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Ovarian cancer progress report & question 16 Jan 2013 12:29 #29282

  • shelfrespect
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For those reading my posts for the first time: I was suddenly diagnosed with stage 3 ovarian cancer on October 1st 2012. In short, after one session of chemotherapy a very good friend put me onto MMS & I abandoned any further conventional treatment. Six & a half weeks of taking MMS my tumour markers went back to the normal range - see below. This story is not over yet. Administrators, please scroll down to see my questions & further comments. Thank you.

As you can see below, they are excellent. The CA-19.9 is now normal.
Tumour markers CA - 125 (normal is anything under 36)
28/9/12 1539
08/10/12 Chemotherapy
23/10/12 1501
30/10/12 383
07/11/12 173
14/11/12 101
22/11/12 57
28/11/12 37
06/12/12 25
13/12/12 17
19/12/12 12
02/01/13 12



Tumour markers CA - 19.9 (normal is anything below 31)
28/9/12 165
08/10/12 Chemotherapy
23/10/12 310
30/10/12 160
07/11/12 78
14/11/12 40
22/11/12 25
28/11/12 23
06/12/12 15
13/12/12 12
19/12/12 6
02/01/13 5

Once my tumour markers went to normal I went onto the maintenance dose of MMS. Today I went to see my GP for the results of a CT scan I had on Monday so that we could a complete picture of my current status. As it stands, I am totally cancer free. However, I do still have a cyst approximately 9 X 7 cm on my right ovary. In hindsight I should have stayed on course with the MMS until I had the scan.

My question is: I clearly need to keep treating myself with MMS, not just the maintenance dose. Whilst treating myself for cancer I was able to get to a very high dose of CDS; 50ml per day in a litre bottle of water. What dosage should I get back on now & what is an optimum time to have another scan to check on cyst shrinkage/disappearance, given that it is radioactive & I would not want one too soon?
I have every confidence that it will disappear. My GP also did a general blood test which showed:
My cholesterol which was once high, is now normal.
My blood pressure which was quite high & which I was taking tablets for is now normal.
As a vegetarian by nature & not choice (I have abhorred the taste & smell of flesh foods all my life) I have for some years been taking an iron supplement. This too was normal which absolutely astounded me as I had stopped taking supplements for the last severl months. I don't know how I can atttribute this to MMS as I know it's not a dietary supplement, but nevertheless it's a mystery - perhaps the MMS corrected an issue of unknown depletion of iron in my body????
Your advice on how to get back onto MMS for cyst treatment & follow up CT scan is greatly appreciated.
Many many thanks for giving me my life back.
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Ovarian cancer progress report & question 23 Jan 2013 04:49 #29535

  • kalylu9
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I too have Ovarian Cancer III C that reoccurred after surgery and chemotherapy in 2009 and 2 years in remisssion. How much MMS etc. did you take to overcome your cancer? My CA 125 has been at 6 for a year after a second round of chemo but it is starting to climb. My last chemo was in March 2012. I am trying the MMS protocol to try to head off a third chemo treatment. I am interested to hear how you implemented the protocol and results.

Thanks for any information anyone can share who has had success with this.

Kalylu9

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Ovarian cancer progress report & question 23 Jan 2013 06:11 #29537

  • shelfrespect
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I simply followed the Protocol 2000 as advised on Jim Humble's website. I started with 1 drop an hour for 10 hours then went up a drop every day. In my case, my body was able to tolerate the MMS very well in high doses. I did switch over to CDS & went up to 50ml of CDS in litre bottle each day over 10 hours.
I do, however, still have a cyst on my right ovary which was revealed in a CT scan I had a week ago. If you watch the following video link you'll see what I'm going to do now. I've just received my DMSO today.



Hope this is of some help.
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Ovarian cancer progress report & question 07 Feb 2013 16:12 #30314

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What a great story! I would like to ask how is it going with the cyst - is it reducing?
Also did you keep using CDS 50ml to a litre of water for 10 hours, or did you use protocol 2000 and DMSO?

Thanks!

