Category: Cancer - Esophageal

Chronic Heartburn Finally Disappears / Child’s Gastritis Improves Overnight

September 10, 2023

I have lived with heartburn as if it had become second nature to my life. I also got used to the foods that made it worse, and I learned to judge whether I really wanted to eat them and suffer afterward, or simply avoid them.

I started CDS low and slow because I was really afraid after reading mainstream media articles claiming it was like consuming bleach. I gradually increased the dosage up to 5 ml in 150–200 ml of filtered water.

Heartburn is now completely gone. What remains is a hiatal hernia, which I need to support by losing weight. I also have chronic damage in my food pipe (esophagus) due to waiting so long and becoming accustomed to living with heartburn.


A 3-year-old had gastritis and had three episodes of vomiting within a 2–3 hour period.
2 ml of CDS was mixed into 90 ml of 7-Up to mask the taste.

The child did vomit once more, but about 10 minutes later, so the CDS had about 10 minutes in the stomach. A good night’s sleep followed, and by the morning there were no signs of gastritis.


Father on MMS for esophageal cancer shows stable tumor, no growth 18 months

January 25, 2012

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.


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