Showing posts with label myofascia. Show all posts
Showing posts with label myofascia. Show all posts

Sunday, January 12, 2020

When Your Frozen Muscles Need Help: Myotherapies for Managing Myofascial Pain



When the myofascia isn’t free to move, other muscle movement is also impaired. This leads to joint dysfunction and chronic PAIN. This pain is universal with distinctive patterns that remain consistent in all people. In some cases, restrictions can be so extensive joints become frozen, meaning joint motion is severely restricted. The goal of all myofascial therapies is to restore normal muscle function. Following are helpful hands-on therapies that work to release restrictions and help our body achieve full normal range of motion.


MYOFASCIAL TRIGGER POINT THERAPY

Myofascial pain syndrome  (MPS) is a constant pain source when trigger points (TrPs) are left untreated.

Trigger point therapy done by a specially trained therapist releases the knotted muscle fiber (TrP) using a compression technique. The therapist will know to look for other TrPs, which are sometimes well away from the one that is causing you so much pain. They know there is a consistent pattern related to the specific location of a TrP in that taut band of muscle. Release TrPs returns muscle to normal function.  That said, the work isn’t all up to the therapist. A good therapist will help you learn the importance of knowing what things are perpetuating your pain. A big one for me is sitting here at this desk staring at my computer screen, or riding in a car for too long.

Chronic myofascial pain from MPS is often accompanied by other disorders, such as fibromyalgia, migraine, spinal degeneration, irritable bladder, arthritis, joint hypermobility, and more. Dr. Karl Hurst-Wicker explains “Fibromyalgia Centralization and Peripheral Myofascial Pain” in an interview I did for Health Central.

Created by Celeste Cooper, The Pained Ink Slayer(c)










Chronic myofascial pain can be the primary source of pain or it can perpetuate pain in other disorders, injuries, or anatomical deformities. The good news is that myofascial pain syndrome is treatable. The goal is to release the trigger point/s so that the muscle tissue returns to its normal functioning position.


MYOFASCIAL RELEASE (MFR)

As so many of us who write about myofascial pain explain, the myofascia is like chicken skin. It’s attached to the muscle, but still moves freely. If you have ever cut up a chicken, you can visualize what that is. Each muscle is covered by myofascia (muscle covering) that draws together on each end to form a tendon. Tendons attach muscle to bone so our joints can function. The goal of myofascial release is to free up myofascial restrictions so our body can function properly.

Developed by physical therapist John F. Barnes, myofascial release is a manual therapy performed by a skilled therapist with the goal of improving movement and promoting wellness.

My personal experience with MFR was enlightening to the physical therapy student following my therapist. During a session, my back starting twitching like a flickering light bulb, the student became tongue-tied. She stated she had not witnessed such a phenomenon. The physical therapist was glad her student was able to see firsthand what restricted myofascia can do and how it contributes to chronic pain.

It’s important to always check the credentials of anyone doing body work. They must have a firm understanding of anatomy of physiology. Here is a directory of myofascial release therapists recommended by John Barnes. http://mfrtherapists.com/


NEUROMUSCULAR THERAPY AND REPROGRAMMING (NMR)

The goal of Neuromuscular Therapy and Reprogramming (NMR), founded by body-worker Jocelyn Olivier, is to balance the central nervous system and the musculoskeletal system by engaging the motor center of the brain.  Therapists specifically trained in NMR treat soft-tissue restrictions, which relaxes muscles, rebuilds strength, improves flexibility, restores venous and lymph flow, and relieves the underlying cause of pain. The therapist will assess blood flow, myofascial TrPs, nerve compression, problems with gait, posture and body alignment, and perpetuating factors.

Other types of bodywork include spray and stretch, Bonnie Prudden Myotherapy, strain counter-strain technique, and deep tissue bodywork, such as Rolfing and Active Release Technique (ART). I caution those with fibromyalgia on deep tissue work. It can be too painful for some. I am lucky to have a physical therapist that does ART. Some chiropractors also use this technique, but the most important thing is to have a working relationship with your therapist and keep the lines of communication open.  


WHAT WE CAN DO

Any myofascial therapy requires us to contribute for the best outcome. We can identify perpetuating factors and practice preventive strategies like stretching and strengthening to maintain muscle health, stamina, and general overall wellness. (Caution: strengthening should be done once the muscle is functioning properly again.) We can be persistent in finding the right therapy or the right therapist. Both are equally important. Maybe you find a therapy you want to try, insurance covers it and all seems well. However, I offer a word of prudence, the type of therapy doesn’t matter if you don’t have a knowledgeable therapist who is willing to work with you and teach you why certain things are important.

A guidebook that focuses on the work of doctors Travell and Simons will help you learn methods of self-treatment and a good therapist will suggest that you do just that. There is information to suggest that when home therapy is encouraged, we do better.


IN CLOSING

Always talk with your doctor for medical clearance. Sports medicine physicians and physical therapists are often a good resource for those of us living with chronic myofascial pain.


Additional Reading:




In healing,

Celeste Cooper, RN / Author, Freelancer, Advocate

Think adversity?-See opportunity!



~ • ~ • ~ • ~ • ~ • ~

Learn more about Celeste’s books here. Subscribe to posts by using the information in the upper right hand corner or use the share buttons to share with others. 

