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» LymeNet Flash » Questions and Discussion » Medical Questions » IV Colloidal Silver feedback please

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Author Topic: IV Colloidal Silver feedback please
Myco
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Member # 9536

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Has anyone on here had success with IV Colloidal Silver/Gold treatments?

I recently met a practitioner who has had success with this and would appreciate any feedback via PM or comments below.

I am aware of purported side effects (agrygaria etc...).

Thanks!

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birdie67
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I don't have personal experience with it, but one of my friends is in remission using that and IV Doxy.

She said it helped her tremendously.

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kellyjk4
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I had Colloidal Silver IVs for two months several years ago.

The first month was twice per week, and the second month was once a week.

At the time, we didn't know I had Lyme. I had tested positive for so many types of bacteria and viruses that my doctor wanted to try it.

I got so incredibly sick - which I now know was herxing.

After it was over, I felt a lot better for a short period of time, but then my symptoms came back.

That's when the doc tested me for Lyme.

Soon after, that doctor was told he couldn't use CS for IVs anymore.

It obviously works, but I don't know how long you would have to continue the treatment to get long term results.

--------------------
Take care -kelly
---------------

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emla999/Lyme
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I had several IV's of the ACS 200 colloidal silver a few years ago and as far as I could tell it didn't help me at all.
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Myco
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Looking for more feedback, thanks!
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Myco
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bump.
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