TOPIC:

So there I was with my situation all laid out, crystal clear & frankly spoken (pardon the pun) in terms that were as unenigmatic as a corpse. So yeah folks, where indeed does one go from here!

Well, I was asked to wait around to chat with a member of my care team, fantastic person, and she also gave me some useful information. For one I was not compelled to accept the traditional medical therapies for cancer, I could not start the treatment and then stop it midway through. She confirmed that there were other avenues open to patients with my diagnosis and that I should investigate them with care and do what feels best for me.

So here I am with my MMS, an ever-increasing mass of personal resolve, a supportive family and some more conversing to do with my medical team to see if we can agree some future dates on which I will be examined to see how things are going. Oh and I have also been connected with a Biochemist, Nutritionist, Naturopath, Psychotherapist who is experienced in dealing with cancers in an altogether different manner. I am somewhat down on my bank balance as a result and wee bit shaky at times when it comes to getting my head around just how 'sick' I am but hey it is what it is.

No, I am not resigned to things progressing as they are till my eventual demise but the hospital plan will subject my body to a quite savage course of treatments that will impair my quality of life right now; and which will possibly cause me future cancers. Yes folks, they asked me to acknowledge that they have informed me of this possibility by signing some documents.

Ah well ...

Hello again & trust that you are well. Am certain that during our engagement with MMS we encounter numerous situations that we want to understand as well as manage so as to stick to our treatment regime. Right now I need some help countering the taste of the activated MMS - I am using the bog standard Citric Acid solution as seen here .

I anticipate that as the number of drops I take increases I will continue to find myself being repulsed by the smell of the activated MMS especially during the short period of time before I add water to it.

I have have worked out that this reaction is to some extent psychological, however the (automatic) mental association of what I smell with an expectation of what I am going to taste is resulting in me experiencing (and having to fight down) a mild gag reaction.I read somewhere on the site that someone had been using a brand of cola instead of water. Any thoughts?

Thanks in advance for any ideas that you have.

Regards

Solomon

My advice is to get used to the taste. It is just psychological matter that can be overcome by everyone if one think of the important to live.

If you are current using citrid acid, then it would be best to change to HCL as activator. The taste will be improved so much.

MMS will be part of our life for very long Year to come, so by getting used to its taste is part of the step to take.

The more one try to develop the alternative way, the more confusion is created, MMS had been around for about 20yrs now, anythings that is capable to be improved had been tried and till now, nothing much is change to claim to give the same effectiveness as recommend in official protocol.

Thanks Edwin3110 I am inclined to agree with you about the getting used to the taste and I have more or less done but the gag reflex exacerbates the "taste anticipation" and this caused me to throw up my MMS dosage immediately on one occasion. Which meant that nothing stayed down that time.

Yes I have ingested more pungent smelling stuff in the past but you know what it's like when you know that something is good for you but you encounter a small hiccup in exposing yourself to it. Yep, you are right that it is mind over matter, but being open about all aspects of my experience with MMS helps me and who knows may also be useful to someone else.

I will investigate the HCL activator (not supplied by the place I got my MMS from & I do prefer to get everything from one place) I also accept that MMS will be part of my life forever more and this is why I am doing a lot of research at this early stage so as to establish a well informed base upon which to build a lifelong regime.

Now that my MMS protocol 1000 is going so well (more about it later) I am now seriously looking for an approved supplier of DMSO to add to the mix by way of moving up to Protocol 1000+. I have read this Protocol works a treat at enabling the MMS to get deeper into our system. My hope is that it will start to work more evidently on reducing my neck tumour. Thanks as always.

regards

Solomon

Hi,
Firstly, I must give thanks for still being here on this side of being, which is no less mysteries than the 'beyond'; so yeah thanks and blessings is due.

Well, one piece of news is that I have not yet started the course of therapeutic treatments the hospital has planned for handling my serious illness. During this delay it has been arranged that I see an esteemed expert at another hospital later this week for a second opinion, more information about my medical situation as well as my health outlook. I have also had more reassurances that we are still in a timeframe during which they feel their therapies will be geared toward curing me. It was also mentioned that once, note not if, the disease gets to my lungs it is an entirely different matter.

So, not to put too fine a point on it, I am dicing with continued life in the hood And yes, I did receive a letter, confirming to all concerned that without treatment my time on this side of being was to be considered in terms of months. So I am in no doubt as to how ill I am.

