Breast Cancer Stage 3 Aggressive

This contribution makes up for any missing ones, Utopia - I'm so glad to see this good news!

Hi Pam, Thank you i hope my post will give others hope to keep on keeping on. By no means is committing to MMS an easy task as it was about 4 weeks to get the diarrhoea under control and most the time mine would come an hour or 2 after my dosing had been done for the day so i never knew if i was over doing the drops or not until later. Learning everything as i went along. Boy it's sure been a ride and a lot of running LOL.

Much love.

Hello Utopia,

Sorry but i am little confused. Are you saying that MMS worked for you? It's confusing because the tumor size remained the same or almost same. Please clarify and sorry for bugging you. Thank you so much

P.S. are you cancer free or you just feel better having normal blood test results and such? Maybe you refer to the tumor markers?

Hi Kulermaster,

Although they believe my tumour may have increased the thing is the original measurement was taken at a different hospital and on a different machine and also only one way measured. The other thing to note is that the day the new measurement of 17 x 12 x 10 was taken was on the same day as all the blood tests. So to me this is an indication that the cancer is below any level able to be picked up from the blood test. From my own research others have had their tumour removed and when tested there has been no cancer in it. These story's I've read from other sites on alternative treatments for breast cancer.

I have had the odd lump in my breast over the years, the first one when i was 19 and this was all clear then in 2005 i had another lump which was again all clear but not removed not was it biopsied, only ultrasound. It was only this year 2012 that that lump from 2005 disappeared and then about a month later i found this new lump which turned out to be cancerous. So it took 7 years from one of my lumps to disappear. Not all lumps are cancerous and we all have a certain number of cancerous cells in our body anyway it's when the immune system can't combat them fast enough that it becomes a problem.

The thing is with cancer you can feel perfectly fine, it's when the cancer spreads or grows that you start to feel unwell. (or your having the conventional treatment) Personally for me i do not believe in what is offered conventionally and more so from speaking with my aunty a few weeks ago when she told me the story of how she met the man who invented it 30 years ago. He warned her not to let her mother have Chemo, which she didn't and lived another 30 years and died of old age.

This journey your own is a personal one by all means ask questions but ultimately trust your intuition for what would be the best course of action for you to take.

I had no signs of being ill or feeling ill, but a number of months before i had been so exhausted all the time but then i was walking long hours, had a puppy from hell to deal with and a hell of a lot on my plate and many huge emotional upsets all through this year. Also in 2005 i sustained a serious back injury that did not get sorted until mid 2009 i kept on working but it took so much out of me and for such a prolonged period of time my body was under so much physical stress and emotional as constant pain takes it toll.

I'm rather a high energy person anyway so i do tend to get periods of tiredness i have found that all the stuff i'm doing can make me quiet hyper and makes it harder for me to slow down and rest.

Maybe if all these test results where a result of treatment via conventional medicine i would be told i was in remission but as it is early days and my consultant and myself are taken these first lots of tests as a bench mark. So in December i go for a follow up and we will see what these tests conclude.

So for now YES the MMS and other things are having a most positive results in dealing with my cancer. Your diet is very important as food should be our medicine, we are what we absorb so if we're eating crap we'll be full of crap. Stay away from any GM foods is a must.

The only way you'll find out if this is the avenue for you is by testing it for yourself. Educate yourself, work on any spiritual lessons, change your life style and lift up your vibrations and stay positive. All this will assist you in your recovery.

Much love & light being sent your way.

thanks, Utopia - this looks like a very positive sign, and would love to have more information when you do your follow-up.


Just as an aside, may I remind the group that this is a support forum, and we are here to support those who are working with their MMS protocols.

That was bizarrrre!

So is the terrible diarrhoea that's kicked in again. I was ok for a number of weeks and the week i was awaiting my test results, week before last. From speaking to someone who's read up a lot on MMS. They said people can be fine for months and then get a bout of it kick in again. I even had to take a break for a couple of days. I am now starting from scratch and building up slowly. I had no issues doing 10 - 12 drop doses for days, but i dropped down to 8 for 10 hours after reading about not needing to be on high doses.

I haven't seen any information on this myself of this happening to others. Has anyone here come across this information or experienced it them self?

