RE: testimonial

[Guest guest]

Hi and all-

I’m new to the group and have

finally read most of the messages in the archives (well, I read forward from

300). I’ve been taking MMS for a few weeks and (very conservatively) am

taking 8 drops at bedtime, increasing very slowly (I tend to get migraines from

too much detoxing at one time). I have Lyme. So far I’ve notice a fairly

significant increase in energy (chronic fatigue has been my main symptom –

Lyme for 20 years).

, would it be OK to share your

testimonial with a couple of Lyme groups in which folks are using MMS?

Thanks,

Dana

From:

[mailto: ] On Behalf Of

I have reported before that MMS made my breathing

easier. Here's what happened last night.

I was born with asthma. Had it all through my

childhood and though I outgrew it as a young adult it left my lungs

compromised--meaning that if I exerted myself I wouldn't be able to

breath deep. There were many times that I'd still have asthmatic spells

of short duration. If I was in a damp environment it would be hard for

me to breath.

I started taking MMS, only 6 drops a day. I noticed

better breathing in just 2 days, but in only less than 3 weeks I am now able

to breath all the way to lung capacity. I can fill my lungs completely

with air and not cough or have that catch that happens. And last night

I went to a concert held in an underground cave. It was quite a ways

down--and going down is always easy. ;-) But coming up, I pushed

myself to keep up with the group as we were leaving so as not to block anyone

behind me. When I got to the surface I had to sit down and catch my

breath for 3 to 4 minutes before breathing slowed down to normal.

BUT--the whole time I was puffing and panting was just from being physically

out of shape and had nothing to do with my lungs, because I, miraculously was

breathing deeply, filling my lungs, no catching, no heat/pain in the lungs

from exertion, no coughing. I was pretty darn impressed!! That

has never happened to me before in my life.

Samala,

[Guest guest]

Of course. The more people know about how many ways MMS can help them, the better.

Samala,

-------Original Message-------

, would it be OK to share your testimonial with a couple of Lyme groups in which folks are using MMS?