introduction, Hep C, and taking MMS on empty stomach
Hello to everyone!
Nice to have found this group and to read and share some information and experiences with MMS.
I started MMS about 3 weeks ago... started with 2 drops and have worked my way up to 15 2x a day. I found that I was having some nausea and am now back down to 12 drops 2 x a day.
Yesterday I tried it on an empty stomach (having read that that was the most beneficial) first thing in the morning and I was feeling pretty bad for the whole day... stomach cramps and overall pretty crappy. Today I have gone back to taking the MMS about 1 hour after breakfast.
I started the MMS because I have Hepatitis C and have been very very sick for the past 4 years. I have been carrying the virus for 26 years (unknown until tested in Jan. 2004). I have not felt to do the interferon treatment but have tried many herbs and supplements (some helped a bit, some did not). A year ago I started on a Raw Food Diet and that has helped tremendously!!! Changed my whole life really... But still I have not regained all my strength and energy, and often feel fatigued and lifeless and dull.
I am hopeful that the MMS will do the trick.
Nice to meet you all. And thank you for sharing your experiences with MMS. I am hopeful that I can report back with some positive results soon.
If you haven't found the post already, you may be interested to know that I have been helping someone with HIV and the MMS seems to be turing it around. He is doing so much better with lab work to back up his good results.
www.HealthSalon.org has a couple of good testimonials on Hep C. so you have every reason to feel optimistic for a positive outcome. One of the testimonials suggests the length of time that may be required. I don't recall how long now so I suggest you look for it.
I keep trying to find testimonials of negative outcomes for mms to put on healthsalon but they just aren't there except for people quiting cause they can't handle the nausea. Nausea is a given with mms if you take too much.
I too have found it intolerable an a fully empty stomach so I take it about 1 to 2 hours after a meal. Jim says its more effective on an empty stomach but its worthless if you vomit it up. Good results are coming in testimonials with using it an hour or so after a meal so I think that is good enough.
__________________ "The nurse should be cheerful, orderly, punctual, patient, full of faith, - receptive to Truth and Love" Mary Baker Eddy
Visit www.HealthSalon.org
Thanks Kevin and Arrowwind09 for the welcome, suggestions and support.
I am thrilled to hear/read testimonies of success, especially from people with Hep C.
Thank you so much for the link (I am looking at it now).
MMS does not normally bother me, even though I have Crohn's disease. But the one time I took it in the morning on an empty stomach, I suffered all day long. I do not recommend doing this. I also take it a couple hours after eating. I can't even tell I took it afterwards.
Between the MMS and the LDN prescription, I no longer have any symptoms of my disease.
I take it on an empty stomach and was doing fine with that until I reached 7 drops. After I did that, I wished I had eaten a little something. I think next time I will do 7 again and eat a handful of dry cereal shortly before, somewhere I read that it doesn't work properly with protein. If I come across that site again I will post a link for you.
Last edited by Liegeman; 04-11-2008 at 06:14 PM.
Reason: goof-up
How are you doing now? Is there a positive result?
I too have Hep.C and trying MMS. I am same with you that I did not know about it until Nov. 2008. I guess I had it for a very long time. I wasn�t feeling well with fatigue, occasional liver pain, and experiencing a mild depression by the time I found that I had hep.C. I now know that the depression is common in people with this disease.
On the second months of MMS, I went up to15 drops MMS 2 times a day, and stayed there for 3 weeks. I was going to do the maximum does of 15 drops 3 times a day ( Jim Humble recommends for Hep. C) , but I have to finish my college going in this spring so I postpone taking 3 times a day. I will not be able to handle the detoxing/ virus killing fatigue while I am in class. Did you notice that taking maximum dose of MMS really wipe person�s energy up even without nausea or big D ? MMS is good but it gives detoxing fatigue.
I plan to resume MMS at maximum dose three times a day after I finished my school this spring. According to Jim, stay there for at least one week. Have you tried that? Right now, I am taking once at night about 10 to 14 drops. I have more energy but I can tell the bugs are still there because my liver aches when I did too much things.