I do think this type of feedback is important as when someone else is going through it, it's ok kind of normal side effect.

Could it also be that the mix of MMS/MMS2/DMSO is getting real deep into the body and releasing yet more hidden toxins.

It would be really interesting to hear anyone's take on this? We are all piloting the uses i guess and paving the way for others. I read somewhere, can not remember where that this intuitive had seen MMS as liquid light. I really like the concept of this.

Sent you a note in the private message area, hope you picked it up.

Sorry it's been so long since i've been here. I'd like to give a follow up on how things have gone since i was last here. I'm a bit baffled really as you may well see. So just to recap on my test results so far:-

Test results to date

Tumour Size: (Aug 2012 - 12mm) ( Sept 2012 - 17x12x10mm) (Dec 2012 - no ultrasound) (Mar 2013 - 20x17x12mm)

Lymph node: (Aug 2012 - 18mm) ( Sept 2012 - 14mm) (Dec 2012 - no ultrasound) (Mar 2013 - 14mm)

Bloods - FBC/Bone/Liver – tested September only - Normal

CEA: (Aug 2012 - no blood tests) ( Sept 2012 - 3.4) (Dec 2012 - 3 ) (Mar 2013 - awaiting results)

CA125 - Normal range <35 U/ml: My results, September 2012 - 8. December 2013 - 7. March 2013 - awaiting results
CA15.3 - Normal range <30 U/ml: My results, September 2012 - 16. December 2013 - 12. March 2013 - awaiting results

An interesting comment was made by my consultant with regards to the first lot of blood tests carried out in September of 2012 was as follows
“As far as you’re blood test is concerned, all tests are reported as normal except two. One is the white cells in your blood stream have increased with more then average number of Neutrophils and Lymphocytes. The cause of this is not obvious but I am of the opinion that we do not need to pay too much attention to it”.

I personally think this may be the result of the MMS2? Or the combination of MMS1 & 2 And at my first consolation with this new hospital I informed them I was using these protocols, so he was aware that I was using MMS1/MMS2 . These tests have not been repeated since this one and only time in September of 2012. I also received lymph node fluid extraction and these showed as no cancer. The previous hospital on two separate occasions only managed to extract fat cells.


Protocol Summary

August 13th 2012 commenced with MMS1. Jumping in at 5 drops an hours and then from there I worked up to around 80 – 100 drops of activated MMS1 a day taken internally. Douching every other day with 20 drops of activated MMS1 and soaking in a bath for an hour or more of either MMS1 or MMS2

August 25th introduced MMS2 pro 78% size 3 caps 3 – 5 a day 2 hourly.

August 31st introduced DMSO into activated MMS1, little water then equal drops of DMSO

While the weather was warm I would also do around 2-4 topical applications of activated MMS1/DMSO on my lower legs. My upper body would react to the DMSO so kept to the low limbs.

The above was carried on until January 10th 2013

I stopped taking the MMS1/MMS2/DMSO while I was trying the Indian mud, This I had come across through one of Jim Hunble’s writings which I have since learnt is also called Bloodroot or black salve.

So from January 11th to February 11th 2013 I did none of the above protocols while I commenced with the black salve OH BOY WOOOOW lol The results of this are rather interesting as this salve pulled out 3 masses from me (I took pictures daily which shows the whole progress of the salve working) BUT what I found odd is that it did not touch the tumour. If you see the tumour measurements from March my tumour actually increased but only on one of the measurements.

Is this because of the salve?

In addition, I feel this is relevant but may be out of most people’s belief system. I have seen a psychic surgeon on 3 occasions since August. The first couple of sessions he commented on that my lymphatic system was very clogged/backed up, when I saw him a couple of days after my March hospital visit. As soon as he put his hands on me he said “wow your lymphatic system is so much clearer”. This gave me confirmation on what I had already been thinking that the use of the salve had pulled out what could of possible been stray cancer cells from around the area and also pulling and cleared out my lymphatic system.

Also I had been thinking and started to research weather a tumour could turn benign as my theory of the black salve is it needs signals to come off the tumour cells and if these cells are dead or not sending off the correct communication signals then it wouldn’t see the tumour?
By having three masses come out this proves the salve was working and out rules the possibility of it being a lesser grade product.

