Hi. My name is Victor Summers and I am suffering from HIV, Severe COPD, as the doc describes it, with emphysema and other stuff I will share as time goes by. Today I started with my first dose of the mms. I have read about half of the posts made and will finish them.

I wanted to use this thread as a way to keep record of my progress and let others use it as a testimonial.

I have been on HIV meds for two years and my viral load is <50 (under 50) which is considered undetectable. My Tcell count is at 500 and something. I just happen to have noticed I have thrush today so instead of using the thrush meds I will look to see the progress I will make with mms. I will also be looking for my COPD to improve which is the biggest thing to me at this point because the HIV is under control but my COPD is really causing me lifestyle problems like being out of breath all the time, plus my chest is very tight to the point it hurts. I also have an enlarged prostate gland and I feel sharp pains coming from that area often (a few times a day.) So will also be looking for that to improve. I would like for this to be documented in the greatest way possible so I will cooperate with anyone in making that posible so we can have the proper documentation to prove the claims I believe I will be making :) I'm going to stay on my HIV meds for now just to see how this first step goes. I took 1 drop in citric acid with apple juice about three hours ago now and will determine tomorrow if I am going to increase it or not and will keep my progress posted here. There are other things wrong too and will mention them as I discover them improving (like my energy.) After reading so many of the posts already, I feel I know some of you and I am very impressed and am so very happy to make your aquaintance. {5/1/08} Day 2 of my MMS experience. Well, I woke up this morning feeling like crap. I could barely get out of bed. After taking my son to school I came home and slept till 2:45 pm. I havn't slept so soundly in a very long time. It reminded me of how I slept when I was a teenage boy. After being awake for a while I started feeling better and I also noticed my lungs seemed to be working better. I have not taken any of my albuteral today, which is highly unusual. I decided not to take my Spiriva and see what tomorrow is like. While writing just now I realized that the tightness in my chest is also much better. I also coughed up some nasty mucus today. My sinuses are dripping I think. There is a weird feeling in them anyway. My joints are hurting also. I had a white spot on my uvula which I noticed yesterday while checking to see if this weird looking bubble was still on my uvula, which it was, but the white spot is gone. The bubble (which looks like a blister) looks the same. It has been there for many years now. My doctors could not tell me what it is. They didn't have a clue. I had a brainstem stroke in 1999 so am anxious to see if my brain improves as a result of taking MMS. I have also been diagnosed with Peripheral Vascular Disease and my legs hurt most of the time and both of my feet have numbness in them. I will see if I experience any improvement in that area as well. I am sticking to one drop until I start feeling better. I'm still tired and feeling blah, like you do when detoxifying. The most important thing for me is getting relief from the COPD and emphysema. My lungs do feel better and I haven't ran out of breath today. And I walked up a hill at my son's baseball practice too. I wasn't even sure I was going to go because of how badly I felt this morning when I woke up, but by 5 pm I actually wanted to go with him. For any readers who may think it may be in my head, I don't care if it is so long as I get relief. I'm serious! LOL {5/4/08} Well, this is May 4th, and I am up to three drops and am feeling very well. Still sleeping like a log but my energy is back up. My COPD acted up yesterday and I had to use my albuteral, but today my lungs feel better again. I seem to be able to breath better -- like my lungs are bigger, if that makes any sense. Oh, well that may be because the tightness in my chest has subsided. Still coughing up green mucus, which started soon after I started using the mms. I feel my strength returning. Feeling more normal and more alive too. My brain fog, which I wasn't that aware of, is lifting and I am thinking better. Just now I noticed I am typing this note without any difficulty or hesitation on my brains part happening. I decided to stop taking my HIV meds. I hope that was a wise choice. But I can always resume them. I have stopped them before and restarted them. I have had chronic diahrea for several years so, for me, I will be seeing if in the long run that improves as well. I hope to see dead parasites soon :) I am also entering into this with a good mental state of mind so I have that on my side. I have a doctor's appointment coming up in a couple of weeks so it will be interesting to see what happens when they give me the "blow" test. Not sure what that is called, but it measures your lung capacity by blowing into this contraption. I failed it so badly the last time that I was diagnosed with SEVERE copd. You know. I am a happy fella and I don't like talking about myself so this is a labor of love, in a way, in hopes that it may help others if it helps me. I don't want people to look at me and think I am ill when my state of mind is so positive and, the truth is, I am not afraid of death. I do, however, want to see my little boy raised.

