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Hi ,

> i seen on the website that ddi has a hair mercury test you can do at

home do

> you thin i will get the same results from that as i would some other

type of

> test what do you suggest i could use all the help i could get

> thank you

Any of the hair tests can be accomplished at home. I recommend

that you get the " hair elements test " . It does

require a doctor's signature. You can order it through

Direct Lab Services for $79.

there is more information here:

/files/HOW_TO_hair_test

best wishes,

Moria

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Where do you live?

Do you have any reasonable kind of insurance?

Do you think you can get some vitamin C powder of the buffered kind -

like sodium ascorbate - and put it in his juice or water and get him

to drink 1/8 to 1/4 tsp of that during the day each and every day?

This does sound complicated (and it does not sound like you got very

repsonsible medical help) and will take some effort to sort out.

Mercury may well be a contributing factor.

Andy . .. . . . . . . . .

> hi

> i briefly wrote in the other day and it was suggested that i explain

more in

> detail so here goes. lets see i had a not so normal pregnancy i had

> preclamsia toxemia and had to be induced at 37 weeks for high blood

pressure

> and did receive a rhogam shot. i was on magnesium sulfate for about

4 days

> and then it took a total of 5 to have him. he was fine first apgar a

8 and

> second a 9 everything seemed fine, 6 pounds 8 ounces.

> i wanted to breast feed but for some reason he was not interested i

suspect

> they fed him in the nursery so he went to sleep in his little bed

next to me

> and i woke up and he was blue i got the nurse in time and they

recesitated

> him but no oxygen left his blood. they ran all kinds of tests but

found

> nothing wrong said it was SIDS. so we went home after 3 days had

things as

> normal as could be with that heart monitor contraption lol. at three

weeks he

> got a fever and we took him to the doctors they admitted him and

found he had

> viral menigitis. (all the while i had my second rhogam shot and i am

> nursing). after a few days of antibiotics he came home and they

again said he

> was fine. but he always had problems with spitting up i put him in

his car

> seat to sleep till he did not fit in it anymore. he had phenomena

and milk in

> both lungs at 5 and again at 6 months he was hospitalized again and

after a

> bit came home all the while he never crawled walked sat up or

anything not

> till after a year and they said he will catch up he will be OK.

finally at

> almost 2 i took him to Kennedy kreiger children's hospital and said

he cant

> talk can barely walk i cant take it anymore please help me and they

did a

> full work up found damage to the white part of the brain, he has

cerebral

> palsy it affects the muscles in his face so he cannot really swallow

good or

> talk good but he can walk and all. he has very low tone. he has

awful

> tantrums very bad rages hair pulling of his own head banging and he

is just

> so autistic they say he is not but he knows where everyone lives and

the

> exact way to get there he knows what he wants and fabric and color

trust me

> if it has to be that way it does or else. he sounds to me like he is

mercury

> toxic he has all the symptoms and they seem to get worse. and sadly

to say he

> got all his immunizations i did not know about all of this until

recently and

> after his last set over the summer he went so loopy more tantrums

then ever

> holding his breathe and everything.

> i seen on the website that ddi has a hair mercury test you can do at

home do

> you thin i will get the same results from that as i would some other

type of

> test what do you suggest i could use all the help i could get

> thank you

>

>

>

> [Non-text portions

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hwy

my insurance is not that good they dont want to do anythign that is not a

shot or he will ok .. it is ridiculous you ask about anything like viatmin c

or someting and they say i would give antibiotics or some crap liek that for

everything i can just call and they send big bottles of cough syrup. i meani

dont give it to my kids but that is what they do.. do you think it could be

the mercury i want to get him this test i am ver excited to try for some

help. i am goign to try the vitamin c to thank you for the help keep giving

advice anything you think of thank you very much. joey

i am in maryland

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>>>>>>i seen on the website that ddi has a hair mercury test you can do at home

do

you thin i will get the same results from that as i would some other type of

test what do you suggest i could use all the help i could get

thank you

<<<<<<

This is the test we used (DDI) and it indicated toxicity in both my boys. I

began chelation in June and both have improved significantly. One has

Asperger's the other has Dyslexia. The Dyslexic child is doing very well in

school. My Asperger son has always been a whiz at academics. Like your son

he's had behavioral challenges that are finally becoming under control. He was

originally dx'd as CP with ADD. He has always been challenged by small motor

skills, eating, drinking, hand usage, etc.. Everything has improved through

chelation.

