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Hyperreactive Brain Network May Be Cause of Chronic Pain in Fibromyalgia, Study Suggests

Fibromyalgia is one of the overlapping pain conditions with TMD. This article appeared in Fibromyalgia News Today on January 15, 2018. A new study suggests a hyperreactive brain network may be the underlying cause of chronic pain in fibromyalgia.

Dry Eye Linked to Chronic Overlapping Pain in Veteran Population

There may be a correlation between dry eye and chronic pain in the US military veteran population as is evident by a recent study. Ocular pain was most strongly associated with headaches, tension headaches, migraines, temporomandibular joint disorders, pelvic pain, central pain syndrome, and fibromyalgia in the veteran patient population.

Patients in Los Angeles or New York City Needed for Clinical Study - Comparative Study of Women Considering or Currently Receiving Botox© Injections for TMJ Pain

Are you a woman with "TMJ" pain in facial muscles, who has either: a. recently had Botox© injections for your pain or b. not had Botox© for your pain but has thought about such treatment? If either is true for you, you may qualify for an observational research study centrally administered by the NYU College of Dentistry. It is funded by the National Institutes of Health (NIH). The purpose of this study is to understand potential health risks that may be caused by treating "TMJ pain" with Botox© injections.

Why Head and Face Pain Cause More Suffering

Hate headaches? The distress you feel is not all in your -- well, head. People consistently rate pain of the head, face, eyeballs, ears and teeth as more disruptive, and more emotionally draining, than pain elsewhere in the body.

Migraine and Coronary Artery Disease: A Genetic Connection

There has long been as association between migraine headaches and vascular (blood vessel) dysfunction of some kind, underscored by epidemiological studies and other research. New evidence for a genetic connection now comes from the analysis of several large data sets of each condition based on Genome Wide Association Studies (GWAS).


  • Mar 2, 2017
It all started with extensive orthodontic work in my early teens--fast forward 20 years and it has consumed my entire life. Last October, I had to have a failed root canal pulled and nothing would ever be the same for me. Five months ago for no apparent reason I had the most severe flare-up where the pain was so unbearable I couldn't think of going on. I couldn't speak, eat, sleep, work, drink or function. I tried medical cupping on my jaw and after several sessions there was slight improvement. Unfortunately I never went back to "my normal" again. I've seen dentists, oral surgeons, acupuncturists, had medical cupping and now I'm trying physical therapy. A neuromuscular dentist wanted to charge me $6,000 to start for very invasive work, which in 5 months I would find out if it worked at all. That was too much of a gamble for me.
I feel completely and utterly alone as I suffer, any joy being sucked out of my life. It affects my right side more than the left. The pain is unbearable, stabbing in my ear, face, jaw, head and neck. The right side of my face goes numb from the TMJ since it's irritating the Trigeminal Nerve. My neck, jaw and face are in constant spasm; also my neck has started jerking to the right. I spend a lot of time not being able to speak mainly just nodding my head.
I used to really love eating but now my TMJ has changed that. I have to eat what's soft whether I like it or not. All my meals/snacks are dictated by what my jaw will and won't allow. I used to love fresh bagels, pizza crusts, hamburgers and subs among other things. Those foods I'll never enjoy again. Sushi is also a favorite but now is cut up into small pieces as I ever so slowly push the food in my mouth. I make constant compromises; do I want to talk that day or eat? Eating is so painful that many times I either spit food out because of pain or I'm almost choking because I can't chew properly. Most of the time I starve because eating isn't an option or if I can eat, I try to eat as much as I can to sustain me for longer periods of time. Going out to eat really isn't an option either since I have a difficult time actually getting food in my mouth, it's very awkward.
I spend a lot of time depressed, in immense pain not knowing how I'll get through every day. The pain I can't escape not even in sleep. My speech has also changed as I slur, hoping people understand me. The pain-killers and muscle relaxants no longer help. Besides the severe TMJ I'm also epileptic and for extra fun throw in fibromyalgia. As I sit here writing this my family is enjoying a movie laughing and relaxing while the right side of my face is numb and in pain (if that makes sense) my neck is jerking and my eyes are filling up with tears. The condition has taken over and happy feelings are fleeting. I could go on and on about all I go through; sorry for the rambling. I pray for all of us that doctors will find ways to better help us and treat this awful disease. I would love to know what a life not affected by TMJ would be like.