Showing posts with label Illinois TMJ. Show all posts
Showing posts with label Illinois TMJ. Show all posts

Wednesday, March 9, 2016

TMJ Illinois: Caniofacial Pain, Orofacial Pain, Headaches, Migraines and Cluster Headaches

Headaches and cranialfacial pain  are all problems related to the Trigeminal Nerve, also known as the dentist's nerve it is involved in almost 100% of all headaches and migraines.  Trigeminal Neuralgia and trigeminal neuropathies are also part of the same problem.

Though patients are usually unaware of the trigeminal nerve dentists, ENT's, Neurologists all know it to be the key input to brain and is involved in 100% of all headaches.  Neuromuscular Dentistry is the best way to decrease noxious input to the CNS.

Treatment usually includes a Diagnostic Neuromuscular Orthotic often received by the patient on their first visit after their consultation visit.  Long distance patients can receive at the same visit of initial consultation.

Visit www.ThinkBetterLife.com to start a process to eliminate and or alleviate (some, most, or all) of  your pain.

Dr Shapira see's patients from across the Chicago metropolitan area, the midwest and across the country.  Special arrangements can be made for long distance patients.

Listen to actual patients on you tube videos describe treatment with Dr Shapira.

Wednesday, September 9, 2015

Find A TMJ Dentist: Who is The Academy of Applied Myofunctional Sciences and where do they fit in TMJ treatment?

There are several excellent ways to locate a TMJ Dentist.

There are several schools of thought in TMJ Dysfunction.  The Alliance of TMD Organizations represents all of the major groups who treat TMJ Disorders.

I am current the Chair, Alliance of TMD Organizations.  It represents groups with several schools of thought.

Personally, I would recommend starting with a Neuromuscular Dentist who is a member of ICCMO.  These doctors are dedicated to the neuromuscular concepts discussed throughout the I Hate Headaches website.

I also belong to the American Equilibration Society and the American Academy of Craniofacial pain, both groups have wonderful courses and I love seeing problems from all angles.  I find I learn more from people outside the primary focus in my practice.  The AES is primarily centered on Centric Relation as a starting point for treatment.  While I don't agree with Centric Relation as the best starting points there are excellent doctors who are well trained in treating TMJ disorders.   The AES puts on a fantastic yearly meeting but the underlying focus is CR as taught by Peter Dawson.  That will change gradually when Dr Dawson retires and leaves the field.  He is much less visible than in the past due to increasing age.  Centric Relation is losing popularity in the age of precise measurement.  The concept of CR has had at least 26 different definitions over the years.

The American Academy of Pain Management is no longer a member of the Alliance but dentists who are also Diplomats of the AAPM tend to be very knowledgable on medical aspects of pain.  The problem in recent years is the AAPM has moved further in the direction of medication as a primary treatment rather than correcting underlying pathology.

The Academy of Orofacial Pain takes this type of treatment to the extreme.  There is a tendency to ignore the physiology of the muscles, TMJoints and Occlusal factors.

The International Association of Physiologic Aesthetics also holds excellent meetings.  It tend toward being a user group of LVI, The Las Vegas Institute that teaches neuromuscular dentistry primarily for use in esthetic dentistry.  LVI teaches excellent cookbook neuromuscular dentistry but does not delve into the science like ICCMO  does.  My preference is find a neuromuscular dentist who belongs to IAPA and ICCMO.

All of the basic principles and top educators at LVI are ICCMO members.  LVI recruited from ICCMO specifically due to their excellence in Neuromuscular Dentistry.  Many ICCMO doctors, myself included went to LVI to increase efficiency in reconstructive dentistry.

The Kois Center and Dr John Kois are similar to LVI in teaching his version of Centric Relation as a way to reconstruct patients.  Interesting, is that while he calls it CR it is actually very very similar to the neuromuscular position.   Dr Kois give excellent courses on technical aspects of dentistry.  

There are other groups teaching Neuromuscular Dentistry.  OcclusionConnections is one such group, its founder learned neuromuscular dentistry at ICCMO and later taught at LVI before going on his own.  Clayton teaches his form of neuromuscular dentistry and I again suggest seeing doctors who also belong to ICCMO.

Ther are other groups who belong to the TMD Alliance including Sacro Occipital Technique Organization or SOTO an excellent Chiropractic group very interested in TMJ treatment as part of whole body biomechanics, Tennessee Cranio and The International Association for Orthodontics who teach functional orthodontics to create healthy physiology and TMJoints.

