Colloidal Silver and Lyme Disease

[SirSilverOzzyyzzO]

This post is one more for support, rather than me posting information. A very dear friend of mine is suffering from, lyme disease. I was reading through some uses for, colloidal silver and lyme disease was mentioned. But nothing more that I could find.

I was wondering if anyone had (Or would be willing to share?) any luck with, colloidal silver and this disease?

I'll be sure to have her visit this site/forum, if anyone can help? Thank-you in advance, for any help.

[G-khan]

This post is one more for support, rather than me posting information. A very dear friend of mine is suffering from, lyme disease. I was reading through some uses for, colloidal silver and lyme disease was mentioned. But nothing more that I could find.

I was wondering if anyone had (Or would be willing to share?) any luck with, colloidal silver and this disease?

I'll be sure to have her visit this site/forum, if anyone can help? Thank-you in advance, for any help.

I would tell her to make sure and see a Dr. and do what they say. Colloidal Silver can be taken with anything that a Dr. prescribs .. tell her to buy a CS generator and she can make it for under a buck a gallon.. I will give you some links on it for her and a link to a generator she can buy... It seems it is bacterial and if it were me I would take the antibiotics the doc gives plus 4-6 ounces of 10 PPM everyday with it..

http://www.cs.cmu.edu/afs/cs.cmu.edu/user/jake/mosaic/lyme.html

http://www.oikourgos.com/silverworks/cs-info1.html

I have the below generator and it comes with the Silver and if she sets it at about 5.5 on the dial she will produce 12-13 PPM CS I had mine tested..

http://www.wishgranted.com/Colloidal_Silver_Maker_777_AC.html

Don't mess around with this - very bad disease......

[SirSilverOzzyyzzO]

G-Khan,
Thanks for the advice. I can tell you that, my friend is seeing a doctor. I don't want to get too into details. But in short, my friend has done/seen all that conventional medicine can offer. Seems that this disease is something of a, grey area issue.
Myself as a friend. I'm really seeing the affects/effects of it, from an outside view. It is rather discomforting. Nonetheless, my friend is a, fighter. I know from being around here for a while that, people have good intentions and like to help. So I thought it would be a nice gift, if I could one day say, hey log onto this site, it has some good refererences specifically for you. For others as well.
It seems a common denominator with this is, being un/misdiagnosed initially. Then when someone is, a host of, antibiotics, again and again. I was ignorant to, lyme disease. Whereas, not so much anymore. I know my friend is, uneasy with all the, antibiotics. Colloidal silver seems to be a good substitute on paper, so it would be wonderful to hear it helps/ed someone with this disease?

[Jasper]

A good list your friend might consider joining is:

http://groups.yahoo.com/group/colloidalsilver2/

There are probably people there with experience of using CS to treat lyme.

[demosfen]

CS isn't the only option your friend has. One other thing I'd consider is ozone therapy. Ozone generators cost a few hundred and are very useful for A LOT of conditions. Here is a good book to read - 'Lyme disease and Rife machines' by Rosner.