Sunday, June 12. 2016100% Recovery from the symptoms of 'Chronic Fatigue Syndrome'
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. 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. With kind regards, Caitlin" Update: And here is a graph of her progress - 100% recovery 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 fraudulent 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." 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". Follow @divinesymmetryIt 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. ------------------------------------------------------------------------------------- Reviewed January 2021, ©2016 -2021 Dr. M. Amir. All rights reserved.Friday, July 3. 2015Recovery from Chronic Fatigue Syndrome, Myalgic Encephalomyelitis and Fibromyalgia
The following data demonstrates how patient, Hannah Gay, eliminated almost 100% of her symptoms associated with ME/CFS with only 7 months of treatment. Hannah was lucky that she discovered our treatment within a few months of falling ill. The article quotes a study making stupendous claims, which I fail to understand having successfully treated very many ME/CFS patients, how killing someones immune system can possibly make them better. Here is what Amy had to say: "This makes me very angry and concerned about the safety of anyone vulnerable and desperately ill enough to be a guinea pig for this very serious and dangerous sounding drug!! As is obvious in the article it simply masks the immune system dysfunction without addressing the fundamental root cause which cannot be cured with drugs and after stopping it the participants simply become sick again. Tuesday, May 5. 2015Post Viral Fatigue Syndrome or a Jaw problem - You decideSunday, March 15. 2015How to save billions for the NHS
"Here's to the crazy ones, the misfits, the rebels, the troublemakers, the round pegs in the square holes... the ones who see things differently -- they're not fond of rules... You can quote them, disagree with them, glorify or vilify them, but the only thing you can't do is ignore them because they change things... they push the human race forward, and while some may see them as the crazy ones, we see genius, because the ones who are crazy enough to think that they can change the world, are the ones who do." I suppose the simple answer is to close all speciality services in the hospitals who diagnose patients into various syndromes like Chronic Fatigue Syndrome (CFS), Irritable Bowel Syndrome (IBS), Ehler's Danloss Syndrome (EDS) and Fibromyalgia Syndrome (POTS) and other 'cooked up' illnesses for which they have no answer and yet set themselves up as "specialists". They often dispense out useless and often dangerous drugs flanked by their 'consultant' status. This would also cut down on the millions of pounds worth of useless scans, tests and hospital appointments. Take this example of a patient who was referred by her GP for umpteenth medical tests costing 10's of thousands of pounds before being diagnosed into ME/CFS: Another example of dastardly care: Father forced to Google his symptoms after 150 GP appointments failed to correctly diagnose his rare throat syndrome • Carl Holt, 34, developed a constant sore throat after returning from holiday • He also lost more than four stone in weight and was permanently fatigued • Over a period of two years, he attended 150 GP and hospital appointments • None of the doctors was able to provide a clear diagnosis • Googled his symptoms and discovered a condition called Eagle syndrome • It is characterised by hardening of a ligament at the back of the throat or by elongation of a bone at the base of the skull which causes discomfort • Mr Holt paid for private tests which showed he had the syndrome By Emma Innes Published: 14:21, 24 June 2013 | Updated: 15:53, 24 June 2013 A couple of the symptoms most patients have in common are an inability to breathe deeply and IBS symptoms of constipation. These symptoms are often treated with Morphine and Codeine which suppress breathing and gut motility and yet patients are being prescribed vast quantities of these drugs making their condition far worse and also getting them addicted to these opiates. Just preventing GP's and hospital specialist services for these three conditions (ME/CFS/FM) alone would save some 5 to 10 billion pounds per annum. Not only that there will be far fewer patients who are chronically ill with these conditions saving further 10's of billions on social security costs. Today the Royal College of General Practitioners asked "for an army of pharmacists to step in to help GPs". This is extremely suspicious. I think the call should be for an army of civil defence forces to protect the patients from big pharma and their toxic wares which have removed almost all semblance of altruism in the medical profession and instead made them into pharmaceutical snake oil agents. "Medical Care Is the Third Leading Cause of Death in the US according to Dr Mercola When you add up medical errors, drug interactions, and hospital-acquired infections, medical care is the third leading cause of death in the US, right after heart disease and cancer. Preventable medical mistakes account for one-sixth of all American deaths. Unfortunately, Covid 19 has rattled these figures. According to the latest estimates, 210,000 to 440,000 Americans die from egregious hospital errors each year, with hospitals that cater primarily to Medicare patients tending to rank the worst." This surely means that to get the best benefit extreme checks must be put in place to curb the ghastly influences of medical commercialisation. Presently if any fraud by the medical profession like 'inventing disease' to sell expensive drugs as happens with MOST major illnesses is discovered the fraud squad is powerless to intervene and have to pass on their concerns to the governing authorities who are often under the corrupt influence of revolving door appointees. This is the major reason why our health service is a bottomless pit! Revised January 2021 ------------------------------------------------------------------------------------- This article may be freely reproduced on social media or copied onto your website provided proper acknowledgment is made and a link provided back to this website. Sunday, March 1. 2015Morphine and Codeine overdosage of ME/CFS and fibromyalgia patients
