Most Recent Testimonials

Here you’ll find the most recently published testimonials on CDTestimonials.com. This includes both newly submitted entries and older testimonials that had not yet been published from the previous site while it was in limbo.

Many of these updates involve video content. On the previous site, videos had to be downloaded before viewing and did not include searchable transcripts. We are now converting those videos so they can be viewed instantly and searched more easily. Because this process takes time—and we have several hundred videos to complete—content is being released gradually.

As a result, the “Published” date shown for many testimonials reflects when the content was added or updated on this new site, not necessarily when it was originally submitted.


Release Date on This Site: March 29, 2026 5:12 pm UTC

Symptom Relief for Yeast Infection

As a woman, yeast infections can be recurring.

So I usually put 15 drops into a douche that you buy at the store, so I empty the bottle and put water and 15 drops and douche a few times a day and I also do the 1000 protocol and drink that, and that usually goes away for a little while and smell so clean down there after.

So MMS is pretty good for yeast in the body and yeast infection, but don’t put too many drops often during the day you can get very irritated down there.


Source: CDTestimonials.com
ID: 321138
Release Date on This Site: March 29, 2026 5:08 pm UTC

Symptoms Gone by Next Day

Category(s): GonorrheaSTD

I had a partner who had gonorrhea, I only noticed the next day that something was off.

And I am a sex worker so I know about sexually transmitted diseases. So I knew something was off and I had something and it was bacterial. It’s the only diagnosis that fit. I had it in my throat and private area.

I drank the MMS and douched myself a few times during the day with MMS, maybe about 15 drops every hour or two and made sure I splashed it around my private area. 1000 protocol for the mouth.

The next morning I went to the clinic to get tested. I had nothing. The tests were negative. But they still treated me.

But tests were negative and yes I know I had something, not making it up. I know what I’m talking about.

But in only one day, it was gone. So it works! Good luck!


Source: CDTestimonials.com
ID: 321139
Release Date on This Site: March 29, 2026 1:39 pm UTC

Gerald's update from March 2015

Name: Gerald McClellan

Hi this is Gerald McClellan of Monroe, NC and this is a followup of my posting to Jim Humbles site in March 2015. I am now 79 yrs old and will be 80 in June.

It was Jan. 2014 that I received Jim Humbles book Master Mineral of the 21 Century and when I first learned and started using the drop per drop method of CD but being that I have A-Fib and am on a blood thinner, I couldn’t do the recommended protocols when I tried like I mentioned in my previous posting.

So I tried other natural remedies to fight my cancer. I was skeptical at first with CD until I started using Kerri Rivera’s method of drinking it from a baby bottle and did until I learned the VA Oncology’s protocol.

And then on the newest method that is Chlorine Dioxide Solution (CDS) with no side effects and neutral PH of 6.7 to 7.4, a alkaline base that made it very easy to consume. I learned of this when accessing Andreas Kalcker’s web site and used it to control and rid my body of a very aggressive Gleason 8 prostate cancer that metastasized first to my lymph nodes then to my bones creating me to stage 4 prostate cancer and creating a very high PSA reading of 38.

On Webster Kehr’s web site I found out all about what cancer really was.

Being I have A-Fib which earlier forced me off of the old drop per drop method CD protocol in 2015 to 2016 and I was not taking much CD and my cancer metastasized from my lymph nodes to my bones and then in 2017-2018 and I recovered down to a 0.45 PSA reading from just being on the Bitter Apricot Seed vitamin B17 protocol for 6 weeks.

Then after several months of not taking anything and as I mentioned earlier I found my cancer was getting really aggressively bad again from the Sept bone and body scans done by the VA hospital my PSA reading grew back up to 38.

Then in late 2018, by the advise of my VA oncologist, I went on a protocol of Abiraterone Acetate, 5mg of Prednisone and a hormone injection (that caused me to gain 20lbs).

The Abiraterone Acetate is a low dose chemo pill that at first caused me to suffer of liver damage putting me in the ER at the Presbyterian Hospital of liver damage. My dosage was then lowered from 1,000 mg a day to 500 mg while being closely monitored by the VA then to 250 mg which I was on from early 2019 to April 2020.

Now is the PSA a true marker for cancer? This is a question I am not truly believing in and having several different thoughts with my oncologist and him explaining to me that testosterone is what really feeds cancer cells.