Sunday, May 27, 2018

12 Months and 14 Fibro Musings by The Pained Ink Slayer



As fibromyalgia awareness month winds down, I am reminded of all the wonderful work of advocates and fellow bloggers. However, this month is a difficult one for me personally, because I also have chronic migraine; and the unstable atmosphere of spring weather is a trigger I cannot control. Fibromyalgia and its partners can be more than a physical challenge. For instance, a special PAINS-KC meeting I looked forward to attending was side railed because of what would end up being a 14-day status migrainosus. And, I can’t remember doing an interview for May awareness that I did not have migraine. Unintentionally, this introduction is also a segue to June headache and migraine awareness month, stay tuned.

What I write is rooted in my personal quest for help. I have learned to forgive myself for the things I can’t control and to embrace adversity. I realize that good days for others are spectacular to me. I hope you find something that is helpful for you.

Note: For future reference, archived blogs are in the right column of this page, Celeste’s freelance articles are in the header tab Celeste’s Publications, and this particular blog will be linked in the header tab Fibro Musings.


  

Ways we can manage the effects of fibromyalgia on our central, autonomic, metabolic, and immune systems…



Explore the types and benefits and practices tai chi, dubbed “medication in motion” for those of us living with chronic pain…




There is a well-documented bidirectional pathway between the brain and gut. Read about fibro-mates, IBS and GERD, and evidence on supportive therapies of the mind…





Determining the most beneficial type of therapeutic massage or bodywork relies on our understanding of the differences between fibromyalgia and myofascial pain syndrome. What massage techniques can help?...



What type of movement is showing promise for managing our fibromyalgia? You might be surprised to see the recent evidence…






Fibromyalgia and EDS (hEDS = EDS hypermobile type) share connections you might not have considered…





What you may not know about your symptoms, stressors, and management tools…




About the male and female fibromyalgia pelvis, pain and the myofascia, diagnosis to treatment…





Genetic studies on fibromyalgia are underway with the assistance of the University of California, UCLA, and University of Illinois at Chicago using the FM/a blood test to identify participants.



Thyroid problems can co-exist with and/or sometimes mimic fibromyalgia, the science, medicine, and awareness...





To understand why manual lymphatic massage is beneficial for those of us with fibromyalgia, we must first understand how it works.





Why does myofascial pain become chronic? What causes the chronic pain of fibromyalgia? Does myofascial pain sustain fibromyalgia pain? Difference between a trigger point and tender point, and more...




The FDA "Voice of the Patient", getting unstuck, the biology of body matter, immune cells, and noteworthy news...





Are your arms and legs like battlefield magnets? Do your extremities look like a world atlas? For those of us with fibro, there might be an explanation to why that is.





Disparity, agreements, 2016 Revisions to the 2010/2011 Fibromyalgia Diagnostic Criteria appear to address previous concerns, and now conclude...




Don’t miss:
The Pain Advocate’s Corner: How to Raise Your Voice
(also permalinked in the header tab of The Pained Ink Slayer).


“To unleash victory, I must have an open mind and willing heart,
judge not, embrace change, and be a steadfast observer of self.”


In healing,

Celeste Cooper, RN / Author, Freelancer, Advocate

Think adversity?-See opportunity!



~ • ~ • ~ • ~ • ~ • ~

Learn more about Celeste’s books here. Subscribe to posts by using the information in the upper right hand corner or use the share buttons to share with others. 

Tuesday, March 12, 2013

What the heck is a syndrome?


A syndrome is a collection of symptoms that remains the same throughout a particular patient group, but the cause is unknown. These might include fibromyalgia syndrome, chronic fatigue syndrome, Cushing’s syndrome, irritable bowel syndrome, AIDS, Asperser’s syndrome, Barrett’s syndrome, carpal tunnel syndrome, leaky gut syndrome,  paradoxical orthostatic tachycardia syndrome, Sjögren’s syndrome, Ehlers-Danlos Syndrome, urethral syndrome,  restless leg syndrome, Raynaud's syndrome, CREST Syndrome (a form of Scleroderma), complex regional pain syndrome, and many more. You may not realize it, but even rheumatoid arthritis is considered a syndrome. 

Some disorders are confusingly called diseases, when they are actually syndromes.  Diseases generally have a known cause. And syndromes, even when we know something about them are still syndromes. For instance, research shows there is an excessive release of acetylcholine at the neuromuscular (nerve to muscle) junction of a myofascial trigger point, but myofascial pain syndrome is still considered a syndrome. This is because we don’t know what causes the excessive release of acetylcholine, a neurotransmitter, the chemical messenger between the body and the brain.

When invisible disorders have no biological marker, a test that says you specifically have the disorder/syndrome, and sometimes when they do, there is always the doubting Thomas.  We think these folks mission in life is to prey on our psyche.  Why is this? Pretty much the answer is simple; they don’t experience our pain, lack of restorative sleep, life altering fatigue, severe chronic headache, a bladder that is constantly on fire, constantly cold extremities, or feel like everything they touch is barb wire, just to mention a few symptoms of invisible illnesses. Syndromes are not seen as real because some people operate on the assumption that if you can’t see it, it isn't so, even some healthcare providers migraines were once attributed to a woman’s frenzied inability to cope with stress.

Newer research into genetic markers will plow under the misconceptions of those who do not share our syndrome. In the mean time, it is up to us to support those who support the research.  Orphan disorders of all sorts face the same challenges.

In healing and hope, Celeste Cooper, RN author, patient, activist

All blogs, posts and answers are not meant to replace medical advice.  www.thesethree.com

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