Re: Desperate for Answers...going crazy! - Tickborne Infections

[Guest guest]

What appears to be going on with children with autism, is that they

have immune dysfunction, and have many and varying pathogens and

toxins. What I am seeing is that most seem to need to be treated

for all pathogen types. One can not see bacteria unless they

use a microscope. I have seen others describe what you are

describing in forum posts. I think the medical world is extremely

lacking in parasite (mostly the word parasite is used to describe

worms, protozoa, and amoeba) identification and knowledge in

general. I am seeing many report their children with autism are

testing positive for many of the tickborne infections. The parents

are testing positive as well, even though they have so few symptoms

that they felt they were healthy. It appears that many are carriers

of tickborne infections (can be obtained from sex, during pregnancy

and from lice, fleas, etc.) but only some show major symptoms.

Infants and children seem to be much more likely to show symptoms

from tickborne infections and parasites than adults. Some children

do recover just from treating the tickborne infections, but a lot

also need other treatments for viruses, and the various other

treatments you see in the autism arena. Yes, I would absolutely

seek out treatment for tickborne infections. Join some Lyme forums,

like this one: "BorreliaMultipleInfectionsandAutism" and seek out

docs that know how to test and treat such. Your average doctor is

usually not considered helpful or knowledgeable concerning tickborne

infections, according to my personal experience and what people

report all over this Internet. Many of the autism doctors are aware

of tickborne infections being part of the autism symptoms, some even

feel it's the main part. LLMD's (Lyme Literate Medical Doctors) are

what are considered knowledgeable concerning tickborne infections,

but they may not be knowledgeable about autism. So, you will need

to do more information gathering on what you can afford, have access

to, and believe is the best way of treating for your family. There

are many different ways being used to treat tickborne infections,

just like with autism. As a matter of fact, many, if not most, of

the autism treatments and diets are used by those with chronic Lyme

disease and other tickborne infections.

Love and prayers,

Heidi N

Amidst all the clamor to buy iodine, and take all

kinds of wormwood, black walnut, and olive leaf extract, I passed a

parasite. I did not know what it was. I had seen this for years and

I always

thought it was a piece of undigested cereal floating in the toilet

after I

went. It was yellowish and puffy and the size of my pinkie nail,

only

roundish.

So - I don't eat cereal for the past year -, I am

squeamish but decided for my family's good to look at it closely.

Half of it

had these spider legs looking things all attached in it and through

it. I

looked on the web and found out what it is.

Borrelia Burgdorferi is the name. It is the

bacteria that causes Lyme disease.

There have been a few post on here, I recall, that

discussed Lyme disease. Please can someone answer this post. Please

help me.

I've not been bit by a tic since I was 7 or so. I have 3 children,

and my

oldest has autism.

The site that made most sense to me said that high

dose of vitamin C, coupled with high doses of salt treats it.

Please someone respond to this and tell me what you

know. What does Lyme disease and salt cure have to do with autism.

I'll feed

my son salt all day long if that's what it takes. I just want my son

well. I

want all of our children well.

God bless, Goodman

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