TOPIC:

Does anyone out there know of a protocol 'designed' with cancer of the tonsil/throat in mind that requires a user to retain the solution in the mouth for as long as possible?

Top of page 5 here might be what you are looking for.

Having had some practical experience of MMS prior to purchasing the book, I am now able to make adjustments to my doses and understand a lot more about the MMS regimes and how I can fit them into my overall health recovery efforts.

Regarding adjusting MMS1 doses, you will note that Edwin has an experimental protocol "CDH Plus 1000" where he shows how he can adjust CDH doses by adding SC. Another way to adjust CDH's SC to CLO2 ratio is to make CDH using 1%, 2%, 3% or 4% HCL. One only needs to have 4% HCL and dilute it down for 1%, 2% or 3% HCL.

CDS can also be adjusted by adding SC to ingested doses as I show in my experimental " Protocol 102 ".

While CDH and CDS ingestion dosing can be adjusted quite easily, MMS1 can not. We are quite fixed in using 30 seconds activation time. To see MMS1's ratio of CLO2 to SC, check out my testing here .

Notice at 30 seconds activation time using 50% citric acid, only 1.5 mg of CLO2 is released from a possible total of 20.1 mg. Most of MMS1's SC is sent to the stomach and beyond for activation.

Reiterating my thanks to CL02 for that but phew! my head is spinning from all these acronyms and percentages .

Truthfully speaking MMS1, MMS2 & DMSO are the products that I currently have in my medicine cabinet and use as part of my health restoration efforts;. Administering these, as we all know, is nice and simple just like me. Conversely, for now, talk of ppm and the like etc sends me dizzy but I will never say never because necessity always provers herself to be the mother of invention. So I will settle down and review the information you have shared as I do want to overcome my illness. Thanks again.

Typically, I like to take my time to research and understand what I am doing before I make any move.
Some of my acquaintances and family members see the cautious, deliberating aspect to my personalty as being at odds with my evident quick wit, speed of thought, inexhaustible capacity for wordplay, and easy ability to brainstorm complex concepts and new information. I try to reassure them that my tendency to ponder deeply is neither burdensome, nor does it give rise to head-ache, however it is still a challenge for many to see that the (at least) "two natures' are part of one wonderful whole.

So SAS here's lil ole Solomon The Unwise" coming at you with a will to comprehend & chock full of ememessence.

Whilst tootling around the forum I came across the Breast cancer topic where we can read it mentioned that having to deal with a large-scale & rapid cancer cell die-off was NOT desirable. Based on my shallow knowledge, theoretical conjecture & personal experience the caution made sense, but as I become more comfortable using the products we discuss I find myself seeking to understand a wee bit more about how they (might) go about ‘dealing’ with whatever ‘illness’ they encounter within us.

So the following questions came to mind:

1. What are the typical signs of cancer cell die-off?
2. Are these signs unique to each individual and/or type of cancer?
3. If taking MMS//MMS2/DMSO brings about some gradual improvement in our liver,
kidney function does die-off continue but the signs become less apparent?

Relating these aspects to my own personal experience, curiosity got the better of me so I took the plunge and opened up about my wonderings to a forum buddy.

Notwithstanding that I do not possess an MD qualification I was glad that I made the approach and found the feedback quite informative, covering aspects related to:

4. Pathways in the body that handle detoxing
5. Potential for overload & possible impact on these pathways if die-off is too fast
6. The sort of medical support that may be required to deal with detox overload
7. Possible - hopefully temporary - issues arising from large scale & rapid cancer cell die-off
8. Possible Impact of large-scale & rapid cancer cell die-of on tumour(s)

Admittedly my conjecture could be naught more than a lot of chat about nothing given the wide ramge of cancers there are, nonetheless though this all gets my attention when I reflect on my own observations since I started taking MMS.

(to be continued)

The way that my mind works here is a link to a youtube video that deals with aspects of my experience hinted at in the above post. G2Voice #026 You need a healthy liver to live healthy, How to cleanse the liver .

It is a long listen covering many aspects besides however given that I am dedicated to getting as well as I can I find it informative.

From practical experience I would add that colon cleansing is also important.

RevPaul wrote:

Add DMSO after you added the water then drink, but if you are making a daily bottle, don't put it in until you are ready to take a dose.

Thanks RevPaul, I found your feedback elsewhere helpful & wanted to share a bit of my experience. I combine your suggested method with the dosing guidelines mentioned in the Health Recovery Manual i.e for every drop of activated MMS I add three drops of DMSO (NB: I think the manual advises up to 3 but I encourage interested people to invest in the book. Good luck)

My current circumstances allow me to make & take each dose as and when required. Insofar as my use of DMSO goes, I have found that at the lower doses of MMS (<6) this 3-to-1 ratio works for me. However on my first day of using DMSO I did start out with a one-to-one ratio and work my way up gradually.

