hi... never any signs of argyria...so far, so good. tests prior to 7/06 only indicated alt/ast, no viral load and genotype wasn't determined. the 7/06 test is where i requested the bug count and genotype determination. i declined to have a biopsy since they're pretty unreliable and have their own small but real danger of causing cancer to get loose into the body if it hits on some. this is with the VA. i started the CS in early september '06
it wasn't really hard to quit tobacco, except i didn't really want to since that was my main remaining pleasure in life. i only smoked imported handmade cigars, and cheaper ones made from the scrap from the handrollers trimmings. no american tobacco co. drug additives. didn't inhale but chewed on them a lot yum yum. they were effecting my mouth and throat pretty bad. a Sota mag pulser and microcurrents seem to really help the whole neck are recover. i think i'd gotten into a early cancer situation. they no longer appeal to me. i used a beck/Sota brain tuner quite a bit too...can't really say it did anything, but well might've... no strong craves at all. yeah, raw foods are where it's at! > -----Original Message----- > From: Clayton Family [mailto:clay...@skypoint.com] > Sent: Thursday, October 11, 2007 11:37 PM > To: silver-list@eskimo.com > Subject: Re: CS>Hepatitis advice sought > > > Thanks Bob, that is very helpful. Have you had any problem with > argyria, or even blue fingernail moons? I am assuming not, but want to > ask to be thorough. Also, how high was your viral load or did you > know? It sounds like you have been taking it for over a year. > > Congratulations on giving up tobacco, and getting your diet improved. > Just that can be a great help in taking a load off the body. Good for > you! > > Kathryn > > On Oct 11, 2007, at 6:54 PM, bob Larson wrote: > > > i'm also type 1a, and last summer was symptomatic to the point of > > having to > > do something just to keep on keeping on. i started right off by > > buying a CS > > generator, since i got one cheap on ebay and had faith i could at least > > resell it. started out with 4-6oz/day divided into 3-4 shots, at about > > 14ppm (as measured with a cheap TDS meter). major huge turnaround in > > 24 > > hours, but didn't last...symptoms came back but not as bad, but > > progressively better for a month at which time i felt reborn. > > other problems also cleared up over the next several months, like gum > > disease and toenail fungus (almost). > > i started making it at twice the strength and taking half the qty at 2 > > shots/day...and that turned out to be a mistake. symptoms started > > showing > > themselves very slightly again after awhile, and where the toenail > > fungus > > only had 1/8" to finish growing out clean, it started coming in > > discolored > > again from the base on both big toes. > > so at about the 6 month point i started making it stronger yet, and > > doing > > 6-8oz/day, divided into 3-4 shots. by this time i had accumulated Beck > > Protocol tools which i use sporadically. i'd also accumulated various > > herbs > > per stephen buhner's "herbs for hep-c and the liver" and had revamped > > my > > diet a lot, and started doing the herbs and other supps regularly. > > this seems to have me back on top of the virus, but still not feeling > > as > > amazingly well as last fall. the toenail fungus is again almost all > > grown > > out, gums are great, and my eyes have turned almost pure blue. in > > july my > > viral load was 1.3 million, and alt & ast were still above > > normal...also AFP > > has gone above normal, and while that's a cancer indicator it also > > happens > > with smokers and can coincide with treatments being effective > > according to > > something i read on the web...in june i quit tobacco, so at the time > > of the > > blood test i was probably still purging that. > > > > also this spring i started adding in Tetrasilver Tetroxide at about > > 10ppm. > > i have no way of knowing if the HCV has become wise to the CS and the > > control i now get may be due to the TT and herbs. i have no way of > > knowing > > if the herbs and either/both the CS & TT are mutually beneficial, > > cancelling, detrimental, or no effect. > > > > if i had it to do over, i'd start the CS at 8oz/day, at least 25ppm, > > and > > keep it up steady. i'd also start right off juicing raw organic > > fruits & > > veggies, esp carrots and beets, daily and do plenty of chlorella, > > spirulina, > > C, E, selenium, MSM as they're all great supps and are the base of the > > argyria cure case posted on the web, so they should be a good idea to > > help > > keep the silver moving on through and not accumulating in tissues. > > > > last week i've added in the MMS chlorine dioxide and am up to 15 drops > > several times daily, timed from 8pm to 6 am so i can take all my high > > C and > > antioxidant foods and supps during the day without neutralizing the > > MMS. > > too soon to tell what's happening with that, except i've had no herxing > > aside from some stuffy nose in the morning that clears when i arise... > > have > > had none of the nausea/vomiting/diarrhea that others have experienced > > with > > increasing the MMS, but i ramped up steadily for a week. i think i'm > > probably very pathogen free except for the hep, and folks seem to > > think the > > funky rxns to the MMS come from it killing off stuff... i don't know > > that i > > agree with that yet. once i hit the 15drop point (this morning) i have > > finally experienced significant loosening of stools, and farting all > > day. i > > used to fart kinda pungent the first couple weeks of doing all the > > herbs, > > but that tamed down. > > i'm going to be doing 15drop doses at around 8 and 10pm, then again at > > 4 and > > 6am steadily now for the next several weeks (unless i get the nasty > > sides > > and have to back down for a bit), then stay at 6drop/day after that > > for a > > couple months. somewhere in the next couple months i'll get another > > blood > > test and see how the numbers are doing. > > > > hope that's some help. > > > >> -----Original Message----- > >> From: Clayton Family [mailto:clay...@skypoint.com] > >> Sent: Thursday, October 11, 2007 2:29 PM > >> To: silver-list@eskimo.com > >> Subject: CS>Hepatitis advice sought > >> > >> > >> Dear List, > >> > >> I have a good friend that is taking a little CS for her hep, and > >> would > >> love to have more info. In particular, she is concerned about larger > >> amounts of CS conflicting with her herbs and chinese > > > -- > The Silver List is a moderated forum for discussing Colloidal Silver. > > Instructions for unsubscribing are posted at: http://silverlist.org > > To post, address your message to: silver-list@eskimo.com > > Address Off-Topic messages to: silver-off-topic-l...@eskimo.com > > The Silver List and Off Topic List archives are currently down... > > List maintainer: Mike Devour <mdev...@eskimo.com> > >
