Hello again. YES - this is my family. It's 18 months since we began this journey. We are back to normal life again. There is no miracle in this - just the desire to get better - something i'm sure that every one of you has.
I guess it's best to spare you from posting the photo of my family six months prior to this one. It's probably not very different from the look of your own face in the mirror when brushing your teeth every morning. I hope you enjoy our story below. I'm sure it's not very different from yours at least initially...
It all started back in early 2013 (or should I say sometime in 2012 since I have no direct recollection of being bitten by a tick other than recovering a dead and squashed one from my cloths) - with my very first symptoms of Lyme disease.
This was at the time when we were living in Sydney, Australia with my wife and our little daughter. It is also where I believe I got infected with Lyme disease, working as a surveyor in and around Sydney.
Having undergone hip replacement surgery in December 2012 - soon afterwards I started experiencing excruciating stubbing spinal pain located between my shoulder blades (for over two months) as well as starting to develop a numbness in my upper limbs. It was not a funny feeling - my biggest fear was that it might be Multiple Sclerosis.
Not waiting too long, I met again with my surgeon, who requested an MRI scan of the upper section of my spine. We were both nicely surprised that the MRI showed absolutely nothing to worry about.
The pain slowly disappeared and the numbness decreased to little or nothing. Only for a short period of time.
But this was only the beginning. Over the course of the following three years, I visited GPs and underwent dozens of tests for dozens of things.
The symptoms I experienced were ticking off almost all boxes as per below:
This web site was actually what saved my life, since NHS guidelines on Chronic Lyme Disease are incomparable.
More importantly - in my personal view - the only blood test available at NHS (ELISA) is probably as good as 40%. There is no proof on how accurate the test is and any claims that ELISA is 75% or better are unproven. Critically - once your results come back negative you are unlikely to be advised on the limitation of ELISA by NHS. At least I wasn't.
In case you've been to Australia, it is shocking that the Australian government still claims that Lyme Disease is not present there. You cannot be further away from the truth. Surely this will change in the coming years.
September 2015 - my Lyme started to make serious advances. I could not remember the names of my kids and my anger management was at the peak of a struggle. It was the point in time that I started to read about what can be causing all these conditions.
Since my GP advised, that all he could see wrong with me was iron deficiency, I was left with little option but to read all possible sources on everything. So here it is - my life saver web site again:
As soon as I read it, I was on the phone to my GP again. I went through all the symptoms on the phone and requested the blood test to confirm. No surprise I was asked if I remembered being bitten by a tick and when I said, "Not quite", I was advised by my GP I should see a neurologist instead.
In his skepticism, he commissioned the blood test. Two weeks of waiting and what a surprise - the test results came back negative! It was devastating news.
I was almost certain I had Lyme. Not to my GP though. Still, in the meantime, while waiting for my blood test and being more than certain I was Lyme positive, I started to read more about it. One of the very common comments was that the antibiotics often fail to cure Lyme. How is this possible??
I started to read more and more and, with my foggy head, I came across the so-called 'Salt and Vitamin C Protocol.'
Not waiting too long, I had no hesitation to try out this method. I purchased both salt and vitamin C as described on various web sites and started the protocol.
I MUST STRONGLY ADVISE THAT THE INFORMATION ABOUT THE SALT AND VITAMIN C PROTOCOL IS INCLUDED IN THIS STORY ONLY TO EXPLAIN HOW I BECOME CONFIDENT I WAS LYME POSITIVE BEFORE SEEING THE CONSULTANT. I THEREFORE DO NOT RECOMMEND LET ALONE ADVISE TO TRY THIS METHOD ON YOUR OWN. ANYBODY WHO ATTEMPTS TO SEEK SIMILAR PROOF OF BEING LYME POSITIVE DO SO AT THEIR OWN DISCRETION. SIMPLY - DO NOT DO IT AT ALL AS THIS MAY LEAD TO OTHER SERIOUS MEDICAL CONSEQUENCES!
To continue the story - very soon (within a day or two) my body's reaction started to make me feel like I was going through an exorcism. It's often describes as 'Herxheimer reaction' in most literature. It felt almost like a Near Death Experience.