But after reading the findings on the referenced web site of what caused me to question my oncologist’s explanation and description of cancer, I had body imaging and bone scans done in Sept., 2018, 2019, the cancer kept growing to almost all of my bones even though the hormone injections did lower my testosterone and PSA readings.

Then in April of 2020 I stopped the VA protocol and on May 17 of 2020 I started on the newly form of taking CD which was CDS and by Sept of 2020 and of only being on CDS for 4 ½ months my cancer showed from the Sept scans that it has regressed to almost half.

And now in the most recent scan of Sept 2021 it showed my cancer being undetectable.


ID: 201304
Release Date on This Site: March 29, 2026 1:29 pm UTC

MMS Helped My Dog Who Went Into Anaphylaxis Shock From A Bee Sting

MY dog was stung (second time) on the lip by a bee in February 2021 and went into anaphylactic shock with the following signs: vomiting, sudden defecation, weakness, heavy/labored breathing, pale gums, salivation, runny nose, restlessness, and hives. All signs of a severe allergic reaction and possibly life threatening.

I mixed a two drop dose from the 6 and 6 protocol for dogs (her weight is 2 drop dose). I only used a 1/4 cup of water (not the 1/2 cup) and administered it via syringe. Even with her issues and weakness she still put up a bit of a struggle with the syringe so using less water I could get more MMS1 into her faster and time was of the essence.

I did another dose same as above 30 mins after the first dose. Within an hour of the second dose she was more alert raising her head to listen to activity outside (it was like I could see the life returning in her) and about half an hour after that she moved herself to the front bedroom to watch the outside activity so she was much more alert.

I gave her a third dose several hours later as other signs (restlessness, curled up and shaking, and hives) appeared.

Additional treatments I administered were: I used the unactivated MMS on her lip and around that area, I gave her an apple cider vinegar rinse (at that time I was not sure if it was a bee, wasp or fire ants and I thought she was stung her leg at first), CBD oil internally for pain, inflammation, and itchiness. I boiled 1 chamomile tea bag with 1 cup of water let it cool then dabbed it on her hives, which were all over her back legs upper and lower (no rinsing the tea off).

About two hours later she was drinking some sardine water I left her with the remaining MMS in it. By evening she had her appetite back and ate a full meal.

Around 9PM the hives were gone and she appeared to be relaxed, breathing fine, and not in pain or other distress—back to her normal self. One would never know the ordeal she suffered only hours before.

Having MMS on hand to treat my dog was vital to my dog’s recovery and for saving her life most especially when time is of the essence and may make the difference between life, death, and/or internal organ damage.

I take MMS with me now whenever I am out for walks/hikes, visiting family and friends since I know my dog is allergic to bees.

I thank Mr. Humble and all who work hard to ensure that the public has access to MMS protocols and information.

Regards,


ID: 201301
Release Date on This Site: March 29, 2026 1:25 pm UTC

Guillain-Barre syndrome (GBS) / Miller Fisher Syndrom (MFS) / Chronic inflammatory demyelinating polyneuropathy (CIDP)

Name: Paul W

BACKGROUND: I was diagnosed with Guillain-Barre syndrome (GBS) / Miller Fisher Syndrome (MFS) / Chronic inflammatory demyelinating polyneuropathy (CIDP) in April 2014 which I caught from a respiratory virus, which later developed into GBS/MFS/CIDP.

I woke up one morning in early April 2014 and had double vision, photophobia (eyes very sensitive to light) and incredible pain throughout my body (this was the CIDP). This very quickly developed into paralysis down my right side, and I had breathing issues and had trouble swallowing. Eye paralysis followed – it was terrifying.

CIDP, which is sometimes called chronic relapsing polyneuropathy, is caused by damage to the myelin sheath (the fatty covering that wraps around and protects nerve fibres) of the peripheral nerves. My own immune system had basically attacked my nervous system.

It took almost 2 years for me to be able ‘self sufficient’ having had to learn to walk again. My balance is shot and going down stairs is very difficult – even now. I suffer from bouts of acute tiredness if I over do things – I build web sites, and if I have to concentrate quite intensely – sometimes I lose my speech, and feel like my head is going to ‘blow up’.

I found MMS / CDS just 2 weeks ago and in the short time that I have been taking it, my balance has improved 100%, and I feel generally so much better.

In the last 2 weeks I have not lost my speech – which is a MIRACLE.

I know that MFS / GBS / CIDP is rare and I am new to MMS / CDS, but I hope that this short testimony will help others.


ID: 201327