Basic Digestion

Protocol

The chlorine balance kit is a set of chlorine donor salts in a seven day package. Each day-compartment contains four capsules. Each capsule contains a mineral salt.

Do not take all four capsules at once. This much salt will give you a stomach ache or nausea.

Taking 2 capsules 30 minutes apart with at least 8 ounces of water is advised. If this creates discomfort, then take 1 capsule every 30 minutes. Drink at least 8 ounces of water for each capsule you take. The water will help your body absorb the salt, and will support your kidneys. Drink at least 6 8 ounce glasses of water throughout the day to support the kidney flow and limit stress.

The four capsules are each a different salt:

• 700 Mg Magnesium Chloride
• 700 Mg Ammonium Chloride
• 700 Mg Potassium Chloride
• 700 Mg Ammonium Thiosulfate

Monitor your pH. It should swing acidic as a result of the salts.

This experimental protocol targets two different aspects of chlorine imbalance.

1. Open the toxin exit path.
2. Supply chlorine.
3. Supply bivalent-negative sulfur.
4. Supply Potassium chloride as a sodium exchange agent.

Protocol Schedule

This protocol is designed as a 7 day procedure. It may cause diarrhea, and symtpoms that accompany elevated NH4 and NO3 Urea mobilization and liver flow..

The titration uses urinary and salivary pH to adjust systemic chlorine levels to normalize metabolism. It uses both saliva and urine pH as a guide to administer sufficient chlorine to re-balance chlorine levels.

Saliva and Urine pH should average to 6.4. To calculate balanced pH multiply saliva pH by 2 add urine pH and divide by 3. If this number exceeds 6.4, then alkalosis is present, otherwise acidosis is present. Ammonium chloride is documented as a treatment for systemic acidosis.

Instructions:

Urinate into a cup or glass;

• Check urinary pH;
• Check saliva pH at the same time;
• Double the saliva pH and add urine pH;
• Divide by three;
• If number is greater than 6.4 then use the protocol that day;
• Drink at least 6 - 8 ounce glasses of water that day;

Detoxification indications suggest that the body has reached its present ability to detoxify noxious agents released from cells. Continuing the program before the body is able to dispose of these agents creates unnecessary and potentially harmful discomfort.

Suspend the detoxificaiton when any of the following symptoms occur:

• Diarrhea
• Gastric distress / pain in the stomach
• Discomfort in the liver/gallbladder region
• Urine pH drops below 5.5
• Dizziness, nausea or headache occur

Normally the Urine pH and Saliva pH will drop. A typical response is an increase in energy.

Discussion:

1. Pathogenic/stress processes generate abnormal cellular lipids. The body uses chlorine to neutralize/oxidize these lipids as a first priority. This priority outranks digestion as a protective function, so chlorine is utilized for detox first. This explains the cellular redirection of chlorine away from digestion.
2. A protocol which accelerates cellular clearance of these agents should first ensure an open exit path. Accelerating cellular releae of chlorine fixed lipidic agents without enabling body clearance, will probably produce adverse response, including but not limited to a severe Herxheimer's reaction.. This protocol should not be utilized until after a successful Liver Flow Detox where the individual was able to complete the 4 hour program without gall bladder discomfort.

Background

Chlorine plays a major role in metabolic process including immunity and stress management. Revici documented that creation of certain fatty acids in abnormal cells consumed very large quantities of chlorine causing systemic deficiency both under stress, or shock, and as a component of pathogenic process.

Most individuals chlorine imbalance tend to have an elevated urinary pH, and salivary pH presenting as systemic alkalosis.

It is unknown if the chlorine dysregulation is pathogenic effect, or a response to pathogenic effect. It seems likely it is a response, because of similarity of the physiological condition across pathogenic and non-pathogenic challenge. Experience suggests mobilization of NO3, toxins having an acidic character, likely indicating enhanced cellular release of acidic toxins.

Regardless of cause, iIt is clear however that chlorine depletion presents chronic, escalating and often dangerous, consequence of physiological challenge. This protocol is designed to address both chlorine deficiency, as well as restore chlorine/sodium balance in the digestive system.

