There is a scale up method that was developed at a group called lymestrategies, a yahoo group. You would start out at low doses,how much depends on your situation, how sick you are, body wieght, etc. It would depend on what other meds you are taking, as to when to take the salt/c.
Kurt ---- G Murray <healthl...@gmail.com> wrote: > > What is the amounts of Vitamin C and Salt regime? What are the > quantities and are there certain times to take these compared with other > Lyme meds? > > G Murray > . > sol wrote: > > kmilkow...@cfl.rr.com wrote: > >> They sure do have an awful lot of names for lyme disease, don't > >> they? I think it was Richard?? that put up the origional thread. > >> Might be a good idea to get on the salt/c protocol with a little MMS > >> and some CS mixed in, what do you think? > > I'm seriously thinking of lyme. I'm on a fibromyalgia list and a lot > > of people there have been found to have chronic lyme after suffering > > for 20 or more years with typical "fibro" symptoms. I just read a post > > from a person on different fibro list who says over 50 list members > > with progressively worsening "fibro" symptoms were tested for lyme and > > found positive. But the tests are expensive, and often not conclusive, > > I've read some lyme tests have 50% false negatives. So I'm thinking of > > a trial of salt/C. > > If anyone here has done salt/C with success, I'd like to know how long > > to see any improvement in symptoms? > > sol > > > -- > 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> > >
