Solomon's Hail: These past two years ... & then some

Protocol 2000 on the MMS wiki mentions adding MMS2 to our regime.

Can someone help me with info on:
Why is this suggested?
Is there a way to get the correct dosage without fiddling around opening capsules and measuring 7/8's and 1/4's of the substance?

That MMSwiki page says: "PROTOCOL 2000 (Last update: 25th of August 2012)" and at the bottom of the page it says: "This page was last modified on 17 November 2014"

The latest update for all protocols including Protocol 2000 are in Jim's latest book .

The idea suggested is to slowly increase MMS2 dosing and assumes you have purchased MMS2 in capsules. That would require removing some MMS2 powder from capsules to take less than full doses.

If you have purchased MMS2 powder in bulk, then you can fill capsules however full you want them.

I believe the MMSwiki pages will someday be updated to agree with the latest book.

Thanks for the feedback. Sounds like I will need to buy myself the book with the latest protocols.

regards

solomon

Is a good practice to always have the latest updated of the protocol.

At the same time, you can help Genesis II good cause to continue by buying the e-book.

Good Luck Always.

Solomon thanks for all your posts. I am following your story with interest. Regarding the MMS2 my understanding of why all the partial doses is for caution, to make sure your body does not have an adverse reaction. I bought my MMS2 from an approved supplier and started right off taking a full pill. I did not want to fiddle about with caps and powder. However, one can easily pull the caps apart and pour a little out if they want to be safe. The only reactions I had to a full pill is what others have also described as "belching pool water".

LaKidd wrote: Solomon thanks for all your posts. I am following your story with interest. Regarding the MMS2 my understanding of why all the partial doses is for caution, to make sure your body does not have an adverse reaction. I bought my MMS2 from an approved supplier and started right off taking a full pill. I did not want to fiddle about with caps and powder. However, one can easily pull the caps apart and pour a little out if they want to be safe. The only reactions I had to a full pill is what others have also described as "belching pool water".

As mention, we dont encourage anyone to start taking full pill right off. Especially the beginner.

Hello all and as always thanks for passing by. I have been busy with stuff over the last couple of days and so have not been able to maintain the number of daily MMS doses as directed by Protocol 1000. However on Monday I gave 7 drops a try for 4 doses which seemed to trigger more tingling in my tumour area as well as some of the 'die-off' symptoms I mentioned earlier. So from my personal MMS experience at this stage it seems that a 7/8 drop serving sends me 'tripping to the toilet' but as i said I am not alarmed. I think that I will keep up with the MMS and consult the latest protocols before trying anything more 'exotic' at this time.

I love music and typically that which we profess to love sort of seeps out of our psyche and manifests in a way that underscores the intrinsic aspects of our personality. As I start to compose this post, i hear the lyrics from a song entitled, "Where Do We Go From Here" performed by the late Bobby Womack, in my mind as a backdrop. Btw doesn't it pull you up short when you hear news that another one of the childhood heroes from your record collection has passed on over from this side of being alive. Damn, aint none of us gonna live forever.

Last week, (Wednesday/Thursday) were two big days for me for I went and got myself all uppity and announced to my personal doctor and my oncologist that the course of therapies they had mapped out for me were none too attractive & I did not feel ready to put myself through it. Damn talk about a one-person game of Russian Roulette ... but hey I was just being truthful with them.

Fact is that my medical team has been great! Things have progressed quickly and I have been in and out of hospital waiting rooms and machines every week almost since December 2016. I can not nor will I fault them and I do make sure that they know how pleased I am with the service I have received. When I met my oncologist to outline some of the stuff that contributed to my unreadiness, she sort of put me more in the picture regarding exactly how ill I am.

ooooopppppssss I kid you not, there goes my alarm for my next serving of MMS

brb

regards

Solomon

Six drops down the hatch so to speak and am back. Oh in case anyone out there is all a wonder I am on the 1 drop MMS & 1 Drop of the Activator regime. Where was i? Ah yes, dicing with death.

Well by the end of my conversation with my oncologist I learnt a few new things about my state of health. For example I learnt that the medical team felt that they had a very small window in which 'curing' my disease was a viable prospect.

I also learnt that further delay would put me at rusk of the disease popping up elsewhere in my body e.g my lungs at which point I would be classified as incurable. I was told that I was otherwise fit, healthy, articulate and with their support should come through the treatment just fine.

And then we started to talk about compromises ...sort of like, "well the blah blah therapy adds about a blah blah percent factor to the 'cure' possibility so as it is so small we might consider taking it off the agenda." (.... of course doctors don't speak like that so you can take it that I am paraphrasing)

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