Fibromyalgia Symptoms
I don’t get many comments on this blog, and by many, I mean any, but if I did, I’m sure at least some of them would say “fibromyalgia isn’t funny”. I know, I live with it, but I still like to laugh and make other people laugh. So I’m attempting to provide useful information along with my own insights. For a more complete list of 63 symptoms click here. Now on with the article.
“The primary symptom of fibromyalgia is widespread, diffused pain, often including heightened sensitivity of the skin (Allodynia), achiness around joints, and nerve pain. Chronic sleep disturbances are also characteristic of fibromyalgia, and some studies suggest that these sleep disturbances are the result of a sleep disorder called alpha wave interrupted sleep pattern, a condition in which deep sleep is frequently interrupted by bursts of brain activity similar to wakefulness. Many patients experience “brain fog”, also known as “fibrofog”, which is objectively proven abnormally slow brain waves and objectively proven cognitive deficits. Many experts suspect that “brain fog” is directly related to the sleep disturbances experienced by sufferers of fibromyalgia.
Interpretation: Apparently going years without deep sleep makes it difficult to think clearly sometimes. Imagine that.
Other symptoms often attributed to fibromyalgia (possibly due to another comorbid disorder) are physical fatigue, irritable bowel syndrome, genitourinary symptoms such as those associated with the chronic bladder condition interstitial cystitis, dermatological disorders, headaches, myoclonic twitches, and symptomatic hypoglycemia. Although it is common in people with fibromyalgia for pain to be widespread, it may also be localized in areas such as the shoulders, neck, back, hips, or other areas. Not all patients have all symptoms.
Interpretation: Fibromyalgia messes up your body, sometimes a little, sometimes a lot, depending on the person.
Fibromyalgia can start as a result of some trauma (such as a traffic accident) or illness, but there is currently no known strong correlation between any specific type of trigger and the subsequent initiation of fibromyalgia. Symptoms can have a slow onset, and many patients have mild symptoms beginning in childhood, such as growing pains. Symptoms are often aggravated by unrelated illness or changes in the weather. They can become more tolerable or less tolerable throughout daily or yearly cycles; however, many people with fibromyalgia find that, at least some of the time, the condition prevents them from performing normal activities such as driving a car or walking up stairs. The syndrome does not cause inflammation as is presented in arthritis, but anti-inflammatory treatments, such as Ibuprofen and Iontophoresis, are known to temporarily reduce pain symptoms.
Interpretation: We have no idea where the crap it comes from.
The following factors are said to temporarily increase the suffering of patients:
Cold weather, especially when damp
Malnutrition, hunger, or starvation
Physical activity of any kind, including minor tasks such as writing.
Some patients have reported a near-complete remission of their symptoms within several weeks of traveling to a warm, or tropical climate, and the complete renewal of symptoms upon returning.”.
Interpretation: Physical activity of any kind? I’m the queen of sarcasm and pessimism (I really am, I have a crown), but why do the dr.’s always tell us to exercise. You can move, try to move as much as possible, you should move. Although that excuse will come in handy next time I’m supposed to vacuum “Is that physical activity? I’m allergic to that. “Starvation is bad for fibro, because it is just so healthy for everyone else.
This article is licensed under the “GNU Free Documentation Licenserel=”nofollow”“. It uses material from the Wikipedia article “Fibromyalgia .”




August 15th, 2006 at 2:28 am
My daughter created a wonderful excel file for me that would evaluate any task in terms of requirements in energy, acuteness of thinking, pain level etc. It is a great possiblity to be able to pull up a list and find tasks I can accomplish no matter what is going on with my fibro. But I haven’t built it yet — because I have fibro LOL. Right now I am in a super flare and just trying to get this house a bit clean is kicking my butt. I have a stretch of time to try to get that done, so I have hopes.
My long term goal is really a gift from my guy. He said the two things I am better at than anyone he knows (grain of salt needed here) are being a psychic and writing. The writing is impacted by my exhaustion, pain level and fibro fog. Acting as a psychic somehow bypasses all of that and still works. So, long time goal is to set up small shop to offer readings to the public and write while I wait for my clients to start and build over time.
Not too long ago I found that I also suffer from PTSD from some years of military service. That has thrown a wrench in the works for a couple of reasons. One is that my fibro expresses itself a lot in muscle spasm and its byproduts of rigidity and avalanching of pain symptoms. That can be initiated by overspending my available physical energy and strength but also by getting emotional. A good cry is so. not. helpful for me. This new wrinkle has made management more challenging but I am working with a MSW who has a specialty of Vets with PTSD.
A question I would love to ask you is if you have managed to figure out how to maintain a slightly clean house with fibro. I have no hope of sparkling, but just not grubby would shake my world.
Gillian
August 15th, 2006 at 11:14 am
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March 2nd, 2007 at 6:37 pm
I have also heard that consuming dairy products too much can also increase suffering. Can anyone shed light on this?
October 29th, 2007 at 2:35 am
Hello, and I must say what a refreshing and enjoyable way to interpret the hell I have been living in!!
Since I couldn’t sleep (imagine that) I was sitting at the computer trying to figure out why there are no major corporations educating and fundraising for this disease. My eldest daughter works for the M.S. Society in Toronto Ontario where there is constant funds being raised for public awareness and most important to fund research into hte disease. I wondered why there is nothing in place for fibromyalgia…is there no celebrity with the disease perhaps??
In trying to learn a whole new way to live, horribly traumatic this disease, I am beginning to find a way to continue with a life that is sleep deprived, painful and causes numerous other slightly disabling issues (like the lack of memory, horrible reflux, sleep deprivation etc.).
Any good direction would be welcome, I am trying to finish a degree and having a wonderful time with the memory hah!!! The part about trying to function while sleep deprived or at times unable to wake for any period of time is also messing with my schudule!!
Thank you for the article, I was actually able to get a laugh!!
Diana
April 15th, 2008 at 7:15 pm
I’m with Diana on this one! My motto (after suffering a decade and a half with this chronic pain) is ANYTHING for a laugh.
I think I’ll enjoy reading your blog.
3T