TOPIC:

I have a number of queries to post today:
First, some background.
I've been using MMS1 & 2 since October 2012 to treat stage 3 ovarian cancer. I had an outstanding result with my blood tumour marker going from 1800 to12 (anything below 36 is a normal reading). However, there have been a number of developments since then which leave me with my cancer still not clear & in fact spreading again – my markers have gone from 33 to 81 in the last 3 months or so. I also have a cyst on my right ovary which is growing in size. Regarding the cyst, I was not able to successfully implement the regime Kashambra undertook (refer to YouTube clip) due to my age. I also tried (without success) Iodine for about 3 months as per instructions by Walter Last (taking about 10 drops in water 3 to 4 times per day). The cyst hadn’t shrunk. Perhaps I should have persevered for longer?
I do acknowledge that some of the reasons I’m in this situation are of my own doing (I’ve touched on these previously).
I’ve learned over time to intuit how my body reacts to the MMS & have recognized some to do/not to do things, e.g.; not take it on an empty stomach and so on.
I enlisted the services of a naturopath who has written a book on alternate means of treating cancer & who is familiar with MMS. He prescribed various drops and tablets which he claimed would support the work the MMS was doing. One in particular would starve the blood supply to the cyst. However, I found that the tablets themselves, not necessarily the contents would bring on nausea & at times vomiting. It was just too much for my system.
Apart from the naturopathics I’ve been experiencing a marked increase in the vomiting. As is well documented this is not a good sign & does interfere with the regular dosing. I was up to 18 drops an hour when this adverse reaction was taking place. I’ve now dropped down to 9 drops & trying to slowly work my way up again. The MMS2 is also difficult as I often feel immediately nauseous after ingesting the capsule & have to wait it out wondering if my body can ride out the nausea/need to vomit.
I have continued to work during all of this. I’m a teacher so taking the MMS regularly has been challenging to say the least. One good thing is that I work with adults & have explained that I need to stop to medication. Although the constant worry about whether or not I’m going to throw up is ever-present.
I’ve seriously considered reverting to CDH to combat the problem issues. But then I remembered the one time I did try it the throat burning was the reason I couldn’t persist with it (especially as my job entails talking all the time).
In conclusion, I’m feeling somewhat desperate & anxious. So much so, that I’ve begun to contemplate the option of surgery – in my case a hysterectomy along with removal of the omentum. I would definitely NOT consider chemotherapy, but would continue to use MMS. I am also keen to use other anti-cancer agents such as turmeric, soursop, and apricot kernels etc as supplements to MMS.
I am prepared to seriously consider the possibility of stopping work for a few months, if able to do so.
I’m due to have another scan in the next few weeks (haven’t had one since August) & another blood test next week. My body is telling me the cyst has grown as I can now feel its presence & as the blood test results are creeping up I’m not expecting good news.
Following are my questions:
1. As my tolerance level of MMS has reduced, does the vomiting mean that it’s just my body reacting to something that simply tastes awful & is therefore not able to be effective in combating my cancer? I’ve been taking MMS for 18 months now. Or does it simply mean all is OK & that I have to remember the rule of thumb: take as much as your body can tolerate without getting sick? I should & am slowly trying to work up levels again.
2. The cyst. The MMS alone can’t get rid of the cyst, right? Is this because the cyst is a bubble with fluid in it, the fluids being the pathogens which the MMS can’t get to because of the sac they are contained in?
3. Where would I find the list of foods to avoid & those to embrace?
4. Any opinions on supplementing the MMS with the barrage of ammunition I’ve mentioned?
5. Any other comments/suggestions?
In gratitude
V Melbourne, Australia

Hello V.

Discomfort when taking MMS1 may not be caused only by it killing off pathogens, contrary to what we believe. I would try CDS or CDH for a while. Please try 4% HCL instead of citric acid.

I would also suggest to try CDS or CDH with added Sweetleaf brand SteviaClear drops at 1 drop per ml of CDS or CDH. It really tastes good!

Using the MHM (Mouth Holding Method) helps a lot to reduce throat burning. Yes, it takes longer to get a dose down.

You did not mention using DMSO. DMSO can help get the CLO2 where it might normally not reach. Be sure to check if you have a reaction to DMSO before using it.

Using capsules might work for you. You can use MMS1/CDS/CDH plus DMSO.

MMS2 nausea could be caused by taking too much of it. You do need to drink a lot of water with the capsule.

