Neurological

What we will discuss here are our ideas and experiences based on logic and observation. These ideas are not accepted by mainstream medicine, but all mainstream medicine has to offer is palliative treatment until death.

Multiple Sclerosis, Alzheimer's, Parkinsons, Motor Neuron Disease, Autism and it's variants are all relatively new conditions.
Alzheimer's was first described in 1903, MS in the 1860's whilst the MND rate has exploded in the last half century.

Neurological afflictions are increasing dramatically across the Western World. If the current rate of increase is sustained, neurological conditions alone will cost more than the whole of the present health spending within 15 years.

None of the conditions is considered curable and all have an unknown aetiology, that is, no-one knows what causes them.
We do not offer or claim cures for any of these conditions.
Whatever the cause of these conditions is, we will discuss this later on, by the time the condition has been diagnosed it is already fairly in a fairly advanced state.
Parkinsons' for instance only manifests the first symptoms after 70% of the cells are affected. The first signs of MS and MND are often ignored until the severity of the symptoms forces action. By then many years can have passed since the first onset thereby reducing the likelihood of any significant recovery.

All attempts at treatment are therefore on a long established condition which is why most end in failure.

However, there is room for hope.
There have been reported and recorded two cases of recovery from MND , many cases of MS. Autism and some Parkinsons recovery have been reported in the literature as well after starting mercury and other metals detoxification regime. In the case MND we never seen a recovery. Patients have reported that they feel more comfortable on the regime but all have deteriorated over time.
It would seem logical that there must be a strong environmental proponent of these conditions considering their newness and the toxicant must be personal in nature as the conditions are spread evenly over the whole population. No infective cause has ever been found despite rigorous searching.

In our opinion, in order to contract one of these Neurological conditions you must fulfil the following criteria:

Have a chronic exposure to a neuro-toxicant or excitotoxant.
Be the genetic type that is sensitive to the neuro-toxicant or excitotoxant, which in turn leads to:
A reduced Immune System
A compromised Gut function
Establishment of a deep seated Secondary Infective Agent (Lymes being the one most frequently brought to mind).
Low threshold tolerance to other pollutants notably Pesticides and Herbicides.

Mercury from dental amalgam fillings, and as a preservative in Vaccines (thimerosal) is the neurotoxicant that is most likely to be the culprit.
We can recommend the article by Prof B Haley, Medical Veritas 4 (2007) 1510-1524 for a more in depth look into the subject.
We know that:
Mercury in very low doses is a potent neuro-toxicant and neuro-excitotoxicant
Dental Amalgam is the largest source of mercury
Mercury from Dental Amalgam causes the same changes in brains as seen in Alzheimer's brains and only mercury can do this.
Mercury from Dental Amalgam causes neuron death by stimulating the build up of Glutamate in the brain (MND).
Mercury from Dental Amalgam can reduce the function of of cellular mitochondria in the citric acid cycle (ATP and NADH). This reduces the energy available to the cell and lowers overall resistance in the body.
Neurological Conditions show greater oxidative stress in the brain. Mercury is preferentially absorbed by the brain and is a powerful oxidising agent.
Mercury, when in contact with certain micro-organisms, will combine with the toxins released by the micro-organism producing di-methyl mercuric compounds of extreme toxicity to neurological tissue.
Mercury can be bound to tissue by certain anaerobic bacteria increasing the mercury load sometimes by a factor of 22,000 (yes, 22,000 times)
Diet alone cannot provide the amount of mercury required for these changes.
 

In Neurological Conditions a frequently seen genotype is the APO-E-4 allele. APO-E-2 is seldom seen and APO-E-3 is seen more than APO-E-2 but less than APO-E-4. This is especially prevalent in AD and Autism.
Why is this significant?
The answer is Mercury.
APO-E-2 & 3 has cysteines that bind mercury and remove mercury from the brain. APO-E-4 has no cysteine and cannot remove mercury.
Mercury is allowed to build up in the brain over time eventually causing the symptoms which are then labelled as diseases.

In Autism the mercury is delivered to the child in vaccines and from the mothers amalgam fillings in utero and when breast feeding.
These children are born with no means of excreting mercury, hence low hair levels of mercury. Low hair levels does not mean low levels of mercury in the body, it signifies that there is no way of excreting the mercury. It is in the genes.
However, they do respond well to a mercury detoxification if started early enough. Indeed the American Autistic Society on it's web site calls Autism a symptom of mercury poisoning.

