Is there anyway to calm down mercury after it's been stirred up in the body?

[Guest guest]

This week I had the sharpest increase in mercury symptoms since I got

my fillings removed (over 6 months). I didn't do anything, I don't

get it? It was actually so strong that my driving was impaired.

Anyways is there anyway to speed up the process of calming stirred up

mercury? It usually takes 5-7 days for me to feel better when this

happens. Some times more.

[Guest guest]

>

> My symptoms were severe mental health problems. I'm currently taking

> a two week break from chelation that's why I don't understand why I

> had such a huge surge in symptoms.

>

It seems that while chelating with Andy's protocol (taking small doses

of chelators at the half life) the metals keep moving constantly. It

is when chelation stops that the moving metals latch on to sites in

the body where they weren't before (redistribution) starting up

symptoms. This has been my experience exactly. I feel fine as long

as I keep chelating. Every single time I stop chelating I get huge

symptoms, always the same ones so it is completely reprodicible. I

have found that some of the symptoms hit the day after I stop and some

(like pain) hit a week or so after I stop. That's why I decided to

chelate continuously for now.

J

[Guest guest]

This is only my opinion, but I believe that it is not a good idea for

a person who is metal poisoned to be using more metal, even to relieve

symptoms. My entire family has extremely high silver according to our

hair tests. I don't know for sure why this is, but we have, perhaps

twice a year over the past 7 years, used a bit of colloidal silver for

sore throat or flu symptoms. Silver poisoned people have very

uncomfortable symptoms too. Also, I wonder if the mercury causes the

silver to stay in the body more than if there were no mercury? Be

careful not to make yourself sicker.

Cutler says, " The effectiveness of chelation for removing silver is

unknown but it can be tried using DMSA or DMPS with alkalinization of

the urine, along with ALA. " page 249 in Hair Test Interpretations.

>

> Okay, I am going to tell you what I have done in thepast and I'm

okay with you giving me feedback, etc. I can relate to this also. I

have come to the tentative conclusion that it is fungus, yeast,

bacteria, or whatever that is getting into the brain or is already in

the brain. The way I solved this problem was to make my own colodial

silver (remember to strain it in coffee filters. This is very

important.) I put it in a spray bottle and squirt it into my mouth

when I get those kinds of symptoms. I was breaking the protocol rules

for awhile because the symptoms were so bad and I'd stop whenever they

got real bad usually cutting my round short and not doing three days.

I did this for about a month until I started supplementing with

silver. Now I'm on a round and this is my fifth day and still no

symptoms. I'm doing 200 mg of the R-alpha lipoic acid which is

supposed to be equivalent of 400 mg of regular alpha lipoic acid. I

use no DMSa or DMPS. This is what worked for me.

[Guest guest]

This is only my opinion, but I believe that it is not a good idea for

a person who is metal poisoned to be using more metal, even to relieve

symptoms. My entire family has extremely high silver according to our

hair tests. I don't know for sure why this is, but we have, perhaps

twice a year over the past 7 years, used a bit of colloidal silver for

sore throat or flu symptoms. Silver poisoned people have very

uncomfortable symptoms too. Also, I wonder if the mercury causes the

silver to stay in the body more than if there were no mercury? Be

careful not to make yourself sicker.

Cutler says, " The effectiveness of chelation for removing silver is

unknown but it can be tried using DMSA or DMPS with alkalinization of

the urine, along with ALA. " page 249 in Hair Test Interpretations.

>

> Okay, I am going to tell you what I have done in thepast and I'm

okay with you giving me feedback, etc. I can relate to this also. I

have come to the tentative conclusion that it is fungus, yeast,

bacteria, or whatever that is getting into the brain or is already in

the brain. The way I solved this problem was to make my own colodial

silver (remember to strain it in coffee filters. This is very

important.) I put it in a spray bottle and squirt it into my mouth

when I get those kinds of symptoms. I was breaking the protocol rules

for awhile because the symptoms were so bad and I'd stop whenever they

got real bad usually cutting my round short and not doing three days.

I did this for about a month until I started supplementing with

silver. Now I'm on a round and this is my fifth day and still no

symptoms. I'm doing 200 mg of the R-alpha lipoic acid which is

supposed to be equivalent of 400 mg of regular alpha lipoic acid. I

use no DMSa or DMPS. This is what worked for me.

[Guest guest]

>

> So are you sayin it could be the two week breaks that is the problem?

> And I should only take 4 day breaks.

>

> I was actually considering chelating every other weekend.

>

I am saying that what worked for me was to chelate continuously with

DMPS. I still consider what I am doing to be a variation on Andy's

protocol - I got the idea from him. I think I might be the only

person on this forum chelating continuously, so I probably am

confusing people when I talk about it.

