Re: Don't piss your life away.....drink it.

[Guest guest]

I also had a strong reaction about a month ago, really unpleasant,

and it took a week before I got up the courage to try any at all

again. It felt like my electrolytes were messed with. It all started

when I tried a day time dose, all my other doses are at night. About

2 weeks ago, I started again with one drop and kept at one drop for

at least a week. No cramps or runs or nausea. So far so good.

In November when I started MMS, after the first few days of the

jumpy feeling, it really helped my sleep. I have had sleep problems

for years due to hormone changes with menopause. The one or two

drops was not helping my sleep and I was waking at around 2 a.m.

Then I remembered that at about 4 drops I slept like a log. So for

the last 2 nights I have upped it to 4 and slept the best in a long

long time I am a big believer in the healing power of sleep,

good sleep that is.

Best of luck,

Jill

[Guest guest]

Hey Ballady,

I am doing UT still. I do the first morning catch also. I have noticed

that now that I am doing MMS with the UT that sometimes the morning

blast of UT will cause me to be a little queazy. I think I am

recycling some of the MMS back in. Has this ever happened to you?

Olive

---

In , " ballady4 "

<ballady4@...> wrote:

>

> Hi Olive!

>

> This is so great to hear! I am happy for you as I know you have had

> chronic problems with your neck since developing LD.

>

> I am finding that I do better with small doses of MMS, not more than 6

> drops once a day, and after I do this for a week I take 3 or 4 days

> off before resuming. I had a very strong reaction a month or so ago

> and it took me a long time to receup from it. Since that episode, my

> body cannot tolerate higher doses.

>

> Are you still doing UT?

>

> I celebrate your success with MMS!

>

> Ballady

>

>

> > > > >

> > > > > Yes, I have been doing urine therapy (UT) for about 8 months.

> > > > >

> > > > > Ballady

> > > > >

> > > > > --

> > > >

> > >

> >

>

[Guest guest]

No, but I take MMS in the late morning, not in the evening as many

here do. Maybe it is mostly out of my system by the next morning.

Ballady

> > > > > >

> > > > > > Yes, I have been doing urine therapy (UT) for about 8 months.

> > > > > >

> > > > > > Ballady

> > > > > >

> > > > > > --

> > > > >

> > > >

> > >

> >

>

[Guest guest]

I like the link mineral deficiency the cause of many desease but taking 10g of salt per day for lyme that news to me. I accasionnaly take 2 g of natural salt in a glasss of water and my body tells me I am doing the right thing. I have more than a few floaters in my eyes and from the look of them they remind me of morgellons or those lyme fibers.

[ ] Re: Don't piss your lifeaway.....drink it.> > > salt/c is a protocol for Lyme Disease> > Ballady>