Peter Marshalton adds the following to his previous post:
"I was prescribed morphine after I was diagnosed with very painful IBS, fibromyalgia and M.E at the age of 20. Over the next twelve years as the pain got worse, the dose was increased and increased again until I was taking almost 1000mg of morphine a day. For the first couple of months on the increased dose, it would work, but then the pain would come back, even worse than before. By this time, the side effects of constipation, brain fog and poor memory were very severe. But so was the pain. I felt stuck between a rock and a hard place. Trying out drug-free ways to manage the pain I found a TENS machine which was the most effective for the M.E and fibro pain. A gluten-free diet and taking oral clay helped the IBS. Comment: Patients are being prescribed vast quantities of these drugs while the medical profession admits that they have absolutely no understanding of the cause of these illnesses. Reviewed January 2021 ©2014 - 2021 Dr. M. Amir. All rights reserved. ------------------------------------------------------------------------------------- This article may be freely reproduced on social media or copied onto your website provided proper acknowledgment is made and a link provided back to this website. Friday, February 20. 2015ME diagnosis as per Canadian Consensus Document (CCD) or TMJ Dysfunction? - You decide
My name is Peter Marshalton. I am 36 years old. I live in London. When I was fourteen years old I was told my teeth were overcrowding my mouth and I needed braces. For the next two years, I had a series of them including headgear worn for 14 hours a day. I also had two teeth removed. Two years later, at eighteen, I had recovered enough to go to work but I always felt tired. Then at twenty-one after working a hard job and long night shifts I fell ill with M.E again. This lasted for fifteen years. Over time I gradually got worse, needing a wheelchair, and often being bedbound. I developed around thirty symptoms and was in constant, often severe pain. It was a struggle just to do basic daily tasks. Then my mother discovered Dr Amir's website while googling ''treatment for M.E'' where Dr Amir explains that dental and jaw asymmetries could be the cause of most symptoms. It seemed incredible that I could be so ill for so long all because of the asymmetry of my teeth. But I felt it was worth trying. Just hours after having it fitted my body felt lighter. Usually, it feels heavy, as if I was filled with lead. My breathing started improving which had been my worst symptom because I could barely breathe prior to this treatment. ©2014 - 2021 Dr. M. Amir. All rights reserved. Friday, October 31. 2014How to avoid the diagnosis of ME, CFS, FM, MS or Mental illness
 Article submitted by patient's mother to Positive Health magazine December 2014 One clinician who examined her right-sided weakness referred her to a neurologist. With a small family history of MS, this was mentioned as a possibility - a devastating prospect for a 19-year-old. An urgent MRI scan was undertaken. Seeing the neurologist the next day privately and anxiously awaiting the outcome is one of the worst experiences of our lives. To our great relief, she did not have any 'brain lesions' and with greater understanding, we now believe that she narrowly escaped being labelled into Multiple Sclerosis. During this period, fretfully searching for an answer, Hannah continued to deteriorate and became virtually housebound. She struggled to walk up the stairs. She was very distraught at what was happening to her. Ultimately at the end of the three months when the myriad of tests were all negative Hannah was finally given a diagnosis of ME/CFS or Fibromyalgia - a diagnosis by exclusion! Hannah was further alarmed at the stories she read on the internet about people having these illnesses and how badly it impacted their lives. Every website said, “The exact cause of ME/CFS/FM/MS is unknown and that there is no cure for any of these illnesses but there were lots of drugs to control the symptoms”. Her plight caused severe upsets in our family. Hannah believed that her life was over as she had known it - her sports, her social life, her love of studying and a future career as a mathematician was all over. Throughout the whole process, whenever we mentioned the change in her facial features or the rib abnormality it was neither acknowledged nor considered by the medical professionals we saw. Indeed there was more focus on anxiety as a potential cause. We were perhaps heading for a dreadful calamity of mental illness! On reflection, we now realise that her facial changes were a key observation and this was always on our minds. We continued in our quest to find some answers. As fate has it, we finally hit Dr Amir’s website. He tells us that he had just started advertising his website and we were amongst the first to call. Thankfully he agreed to see Hannah immediately. Despite our initial scepticism, we listened intently as he spent a full hour with Hannah listening to the story going through the questionnaire (which we had completed online via his website), physically examining Hannah from head to toe and at the end of the hour showed us his findings. He found that Hannah had: • A severe jaw displacement; • Misaligned ribs – causing the rib pain; • Very asymmetric hips – this was a complete shock as Hannah had no hip issue; • Severe breathing problems; • Extreme muscle weakness. Dr. Amir was able to show us how all the symptoms were related to previous extraction orthodontics and the asymmetry of her jaw. He showed us Hannah’s very misaligned jaw which was affecting the vertebrae in her neck, lower back and the hip bones. He showed us how the jaw was affecting the ear organ causing the dizziness. How