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.
Severe candida reduced with MMS; dietary shift sought
My main problem is severe systemic candida. I started taking MMS about 4 weeks ago and gradually increased dosage from 2 drops to 15 drops. I have been taking MMS 15 drops 1x per day at bed time for the last three weeks.
MMS worked like magic. It killed a ton of candida (I can see this from the loose and fuzzy stools I passed). My candida symptoms are much better now. I have much more energy. But the battle is not over yet. I still have candida in me and still have candida symptoms.
I plan to take MMS 15 drops 3x per day starting today and stay at the dosage until I am candida free.
Because of my candida condition, I am very sensitive to food. I can only tolerate meat, non-starchy vegetables, and oils. The only foods I am currently eating right now are chicken, fish, shrimp, vegetables, coconut oil, olive oil.
I’d like to switch to a more alkalizing diet. I’d like to stop eating meat. Anybody please help! Any ideas on a balanced candida diet that is more alkalizing? I’d like to stop eating meat if there are alternatives.
Thank you!!
MMS allowed bowel movement without laxatives for two days
Hubby quit taking his MMS for a couple of days because it was upsetting his tummy even more than it usually is, but even so, in that two-day period, he was able to “go” without taking any laxatives or senna tea for the first time in YEARS! It’s the first clear proof we’ve had that it’s really working. It might not seem like a big deal for most people but we’re in shock.
He’s gone back to taking it, starting tonight, and I think that he’s beside himself that finally, after all this time, money, useless doctors and their endless tests and running around trying one thing after another, *something* is making a real difference.
MMS use linked to reduced PSA and cleaner bowel in tested individuals
My son introduced a friend (55 y.o.) to MMS. He has an hereditary cancerous bowel condition requiring 6-monthly colonoscopies and diathermy of cancerous polyps (up to 40 each time).
After 3 weeks of MMS (as per protocol) his doctor has declared him to have a “clean bowel” and doesn’t need to see him for at least 2 years.
The same man also had a PSA reading which had increased sharply over the past 12 months, up to the point of recently being scheduled in for surgery for prostate cancer, something he did NOT want to do.
After 10 days of MMS, his reading came down into the normal range and so amazed his doctor that the doctor demanded to see all the literature he had on MMS. The patient, of course, is very happy that he didn’t need the operation after the MMS.
My son (35 y.o.) has suffered with debilitating prostatitis for 15 years. He took the MMS drops as per the protocol and after 10 days he has declared himself 100% cured.
His daughter (3 y.o.) went to a child’s party and caught a very bad throat infection. He and his wife thought long and hard about giving her MMS, as he said “It’s one thing to take it yourself, but another to give it to a child.”
After careful consideration they started with 1 drop, then 2 drops, then 3 drops, and after the 4 drop dose two days later she was up and running around. Normally a similar infection would have required heavy doses of antibiotics and a spell of 7 days or longer in bed. They weighed her and followed the protocol.
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 discernible improvement, but we are 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.”
MMS use linked to rising blood pressure and blood sugar levels
Although I remain a big supporter/believer in MMS and what it can accomplish in the body,
I am going to go off it for a while (at least.) At only 6 drops once a day, it seems the MMS is
neutralizing blood sugar and blood pressure medication because both are going up.
I have been feeling more pain and other all-over crappy feelings, easily stressed out, with
palpetations at times.
My bp has been inching up steadily with no change in medicine. I have had my blood sugar medicine
changed because the one I was on was causing pitting edema. It seems that the new medicines have
had no effect since I was on the MMS at the time of changing.
Since I feel so bad, I am dropping the MMS and continuing with other good supplements.
Hopefully, this will help.
Just a “heads up” to those on medication.
MMS use linked to improved breathing capacity and physical endurance
I have reported before that MMS made my breathing easier. Here’s what happened last night.
I was born with asthma. Had it all through my childhood and though I outgrew it as a young adult it left my lungs compromised–meaning that if I exerted myself I wouldn’t be able to breath deep. There were many times that I’d still have asthmatic spells of short duration. If I was in a damp environment it would be hard for me to breath.
I started taking MMS, only 6 drops a day. I noticed better breathing in just 2 days, but in only less than 3 weeks I am now able to breath all the way to lung capacity. I can fill my lungs completely with air and not cough or have that catch that happens. And last night I went to a concert held in an underground cave. It was quite a ways down–and going down is always easy. 😉 But coming up, I pushed myself to keep up with the group as we were leaving so as not to block anyone behind me.
When I got to the surface I had to sit down and catch my breath for 3 to 4 minutes before breathing slowed down to normal. BUT–the whole time I was puffing and panting was just from being physically out of shape and had nothing to do with my lungs, because I miraculously was breathing deeply, filling my lungs, no catching, no heat/pain in the lungs from exertion, no coughing. I was pretty darn impressed!! That has never happened to me before in my life.