The lyme tests all suck by design. If they were accurate, there'd be big problems, everybody might figure out where they get it from. Look up Dr. Lida Mattman?? I think that's how to spell her name. She just died last week, she was in her 90's. She developed an accurate lyme test and was run out of business by good ol' uincle sam. She kept on fighting anyway, her work is still ongoing. You can look into Central Florida Research lab, for testing. They have one of the most accurate tests. Lyme, is a clinical dx anyway, it's diagnosed by symptoms. There aren't any tests for MS or Parkinsons either, people just accept the dx from the allopathic quacks.
I have been on the salt/c protocol for over 2 years along with other various non-pharmaceutical adjuncts. Seems to be working out well for me. In March of 06, I could barely walk up a flight of stairs at sea level. This past March I went skiing in Colorado and had almost no problem hiking up 13,000 feet carrying my skis. I was starting to develope Parkinsons 2 and a half years ago, and had I followed the allopath I'd probably be in the same boat as Micael J Fox?? Who incidently was treated for lyme years before his Parkinson's dx was given. Kurt ---- sol <sol...@sweetwaterhsa.com> wrote: > kmilkow...@cfl.rr.com wrote: > > They sure do have an awful lot of names for lyme disease, don't they? I > > think it was Richard?? that put up the origional thread. Might be a good > > idea to get on the salt/c protocol with a little MMS and some CS mixed in, > > what do you think? > I'm seriously thinking of lyme. I'm on a fibromyalgia list and a lot of > people there have been found to have chronic lyme after suffering for 20 > or more years with typical "fibro" symptoms. I just read a post from a > person on different fibro list who says over 50 list members with > progressively worsening "fibro" symptoms were tested for lyme and found > positive. But the tests are expensive, and often not conclusive, I've > read some lyme tests have 50% false negatives. So I'm thinking of a > trial of salt/C. > If anyone here has done salt/C with success, I'd like to know how long > to see any improvement in symptoms? > sol > > > -- > The Silver List is a moderated forum for discussing Colloidal Silver. > > Instructions for unsubscribing are posted at: http://silverlist.org > > To post, address your message to: silver-list@eskimo.com > > Address Off-Topic messages to: silver-off-topic-l...@eskimo.com > > The Silver List and Off Topic List archives are currently down... > > List maintainer: Mike Devour <mdev...@eskimo.com> > >
