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Circumstances dictate that I now be on a 'bottle protocol' most days, but I hope to get back to mixing my doses fresh before too long. As a consequence I can add DMSO to my MMS only on my days off work.
Truth is that though I do have all manner of support from family, I feel blessed to be able to "earn my keep" at this stage of my illness, One upside of being able to work is that it helps someone like me to maintain a broad perspective despite my diagnosis and the typical dread and foreboding that can engulf one who finds themselves wearing "cancer's sinister cloak". But I do admit, that I have to keep an eye on this 'desire to be independent for as long as possible' because it could well mask avoidance and a tendency to downplay the significance of my diagnosis and the consequent need to focus al I can on health recovery.
No, I haven't totally ruled out chemotherapy/radiotherapy and so I am constantly re-appraising my situation in the light of stuff that I can see happening in my body. As I mentioned, my neck lump is much, much smaller than it was back in November when all of this started and even in as it was back in early March just ahead of the time I was due to start my course of chemo & radio therapy.
Fingers crossed & hands firmly, earnestly clasped in prayer that the remainder of my body continues to be free of signs of abnormal cell growth! Given that I continue to read-up on it whenever I get the chance, the illness itself has lost some of its mystique. I am now more certain that the standard medical response to treatment of cancer is not the only worthy avenue. Am also certain that doctors themselves are fully aware of the alternative possibilities. But hey, this is the world we live in so we each have to find a way to act on our convictions.
A positive attitude and constantly gaining knowledge are key elements within the foundation of my strength and faith that things will be as they will be. So it falls upon me to remain flexible, ever-ready & retain trust in my instincts.
Thanks for passing by & expending some of your time to read this. Wishing you well in all that you do & on a personal reflective note "may the spirit of liveliness continue to ring out in Solomon's Hail.
New to mms I want to help my dogs mouth infection.
Thank you received: 3
I found this very comforting, I am presently treating my rescue dog for a severe mouth infection and this is the first time I have seen severe infections mentioned! As soon as I began adding DMSO to his protocol 1000 yesterday after just one day swollen areas above and below his eye got much worse! I became extremely concerned. I have drastically reduced DMSO today, hoping for better tomorrow morning. I have to say all the tooth extraction site looks completely free from bad skin overgrowth now thanks to protocol 1000 now I am hoping to keep on 1000 plus. Very good luck with yourself.
The following user(s) said Thank You: fourfingerz, Solomon
Hello Kathy Hs thanks for passing by & trust that all is well.
Given the sense of community that characterises this forum, you will not be too surprised to read me confess that I had read your topic and noted your experience with your beloved pet dog. I don't have any experience dosing four-legged animal's with DMSO (or MMS) but hope someone who has will turn up soon to share what they have learnt. I have seen videos in which people mention having treated their animals with MMS, so it is an avenue worth investigating.
In the latest edition of Jim Humble's Health Recovery Manual there is a guide as to the number of DMSO drops that can be added to our MMS mixtures. For myself I never exceed a 3-to-1 ration i.e for every drop of activated MMS i add between one and three drops of DMSO and stir very well and keep stirring between every mouthful till finished. For an animal I would be inclined to start off with fractions of this amount and go really slowly.
I am inclined to think that you have done the right thing by pulling back a bit on the quantities you are using with your pet - I think that most of us engage with these products in this constructive and evidence-based way. In my own 'severe case' the stuff I am doing can all be seen as a great big experiment, and though I keep an open mind on conventional treatment options, thus far I am content with all that I am learning about the body.
To end, I will also confess that since I learnt of MMS and the fact that some owners do engage with the products to treat their pets, I determined to mention MMS to a good friend who has an ever-sick pet husky! Despite spending lots of money at the vets and on specialist food/medicines nothing has worked to improve the dog's health health. To see such a beautiful, majestic looking animal suffer from a recurrence of mystery complaints is indeed heart wrenching. Good luck and keep at it.
Can you share with me how you are at the moment please? My partner has just been diagnosed with inoperable throat cancer. We already have MMS1 and he is starting the protocol today. Any help and advice would be well received
The following user(s) said Thank You: Solomon, Ellora
Hello healedin5 my thoughts and good wishes to yourself, your husband and family as you face this situation. Similar to your husband my cancer has also been classed as being 'of the throat' so we share that in common.
Given that I sincerely regard all of us on here as being part of a community, I hope that It does not seem like I am 'backtracking' when I state that I am not at all qualified to 'offer advice' on this or any other topic. I openly confess to this lack of qualification by signing off my posts as 'Solomon the Unwise'.
