TMJ 'dysfunction' - Health implications

Within this forum, you will discover valuable insights on how a 'dysfunctional' jaw, dental arch anomalies, and various body asymmetries can contribute to illness from a unique perspective. This is your go-to resource for finding effective solutions and achieving lasting relief.
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PostPosted: Thu, 25 Oct 2012, 12:45 pm 
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Joined: Thu, 25 Oct 2012, 12:14 pm
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I have never been diagnosed as having ME or Chronic Fatigue. But I have had a history of vague symptoms that chime with these two illnesses: depression, low energy, cold hands & feet, poor digestion, slow metabolism, low blood pressure & an eating disorder since I was 14/15.

I always suspected something was wrong, but any medical professional I have ever been to never took my symptoms seriously. I stopped having periods for a number of years - again, this was because I wasn't eating properly.

However, my problems started years before my eating disorder took hold. When I was born, I was born in the 'brace' position - my head was face up, rather than tucked into my chest like normal births. My first memory is of physical pain in my neck & no strength in my neck. I did not start to walk until I was almost 3. My mother eventually took me to see a Consultant, who examined me and pronounced me as 'lazy'.

Aged 33, I discovered Dr Amir at Atlasbalance. I went to him because I was suffering a lot from neck pain. He told me my Atlas Vertebra was improper. He had a look at my teeth. During my teens, I was sent to a total cowboy of an Orthodontist who took two of my teeth out and whacked a brace on my teeth. Dr Amir asked when I began to have Orthodontic treatment - it was aged 14/15 - exactly coinciding with the onset of my eating disorder. He made the connection between the two. I was more dubious.

From that initial consultation, it took me 18 months to pluck up the courage to begin having treatment with Dr Amir. I was worried about the cost/time involved.

I have been wearing a brace now for 1 week to realign my jaws. In that short time, I have experienced a huge shift. My energy level is better than ever before. I now realise how ill I was. I always wondered where the surrounding others - my siblings & friends - got their energy from.

I was literally dragging myself around, but because it had always been that way, I didn't know that life could be any different. Furthermore, I feel like a different person - I am on better form, more positive, I feel more able to cope. I feel less daunted by working & holding down a full-time job (I have always only been able to work part-time & felt such a failure about that without realising it had so much to do with my energy levels).

Furthermore, I am hopeful that my problems & fear connected to food may well be because I put on weight so easily due to such a slow metabolism. I am excited now that I may have got to the root cause of it. I always thought the root cause was psychological - what had happened in my childhood to make me like that? But now, Dr Amir has helped me to see there was a physical problem to begin with.

Wearing this brace has been a huge breakthrough for me.

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PS: Taking a stand against the existing paradigm of dental and medical care is very costly. My website has highlighted the practices of those who knowingly or unknowingly perpetuate illness. This is not acceptable to the power structure controlling our health. To continue to produce evidentiary articles on my website and this forum - which have enlightened thousands of health practitioners and patients all around the world, to keep my staff employed and my offices viable, we request a little help. If you feel that this article has made an astonishing change in your symptoms, please donate through a window that comes up after a few seconds at dramir.com.

CONDITIONS OF USE AND IMPORTANT INFORMATION: This article is for educational purposes only. The improvement or benefits identified in this article or on this site are based on individual experiences which are dependent upon the patient’s unique health condition, medical history, and other individualised factors, and should not be considered representative of all treatment outcomes. You must do your due diligence by consulting your physician before embarking on what may be suggested here. This information is meant to supplement, not replace advice from your doctor or healthcare provider, and is not meant to cover all possible uses, precautions, interactions or adverse effects. This information may not fit your specific health circumstances. Never delay or disregard seeking professional medical advice from your doctor or other qualified healthcare provider because of something you have read on this forum. You should always speak with your doctor or health care professional before you start, stop, or change any prescribed part of your health care plan or treatment and to determine what course of therapy is right for you.


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PostPosted: Fri, 14 Dec 2012, 4:04 pm 
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Joined: Fri, 14 Dec 2012, 4:01 pm
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ME/CFS has nothing to do with "Depression/Low Energy".

It is a well defined disease the principal symptom of which is post-exertional malaise or post-exertional neuro-immunological exhaustion. If you do not have those symptoms you do not have ME/CFS.

This is the most up to date definition/criteria for the disease: http://www.meassociation.org.uk/?p=7173


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PostPosted: Fri, 14 Dec 2012, 4:31 pm 
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Joined: Mon, 01 Oct 2012, 4:35 pm
Posts: 35
Vitalic
By now I have treated very many patients who had been OFFICIALLY diagnosed as suffering from ME/CFS. Almost every patient walking through my door with that label has mostly recovered from all their symptoms with a very large number who went back to work during treatment.

Either they were all misdiagnosed or the ME/CFS label is another name for TMJ Dysfunction. Please visit this temporary website: mecfs.com to read some more testimonials.

Here is a graph of a new recovering patient with more comprehensive symptoms which would enable a confirmation into the rather dubious label of ME/CFS. I thoroughly and unequivocally have disputed this assertion since 2004. I have written extensively to the promulgators of the Canadian Consensus Document which is largely being followed around the world and from which you quote:

Attachment:
Kirsty line graph.png
Kirsty line graph.png [ 256.36 KiB | Viewed 17229 times ]


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PostPosted: Fri, 14 Dec 2012, 6:32 pm 
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Joined: Fri, 14 Dec 2012, 4:01 pm
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Hi Dr Amir,

The key thing that seems to be overlooked is post-exertional malaise. This is the only aspect of the illness which is unique to ME, and if it's not listed as one of the symptoms we cannot know if that person really had ME/CFS. It is defined as:

Code:
1. Marked, rapid physical and/or cognitive fatigability in response to exertion


It has been shown repeatedly that ME patients respond differently in the 24-48 hour period following exertion compared to sedentary controls and even patients of other diseases like MS. What is important to know is not whether the patient's fatigue has diminished but has their tolerance to physical exertion increased?

I do not understand why the ME associations have not responded to your letters and I certainly agree that patients should at the very least be made aware of the potential link between ME and cranial issues. The information is slowly starting to become available though, indeed I found your work only after seeing a link in the following ME/CFS treatment roadmap:

https://docs.google.com/document/pub?id ... TiJk9QIeY0

Temporomandibular joint dysfunction is not mentioned until the very end however! Perhaps this should be one of the first things to be checked.


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PostPosted: Fri, 14 Dec 2012, 8:47 pm 
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Joined: Mon, 01 Oct 2012, 4:35 pm
Posts: 35
Excellent response.
Please note that TMJ Dysfunction causes very many disorders. This forum covers only about half. The questionnaire was originally designed to cater for everything in a more generalised manner.
We recently added a section where patients are asked to name the illness they have medically been diagnosed with. This warrants that we add every 'fashionable' symptom, like you admirably point out, to the questionnaire and this will be immediately added.

I can assure you that if I had this question in my original questionnaire most patients would have said a most definite YES to it. I have been seeing this symptom in many patients and it is one of the hall marks of the illness as you rightly point out.

We will be presenting more graphical information in the coming months which hopefully will conclusively dispel the myths about ME/CFS in a vast majority of cases.


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