TOPIC:

Posting below some emails sent in to an MMS yahoo group. This man is taking chemo for lung cancer that has spread. He was in a lot of pain but MMS1&2 have eliminated the pain, and swollen lymph nodes have shrunk 80% also.

i want to relate my story to all of you , i have lung cancer that spread to other parts of my body . (one of them being my Pelvic Bone)
in november i went to my Dr to prescribe me some Tylenol3 for the pain in my hip was becoming terrible, and i started taking 2 tylenol 3's immediately, it eased the pain but not completely. then someone told me about MMS1 and MMs2, i started taking it and increasing the dose to 11 drops 4 times per day and 4 MMs2 4 times daily also, after 2 weeks i noticed the pain was gradually less every day, eventually i did not need the pain killers anymore. but then i got diaria and quit MMS because i thought that is what caused it . soon thereafter the pain to my hip returned, in the mean time i started taking antibiotics for a bug that i had got, after taking the antibiotics the diaria stopped , i was already taking the pain killers again , 2 pills every 4 hours and the pain was still intense, but then i thought about starting on the MMS again , well................after 8 days of taking it , i no longer required painkillers anymore , after another 3 weeks of MMS , ALL my pain is gone, i have been pain free now for over 40 days , i also could feel swollen Lymph Nodes in my neck and now those have shrunk by maybe 80%, i dont know if its because of MMS or despite of it as i am also on chemotherapy, i dont know how the Lung tumor is doing , but i will have a CT Scan in 3 weeks or so, i will report on it as soon as i know the results . thank you for the opportunity to tell my story

Pedro

the Chemo is " Carboplatin-Gemcitabin" combination, it is the 4th different kind of Chemo i take intravenously at the Cancer Clinic. MMS1 and MMs2 i take at home and have been taking at different dosages since November 2011,
Yes i have blood work done the day before every Chemotherapy session, the red blood cells have only been too low the last 2 chemo , i will have blood work done again next tuesday so i will know the results the next day . i will post the results

it might be of interest to readers that i was on Chemo AND mms 1 &2 for 4 months before my red cell count went down too low , but until January 12th i was only taking 8 drops of MMS1 4 times per day. i started increasing the dosage to 9- 10- 11- and 12 drops after that date , so the dosage MIGHT have something to do with decreased red cells . but like i said before , it could be from a combination of Chemo and MMS , there are too many variables to make an informed decision at this time

Pedro

Hello all, i have my blood work results back and now i can safely say that it is NOT MMS that gets my red cells down to such low level,
i stopped taking MMS on the 4th of March, on the 6th of March my red cells were at 86 on the 13th of March the red cell count was at 81!
i have started taking MMS1 again at the rate of 9 drops every 2 hours 4 times per day and MMS2 every 2 hours 4 times per day also.
for those that are wondering , even if the red cell drop had been from MMS, i would still resume taking it as i feel that the positives are more than the negatives were . Just the fact that i am in no pain is worth the MMS weight in gold. also, we know that Chemotherapy does a lot of harm to the body but we keep ( i do anyways) keep taking it as we hope it will prolong life to a certain extent. even if the quality of life isnt as good as it would be without it !

Pedro

Hello Jurgen, i dont know of any "field studies" about MMS but i can tell you about my experience with it.
I was diagnosed with stage 4 lung cancer in december 2010, i was given 8 to 10 months to live if i didnt do anything , and 12 to 18 months to live if i had chemotherapy, i chose chemo . i was told that they could not cure it , that they could only prolong life by a few months.in september 20011 i was feeling pretty bad ,physically and mentally because the cancer had spread to my Liver and to my Pelvic bone. in october i started taking Pain killers for the pain in my bone.
And then i heard about MMS1 and MMS2, since i had nothing to lose , i started taking it. after 3 weeks the pain was starting to be less and less until one day i didnt feel pain anymore, i attributed it to the use of MMS, but i wasnt completely sure that's what was doing it.but i came down with a bug and quit taking MMS for 3 weeks . the pain came back so bad that i had to go back to the strong pain killers .once the bug was killed i went back to MMS and within 1 week i was able to go off the pain killers, and after Christmas i no longer felt ANY pain . now i am sure it is the MMS that is doing it. i also had some Lymph Nodes that were really badly swollen , they have now shrunk by what i think is around 70-80%, i can not attribute that to just the MMS as i am still in Chemotherapy,i dont know what the tumour is doing yet but i am going to ask my Oncologist to give me a CT scan, i hope she will give it to me within 4-6 weeks , as soon as i have it i will publish the results .
I hope this will help you in some way,
Pedro

Michael