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i’ve been taking mms for about a week……i take it with knudsen’s pineapple juice…….i am up to 15 drops 3 times a day, but when i take it without the juice it makes me puke and have serious debilitating nausea….

could it be that the juice is neutralizing the mms???????????????? at any rate,

it is clearing up some symptoms…..i am impressed……i am staying on the protocol with juice…….it is super easy with juice…….eventhough i have a bad stomach ulcer……

later, superpes

{Part of original post}

I am a seriously ill person who has been diagnosed with both ALS and Lyme Disease…

I thought I had better qualify my previous statement. I now realize it sounds like I have both diseases whereas it is actually more of an either/or situation:

I am not sure if I have ALS or Lyme disease. I was diagnosed with ALS by a neurologist last May but 2 months later, I took antibiotics for an unrelated ailment (swollen glands) and I had a “Herxheimer reaction” (which should not happen to an ALS patient). Since August, I have been also given a working diagnosis of Lyme by an infectious diseases doctor (it can sometimes imitate ALS) and have recently had a weak/borderline positive Lyme test result from IgeneX labs in CA. So, my feeling is that I do have Lyme (with severe neurological manifestation of symptoms) and not ALS, even though I have been diagnosed with both.

{2/8/08}

I have been taking MMS for 1 month now. Currently, I am at 10 drops twice a day. I have had to stop and re-start twice due to extreme “herx” reactions. My goal is to get up to 15 drops 2x a day WITHOUT nausea. I got up to 15 drops before and had a violent reaction (the usual- vomiting and diarrhea) BUT I felt great for several days after the reaction subsided. I DO feel like it is getting to something toxic in my system and killing it.

I am still weak, have trouble walking and my hands are crippled from nerve damage. I do notice that some of my other symptoms are better or gone.

Better: fasciculations (twitching muscles), fatigue

Gone: tingling, facial numbness, blurred vision

I finally broke down and purchased MMS and citric acid. Began taking it starting at 1 drop and quickly got up to 8 drops by the end of the week which is where I began experiencing the much-discussed diarrhea. However, I was forced to stop, not because of the MMS, but because the citric acid was doing a number on my teeth. My teeth got so sensitive that anything I ate or drink would cause my teeth to hurt. So, I was forced to stop. Interestingly, the diarrhea lingered for another day or so after I had stopped but not as frequent as the last day of taking MMS. My teeth, however, are still experiencing sensitivity a month later.

I should note that I am in fairly good health and not dealing with any illness or ailments at present. But I am a follower of alternative medicine and like to read up on the latest alternative health protocols.

That is my MMS experience thus far.

FWIW.

I have been noticing that since starting mms over a week ago, that I am having bladder irritation. I assume I need more h2o.

{2/9/08}

update… I have been taking mms for about two weeks now. I stopped for just 2 days(1 after yukky nausea and one when I suspected I had a bladder infection or irritation. I am back on 3drops in the am and 4 in the evening. My arthritis pain is gone in my fingers and toes!! I sleep like a baby when I take the mms. when I don’t it is my usual fragile sleep pattern of the 57 y.o. women. The bladder pain was not bladder pain but uterine. I had stopped progesterone creme and it came back after a few weeks. I am back on that now. My husband is sketchy about taking it because he is herkzing more than me. He has bad sinus, arthritis, and some kind of weird gut problems. His daughter has Lyme and we are trying to get her and her mom on board with the mms. she sees dr. diamond and my husband is going to go to next appt. to suggest the mms and see what he has to say. My step daughter got lyme last summer and has been quite sick on and off with flus colds, and aching and poor sleep. I will keep you posted on that progress.

the other thing I notice is a reduction of my attachments to food. there are times when I forget to have my 2nd cup of coffee(never the first)!!I am sold. I am a therapist and work with lots of clients who have med. issues like fibro. I am referring them to the web info that I found and am being their guinea pig.

I am excited.

I have stopped using MMS and here is why.

I had just reached the 15 drops two times a day, and had been on MMS for about 15 days days slowly increasing my dose by one drop per day. In the meantime my daughter got a pretty bad cold virus. I…fool that I am…took very few precautions when around her believing I would be able to withstand the virus.

About 6 days ago I could feel myself coming down with the head cold, but I continued to take the MMS two times a day. Shortly after the cold symptoms I began with the diahrea. Thinking that this was maybe jsut a side effect of the MMS a continued for another day….and then stopped…because the diahrea did not.

Five days I had the worst diahrea I can remember…not fun…as far as going back on the MMS…no thanks!