Re: CS lyme and fevers
Hi Tami tm4...@aol.com wrote: I've been CS 6 months and worked up to a cup a day for lyme. I spent 9 months on IV rocephin and started Flagyl/Doxycycline 2 months ago. You've been on some tough meds! I took Tinidazole/Tetracycline 2gms each / day. This was the most effective antibiotic combination I had found after 10 years of Lyme. (Tinidazole and Flagyl are very similiar) I just couldn't stand the overall toxic effect. I'm now taking only CS and find it equally, if not more, effective. And I have no stomach upset, more energy, quit amphetamines, almost completely off of antidepresents, and everyone around me notices the improvement. I've been a slave to pharmacuticals. My gole is to take no pills! I had no fevers on IV but they started back in after stopping IV and going to oral meds. I run a low grade fever every single eve from 5-8 pm and it feel like sitting in a oven. It will then break then chills and exhausted. Docs don't know why this is and don't seem to care. IT'S NOT NORMAL TO HAVE A FEVER EVER NIGHT! You'll find that daily fevers and periods of fatigue are common with Lyme. I notice them more when I am actively treating the disease. This may be due to the bacteria die-off. Research shows that Bb can mutate, such that it is unaffected by many antibiotics. This mutated form is referred to as a cyst. It has been shown (in vitro) that flagyl is one of the few antibiotics that kill the cyst form. The doxy then mops up the free spirochetes. So, one theory could be that the IV meds killed the free spirochetes and caused others to encyst, where they were safe. The change to flagyl may be now going after the cysts, and thus killing them and releasing their toxins (herx) in the process. I'd love to see an in-vitro study of CS and it's effect on the mutated forms of Bb. You are exactally right, most doctors don't know and don't care. Everything revolves around money...the golden rule he who has the gold, makes the rules. The same Dr that is treating you may be getting paid $500/hr+ to consult with your insurance company as to appropriate cost effective treatment for you. Your well being is not part of the picture. This is a criminal conflict of interest IMO! Doctors are highly discouraged from treating Lyme Disease. This pressure is not only from insurance companies, but from government as well. Doctors that stray from the pack, and treat Lyme are often persecuted and end up losing their license to practice. Interesting thing is, it's a certian group of Dr's that continue to carry out the persecution. This group of Dr's also get most of the NIH funding for Lyme research. If you follow the money train, you'll see that these Dr's are using the results of the NIH funded research to their own financial gain. They patent various antigen candidates for vaccines and develope useless test kits to be manufactured under their private business. Funny how Gulf War Illness and Lyme are similiar. Odd how lyme is endemic on the LI and CT shore, and that Plum Is. is in between. And who sold weapons to the Gulf countries before the war. I don't think that the US wants the embarassment of having to admit that they do have a bio weapons program and that these weapons have been tested on various populations. I'll get off my soapbox now. That's about all I know. Is this my body fighting,a CS effect,toxins? Anyones's info would be of help- Tami M Tami, I wish there were answers. I don't think we know exactly what the extent of Lyme disease really is...it has so many symptoms and can cause anything from a simple anoyance to incapacitation to death. For me, eliminating the abx, and taking CS has proved the most helpful so far. The other thing to realize is that it takes a long time to get well, when you've been sick for a long time. One last word from my soap box: Don't ever consider the Lyme Vaccine. I've seen and heard of too many lives devistated by it. The adverse effects go unreported. These very sick people are told that what they have is all in their head, and that it couldn't possibly be the vaccine. Now they're testing it on children! ...time is short IMO... God Bless, Jeff -- The silver-list is a moderated forum for discussion of colloidal silver. To join or quit silver-list or silver-digest send an e-mail message to: silver-list-requ...@eskimo.com -or- silver-digest-requ...@eskimo.com with the word subscribe or unsubscribe in the SUBJECT line. 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...@id.net
Re: CS lyme and fevers
