[email protected] wrote: As a first approximation, I'll assume that by the 96th day after stopping CS
> ingestion all remaining silver in my tissue was eliminated. (This is a > reasonable assumption, but you would have to see the report to know why.) > Numerical integration of the graph on page 7 of my report would indicate that > the maximum amount of retained silver in my body which, of course, occurred > on the last day I took CS before stopping, was 159 mg. At that time I weighed > about 104 kg. (pure muscle, of course). So in terms of body mass, I had an > average of 1.5 PPM CS. (This figure may be higher if there was still a > significant amount left in my body AFTER the 96th day, but it is doubtful > that I am off by more than 20%). Now, most people who take CS don't take > anything near the 2.3 mg/day that I took for the prior 5 1/2 months, and, > therefore, their CS concentration on body tissue could be much, much lower > that the 1.5 PPM I've estimated here. So their degree of systemic protection > could be proportionately less, particularly if you take into account local > levels of CS depletion where an infection has already started to multiply > rapidly. Since there is good evidence that I was saturated in CS, while most > CS takers are not, it is quite possible that an infection could get a > foothold for many despite daily CS ingestion. Incidently, I don't recall > being sick during the entire period (~9 months) I did this study. I wonder if there is any difference between CS you have just taken, and CS that is still around after a few days. What I am thinking is that CS that was taken recently will be in the blood, where it can do the most good in most cases. Now my guess is that it will quickly be either eliminated by the kidneys, or get trapped somewhere, in tissue perhaps, or bound somehow. This CS is not quickly released, and likely is only released when a chelation agent is eaten (there are many, ie. garlic). Chelated metals often tend to be eliminated by the liver. If that is the case I think it would explain several things. ie. 1. Why the effectiveness of CS seems to drop off rapidly after taking. All the CS in the blood is essentially elimated in 24 hours or so by the kidneys. 2. Why you saw a long term storage of silver. 3. Why initially you saw most silver in the urine, but later in the feces. What do you think? Marshall -- The silver-list is a moderated forum for discussion of colloidal silver. To join or quit silver-list or silver-digest send an e-mail message to: [email protected] -or- [email protected] with the word subscribe or unsubscribe in the SUBJECT line. To post, address your message to: [email protected] Silver-list archive: http://escribe.com/health/thesilverlist/index.html List maintainer: Mike Devour <[email protected]>
