{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’m using MMS for Lyme. I started it on 10/4/07, worked up to 15 drops 2x a day, am & pm. When I experienced no nausea or diarrhea, I began to wonder if it was doing anything. Well, 15 drops 2x day didn’t last long. Walking got more difficult, started taking 2 hr naps, lots of pain in jaw/teeth/neck area and down spine, swelling in cheek, nerves in limbs screaming. Agony everywhere! Well, maybe not everywhere. It just felt like everywhere. But at least it became obvious it wasn’t doing nothing. Dropped back drastically on # of drops and some days went off entirely. Dropped salt/vit c protocol and supplements. I couldn’t think what to take or not to take or when to take it and couldn’t keep track even when I tried.

What I think is happening is that the MMS got to the spine where the dastardly little beasties had been successfully hiding out escaping the salt/vit c. I also consider this experience further confirmation that it was dental work that provided the major opportunity for this invasion. (If it hadn’t been for our ‘state of the art’ American medical profession I’m sure I could have negotiated this life much more successfully. Grrr!!) Anyway, I’m still miserable. but plodding on. Presently doing 15 drops once a day. Would like to try fewer drops at a time and more often during the day, but the taste/smell grosses me out so that I prefer to do it once and get it over with. I also added to my misery by using the Indian Herb, (otherwise known as black salve) recommended by Jim Humble on a couple of little crusty spots on my skin which, judging from how angrily they are reacting, I’m now convinced they are skin cancers. I also got the life-line water from the Indian Herb lady in hopes it will help hydrate as she says it will. So the experiment goes on.

Thanks to all of you for being here.

I also experienced that same thing using MMS for lyme. I worked to 15 drops twice a day and was fine for a while and started to notice fatigue and nausea building and stopped the mms after about a month. It became tough to tollerate the mms. 5 days later I started it up again because the fatigue worsened. 4 days after that i started feeling ok again. At 10 drops a day I leveled off as it was to much to go to 15 drops again. I finished half the bottle and have stopped for now. Most of the infections I have had are gone. After dermal testing the lyme was gone also but may be dormant. I had a lyme test three weeks ago to verify that I have beaten the bug.

If MMS can beat lyme this would be god sent.

I have been on it for almost 3 months now being careful to follow the directions exactly as told in the protocol. I have Lyme Disease, and I was infected in April 06 and have been virtually bed ridden since. I was treated early when the rash was first found and I never recovered, which they now suspect I got more than one tick infection. I now have been diagnosed with Neurological Late Stage Lyme Disease with nerve and muscle damage in all of my extremities. Within 2 days of taking MMS I had some energy, the first I have had since I was infected. I have continued with the protocol and am up to 15 drops per day. I did experience some nausea and diarrhea at about 6 drops and no it isn’t pleasant but the feeling after the toxins passed was like a cleansing. I almost felt like my old self once the toxins left me. I also took the MMS while on mega doses of antibiotics for a while and also experienced 3 terrible herx reactions, and honestly I felt like I was going to die, my husband was wanting to take me to the hospital. But after a couple of days, it finally passed, and I could tell I was better after each herx reaction. It sounds like the poster above is experiencing a herx reaction, and you have to get through them and continue, your body has to expel the toxins and it’s painful and that’s really an understatement on how bad the toxins leaving your body feel. But for the first time since I was infected I have energy, and I’ll take whatever energy I can get and I’ll put up with the herx’s from the toxins leaving to get that little bit of energy each day!

My mom has diabetes, and I got her to try it. Day one was 2 drops, day two was 3 drops, when she awoke the third day she said she hadn’t felt that good in years. Needless to say she had us online ordering her a bottle of her own. I’m anxious to see what it does by the way of healing her pancreas and improving her diabetes that she has been dealing with for 15 years. We also activated a small amount of the MMS and I applied it to her scraps on her head that haven’t healed in months, and within 3 days they were almost healed completely.

MMS works, and you will get sicker before you get better, but that’s true of any prescription or protocol that clears toxins from your body. Just bear through it, it’s worth the reward of some of your health back.

