Monday, February 13, 2012

Myofascial Pain Syndrome

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Ravin

Ravin

Fri, March 14, 2008

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Myofascial syndrome is a pain disorder that affects the muscles and fascia throughout your body. Fascia is like a web that surrounds the bones, tissues, organs, and blood vessels throughout the body. Myofascial pain syndrome can attack and cause degeneration of certain areas of the fascia, resulting in chronic pain and a variety of other symptoms. Myofascial pain disorder is very common in fibromyalgia sufferers. It was once thought that myofascial pain syndrome was actually a kind of fibromyalgia. However, this is now known not to be the case. It is possible to have both fibromyalgia and chronic myofascial syndrome, and therefore it is important to be diligent when analyzing your symptoms. If you notice myofascial syndrome symptoms, record them and report them to your doctor.
Signs and Symptoms of Myofascial Pain Syndrome
The most common sign of myofascial pain is the presence of palpable trigger points in your muscles. Trigger points are areas of extreme tenderness and sensitivity, and usually form in bands of muscle underneath your skin. They are similar to the tender points caused by fibromyalgia, only trigger points can be felt beneath the skin. When touched, trigger points will produce pain and twitching in the muscles. Often, pain is felt in an area distinct from the trigger point that is actually affected - this is called referred pain. The pain of myofascial syndrome is typically a dull ache, but can also produce a throbbing, stabbing, or burning sensation. Pain is often located in the jaw area, though any part of the body can be affected. One-third of myofascial pain sufferers report localized pain, while two-thirds report having pain all over their bodies. Myofascial pain can also produce a variety of other symptoms, many of which may appear unrelated.
These include:
numbness in the extremities, popping or clicking of the joints,limited movement of joints, particularly the jaw,
muscle weakness(manifested in dropping things),migraine or headache,disturbed sleep,balance problems,tinnitus and ear pain,
double vision or blurred vision,problems with memory,unexplained nausea, dizziness, and sweating.
Aggravating Factors: Symptoms are often aggravated by specific factors. Stress and anxiety contribute to muscle tension and can irritate trigger points. Changes in the weather, including sudden coldness, high humidity, or extreme dryness can also exacerbate symptoms. Physical activity can also trigger symptoms.

Causes of Myofascial Pain Syndrome: There are numerous proposed causes of myofascial pain:
Muscle and Skeletal Problems: The causes of myofascial pain dysfunction syndrome can be numerous and depend upon the individual. Generally, myofascial pain is caused by some sort of trauma to the muscles and skeleton in the body. Overworking of the muscles can cause damage to certain areas resulting in the development of a trigger point. Poor posture can also trigger myofascial pain in certain individuals. Skeletal abnormalities, such as having different sized feet, toes, or legs, can also contribute to the development of myofascial pains. Frequent exposure to cold weather may also increase the risk of developing chronic myofascial pain syndrome.

3/15/08 8:48pm

Raven

 

That was a really good and informative share post and I thank you for the great information. 

I don't quite understand alot about myofacial pain and your post helped clear a few questions up for me.

 

Do you have Myofacial symdrome?  I've never been told that I do, but think that it's quite possible.  I have had a message therapist do some myofacial release therapy on me and it felt great when she was working on me, but It liked to kill me off the next seval days afterwards, so I'll not be doing that again.  It caused the worst FM flare that I've ever had.

Thanks for sharing this information with us

Betty

3/16/08 11:52am

Yes, I do have MPS & FMS. Some Physicians will tell you that you have FMS, in my case. I needed a Medical note for a Court hearing, on it, it stated I have MPS & didnt mention FMS. I questioned my pain Specialist about this, as to why it stated MPS & not FMS. He basically told me, they are nearly one in the same. Except that I unfortunately had both & it was easier just to put one on the document.

I have a tens unit which helps some & get injections, which dont help, really much at all. I get them in my legs & arms the most & have people push on the trigger point until it releases. It hurts so bad yet feels so good at the same time & then leaves bruises & soreness. Thank-you for any comments.

4/ 6/08 11:39pm

Hello Raven Star, I have now more questions for my doctor that she wont be able to answer. She is finally sending me to a rhumatologist, have been waiting forever and still have over a week to wait, then to a chronic pain counselor at the end of April.

I have a back injury from 2000. L4/L5-- SI JOINTS, DDD, BULGING DISK, FIBROMYALGIA= ??? since Jan. The doctor said i had 8 tender points. She wants me off the percocet and i told her that is the only thing that keeps me moving around. I was on the Lyrica and stopped taking it because my fingers and knee's hurt/swealed so bad. It's only been a couple weeks since i stopped the lyrica and seem a bit better. Im confused now thoe after i read about the MPS. I have most symptoms of FM, and i c a few from MPS, like the numbness is constant in my fingers, memory,sweating,sleep,headache,limited movement in joints,weather-physical activity-stress trigger symptoms. The numbness is out of contol, eating is a problem or holding anything. I have this huge bump on the inside of my right shoulder blade(size of a softball) and it causes neck pain, can't turn head at times, cause headachs. My boyfriend uses his elbow and pushes as hard as he can and it feels so good, like i can feel blood flo to my brain and i can crack my neck most the time after that, but it feels so good, so much relief. But he has to constantly do this and is so sick of it. So does that sound like a symptom? Now i will be doing more research and hopefully one of these doctors can figure this out. Hope to hear back from you. - so confused.....

4/10/08 5:03pm

Yes, bulging muscles, hard, tender spot accompany MPS. I get them in my arms, legs, Mid-Back & Shoulder blades. I am on different meds, the med that helps me most is Ultram/Tramadol 50mg. 2, 3xs day. The only thing I dont like about it is, I cant take them late at night or past 6P. or I am wide awake with insomnia.

There are alot of symptoms that act like or mimic other conditions, such as Lupus, FMS, CFS/ME, MPS Etc. I have a Tens Unit which helps some, for all of my conditions. My Spouse presses on mine as well, even though it hurts it also feels good, if that makes any sense. I get injections as well, but they dont last long at all. I am thinking of getting a pain pump insert to my spine. Hope this helps you out.

4/ 4/10 9:27am

I have had this for 3 yrs. I feel like bugs are eating me alive on my back I went to the dr and was prescribed lyrica all it did was make me dizzy 1st dr prescribed 50 mg the 2nd dr 150mg the 1st nite I took it I landed up in the emergency room I nearly died I am a small person  and the dr was all wrong about the dosage I threw all the pills away today I just live with the pain I hurt so bad I feel like stepping out in front of a  car to get relief thats how bad I hurt and I am not a crazy person my pain is 24/7 and I even feel the pain and the crawling in my sleep I am stiff as a poker when I try to get out of bed in the morning my wish is that someone   will find a cure for  in the meantime the way I cope w/it is to ignore it  pretend it's not there ohhhh but it is and I just push and go on even though I hurt like a big dog .             

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