of GBS and

[Guest guest]

funny how, when you start talking to parents, all of a sudden

you start comparing the similarities .. the couple who introduced us

to Dr G have 3 kids ... they also have a family history of

autoimmune disorders.

I often tell my husband that I'm kind of glad he got GBS.

Otherwise, we would still be doing DAN, probably chelation or transfer

factor ... of course, we're still disappointed with thepediatrician

had

then who told us that there was no way in the world would ever

be affected. My research was saying otherwise ...

but making lemonade out of lemons, we found Dr G.

And quirky that he may be, he's able to connect the dots.

And from what I hear, things are looking very promising.

If you're unable to get out to Calif perhaps Kathy and her folks in NNY

might be able to get you started ..... or even better ...

put Kathy in touch with your local pediatrician. See if you can start a

local

movement ...

doris

-maryland

Posted by: " Rene " joeandren@...

<mailto:joeandren@...?Subject=%20Re%3A%20Trolling%20%2E%2E%2E%2E%20%\

20doctor%20in%20Michigan%3F>

yotengodos <yotengodos>

Mon Jul 16, 2007 5:58 am (PST)

Hi not trying to intrude but, I just read your story and am

flabergasted since it mirrors ours. My son was 8 months when my

husband came down with GBS.

We've only confirmed in the last 2 months that at four he has

autism....but it was shortly after my HB illness that I started

noticing things about my son that doctors kept dismissing when I

brought it up.

How do I go about finding a doctor close by? I've been

searching and haven't come up with anyone. We've been doing DAN in

the meantime (since I can do that at home) with some sucess.

Definetly not as spacey and some pretend play with his twin sister.

I am so mad at myself that I did not push the envelope sooner and do

more research, although I was taking care of my husband so I guess i

have to cut myself some slack....

H