The newest member is the Academy of Applied Myofunctional Sciences. Their first meeting is September 9-13.  I have been very impressed with their organization and I am enjoying the meeting.  I really belong to too many organizations but feel this is one more I must join not because of the work with adult TMJ patients but because of their commitment to grow healthy children into healthy adults without TMJ, sleep or breathing problems.  I expect great good to come from their efforts and I am proud to be at their first meeting.

Myofuntional Therapists work with patients oral habits and oral function and treat patients by correcting pathological patters.  regardless of which doctors are treating you Myofunctional Therapy can help the process.

Sunday, August 9, 2015

Severe Exacerbation of Lifetime Headache Problem: Migraines, TMJ, TMD, MPD or other problem. All tests are negative but quality oof life is being destroyed and medications are no help.

Paul's Question for Dr Shapira
Tell us about your headaches...:    I remember my mother taking me to the doctors when I was a child for random tension headaches. I've always been an over-thinker, which can cause anxiety and stress, potentially leading to headaches. Throughout my childhood and adult life, I had headaches hear and there (more frequent than the average person, I'd say), but nothing that a an OTC and a little time couldn't handle. It was never chronic or debilitating. All that changed on October 25th, 2014...

On that day, after a stressful year and a half, I was knocked down by the worst headache/migraine I'd ever had. I didn't know what it was, but I feared for my life. It was as though something was going to explode in my head at any moment.

In the months that followed, it never went away, and I was plagued with off neurological symptoms (felt like someone was pouring cold water on my head at times, odd sensations in random parts of my body, my eyes would hurt at night) but the most difficult thing was the pressure. Every day it felt like my head was going to pop. I was living as though any second I could die.

Though the some of the strange symptoms have subsided, the pressure and fatigue remain. The emanate from the base of my skull where my spine meets my skull. That seems to be the centerpiece, but it moves to the sides of my head just above the ears, and sometimes the top. Different positions rarely help.

I've seen two neurologists. One said it was atypical migraines. She's wrong, though they can rarely turn into migraines, that's not what they are. She started me on magnesium, melatonin and riboflavin as well as topamax to no avail. I moved on to another neurologist who's DX was Chronic Daily Headaches, and does nothing but through pills at me. I'll admit that the only thing that relieves the pressure and makes me feel somewhat normal is Soma, but it's short-lived, tolerance builds fast, and I feel we are not getting to the root of the problem. Klonopin also seems to help, which makes me think it's a muscle tension, possible TMJ issue.

I had a decaying tooth, so I even saw the dentist, who wound up doing 2 root canals and I went through a round of amoxicillin just in case there was an infection. I can say my teeth are now the best is town (after a whole summer of treatments), but dental stuff doesn't seem to be the issue. She just gave me a referral to be evaluated for TMJ.

I also saw my optometrist, he said everything looked fine; however, my vision had improved, and I had been wearing contact lenses that were too strong for awhile. He said this isn't the cause of my headaches, but it certainly isn't helping.

I am now seeing a Chiropractor 3x/week who says I have an Atlas Sublaxation, and a bone in my neck/base of skull is out of place and could be pinching nerves. Over time, he plans to put that bone back in place. I'm skeptical.

I have had a CT and MRI of the brain, all unremarkable. Last week I went for a Lumbar Puncture to rule out other things. I go over the results with my neurologist on Tuesday.

I'm growing weary, and this is all making me depressed. The side-effects of the meds also make me depressed. I'd love some input.

I have a past history of substance abuse, and have kindled with benzo's and other GABAergics. In fact, right before this happened, I was taking a substance called phenibut for my anxiety, and coming off of a high dose of gabapentin (which i was put on after coming off of Klonopin). My abuse days are over, but I wonder if it plays a role.

I am currently on the following medications:
Vyvanse (70mg/daily) - a mild amphetamine for ADD and unresponsive major depression
Klonopin .5mg 3-4x/daily PRN
Baclofen 10mg 4x/daily PRN
Soma 350mg 4x/daily PRN

I also take melatonin, magnesium, a B-complex, Fish oil/omega-3's and a multivitamin.

Any help, direction, or input would be greatly appreciated, as this leads to such a poor quality of life that living seems useless at this point and I think about death far too often.

Tell us about your headaches...:    I remember my mother taking me to the doctors when I was a child for random tension headaches. I've always been an over-thinker, which can cause anxiety and stress, potentially leading to headaches. Throughout my childhood and adult life, I had headaches hear and there (more frequent than the average person, I'd say), but nothing that a an OTC and a little time couldn't handle. It was never chronic or debilitating. All that changed on October 25th, 2014...

On that day, after a stressful year and a half, I was knocked down by the worst headache/migraine I'd ever had. I didn't know what it was, but I feared for my life. It was as though something was going to explode in my head at any moment.