{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

why do i never get any reply from wanting to ship the book to the UK….

and by the way, i have been taking this product for almost 4 months and the results are like nothing else i have experienced with other health products.

this product is not going to be wanted by not only the pharmaceutical companies but its not going to be wanted by many of the other products that do not do what they say on the bottle….

what i noticed real and objective.

7 drops for first three months apart from 1 day when i had flu so tock 45 drop and the main symptoms where gone in 5 hours.

1. irritable boul gone, had this for over 20 years.

2. massive increase in breathing.

3. indefinitely stronger.

4. improvement in my eye sight.

5. many other little things.

6. brother almost has no asthma now after 3 months.

i was so impressed with this product, i realized that people need it.

i have now started providing it for other people and the feedback i am getting from people that have tried many things for years, but nothing like this……and the people with the more serious illnesses that follow the protocol correctly are seeing wonderful improvements.

I wonder if Jim Humble is fully conscious of what he has let loose in the world? and how this accidental discovery is going and is changing the way people think about illness and disease.

I AM 41 AND I HAVE NOT EXPERIENCED THE HEALTH I HAVE NOW SINCE I WAS IN MY EARLY 20S………………………………………………. physical mental health has improved more in this last 4 months then it ever has in the past…………

i would like to contact Jim Humble for someone that is close to him……

please get in touch ellis_derek@hotmail.com

I am on my fith day of using MMS and here is what I am experiencing so far. Any input anyone has to give would be appreciated.

– I started with 2 drops and stuck with that for my next dose. After that I started going up by one drop each time I take it (twice a day)

– For about the first hour after I take it I feel like like I have a slight buzzing in my head. Also if I do anything like run up the stairs…or lift anything (anything that causes your heart rate to go up) I notice that I get winded a little faster.

– I know I am detoxing because I am a smoker and a heavy coffee drinker and when i wake up in the morning I can feel the lack of caffiene and nictotien in my body.

-However I have not experienced any diarrhea, in fact I did not go at all until the third day of being on this stuff and I consumed quite a bit of fiber to make this happen. But since then I am pretty regular.

-Morning breath is almost non-existant.

{1/18/08}

I will say though that I feel great. I have a 15 month old daughter who has a bad cold and has been sleeping very poorly..which means I have been sleeping very poorly. Not only do I not have the cold, but based on my energy and alertness you wouyld never guess that I am pretty sleep deprived!

Dear All,

Followings were my previous posts:

[This was my post on 1-8-08:

“I have been taking MMS for ulcerative colitis for past 20 days at 5 drops a day and have seen very little/none improvement for which I want to go slow.

The real reason for the post is my mom’s Breast Cancer in her left breast about 3cm. She has started mms with cancer protocol. She is at 18 to 21 drops a day. She had lots of D and nausea. We thought of checking cancer marker CA 27.29 and we did and the results are 86.8 on 12-28-07 and 96.8 on 1-7-08. The mms was started on 12-19-07.

The question is the increase in the reading. Why? She is scheduled for chemo in a couple weeks. We are very much in disappointment.”

Following is the update as of 1-24-08.

My mom is at 6+3+3+3+3+9 drops a day for past two weeks. She had done another CA 27-29 blood test on 1-22-08 and the reading came out to be 87.4. I am not sure weather to call it a improvement for sure. She is also taking the Indian Herb at dinner time only. She has stopped seeing the oncologist for chemo for the time being.

I am at 3+5 drops and yet to see an improvement. My mom stays with me and I am looking for improvement in her situation first. We may continue with the drops and increase a bit for her and then check again.]

My mom had another blood test on 2-12-08 and the reading came out 91.2. She is at 3+3+3+3+3+3 drops a day. She could not handle more drops. She is thowing up, big D and lots of weakness. She was on the Indian Herb but she has stopped since last few weeks due to heavy nausea. At the 18 drops a day she does not have nausea, very little D. Just to keep the track, the readings are 86.8, 96.9, 87.4 and 91.2. I did not see any improvement. Please help. Can she increase the drops and take Imodium(for big D), Tylenol(for strength) and something (?) for nausea. We want to increase the drops and control these symptoms at the same time.

Thanks.

