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Re: need advise on ALA

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>

> This is my first post, I am new to this group.

>

> I suspect Hg toxicity even though my CaEDTA/DMPS challenge test had

> nothing in " red " , but many in " yellow " .

Don't let the results of this test confuse you, the numbers are not

useful to make any conclusions about anything (except that you do have

metals in your body, which most people do).

> The test was done before the

> amalgam removal.

You will find that we advise against taking any type of chelator with

amalgam in. What has happened in the past cannot be changed, but

please check with this group before trying anything that this doctor

recommends. His/her methods are harmful.

> I had one mixed-metal amalgam filling in a gold

> crown and 6 " regular " ones.

>

> I have been on ALA (300mg/once day)

I'm sure you know by now that we also recommend against taking

ALA(which is a chelator) with amalgams in and that the only safe way

to use ALA (after amalgams have been removed and sources of exposure

stopped) is in small doses every 3 h per Cutler protocol.

> since mid July 2007, per my doctor

> who said it will help with neuropathy. Since then, my neuro. symptoms

> got worse: ringing in ears, muscle vibration at night. At the end of

> Aug. 2007 I had my first 3 amalgams removed. Tomorrow I am removing

> the last 4.

>

> After reading your postings today, I have stopped taking ALA for now.

Good.

> How do I safely get on a frequent dose protocol after my ALA

" adventure " ?

>

While your amalgams are being removed avoid all chelators.

During this time you can get on a good supplementation program. See

pages 133-134 of " Amalgam Illness " and the " Andy index " (links

section). As you are starting supplementation members of the group

can help you to prioritize.

You may find that dietary changes will help with symptoms. See Andy's

" Diet - How to pick the right one for your kid " in the files section

and ask questions of the group if there are things that you don't

understand yet.

Many people have specific problems that need to be addressed. A hair

elements test from DDI would be the first place to start and possibly

other tests depending on symptoms.

After amalgam removal chelation can begin - see TKs general

recommendations in the files section and Andy's " Amalgam Illness " book.

The only way to reverse the damage that was done with the challenge

test and the improper ALA use is to chelate properly with Andy's protocol.

Good luck

J

> Many thanks,

> SN

>

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TK--- we use hair elements testing for the protocol here - challenge

testing is not informative and very dangerous

>

> This is my first post, I am new to this group.

>

> I suspect Hg toxicity even though my CaEDTA/DMPS challenge test had

> nothing in " red " , but many in " yellow " . The test was done before

the

> amalgam removal. I had one mixed-metal amalgam filling in a gold

> crown and 6 " regular " ones.

>

> I have been on ALA (300mg/once day) since mid July 2007, per my

doctor

> who said it will help with neuropathy. Since then, my neuro.

symptoms

> got worse: ringing in ears, muscle vibration at night. At the end

of

> Aug. 2007 I had my first 3 amalgams removed. Tomorrow I am removing

> the last 4.

>

> After reading your postings today, I have stopped taking ALA for

now.

> How do I safely get on a frequent dose protocol after my

ALA " adventure " ?

>

> Many thanks,

> SN

>

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Share on other sites

TK--- we use hair elements testing for the protocol here - challenge

testing is not informative and very dangerous

>

> This is my first post, I am new to this group.

>

> I suspect Hg toxicity even though my CaEDTA/DMPS challenge test had

> nothing in " red " , but many in " yellow " . The test was done before

the

> amalgam removal. I had one mixed-metal amalgam filling in a gold

> crown and 6 " regular " ones.

>

> I have been on ALA (300mg/once day) since mid July 2007, per my

doctor

> who said it will help with neuropathy. Since then, my neuro.

symptoms

> got worse: ringing in ears, muscle vibration at night. At the end

of

> Aug. 2007 I had my first 3 amalgams removed. Tomorrow I am removing

> the last 4.

>

> After reading your postings today, I have stopped taking ALA for

now.

> How do I safely get on a frequent dose protocol after my

ALA " adventure " ?

>

> Many thanks,

> SN

>

Link to comment
Share on other sites

TK--- we use hair elements testing for the protocol here - challenge

testing is not informative and very dangerous

>

> This is my first post, I am new to this group.

>

> I suspect Hg toxicity even though my CaEDTA/DMPS challenge test had

> nothing in " red " , but many in " yellow " . The test was done before

the

> amalgam removal. I had one mixed-metal amalgam filling in a gold

> crown and 6 " regular " ones.

>

> I have been on ALA (300mg/once day) since mid July 2007, per my

doctor

> who said it will help with neuropathy. Since then, my neuro.

symptoms

> got worse: ringing in ears, muscle vibration at night. At the end

of

> Aug. 2007 I had my first 3 amalgams removed. Tomorrow I am removing

> the last 4.

>

> After reading your postings today, I have stopped taking ALA for

now.

> How do I safely get on a frequent dose protocol after my

ALA " adventure " ?

>

> Many thanks,

> SN

>

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