Pain is an unpleasant sensory and emotional experience that signals actual or potential tissue damage and serves as a protective warning mechanism for the body. It can be acute, arising suddenly from injury, inflammation, or illness, or chronic, persisting for months or longer and often associated with ongoing medical conditions. Pain may be localized or widespread and described as sharp, dull, throbbing, burning, or aching, depending on its cause and the nerves involved. It can originate from musculoskeletal injury, nerve damage, internal organ disorders, infections, or inflammatory diseases. While pain is a normal physiological response, persistent or severe pain can significantly affect physical function, mood, and quality of life and warrants medical evaluation to determine the underlying cause.
MMS use reduces tooth and head pain after root canal
Hey I got some mms success
Should not have ate those cookies:
I got a root canal started, which cost alot, but was unable to finish it due to cashflow. They opened the tooth and did whatever they had to do, and then patched it up with the porcellin filling, but left the nerve in, which they were suppose to take out on round 2. Had a bad tooth ache all day yesterday could not even bight down, which lead to a bad head ache.
No Problem, whipped out the mms, put some in my mouth and let it sit on the tooth for about 5 minutes. Did this a few times, pain is gone, no more head ache, no more tooth ache, well its about 95% gone, i just fill a little tention but i can still eat on that side now.Should not have ate those cookies:
Stomach tumors reduced; pain disappeared within days
A couple of months ago i was informed a good friends wife had been diagnosed with stomach Cancer. She had several Tumors in her stomach. 1 as big as an Orange, another Egg size and several others Olive size. She was having lots of pain. I told them to check out MMS as I thought it would help. They read up on it, found the product and activator the Citric Acid and started taking it right away 2 times per day worked up to 3 x 2 per day. With in a very short time 1-2 days the pain was gone. After 2-1/2 weeks she had acquired a lot more energy. I think this means she is winning??
PGH 7-17-08
Flickering vision improves significantly after MMS and salt C use
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.
Incredible energy, like never before since taking MMS.
My husband and I have been taking MMS for just over a week. We have tried all sorts of things for our health before, but this MMS has been the best so far. We started off with 2 drops + 5 drops citric acid + wait 3 minutes then added water. Almost straight away we felt something. It almost felt like we were ‘out of it’. We could feel it moving around the body with obvious sensations.
By that evening after having another 2 doses, our eyes felt like they were really wide open. Each day we have been increasing our dose. I got to 5 doses but then felt extremely nauseous and dizzy. So I cut back on the amount. We continue to take it and I am slowly increasing the doseage. We have incredible energy, like never before since taking MMS. My head experiences large moments of clarity instead of the foggy mist it normally feels like.
I am very excited about it. My friend who had a sore tooth for quite awhile now, swirled it around in her mouth and straight away the pain went.
Woman recovers mobility after using MMS supplement
The case of the lady that lay in bed unable to move for 8 years.
This is May 1, 2008. About one month ago there was a knock at the door here at my friends place in Mexico and in walked a very pretty Mexican lady. She was carrying a large envelop which I recognized as such an envelop that would have x-rays and other records. And that was exactly what was in the envelop. She said that she wanted us to see that she had evidence to back up the story that she was about to tell us.
There were quite a few x-rays of her back and legs and other bones. These x-ray showed the evidence why she was unable to walk and move to any extent for 8 years. In the year 2000 she had been 47 years old, now she was 55 and very happy.
She said that in the year 2000 she began to get back pains and leg pains. The doctor said it was rheumatoid arthritis. Her pains continued to get worse and finally she had to take to her bed during the year 2000. It continued to get more painful to move and the muscles drew up so that she couldn’t move much anyway.
Her hands started to resemble birds claws and she could not use them. Her eyes dried up requiring someone to drop tears into her eyes on a continuing basis, and her mouth went dry so that she also need continuous water for her mouth. She told us that she no longer wanted to live. The pain and constant need for help was more than she could stand. She wished for death.
Then only one month before she came to see us, someone took a bottle of MMS to her and suggested that she take some according to the instructions on the label which was to start at one drop and increase one drop each dose if possible. Well, she worked up to 7 drops only, but in one month she was back on her feet, walking normally, and when she walked into our house here no one would have imagined that she had been in bed for 8 years.
She looked very good. She was taking 7 drop doses twice a day, and she told me she intended to continue right on up to 15 drops twice a day. She shook my hand and gave me a big hug. She said that we could have her records but we didn’t have a place for them. She said that she would keep them and that if anyone ever wanted to ask her about her experience she would be happy to show them.
She left walking normally without even a limp. The only thing left was that she still needed to put artificial tears in her eyes from time to time. She had been a law student in 2000 and she wanted to return to her studies.
So do you see why I called the MMS a Miracle Mineral?
MMS use reduced ingrown hair swelling and improved clarity
I have been reading the post for a week or so. I just got my mms yeasterday. I started last night with one drop. This morning I ended up taking more like 5 or 6 drops. I am a 39 year old with no large known medical problems. I do suspect that I have quite a problem with candida, and my lung collapsed a couple of years ago. I also have a mouth full of metal fillings.
When I woke up this morning I did notice that an ingrown hair that I have (in my underware line area) doesn’t seem to bother me today, and the swelling seems to be down from yesterday. I have had them pretty persistantly for several years….could be candida related?? I also feel as though I have more clarity then I have had for a long time. I smell completely different. I got out of the shower and smelled pool!!! I am a smoker (bad I know)and I smell so different!I also feel as though I am extremely bloated tody.
I was a little quesy yesterday with one drop, so far no big D. Yesterday I mixed with a lime I had around, I mixed todays with a bottle of lemon juice and was wondering if anyone could tell me if that is okay. I didn’t seem to get as quesy so I am wondering if it counteracts at all. I am using distilled water until I can’t take it, then I will switch to juice.
{4/21/08}
I have been taking mms for 4 days or so. I ramped up fairly fast and took 1 drop first time, then 6, and 8 the next day, 8 and 10 the day after that, 10 and 11 the next day. This morning I skipped. I only had intestinal cramping one day (day before yesterday), and mild d the same day.
I ate an orange today, I hadn’t had any mms for 12 hours or so but my stomach really cramped up and I thought I was going to be ill. It passed after a few minutes, but I wouldn’t consume oranges while taking the mms.
I really didn’t realize how often I eat! It is hard to find anytime other than first thing in the morning that I have an empty stomach.
I have no major known illnesses but my lung collapsed a couple years ago, and suspect I have a candida issue. Yesterday I had the thickest mucusy taste all day. I was also coughing and it felt thick. I really think that it does go right to the area that needs help.
I am getting ready to go in and take it, but I am having to make myself do it despite feeling it is doing good work.
Also the tip about immediately rinsing your mouth really does help! Thanks again
Lyme disease with neurological symptoms shows improved fasciculations and f
{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
Cancer marker levels rise despite MMS supplementation and symptom escalatio
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.