Hep-C does mms get rid of this monster?

I wish you both good fortune in your journey. As you have probably read on another thread, there's a parasite protocol coming out soon from the Autism work. It's a year long, (although I could be wrong, so don't quote me ) I had been on CDS for several months before I had my first parasite "evidence" - and I'm sure there's more to come .

P

I started taking MMS now 6 months ago. I have Hep C Type A. My viral load when i started was 400,000 after taking protocol 1000 for 3 months i did blood again and viral loads came back 2.5 million. Well i knew this was suppose to happen so no biggy. The mms is pulling the virus into my blood to clear it. I still remained on protocol 1000 and in another 3 months took it again. It's now 1.3 million. I have not been in touch with Rev Joe who has cleared his hepC back in 2010. This gave me hope. I am now on protocol 2000 and now doing the CDS. I will test again in 6 weeks. I have heard people say it may take protocol 2000 to clear most hepc people. I have had hep c from a blood transfusion at 16 but did not pop it's head out till i was 46. I have been working for years on a cure...I have tried ozone therapy. I have the machine and tent. I have also put the ozone gas into the vein. Nothing has worked so far but am thinking that 2000 will with the CDS. It is easy to make NO taste at all so easy to take. Just water back. Crossing my fingers and hoping in 6 weeks i'm clear. If there is anyone else out there that has healed themselves. Please contact us.

I was also contacted by a guy name Don they other day that i met on the internet. He had asked me what i was doing and i told him about hydrogen peroxide and ozone therapy and MMS. He decided to do the peroxide therapy and just called me the other day to tell me he cured himself in 4 months by drinking 35% hydrogen peroxide food grade.through out day..but only wanted to let me know because he liked me. He does not want to talk to anyone or broadcast that he is cured. Why do pepole do this? There are so many of us out there that need help and would like to know what cures. If your out there please let us know who you are.

Hi Pam. Are you a doctor? Just wondered. How much CDS should i take each hour. Right now i'm doing 2000 and doing 2 ml per hour of CDS. Should i continue to up the dosage each day. It would be easy to take since there is no taste with the CDS.

Not a doctor, Debi -
2mL an hour, if you're doing the 3000, is a 6 drop equivalent.

On 2000, you can go higher than that. I know of a woman with cancer doing 12mL an hour - I've never gone that high, but have done a 12 drop equivalent - (which is 4mL an hour)

Hi Bob i also have hep c and have been doing the 1000 and the 2000 and the 3000. the 1000 for 7 months the 2000 for 2 months and still my loads went down from 1.3 mil to 542,000 then the next test after doing the 2000 protocol the loads went back up to 1.5 mil. Very frustrated. Working with a few of the Rev's on this now. Still working on it with no success yet. I feel fabulous but still not gone.

Debi in response to your post. For what it's worth my experience has been what ever method I've used to knock the virus back as soon as I stop the treatment it bounces right back to the old level. Homeostasis I believe they call it in science. So since this Hep C virus is so creative personally I believe the only way to get it is to continue the protocol. You might look into CDS it's much easier to take and easy to make. It doesn't have that terrible taste that gets hard to handle after a few weeks. Just an idea. Ask the Ministers if the CDS is just as effective as the MMS for Hep C. I've heard it is.

yes i too am looking for someone to say their loads are 0! I have been on mms and cds for a 1. I found out that everything i was doing was proventing the mms from working. I'm a vegetarian (not good everything i eat is antioxidants). MMS does not like this. I was also for the first 4 months doing it with Alkaline water ...MMS does not like this either. I now have to start eating meat (first time in 10 years and the fact that the liver hates it. It cannot process the protein and makes it toxic) So how do i eat red meat (high in iron which is toxic to the liver again.. eat meat and root vege. I use to juice greens all day long not realizing this was killing the mms. I'm still praying and i'm going to keep trying till i am a zero..have faith or it won't work.

Yes i have been corresponding with Joe Plocovich. He told me he cured his HepC in 2010. I have asked him but have never received his blood work. I'm still waiting...he has been real busy with his dad's illness and taking care of him. Not sure if he has papers stating this but i will ask again. I know what you mean and I to am always wondering if i can talk with someone who has cured their HepC. Joe did give me his protocol that he did for 1 year. I have not been doing it right because of all the antioxidants I take. I'm now off everything for at least 3 months. I have emailed Colleen from the Church of Genisis and she says that she has heard of many people that have. I would love to hear from them myself. I have also talked in person with a man by the name of Doug. He says he travelled with Jim for 10 years. He had some health issues and said it took him 3 years. He did the MMS and a few other things along with it. The hardest thing for me is i'm so healthy eating that it kills the MMS. I will have to eat like a Cave man for 3 months and see what happens. Just got my loads back 730,000 down from 2 million 4 months again. Yes they do bounce around. I know when the went from 320,000 to 1.2 mil the mms was working pulling the virus into my blood. It's working you have to just keep going. Everybody is different. Some take 3 months and some take 3 years. I think if it's not curing us it's because of how your taking it. I have also done protocol 2 also. I did it for the last month of the last year. I was thinking my blood work would be zero but came back 2.1mil. I was so bummed. Now it's down again. I have also made and done the CDS. Yes it's much easier to take for sure. I was just wondering if it's as effective. I stopped after my loads went up but am now doing mms 6-8 doses per day. I think i will make some CDS ...my husband is sick and he won't do the mms because of the taste. Bronchial's and coughing. I will do Protocol 1000 with this. God Bless and hope there is someone reading this that will decide to share their stories also.

Hello Debibrown

I started this topic last year and began the Pro-1000. About 1 week ago I visited my clinic and had another blood draw. I was disappointed that my AST & Alt had gone up some. My Amylase actually came down about 23 u/l. They did not do another viral count as that is expensive to do and I'm going through the VA.

As far as my AST & ALT goes I was surprised to find that anyone that has had HCV will usually show an Elevated level that can be as much as 5 times the upper normal amount and still be considered slightly above normal. My AST was 143 and my ALT was 160. So I'm well within the 5 times category.

I did the Pro-1000 for three weeks. Since then I have been doing a 3-4 drop maintenance dose everyday. My schedule with work etc. does not allow me to do the Pro-1000 full time as I can not seem to keep from getting the nasty symptoms that force me into the bathroom in a hurry.

I will visit my Dr. tomorrow and one of my main questions will be what is considered to be a life threatening level with regard to AST & ALT, etc. The last thing I want is having to go thru the Interferon treatment and since I'm a type 1 it would be iffy at best.

I hope everyone reading this has success in their use of MMS.

Michael