right now, the majority of the population believes in scientific realism and have no idea that biology/medicine are systems with rough edges that cannot understand everything.
I imagine the humility for doctors would be a benefit. The general population would be more likely to work towards developing solutions and trying things rather than expecting a simple solution.
But again, I have no idea how to actually do this. It took almost a decade of reading to learn about these concepts, and it took humanity ~2400 years since Plato to figure this out.
Re: As a linguist, I want to find the words to measure chronic illness
#16After skimming this article, it drove me to search for the term “hypochondria” which this article suggests afflicts 5%-10% of the population. https://www.psychologytoday.com/us/basics/hypochondria Those afflicted with hypochondria spend 10x more on health care than the average individual, according to this article. May be a relevant driver for health care costs, and thus insurance costs. I’ve heard that every medical…
I was diagnosed with Celiac disease in 2014 via blood test and upper endoscopy. Before I was diagnosed I went to at least 5 doctors (that I can remember) complaining of symptoms. When I said that I felt fatigued, I was told to sleep more. When I complained of joint pain, I was told that I was just typing too much. When I complained of mood swings, I was told it was just being a teenager. Doctor after doctor told me t…
> European Union has suggested that between 6 and 8% of the European population could be affected by a rare disease sometime in their lives.
Obviously some of rare diseases are quite visible and obvious, but I wonder how many aren't.
Re: As a linguist, I want to find the words to measure chronic illness
#17People (even from the same culture, with the same native tongue) use words differently. It is one of the reason for which I am mildly skeptical about all such things as "How happy you are on the scale 1-10?" - no matter what is the sample size (it could be a billion), it depends on one's inner definition of "happy" and on the numbers attached to it. Words are virtual. At the same, experiences are real. Also, real is…
In my experience if they see someone struggling to move around and follow instructions in the hospital then they will just pump some morphine in so the patient can comply and they can quickly get on with things but its not driven by the level of pain the person is actually in when left alone in their hospital bed or at home.
Re: As a linguist, I want to find the words to measure chronic illness
#18I'm not entirely sure how to do this, but I think it would benefit society to have Wittgenstein's Tractatus Logico-Philosophicus taught, and probably William James's Pragmatism. Wittgenstein is a difficult read, Pragmatism is not difficult, but I feel like many people wouldn't understand what is being said. The goal of this would be to teach how language is the basis for all science, and as a result cannot explain wh…
This happens in every single disease, ME/CFS is 280 symptoms yet its defined by 4 despite the fact that only seems to match about 90% of the patients but they have other combinations. We are dealing with both the imprecise nature of language and a lack of common experience with which to convey understanding but also a medical system that has drastically simplified diseases to the point where its descriptions and diagnostics are incomplete. Its going to take a very long time to correct it all assuming we can get medicine to once again follow the scientific findings, which remains a big if at this point.
Re: As a linguist, I want to find the words to measure chronic illness
#19Next week it will be twelve years since my wife killed herself due to Chronic Pain. Willing or not thrusting me into being an advocate for those with Chronic Pain. Most specifically advocating for those with Intracranial Hypotension due to Cerebrospinal Fluid (CSF) Leaks and those poisoned by Fluoroquinolone antibiotics such as Levaquin, Cipro etc.
See our documentary Pain Warriors about the whole saga of my late wife. It is free to watch many places. I get no remuneration of any kind from Pain Warriors.
As someone with Lupus "The Spoon Theory" was created by Ms. Christine Miserandino.
Anyone that spends time in Social Media related to chronic health issues is going to come across someone talking about 'Spoons'. Yes, the utensil that you eat with.
A normal health person has an unlimited number of spoons per day. Someone with a chronic condition may only have five or ten if they are lucky.
Each 'Spoon' represents a task of daily life. Say just getting out of bed, taking a shower or eating a meal, each being one spoon.
When you run out of spoons for the day your day is over, or you start paying by borrowing spoons from tomorrow, which makes tomorrow a worse day than today.
So the linguistic words being looked for are already being measured by the community itself in a scale of Spoons. As silly as it might sound.
Ms. Miserandino explains how this all came about here:
https://www.butyoudontlooksick.com/articles/written-by-chris...
Something I need to add, because I mentioned Lupus, is that food sensitivities to Nightshade plants, common in our diets, can mimic the systems of Lupus and Rheumatoid Arthritis. If you or a loved one has those, eliminate the Nightshade family from your diet for a while and see if there is any improvement.
Re: As a linguist, I want to find the words to measure chronic illness
#20After skimming this article, it drove me to search for the term “hypochondria” which this article suggests afflicts 5%-10% of the population. https://www.psychologytoday.com/us/basics/hypochondria Those afflicted with hypochondria spend 10x more on health care than the average individual, according to this article. May be a relevant driver for health care costs, and thus insurance costs. I’ve heard that every medical…
I was diagnosed with Celiac disease in 2014 via blood test and upper endoscopy. Before I was diagnosed I went to at least 5 doctors (that I can remember) complaining of symptoms. When I said that I felt fatigued, I was told to sleep more. When I complained of joint pain, I was told that I was just typing too much. When I complained of mood swings, I was told it was just being a teenager. Doctor after doctor told me t…