DMSO and MMS/CA spine rub gone wrong...has burned my back

Blessed/smartyme,

Try putting some wet clay on your out break, and then going to sleep ... they will dry them up and inactivate them.

C

Blessed.

I just sent it to you. Check your email. Once you have the English version, we need to figure it out how to make it public. It has some graphic pictures.

Update:

I have been problem keeping up the 15 drops of mms, before there was no problem I threw it up 2xs, yesterday possibly because I ate bread and cheese and dairy does not mix with mms, and today because I did not have enough food in my stomach. I don't know what to eat in the morning, usually it was cereal or oatmeal (without milk) never any meat etc, I don't know what to eat this has been a very lengthy journey... I wonder why other people are able to get rid of this in 1 month and it is taking me so long.

I continuously get those nerve twitches, all over my body especially in my face, honestly I feel that I haven't changed at all sine I started mms about a month and 2 weeks ago. I feel the the herpes symptoms have rocketed and have been further aggravated by the mms. I constantly touch my face because I feel something walking like bugs etc but they are the nerve twitches. I continue to take mms because this is the only thing that has cured others, I dont know what to do.

I don't feel 100% right now I am a bit nauseous but in 20 I will take another dose hopefully I can keep it down. ANYONE please let me know what to eat in the morning. Also as part of the symptoms I get nerve pain in my left foot and I also get really itchy on the sole of that foot.

I dont trust Doctors because I went 3 times trying to get tested for hsv, one time I had a sore although not big it was there it looked like a mosquito bite, they doctor took a sample came back negative. The second time the doctor inspected visually, again nothing, the 3rd time they did blood works... really? and nope negative that was about 9 months after expected of exposure and it returned negative. It was deficient in vitamin D, low white and red blood cells and the doctor didn't even prescribed anything, I nurse insisted I should ask him. Also i had to literally fight and argue about getting the suppression drug and they kept telling me that it will get better with time and it will come and go, when this thing can go to my head or kidneys. I really dont know what to do, I dont know what to do now? why am I getting nerve twitches soo bad it's like they are aggravated, and the mms is not staying in my stomach after I was able to before?

I really want these nerve twiches to end and these OBs, I hate it I can't have a normal life. Also I now that organic virgin coconut oil help take the coating of the virus, but since I cannot eat it anymore because of antioxidants that contradict the mms,when I shower I rub it on my spine around my tail bone and around the neck, where the ganglia where the virus lives and I wake up with a MAJOR back pain (observation).

Once again please, what to eat for breakfast. Thanks

Sally

Hi sally,

Try a protein based breakfast, eggs, sausages, bacon. It doesn't sound to healthy but I find protein is better to help the MMS down, but that could just be me.

I just have eggs for breakfast.

The same thing happen to me with the MMS. I was taking 6-drops hourly for weeks and had no problems, then all of a sudden I was getting watery diarrhea, nausea and general malaise. So I cut back on drops, went to 3-drops hourly, but I wasnt happy with it cos I felt I wasnt getting a strongest enough dose, but the above mentioned symptoms stopped.

I have now gone back to 6-hourly drops with no problems.

Maybe you should decrease the number of drops for a week or so. Basically listen to your body.

As for the nerve twitches, the nerve twitches in mt cheek stopped since using the DMSO topically.

I still have the twitch in my knee and in my other foot now but I have been applying the DMSO to those areas too since I notice the difference it made to my face.

I dilute my DMSO and spray it more frequently rather than using it undiluted and causing skin irritation. Using it undiluted caused my skin to burn, scab and then feel like sand paper.
So I rather spray 3-4x daily with a weaker dose that I can manage than 2x a day torturing myself.

@Blessed

I also have had sharp deep pains in both feet that blistered than the 2 blisters went away after a month, same on my left leg near my ankle...and they have never come back.

I agree with Delite's response to you.
Keep eating lots of protein - this helps me keep the mms down too...now if only the nausea, fatigue, potential obs and dizzyness would go away everything would be all right lol!

@ Research,
Why caused those blisters on your feet?

