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[Guest guest]

Hi all! I have decided to get rid of the viruses in my son. I have some

decisions to make though and I need some help. I know I don't know any of you

on this group, other than popping on once in awhile, but this is something you

have all been working on.

I found dr goldberg yesterday and ended up here. I did research and read good

and bad things about the dr.

So I think I have 3 choices:

See if my family dr will work with me, but still I will probably be going it

somewhat alone as far as dosing goes, etc... although I know some of you would

be able to help with that. He may not even be willing.

Find a DAN, there goes alot of money again I am thinking. Been to 2 in my

state so far.

Go see dr goldberg.

Let me tell you a brief history about my son though.

The most important thing is his arachnoid cyst on his left temporal lobe. We

have been thinking, quite a few years have gone by and we should see if it has

grown. We have had 2 surgeons from 2 major hospitals say it was too small to be

causing his seizures and didn't need surgery. Of course meds weren't helping

the seizures either. Dr goldberg would be able to address this for us. I simply

do not want to see a main steam neuro again, it was a nightmare.

They tried 19 different anti seizure meds and at one point he was on 3 different

ones, totaling 17 pills a day. He was a mass of bruises and his hair was

falling out. His eeg was also showing a seizure every minute. He was having

17-25 grand mals a day.

had his first seizure at age 3 and just turned 13. After we ditched the

mainstream drs we started with holistic. We have been to probably 15 and every

single time they have sent us on our way, they could not help us. The monetary

part was huge but most importantly was the time wasted.

Every person we saw claimed they knew how to get better and we had to stop

what we were doing with him. He always regressed. I am afraid of this with dr

goldrberg. We have come to far with to see this happen. I am afraid to

relinquish control. One DAN treated me like I was stupid and even asked why I

had my son on a b-complex. He also asked me who told me to put him on those

supplements. o you can see why I hesitate.

is moving along slowly. He has been on gaps/bed for the last year and we

are seeing slow progress, we never have before. I do not want to give this up

because a dr tells me to.

has no speech, although on a good day he will try to talk. He sits, but on

a good day he will walk around and on a really good day he will fit train track

pieces together. He has zero bowel movements and we give him an enema every

other day. He is not loud, he is never violent, rarely stims, he is very sweet.

He wears a pull up and we feed him. He makes eye contact and he smiles. His

seizures I think are a reaction to the wrong food. Although dr goldberg said it

is an immune response. Maybe that is why his allergies seem to change. I rely

on muscle testing to determine what to feed him. It is not accurate of course,

so he does have seizures, from 0-3 a day.

I would love some opinions and some feed back about the dr.

Thank you so much for your time. No matter what I decide, I am sure I will be

part of this group.

jo