My wife is up to 9 drops and her reactions are now very slight to the treatment.

In the beginning she stopped taking it for a while at three drops because almost all her joints hurt so badly. She described her spinal pain as feeling as if her back was breaking.

Now she only has slight pain in her thumb joints. I am speculating that the MMS has done its job in the main part of the body either eliminating or greatly reducing the Lyme bacteria. Now it is getting to the peripheral areas.

She has not yet had the Diarrhea that almost always happens at some point. If she has it at the same point I did, it should be coming at about ten to eleven drops.

I can only hope that it is killing the cyst form and not driving the Lyme into dormancy. It will be a period of months before I will know the answer to that. But, so far so good. She has more energy than I do and feels well at this time.

I am no longer taking MMS myself as I am now on Low Dose Naltrexone for my Crohn’s Disease.

That is all for now.

……………………………………..

I have been using MMS and Rife Treatment on a friend of mine with

Lyme disease. On her first lyme test she scored the second highest

levels that the lab had ever seen. Her last test shows her levels to

be normal with only the co infections showing up. Those were at a low

level also.

MMS and Rife treatments seem to be getting her lyme to die off! The

results so far a promising!

The rife machine we are using it the Truerife with the foot bath or effectrolysis unit.

Hi everyone,

I started MMS last may 30, and soon went up to 14 drops adding one drop every day without problem. THEN, the morning of the 14 drops, I went through severe Herxheimer reaction. I did a major clean up of Morgellons which I do not have anymore. I expelled a ”silicone river” from both ends. At that point, I was scared to take MMS again so I did not take any for three days. I am a kinesiologist student and had my teacher test me on that and she said I was free of Morgellons. Since I was having the chance of being tested by her (such a great person…) I asked her to test for Lyme disease which I was suspecting and she tested positive on Lyme. So after those 3 days, I thought I should keep on and get back on MMS but was so scared I cut down to five drops (from 14…) and there I go again with the Herx and all. This time, the vomiting was clear mucous and mucus tinted a bright mustard yellow, nothing that I could have eaten the day before. I thought I was clearing from Lyme as fast as I did from Morgellons…nono.

No such luck for me. I wonder if the yellow color could be from being allergic (all of a sudden…?) to citric acid.

Anyways, I keep doing MMS (must be a very determined person) and three days ago got some DMSO and started the protocol from Jim Humble. I don’t like the feeling of doing this one, my skin is breaking out with rashes, I don’t seem to be able to drink enough, I am constipated and do enemas with MMS only, drink prune nectar should get something like All Bran, yeah… Anyways, I keep myself minded on doing the job of getting back my health. I wish I could afford a Rife device. I bought a zapper from dr. Clarke, should come in next week or so. Can someone tell me about Colloidal Gold ? Dr. Clarke is soon going to sell a device to produce your own and I wonder if it will be better than silver as stated on her site.

Thanks for any answer, sorry my post is long. God bless you all fellow sufferers.

I tested positive for Lyme disease and tested negative for all co- infections almost a year ago. I got tested at a reputable lab, but I know all tests are not 100% reliable. My point here is, I believe I had babesia and bartonella. Every morning I got out of bed, the soles of my feet would be very sore and sometimes after being on them for a long time. I understand this is a symptom of bartonella. Since starting MMS, I’ve recently noticed the bottom of my feet are not sore in the mornings. Also, the first day or two I took MMS I had intense aching in the neck, shoulders, and between my shoulder blades, which I never really experienced before, or at least not as intense. Usually these aches would come and go throughout a day, but this ache was constant all day long and lasted into the next. Well, I haven’t experienced this ache since the first day or two of MMS. I understand these is area babesia likes to hang out. So, it looks like I’ve been killing bartonella and babesia, which I didn’t think I had. Very interesting and amazing it if is true……..

I have used it for my Crohn’s and my wife is using it for Lyme disease. It has worked well for both of us. She will require a longer time period to know if it is capable of killing all of the bacteria, but we are hopeful.