Hello All, I have recently been diagnosed with HSV 2. I am extremely scared and afraid of what the future has to bring. I have been doing a lot of research on this virus and I was wondering on what everyone has found for themselves? I have heard and read somewhat about this MMS everyone is talking about and I am completely confused on how, what and where to start.. I have also read about Colloidal Silver which some people have talked about using and came to have negative blood test results afterwards.. Has anyone heard about this and it seems to be the same concept of the MMS.. I look forward to any and ALL help I can get.
I am a firm supporter of MMS but I am not on line much these days to help you. I am directing you to this forum of mms specialists to answer your questions.
Colloidal silver is easy to use, is antiviral, and has no negative side effects unless you use alot. I personally take about 6 ounces of 20 parts per million per day, have done so for years, and have not turned "blue".
It is alot cheaper to make your own than to buy bottle after bottle, so I would suggest buying your own colloidal silver generator.
Also, I would suggest taking 500 mg of vitamin C every 4-6 hours and upping the dose from there to bowel tolerance. Vitamin C is also antiviral.
Straight ascorbic acid (vit C) may cause gas/bloating, so you could use a buffered form of C such as calcium ascorbate, which is pH neutral. That way it won't react with stomach acid.
Thank you for the suggestions. I have currently bought some Colloidal Silver (10 ppm) and I am taking about a Tsp under my tongue every few hours. I have also bought some Monolaurin 500mg and started that today. I plan on continuing the Colloidal Silver.. I am also experiencing some strong burning sensations in the southern region.. Does anyone have any ideas as to how to stop or atleast help that so I can continue my day (Sitting at a desk for work) without being in so much pain.. If I am going to have to "Deal" with this issue for now until there is something that is found to cure this dreaded virus, I would much so rather it be done without so much pain.. IS there anything that I can take to help minimize the OB or atleast make them nonexistant if that is an option. I look forward to everyones comments and suggestions.
I personally take about 6 ounces of 20 parts per million per day, have done so for years, and have not turned "blue".
You've done so for years? No signs of neurologic toxicity? Interesting.
Okay wait, I can't seem get this for some reason. Am I correct in that 100 liters of 10 ppm colloidal silver equals 1 gram (1,000 mg) of silver? If so what is your intake in grams over the span of a year? My brain's not working tonight & I can't figure it out.
I've read that it takes approximately 1 to 5 grams of silver accumulation (over a year span) to produce grey or blue skin.
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Hi, Does anyone have any advice on colliodal silver with monolaurin? I have them both and I have read good things on both.. I am looking for some feedback. These together are suppose to wipe out OB's?
I had to stop the MMS program to go back to work and I'm sad to say that the herpes I had been experiencing seems to be returning. I stopped topical usage as I said. I'm going to start the MMS 1000 protocol again next week but I can say for sure if you DON'T follow the protocol it won't work.
Yeah I'm SUPER bummed that cash trumped reason and I had to go back to work. Also failed at reconciling with the girl that gave me the sh*t in the first place....so my motivation to re-start and finish the protocol is like.....endless.
I've read that it takes approximately 1 to 5 grams of silver accumulation (over a year span) to produce grey or blue skin.
Only improperly made silver can cause argyria.
Improperly means adding something to the solution during production, such as salt, thereby creating a type of silver chloride instead of ionic colloidal silver. These improperly made silver particals are huge in size compared to silver ions, thus, end up under the skin.
Colloidal silver does not stay in the body for long periods since it is constantly being excreeted in the urine, thus, will never accumulate to a toxic level.
Im always reminded of the Nancy Delise case, the woman who cured her MS with CS. She took huge volumes to no ill effect. And then she also took it by IV too.
For herpes, try some lugol's iodine on the lesions and apply as soon as you realize that you are getting an outbreak... generally when the skin starts to itch but no blister yet. Lugols is known to dry up blisters fast.
Hi all! I am very excited to hear about MMS and am eager to try it out! I've been afflicted for over 10 yrs. It was so bad I've had blisters all over my body and even suspect I got viral meningitis from it.
Anyhow, I've had ample time to try different things and so far the one thing that cut my outbreaks by about 90% was.... ready? CLEANLINESS!!!! For yrs I had been getting rashes on my lips from my chapsticks until it just hit me one day when I finally noticed the subtle cause and effect. I have been re-infecting myself everyday of my life via my toothbrushes, lip glosses, left-over foods, pillows, practically anything I got my contaminated saliva on.
As we all already know herpes is EXTREMELY CONTAGIOUS and it only made sense to me how I found myself getting outbreaks anew after I ate contaminated left over food, brushed my teeth, used chapstick and/or came into contact with anything contaminated.
So what did I do? I started washing, with basic soap and water, my toothbrushes, pipes, anything that could be infected and have cut my outbreaks by it seems like 90+%!
Then I started taking coconut oil and have decreased outbreaks further but rarely I still get an occasional blister and have occasional "weeping" from a previous constant blister site when I think I may have had contact since I have not been 100% on top of cleanliness. There's probably a current viral load I also have to contend with which is why I'm excited about MMS. I suspect one will need to be stringent if they are to be rid of the suckers completely if possible.
As time has worn on since I've begun practicing near complete cleanliness I can say that my outbreaks have been reduced dramatically. Could this mean the body is naturally capable of shedding the virus like the cold? I am hopeful and excited to see what will happen when I try MMS armed with this knowledge. Thank you all for the great posts. Hope this helps and goodluck to you all!
No signs of neurologic toxicity? Interesting.
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