Wish you a good health,
I will update my progress when I completed MMS protocol.
There is a negative testimonial on the Rife Forum of MMS not working for Leukemia. The claim is it has never worked for Leukemia to this persons knowledge.
The lady lost her husband to Leukemia and MMS did not help him.
There is a negative testimonial on the Rife Forum of MMS not working for Leukemia. The claim is it has never worked for Leukemia to this persons knowledge.
The lady lost her husband to Leukemia and MMS did not help him.
Dan
I don't believe it is 100% definite with any of it's usage, as all people's body's and overall health is difference which I'd imagine would have it's significant changes to being aided. Did they list this person's applications and diet or anything? Not saying they are wrong, but just as an overall note.
There is a negative testimonial on the Rife Forum of MMS not working for Leukemia. The claim is it has never worked for Leukemia to this persons knowledge.
The lady lost her husband to Leukemia and MMS did not help him.
Dan
I am always astounded that people can think that just one thing might cure their cancer! I do not think that MMS could work unless there is a microbial issue underlaying the condition. Also, the MMS would have to be able to get into contact with that microbe. If the microbe or virus is lodged within a cell it would first have to be able to penetrate the cell membrane to do its work without destroying the cell, and this would be particularly important in leukemia...you need your white blood cells.
When cancer advances so many things go wrong in the intercellular functions and enzymatic workings....the cascade downwards can be hard to forstale, of course, as we all know. I would not expect MMS to manage all of this.
If one is to say that MMS didn't work a list should also be made of all the other things this person did or did not do that did not work. This above mentioned person didn't even bother to mention what kind of leukemia they were dealing with.
I have a dear friend with Luekemia. Now there are different types of leukemia. She has had it for many years and she manages it with proper diet...not what some doctor thinks is proper diet, but what is proper diet for her...a tricky thing indeed to figure out...
Other forms of leukemia are far more dangerous. She has the more desirable type, if you could say that at all. She won't go near MMS with a 10 foot pole. She has found her balance and is not willing to experiment.
.
__________________ "The nurse should be cheerful, orderly, punctual, patient, full of faith, - receptive to Truth and Love" Mary Baker Eddy
Visit www.HealthSalon.org
I am always astounded that people can think that just one thing might cure their cancer! I do not think that MMS could work unless there is a microbial issue underlaying the condition. Also, the MMS would have to be able to get into contact with that microbe. If the microbe or virus is lodged within a cell it would first have to be able to penetrate the cell membrane to do its work without destroying the cell, and this would be particularly important in leukemia...you need your white blood cells.
When cancer advances so many things go wrong in the intercellular functions and enzymatic workings....the cascade downwards can be hard to forstale, of course, as we all know. I would not expect MMS to manage all of this.
If one is to say that MMS didn't work a list should also be made of all the other things this person did or did not do that did not work. This above mentioned person didn't even bother to mention what kind of leukemia they were dealing with.
I have a dear friend with Luekemia. Now there are different types of leukemia. She has had it for many years and she manages it with proper diet...not what some doctor thinks is proper diet, but what is proper diet for her...a tricky thing indeed to figure out...
Other forms of leukemia are far more dangerous. She has the more desirable type, if you could say that at all. She won't go near MMS with a 10 foot pole. She has found her balance and is not willing to experiment.
.
Yea, that's definitely too ambigious for a definite answer like that. One needs to know a lot more background and current state of health before claiming something so definitive.
I have taken it with or without food and have no problems. I made it up to 9 drops and had to back down oh did I ever hurt and the N and V was terrible. The stomach cramps were worse if anyone can make it to 15 I give you kudos. I dont think I will ever get there.
introduction, Hep C, and taking MMS on empty stomach
. Today I have gone back to taking the MMS about 1 hour after breakfast.
, VFH. Thanks for sharing your experience, I'm sure other members can benefit from it. Hope you enjoy your stay here.
Hi!
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