My tumour has always been soft hard, little big throughout the day so it is very changeable.

I also know that the MMS I have been purchasing is of good quality and have been using the same supplier since 2009.

(By the way I also received an email when I first ordered asking me to hand over my MMS to the FDA. I think I still have a copy of that somewhere. I’m in the UK so if they really wanted it they could come knock on the door).

The only side effects I had were diarrhoea, mostly though this would happen a few hours after I had finished dosing the 10 hours of dosing and kind of vanished apart from the odd day now and then since. I was only eve r sick the once after taking MMS1 and once with the MMS2 in the whole time I took it.

I resumed the MMS and the rests from February. A maintenance dose 30 – 40 drops a day.

I have since stopped from April 24th as am seeing what results the supplement Salvestrols will bring. I don’t believe these would interfere with any of the other protocols but I wanted to give it a month or so to see just these along might do and they are said to work on benign tumours and cysts. Gerry Potter from Leicester University was the founder of these. His story is an interesting one and the authorities even had him sectioned when his work was written about in the papers. Very interesting research if you have not come across this yet.
Dan Burke who’s worked with Gerry Potter and below is really good talk on how it all works. Explains it all. Am keeping it brief as I understand this is an MMS forum. But if any one would like further info if it is not etiquette to post here I can email privately. But this is well worth info to know about.


I have been taking the Salvestrols now for about 45 days and have not noticed the tumour shrinking as yet. Can take anywhere from a month to six months.

I believe would work well along side MMS’s protocols, unless anyone would know otherwise?

My diet is pretty health I wasn't eating meat for a while and still not really eating it. I buy mostly organic. Fruits, veg. Not really a big pasta eater or rice. Pulses and sprouts. I do eat a lot of eggs and cheese is a bit to much like chocolate for me.

I have been doing Budwigs Flaxseed and cottage cheese protocol so I know I am getting a good source of EFA’s. I do weaken at the odd muffin.

I am a smoker but my CEA levels aren’t reflecting this as a healthy non-smoker is 2.5 a smoker is 5 I am 3 currently but I do now smoke a 100% additive- free natural tobacco and have cut right down.

I do plan on getting another core biopsy done. I did request this when on my March visit to hospital but they had even cocked up booking me in for an ultrasound and said there wasn’t time. I only go every 3 months and it’s been over 3 months now and two days ago I received a letter from my consultant saying everything was great. But sadly again he did not included any of the tumour makers figures.

I will also add that when I stopped the MMS and the rest whilst doing the Black salve which was for a month. I jumped straight back on the MMS and co at 10 drops a dose 3-4 times a day with no adverse reactions. I also plan on resuming next month once I have finished my 3rd supply of Salvestrols.

Maybe my tumour is none cancerous? and I just have to wait until the body dissolves it. Or another core biopsies is preformed so i know one way or the other.
Thank you for taking the time to read this.

I would be very interested to hear any thoughts and feedback on the above any of you may have, as I am a little baffled as to why this tumour hasn't been effected by any of this?

Hi Utopia,

You are doing great stuff and I admire you for being so determined!
One note of advice please (coming from a holistic nutritionist): please do not drink any amount of alcohol, wine or other. Your liver is the most important organ in dealing with cancer. Believe me you need it 100%, you do not want it occupied with detoxifying alcohol. In the first place the liver is not able 100% to perform its functions if you have cancer.

Your pH results for saliva are very low indeed. Chocolate and wine (any alcohol) are extremely acidifying, so please do not use. You need to take alkalizing ionic trace minerals (are liquid, you add them to your drinking water). You need to do this ASAP, ESPECIALLY because you drink distilled water. Distilled water is robing you of extra minerals, making you body very acidic. Cancer can survive only in an acidic environment, so must alkalize immediately.
If you are not taking any heart medication, take 1/2 tsp of sodium bicarbonate in the evening, before bed time. Must be on an empty stomach and away from MMS1/MMS2.

Be blessed!

Hi
I would recommend ozone water therapy plus ozone air/ dmso mix on the afected area

the mms protocol alternately

fight on the disease .... theres a cure