dose instruction, Questions And Answers
Pancreatin 325 or 1200 is not as effective as Kelley Solozyme in breaking Cancer Cells.
Pancreatin 325 or 1200 contains only amylase, protease and lipase
Kelley Enzyme are more effective with cancer
Kelley Enzymes VS USP Enzymes
Enzymes consumed near food digest the food first. Then cleans the blood, then goes after cancer.
Enzymes consumed well away from food (1 and 1/2 hours) go after cleaning blood then cancer.
The specific dosage for him will depend on his ability to remove the broken cancer cells via the coffee enemas.
Either full 54 grams each day then stop for five days if the enemas will not manage the liver overflow.
Adjust down the dosage down to the maximum level he can manage to consume without the liver overflow symptoms.
Revisit the correct dosage by increasing amount every few weeks, to find the new maximum dosage that can be managed.
Buiding up dosage vs starting at recommended dosage? It is up you to explore what works best for you.
For those who have been told they have cancer, following a modified Kelley Metabolic program. In this modified version we use Pancreatin USP to be taken thirty minutes prior to eating.
Understanding the differences between Dr. Kelley Enzymes and USP enzymes. Kelley enzymes start with the entire organic New Zeland porcine pancreas gland. Freeze Dried with additional chymotrypsin. The USP enzyme is highly refined only contain:
lipase xxx USP units
protease xxx USP units
amylase xxx USP units
The balance of the materials extracted via chemical breakdown is typically sold on to digest clogged drains.
I recommend the Kelley Enzymes taken well away from food three times each day 12 capsules each time for a total of thirty-six capsules (twenty-seven grams.) These enzymes are porcine from New Zealand.
And in addition, thirty minutes prior to eating take nine grams of pancreatin USP to assist in digesting the food. It is important to support your body in completely digesting and extracting all the nutrition from the food you consume. These enzymes are porcine primarily from New Zealand although we cannot guarantee origination.
- You will also need to take coffee enemas as needed.
- Enjoy a vegan diet for at least two months, then as much as five percent animal by calories.
- Practice emotional stress reduction process daily.
- Probiotics reinoculation is essential if you have ingested any pharmaceuticals or you were born cesarean.
From Wikipedia Explaining more about what the differences are.
The pancreas is both an endocrine and an exocrine gland, in that it functions to produce endocrinic hormones released into the circulatory system (such as insulin, and glucagon), to control glucose metabolism, and also to secrete digestive/exocrinic pancreatic juice, which is secreted eventually via the pancreatic duct into duodenum. A digestive or exocrine function of pancreas is as significant to the maintenance of health as its endocrine function.
Two of the population of cells in the pancreatic parenchyma make up its digestive enzymes:
- Ductal cells: Mainly responsible for the production of bicarbonate (HCO3), which acts to neutralize the acidity of the stomach chyme entering duodenum through the pylorus. Ductal cells of the pancreas are stimulated by the hormone secretin to produce their bicarbonate-rich secretions, in what is, in essence, a bio-feedback mechanism; highly acidic stomach chyme entering the duodenum stimulates duodenal cells called “S cells” to produce the hormone secretin and release to the bloodstream. Secretin having entered the blood eventually comes into contact with the pancreatic ductal cells, stimulating them to produce their bicarbonate-rich juice. Secretin also inhibits production of gastrin by “G cells”, and also stimulates acinar cells of the pancreas to produce their pancreatic enzyme.
- Acinar cells: Mainly responsible for the production of the inactive pancreatic enzymes (zymogens) that, once present in the small bowel, become activated and perform their major digestive functions by breaking down proteins, fat, and DNA/RNA. Acinar cells are stimulated by cholecystokinin (CCK), which is a hormone/neurotransmitter produced by the intestinal cells (I cells) in the duodenum. CCK stimulates the production of the pancreatic zymogens.
Pancreatic juice, composed of the secretions of both ductal and acinar cells, is made up of the following digestive enzymes:
Pancreas's exocrine function owes part of its immaculate function to bio-feedback mechanisms controlling the secretion of its juice. The following significant pancreatic bio-feedback mechanisms are essential to the maintenance of pancreatic juice balance/production:
- Secretin, a hormone produced by the duodenal “S cells” in response to the stomach chyme containing high hydrogen atom concentration (high acidity), is released into the bloodstream; upon return to the digestive tract, secretion decreases gastric emptying, increases secretion of the pancreatic ductal cells, as well as stimulating pancreatic acinar cells to release their zymogenic juice.
- Cholecystokinin (CCK) is a unique peptide released by the duodenal “I cells” in response to chyme containing high fat or protein content. Unlike secretin, which is an endocrine hormone, CCK actually works via stimulation of a neuronal circuit, the end result of which is stimulation of the acinar cells to release their content. CCK also increases gallbladder contraction, resulting in bile squeezed into the cystic duct, common bile duct and eventually the duodenum. Bile, of course, helps absorption of the fat by emulsifying it, increasing its absorptive surface. Bile is made by the liver but is stored in the gallbladder.
- Gastric inhibitory peptide (GIP) is produced by the mucosal duodenal cells in response to chyme containing high amounts of carbohydrate, proteins, and fatty acids. The main function of GIP is to decrease gastric emptying.
- Somatostatin is a hormone produced by the mucosal cells of the duodenum and also the “delta cells” of the pancreas. Somatostatin has a major inhibitory effect, including on pancreatic production.
dose instruction, Questions And Answers
P.B. asks Dale Q – Dale, would like to share changes which I felt after reducing PEP from 12 to 5 as per your recommendation. while taking 12 PEP away from a meal, was feeling less energy in the body, less appetite and had a rash on the body, so it means it was working very well. As soon as reduce to 5 more energy level, less rash on body level of appetite as increased, so it means less effective.
I am maintaining five enema/day.
A – As you move through the process of destroying the cancer cells it is many times the case that the enzymes will cause the side effects you have experienced, rash, reduced energy and more.
In Dr. Kelley's book, he advises a twenty-five day on and five days off rhythm at full dose. It is also written and observed that in the early days you may need a five-day break more frequently than every twenty-five days.
You have, by reducing the dosage achieved a similar result.
Your body will change from time to time and you may be able to resume more aggressive dosage amounts as your total cancer load is reduced.
When people return to working full time they often, in order to manage the reduced number of enemas must reduce the total enzymes each day so that they can function well in their job.
As long as you are continuing to ‘push' the number of enzymes toward the therapeutic 54 grams each day the progress toward cancer free is going in the correct direction.
I have seen over the 1000's of cases I have supervised some people cut back too far and they will get a wake-up call (test results not getting better or pain or lump reforming.)
Maintaining the forward motion that moves you toward full recovery is a process I can only witness and advise on.
It is well advised that this recovery process is not a quick fix and will take the time that it takes. Dr. Kelley said that it generally takes six to eighteen months to arrive at full recovery.
You are correct on your observation and are learning well, congratulations. – Dale