We encourage new members to post a short introduction of themselves in this forum category. Get to know your fellow board members and their interests and skills.
Please come and participate in educating people about the healing miracle that is MMS, and join the movement to make it available to the World!
One can see/read many testimonies online from folks who at one stage of their life been termed 'inoperable'. Thus far my approach to dealing with my diagnosis has been highly individual; I do not recommend it. Much to my wife's annoyance I often confess that there is part of my mindset which finds me accepting that I am on the way to crossing over from this side of being to the other side.
MMS1 was the beginning for me, to which I added MMS2 pills as part of my protocol; and after a while I added DMSO. I regard these three as the undisputed 'cancer destroyers' in my arsenal. I will try to post some more over the next two weeks now that I will return to heavily relying on them.
It is arguable that I have the luxury to spout such glib nonsense at this time because I am not in any pain, nor have I been told that my cancer has become inoperable. Truly, I cannot really imagine what it might be like to be in this position, and so from this side of that possibility I extend good wishes & brotherhood to everyone who may pass this way.
nzmaori2017 wrote: How are u getting on soloman? could you give me your number if you have any chance? Cheers would love to hear from you. Duane
Hi nzmaori2017 thanks for passing by. I reckon that the cynical reader will find it somewhat farfetched to read me write that it was without any prior knowledge that a question was being asked of me that I was planning to log on and provide an update. So here goes ....
Well, I am still here on this side of being. Since my last post I have been as consistent as I can be with my health recovery efforts. This week has seen me re-incorporate daily MMS into my regime which still comprises al the other stuff I have alluded to earlier.
About six weeks ago l decided to re-visit my doctor to announce that having tried various alternative methods of dealing with poorly differentiated squamous cell carcinoma in my left tonsil that had progressed to a lump in my neck, I was now ready to fully embrace whatever medical interventions were deemed appropriate/still viable for me six months after I had declined their offer of a six week course of Chemo/ Radiation therapies!
Having had my PET/CT scan early in August it has been a bit of an anxious wait for results and/or some indication of what the medical profession now makes of my case having last seen me at the end of March, by which time I had already received the sobering news that 'without treatment my tenure on this side of existence was reckoned at around six months'
Yeah, I dare you to count out the months out on your fingers ! Peace to all who pass this way having been given a similar prognosis. I have chosen to live this way and loved every moment of it. So it is with a lot of love and joy that hail the known and/or unknown knowns with an attitude of immense gratitude. Que sera sera as I chose to live this life my way!
Today, I finally received an invitation from the hospital to see a couple of therapists who are to advise me on diet, rehabilitative exercises and the like, appropriate for someone scheduled to undergo radiation therapy in the mouth/neck area. So, with no cure expected or implied, it appears that I am 'still treatable'.
I had been this way before earlier in the year so am on the lookout to be invited to attend hospital to sign various bits of paper 'releasing the physicians from responsibility in the event that the treatments do not work'; and to attend for measurements to be taken from which a custom-built mask will be made; and to sign in acceptance of whatever drugs they determine as being best suited to my case.
I approach these upcoming events with my will to linger a wee bit longer on this side of being burning even brighter! I have experienced a lot of great life in the intervening period, and my trepidation regarding the various poisons that I will be administered is no longer filled wth dread.
Having said all of that you can see that I remain most assuredly
Having re-opened the conventional medical avenue to dealing with my cancer it is reasonable to imagine that questions will abound about how it is that I assess the time I've spent engaged with MMS and my assorted alternative therapies.
Since I had my diagnosis back in January everything that I've done has been guided by a desire for knowledge and a sense of calm that has never been akin to what I term meekly surrendering to a fate worse than death itself; nor have I submitted blindly to what others say I ought to do. So in hindsight being informed that a certain part of my body was undergoing the 'cancer process' was sobering but not immobilising.
Disclaimer:The protocols described on this site are official sacraments of the Genesis II Church of Health and Healing. The reader accepts 100% responsibility for any and all use made of any information herein.