A Bad Case of Hepatitis C

Thank you for the testimonials you keep passing our way. I wanted to tell you a couple of things. First of all, I got my little brother on the MMS. He had one month before he saw the doctor regarding his Hepatitis C, but he didn't take the MMS seriously and didn't really get serious about taking it until I got onto him pretty bad. So, just ONE week before seeing the doctor, he got quickly up to 15 drops twice a day. When he saw the doctor, his doctor told him he was "kicking butt". His bilirubin was completely normal!!! My brother called and was crying. It was emotional for all of us. He called three of his sisters and mother and cried with all of us. He is really sticking with it now, because at the end of November he is supposed to meet with one other doctor...the one who was to put him on Chemotherapy to kill the hepatitis C virus. I'm in all hopes that he will not have to take it. I'm very confident he won't. It if were me, I wouldn't do it anyway, but most people have the modern medicine trance. God broke me away from it long ago. I'll let you know just as soon as he has his next appointment with the other doctor. Again THANK YOU from the bottom of my heart for turning us on to MMS.

https://www.miraclems.com/testimonies.html

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because at the end of November he is supposed to meet with one other doctor...the one who was to put him on Chemotherapy to kill the hepatitis C virus.
You have to be kidding Arrow, since when do they use chemo to kill virus?

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If you do what you've always done,
You'll get what you've always got.
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You have to understand that any drug is considered chemotherapy. Chemical therapy! Right? In this case they likely mean interferon but I think they have one or two other nasties for hep C.

Interferon and Ribavirin... used in the treatment of some cancers as well. Treatment is usually about 1 year, and not always an easy journey from what I've read and from those I've talked with. I am so happy to hear that MMS is helping your brother. I am hoping it will do the same for me!

Hi AW,
I am indeed happy for your brother and do hope that you continue to post his recovery, but please try to provide us [that are taking a more scientific approach to MMS] with some numbers....like ALT/AST values and other liver function lab results. What would be more convincing evidence would be viral load/genotype/and ultrasound readings before and after. Surely the Dr's are taking tests before and after recomending a wait and see attitude regatding mainstream tx.
Please,for the sake of us out there that have some doubts about this MMS treatment.......share some numbers.

ps,
I'm on my 2nd week of MMS and awaiting test results that i got yesterday and will post for the sake of others that need numbers to convince [or not convince] them to abandon mainstream.

I can't say for sure because I don't understand what the numbers are. But if the numbers in anyway could reflect a dye off, a stress from dye off, a dye off of sick cells then it could be a positive thing.

One question is how is this person feeling? Does the increase in numbers match how he feels?