From what I've read if you use the right sort of colloidal silver at a controlled dosage that the silver skin condition won't occur and that has only ever happened from poorly made silver used in excessive quantities.
Anyone know of this skin condition ever happeneing from a product such as mesosilver?
I'm looking into this as an adjunct to abx.
Thanks
Kelly
-------------------- Sx Start Jan 08 (test neg, but herxing)Susp Lyme, Bart + Babs??
ABX Doxy 400mg + Amox 1g Jun - Sep 08 Rifampin 600mg + Biaxin 1000mg Tinidazole 1000mg/day - Sep 08 to June 08
Currently taking Salt/C 15g (himalayan salt)
85-90% better Posts: 231 | From Australia | Registered: May 2008
| IP: Logged |
posted
I would not use it..that is just me..
Posts: 593 | From long island ny | Registered: Apr 2006
| IP: Logged |
Pinelady
Frequent Contributor (5K+ posts)
Member # 18524
posted
I am with my regular meds.
-------------------- Suspected Lyme 07 Test neg One band migrating in IgG region unable to identify.Igenex Jan.09IFA titer 1:40 IND IgM neg pos 31 +++ 34 IND 39 IND 41 IND 83-93 + DX:Neuroborreliosis Posts: 5850 | From Kentucky | Registered: Dec 2008
| IP: Logged |
posted
I've been taking "ACS200" for months with no skin issue. It certainly isn't curing my symptoms, but may be having some minor effect.
There is significant evidence to show that high quality, high surface area colloidal silver is cleared from the body rather rapidly, and it is the silver salts that cause arygia.
There is a huge amount of difference in the particle sizes between brands, so this is only an affirmation that this particular brand has been safe in my case. I would not have even tried it had my LLMD not used it himself, and suggested it on an EXPERIMENTAL basis.
I hear that Mesosilver is quite possibly the best product available, but I'd like to hear a personal testimony from a user of greater than 6 months.
Posts: 691 | From East coast, USA | Registered: Jun 2006
| IP: Logged |
posted
There is a letter of endorsement by the guy who named the Lyme spirochete at Invive.com. I have used the stuff. It worked good giving me a God-awful herx when I first got Lyme. It is very expensive though.
-------------------- Dying is easy. Living is harder. Posts: 257 | From owensboro kentucky | Registered: Mar 2008
| IP: Logged |
posted
I use Argentin (sp) 1/2 tsp. once per day. Improvement from it? I can't say for sure as I am on a lot of different things and I am feeling pretty good.
Posts: 103 | From Northern VA | Registered: Apr 2009
| IP: Logged |
posted
That invive site is interesting. Seems they're calling the mesosilver people liars, mesosilver is calling everyone else liars, and its very hard to find unbiased information.
Let me work on this a bit. The Invive site seems to have some logical fallacies. Abigail - what strength, how often, and how long did you take it? I'm assuming no arygia (turning blue)? With the concentrations its talking about, I imagine you'd have to be VERY careful not to let it form any sort of salt.
Posts: 691 | From East coast, USA | Registered: Jun 2006
| IP: Logged |
posted
There does seem to be a lot of conflicting info. Some sites say colloidal silver should be clear, others say it should have other appearances, its just hard to know what is the right thing.
-------------------- Sx Start Jan 08 (test neg, but herxing)Susp Lyme, Bart + Babs??
ABX Doxy 400mg + Amox 1g Jun - Sep 08 Rifampin 600mg + Biaxin 1000mg Tinidazole 1000mg/day - Sep 08 to June 08
Currently taking Salt/C 15g (himalayan salt)
85-90% better Posts: 231 | From Australia | Registered: May 2008
| IP: Logged |
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/
UBBFriend: Email this page to someone!
Printer-friendly view of this topic