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?