Hi Jeannie, I would assume its probably CNS Lyme. That's great the success you had with CS in the past. I would go back to that and stay on it.
Can I ask what ppm you used and what dose? Thanks, Christy In a message dated 6/5/00 4:30:47 AM Pacific Daylight Time, ar...@nf.sympatico.ca writes: << > Hi to all... I just subscribed to this list because I found > colloidal silver (again). A few years ago I was diagnosed with > Lyme Disease, after spending 3 years being misdiagnosed and > almost crippled. After finally receiving antibiotic therapy > and my body not tolerating such after a couple of years, I > turned to alternative medicine. Several homeopaths and > nutritionists had told me about colloidal silver, so I began to > do my own investigation on the limited literature available at > the time. > > I found that it really helped me alot and after about a year, I > fell off the wagon (so to speak) because I was feeling pretty > good. About 8 months ago, I started slipping again into a > stupor, double vision, trouble with speech and gait and once > again started on the travails to find out what was wrong. > > It again is a question mark between MS and CNS Lyme Disease.. I > guess my question right now is, if it is MS, will taking the > Colloidal Silver hurt me in any way. Does anyone know anything > about this? > > Thank you and good health to all of you, > > Jeannie >> -- 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: silver-list-requ...@eskimo.com -or- silver-digest-requ...@eskimo.com with the word subscribe or unsubscribe in the SUBJECT line. To post, address your message to: silver-list@eskimo.com Silver-list archive: http://escribe.com/health/thesilverlist/index.html List maintainer: Mike Devour <mdev...@eskimo.com>
