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in patients with other described symptoms (anxiety, depression, primary ovarian insufficiency, muscle pain, autoimmune disease, family history of mental retardation or
intellectual disability, among others)."View Thread






Yet, so little research has been done. Think about the poor souls who were told their symptoms were purely psychological. Some of these people committed suicide because their friends and family wouldn't honor their suffering.
Now, MRI imaging shows fibro quiets - yes, quiets, pain centers which should be active, and activates pain centers which should be quiet. Even more interesting, brain chemical tracking shows the brains of fibro patients do not produce dopamine. The dopamine center is quiet resulting in thalamo-cortical dysrhythmia - the cause of central pain, tintinitus, depression, and more - yes - a grab bag of problems. So, for those who want to streamline fibro into a simple pain problem, study up.
I believe fibromyalgia is a neurological disease. Did you know rheumatologists now say many people diagnosed with MS have been misdiagnosed; instead, they have fibromyalgia? Think about the respect MS gets as a disease compared to fibromyalgia. It is simply a couple words. The words we use when describing what's happening and has happened to us are extremely important - never forget that.
I believe there are at least two kinds of fibro. 1. Polygenic Fibromyalgia: meaning you are born with it.
2. Secondary Fibromyalgia meaning you acquired it from head or spinal cord trauma. The results of the poll above clearly show about 70% of those who answered suffer from Polygenic Fibro. The rest - Secondary. Researchers need to divide the two groups and work a lot harder to find a cure or at least medication that brings near normalacy.
Personally, I hate catering to my fibro. It's an ongoing regimen of self care that takes up a lot of my time and limits me. I dislike working part-time more than words can say. I would love to be out there with the rest of the movers and shakers but the fact is, this frustrating illness limits me. It limits me physically and financially - which sucks.
Finally, I want to address the idea that it is aging which makes fibro worse not the progressive factor. Well, If you have secondary fibro, I'm sure it seems that way to you. If you have polygenic fibro then you understand the progress as you have accumulated symptoms one by one. I spoke to my 72 year old father about a year ago, before I was diagnosed. I couldn't understand the stiffness and pain I was hit with last year. I asked him, "Do you feel pain when you sit for more than 15 minutes or when you get up to move. His answer, I don't feel any aches or pain at all. Do you??" So, yes, aging can worsen things for some yet certainly isn't the reason for progressing pain in ALL of us, you see. Because everyone does not have more pain with age....View Thread

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