So far this is what's happened. After my liver biopsy and blood tests in February I decided to do the Miracle-Mineral-Supplement in between then and the next set of blood tests as this would provide an experiment with verifiable results.

I did the Miracle-Mineral-Supplement for about 4 weeks. To be honest, I can't say what dose I got to by the end because I realised that the measurements are so imprecise and a "drop" varies greatly according to the dropper!

My kit did not come with a dropper, and it wasn't until 3 weeks into it when I switched to different bottles and droppers, how different the sizes of the drops could be! I think the measurments should be much more specific.

Anyway, I'm pretty sure it was a lot by the end, certainly at least if not more than the 15 drops, and I felt extremely queasy and tired all the time.

I was relieved when I took the next set of blood tests and could stop the Miracle-Mineral-Supplement for a while to see the results.

Well I got the results yesterday and it's NOT GOOD! My live enzymes which have not been bad before were 10 times what they should be. THere was a small reduction in the hep c viral load, but my doctor said that's because I've been "chewing up liver cells" consistent with either having gone on a massive alcohol binge (I didn't although I do drink) or taking poison. He said my liver was most unhappy and I can confirm that I feel like crap. The "normal" hep c symptoms that I now feel (stomach nausea and fatigue) were NOT felt by me until I started taking the MMS and I still feel like shit after 3 weeks of not taking it anymore.

My doctor was so concerned he had me do more blood tests yesterday and I'll get the results in 4 weeks. Hopefully the enzymes will have normalised. It would be amazing if the next tests showed that the viral load was way down and the enzymes back to normal, and then perhaps I'll believe that the MMS had some good effect but for now, I'm not seeing that it was helpful, but rather appears to have been extremely harmful to my liver.

I hope that's not the case, I was really backing the MMS and have told loads of people to check it out, but this is a huge disappointment so far.

I wish you the best of luck. Thanks for the info on the Lloyd Wright protocol, but I think I will try one thing at a time. For what I have read, Miracle-Mineral-Supplement should knock down the virus quickly. By the way, my doctor states that one should get a viral load count after 4 weeks of starting interferon treatment. I wonder why yours is waiting 6 weeks. I will have mine done after taking Miracle-Mineral-Supplement 3 1/2 weeks. Will post the results here. I am hoping for a substantial reduction of viral load. I have bad reactions every time I get up to 12 drops. 11 drops OK but 12 give me bad stomach cramps, really bad diarrhea and mild nausea. I don't think these are Herxheimer reactions because they are happening after 17 days of starting and I understand that herx reactions happen at the beginning of any treatment. I just think my system cannot tolerate very high doses. Anyhow, I hope that the Miracle-Mineral-Supplement has done something to kill the virus during this time.

I, too, used and use Lloyd Wright's recommendations. Even though my viral load dropped, I did have to go on the meds as my liver progressed to cirrhosis in spite of the drop. I used a lot of his & Dr Zhang's supps thru the treatment. I still use Lloyds mixed with Zhang's to get my liver back in shape. I especially like Lloyd's frozen Natcell TLM and Thymus. Expensive, but I can really feel the difference when I take it.

Just know that the viral load, with or without supplements, fluxuates by millions throughout the year. Diet, medications, Antibiotics , shots, stress, can effect it.

It's a nasty, deceptive, humbling disease. Best of luck!

Hi crane99.

sorry to hear the news from your VL test. Did you see any improvement in any of the other blood tests?

I have been on Miracle-Mineral-Supplement also and I am meeting with my med. dr. on the 18th to look at my blood test results (not the viral load however). I am hoping to see some improvement in the liver enzymes and the rest, but I guess I shouldn't get my hopes up...

After 4 years of alternative therapies I am pretty sure I will start the interferon treatment in the fall. I'm just tired and it feels like it is time.

I wish you all the best on your journey.