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, 30 Dec 2021, 12:46 pm 
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Joined: Fri, 28 Sep 2012, 9:08 pm
Posts: 219
Testimonial:
From January 2013 our daughter Caitlin, who was 14 at the time, started suffering from extreme tiredness and fainting episodes. These episodes became more frequent and as a result, she had various blood tests, ultrasounds, MRI Scans, echocardiograms, and an ECG monitor.

None of these gave us an answer and Caitlins symptoms were becoming more pronounced. By October 2014 she was missing large periods of school and sleeping for up to 18 hours, without feeling refreshed. Her complexion was grey and she had very little strength. She also would often feel extremely cold and clammy, particularly her hands and feet. She was susceptible to throat infections, often brought on by exercise, and this would leave her unable to function for weeks on end.

We were extremely concerned for Caitlin and by February 2015 she was given a Chronic Fatigue Syndrome diagnosis.

Whilst we now had a diagnosis, the ‘treatment’ options were limited to managing the symptoms with strategies such as pacing and avoiding boom and bust activity.

Caitlin managed to take her GCSE’s despite missing many days of schooling, and in the summer, when she was able to rest, she seemed to improve. However, by October 2015, she was again suffering from fatigue and at this time I happened to read about some of the work Dr Amir was doing with patients who had been given a CFS diagnosis.

Because Caitlin had been fitted with a brace from age 11 and had continued to wear a retainer at night, we decided to complete the detailed questionnaire required by Dr Amir, and we went to see him at the start of November 2015.

Given the number of consultations Caitlin had already been through, she was a little unsure as to how her problems could be linked to her teeth and jaw alignment, but we felt if we did not try, we would only wish we had.

After examining Caitlin, Dr Amir was absolutely sure he could help Caitlin and this was the first good news we had had in a long time.
Caitlin has been seeing Dr Amir every 2-3 weeks since, and the work he has done has improved her health significantly. The results were not immediate but steady progress has been made, and Caitlin started attending all her lessons which was a massive improvement.

More recently she now can go to bed at 10 pm and gets up for school at 7.15 am, having had a refreshing sleep. This may not sound life-transforming, but having seen how hard it was for her to get up, we know she is back to her old self. Her complexion is also now back to how it was. We are delighted with the treatment provided and we would recommend Dr Amir to any other family in a similar situation."

Chris Ellis - Director
Dip PFS, Certs CII, IMC
12th June 2016
Update:
On Sunday, 16 July 2017, 19:01, C. Ellis <cellis_uk@yahoo.co.uk> wrote:

"With regard to our daughter, Caitlin at no point during the countless consultations and tests performed by the NHS was there any mention of the possibility that her problems could stem from previous dental work.

Had this been mentioned at an earlier stage we could have saved ourselves and Caitlin at least 1 year of suffering the debilitating symptoms, and the NHS considerable money and resource.

The results being achieved by Dr Amir surely deserve some attention from the wider medical world as Caitlin's symptoms, as with countless others could be treated more widely, with more success and cost-effectively."

Chris Ellis

22nd February 2020
Here is the latest feedback from Caitlin:
"Hi Dr Amir,

I have completed the questionnaire for you.

I’ve been doing really well, I’m studying Urban Planning at Newcastle University. I’ve been able to do everything that I’ve wanted to.

I’m forever grateful for all that you’ve done for me.

With kind regards,
Caitlin"
Update: And here is a graph of her progress - 100% recovery. Please click on the graph to enlarge it.
Attachment:
Graph Ellis CFSME.PNG
Graph Ellis CFSME.PNG [ 180.03 KiB | Viewed 3506 times ]

Graph of ME/CFS Progress

Comment:
Over the last 25 or so years I have seen very many patients suffering from the mythical "Chronic Fatigue Syndrome" who have been on the medical merry-go-round for years. The patients have never benefited from any medical intervention in any shape or form whatsoever.

NHS Choices website describes CFS as:


"Exactly what causes chronic fatigue syndrome (CFS) is unknown, but there are several theories. Some experts think a viral infection such as glandular fever can trigger the condition. Certain bacteria have also been suggested as a cause of CFS in some people, including types of bacteria responsible for pneumonia."

