I had a prostate biopsy in November 2016, with the results explained at a later date as an aggressive cancer (4 out of 5). The doctor wasn't impressed when I told him that I would not subject my body to chemo, because I was interested in a natural cure. I didn't want to let on about MMS, because he would not believe me because of his tunnel vision (training). He then said that there were other options before chemo like surgery and radiation. Great choices!!! I have since been given an appointment on Jan 9, 2017 for a scan to see if it is localized or spread. I was unsure as to whether to keep this appointment or not, as it will not affect the way MMS works. The appointment will be kept because I will need him for other tests later to check for the improvement.
I recently started my MMS treatment with the CDH I had made (22+1+1). I started at 1 and progressed without any issue to 10 during the third day. At 11, the next level (2nd last for day) I felt a bit squeamish so decided to drop back to 10 for the last. During the taking I was only advancing by 1/2 to 1 drop at a time. Maybe I should have dropped back more as after about an hour or so I had bad diarrhea for the next 2 days and stopped taking the MMS as I couldn't stomach the thought of it. During the time I was taking the CDH I had no issues toward taste as I was using peppermint extract 1 to 1. At 10 drops I started to use a drop of stevia instead. So it really caught me by surprise. I can assure you I was not trying to be a hero. It is just that because of the cancer I was trying to get to a reasonable working level, having just received the MMS 2 in the mail. At the moment I feel very nauseous at the thought of MMS.
Has someone experienced a similar situation or can advise me of the course to take before re-commencing the protocol. I know I should not have stopped, but as I was very nauseous I had to stop and re-evaluate the situation. I have thought of leaving it until after the scan on Jan 9, 2017 and hopefully letting my stomach etc settle down fully. Is this a good idea? I feel it may be better in the long term, as I feel my body may accept it better than it would at the moment. Also I don't want to offset any chance of re-commencing the protocol. On re-commencing I will certainly stay on levels longer for a time to evaluate.
If you are about to use any Protocol, please use this experience for your own guide and pause on levels each time to really evaluate the situation before advancing.
jolly roger, you say you used CDH and dosed by drops. CDH is usually dosed by milliliters if made using the one bottle method. Please clarify.
It is possible that the peppermint extract used reduced CLO2. Have you tested peppermint extract to determine if it is compatible with CLO2? Also, some stevia is okay with CLO2, but some may not be. Sweet Leaf brand of stevia drops does not reduce CLO2 in MMS1/CDS/CDH.
It does seem you have overdosed and were rewarded with some Herxheimer reactions.
Increasing dosing is usually done on a daily basis, not hourly. And when you take too much, immediately reduce dosing 50%. Sometimes one has to stop for the day and start again the next day.
Yes I was dosing 1 ml CDH as 1 drop. How would I test peppermint extract (natural) or any other additive to see if compatible with CDH? Would I put some drops in with CDH (without DW) and see if it holds colour?
I was concerned because of the cancer and trying to get on top of the situation, but will be increasing dosing on a daily basis now not as before. I hope I can still nullify or eliminate the problem, as it is said that it is never too late. Hope that is right.
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