My doctors have as much as said that my refusal to accept the course of chemotherapy and radiotherapy they had mapped out for me is most misguided and they do not expect anything good to come of my 'nutrition approach' to dealing with my illness. I cannot begin to really express to another human how sobering it is to get a letter from your oncologist advising that if you do not do anything about your cancer you will be dead in in three months. So I guess that we can add 'Solomon the Condemned' to the 'Solomon the Unwise' tag. In light of that correspondence one of my short term horizons is to hopefully wake up on this side of existence at the end of come 1st September.
On the face of things I continue to feel 'fine' notwithstanding that I have been diagnosed with a serious chronic illness. One of the reasons why I chose to delay submitting myself to the 'chemo/radio therapy twins' back in February was because i wasn't physically or emotionally ready to have my quality of life impaired. The medical team had done a very good job painting a picture of what it was going to be like, and the trade-off did not appeal to me at the time.
So, having parked the conventional approach I decided to continue to learn as much as I could about cancer and to continue to consult with my allopath. Back in April she got me to submit a sample of blood for analysis - such things as P53 GENE EXPRESSION, P53 PROTEIN LEVEL, BCL - 2 GENE EXPRESSION, BAX GENE EXPRESSION, SURVIVIN GENE EXPRESSION, VASCULAR ENDOTHELIAL GROWTH FACTOR ( VEGF ) GENE EXPRESSION, MATRIX METALLOPROTEINASE 2 ( MMP - 2 ) GENE EXPRESSION were all measured.
Of course I knew beforehand that whatever was being tested would come back positive for whatever it is could be detected insofar as the the traces of cancer goes. Based on her feedback and my research I would say that the results were 'mixed'. I have had some additional supplements added to my list and she has reiterated that I need to have as much juices as I can get down me - a masticating juicer being the machine of choice.
I have drastically reduced my intake of MMS over the last month - see what I mean about the Solomon the Unwise tag?? - but this is all in keeping with my ongoing efforts to keep respond to my situation as seems best for me. As long as I remain peaceful with whatever decision I make then all is good in my world.
Back in May I noticed that the combination of the vegetable juices and MMS did not sit well in my stomach! Even with a two hour interlude betwixt the two I found that I was upchucking the lot as soon as I swallowed the MMS.
I discussed this with my allopath and the advice was to go full steam ahead and have as much as a litre of fresh vegetable juice per day even if it is mainly carrot juice, prior to this clarification I was concerned about the carrots and avoided using lots them because of their relative 'sweetness' (some of you may have read research that cancers find sugars and carbohydrates very, very yummy).
Right now the plan is to go back on the MMS as strictly as my circumstances allow till I can afford to re-stock my medicine chest with some of the pills and supplements that I have run out of - yep this approach of mine makes a big dent in the pocket. I anticipate that this will be a two week spell. I will then try to re-incorporate MMS with the other stuff I am doing and re-assess my situation during August.
Unfortunately, over the months I have noticed what appears to be another swelling has appeared just below my left earlobe ggggrrrrr. Yes. it is a cause for concern! To the touch and by all appearances the initial swelling that made me go to the doctors has decreased in size but as I may have said earlier I can't make too much of this because the doctors pointed out my weight loss may have caused me to shed some of the fatty tissue around my neck hence we can now see the real size. I assess that my weight loss is due to my very restricted diet.
Because of the location it could be that these two swellings are merging or I have a brand new outbreak!
What is interesting is that my allopath is adding many of the things you would have come across in your cancer research to my list of 'supplements' to take. Organic apricot kernels, Colloidal Silver (finally) which I am spraying directly into my throat. Curcumin pills (I have been adding organic cumin to my juices also).
I have been instructed to increase my daily intake of pancreas capsules to 90 per day; and have also upped my enemas to two litres twice daily! Confession: I have become quite fond of enema's and I use the time to clear my mind of negativity and repeat to myself some great affirmations/prayers I have come across. For those of you who haven't ever tried the enema I would suggest that you do some research on the topic. I will keep doing enemas regularly for as long as I am on this side of being.
As I mentioned earlier during my feedback on DMSO plus MMS, the roof of my mouth and my throat as far as I can see continues to improve in appearance. Admittedly, I might be in that stage before the cancer wreaks complete havoc in my oral cavity but I do not feel down in the dumps when I look into my throat. I am also acutely aware that there may be things going on my body that my eyes can't see so I don't get over excited by the stuff I can observe.
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