The following are pieces from Eric’s website (www.ericswinning.com) that serve as a testimonial from his own experience successfully fighting ALS using numerous strategies including MMS:

In 1990, I developed ALS, a 100% fatal disease with no cure or treatment. In 1995, four different MD’s told me I had six months to live, I PROVED THEM WRONG. I am an ALS survivor of 21 years from the date of my first symptom; my doctor told me that 90% of people with ALS die within 1-5 years. He also told me that there was NO CURE and they had NO CLUE as to the cause of ALS. Now, that was either a lie or he was a bone head. I now know that a NEURO-toxin, such as Mercury, will cause damage to your NEURO-system, resulting in PARALYSIS. Now, what is ALS? Nothing more than damage to your NEURO-system, resulting in PARALYSIS. Now, don’t tell me that the MD’s don’t know that.

For more details about his regimen, go to his website. Also, watch his movie trailer…

This was a Mexican lady about 60 years old. One evening about 6 PM we got a call from a Mexican gentleman who said that he would like to bring his wife over right away. We always try to accommodate anyone that we can and so he was invited over. When he arrived he helped his wife through our door. She could not hold onto the walker that she was using, so her husband was holding her to it from behind. It was a chore to see them squeeze through the door together.
They inched over to a living room couch and sat down. She explained that her right hand was totally paralyzed and numb from the wrist down for over two years, her foot was paralyzed in the same way. The paralyzed hand kept her from holding onto the walker, and the paralyzed foot made it extremely hard to walk even with the walker. In addition she had terrible back pains and leg pains that also limited her walking. She could barely get around the house.
Well, Clara always trains anyone who comes here by first giving them a six drop dose of MMS explaining exactly what she is doing, and then has them wait for an hour. The second dose she has them mix, wait the three-minute wait, and pour their own drink. That is, of course, so they will be able to make their own doses at home. In this case the lady said, about 1/2 hour after taking the first dose, “I think some feeling is coming back to my hand.” She also mentioned that the back pain seems to be less. Clara had the lady mix and take the second dose after an hour.
In just about another hour (it was two hours total) Clara called me. She said, “Jim, come here. You will want to see this. I quickly walked into the room. The lady was exercising her paralyzed hand. All of the muscles were moving correctly, and she had her shoe and sock off and was also exercising all of the muscles in her food. In fact the muscles in my foot don’t move that well. When this lady left our house she was still using the walker, but her husband was not holding her onto it, and one could see that she would not be using that walker for more than a day to two.
Let me say here that so far as I have been able to determine once these things go away, they seldom return. I believe that it is important to continue taking the MMS until one is sure the microorganisms are dead. Then maintenance doses are important to keep the immune system tuned up.

I started using this Mineral from Heaven 10 months ago. I Was suffering from Ramsey Hunt Syndrome (Shingles in my ears). Which left every nerve in my being  (entered the spinal column ) ravaged and wracked with chronic pain. Physical tremors and shaking. Terrible Anxiety. Depression. And  the virus kept coming back every 3 weeks  for 5 years (while using antiviral). GONE It has taken a good 6 months to work it out of my system. Bonus!: warts, gone. Skin pre cancer sun damage, dried up and fell off. Major fungal infection of sinus and skin Tinea Versicolor, gone. Dark spots and overall weird skin thingies, gone. Body odor, gone. Teeth And gums, awesome. Pink eye, gone. Bronchitis, gone. Sprained ankle wrist, no bruising and healed in a week. Chronic heartburn, gas from any foods. No more.

Hi lovely family. Am been closely following videos on YouTube of how mms cures diseases and this mms saved my life coz I was like epileptic….but thanks to mms which I bought from South Africa saved me. Suppose, I start your course and finish would you by any chance conduct a seminar here in Zambia because the community is dying from these chronic diseases. Waiting to hear from you

I have my own testimony for the treatment of lung cancer. I have my own medical diagnosis ‘Inter DiaCor’. Having problems with sweating, dry cough, fatigue, nervousness, severe pain in the middle of the back, hard to sleep and pain when lying on the left side. I decided to do a complete analysis of the organism. I found a great contamination of bacteria and viruses in each lung, but really on the left. Also was weak and small alveolar gas exchange. Urgent I started using MMS protocol 1000. Kontrol analysis I have worked for 15 days and the result was 50% less microorganism, still I spent MMS. I’ve done the analysis for 30 days and the result was 100% clean lungs. I continued to drink MMS for 20 days due to parasites in the cerebral cortex, the brain, and by the end I was able to repair all the problems in 52 days. Initially, the viral load was 86.1%, and finally 4.6%. I have all the images of such evidence for other people or seminars. Health resort I have other patients with bone cancer, severe toxemia, depression and the like. The success was great for 30 days. This is truly amazing!

Hi there,

I am insulin dependant (Type 1) diabetic and have been on insulin for nearly 21 years now (I am nearly 50). I understand that there may be several causes to the disease which may explain why the MMS cure only works 50% of the time.