I feel really week because I threw up so much today, I drank some water with calcium clay and that helped a bit, just now. I just don't know why after a month and 2 weeks I am still getting OBs, this is ridiculous, I will back down on the dosing. But also this damn nerve twitches, my eyes where moving by themselves and today after I threw up I saw what seem to be a vein in my hand twitching, I mean you can literally see the parts twitching on your body. I some times get nerve pain.

Sall

Blessed,

not sure what it was...maybe a mini ob or hopefully die-off...who knows.

I also get twitches on my legs and arms it`s weird ...your doing something then a twitch comes on and it continues for quite a while amazing....these things never happened to me when i was not taking mms. I believe its a good thing, it has to be the mms duking it out with herpes. The nerve pain is the worst...the pain is brutal!

your eyes were moving by themselves!!...what the heck is that all about!!

Maybe you should cut back a bit...its a nasty thing but you can beat it.
hang in there! You will win.

lmao...."your eyes were moving by themselves!!...what the heck is that all about!!"..
lol..hahah funny, I mean my eye lids, you know when you feel your eye twitching, well you can actually see it, its funny per se, but it is scary and disappointing when this happens. May I ask you, where you able to get rid of hsv if you did have it? I just wonder because it is taking be long and my symptoms are increasing, as I type I have to stop to scratch my face because I feel these nerve twitches... so annoying.

Update:

If anyone can help me please help me, I am documenting my use of mms of if you can help please do so.

Today I did not take mms, I don't know if you can reach a point where enough is enough because I can't even smell it, I have been taking it in capsules to avoid the taste. Yesterday I was in pain and three up 4 times, I had a horrible night and woke up a lot, I woke up very late today since I was unable to sleep. I had weird dreams involving a colorful snake that bite me while I was trying to give an antidote to some children that where infected and then I tried to take the antidote myself..loll so weird. Also yesterday before bed since I kept throwing up I took organic extra virgin coconut oil and put 2 to 3 drops of DMSO and rub it around my lower back and around the neck and the ganglia where the hsv virus hides, supposedly the this is good against herpes internally but since I cannot consume it due to antioxidant properties I did it topically

As I said I did not take mms today, I have been taking this for over a month, close to 2 months and suddenly I am not able to take the large dose that I worked so hard to try to get up to. I really hope that I don't have to start from the beginning ...loll I understand that other people my have more serious illnesses but I just refuse to share my body with this nasty virus, when this was done in such a bad way to me. I have so much nerve feeling all over my face, I feel little bigs or something especially on my legs and face. since I was 7 years of I have always wanted to get married and be a mother, that's why I went into education, I refuse to leave my goals.

I will continue mms for 3 more weeks and them I will be doing one of those 7 days protocols.
I will continue to post my progress, I currently continue to feel these annoying nerves, I feel like I might be getting an OB on my mouth.


sally

Hello,

Herpes is one of the hardest to get over. It does take more time with some people.

With MMS try to make a full days dose so you can add your 1/8 teaspoon of baking soda, which will help than taking it without. Also adding your dmso drops will help as well as you are doing.

Try not to do more than 3 activated drops per hour. doing 10 or 15 drops a couple or a few times a day in a herpes protocol will take forever and ever from my results of people who have done this. Herpes needs to be attacked for as many hours per day as possible. Only way to get it gone especially in bad cases. If MMS gets to be too much try to take CDS doses for half your doses per day, keep in mind to always take MMS2 with Herpes if possible. Some people disagree with this and that is fine....many people are different. If ways work for you....then do it!

It seems from your previous statements that you angered the heck out of the herpes to where you are getting horrible breakouts. This usually occurs in the first 2-3 weeks of a protocol depending on the strength of your herpes. However yours came in the 6th week (give or take) which means " You were driving it out " and it cannot stay in your body. You were and are doing so great....do not give up. It is a nasty thing having this disease...you are right.

Stay on your protocol...whichever that may be....but try to take as many small doses per day as possible. When you get up in the night to go to the bathroom or wake up with a bad dream...take another. Gotta get em and get em and get em til they cant take it anymore and you will WIN.

It gets very depressing for some like your self when you've tried so hard for the last 1-2months and you still have OB's. It dose get everyone down. Just keep in your head that this will work and it will. Stay positive. Stress causes your immune system to go down and the herpes will stay strong. Try to be positive and keep up all of your good work! You can do this!

Take Care as always,

John