Do you use enemas, tub baths, external application of CLO2? Anything to get CLO2 inside that you can tolerate.

If you have not seen this Newsletter, it may provide some info on why you have not been 100% successful, yet. mmsnews.is/all-newsletters-list/175-29-reasons-why-mms-is-not-restoring-your-health-06-16-2013

Also, read all the posts from forum member gefeu2.

Let us know if any of these suggestions help you. Don't give up!

Dear JB13
Thanx so much for your informative & instant reply. It has done its job of restoring my faith in this process & to make necessary amendments.
I didn't know that CDH can be sweetened. I will go for this option! I'm going to order it immediately (from my approved supplier).
I do have DMSO. How & how much to add to the CDH please?
What is CLO2?

Regards
V

CLO2 is shorthand for chlorine dioxide. There is a glossary now at mmswiki.is

I believe you would add 1 drop of DMSO for each ml of CDH, and wait 3 minutes before enjoying your cocktail of CDH. It needs to be added to each dose and not to a daily bottle as it will reduce the CLO2.

Be sure to use 4% HCL to make CDH for the best flavor. Yum, yum!

yum yum indeed!
If ever you get tired of the delicious taste of CDH, you can put CDH in capsules.
See Zero taste thread for details.

Hi ShelfRespect,

I would also recommend the DMSO as JB13 has. Please read the following:

www.cancertutor.com/dmso/

About the throat burn with CDH, whatever amount you're taking hourly could be divided in half and taken every 1/2 hour but with the same amount of water or whatever amount of water works to stop that throat burning problem. So as an example, instead of 10ml CDH in 300ml of water every hour, a person could take 5ml in 300ml every half hour. That will greatly reduce or stop that throat burn problem.

And last but certainly not least, in order to help your immune system to heal your body, I'd recommend following the parasite protocol that Kerri's autism families do. I think that this will really help you to have the best fighting chance. You can get her book here:

mmsautism.org/bookstore

Kerri also talks a lot about doing enemas as a part of her protocol, and the bowels being so close to the ovaries, I would think that would be a good way to bring the CLO2 into your body very near to where it's needed the most.

Hope that helps,
Scott

Hi shelfrespect, My girlfriend recovered from vagina cancer that was caused by HPV (the wart virus)using protocol 1000 plus mms douches. She used 8-10 drops activated in 1-1/2 quarts H20. Plus fireweed tea to drink and some other supplements. I think the 1000 and douches are what really did the trick. Maybe add that to your protocol? Blessings, Suzanne

I’d like to thank everyone for all the support & invaluable advice when I fell into a chasm of doubt.
I’ve taken onboard most of the suggestions made – am using CDS with DMSO; am working on the parasite issue now.
I chose CDS as I have to talk all day in my job & couldn’t deal with the throat burning side effect of CDH.
Today is day 7. I haven’t experienced any nausea or vomiting to date (am over the moon about this!). Today I’m up to 70ml in a litre of H20, with at least 1 drop of Stevia per ml as prescribed. I also saw my doctor today for blood test results from Friday. Not surprisingly, due to all the vomiting & the consequent sporadic dosages of MMS my levels have increased considerably, from 81 to 157 in a one period (anything below 35 or 36 is considered normal.
However, I find it ever so much easier to just function in the world by being able to drink the CDS. It’s a pretty strong cocktail but not having to worry about debilitating side effects restores my resolve.
A few quick questions:
Sometimes, particularly when I’m working, I prepare the mixture & let it sit for 3 minutes before drinking. I get on a roll & then find that I’ve let 10 minutes elapse before drinking. Does this affect the potency at all?
Is it OK to increase the amount of Stevia as I’m taking quite dosages I think? That is, more than I drop of Stevia per ml?
Putting the CDS into a gelatin capsule. Does it need to be taken within 2 minutes so the capsule doesn’t dissolve?
In gratitude
V

More questions:

I think I mentioned that I've chosen CDS because I couldn't cope with the throat burning issue in my job.

In any case, I still find the taste difficult & immediately eat a couple of grapes to rid the aftertaste. Are grapes OK? Or. should I use something else such as grated apple?

Also, I was using organic apple cider vinegar for another (minor) condition which has been working really well. I've stopped because I'm unsure whether it has a negative effect on the CDS. Could you clarify this for me please?

Will keep you posted. Thanks in advance. V