All organs and every part of my body became so painful it was hard to survive the first few night. Luckily, not all parts of my body and organs attempted to release the demon simultaneously. I lasted doing this protocol for two months or so.
In the meantime, my neurologist appointment came up - the 2nd December 2015 - in my local hospital in Norwich.
Very simple process: I went through the symptoms with the medical professional and, after 40 minutes of conversation, I heard the most astonishing thing in my life - I was diagnosed with Functional and Dissociative Neurological Disorder (FND). Link to the educational link below.
I would not be surprised if some of you reading this have got a very similar story to tell. I was assured by the NHS neurologist that he had 3 in every 10 patients with identical symptoms, so I was not alone. I was actually belonging to the large group of people with the medical condition you can easily live with.
And here is why I have little respect for the views of the NHS neurologist: when, during my appointment on 2nd December 2015, I questioned him as to whether I might have Lime Disease, he said that he could not discount the possibility and, instead, said that he was confident that my condition was 'Functional and Dissociative Neurological Disorder'.
When I mentioned to him about the salt and vitamin C protocol and my body's reaction to it and that it was the proof that I had Lyme disease, he did not want to hear about it.
So, I got no further advice from him as to other possible tests that could be undertaken, whether at NHS or privately and I was simply kicked out of his office! Mainly because I exceeded my 30 minute appointment by further 15 minutes, and I'd probably pushed his schedule into his lunch break. All I can do is take this chance to apologise to him in my story. The letter with his diagnosis appended below.
Most people, I imagine, who would've been sent off by this professional must have entrusted his diagnosis beyond any doubt. I feel very sorry for his 3 in every 10 patients who get diagnosed with FND.
It is in my view that if there is only two thousand cases of patients misdiagnosed with Lyme Disease in the UK on annual basis, then the number over the past three decades would've accumulated to sixty thousands. And this number could be as high as five or ten fold. Especially if below scientific research was proven one day to be correct - please read the below article:
I do not try to say that all these patient with FND are Lyme positive, but if my story is being repeated daily amongst every 3 in 10 neurological patients, then in my view, if only 5% of those patients are Lyme positive without being given a brief on that they might be Lyme positive, then there is something fundamentally wrong with all medical professionals who perform their duties in similar ways.
To continue the story - as I never give up on anything, I was not waiting much longer and I booked my flights over Christmas 2015 to Europe where I knew there were a number of clinics dedicated specifically to Lyme disease. I had to know. I needed a prove my Herxheimer reactions were linked directly to Lyme Disease.
Surprise, surprise - two clinics and two bull's eye hits! Both tests positive for Lyme. This is obviously hard to define whether this is good or bad news. Probably both at the same time, which is very ironic! At least it was not MS. The records of tests with two different types of equipment as well as two different methods - Volla/Vega-test and MORA appended below:
Additionally - the medical doctor that we met at the Novaclinic completed the symptom check for clinical diagnosis. Although having already the results with Bioresosnace, it was a routine protocol to fulfil. The diagnosis - Chronic Neurological Lyme Disease - letter appended below.
To make it even more ironic my wife tested positive for Lyme as well, although she was confident she didn't have it. And my two year old son may be positive with Lyme but we still do not know since he was too little to undergo the bioresonance diagnosis with Vega-test. His behaviour was very suspicious over those few weeks leading up towards Christmas - so I suspect my wife may have been infected by myself just before our son was conceived. Hence my son may have been born with Lyme. We will probably never know...
In addition to Lyme we were diagnosed with other pathogens like: Candida, Aspergillus, Chlamydia Pneumonia, Chlamydia, Tapeworm, Yersinia, Staphylococcus, Streptococcus, Herpes. All blood tests for the Candida, Chlamydia, PCR and Western Blot came back negative. Only Chlamydia Pneumonia test came back positive. The proof appended below:
The great thing at that time was that we knew what we had and we were very astonished that the bioresonance can also be used as a treatment to fight it off.
So we are now 2 years later having uncovered around 100 Lyme coinfections on top of Borrelia Burgdorferii. It was a very interesting two year with many ups and downs mainly as we continued to identify new Lyme coinfection every few days.
IT IS EARLY 2018 NOW AND OUR LIVES ARE GOING BACK TO NORMAL ROUTINES. THE LYME SYMPTOMS HAVE FADED AWAY.