The protocol was developed in response to the inability to restore digestion in certain individuals with acute chlorine deficiency. These individuals took 50 betaine tablets, and still did not seem not to have restored the acid component of digestion.

This inability suggests that other methods are needed.

Chlorine Dysregulation

Chlorine dysregulation has been observed frequently. Individuals usually report upper GI discomfort. Doctors respond by using a scope to search for blockage. Normally none is found.

There are several typical complaints:

• Heartburn or acid reflux (see betaine page);
• Chronic bloating below center/left rib cage;
• Poor digestion/flow in the upper GI tract.

Long term chlorine deficiency may result in uncomfortable esophogeal lesions, irritation, and in severe chronic cases may result in cancer as chronic lesions mutate into cancerous tissue.

Evidence of Chlorine Accumulation

This research is supported by Chinese practitioners who use electric currents to treat cancer tumors, who report that treatment releases large quantities of chlorine into the air during treatment. This chlorine release is not consistent with electrolysis which would cause salt to precipitate.

Individuals with acute chlorine imbalance often report digestive stress with excessive bloating in the upper GI tract, typically below the rib cage.

Probable cause of digestive issue, upper GI bloating/distension:

• Long term stress has triggered overproduction of abnormal UFAs in cells throughout body;
• These UFAs absorb huge quantities of chlorine causing systemic chlorine deficiency;
• The chlorine deficiency imbalances Sodium, (Sodium Bicarbonate) in the pancreas and upper small intestine
• Creating persistent, and often acute, inflammatory constriction of the upper GI;

Stress, from any combination of physical trauma, disease, or psychological challenges, are a big factor in the phenomenon. 

Revici documented that the upper GI inflammation, top part of the small intestine, was a universal autopsy finding, in animals which were “stressed to death”.  He asserted that stress triggered creation of anti-fatty acids UFAs, which absorbed sufficient chlorine to trigger systemic jeopardy and accelerate death from other factors.  See P-230 Revici Guided Chemotherapy.

So… The immediate problem appears to be to restore chlorine/sodium balance. There are at least three potential agents for this job.

Settling the imbalance should normalize the ionic balance in the Small Intestine and the inflammation should reduce.  Salt, NaCl is a poor option because it contributes Sodium, which is part of the problem. The chlorine is used as needed, but the sodium contributes to the imbalance. This means that either:

• Add Chlorine
• Remove Sodium
• Or Both

Available Chlorine reagents:

• Betaine-HCL – Included in the kit we sent.  Betaine is TMG, from sugar beets bonded to Hydrochloric Acid.  Betaine performance is usually good for moderate chlorine deficiency. In severe cases, individuals took up to 50 capsules without restoring digestion, often creating nauesea, etc. This suggests that the amount of chlorine in Betaine sometimes isn’t enough to get the job done.  This is frequent with individuals cancer, or acute stress.
• Magnesium Chloride - Is a preferred reagent with elevated urea levels, which are a typical response. Elevated chlorine, with sulfur enable cellular mobilization of lipids, and increase NH4, which are part of the detox
• Ammonium Chloride – Is a preferred reagent because the NH4 is rapidly converted to Urea, which have simple detox paths. This is the simplest way to settle the imbalance because it contributes a lot of chlorine without creating a strong anionic imbalance.  NH4 is a weak base that’s easy to dump.
• KCl – Potassium chloride – Is a backup option.  The good news is that you can buy it in the grocery store as “Sodium Free – Salt substitute” .  This strategy presumes blanaced potassium metabolism, with functional potassium release. Some research references suggest that Potassium may swap with sodium. In this case, KCl, will reduce the sodium side of the imbalance. If not, there is a good chance it will likely help. 
• Ammonium Thiosulfate - is a catalyst for cellular chlorine binding. It also aids in liver flow.
• Ammonium Cations are preferred in this model because they provide a weak base with a stable exit path, and no toxicity. Ammonium is used in the body to bind noxious acids and is a primary a detoxifying agent.