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In fibromyalgia, cognitive symptoms are worse than in rheumatoid arthritis

Published 28 Jun 2016

In fibromyalgia, cognitive symptoms are worse than in rheumatoid arthritis
A team of researchers from Rush Medical College, Chicago, and colleagues at other institutions recently did a comparative study of the cognitive functions of fibromyalgia (FM) patients versus rheumatoid arthritis (RA) patients. The study, which was called “Cognitive Symptoms in Fibromyalgia Patients Compared with Rheumatoid Arthritis (RA) Patients”, was presented at the Annual Meeting of the American College of Rheumatology, in Boston.
 
A disease caused by abnormalities in the way the brain processes pain signals, FM is characterized by widespread chronic muscle pain. The associated symptoms of FM are fatigue, poor sleep, hypersensitiveness to pressure, memory problems, as well as other mental impairments. Currently, an estimated 5.8 million Americans suffer from fibromyalgia.
 
The strategy the researchers adopted to address the cognitive impairment of FM patients, was to compare the symptoms of FM with the symptoms of rheumatoid arthritis, a chronic inflammatory disease that starts off with pain in the joints followed by joint deformity and finally, immobility of the joints. In addition to the joints RA patients also exhibit significant cognitive impairment.
 
As part of the study, the researchers studied 211 patients of whom 150 were FM patients and the remaining 61 were RA patients. The cognitive functions of both the groups group were assessed by a questionnaire where the severity of the symptoms were rated from scale one (symptoms never occurring) to five (symptoms occurring all the time). Overall, the researchers found that the symptoms of cognitive impairment were worse in FM patients than in the RA patients.
 
Cognitive symptoms in fibromyalgia
 
The researchers observed that a state of clouding of consciousness, termed ‘fibrofog’ (brain fog) is worse in the FM patients than it is in the RA patients. Fibrofog encompasses difficulties using language, difficulties with learning, and memory loss. These symptoms tend to descend in a haze or “fog,” around the sufferer, and hence the name. Both women and men who have fibromyalgia pain, present with fibrofog, though it tends to hit women more often, especially women between the ages of 30 and 50 years. Symptoms of brain fog can range from mild to severe, varying from day to day, and from person to person. The symptoms include:
 
Poor word use & recall: The patient experiences a difficulty in recalling known words, and names and often uses incorrect words in sentences. Short-term memory problems: Forgetfulness, inability to remember what’s read or heard.
 
Directional disorientation: The patient does not recognizing familiar surroundings, and easily loses his way in his own surroundings. They very often also have trouble recalling where regular everyday things are kept.
 
Inability to multitask: More often than not, people with fibromyalgia cannot focus on more than one thing at a time, and tend to forget the original task when distracted with another.
 
Depleted focus: These patients are very often confused and have a lot of trouble in concentrating and processing information.
 
Number difficulties: This is a common feature of people with FM and they find it extremely difficult to perform basic math problems involving addition, subtraction, division etc. The also fail to remember numbers,
 
In addition to the above symptoms, FM patients also have a difficulty with language, including trouble holding conversations, understanding conversations, and expressing thoughts. The often struggle to find the “right” word to use in conversation.
 
People with fibromyalgia are faced with special demands. Given the task of coping with the pain and fatigue each day, patients need to prioritize and adjust their lifestyle according to the demands of fibromyalgia. Having said that, it does not mean you become a slave to the condition. The limitations of fibromyalgia can be lessened if you get the facts. So arm yourself with all the knowledge about the condition, get answers to all your questions and, instead of focusing purely on fibromyalgia, try steering the knowledge seeking process to “fibromyalgia and you”.
 

Belmarra Health

21 comments


Suzhannah
on 26/07/2016

Hi painnow

You can ask for a referral to a Rhuematologist... They diagnose Fibromyalgia as a neurologist diagnoses ME.... Lyme disease and lupus are also similar in symptoms so you do need a referral to a specialised consultant. 

Most GP's have no training for diagnosing these illnesses but they can be aware of changes they deem to be symptomatic  to be further assessed by an appropriate consultant. 

Hope this helps 


avatar
Unregistered member
on 27/07/2016

Thanks for the answers yes I will talk to my GP can't go on like this really had enough thankyou


raining
on 29/07/2016

I have fibromyalgia, underactive thyroid and osteo arthritis. I look after my husband who has rheumatoid arthritis. I am very tired. my husband has begun correcting me when I say a word wrong and my son is too. This makes me feel demoralised as I am a very intelligent woman and held down a very responsible job until I retired.  this article makes me feel better thankyou


lildav
on 31/07/2016

I have had fibromyalgia for nearly 20 years now and apart from the continuous pain I have what I term 'unplugged episodes' where I am doing something and then suddenly I lose all my energy and will not be able to do anything more.  I just sit or lie and have no energy to get up, walk or carry on with the task in hand.This is bad enough at home but if i get this unplugged feeling when i am out I feel like just sitting or lying down where I am and it is very distressing.


avatar
Unregistered member
on 08/08/2016

lildav, I know exactly what you mean about your "unplugged episodes." I have them to and usually explain them to people as "like having a sink plug in my feet, the plug is pulled and I can feel my energy pouring out of my body from the head down." I too, worry about this happening when I'm out and about, especially if I'm on my own and have to drive to get home.  As far as the Fibro fog goes, I find it gets worse the more exhausted I get.  I'm lucky that I'm self employed and can work my own hours.  This enables me adjust my work around my sleep, which is very useful as I rarely get to sleep before 4am! 

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