TOPIC:

I was diagnosed with RCC (Renal Cell Carcinoma) cancerour tumors in my 2 Kidneys, feb 2010.
I had a CT Scan done Feb 2010, Left Kidney Tumor 20mm in size, Right Kidney Tumor 11mm in size.
I started researching and found our about MMS Aug 2010 or so.
I had another CT scan done roughly in sept 2010. Both Tumors, no size change.
I also had a Needle Biopsy that confirmed cancer in the Left Kidney Tumor.
I started eating better, i also cut my sugar intake 90%, dropped my POP intake 90%,
i ate foods that claimed were Anti Angiogenisis (Cancer starving foods)
But the main thing is....I started MMS.
I started MMS2 Capsules around sept 2010 after my second CT scan.
I found the Calcium Hypochlorite in a Pool/Spa store, $4.29 for a small bag.
I bought empty capsules from my local pharmacy.
1 week later I bought MMS1 Liquid from an online dealer.
Here I started a 3 week protocol.
every day for 3 weeks. from 8 am to 8 pm (8am, 10am, Noon, 2pm, 4pm, 6pm, 8pm) i would take both MMS1 and MMS2.
I took Size 0 capsules full of 73% Calcium Hypochlorite granules. Every 2 hours as listed above.
I took MMS liquid 15-20 drops. Every 2 hours as listed above.
I only felt nautious 3 times in the 3 weeks, and it was mild and i just drank a big glass of water. I never once vomited.
Oct 2010, i had a CT Scan for my Chest. After I got my CD-ROM of my CT Scan and Dr,. Notes. I realize that the SCAN has caught part of my kidneys too. and low and behold, from looking at my CT Scan, my tumor on the left kidney shrunk from 20mm to 14mm. The Scan didnt get all of the kidneys in teh scan.
BUT, i was amazed that just 3 weeks of taking the MMS , my tumor shrunk. I was so happy.
I was then not so happy because no one believed me, my family had excuses as to why it was smaller, some friends denied it,
many i share info with think i am crazy, my own family urged me to "Stop taking that crap" but they dont realize its helped.
One family member used excuse that maybe the tumor that shrunk was from my Needle Biopsy, leaking it out.
I never believed that, i whole heartedly believe MMS worked.
I was shot down, overwhealmed and frustrated by negativity from people.
I stopped taking MMS, i became depressed, i had no encouragement, DR never wanted to hear what i was doing, 2 doctors never even explained to me why my tumor shrunk at all. I gave up. I ate crappy foods, lots a pop and sugary foods. Stuff i surely thought would make my cancer grow worse.
months of giving up, accepting cancer, no one cared if my protocol was working, some did, on my facebook circle of friends,
but even they must truly not realize what MMS did.
March 2011 my recent CT Scan, Abdominal to measure if my Tumors in my Kidney have grown or spread.
Results are amazing.
Left Kidney Tumor 20mm, now 14mm.
Right Kidney Tumor 11mm, now 8mm.
BOTH shrunk , from using just 3 weeks of MMS1 and MMS2.
Even after i stopped and gained weight and ate junk foods , my tumors neber grew.
and now i have proof that not one but both Shrunk.
I am now energized to start back to using MMS1 and MMS2 FULL FORCE and cancer protocol for 1 month.
then taper down to a strong dosage of both, 3 times a day, morning , noon, night for another month or 2.
and i wana get a second opinon from new doctors, and get another CT Scan.
I hope that after my second MMS protocol plan, my tumors will be so small , or gone, that i will be cancer free.
I will keep you all up to date.
Feel free to email me davidvoy at g mail dot com.

I am proof that MMS Works! I aim to try and inform as many as i can.

MY CT Scans. From 6 monhs ago around (Sept 2010)

My measurements are not 100% on these images, 20mm for left kidney, 11mm for right kidney.

I plan on uploading my NEWEST CT-Scans from (March 2011) showing the shrunken sized Tumors soon.


Software I use is for iMac, called OsiriX.
and i requested my Scans on CD-ROM, from my hospital.

I also plan on breathing in MMS1 Liquid using a Neblizer .
I will read more in Jims book about more methods of administering MMS and report back.

Hi David, awesome testimonial!! Thank you for sharing it with us. I'll bet it was the MMS that was mainly responsible for shrinking the turmors also, but the dietary changes were probably very helpful to your body as well.

I would like to verify, just to make sure, you took 10-15 drops of MMS1 liquid each time you took a dose, ie every two hours? If so, that was a lot of MMS. Some people can do it.

When you start the MMS again, you want to use protocol 2000 which is here jimhumble.biz/index.php?option=com_content&view=article&id=34&Itemid=61. On that protocol 2000 you take the liquid MMS1, maximum dose you can, every hour for 10 hrs, and the MMS2 capsules every 2 hrs. for a total of 5 caps each day.

I should also mention, when it comes to the tumors, your body can also kill them and then encasulate them without shrinking or absorbing them. This sometimes happens with cancer, and in that case the tumors will no longer shrink or grow because they are dead. So if you don't get any further shrinkage after the protocol 2000, I wouldn't be too concerned. I would encourage you to keep up with the dietary improvements, and definitely don't listen to the naysayers. You are doing a great job partner, keep it up!

When it comes to nebulizing the MMS1, be careful. It made my asthma worse when I did it.

My prayers are with you,
Michael Harrah

Yes, thanks, David!

Incredible example of initiative and perseverance. To be using both the Cal Hypo and the MMS1 at those levels without a Herxheimer/detox reaction indicates that your levels of toxicity are probably generally pretty low. As Michael said, you'll probably benefit from taking hourly doses of MMS1 - for Protocol 2000 Jim Humble's recommendation is for up to 10 activated drops per hour. You can mix up a day's (10 hourly doses) batch of measured doses and put them in a sealed bottle to take with you for convenience.

This shows us what a commitment to Wellness Self-Responsibility looks like. Too bad those around you don't "get it." But, it can be very hard for people to free themselves mentally from the straight-jacket of "medical expertise."

Regarding MMS1 and lung conditions (congestion in particular), my experience personally and with people I've worked with is that it can increase the congestion. I suspect strongly that this doesn't mean that it's "getting worse," but that some kind of healing crisis is ongoing. The nebulization is probably helping. Using the MMS2 is a powerful way of reducing lung congestion, I've found it quite amazing.

Please keep us posted! --Bruce

I dont have athsma or any congestion that i know of, i just thought that if one uses a nebulizer its is one of the most direct to bloodstream options, breathing it into lungs. I have a friend who has a nebulizer that i can try.
is this a very effective method to administer MMS1?

Michael, Thanks, so basically my tumor , or a mass may still be present in 6 more months, but they maybe dead of cancer. Great. Next would be a needle biopsy to confirm any cancer.
Isnt it amazing how my Dr.'s havent evem commented to me about why or how my 2 tumors shrunk?????
i feel my University DR are cold and uncaring and frustrated that i just havent got on the operating table .
wana hear the consultation? i recorded a 3 or so minute cosult after teh lastest CT scan. my dr even forgot i was confirmed cancer. How unvelievable.

Audio on Youtube from my Appt.

Bruce

did you mean taking MMS2 orally could improved lung congestion as well?

Thanks for sharing.

I dont get your question. I dont or never had lung congestion. and never mentioned i did.