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Re: UT for HVC was Frustration setting in.

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--- In , " Kat " <makiah@...>

wrote:

>I'm beginning to give up hope here.

>

> I feel like I should just accept the inevitability that HCV is not

> going to get killed by MMS and I should just learn to live with

that.

>

> I know I've been so positive. But right now I'm feeling hopeless.

>

>

Hi Kathy,

Since there as been some discussion on urine therapy, I thought I'd

tell you about a woman who has hcv that does UT and says she is only

get better and better, plus she spends her time taking care of her

disable husband.

If interested, look more into it. Sometimes there is an adversion to

the thought of it, but for those that it works for, they swear by it.

I have tried it in the past. You can ease yourself into it by

collecting you urine first thing in the morning and safe until you

are ready do to any enema. Do a water enema first to clean the

bowels then follow that with an urine enema and retain it for 20-30

minutes as possible. Sometimes you will be able to retain it that

long, other times you will need to eliminate quicker. Just relax and

go as you body allows. IF you are thorough with the water enema

first, you will have more success with the urine enema. Might want

to just put your feet up and take a nap.

The woman I mentioned says she does this several times a week, and

only is getting better and better.

Worth a try.

Gail

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>

> Hi Kathy,

>

> Since there as been some discussion on urine therapy, I thought I'd

> tell you about a woman who has hcv that does UT and says she is only

> get better and better, plus she spends her time taking care of her

> disable husband.

>

>

ps. She also uses DMSO with the urine for better results. gail

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Now that does sound interesting.

I'm very good at enemas, but the last time that was mentioned, it

went in one ear and out the other. |:-0

How does she know she is getting better?

Kathy

> >I'm beginning to give up hope here.

> >

> > I feel like I should just accept the inevitability that HCV is not

> > going to get killed by MMS and I should just learn to live with

> that.

> >

> > I know I've been so positive. But right now I'm feeling hopeless.

> >

> >

> Hi Kathy,

>

> Since there as been some discussion on urine therapy, I thought I'd

> tell you about a woman who has hcv that does UT and says she is

only

> get better and better, plus she spends her time taking care of her

> disable husband.

>

> If interested, look more into it. Sometimes there is an adversion

to

> the thought of it, but for those that it works for, they swear by

it.

>

> I have tried it in the past. You can ease yourself into it by

> collecting you urine first thing in the morning and safe until you

> are ready do to any enema. Do a water enema first to clean the

> bowels then follow that with an urine enema and retain it for 20-30

> minutes as possible. Sometimes you will be able to retain it that

> long, other times you will need to eliminate quicker. Just relax

and

> go as you body allows. IF you are thorough with the water enema

> first, you will have more success with the urine enema. Might want

> to just put your feet up and take a nap.

>

> The woman I mentioned says she does this several times a week, and

> only is getting better and better.

>

> Worth a try.

>

> Gail

>

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