Actuallyl, Tami, from what I've read, it's good that your body is able to run a fever. Lyme doesn't like the heat, so this will help kill it off too. Since I had Lyme, I have not run a fever in at least a year.Sometimes I WISH I would get the flu or something to crank up body temperature. I'd look at it (fevers) as a good sign. Sparrow I've been CS 6 months and worked up to a cup a day for lyme. I spent 9 months on IV rocephin and started Flagyl/Doxycycline 2 months ago. I had no fevers on IV but they started back in after stopping IV and going to oral meds. I run a low grade fever every single eve from 5-8 pm and it feel like sitting in a oven. It will then break then chills and exhausted. Docs don't know why this is and don't seem to care. IT'S NOT NORMAL TO HAVE A FEVER EVER NIGHT! That's about all I know. Is this my body fighting,a CS effect,toxins? Anyones's info would be of help- Tami M -- The silver-list is a moderated forum for discussion of colloidal silver. To join or quit silver-list or silver-digest send an e-mail message to: silver-list-requ...@eskimo.com -or- silver-digest-requ...@eskimo.com with the word subscribe or unsubscribe in the SUBJECT line. 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...@id.net
Re: CS lyme and fevers
sauna? Dennis 51/50 24/7 ---BeginMessage--- Actuallyl, Tami, from what I've read, it's good that your body is able to run a fever. Lyme doesn't like the heat, so this will help kill it off too. Since I had Lyme, I have not run a fever in at least a year.Sometimes I WISH I would get the flu or something to crank up body temperature. I'd look at it (fevers) as a good sign. Sparrow I've been CS 6 months and worked up to a cup a day for lyme. I spent 9 months on IV rocephin and started Flagyl/Doxycycline 2 months ago. I had no fevers on IV but they started back in after stopping IV and going to oral meds. I run a low grade fever every single eve from 5-8 pm and it feel like sitting in a oven. It will then break then chills and exhausted. Docs don't know why this is and don't seem to care. IT'S NOT NORMAL TO HAVE A FEVER EVER NIGHT! That's about all I know. Is this my body fighting,a CS effect,toxins? Anyones's info would be of help- Tami M -- The silver-list is a moderated forum for discussion of colloidal silver. To join or quit silver-list or silver-digest send an e-mail message to: silver-list-requ...@eskimo.com -or- silver-digest-requ...@eskimo.com with the word subscribe or unsubscribe in the SUBJECT line. 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...@id.net ---End Message---
CS lyme and fevers
I've been CS 6 months and worked up to a cup a day for lyme. I spent 9 months on IV rocephin and started Flagyl/Doxycycline 2 months ago. I had no fevers on IV but they started back in after stopping IV and going to oral meds. I run a low grade fever every single eve from 5-8 pm and it feel like sitting in a oven. It will then break then chills and exhausted. Docs don't know why this is and don't seem to care. IT'S NOT NORMAL TO HAVE A FEVER EVER NIGHT! That's about all I know. Is this my body fighting,a CS effect,toxins? Anyones's info would be of help- Tami M -- The silver-list is a moderated forum for discussion of colloidal silver. To join or quit silver-list or silver-digest send an e-mail message to: silver-list-requ...@eskimo.com -or- silver-digest-requ...@eskimo.com with the word subscribe or unsubscribe in the SUBJECT line. 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...@id.net
Re: CS lyme and fevers
I would personally give the Beck 4 step program a try. That is what cured my sister of Lyme. Marshall tm4...@aol.com wrote: I've been CS 6 months and worked up to a cup a day for lyme. I spent 9 months on IV rocephin and started Flagyl/Doxycycline 2 months ago. I had no fevers on IV but they started back in after stopping IV and going to oral meds. I run a low grade fever every single eve from 5-8 pm and it feel like sitting in a oven. It will then break then chills and exhausted. Docs don't know why this is and don't seem to care. IT'S NOT NORMAL TO HAVE A FEVER EVER NIGHT! That's about all I know. Is this my body fighting,a CS effect,toxins? Anyones's info would be of help- Tami M -- The silver-list is a moderated forum for discussion of colloidal silver. To join or quit silver-list or silver-digest send an e-mail message to: silver-list-requ...@eskimo.com -or- silver-digest-requ...@eskimo.com with the word subscribe or unsubscribe in the SUBJECT line. 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...@id.net
