Hi Christy... I was using only 10ppm two times per day. It took about 2 months for me to start really feeling its affects. Although I was also taking a number of other supplements, some of which I have returned to, such as pantothenic acid (up to 1500 mg/day), CoQ10, primrose oil, calcium/magnesium supplement, garlic tablets, B-complex, flax seed, and fish oils.
A nurse practitioner who knows about these problems also believes that it's probably CNS Lyme. The only thing is that when this 'episode' started similar symptoms began, but showed themselves in slightly different ways. Because of my long term experience with this, it completely threw me. I will have to wait and see. But I certainly won't sit back and wait. Thanks for the message. Jeannie -----Original Message----- From: ritz3...@aol.com [mailto:ritz3...@aol.com] Sent: Monday, June 05, 2000 10:14 PM To: silver-list@eskimo.com Subject: Re: CS>New to List 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>
