Most Recent Testimonials

I had shingles for more than 30 years, having a break out at least once a month during those 30+ years. A year and a half ago, I did the Protocol 1000 for 3 weeks and have not had 1 single break out of shingles since!!

Haven’t even been doing a “maintain” program since those 3 weeks and STILL haven’t had a break out of shingles – YEAH for ME!!

Dear Jim,

In 1997 I was diagnosed with a Gleason 7 prostate cancer having a 1.5 cm tumor.

My healing modalities at the time did not include mainstream medicine but was expensive. For the last 6 years my AMAS tests were negative.

July this year my AMAS test had a Net Tag of 158 which was elevated cancer; on Aug. 2 the Net Tag was 181 and finally on Sept. 21, 2011 my Net Tag was reduced to 81 which is very low and well in the normal range.

I used MMS1 and MMS2 protocols with MMS enemas.

What cost me last time over $50,000 I did this time for $50.-.

I am ever so grateful for your work, Jim, facing challenges with tenacity and bringing a better and better understanding to how MMS works.

On your old program I got rid of a stubborn case of candida [yes, us men have that too] where for 10 years I tried everything and nothing worked until I took MMS for 3 weeks and the follow-up tests had me clear.

I had a hard time taking the MMS the old way and was delighted to be able to take it in capsules now.

I encourage anyone with a serious disease to study MMS; it helped me two times so far.

I will now stay on a maintenance protocol. The above mentioned tests and my daily MMS consumption protocol are available on request.

Many thanks again

John Bastian

I lost my mother to cancer – didn’t know enough about MMS at the time to use it.

Am now trying to help my father overcome cancer of the esophagus. He was diagnosed 18 months ago; he is 82 and the docs were pretty grim faced about it all. But 18 months on here we are. I think the reason he is doing so well is because 2 years before he was diagnosed he was taking MMS off his own back, on the old regime of a 15 drop dose in the morning and one in the evening. I believe that has stood him in good stead. His tumour has not grown or spread since diagnosis. Doctors are a bit confused. BUT the tumour is still there and still dangerous. I have only recently got him back on to MMS – protocol 2000 without the MMS2 as he can’t swallow the capsules. Am persevering but it is hard sometimes and easy to give up when the MMS is making him feel bad. Sometimes the amount of things one could try with MMS is overwhelming too for the carer – should i do this or that etc. MMS1/MMS2/CDS/DMSO…swallowed, bathing, enemas etc. Great to have such choice but overwhelming sometimes too.

My name is Jason, I live in the US in the state of Michigan. I was born with the supposedly incurable disease: X-linked_agammaglobulinemia

I am entrapped into a system of health care and cannot seem to free myself, I have scoured the internet in search of a cure for my condition or at least a means to survive once Obama Care comes into play. My first success with MMS was with an abscessed tooth where the infection had spread down my neck and into my ear. It was extremely painful, and thanks to the wonderful governor Granholm of Michigan who cut out dental care from the medicaid program I had no dental coverage. The MMS worked within a few days I was mainly without pain but the herxheimers were bad. I quit taking MMS at that time because my doctor wanted me to take a large dose of antibiotics before he pulled the tooth, which I had to do if I wanted it out. Since the tooth was a wisdom tooth and more than 2/3 rotted/broken out I complied. After this I felt relatively healthy except for catching roto-virus twice (which I realize now was do to my stopping the MMS). I felt better after the tooth was pulled and I thought the MMS might have made me ill.

My second success so far came for me after much study of MMS & chlorine dioxide; when I tried to convince my mom that it would cure her diabetes which is steadily getting worse. She refused to take the MMS because its not FDA approved… So to show her that it works I will do everything I can to cure myself of this dreaded illness. So far I have been following protocol 1000 as close as I can and taking 20-25 drop MMS baths twice a day, in addition to putting MMS drops in my eyes ears and nose. The baths were absolutely the breaking point. I awoke the next morning with 2x more energy than the previous day. I am fairly certain I am awash in virii,bacteria,yeast etc you name it. I have been on so many antibiotics and I get infusions of gamma globulin each month. I am keeping track of my counts and so far they have slowly gone up. I will continue to track this information and I will let you know asap if somehow I am cured. I have added a couple 1/4 capsule pills of mms2 during the day but so far it really upsets my stomach.

Due to my own diligence in trying to find real answers about my condition I found the average lifespan of a PID patient was 42 years. I want to thank Mr Humble from the bottom of my heart. I struggle to find the words that properly convey my appreciation for his selfless acts. For the first time in 15 years I can breath through my nose for at least 90% of the day. I have more energy than I ever remember having and I can breath deeply into my lungs without feeling like someone is sitting on my chest. I pray for all of you every night and will continue to do so until we are free or we are dead. Thank you Mr. Humble for giving me hope for the future and the possibility of seeing my children grow old.

I purchased your book and wish I had the funds to help more, however I am on a fixed budget of less than 800 a month so things are very tight I will help somehow even if its only by spreading the word and sharing your book. I encourage everyone to buy it and I will continue to discreetly help as much as I can.

Take care and God Bless You All

Jason

{2/29/12}

…I worked my way up to protocol 1000 for about 5 weeks along with a full size 0 mms2 capsule 2 – 4 times a day. Also a 20 – 30 drop bath usually at least once a day sometimes only every other day. Then at the end of January I took a break for about a month to let my system clean itself out and I wanted to see if my nose would stay clear.

My nose did not fully clear up and I am also still very tired. So 3 days ago I started back on the MMS but I have gone to 6 drops an hour of just mms1. So far no diarrhea but I am a little tired. I will add more to this but I have to go for now.

“Yes, and must tell you I think there is an unexpected result. For several years I’ve had the feeling of something stuck in my throat and a couple years ago I had a throat/thyroid exam which revealed little seed lumps on the thyroid and I was iodine deficient. Increased Iodine intake and things got better, but not gone.

However I noticed these last few days that the lump feeling in my throat is gone! Hope the CDS will migrate over to the carotid arteries that run up each side of the neck and carry blood/oxygen to the brain. (both blocked 75%.) Anyway thought you would like to know.”

Barbara

(Barbara has been taking CDS for the past two weeks using 2400 ppm CDS at the rate of 2 ml in 4 fl. oz. water/hour x 8 hours/day.)