In the months that followed, it never went away, and I was plagued with off neurological symptoms (felt like someone was pouring cold water on my head at times, odd sensations in random parts of my body, my eyes would hurt at night) but the most difficult thing was the pressure. Every day it felt like my head was going to pop. I was living as though any second I could die.

Though the some of the strange symptoms have subsided, the pressure and fatigue remain. The emanate from the base of my skull where my spine meets my skull. That seems to be the centerpiece, but it moves to the sides of my head just above the ears, and sometimes the top. Different positions rarely help.

I've seen two neurologists. One said it was atypical migraines. She's wrong, though they can rarely turn into migraines, that's not what they are. She started me on magnesium, melatonin and riboflavin as well as topamax to no avail. I moved on to another neurologist who's DX was Chronic Daily Headaches, and does nothing but through pills at me. I'll admit that the only thing that relieves the pressure and makes me feel somewhat normal is Soma, but it's short-lived, tolerance builds fast, and I feel we are not getting to the root of the problem. Klonopin also seems to help, which makes me think it's a muscle tension, possible TMJ issue.

I had a decaying tooth, so I even saw the dentist, who wound up doing 2 root canals and I went through a round of amoxicillin just in case there was an infection. I can say my teeth are now the best is town (after a whole summer of treatments), but dental stuff doesn't seem to be the issue. She just gave me a referral to be evaluated for TMJ.

I also saw my optometrist, he said everything looked fine; however, my vision had improved, and I had been wearing contact lenses that were too strong for awhile. He said this isn't the cause of my headaches, but it certainly isn't helping.

I am now seeing a Chiropractor 3x/week who says I have an Atlas Sublaxation, and a bone in my neck/base of skull is out of place and could be pinching nerves. Over time, he plans to put that bone back in place. I'm skeptical.

I have had a CT and MRI of the brain, all unremarkable. Last week I went for a Lumbar Puncture to rule out other things. I go over the results with my neurologist on Tuesday.

I'm growing weary, and this is all making me depressed. The side-effects of the meds also make me depressed. I'd love some input.

I have a past history of substance abuse, and have kindled with benzo's and other GABAergics. In fact, right before this happened, I was taking a substance called phenibut for my anxiety, and coming off of a high dose of gabapentin (which i was put on after coming off of Klonopin). My abuse days are over, but I wonder if it plays a role.

I am currently on the following medications:
Vyvanse (70mg/daily) - a mild amphetamine for ADD and unresponsive major depression
Klonopin .5mg 3-4x/daily PRN
Baclofen 10mg 4x/daily PRN
Soma 350mg 4x/daily PRN

I also take melatonin, magnesium, a B-complex, Fish oil/omega-3's and a multivitamin.

Any help, direction, or input would be greatly appreciated, as this leads to such a poor quality of life that living seems useless at this point and I think about death far too often.

Dr Shapira's Response:


DEAR PAUL,

You have been through a lot and even though non-diagnostic MRI and CT scans can be disappointing they are actually very good news.

Most chronic pain is from causes that are not visibile in those tests.  The number one source of pain is MPD or Myofascial Pain and Dysfunction which is always a major portion of all Temporomandibular Dysfunctions.  

These conditions were well described by Dr Janet Travell in her landmark text 
"Myofascial Pain and Dysfuntion:   A Trigger Point Manual"

You did not mention having SPG blocks which may help butare not the ultimate answer.  Atlas /Axis problems with the first two vertebrae can give a host of strange symptoms.
The SpenoPalatine Ganglion is the largest parasympathetic ganglia of the head and neck and is implicated in a wide variety of wierd and inexplicable cases of chronic pain and dysfunction.  It was made famous in the best selling book "Miracles on Park Avenue" which is a worthwhile read.

The Trigeminal Nerve is responsible for over 50% of input to the Central Nervous System after amplification in Reticular activating System.  It is an oversimplification to call it a TMJ problem but more accurate to call it a musculoskeletal/ trigemino-vacular and trigeminal nervous system dilemma.

I frequently hear stories that are similar yet different.  I assume the lumbar puncture will be negative but it is good to rule out all organic problems.

I am located in the Chicago ara but I frequently see long distance patients.

Visit my website www.ThinkBetterLife.com to learn more.

I will put some links to patients testimonials for you.  Each and every case is unique and different, but you have already ruled out all the worst alternative causes and probably are dealing with a functional issue.

Ira L Shapira DDS, D,ABDSM, D,AAPM, FICCMO

Chair, Alliance of TMD Organizations