Am now up to 9 drops as often as I can take during the day - over this past weekend I have been able to advance from seven drops. On Saturday, whilst out, I had my first full-on hit of feeling extreme nausea whilst out in a public space! Wow, I only just held it together. My head ached. I felt weak in my stomach (which all reminded me of one of my terrible hangovers from many, many moons ago) but I made it back indoors ok. Talk about relief.

From personal experience I can add my testimony to the observation that the body seems to need a few 'shots' to adjust to each increase in the number of drops one takes. This morning 9 drops was a cinch but last week there were times when I could barely stand the smell of the seven drop mixture! My stomach would churn and I would physically shudder once the smell hit my nose - much to the hilarity of my family members Still experiencing Herxheimer reactions but not with every dose.

Think I mentioned earlier that I have seen Naturopath. This person has put me on various supplements and outlined dietary changes I ought to make. I am following this advice with the loving support of my family members - thanks to them. Being close to them is a big tonic for me as I go through this experience.

I am doing enemas twice daily, sometimes just with coffee and at others with the addition of tea. Talking of which it has been suggested that I drink as much tea as I can but I am very concerned about this because I read that tea ought to be avoided when one is on MMS. So I need to do more research on this aspect. So as you can see I am juggling a few 'treatment pathways' towards restoring my health. I am also reading up about cancer and so continuing to learn.

Have been practically vegan for nigh on thirty years, so while the dietary changes are not too drastic, I am eating lots more raw/barely cooked veg. It has been decades since I stopped boiling my veg so our steam pots are working overtime. I have been advised to go the organic route for all sources of food and to wash stuff carefully.

The detoxes are easily manageable and it is very interesting to observe how the MMS plus the enemas seem to amplify die-off symptoms. Doubtless to say that am very pleased to see what is expelled from my body when I get off the toilet - I will spare you the detail but I have not yet seen any foreign living organisms. However the debris that is being purged from my system is beyond anything that I could ever have imagined. I take this all to be positive and continue to remain highly motivated to do all that I can to get better.

Anecdotally, I feel that the MMS has brought about some changes in my physical condition.Now that I have added the dietary changes, supplements and enemas to the mix I am gaining more of an understanding of how my body works. I will avoid saying too much about my 'feelings' on this score right now but will when the time is right.

Now for an issue that has been running around my head ...

Glad to hear your good progress.

Have you ever think of moving into Protocol 2000?

I would believed that your situation is best to be on Protocol 2000.

Yeah, by now you would have got some inkling that not only am I a wee bit crazy, but am also creative in my approach to stuff that I encounter on this side of being. I swear that the inside of my psyche is a mass of unpredictability but it feels good to be me and I hope you don't mind me wishing that you feel the same about being you . We are all unique and the world would not be the same without each of us. So live strong and smile always.

Where were we?

Ah yes. I have been musing on a particular aspect of my engagement with MMS but the way my mind works I have an inkling that I would have encountered this whatever treatment path I undertake. I will try to share the essence of this mindlessness with you but first I have to confess that in this context S.A.S does NOT stand for the Special Air Service but rather Symptom Anxiety Syndromes. With that said let's a re-branding of this post would read "Daring to prevail against the Symptom Anxiety Syndromes during health restoration!" ... but hey it is still a form of combat ain't it?

Since I started to take MMS there are times when I find myself getting anxious when I don't experience the typical 'positive' symptoms that the solution is renowned for. Deep down inside I know that this anxiety is no good for me, but it is a sort of auto response born out of the need to find something to relate/cling to! Something, be it imaginary or potentially downright misleading, that can keep me buoyant in this sea of uncertainty. But truth is that there is no certainty! So I am left with toying with the idea that part of my 'battle' is with the self NOW. Ans so I let go of anxiety and questions during my treatment.

I welcome the symptoms whenever they appear but till they do I rest on the assurance that MMS is doing it's thing just like the chemotherapy and radiotherapy do their thing. Right now I prefer therapies which afford me the chance to experience 'this' quality of life.

Yes, my feelings may change in a week or a month but hey till then I will just keep on living as I am, combating unnecessary anxiety and getting on with the medicine taking; because after all getting me better is its job. Put another way: I do dare to prevail against the S.A.S during my health restoration!