My husband Jan has liver cancer in IV stage, the doctor said he should not live longer than end of january or february. In fact he come back home alone with corticosteroids to control high fevers who suffered from cancer.

In addition to liver cancer, has liver cirrhosis.

He began taking MMS1 on 9 January and began to feel better, but again and again high fever so he is back taking steroids. Two days ago has begun to take MMS2. I noticed a big change and I have high hopes for this treatment, but do not know if he should leave the steroids again.

I had stomach cancer and lever cancer in an early stadium – and aspergillus fumigatus. With the help of “zapper” and “MMS” bott cancers vanished and aspergillus became less.

MMS: started with 1 drop (morning and evening), up to 6 – and this for 6 weeks.

{In response to an Anti-MMS post by Anonymous Coward 944207}

Well you are totally uninformed. A close personal friend of mine who is a pathologist and a Toxicologist RECOMMENDED MMS to me. He was taking 15 drops 3 times a day for almost a year and it cured his liver cancer as proven by a PET scan. So take your MMS fraud bullshit and stick it where the sun does not shine. I suffered from massive bouts of dizziness for 2 years and after ONE day on MMS it was gone and has not returned. My friend the Toxicologist told me “Big Pharma” will suppress any treatment for any disease no matter how effective it may be if they cannot make money on it.

09:11:09 Mrs. R.K. tells us

Can love be published, but with initials please.

Thank you.

Hello, thanks for the quick delivery and for the addition.

I would like to share my experiences. I purchased in September 2008, MMS, arrested and increased over a period of 10 days on a total of 23 drops. Have taken it for many years and over again emerging bronchitis (in a year x 4 – 2 x combated with antibiotics, but they kept coming back). For MMS, I have not had bronchitis more. My brother was very ill in January 2009 (he could no longer stay with him and took extreme). At the hospital it was found that it is up to the intestine and liver. He was taken out and put a piece of intestine, a second output. In the liver, he had a filled with 1/2 liters of pus bulge, which went away despite drainage for weeks. The doctor said, without further surgery on the liver, my brother would not be healthy. We said to my brother: Now is the time to take MMS. Three weeks ago, he has taken it every day. In the next operation n othing more was found. Since then, he is symptom free. The output was transferred back and only the surgical scar, which makes him even more to create. I tell you, you deal with Hamer, with MMS, with Vitabiosa, with EM, with Dr. Schnitzer, with synergetics – seeks out the best of you, even take over the responsibility for yourself and decide yourself

R.K.

Drs all across America are now standing up against mms as

many americans livers are turning color and sometimes becomeing cancerous. They claim the liver is supposed to cleanse the blood of impurities and mms seems to be hanging around in the liver and sometimes dyeing urine as it gets into the kidneys as well. In Sept edition of Physcians Journal they showed the jump and rise in americans coming into emergency rooms with cancerous and ill looking livers that are no longer fully functional. I had been takeing it just a few times and mention it to my Doc and He wanted to know how long i was on it,and a biopsy was conducted later in the week to see what damage could have been done. All though i havent phoned them back they have left 2 messages on my answering machine.

Hi’ve been taking the MMS since the end of november. I have Colon Cancer with multiple mets in the liver. I was diagnosed last July and my oncologist started chemo a week later. I had chemo from july to november. I decided to stop the treatment in November even though I was responding very well to it. I started to take the MMS at that time. At first, I took 10 drops every hour, then 25 drops 3 time a day. When I went back to see my oncologist on January 9th, my CEA was down to 10. At my next appointment 3 weeks later it was at 8, then 7 then 6. My husband who’s a physician and doesn’t believe in any alternative treatment was very surprise. On february 15th, I started using the Molecular enhancer along with the MMS. 5 days later I had to see the oncologist and to my surprise my CEA was up to 7. I was disapointed but my onco told me that from 6 to 7 it doesn’t make a diffrence. At my next appointment it was at 10, and now according to my last lab test it is at 16. I realy don’t know what to do now. Should I increase my intake of MMS? Is it the Molecular enhancer? I was doing so well with the MMS alone. I also took the indian herbs and everything was always fine. The good thing is I feel good. I have enough energy to take care of my 3 kids (5 yo, 3 yo and 9 months)but I am wondering what’s happening in my body.

{4/20/08}

The molecular enhancer is some kind of electromagnetic machine. It has the reputation too boost the sick cells too normal function and make them kill themself.

I don’t know about a delayed effect from the chemo but my husband think that there is a possibility. I’ll ask my onco on my next appointment.

I am pretty sure I am activating the solution well. I had every side effect at the beginning, diarhea, nausea, vomiting etc

I took the indian herbs for 21 days, then stop for 5 days and started taking it again but after 10 days my foot was aching me so bad that I had to stop it. You know the kind of pain you experiment after a very long walk. It was terrible.

My onco is thinking about doing a CT scan too see what’s happening. I red that when we are killing a lot of cancer cell they are circulating in our blood stream before we evacuate them and that can make the cancer marker goes up. I will be so happy if it was my case

{James Ellison (OP) 390448}

…Update.

lady with the breast cancer, her husband called ma again to update me with more details.

Before she started taking the MMS her doctor told her that the cancer will spread from her breasts to her liver and then to her brain. she would only live for another 6 to 8 weeks.

before taking the MMS the tumors in her breasts were 5cm and the other was 3cm.

now after 2 months of taking the MMS she went for her scan and the tumors have reduced, the 5cm to 2cm and 3cm to 1.6 cm.

this woman is another life saved by using MMS………dont believe anything here, just get it and use it. you can save your own life or that of a loved one……

My son (35 y.o.) has suffered with debilitating prostatitis for 15 years, and since taking MMS (as per protocol) for 10 days has declared himself cured! He has been on the strongest antibiotics for most of that time, which of course has had lots of side effects.

His daughter (3 y.o.) developed a severe throat infection and he said ‘it’s one thing to take MMS yourself, but another thing to give it to a child’. However, after careful consideration he and his wife decided to give it to her. She took 1 drop, 2 drops, 3 drops and after the 4 drop dose on day 2, she started playing and felt fine. Normally such a situation would require antibiotics and bed rest for at least 7 days.

My son’s friend (55 y.o.) has had an elevated PSA count for the last 12 months to the point where prostate cancer surgery was planned. He started taking MMS and after 10 days his PSA count had returned to within normal limits. His doctor was so amazed, he said ‘we have never seen this happen before’ and demanded to know what he had been taking. He also suffers with an hereditary cancerous bowel condition, requiring very regular colonoscopies for diathermy of cancerous polyps. He had a colonoscopy after 2 weeks of MMS and the doctor declared his bowel to be ‘clean’ and not needing to see him again for 2 years.

My partner has metastatic melanoma Stage IV with secondaries in lungs, liver, bones, chest wall and groin lymph nodes and began on MMS about 4 weeks ago. So far no discernable improvement, but we are ever hopeful and I will report his results as time goes on. We understand there is no simple test to undertake to determine if the MMS is actually working on him or not, but he says, ‘where there’s life there’s hope’.

I would encourage everyone on these forums to keep posting their findings. And I say, What a miracle!!!!!