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deepblue
06-24-2013, 11:56 PM
I don't have fibromyalgia, but I know a couple people who do, so I thought I'd pass this on here- in case there are those here who suffer from it.

Science has discovered the source, and it's not the brain.

Fibromyalgia Mystery Finally Solved!
Researchers Find Main Source of Pain in Blood Vessels

From here: guardianlv.com/2013/06/fibromyalgia-mystery-finally-solved/


Researchers have found the main source of pain in Fibromyalgia patients, and contrary to what many believe, it does not stem from the brain. The findings mark the end of a decades-old mystery about the disease, which many doctors believed was conjured in patients’ imaginations. The mystery of Fibromyalgia has left millions of sufferers searching for hope in pain medications. Up until recently, many physicians thought that the disease was “imaginary” or psychological, but scientists have now revealed that the main source of pain stems from a most unlikely place- excess blood vessels in the hand.
The discovery may lead to new treatments and perhaps even a total cure in the future, bringing relief to as many as 5 million Americans thought to have the disease. To solve the Fibromyalgia mystery, researchers zeroed in on the skin from the hand of one patient who had a lack of the sensory nerve fibers, causing a reduced reaction to pain. They then took skin samples from the hands of Fibromyalgia patients and were surprised to find an extremely excessive amount of a particular type of nerve fiber called arteriole-venule (AV) shunts.
Up until this point scientists had thought that these fibers were only responsible for regulating blood flow, and did not play any role in pain sensation, but now they’ve discovered that there is a direct link between these nerves and the widespread body pain that Fibromyalgia sufferers feel.
The breakthrough also could solve the lingering question of why many sufferers have extremely painful hands as well as other “tender points” throughout the body, and why cold weather seems to aggravate the symptoms. In addition to feeling widespread deep tissue pain, many Fibromyalgia patients also suffer from debilitating fatigue.
Neuroscientist Dr. Frank L. Rice explained: “We previously thought that these nerve endings were only involved in regulating blood flow at a subconscious level, yet here we had evidences that the blood vessel endings could also contribute to our conscious sense of touch… and also pain,” Rice said. “This mismanaged blood flow could be the source of muscular pain and achiness, and the sense of fatigue which are thought to be due to a build-up of lactic acid and low levels of inflammation fibromyalgia patients. This, in turn, could contribute to the hyperactivity in the brain.”
Current treatments for the disease have not brought complete relief to the millions of sufferers. Therapies include narcotic pain medicines; anti-seizure drugs, anti-depressants and even simple advice such as “get more sleep and exercise regularly.” Now that the cause of Fibromyalgia has been pinpointed, patients are looking forward to an eventual cure. Other expressed frustration about how much they had suffered already:
“When are they ever going to figure out that things are never “all in your head?” said one commenter. “Whenever something doesn’t fit in their tiny little understanding, they belittle the patient and tell them they are crazy. People have suffered through this since they were invented. Prescribing SSRIs for everything is not the answer any more than a lobotomy or hysterectomy was.”
The announcement has the potential to unlock better future treatments and undoubtedly has patients all over the world rejoicing that the mystery of Fibromyalgia has finally been solved.



Sources are at the link, under the story.

Aziara
06-25-2013, 09:24 AM
oh wow.... so it's circulation, not neurological. That's amazing. I've long suspected I might have it, I've always had low-level pain randomly throughout my body. When I was a kid, it was dismissed as 'growing pains'. Now to go hunt down a circulation tonic from my ND mother...

Aziara
06-25-2013, 09:25 AM
Uhm, page cannot be displayed for the link.

deepblue
06-25-2013, 12:44 PM
Looks like it's nerve fibers more than circulation, at least that's the impression the article gave me.

The forum keeps putting in http and the link doesn't have that. Here you go:

guardianlv.com/2013/06/fibromyalgia-mystery-finally-solved/

(http://guardianlv.com/2013/06/fibromyalgia-mystery-finally-solved/)

Echidna
06-25-2013, 02:14 PM
My mother is diagnosed with fibromyalgia, but she also has had Lyme for years.
So have many others who have been labelled with fibromyalgia.

Symptoms of fibro include not only pain and "tender points", but fatigue and in some cases, vertigo and nausea.
At that point it's really difficult to say whether the symptoms are caused by one or the other.

I used to think fibromyalgia is just a misdiagnosed Lyme.
Lyme gets worse in colder weather too, because borrelia like cold.
Should also add here that all the "fibromyalgia symptoms" appeared only after the tick bite.

So, I'm a bit sceptic here.

Edit: For both my mother and me, ALL of the alleged fibro symptoms get better when we take antibiotics or anti-inflammatory meds^^

AniaR
06-25-2013, 05:03 PM
this makes so much sense. All of my fibro problems are mostly in my hands. And like, this describes how I FEEl lol. I can't wait to show it to my doctor hahaha

deepblue
06-25-2013, 05:11 PM
I used to think fibromyalgia is just a misdiagnosed Lyme.
Lyme gets worse in colder weather too, because borrelia like cold.
Should also add here that all the "fibromyalgia symptoms" appeared only after the tick bite.

So, I'm a bit sceptic here.

Edit: For both my mother and me, ALL of the alleged fibro symptoms get better when we take antibiotics or anti-inflammatory meds^^

I can understand that, esp when lyme is so often misdiagnosed. A family friend died of lyme because she'd been misdiagnosed for so long- absolutely heart breaking. But when they have the physical evidence of more nerve endings in fibro patients, not just symptoms, that makes a huge difference.

Echidna
06-25-2013, 05:17 PM
I can understand that, esp when lyme is so often misdiagnosed. A family friend died of lyme because she'd been misdiagnosed for so long- absolutely heart breaking. But when they have the physical evidence of more nerve endings in fibro patients, not just symptoms, that makes a huge difference.

Yea, there is nothing worse than being called mental while your illness gets ignored.
This goes for Fibro, Lyme, MS, whatever.

I have been declared to have fibro too, but I scarcely- if ever- have any problems in my hands.
Same goes for my mother, who is even prescribed stuff against fibro (she declines it, rightfully so.
Take antidepressants if you have a depression :rolleyes:)

It's an interesting development for sure, but misdiagnosed stuff aside,
I wonder whether they have found the CAUSE of the illness, or just a symptom.