Re: Re: Anyone ever heard of PCA RX chelation treatment?

[Guest guest]

,

I am going to buy the book --actually I think I have it and need to find it

and re-read it.

My questions is:

We went to DAN docs and tried various forms when our son was younger. They

didn't work --very little came out. Then finally we did IV for seven

months, and tons of mercury, lead, aluminum, arsenic, and even uranium came

out. but sadly our son started to have asthma attacks after the treatment.

The first time the doc said it was " coincidence. " (Gee, where have i heard

that before?). so we went back two weeks later and did IV DMPS/EDTA again

and sure enough, he had another asthma attack. So we took a break, but over

time I could see my son regressing in certain areas (stimming mainly). Then

in June of this year we went back and just did IV EDTA, and we noticed gains

and a lot of lead, arsenic, uranium and other stuff came out, but after a

month of treatments (once a week) our son had another attack!

So now what? It seems he developed an allergy to sulfa in '07 when the

first attacks started because after that he broke out in hives after eating

broccoli and since he gets infections easily, he was put on Bactrim for

something and broke out in hives!

So how are we going to safely do Andy's protocol? Do parents just do it or

do they have a doctor oversee it and check blood work routinely. I know my

son is high in heavy metals (he was even diagnosed with this quietly at our

major children's hospital). They were so " hush-hush " about it.

I know we need to chelate, but how do we do it if our son is allergic to

sulfa drugs and even some sulfur containing foods? He eats eggs and doesn't

break out. I just don't get it.

Any info you could send me would be appreciated.

Thanks,

Haven

[Guest guest]

Dear ,

I can't thank you enough! I will find info on the sulfur exclusion diet,

and then order the hair test.

We had one done when he was two, but he is now almost eleven, so I am

guessing we need to re-do it. Once I have instituted the diet and get the

hair test results back, I will post the results, and in the meantime I will

be reading Andy's book like crazy.

For the tests that do need to be run, who do families usually turn to?

Ethan had low neutrophils after regression, and he had hyperbilirubin anemia

after birth and had to be hospitalized for it, so I worry about kidney and

liver function as well as the neutrophil count. He has been diagnosed with

a non-specified immune disorder, so I just want to proceed carefully and

know hat to do, but I know one thing for sure:I want to get this toxic

overload out of my son's body!

My son swallows capsules easily, but is there a way to do both oral and

transdermal? I was just wondering if we could o capsules during the day and

transdermal at night so that I don't have to wake him up (he has sleep

issues, and if I wake him, he may not go back to sleep). I am assuming we

get the capsules at a compounding pharmacy. Don't we have to have a

prescription? Who would write this for us?

His DAN gave us Natural Cellular Defense drops to put him on. We have not

started this.

Also, is a urinary porphyrins test not reliable?

Thanks so much for all your help.

Haven

[Guest guest]

Thank you for all the answers. His urinary porphyrins always have shown him

to be moderately high in mercury and very high in lead.

I will did out his first hair test and post and see what you all think.

So, Andy, if we just choose to go with the transdermal --mainly because then

we would not have to wake him and I could just wake up and rub it on him

during the night, and that way I am thinking we would go with a four hour

interval all through -- is this amenable or should we just realize we need

to do it every three hours. I can do this. How much less effective is

transdermal than oral? Are they equal in efficacy?

Thanks so much.

Haven

[Guest guest]

Andy,

I am anxious to get started but I do have to look at the sulfite issue and

the high molybdenum, and get him in the right place. I need to read and

study!

I still need an answer as to how I get the right transdermal at the right

dosage. I know I go to the compounding pharmacy, but do I need a script?

You say not to go to this doctor again, and to tell you the truth, I have

many reasons why that is a good idea, but then who do I take him to to do

testing? Does anyone on this board know for a doctor in the DFW area who

will order the tests as I need to get them done?

Andy, I am kicking myself. I spent a lot of time on this board in the

beginning and just got so side tracked and busy, and now I have come back to

the realization that I wish I had started with your protocol. My son has

improved so much, I do feel blessed, but his immune issues and stimming

remain, and he continues to store toxins from the environment. I think he

will probably need to do chelation all his life ---maybe not as often, but

when we chelated regularly (before the reactions) the levels came down, and

when we stop, they go back up. This tells me his body just can't do it on

its own.

Thanks for all your help, Andy.

Haven

[Guest guest]

So I would use only ALA with him and not DMSA or DMPS?

Haven

[Guest guest]

Dear Andy,

Your answer to Haven about* testing*:

" If he needs testing, see a regular health plan doctor.

No testing is necessary to 'track' proper chelation. "

makes me think about my situation. We are stuck and we haven't started yet

chelation with my almost 5 year old son

only because of testing.

First his zinc levels (low red) that aren't changing from 2 years even with

high supplementation,

and now his inflammatory small bowel disease that we have to treat with

Prednisolone and Entocort.

What do you suggest me to do.

Can we start chelation using AC protocol in this situation?

Thank you so much,

God bless you

Mimoza, 's mom

On Tue, Aug 3, 2010 at 12:18 AM, andrewhallcutler <AndyCutler@...>wrote:

>

>

>

>

>

> >

> > Andy,

> >

> > I am anxious to get started but I do have to look at the sulfite issue

> and

> > the high molybdenum, and get him in the right place. I need to read and

> > study!

> >

> > I still need an answer as to how I get the right transdermal at the right

> > dosage. I know I go to the compounding pharmacy, but do I need a script?

>

> Just mix the contents of some ALA capsules in hand lotion.

>

>

> > You say not to go to this doctor again, and to tell you the truth, I have

> > many reasons why that is a good idea, but then who do I take him to to do

> > testing?

>

> If he needs testing, see a regular health plan doctor.

>

> No testing is necessary to 'track' proper chelation.

>

>

> Andy

>

> http://www.noamalgam.com/index.html

> Amalgam Illness: Diagnosis and Treatment

>

> http://www.noamalgam.com/hairtestbook.html

> Hair Test Interpretation: Finding Hidden Toxicities

>

> http://www.noamalgam.com/nourishinghope.html

> Nourishing Hope for Autism: Nutrition Intervention for Healing Our Children

>

> http://www.noamalgam.com/biologicaltreatments.html

> Biological Treatments for Autism and PDD

>

>

>