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RE: chelation questions - Rochelle

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Hi , thanks for the reply!! I am so glad to hear that your son

is doing so well. I am so anxious to see some results. I am also scared

that I will get my hopes up and nothing will happen. It seems like that

is the way it always goes with Cayla. I have tried so many things with

really no progress. I have always known she was mercury poisoned. Now

that I am finally doing the ALA it really gives me hope. How long

before you started seeing results?? I will end up doing the DMSA at a

later date, but just wanted to start with ALA first.

Rochelle

Re: [ ] chelation questions - Rochelle

Rochelle,

ALA should work for your daughter. I don't think it matters if ASD is

regressive or not. She was obviously exposed to mercury during your

pregnancy or in

her early days. My 5 year old is not regressive, yet ALA has helped him

tremendously. We started with DMPS for three months and when we added

ALA, really

great things started happening for him. We're on round 22 now, and he

is

really doing great.

Jukoski

In a message dated 10/30/2004 1:38:01 PM Eastern Standard Time,

writes:

> Hello I started chelating my daughter yesterday with ALA only. I am

> doing every three hours 3 days on 4 days off. I was wondering if

I

> started at 8 am Friday morning and I end on Sunday night is that ok,

or

> should I go till 8 am on Monday. I know that is probabley a stupid

> question but just wondering. Also yesterday she had bad diarreah

three

> times. Could this be from the ALA. I am giving her 2.5 mg every three

> hours. She is 22 lbs 23 months old. Also I was kinda looking for

> support. I was wanting to hear some stories of people that have used

ALA

> only with an ASD child that does not have the regressive type ASD. My

> daughter showed signs from three weeks old. Does this usually help

with

> this type ASD?

>

> Thanks for the help!!!!

>

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, when you added the Ala, what did you notice? Are you doing the

transdermal DMPS along with the ALA? Did a doctor recommend this or

did you decide to try it? Kristy

On Oct 31, 2004, at 8:32 PM, JLJukoski@... wrote:

> Hi Rochelle,

> I have worked very hard to find the right answer for my son.  We've

> been

> trying to figure it out since he was two, and now he is five.  He has

> been doing

> the Feingold Diet for almost two years and " biomedical " treatment for

> over a

> year.  I was very excited to begin chelation with him, which we

> started in May. 

> But even though I had read so much great stuff about it and even

> though I was

> very dedicated to following through completely with chelation, I was

> still

> not sure if it would really work.   The whole concept can seem a bit

> unbelievable.  My husband didn't believe in chelation or any other

> biomedical treatment. 

> He kind of viewed it as my hobby!  But now that my son is doing so

> well, my

> husband does believe in chelation and other biomedical stuff.  You

> just have to

> have faith that it will work.  Cayla is very likely going to be

> helped with

> chelation.  Most kids like her are.  And since she is so young, I

> think you

> will see results more quickly.  My son has received every ASD

> diagnosis, but I

> think that PDD is what fits him best.  He has responded to chelation

> very

> quickly - not quite sure why, but we are pleased.  Part of the reason

> may be that he

> has never had yeast and has never had gut issues.  With DMPS, we saw

> gains

> with every round.  After round 10 of DMPS, the total of the gains was

> pretty big

> and continued getting bigger quickly.  We added ALA at round 12, and

> after a

> couple rounds with ALA, he started becoming quite normal.  With every

> round of

> ALA, he is more and more normal - really more than I ever thought he

> could

> be.  He is on round 22 this weekend.  We will continue for the full

> two years. 

> Also, ALA alone can be difficult on the child because of

> side-effects.  We use

> very high dose vitamin C to eliminate the side-effect issues.  Hope

> this

> helps you!

> Jukoski

>

> In a message dated 10/31/2004 8:55:05 AM Eastern Standard Time,

> writes:

>

>

> > Hi ,   thanks for the reply!!  I am so glad to hear that your

> son

> > is doing so well. I am so anxious to see some results. I am also

> scared

> > that I will get my hopes up and nothing will happen. It seems like

> that

> > is the way it always goes with Cayla. I have tried so many things

> with

> > really no progress. I have always known she was mercury poisoned.

> Now

> > that I am finally doing the ALA it really gives me hope.  How long

> > before you started seeing results??   I will end up doing the DMSA

> at a

> > later date, but just wanted to start with ALA first.

> >

> >

> > Rochelle

> >

>

>

>

>

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julie and rochelle,

thanks for sharing! julie, your story sounds so familiar. my daughter is

also 5. she became autistic with her 18 mo vaccinations. i have tried everything

out there since she was 2 to get the mercury out. unfortunately, she has the

yeast and gut issues. she remains nonverbal. i signed the papers last week for

DMPS and am doing the waiting game. i pray that this is our answer. thanks

again! angie from ohio

Kristy <K@...> wrote:

, when you added the Ala, what did you notice? Are you doing the

transdermal DMPS along with the ALA? Did a doctor recommend this or

did you decide to try it? Kristy

On Oct 31, 2004, at 8:32 PM, JLJukoski@... wrote:

> Hi Rochelle,

> I have worked very hard to find the right answer for my son. We've

> been

> trying to figure it out since he was two, and now he is five. He has

> been doing

> the Feingold Diet for almost two years and " biomedical " treatment for

> over a

> year. I was very excited to begin chelation with him, which we

> started in May.

