I don't think it's the least bit odd that people are posting breathing
problems. When I first found this board in early December there were many
posts about people getting bad colds and a lot of the "supporters"
replying to the effect that "it's just a healing crisis" or some such
thing. It is remarks like that which cause people to refrain from posting
I too had breathing difficulties at the 15 drop level with a vinegar
activator. Yet I don't see that as a real problem because it only lasted
for a few minutes, but it was definitely there. I'm not going to press it,
but I am much more in touch with my body than a lot of folks and I can feel MMS
entering me through my tongue and throat. When it hits those places at the
high dosage, that's when it also odor wise, affected my breathing for a
while. A portion of the MMS solution stays in that area, and that's what
caused my breathing problems, the continuous vaporization from those places
which got into my lungs.
I have granulomas in my lungs which are what my body created to surround and wall
off the active TB that entered there. The TB germs are still alive and
active even after more than 70 years. My condition is not unique.
Many people have active TB in lung granulomas decades after their
exposure. However, if in fact MMS breaks down those walls, then it is
capable of releasing active TB in me and anyone else who has them.
I think that by chastising people on this forum who have negative experiences
with MMS, it discourages the posting of negative experiences. This is a
support forum - for both negative and positive outcomes.
I'll probably continue to use mine as a mouth wash - it is a good plaque