Selecting a few symptoms, clustering them into a group and then calling them a disease is the modus operandi in many illnesses and syndromes. Then the next step is to feign that we do not know what causes this disease. or syndromes is a very profitable industry. This allows the medico industrial complex to grease its wheels by putting patients through multiple very expensive scans and tests. The usual outcome is that nothing abnormal was found and we shall repeat the tests and consultations in six months again!

In the meantime take this drug!

Imagine a scenario where the patients had to pay for all the consultations, tests and scans. The cost to each patient could reach many thousands of pounds each year with no resolution in sight. This is perhaps what causes many families to go bankrupt across 'the pond' from these illness labels.

Ironically I was recently informed about a patient who has had braces for many years, This, in extreme cases, may cause cervical instability which is a serious consequence.

The patient has, however, been diagnosed with Ehler's Danloss Syndrome, (the keyword is 'syndrome') and this ONE single patient is costing the health service half a million pounds a year which you and I are paying for! There are thousands more like her in the clutches of the medical profession busting the NHS in this country and bankrupting families in other countries.

Almost every hospital has a CFS speciality department. The word 'Syndrome' fundamentally means that your doctor knows nothing about the illness. Yet we have many specialists who are consultants in this 'syndrome' which they know nothing about!

A recent report in the Positive Health Magazine says:

"A Press Release received two days ago (12 Sept 2016) announced data of the PACE study on myalgic encephalomyelitis / chronic fatigue syndrome, re-posted to the Letters to the Editor, Issue 233:

“The new analysis of the PACE trial appears to confirm the consensus view that CBT and graded exercise therapy were associated with a mild placebo effect.” and “The release of data from Queen Mary University of London’s PACE study into Myalgic Encephalomyelitis proves that graded exercise and cognitive behavioural therapy were never effective treatments for those suffering from ME."

"just 21% of patients found improvement with graded exercise, as compared to the 61% they originally reported in The Lancet.

Critics think that when the data is independently analyzed, it will show that exercise has no positive benefit at all.. Graded exercise is a commonly prescribed treatment for ME/CFS but many patients and researchers believe it can make symptoms worse, sometimes permanently."

It was also announced that Queen Mary University spent over £200,000 on legal fees on a tribunal appeal to try to prevent the data’s release." Further proof of medical corruption which harms patients and the GMC did nothing about it.

In brief, I have never found any patient who presented with 'CFS' to actually have 'CFS'. It is nearly always jaw symmetry problems and the patients rapidly start recovering from THEIR SYMPTOMS once proper treatment is instituted.

'Experts in 'CFS' attending to these must refer them to a dental specialist at the outset for a differential diagnosis before diagnosing them into this mythical illness and before telling them that "there is no cure for 'ME/CFS', but drug treatment can ease some of your symptoms and improve your quality of life".

It is almost criminal for the medical profession to monopolise these patients without excluding jaw dysfunction in their differential diagnosis. Not to get clearance from a dental specialist is tantamount to gross medical negligence and actionable in a court of law.

Their ego trips, by design or idiocy, achieve nothing other than bankrupting the NHS, the social services and the patients whose pain, suffering, lost careers and lost futures continue unabated.

There are hundreds of thousands of patients like this all around the country keeping our hospitals abuzz with FUTILE activity and the patients in a lifelong limbo. Imagine what would happen to the waiting lists and the doctor's surgeries who are too busy to give you an appointment if they were banished from 'treating' this and other fictitious syndromes.

-------------------------------------------------------------------------------------------NOTICE-----------------------------------------------------------------------------------------------
This article is written under the Human Rights Act 1998: UK Public General Acts 1998 c. 42 SCHEDULE 1 PART I Article 10 for of the long-suffering British public.
The law specifically states that "Everyone has the right to freedom of expression. This right shall include freedom to hold opinions and to receive and impart information and ideas without interference by public authority".
Any harassment, direct or indirect, by the ruling bodies or their cronies, will be vehemently pursued through this act and the freedom of expression laws.
Any breaches of the Data Protection Act shall also be brought to the attention of the Information Commissioner's Office and The Law Society.
.................................................................................................................................................................................................

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.
A paradigm shift in the care of ME/CFS patients.
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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