Re: Don't piss your life away.....MMS

[Guest guest]

Hi Olive,

So good to hear your report! I'm happy for you. I know you didn't see

much result from salt/c so this is encouraging for you.

I just started a couple of weeks ago on MMS. I'm on a low dose,

trying to work up. I still need to take a couple of days of break

from it because of herxing.

Blessings,

Avril

In , " oliveo13 "

<oliveo13@...> wrote:

>

> Hi Ballady,

>

> I just wanted to respond here with an update on my condition as you

> and I are on about the same therapy. We started UT about the same

time

> and when you posted back in December with your improvements from

MMS I

> started that also. As of late I have really been having some great

> improvements and it is so exciting.

>

> The muscles on the right side of my neck have been useless /infected

> /atrophied since early 2003. About a year ago I started having a

> little bit of muscle or tendon movement in my neck again. Just very

> little. After starting UT in July of 2007 I made some big gains and

> had quite a bit more muscle response.

>

> I started MMS the end of December, slowing increasing to 4-6 drops

3x

> a day. Yesterday, for the first time in 5 years, the large muscle in

> my neck, called the SCM, started moving. It feels so wonderful.

Today

> I had even more movement. It is very sore as this muscle has not

moved

> in 5 years but ITS ALIVE!!!!!

>

> As far as the salt/c, I pretty much have abandoned it but do salt my

> food liberally (very, very liberally sometimes) and eat 1-4 servings

> of vitamin C fruit daily.

>

> Thanks so much for sharing your MMS experience, Ballady as that is

> what really got me started on it. Life is getting easier!

>

> Olive

>

[Guest guest]

Hi Avril,

I did have some benefit that I attribute to salt/c but I was on it for

about 16 months and did not have enough improvement to convince me

that it would totally get me better. How much improvement did you have

on the salt/c?

When I first started MMS I had a lot of diarrhea which I still get

every few days or so but not everyday like I was having. I think it

will take me awhile to get up to a full dose although I'm not exactly

sure what a full dose would be. I am thinking for me maybe 8-10 drops

3x a day. It seems I do better when I take the MMS every 4-6 hours so

that is why I want to do it 3x a day. As we take this journey I'm sure

there will be variations in how each of us handles it and people also

seem to vary quite a bit how much they do depending on the herx and

how they otherwise feel.

Nice to hear from you, Avril. I look forward to reading your progress

reports in the future.

Olive

> >

> > Hi Ballady,

> >

> > I just wanted to respond here with an update on my condition as you

> > and I are on about the same therapy. We started UT about the same

> time

> > and when you posted back in December with your improvements from

> MMS I

> > started that also. As of late I have really been having some great

> > improvements and it is so exciting.

> >

> > The muscles on the right side of my neck have been useless /infected

> > /atrophied since early 2003. About a year ago I started having a

> > little bit of muscle or tendon movement in my neck again. Just very

> > little. After starting UT in July of 2007 I made some big gains and

> > had quite a bit more muscle response.

> >

> > I started MMS the end of December, slowing increasing to 4-6 drops

> 3x

> > a day. Yesterday, for the first time in 5 years, the large muscle in

> > my neck, called the SCM, started moving. It feels so wonderful.

> Today

> > I had even more movement. It is very sore as this muscle has not

> moved

> > in 5 years but ITS ALIVE!!!!!

> >

> > As far as the salt/c, I pretty much have abandoned it but do salt my

> > food liberally (very, very liberally sometimes) and eat 1-4 servings

> > of vitamin C fruit daily.

> >

> > Thanks so much for sharing your MMS experience, Ballady as that is

> > what really got me started on it. Life is getting easier!

> >

> > Olive

> >

>

[Guest guest]

Olive,

I was on salt/c from August 2006 to March 2007. When I was tested on

a Voll type diagnostic machine all my systems showed up better than

they had ever been. Later, a similar machine did not show up Lyme so

much as Babesia. I never got beyond 5 or 6 grams a day because I was

interrupted by a huge mistake made when we repaired a bathroom. We

used regular grout sealer which made the whole house toxic to me. I

ended up living in the mountains with friends from May to September

and this made it difficult to keep up with detox, etc. I did notice

less sinus infection and some infections on my face went away...while

on salt/c.

When I came back to Lymestrategies, I found everyone raving about MMS

so that led me here. I have been slowly trying to ramp up on salt/c

but can't seem to do it very well. I'm also slowly ramping up with

MMS. So we'll see. It seems like a constant dance of killing Lyme &

Co., detoxing and nourishing organs that have been compromised by

Lyme.

You sound you're well on your way with this protocol. I look forward

to your progress reports, as well.

Avril

In , " oliveo13 "

<oliveo13@...> wrote:

>

> Hi Avril,

>

> I did have some benefit that I attribute to salt/c but I was on it

for

> about 16 months and did not have enough improvement to convince me

> that it would totally get me better. How much improvement did you

have

> on the salt/c?

It seems I do better when I take the MMS every 4-6 hours so

> that is why I want to do it 3x a day. As we take this journey I'm

sure

> there will be variations in how each of us handles it and people

also

> seem to vary quite a bit how much they do depending on the herx and

> how they otherwise feel.

>

> Nice to hear from you, Avril. I look forward to reading your

progress

> reports in the future.

>

> Olive