Fibromyalgia: The Invisible Disease | Arthritis Information

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Drug approved. Is disease real?”

“Does it really exist or is it all in women’s heads?”

“The doctors are in. The jury is out. “

The New York Times headlines rankle Barbara Keddy. For more than 40 years, she has suffered from fibromyalgia, a chronic disorder characterized by widespread pain and fatigue. But the condition is little understood and difficult to diagnose. As borne out by the headlines, some doctors are hesitant to acknowledge it even exists.

After retiring from teaching at Dalhousie University four years ago, Dr. Keddy decided it was time for an in-depth investigation of fibromyalgia, which is much more common among women than men and so has become known as primarily “a woman’s disease.” As a nurse, medical sociologist, university professor and researcher who suffers from the condition herself, she has a unique perspective to offer.

Drawing on her own experiences as well as those of 19 other women, Dr. Keddy discusses current theories of causes and treatments in her book, Women and Fibromyalgia: Living with an Invisible Dis-ease (iUniverse Co.). She also maintains a blog (http://www.womenandfibromyalgia.com) exploring the daily difficulties faced by fibromyalgia sufferers.

“When I became affected by this (after the birth of her first child by Caesarian section), they didn’t know what to call it,” says Dr. Keddy, professor emerita with Dalhousie’s School of Nursing, who was finally diagnosed with fibromyalgia 30 years after first experiencing the symptoms. “All I knew is that I was sore all over.”

“Sore all over” is a refrain among fibromyalgia sufferers, who have been stigmatized as chronic complainers, says Dr. Keddy. Other symptoms include generalized stiffness, sleep disturbance, fatigue, depression, lack of concentration and digestive upsets. The musculoskeletal condition is aggravated by dampness and difficult weather conditions. The pain can be managed—climates with dry heat help, as do some medications—but it doesn’t go completely away.

“The audacity! The women who have this condition hurt in all the same places and have the same symptoms. So how can they say that it’s all in women’s heads?”

She suspects many more women have fibromyalgia than have been diagnosed. Called “the invisible disease,” fibromyalgia doesn’t affect the major organs, can’t be revealed with x-rays or blood tests and isn’t life threatening.

Because of the soreness and pain it causes, fibromyalgia has come to be associated with arthritis and rheumatism. But Dr. Keddy believes the condition is a neurological hypersensitivity, caused by an over-stimulated nervous system.

“Fibromyalgia involves pain in the muscles, whereas arthritis is in the joints—but somehow fibromyalgia has landed there (with arthritis) as a home base,” she says. “My thinking, and I’ve interviewed hundreds of women not just the 20 who are profiled in the book, is that it’s due to a hyper-aroused nervous system.”

Dr. Keddy believes women are more susceptible because they are caregivers, thinking about others before they think of themselves. “Some women have highly developed intuitive skills honed to such an intense stage that the nervous system becomes highly sensitive and hyper aroused,” she says. “Then, there’s a trigger, a dramatic event—perhaps the death of a loved one or an operation such as a hysterectomy—and the nervous system is pushed to the extreme.”

http://www.sciencedaily.com/releases/2008/05/080513191552.htmInteresting article.  I had a hard time getting fibro dx.  I only learned of it from my cousin who has it, is an RN married to an MD who got the dx from medical school friend of her husband.  It is hard because no physical lab test confirms it, only physical exam.  Maybe some day.

 
Jan
It's all in a guy's head too. Yeah right Interesting little thread and helps me to  understand what I have been thru.

Over the past eighteen months of this RA stuff I have also had a different type of pain/discomfort that I could not pin to RA, it just felt different.

What I was experiencing was muscle type pain across my shoulders, neck, upper arms.
At times this would become debilitating to the point that I could not raise my arm.
The only way to get some sort of relief was to (and still do) lay down for 30 minutes.

I can also get the shakes at the slightest sign of stress and become very nervous.

I have always been a bit of a stress head but since getting this condition (RA) I seem to smell a stressful situation before I actually know whats coming around the corner.

All this leads to the fact that I have mentioned all these things to the Docs many times.
I say to them, it feels like my nervous system has been fried, iether the drugs or the RA has/is doing something to my nervous system as well.

Nope, not the drugs, nope not the RA, lets try you on some antidepressants.
Four docs have all said that it is in my head and that needs some therapy to get it (your head) right...

You do end up having a lot of self doubt  which does not help the situation and then it becomes a matter of, it's in your head stuff.

I'm a bloke and they want to push more antidepressants down my throat, I have an unfilled script for Zoloft at the moment.

Not to sure what I set out to say now, ah yes.
I just feel I have had touches of this and at least for me, is real.


[QUOTE=mab52]It's all in a guy's head too. Yeah right [/QUOTE]You put this up while I was trying to compose my little piece above but you and I seem to think along the same lines and run into the same trouble trying to explain things to the experts.
Bodak2008-05-14 12:28:12Bodak
I think if you write all of your symptoms down daily like I did, you might be able to discern a pattern for FM that has been cloaked behind your RA. If this is so, you might need to be assessed for that as well. Once I wrote everything down it practically screamed FM.

There's enough differentiators for FM so that you can mark them.
Mike

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