the shallow breathing was affecting her energy system and causing her belching. He also reassured us that Hannah did not have any disease process going on and the entire list of symptoms emanated from the asymmetry of her jaws and teeth. He had seen this many times before. Dr Amir speculated that her problems started with the removal of some teeth and the wearing of braces as a teenager. It had also caused a change in her facial features. He explained that the illness hits anytime between 17 and 25 and can come about all of a sudden with a myriad of symptoms. He has successfully treated very many patients over the last 20 or so years. It all made so much sense. This was perhaps our last chance to find an answer and here was someone who had all the answers. We were desperate. We did not wait and decided to embark on the treatment immediately. Hannah started an extensive course of treatment to reposition her jaw using Dr Amir's custom made appliances. The improvement in Hannah's health in the first few weeks of treatment has been remarkable. The symptoms that have disappeared completely are: • Dizziness; • Belching; • The cold feeling trickling down her right arm; • Pins and needles in right foot; • Tendency to feel faint, syncope and dry eyes. The fatigue has virtually disappeared and the weakness in her arms and legs are much improved. Interestingly Hannah's ribs no longer protrude and her hips are visibly completely aligned. She has a few problems sometimes but these are almost immediately resolved by Dr Amir changing the appliances or his strategy. At just over three months into the treatment, Hannah has recovered a lot and has been able to return to university and is getting stronger with each passing day. She is also back to her noisy, bubbly self! The family is so relieved. Hannah and her family are eternally grateful to have found Dr Amir so early in her illness as she was physically deteriorating so rapidly that walking was becoming a significant concern and disability a real possibility*. We would encourage anyone with these symptoms or with such a diagnosis to see Dr Amir determine if the cause is the same as Hannah’s so he can work his magic on them. We believe that Hannah has been saved from being drawn into a “chronic incurable illness” like CFS/ME/MS or Fibromyalgia. Our advice to everyone with these or in fact many chronic disease labels is to have their jaws checked. You may have a chance to recover fully. If any family or individual wants to discuss this with me I would be more than happy to help. You can phone me on 07436037332 Mari Gay 31st Oct 2014 *Comment:MS patients - Please note that the jaw problem was going to cause her complete walking disability and probably make her wheelchair-bound. This phenomenon needs careful evaluation to see where this disability actually emanates from.Presently, the walking disability is one of the cardinal signs - a fait accompli, in the diagnosis of the mythical 'MS'. I have serious reservations about that. Here is a graphical representation of Hannah's recovery:  Email received from patients mother Xmas 2014:
Hi Dr Amir, "Once again I want to thank you for all you have done for Hannah. She is now completely back to the girl we knew and is walking long distances with no problem and the strength has returned fully in her arms and legs- I would go so far to say she is stronger than she was before. I know I was very sceptical at first but have seen first-hand the changes in Hannah’s body as a result of your treatment. I am continuing to spread the message and will make a concerted effort next year to influence where I can. Hope you and all your staff have a lovely Xmas and a well-deserved break. Sincerely," Mari Gay. On 20th April 2015 Mari wrote: "Have to once again thank you. This time last year we were so upset and worried about Hannah. She was very unwell with all those awful symptoms and she was so quiet that it was heart-breaking. This weekend we spent in Liverpool and the strength she had was amazing and is clearly able to do what she wants now, and she was very noisy!!!! It was brilliant and she really enjoyed it. [Furthermore,] One thing I have definitely noticed with Hannah is that she has lost her clumsiness she developed in her teens and her tendency to walk into any door frame around. She just seems more controlled now!" 14th July 2016 Mari writes: "Had to show you what a wonderful day we have had today for Hannah's graduation. Several times today we have remembered that this day would never have been possible without your treatment. Thanks so much once again from our family!!!!! She's had a great day!! Update January 2020: Mari writes sending me a photograph: "Had to show you this. Hannah has turned into an excellent netball player - all because of you.Hannah remains well and very bubbly." Reviewed January 2021 ©2014 -2021 Dr M. Amir. All rights reserved. Sunday, August 17. 2014The myth of mitochondrial imbalance in ME/CFS & Fibromyalgia
"The causes of ME/CFS and Fibromyalgia are unknown", is the usual mantra which is also applied to most other medical syndromes. Some "charitable societies and associations" are happy to fund these futile studies the outcome of which is usually a foregone conclusion. Many practitioners have already become experts and have started treating patients by "rebalancing of the mitochondria using a recipe of multivitamins and minerals at enormous cost to the patients with questionable outcomes as one of my patients, who recovered with Jaw symmetry treatment, commented: In our practice we have demonstrated time and again, with hardly any exceptions, for over 30 years, that the cause of ME/CFS is Cranio-dental jaw and spinal asymmetries. I have never come across any patient who did not fit into this criteria. Sunday, May 25. 2014Suffering for 'ME/CFS' patients deprived of proper and timely TMJ treatment
I recently saw a new 22-year-old patient who soon after her 9th birthday during 1999 became very ill unable to go to school with the following symptoms: |
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