> But even though I had read so much great stuff about it and even

> though I was

> very dedicated to following through completely with chelation, I was

> still

> not sure if it would really work. The whole concept can seem a bit

> unbelievable. My husband didn't believe in chelation or any other

> biomedical treatment.

> He kind of viewed it as my hobby! But now that my son is doing so

> well, my

> husband does believe in chelation and other biomedical stuff. You

> just have to

> have faith that it will work. Cayla is very likely going to be

> helped with

> chelation. Most kids like her are. And since she is so young, I

> think you

> will see results more quickly. My son has received every ASD

> diagnosis, but I

> think that PDD is what fits him best. He has responded to chelation

> very

> quickly - not quite sure why, but we are pleased. Part of the reason

> may be that he

> has never had yeast and has never had gut issues. With DMPS, we saw

> gains

> with every round. After round 10 of DMPS, the total of the gains was

> pretty big

> and continued getting bigger quickly. We added ALA at round 12, and

> after a

> couple rounds with ALA, he started becoming quite normal. With every

> round of

> ALA, he is more and more normal - really more than I ever thought he

> could

> be. He is on round 22 this weekend. We will continue for the full

> two years.

> Also, ALA alone can be difficult on the child because of

> side-effects. We use

> very high dose vitamin C to eliminate the side-effect issues. Hope

> this

> helps you!

> Jukoski

>

> In a message dated 10/31/2004 8:55:05 AM Eastern Standard Time,

> writes:

>

>

> > Hi , thanks for the reply!! I am so glad to hear that your

> son

> > is doing so well. I am so anxious to see some results. I am also

> scared

> > that I will get my hopes up and nothing will happen. It seems like

> that

> > is the way it always goes with Cayla. I have tried so many things

> with

> > really no progress. I have always known she was mercury poisoned.

> Now

> > that I am finally doing the ALA it really gives me hope. How long

> > before you started seeing results?? I will end up doing the DMSA

> at a

> > later date, but just wanted to start with ALA first.

> >

> >

> > Rochelle

> >

>

>

>

>

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Hey , thanks for emailing me back. Well we just finished round

one last night, and overall she tolerated it very well. You mentioned in

your email about side effects with ALA only. What are they?? Is it

normal for the child's first day off the round to be a bad day. My

daughter is not eating well today and crying a lot. Her dark circles

look a lot worse also. Last night she was in her swing (Yes She still

likes to swing) and she was laughing non-stop for about an hour at

nothing. I know this is yeast, and I upped her GSE. I also have her on

Olive leaf Extract. I hope it helps. Anyway I appreciate the advice.

Thanks for listening. Rochelle

Re: [ ] chelation questions - Rochelle

Hi Rochelle,

I have worked very hard to find the right answer for my son. We've been

trying to figure it out since he was two, and now he is five. He has

been doing

the Feingold Diet for almost two years and " biomedical " treatment for

over a

year. I was very excited to begin chelation with him, which we started

in May.

But even though I had read so much great stuff about it and even though

I was

very dedicated to following through completely with chelation, I was

still

not sure if it would really work. The whole concept can seem a bit

unbelievable. My husband didn't believe in chelation or any other

biomedical treatment.

He kind of viewed it as my hobby! But now that my son is doing so well,

my

husband does believe in chelation and other biomedical stuff. You just

have to

have faith that it will work. Cayla is very likely going to be helped

with

chelation. Most kids like her are. And since she is so young, I think

you

will see results more quickly. My son has received every ASD diagnosis,

but I

think that PDD is what fits him best. He has responded to chelation

very

quickly - not quite sure why, but we are pleased. Part of the reason

may be that he

has never had yeast and has never had gut issues. With DMPS, we saw

gains

with every round. After round 10 of DMPS, the total of the gains was

pretty big

and continued getting bigger quickly. We added ALA at round 12, and

after a

couple rounds with ALA, he started becoming quite normal. With every

round of

ALA, he is more and more normal - really more than I ever thought he

could

be. He is on round 22 this weekend. We will continue for the full two

years.

Also, ALA alone can be difficult on the child because of side-effects.

We use

very high dose vitamin C to eliminate the side-effect issues. Hope this

helps you!

Jukoski

In a message dated 10/31/2004 8:55:05 AM Eastern Standard Time,

writes:

> Hi , thanks for the reply!! I am so glad to hear that your son

> is doing so well. I am so anxious to see some results. I am also

scared

> that I will get my hopes up and nothing will happen. It seems like

that

> is the way it always goes with Cayla. I have tried so many things with

> really no progress. I have always known she was mercury poisoned. Now

> that I am finally doing the ALA it really gives me hope. How long

> before you started seeing results?? I will end up doing the DMSA at

a

> later date, but just wanted to start with ALA first.

>

>

> Rochelle

>

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