Hi Tony Yes, I agree with you. I didn't know you have discussed this - I have only recently joined. Unfortunatelly, after that mother trying the DMSO on the sputum of her Cystic Fibrosis son (when the sputum got very thick) everyone is scared to try Silver + DMSO on a real person. So unless we find some papers published and talk to CF people that have tried DMSO and are still alive :) we are scared... BTW, there is no DMSO in Bulgaria so I can't even try on myself...
Maia --- Tony Moody <a...@new.co.za> wrote: > Dear Maia, > This list has discussed why CS doesn't work and it > seems quite well > established that CS does not work if it can not get > to the offending > organism. It seems that if the organism is covered > in a layer of fat or > mucous or if the area is fairly dry then there is > less chance of CS working. > So whatever could be used to cut through the mucous > and carry the soluton to > the pseudomonas may work. > > DMSO may overcome these barriers. I have had > excellent success using very > small amounts of DMSO. In the order of a drop per > cup of CS, or CS and H2O2. > The ghastly smell is replaced with delightful woody > aromas which change > constantly. > Tony > > Maja Hristozova wrote: > > You would be surprised.... Cystic Fibrosis people > have > > tried many things... > > > > -- > The silver-list is a moderated forum for discussion > of colloidal silver. > > Instructions for unsubscribing may be found at: > http://silverlist.org > > 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> > __________________________________________________ Do you Yahoo!? Yahoo! Tax Center - File online, calculators, forms, and more http://tax.yahoo.com
