Dear Peter, Just a quick note to let you know my experinces I have had with colloidal silver. I didn't catch whether you have M.S. or Lyme Disease. I have been taking CS over 2 years and definitely feel it is working. It is a slow process so patience is the key word. I have gradually tapered down on the antibiotics I was taking. I have come from 12 different antibiotics to 4 daily and then I was taking the penicillin shot every week and now every 3 weeks. So, that is quite a sizeable drop. I was curious about the mitoxantrone course. What is that? I was also taking the Mild silver protein so I don't know if you are making your own or ordering. I do feel it is very important to get a good reliable source in the beginning at least. If you want to E-mail me I would be glad to discuss CS with you. For pain -- Try getting Myoflex to rub on the areas. It won't hurt clothing or no odor so it can be put on anytime. Then, if you can take a muscle relaxer that helps a lot because that is one our main problems is muscle spasms. Try some otc Percogesics and see if it helps. That is what I took before I got a prescription. Also, Try massaging the points, that will also help a lot. Hope this helps. Vanita. I am connected with the Lyme Association of Greater Kansas City, Inc.
-- 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: [email protected] -or- [email protected] with the word subscribe or unsubscribe in the subject: line. To post, address your message to: [email protected] List maintainer: Mike Devour <[email protected]>