In Multiple Sclerosis the myelin sheath covering the nerves is eaten away by a mis-directed immune system. Mercury is attracted to fatty tissue such as Myelin which surrounds the nerves. The immune system scouts, the B Lymphocytes, recognise mercury as as an intruder and signal the immune system attack it. Unfortunately the attackers target not only the mercury but the myelin sheath as well. This is an autoimmune diease.
The Melisa Test of Prof. Stejskal can detect such a sensitivity to mercury.
The proper removal of mercury and infections is logical in such patients as is a gut cleaning programme and Dr Klenner's Protocol.

In MND The proper removal of mercury and infections is logical in such patients as is a gut cleaning programme and Dr Klenner's Protocol. There are specific supplements like carnitine recommended by some neurologists, also see the book "Eric is Winning". MND is is the result of an excitotoxicant unbalancing the Glutamate pathways. Z
 

All this information is fine but what should be done?

Firstly, whatever the diagnosis, have hope but no illusions as to a miracle cure.
Removing mercury from the teeth, remove dental metals (they reduce the immune system), remove infections and optimise gut function is the first step.
Start a long term safe mercury removal programme from the body using supplements and Intravenous High Dose Vitamin C.
Try and identify any deep seated infective agents and attack them using the electronic machines available from the Lymes community.
Have a blood test - a Neurological Profile - from Biolab.
Adapt Dr Klenner's Protocol in the light of the deficiencies illustrated by the test.
Have a fat biopsy for pesticide and herbicide residues.
Consider a Phospholipid exchange programme to remove such residues.
Have a metal and physical exercise programme and stick to it.

We can guide patients through such a programme supplying what they require.
It is time consuming and requires commitment. It all has to to be funded privately as well, expect no official help.

Dr Klenner's Protocol

The protocol of Dr. Klenner's consists of:
(1) a daily intramuscular injection of vitamin B1 of 300 to 400 mg. The correct dosage can be determined by the level of fatigue the patient experiences. Some patients require 300 to 400 mg daily to experience relief of fatigue symptoms. The B1 is available in a strength of 200mg per ml. So a 200 mg injection would be 1cc.
(2)Twice weekly 1cc of liver extract is added to the B1 injection so extra injections aren't needed. The B1 injectable comes in a 30cc bottle and lasts for two to four weeks. The liver extract comes in a 10cc vial and lasts 5 weeks. The syringe is a 25 gauge by five-eighths inch 3cc syringe.

Note: B1 is not well absorbed in oral form ­ the daily injection is required for life for successful treatment and recovery.

Oral Vitamin Regimen (Varies a little from Patient to Patient)
1. 5 grams daily in divided doses of Calcium/Magnesium Ascorbate (buffered Vitamin C). This boosts the immune system and eliminates or shortens recovery time from colds and flu.
2. Vitamin E 400 to 1000 IU daily
3. B-100 tablet. This tablet contains 100mg of all of the B vitamins.
4. B12 ­ One tablet (sublingual ­ dissolved under the tongue) daily. One to 2mg strength.
5. Niacin. Once or twice weekly, 100 to 300mg before breakfast. This is a vasodilator and opens the blood vessels allowing the nutrients to rebuild the myelin sheath damaged by MS. This will produce a flush and reddening of the skin for about 30 minutes, which most patients say they enjoy. It is advisable to lie down and cover up for the period of the flush.
6. B5 & B6 daily tablets 200mg.
7. We add a Canadian Supplement called GSH which is a Glutathione derivative.

Diet or a diet advised by the patient's Metabolic Type.
A high protein diet is required to rebuild the myelin sheath. Examples: Breakfast ­ 1 or 2 eggs poached, with fruit and cereal. Lunch ­ fish and vegetables (steamed) and fruit. Supper ­ chicken or beef with vegetables and fruit.

One 500mg digestive enzyme tablet taken with each meal can often improve digestion and absorption.

REMEMBER THAT THIS IS A DAILY REGIME THAT COULD BE LIFELONG.

Typical Neurological Profile Test Result:

Typical Pesticide/Herbicide Residue Result: