TOPIC:

I have stage 3 ovarian cancer which was suddenly diagnosed on October 1st. Being in a state of shock I was swept up in the medical system & went to hospital. In addition to this I had a pulmonary embolism on my right lung. This made immediate surgery risky & it was decided that I would require 2 to 3 sessions of chemotherapy prior to surgery. During my stay in hospital I had the first of these sessions & was then discharged scheduled to have the 2nd session on October 30th.
Having survived the feeling of illness, weakness & general debilitation of the chemotherapy I had time to think & reflect & decided not to pursue this path of treatment & so did not proceed with the 2nd session. A very dear friend put me onto MMS which I started on October the 20th.

Below is an extract of a journal I periodically send out to friends & family:

Beginning of extract:
"I saw my GP this morning for my weekly blood test result. For those new to this journal (which is confidential so please don't forward without my permission), I think most of you know that I have put on hold the treatment path of chemotherapy/surgery & am treating myself with a solution known as MMS.

As I'm not in any pain or discomfort I'm monitoring my progress via the blood tests constantly so that I can make an informed decision if & when need be. I asked my GP to print off the oncologist's report for me also as I've not yet seen it.

I haven't yet furnished my journals with data but I think today is the day for this.

To quote my oncologist's report of Oct 16th:

"The clinical picture was one of advanced ovarian cancer."

What is looked for in the blood tests are the Tumour Markers, called CA -125. In a healthy person this reading is 10. On the 28th of September mine was 1539. My blood test of last Tuesday, the 30th of October was 383. My doctor was extremely pleased with this result & just encouraged me to keep on doing what I was doing." End of extract

It should be noted that the session of chemotherapy would have some impact on the results; the next few blood tests however will be all about the MMS. The doctor did note that the cancer marker reading was extremely good so I'm quietly confident that the MMS is already doing its work.

I'm now taking 1/2 a capsule of MMS2 5 times a day & still incrementally taking higher doses of CDS - tomorrow will be up to 4.5ml for the day.

I'm also doing the following to support the MMS regime:
Each AM & PM am drinking a glass of bicarbonate of soda (called baking soda in the US I believe)
Eating a very alkaline diet - I am by nature a vegetarian/vegan as I have always abhorred the taste & smell of flesh food so this is not part of my dietary plan.
I purchased a water unit which creates water with a PH value of 7.2 as well as cleansing the water.
Meditation & walking.

I can also intuit/detect certain changes/sensations within my body; for example, on the right side in the area of the ovary I once constantly felt a pulsing sensation. This has now disappeared.

My next appointment with my doctor is on November the 14th. I will keep you posted with the results of today's blood sample taken.

I'm eternally grateful to Jim Humble & his great work.

The CDS I'm using is from a supplier recommended by Jim Humble - the 100ml bottles (1ml of CDS is equivalent to 3 drops of MMS).
I'm taking it 10 times per day.
Today I've put 4.9ml in a litre bottle of water. If all goes well after a couple of hours I'll increase to 5ml.

How are you doing?

Thank you for your regard. My sincere apologies for the tardy reply but it has not been because of forgetfulness that it’s taken so long.
I don’t know where to begin with updating you with this journey that began in October 2012. In short, I’m still not in the clear. Many factors contribute to this outcome & these are:
• My own ignorance about this type of cancer. I was unaware for some time that there is no devised screening process for ovarian cancer; that the only way to monitor it are blood tests and CT scans. When my blood test result had a normal reading I went onto a maintenance dose of MMS. Almost 3 months had elapsed before I had a CT scan which revealed that there was still residual cancer as well as a cyst.
• After that followed several fits & starts with MMS. At one point I just went into a meltdown psychologically keeping up the hourly doses (I’ve been back at work since January 2013). For several weeks I was taking it sporadically. Then, late last year for a period of about 6 weeks I experienced a great deal of nausea and vomiting without increasing the dosage. This eventually ceased of its own accord. However, during this period it was difficult (if not impossible, really) to keep up with the hourly dosages.
The last CT scan I had was in August 2012. This showed an increase in the size of the cyst and some spread of the cancer. This wasn’t surprising given my psychological meltdown & the period of vomiting which ensued.
I had 2 blood tests in December, both of which showed the tumour marker to be a little outside of the normal range. The one encouraging thing to be noted here is that the markers were the same, indicating some stability. Since then I’ve been far more vigilant with sticking to the hourly doses. To date I’m taking about 18 drops an hour. I’m still experiencing frequent nausea & vomiting about once a week, so I know I’m peaking with what my body can tolerate.
I was referred to a naturopath who is based in another state to me but does long distance consultations. He has written a book on alternate treatments of cancer & is familiar with MMS. He has a somewhat scientific approach & does an analysis of one’s blood. I’ve purchased several products he’s recommended & have been taking them since early January. He claims these will help MMS do it’s work.
I recently had one attempt at CDH. This wasn’t successful but I’m thinking of giving it another go as I suspect the recommended amount of stevia is not to my body’s liking & I may need much less.
I’m seeing my GP on Wednesday for blood test results. My plan at the moment is to have another scan in March & also another follow up consultation with the naturopath.
In conclusion, my resolve is strong & I’m committed to continuing with MMS. If it was available in vanilla, I’d be in heaven.

Ah, but stevia i s available in vanilla <G>.

Hugz - you've definitely got your hands full - my thoughts and prayers are with you.