Hello to everyone here at the forum,
I am new and just last month i was introduced to MMS.
A brief synopsis of me.
1988 i was a passenger in a motorcycle wreck.
I suffered with multiple traumas and much blood loss.
Recieved life saving blood transfusion which later turned out to be tainted with HCV.
Intially my Hospital stay was 3 months then over the next 20 years surgeries, skin grafts and total knee replacement, battling hcv and a non responder to conventional treatments i am and have been for 5 years stage 4 cirrhosis.
Transplant being my only medical option i have been struggling with brain fog , fibro pain through my body,chronic fatigue all kinds , low blood sugar to name a few. All the things associated with chronic hcv cirrhosis and multiple traumas to the body.
I recently went to my Natropath and she told me about using MMS. I was most excited and could not wait to try it. I carefully read all the instructions and researched the web about it. I saw many good reviews and many unanswered ones. Folks saying they went on it and never followed up with what happened later in their treatment. Some reports were negative but i can read between the lines with all that.
I began with protocol 1000 and worked up to MMS2. I wrote Mr. Humble and asked him questions on what dosage and all for my illness.
He wrote back and was very nice. He thought i should go on MMS2 and 3 drops every hour for ten hours and add a drop more or until i start to feel it is to much and back off. He said i might want to try the Calcium Hyperchlorite tabs and sent me a link to his website on the instructions for that. I have yet to do this and will add it soon.
I have been on MMS for 1 month. I went through the initial nausea and die off but went away in a few days. I felt more energy and i am cautiously optimistic with how i am feeling.
I must admit my pain levels have dropped and my brain fog is clearing. I also notice my sugar levels have been more stable especially after eating. I can breathe better and smell better also.
I mix my MMS in the morning with distilled water 30 MMS drops to 30 citric acid activated solution and then into 1 quart measured container for the day after the 3 minute wait of course. Been struggling with trying to eat around dosing and some hours I end up late taking it because i don't want the food to interfere with MMS. Also hard to take other vitamins close to dosing but i am managing. I noticed my urine is clearer as i measure my output daily.
Overall I am happy with the results and will continue to use it. I still need to find out how long i should be on this dose before i go to maintenance dose ? I am moving cautiously as with my cirrhosis and all. Not sure if it will kill or quell the hcv but i have little recourse.
Looking forward to meeting new folks here and keeping updates about my progress.
Thanks for reading and Godspeed
Dan