MAKE NO MISTAKE THIS STORY IS NOT ABOUT GOING INTO REMISSION THIS STORY IS TRUE AND IS ABOUT HAVING COMPLETELY ELIMINATED LYME COMPLEX WITH RIFING. THIS STORY IS ABOUT ERADICATING LYME WITH VEGA TEST AND MY RECOVERY AS A PROOF TO THE WHOLE WORLD.
DID YOU KNOW?
LYME STATISTICS (TICK RELATED ONLY) - USA - 300,000 cases each year, Germany - 80,000 cases each year. UK - NHS estimate 2000 - 3000 cases each year. How does it add up? If only 20,000 - 30,000 of Lyme cases were presumed in the UK each year then over 4 decades the total of people living unknowingly with Lyme disease in the UK would exceed 1 MILLION. And this number would not even account for STDs and congenital infections!
Thus far we have not identified a single person with formally diagnosed neurological condition - e.g. MND, MS, Alzheimer, Parkinson, FND - who would not be Lyme Complex positive. It is our view Lyme Complex is the root cause of all neurological diseases.
Lyme Disease is the most serious of all sexually transmitted diseases. In our research we have identified Lyme Disease is passed from male to female partners. We have not identified any cases of this STD transmitted in the opposite direction which does not mean it is impossible.
The above fact explains why the ratio of women to men amongst all neurological diseases is approximately 3 to 1.
Lyme Disease is transferred through congenital means as well. So if you were Lyme positive during pregnancy your children are almost guaranteed to have Lyme as well. This may explain why ADHD or Autism numbers are on huge rise.
ELISA test - the blood test for detection of Lyme Disease is probably as inaccurate as 8-12%. The truth is - nobody knows how accurate this test really is. And for that reason Lyme Complex have been denied to be linked as a root cause to all neurological conditions. Lack of testing is another serious issue and injustice to those patients.
Practically all GPs and neurologist in the UK think that if your Lyme ELISA test results are negative you do not have Lyme Disease. Hence you have to be labelled with another medical condition. In other less developed countries (e.g. Poland) Doctors know this fact and often complete clinical diagnosis to confirm Lyme Disease. In the UK clinical diagnosis is called FND - Functional Neurological Disorder. In our view there is no such thing. FND diagnosis is simply a death sentence.
To have your ELISA test commissioned by your GP you need to remember to be bitten by a tick - NHS Guidelines. The problem is - majority of Lyme patients do not remember being bitten by a tick. Another half of those who remember will never go on to developing the rash or a bulls eye confirming infection with Lyme Disease. And these are only about a third of all cases. The other two thirds are STD and congenital infections. Your chances of being confirmed Lyme positive by NHS are in our view less than 2%.
We know this fact from our research. Additionally - there is a growing scientific evidence that Alzheimer Disease and many other neurological conditions could be triggered by various pathogens, in particular: Chlamydia Pneumonia, CMV, Herpes Virus and the main suspect - Borrelia (Lyme Disease). Not surprisingly - the funding for those researchers has been ceased by obvious grant providers. There is no need to comment any more on this issue...
Are tick the only creatures carrying the disease? Wrong! Mosquitoes, spiders, fleece and many other ectoparasites also carry this deadly disease.
So - what is our evaluation of how many people are positive with Lyme in the UK. Well - double the number of tick related cases up to two million. Double that to account for STDs. And add another 2 million to cover congenital cases. And the number should be 6-7 MILLION. If you compile all neurological diseases, fibromyalgia, ME and unreported cases - then 2 + 2 = 4. In our view - at least 1 in 10 people is Lyme positive and these numbers will double very quickly over the next couple of decades.
Dirofilaria Immitis, Dioctophyne Renale and Trypanosoma Cruzi are standard Lyme co-infections confirmed in all our cases thus far. Any of these parasites will protect Borrelia and other Lyme co-infections from eradication. The starting point of treating Lyme Complex should be by removal of these parasites. This can only be done with Vega Test and Rifing.
The final question - do antibiotics work in curing Lyme? Well - see our Lyme Complex Table and answer this question yourself...
LYME DISEASE IS THE BIGGEST GLOBAL PANDEMIC AND IT IS UNSTOPPABLE!!!