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Ovarian cancer progress report & question 14 Aug 2013 15:15 #35275

  • Sorraia
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Hello-

I was wondering has anyone else been successful using MMS for cyst and or fibroids besides Kashambra?
I don't mean to sound discouraging but one or two people coming forward with their success is not a very good
success rate to me. Not to discourage anyone from trying it out for themselves but for myself I would like to see more proof in the pudding so to speak. I do want to say thank you to Kashambra for sharing her story.

I have also looked on the internet and You Tube and so far not much evidence that MMS works for this type of dis-ease in the body.
Now I Know there may be people out there who have had success but wish to remain anonymous ( and that is understandable) but I would think with over 400 members and thousands of people using it ( and the high prevalence of ovarian cyst/fibroids) we would here more success stories either here or somewhere on the internet you tube face book etc.
Any thoughts and ideas and experiences are very much appreciated.

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Ovarian cancer progress report & question 14 Aug 2013 16:04 #35278

  • fourfingerz
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MMS and CDS when taken as directed have no negative side effects.

Why would you not try it to see if it might help you?
Martin
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Ovarian cancer progress report & question 15 Aug 2013 02:03 #35292

  • Arrow
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Personally I would not use mms for ovarian cysts and breast fibryoids. these issues are clear indicators of iodine deficiency. Supplementing with Lugol's iodine will get rid of them in 3 to 6 months . I had fibrocystic breast disease but no more. Iodine is essential to reproductive issues and when supply is low cysts form. It also got rid of my thyroid cysts at the same time. Although mms may have eleminated the cysts for some people it will never address the difficiency issue.
For cutting edge updates in Alternative Medicine visit www.HealthSalon.org
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Ovarian cancer progress report & question 15 Aug 2013 13:24 #35306

  • Sorraia
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Hey Fourfingerz thank you for your comment.

To answer your question there is not enough evidence to encourage me to try it for my situation. I
I trust very heavily on my intuition......and for me with MMS the message has not come through to give it a try.
I do believe MMS has it's place and there are MANY applications for it's use for example if I had malaria or some type of
horrible virus or cancer I would be all over it.

Now regarding the Lugol's Iodine.....this makes sense to me. Based on my research and talking with
a health consultant friend who personally knows many people who have had success with lugols for cyst.
I just started applying the Lugols to my skin about two weeks ago. I think I will alternate this with ingesting it as well.
I tried the Iodoral which is Iron and potassium in tablet form a few years back and it didn't do anything but then again
I don't think I stayed with it long enough....I only took it for three months.
I do believe the Lugols supplementation will assist with the removal of the cyst/tumor. I am also taking a supplement called Trevinol
that helps break down fibrin/scar tissue through the use of enzymes.
A few other things ( amongst many) that are known to assist the body in the removal of fibroids include
the herbs Vitex ( Chaste tree), Red Clover and sea vegetables such as kelp and dulse.............which just so happen to be a good source of natural Iodine.
And of course it goes without saying diet plays a huge role as well as insuring the organs are clean and working well.
Getting back to the MMS I believe it could very well breakdown the fibrin tissue whether through supplementation or as a douche and it may be something I will try down the road but since I am already taking the Trevinol and Lugols amongst a whole host of
other things I am going to hold off for now. Many thanks for your suggestion Arrow. I am hoping the Iodine assist with my hair thinning out as well.

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Ovarian cancer progress report & question 15 Aug 2013 14:53 #35309

  • pam
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I want to mention that we are a fairly small forum, and thus we don't have a huge database of people who have done specific cures for specific things. And, as stated, some people are not comfortable talking about their medical issues. Soraia, I'm not sure why you are on the forum at all, since you don't seem to believe in MMS.

Until one TRYS mms, one doesn't know if it will help at all. The issue, bottom line, is what is causing the problem. To assume that all fibrocystic breast issues are iodine deficiencies begs several questions - 1. what is causing the iodine deficiency (is it some sort of pathogenic problem with the thyroids) and are ALL fibrocystic breast issues caused simply by thyroid - I had fibrocystic breasts for 40 years, exacerbated by caffeine, with absolutely no thyroid issues (verified by blood tests), once I hit menopause they went away - so there is something else there. I have had no uterine or ovarian issues.

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Last edit: by pam.
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