Interesting symptoms taking MMS anyone had this or can anyone comment?

Darren
I got over the allergies rather quickly.
Started getting better with first drop.
That was a Friday. Monday I could breathe thru nose 1st time in 15 years. Tuesday I was at 12 drop doses. About ten days later I stopped using MMS.
Waited several weeks and restarted.
But it would have been in the first 10 day period that many issues receded for me, including allergies or level of reactions to allergens. Receded enough that I could break from MMS therapy and rethink my position.
6 weeks later I began my 1st 100 days...

Rev Ray
That's awesome, sounds like your allergies were as bad as my brother's. He can only breathe through his nose after a couple of weeks of eating what his body allows, which isn't much of a selection, so he lives with the blocked nose. Hopefully soon he will make the 12 hour drive out here again and I can get him on the protocol. I will post the results when the time comes.

Darren70

One of the first changes in my body was my Sinus. Normally I got sinus infection in Ohio during the winter time. After my first three drops, the first reaction was my sinus that clear with the first shot. And never be a problem after that. I finished protocol 1000 in two weeks period because basically Im not really sick, so then i continue with the maintenance 6 drop (12 after activation) shot every night. And now every morning I wake up breathing clear.

FWIW = "for what it's worth"

Rev Ray - this is certainly in line with my thinking. Previous to becoming unwell I didn't have any allergies etc then after whatever happened I seemed to have issues with all sorts of things. I figure getting rid of the core underlying issue would be the way to go, still avoiding foods etc i react to in the mean time.

Thanks Suzanne, this is in line with what I have been thinking.

richiek wrote: Hi there

I have had Chronic Fatigue type symptoms for over 15 years which has been incredibility frustrating. My symptoms seem to get worse in the winter time which seems odd to me. Last winter things got really bad, extreme fatigue, very blurry vision, a lot of mucus type discharge coming out of my eyes, difficulty concentrating etc. A friend had told me about MMS so i decided to take it. After about 3 days my vision had become clear and i started to have much more energy. After about 3 weeks I was feeling quite a bit better, not perfect but decided to stop taking it to see what happened. After a while my symptoms got worse again.

Best regards

when you wake up after sleep (5 or more hours) check in the mirror if your tongue is white.

any doctor can argue to you against this practice of take medicine some days "only for see what happens", virus and co. not are idiots and learn to defense so doing this you are working for your enemy. I do not believe in antibiotics so I don't take this sh?t in a silly game with my and others health.

richiek, I to have had the same symptoms with fatigue and my main issues were breathing. Shortness of breath, pain in my chest, burning sensation in my throat along with lots of mucus. I was afraid to go to the doctor because I was afraid he would tell me I had cancer. I was so sick. I thought maybe to it could be horrible allergy reaction to mold in the house we were renting. In December we moved into a new home and made sure we check for any dampness and there wasn't any. I also started taking mms. Slowly things began to improve and I actually felt healthy again. I did the 3 week protocol and felt normal again so I stopped taking it. I had developed a strong dislike to the taste and smell. After being off a few weeks the symptoms began to slowly reappear. And before long they were back with a vengeance. Also having extreme fatigue. The dr thinks maybe reactive hypoglycemia. I am back on mms and mms2 now (protocol 2000). It took about a week but I'm starting to feel human again. Not sure what's causing my symptoms but I do know that now that I have discovered MMS0 (thanks Ray) I will never be off mms ever again. Hope this helps you. And get you some gel caps and an eye dropper (I use a small syringe) and go MMS0 (tasteless).

Now faith wrote: Now that I have discovered MMS0 (thanks Ray) I will never be off mms ever again. Hope this helps you. And get you some gel caps and an eye dropper (I use a small syringe) and go MMS0 (tasteless).

Both MMS original and CDH have great Capsule potential.

I truly believe that MMS capsules will be the Future delivery vehicle of choice, that can bring back so many users of MMS who have the reaction U&I do to MMS smell and taste, who have quit and even lost the battle now have a real tasteless opportunity for healing.

I think the reaction is cellular.
That whatever bug is inside of us, when we smell it, it smells it, and excretes into our body stuff that makes us ill just to smell CD and that causes the aversion. The bug knows whats in store for it so its defense creates our aversion. I am testing that theory.

This is the first I've mentioned what I think on this and is not G2C position. Just my own thoughts but I'd be happy to hear what others think causes the aversion. Or how.

Post MMS0 to your fave social media sites.
World needs'a healin'.

It's funny that now every time I'm around tap water I smell that smell. Kinda makes me shrudder just to wash dishes or walk into the bath. I am still dealing with sinus issues so I'm trying to also stay with the breathing of the gas but only briefly. And I don't do it as often as I should.