I too have heard that the problem is caused by an inflamed pancreas (actually I heard inflamed nerves in the pancreas) but also that it is an auto-immune disease where your immune systems gets confused and attacks your own insulin producing Islets of Langerhans cells. This theory may be supported by the fact that nowadays they check you actually are Type 1 diabetic by doing a GAD anti-body test (this was invented as originally a lot of people were put on insulin unnecessarily – so the existence of this anti-body supposedly confirms the auto-immune issue).

When I was originally diagnosed back in 1991 they thought diabetes came from either stress (I had a period of extreme stress 18 months before diagnosis), a virus (I had a bad virus in Bangkok 11 months before) or after an extended overseas trip (I had just returned from a 8 month round the world tour when I was diagnosed). Three for three in my case!

I have just completed 3 weeks of Protocol 1000+ and there has been no change to my diabetes and no change to my insulin requirements. This included no change when I have injected which I did at the same time as I took MMS1.

I have 2 other auto-immune diseases (Uvitis in my left eye and CIDP – Chronic Inflammatory Demyelinating Polyneuropathy) so I was hoping that there was an underlying viral cause to these that MMS would sort out.

Not to be beaten and having been advised to do Protocol 2000 I have ordered ready made MMS2 from www.mineral-solutions.net/ and will take a 4 day break while I travel then try Protocol 2000 for a couple of weeks.

I do understand that I may have the “auto-immune” type of diabetes so none of this may work but will give it (and MMS2) some more time and see what happens. I am no doctor but I guess if my issues were originally viral which programmed my immune system incorrectly, MMS’s may well kill the virus(es) but the immune system would still be triggered by my own similar valid tissues like the Islets of Langerhans and the myelin sheaves (in the case of CIDP).

I will update this post if I have any progress. Paul

I have chronic Neuro Borreliosis, in other words Lyme Disease in third stage.

The symptoms (some but not all) are severe headaches, especially in the back of the head. These headaches are caused by massive amounts of ammonia that is produced by the the Borrelia bacteria.

Furthermore pains in mussles, strong morning chills, low temp feavers, very!! foggy brain, paralizing feeling in palm of hands, changes in perception of length of extremities, stumbling walk, loss of congnitive function.

I am using MMS now for two months. The great thing about this product is that it kills the Borrelia quite fast and sufficient to have much less pain in the brain. I have been on painkillers for 18 months and had to stop, so fortunately MMS came allong.

At this moment I use 7 drops 5 to7 times a day, so that is quite a lot.

The last few days I started to note a difficult feeling in the liver, as if too much chlorine (or some chloor product) was accumulating in the liver.

That is why I have started to research what the long term negative effects might be of taking this amount of MMS.

7 times 7 drops is a little more that Mr. Humble suggests, for strong treatment protocol. So I’m taking this daily to have the pain reduced, it is one of the other at this moment.

I have heard and experienced that Phenylbutyrate (Brands: Buphenyl and Ammonaps) is very good in reducing the ammonia ammount in the brain, it really helps. However Phenylbutyrate is expensive – you need 500 – 1000 mg a day – and can only be supplied through MDsubscription.

But MD’s are not knowledgable in this area and refuse to supply this to me. I live in Amsterdam, The Netherlands

So I’m looking for supplier or MD that is willing to sent it to me without subscription for a reasonable price.

Will continue use of MMS, I use ozone sauna for 2 hours a day to feel better when too much regular MMS is getting me ill.

My experience so far is that MMS does reduce very well the pain in the brain but has very little effect of killing the CWD forms as well as the cysts and spores forms that Borrelia uses to hide itself in the body. So it does kill the spyrocheet forms, but leaves the rest allone. This means that after about 3 hours you have to take it again to reduce the pains

I’ve had slow, but steady improvement on salt & C which took me from mostly housebound, on a walking frame & dying, to traveling overseas last year & not well, but actually having a life.Throughout my 29 year Lyme battle I’ve had flickery vision with flashing lights and blind patches. Kind of like a permanent migraine. It has been torturous, very disabling & stopped me driving my car. I could not cope with glare or sudden changes in light & dark. I had to wear sunglasses a lot and also sleep with a small night light on. On waking, the flickering would be very bad and I presumed it was due to poor circulation. Eye docs and neurologists could not explain it, other than a rare form of permanent migraine or spasms in the tiny veins in the eyes. Magnesium did not help the spasms.

I have been on 5 drops of MMS morning & night for 7 months, stilltaking 2 doses salt & C during day.I have to tell you, the 29 year spasms are nearly gone!!!!!!!!! I have slept without a night light for 2 weeks with no problem!!!!!! I am driving again the last few months and finally without sunglasses!!!!!!!! I wake in the morning and can cope if a light is turned on suddenly!!!!!!!

Yahooooooo!!!!!!!!!!!!!!!!

I think the MMS is killing a virus or something that salt & C was not killing. I am also walking miles every day, my cheeks are pink and my circulation is so much better. People everywhere are noticing how much better I look. I am even feeling well enough to look for a part-time job soon.

Persevere. It is worth it.

Rosemary.