My wife is a Diabetic and also has Cancer (Ovarian) and has been taking MMS for about 2 weeks now. She is up to 15 drops a day and has the big D. several times a day. She Kaopeptate to control it so she can sleep without getting up all night long. Her shots were up to 35 Units in the morning and 25 at night. She is now taking only 25 units in the morning and none at night. I will let you know about her Cancer after she gets her next Blood test in 13 January, 2008. Her last test (CA-125) was up from 290 to 430. “We are holding our breath on this test but have our fingers crossed. She has had 2 operations 1 series of Radiation treatments, 4 different Chemo series treatments before we found out about MMS.

… Two days ago, my sister called me and she can feel a cold coming on. She had visited her son’s family who were all very sick for Christmas. Her throat was starting to get very sore, and she could feel congestion starting to happen. Based on previous experiences, she expected to be sick for 4-5 days and have to go to the doctor for anti-biotics.

I advised her to start with 2 drops activated with real-lime and add 4oz of water. I told her to do this twice that day. The next day her sore throat was just a minor lump in the throat, and she expelled some yellowish mucous. She up the dosage to three drops for that day and did two doses.

I talked to her today and she is very impressed with the results. She can feel some slight symptoms, but is almost back to normal (some tightness in throat, and minor nose issues), but she feels about 95% normal. She is a little concerned that it might be coincidence, but she is willing to use it again the next time. She is planning to send an email to all the family detailing the positive results. Her husband (70’s)has problems with sinus infections and using anti-biotics. I suggested that MMS would be great for him. So she is trying to convince him to try it out…

I am doing the detox program. I am 50 and in reasonable health. I started out with 2 drops twice a day and then the next day went to 3 drops. I immediately noticed energy increase etc… I had my first bad reaction at 8 drops (day 6), I had nausea and went with the flow and purged. Felt immediately better. Held at 7 drops for a few days, and then started to increase. The next bad reaction was at 13 drops at night and 10 during the day. Big D for a few days. Left work early one day with massive headache. Went back down in dosage and then started back up. Big D again, no headache, no nausea. I’ve been holding at 13 at night and 10 or 11 during the day. The big D has decreased significantly, brief nausea for the morning dose, but crackers seem to help. Due to holidays, I have gone up to 15 drops at night which my body seems to handle quite well without sideeffects and over the last few days skipping the day dose. Listen to your body and don’t go too fast, this stuff is powerful. Reducing dosage after Big D sideeffects etc… allows your body to recover from the sideeffects. Its not a race, the tortoise will win and be much more comfortable than the hare.

Benefits:

Alertness seems to be improved.

Improved energy, very obvious during the first week. Now my new normal.

Appetite seems to be reduced

Cravings are gone.

Weight loss is increasing.

Keyloids seem to be getting smaller and smoother.

Skin tags are gone.

Skin seems healthier

Elbows no longer rough and dry. I did have some re-tracement with my elbow problem going to my right hand knuckles, but after 5 days my right knuckles are about 70% back to normal

Knees used to be achy but are fine now.

Sinuses appear to be better. A Q-tip seems to get lost in my ear canals, use to be a tighter fit, now much looser.

General aches pains in legs associated with old age are gone.

Still plan to get to 15 twice a day, but I will take my time. 15 at night now seems to not be a problem, and will slowly get my day dose back up. The big D sideffect was always controllable, but be careful passing wind. The nausea during the morning dose was the most annoying, and that is what led me to the different dose at night versus day. Powerful stuff!

I began taking MMS approximately 2 months ago. I am 60 years old and have COPD (Chronic obstructive pulmonary disease) with chronic asthma, chronic bronchitis and emphysema. I was on oxygen 24/7.

I was not bed ridden, but life was a real struggle. To give an example of how weak I was; I had to sit on a stool and lean on my elbows to brush my teeth because I didn’t have the strength to stand or to hold my body upright while I brushed my teeth.

Each day when I opened my eyes in the mornings I dreaded making the effort to get out of bed. But in only one week after beginning the MMS drops I noticed that I didn’t need my oxygen all the time and that I had strength and could walk easily through my home without gasping for air. I was able to remove the stool and stand to brush my teeth. I opened my eyes each morning looking forward to the day. By the end of the second week I was completely off the oxygen.

I am a new person and getting better with each passing day. I do things now that I have not been able to do in a long time. I vacuum, do laundry and am also able to go shopping. I’m beginning to have a real life. MMS has proven to be a MIRACLE for me and has literally given me back my life. God bless and have a wonderful day.