In your case it might help to take 4 day breaks or it might help to

lower the chelator dose. If the dose is lower there won't be as much

metals stirred up during chelation and the end of round symptoms won't

be as severe.

There also may be supplements/medications that may help. To determine

which ones might help a person really needs to review pages 133-167 of

Amalgam Illness - not an easy job, I know.

J

>

> > >

> > > My symptoms were severe mental health problems. I'm currently

taking

> > > a two week break from chelation that's why I don't understand why I

> > > had such a huge surge in symptoms.

> > >

> >

> >

> > It seems that while chelating with Andy's protocol (taking small doses

> > of chelators at the half life) the metals keep moving constantly. It

> > is when chelation stops that the moving metals latch on to sites in

> > the body where they weren't before (redistribution) starting up

> > symptoms. This has been my experience exactly. I feel fine as long

> > as I keep chelating. Every single time I stop chelating I get huge

> > symptoms, always the same ones so it is completely reprodicible. I

> > have found that some of the symptoms hit the day after I stop and some

> > (like pain) hit a week or so after I stop. That's why I decided to

> > chelate continuously for now.

> >

> > J

> >

>

> So are you sayin it could be the two week breaks that is the problem?

> And I should only take 4 day breaks.

>

> I was actually considering chelating every other weekend.

>

[Guest guest]

>

> So are you sayin it could be the two week breaks that is the problem?

> And I should only take 4 day breaks.

>

> I was actually considering chelating every other weekend.

>

I am saying that what worked for me was to chelate continuously with

DMPS. I still consider what I am doing to be a variation on Andy's

protocol - I got the idea from him. I think I might be the only

person on this forum chelating continuously, so I probably am

confusing people when I talk about it.

In your case it might help to take 4 day breaks or it might help to

lower the chelator dose. If the dose is lower there won't be as much

metals stirred up during chelation and the end of round symptoms won't

be as severe.

There also may be supplements/medications that may help. To determine

which ones might help a person really needs to review pages 133-167 of

Amalgam Illness - not an easy job, I know.

J

>

> > >

> > > My symptoms were severe mental health problems. I'm currently

taking

> > > a two week break from chelation that's why I don't understand why I

> > > had such a huge surge in symptoms.

> > >

> >

> >

> > It seems that while chelating with Andy's protocol (taking small doses

> > of chelators at the half life) the metals keep moving constantly. It

> > is when chelation stops that the moving metals latch on to sites in

> > the body where they weren't before (redistribution) starting up

> > symptoms. This has been my experience exactly. I feel fine as long

> > as I keep chelating. Every single time I stop chelating I get huge

> > symptoms, always the same ones so it is completely reprodicible. I

> > have found that some of the symptoms hit the day after I stop and some

> > (like pain) hit a week or so after I stop. That's why I decided to

> > chelate continuously for now.

> >

> > J

> >

>

> So are you sayin it could be the two week breaks that is the problem?

> And I should only take 4 day breaks.

>

> I was actually considering chelating every other weekend.

>

[Guest guest]

>

> So are you sayin it could be the two week breaks that is the problem?

> And I should only take 4 day breaks.

>

> I was actually considering chelating every other weekend.

>

I am saying that what worked for me was to chelate continuously with

DMPS. I still consider what I am doing to be a variation on Andy's

protocol - I got the idea from him. I think I might be the only

person on this forum chelating continuously, so I probably am

confusing people when I talk about it.

In your case it might help to take 4 day breaks or it might help to

lower the chelator dose. If the dose is lower there won't be as much

metals stirred up during chelation and the end of round symptoms won't

be as severe.

There also may be supplements/medications that may help. To determine

which ones might help a person really needs to review pages 133-167 of

Amalgam Illness - not an easy job, I know.

J

>

> > >

> > > My symptoms were severe mental health problems. I'm currently

taking

> > > a two week break from chelation that's why I don't understand why I

> > > had such a huge surge in symptoms.

> > >

> >

> >

> > It seems that while chelating with Andy's protocol (taking small doses

> > of chelators at the half life) the metals keep moving constantly. It

> > is when chelation stops that the moving metals latch on to sites in

> > the body where they weren't before (redistribution) starting up

> > symptoms. This has been my experience exactly. I feel fine as long

> > as I keep chelating. Every single time I stop chelating I get huge

> > symptoms, always the same ones so it is completely reprodicible. I

> > have found that some of the symptoms hit the day after I stop and some

> > (like pain) hit a week or so after I stop. That's why I decided to

> > chelate continuously for now.

> >

> > J

> >

>

> So are you sayin it could be the two week breaks that is the problem?

> And I should only take 4 day breaks.

>

> I was actually considering chelating every other weekend.

>