Even when taking quite low doses of DMSO I have had to stir the mixture quite vigorously - even between mouthfull's - so as to ensure that the DMSO does not 'separate & settle at the bottom of the mixture'. Not taking this step results in me gagging on what feels like 'neat DMSO' at the bottom of glass! Ladies & gentlemen I can assure you that it is not a pleasant experience!

I am currently on a 5-drop dose of activated MMS to which I am adding 13 drops of MMS; this is a step up from 4 drops of activated MMS to which I was adding 12 drops of DMSO.

What else? Oh, though I have also used DMSO topically on my neck lump, I am unsure that this is an effective use given that the location of my cancer is in the area of my left tonsil i.e inside the confines of my throat. Though slightly more 'logical', if equally 'unsupported by any medical authority', I also 'gargle & swish' the last two mouth-full's of each dose much as if I were using a mouthwash. Talking of gagging and keeping things down, I am still grappling with assorted SAS uprisings, however more about those at a later date. I will continue to research & apply DMSO topically from time to time.

Finally, while there is not a second that passes during which I do not do so, I must here record an un-reserved THANK YOU to my family & friends for their love, support and patience. In the presence of their open-hearts & love-full nature I not only find myself blessed with the great fortune of NOT going through this experience alone, but I also have a wonderful now and inspiring visions of a future ... come what may.

And so dear reader, in the spirit of Ememessence I raise a glass and drink-down a wee dram of Dee-em-ess-oh in toast to you, your loved ones & your health recovery efforts.

Yours in sincerely

Solomon "The Unwise"

It was on this day exactly a month that I got a letter from my specialist medical team inviting me for a 'situation update' seven days hence i.e 31st March. For all sorts of reasons you can well imagine that I took that communication as a signal to step-up my health recovery efforts; so my mindset could be best described as placing me determinedly on a seven day countdown to a D-day of sorts.

As things transpired my practical efforts were in fact shaped by all manner of unforeseen circumstances and (very short term) preparation/plans for life beyond the 1st April. When it came the meeting was routine.

Unfortunately I continue to lose weight but seen within the context of my eating regime; I ram still not alarmed by this but admit that I need to keep an eye on this aspect.

Insofar as my emotional state was concerned, I characterised my 'condition' as still being mainly positive; yes there are days/periods of doubt over the course of action I have taken in dealing with my situation, but this is only to be expected.

During a cursory examination of the inside of my mouth & what could be seen of the area down inside my throat, the feedback was "it appeared NOT to have gotten any worse". Much to my later regret (but that's a different story) I feel that I was a bit too forthcoming when asked about what I had been doing to 'treat the cancer'.

Upon reflection I am now acutely aware that 'folks in positions of authority' e.g Doctors/Police/Lawyers and the like must have a whole series of ingenious techniques to get us to open up about stuff. Nodding of the head when listening to a dumba$$ like to me talk about all of the 'nothings' being done to treat a serious chronic illness is a prime example. Having read the summary of our meeting I vowed to never, ever again allow myself - not even subconsciously - to interpret such nods and 'suggestive sounds' as signalling empathy, agreement or confirmation that the listener is hearing feedback that they concur with. In future, I will shut-up real tight like a clam under threat at the very first sign I see of a learned personage nodding and smiling when I speak about matters of personal importance.

Suffice to say that I left the meeting somewhat deflated even though I did not have great expectations of being 'encouraged'. We agreed that I would be signed off from the specialist cancer treatment centre for now and refer any future concerns I may have to my GP, whereupon the next steps will be agreed. Under the circumstances I am happy with this conclusion.

Though the most apparent symptom of my illness - neck lump - continues to decrease in size, I don't know what this means. The hospital's expressed opinion and my own research has encountered information that this does NOT necessarily imply cell die-off or any other 'thing' that a cancer patient should interpret as a 'positive' especially a cancer patient who has refused the offer of free, standard 'therapeutic' therapies.

By the way, anyone in UK read the article on research revealing test results that show that consumption of certain mass-selling 'soft-drinks' and other assorted beverages appear to increase consumer's chances of falling to a cancer! Suffice to say that the relevant 'beverage sellers protection body' counter by saying that such findings are inconclusive .... Whatever! A short time ago I did some research on Aspartame and was horrified at what I read.

So for what it is worth I continue to consume MMS, DMSO, as well as my other treatments. I will always monitor my situation closely and a about to have some other blood tests, geared at helping me to further assess my current status.

Based on their own research, witnessing my growing conviction plus the various positively interpreted consequences of my MMS consumption, a family member has also started to use MMS. I was amazed that for the first fortnight or so this individual DID NOT display any of the telltale signs that the MMS had (or was going to) encounter anything adverse in the person's body. In my case it was on the very first day that I started to experience all manner of 'feedback'.

However a bit beyond the two week mark those lovely classic symptoms of a body experiencing Herxheimer Reaction showed up! Yes the individual does find these discomforting but all in all these experiences reinforce our belief that trying MMS is well worth the effort.