aGet more from the Web. FREE MSN Explorer download :

http://explorer.msn.com

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Fully read and understand what chelation is about. Get yourself very familiar

with it. You don't have to do the test, and if you feel comfortable you can do

this without the help of your doctor. Finding a doctor to assist would be nice,

but many of us have found no one to help. I do this on my own, but I did not

start until I felt comfortable and knowledgeable about what I was doing.

aGet more from the Web. FREE MSN Explorer download :

http://explorer.msn.com

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The first part of your story definitely sounds like metal toxicity.

Plus because he stopped breathing while sleeping, I would suspect

antimony as well as mercury. Scroll down my page here to the antimony

section, and be sure you are not using flame-resistant pajamas for

him, and be sure you wrap his mattress, etc. I have quite a few

informative links under antimony.

http://www.danasview.net/metals.htm

finally at

> almost 2 i took him to Kennedy kreiger children's hospital and said

he cant

> talk can barely walk i cant take it anymore please help me and they

did a

> full work up found damage to the white part of the brain,

This may or may not be correctable or he may or may not be able to

work around it. But even if it is permanent, there are many things

you can do to improve his life in other ways.

>> he has cerebral

> palsy it affects the muscles in his face so he cannot really swallow

good or

> talk good but he can walk and all. he has very low tone.

Some kids have CP, or their CP is aggravated, by gluten. So you might

want to consider removing gluten from his diet

http://www.gfcfdiet.com/

>> he has awful

> tantrums very bad rages hair pulling of his own head banging and he

is just

> so autistic

Remove milk and other high phenol foods

http://www.danasview.net/phenol.htm

You can also consider enzymes

http://www.houstonni.com/

http://www.kirkmanlabs.com/

> got all his immunizations i did not know about all of this until

recently and

> after his last set over the summer he went so loopy more tantrums

then ever

> holding his breathe and everything.

This is your sign that metals are at least part of his issues.

http://www.danasview.net/chelate.htm

Dana

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,Many of us have found that insurance won't cover the things that will

really help and have paid out of pocket for them in order to get better. Sad

and unfair but true. S--- On Sun 12/01, & lt; ummezahid@... & gt;

wrote:From: [mailto: ummezahid@...] @...:

Sun, 1 Dec 2002 07:52:44 ESTSubject: Re: [ ] Re: HELP more info on

my son please help nowhwymy insurance is not that good they dont want to do

anythign that is not a shot or he will ok .. it is ridiculous you ask about

anything like viatmin c or someting and they say i would give antibiotics or

some crap liek that for everything i can just call and they send big bottles of

cough syrup. i meani dont give it to my kids but that is what they do.. do you

think it could be the mercury i want to get him this test i am ver excited to

try for some help. i am goign to try the vitamin c to thank you for the help

keep giving advice anything you think of thank you very much. joeyi am in

maryland

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Hi ,

JMHO, but as well as getting the hair test, I'd suggest his going on a

gf/cf/sf (gluten free/casein free/soy free) (www.gfcfdiet.com) diet and/or

investigating using enzymes (www.houstonni.com). A lot of parents on the

list have found these to be useful before and during chelating, and after

chelating you may even be able to drop the diet and supplements.

Also, pick up a copy of Children with Starving Brains, by Dr. McCandless

(hi Jacquelyn).

http://www.amazon.com/exec/obidos/tg/detail/-/1883647096/qid=1038771909/sr=8-1/r\

ef=sr_8_1/104-9203012-0044719?v=glance & s=books & n=507846

Good luck, my 5 year old regressed at 18 months, we started DAN protocol at

three (diet and supplements with secretin) and now I consider him no longer

autistic though still on the spectrum. The few rounds of DMSA and ALA were

very useful in creating cognitive and allergy improvement and we plan to

continue.

Avril, mom to Gerry (2/19/97)

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