Health
Frequent Contributor (1K+ posts)
Member # 6034
posted
Hello,
Am on antibiotics for lyme, but also doing the collodial silver.
Am on the zithro and flagyl, and take 1 tsp of the CS several hours away from the antibiotics.
The herxing from the CS is worse then the antibiotics... possibly, the CS is killing other infections I do not know I have. I feel it is working, cause the herxing today is much less then 6 days a go.
I joined the silver list, to find out more info, but was worried after what I heard.
First off, I was given this CS for free, and the man is willing to make me more, to see me get better. So, I dont want to give up a good thing.
The CS has a camphor taste. I like it, it is soothing. I asked the man about this, he said it is just silver and water, made it with his machine. I will take a look at his machine, later, I am far too sick to drive at this time.
So, question is, has anyone used CS that is tasting camphor like? It has a yellow tinge, and the only thing I can think of is... it is the yellow silver, and read that this has a bitter taste. MIne is not bitter, more camphor tasting.
Trying to get a hold of man, not home. He is a friend of friends, and drinks it himself.
rosesisland2000
Frequent Contributor (5K+ posts)
Member # 2001
posted
Oh and not as many folks come to this forum...and, the post should've been put in Medical forum in the first place.
Just provided you with that link as you may not want to wait for an answer...weekends are very slow here and everything, well almost everything, around probably 98% of everything, has been discussed here in the past. So, if you want an answer faster, learn how to do a search.
posted
I have used CS for a good bit, off and on. Never more that 15 days a a time. The stuff I have used has always been clear, or a little yellow. With no taste at all. So I am not sure about the camphor taste you are speaking of. I have not turned grey or blue, like some would claim. I used to herx on it quite well. But no so much any more..
greg
Posts: 740 | From frederick,md,usa | Registered: Jun 2001
| IP: Logged |
posted
I cannot take it due to the severity of my herxes on it. 2 hours after taking it I am on the couch with a high fever and cannot move for the rest of the night. I think it works amazing. My body just cannot handle it right now. im not sure about the taste you are talking about either but I didn't turn blue
Take Care Abbie
------------------ You can only see the stars when its the darkest.................
Posts: 149 | From New City, NY USA | Registered: Mar 2004
| IP: Logged |
Health
Frequent Contributor (1K+ posts)
Member # 6034
posted
thanks everyone,
Rosemary, I do a search before I post. Found many posts with CS but NONE with the taste I have in mine. Want to know about the taste, I know that many had good results, but now that I posted this, did NOT know that someone had it work very well and had to stop it.
I am going to stop mine, cause I am waaaaay to sick on it. Want to wait to see how the antibiotics work, I am on a new one, the Zithro and the Flagyl, and the herx from this is so much.
Greg, why do you only do it for 15 days only, then stop. Never read this before...
ABBIE, that is how I am with it now. I am going to stop it, and see how I do with the new round of antibiotics. Am on the Zithro and the Flagyl. I started both at the same time, and just too sick, dont want to live so sick. By stopping it, I will then see what kind of herx I am getting from the antibiotics alone, then after a few days or more, see if I should take the CS. I get afraid that possibly the CS might make the antibiotics not work as well. I read that it does not, but we are all different, so one never knows.
posted
mostly because i feel like it is really only effective durring the week before and after my lyme cycle. I find that i get better hits when i pulse it.
also just so that i dont do to much for to long. just in case..
Posts: 740 | From frederick,md,usa | Registered: Jun 2001
| 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/