Help please

[Guest guest]

ASK YOUR DOC AGAIN IF DIFLUCAN IS BEST FOR HIM......OUR SON WAS VERY BADLY

AFFECTED BY IT AS HE COULD NOT TOLERATE THE FLUORIDE IN IT, AND LOST THE SPEECH

HE HAD GAINED...IT TOOK MONTHS TO COME BACK. HE WAS ALSO VERY AGGRESSIVE AND

SLEPT BADLY, WHICH IS NOT USUAL FOR HIM.

[ ] Help Please

We have a 2.9 year old celating for 6 months in the last month he has

gone backward big time. I know it is yeast and I have had a

dysbiosis done on him, per Dr. Cave. he was high in P-Hydroxybenzoate

(Bacterial/Protozal) and Citramalate & B-Ketoglutarate(yeat/Fungal)

Dr. cave has given him Dilucan(which is really bad on) and when

finished with that a homaphathic Candidia 200c. What has everyone

else have been on when Dysbiosis is like this. I need my child back.

Fill like I have gone back so long. Don't want to celate untill I have

this under control. Andy if you out there please help. If anyone know

a doctor in Penn. that would be great. He has been on pro-gold and

culturelle on the ON days and Diflucan. Is Diflucan the best way to go

and how long is the die off. I have been on Diflucan for 21/2 weeks

and it is not fun. THe child only poops once a day and I have to help

him go poop 4 days out of week.

Any information would be great thank you all

Randi Bell

email @...

[Guest guest]

I think diflucan can be really hard on the liver if I recall correctly. We

use caprylic acid and aloe vera juice. The aloe vera would not only kill the

yeast but would also soften the stools to help with constipation.

Gaylen

[Guest guest]

What chelation protcol were you using?

What are your supplements?

Please describe the problem in more detail.

Andy

> We have a 2.9 year old celating for 6 months in the last month he

has

> gone backward big time. I know it is yeast and I have had a

> dysbiosis done on him, per Dr. Cave. he was high in P-

Hydroxybenzoate

> (Bacterial/Protozal) and Citramalate & B-Ketoglutarate(yeat/Fungal)

> Dr. cave has given him Dilucan(which is really bad on) and when

> finished with that a homaphathic Candidia 200c. What has everyone

> else have been on when Dysbiosis is like this. I need my child

back.

> Fill like I have gone back so long. Don't want to celate untill I

have

> this under control. Andy if you out there please help. If anyone

know

> a doctor in Penn. that would be great. He has been on pro-gold and

> culturelle on the ON days and Diflucan. Is Diflucan the best way to

go

> and how long is the die off. I have been on Diflucan for 21/2 weeks

> and it is not fun. THe child only poops once a day and I have to

help

> him go poop 4 days out of week.

>

> Any information would be great thank you all

>

> Randi Bell

> email @p...

[Guest guest]

Hi, Randi!

Both Diflucan and chelation are hard on the kidneys. Perhaps if you stop

demanding so much of his kidneys for a while, he may improve. Have you had any

tests for kidney and liver function recently? Either one of these may be part

of the problem. Just a thought.

[ ] Help Please

We have a 2.9 year old celating for 6 months in the last month he has

gone backward big time. I know it is yeast and I have had a

dysbiosis done on him, per Dr. Cave. he was high in P-Hydroxybenzoate

(Bacterial/Protozal) and Citramalate & B-Ketoglutarate(yeat/Fungal)

Dr. cave has given him Dilucan(which is really bad on) and when

finished with that a homaphathic Candidia 200c. What has everyone

else have been on when Dysbiosis is like this. I need my child back.

Fill like I have gone back so long. Don't want to celate untill I have

this under control. Andy if you out there please help. If anyone know

a doctor in Penn. that would be great. He has been on pro-gold and

culturelle on the ON days and Diflucan. Is Diflucan the best way to go

and how long is the die off. I have been on Diflucan for 21/2 weeks

and it is not fun. THe child only poops once a day and I have to help

him go poop 4 days out of week.

Any information would be great thank you all

Randi Bell

email @...

[Guest guest]

Randi:

What part of PA do you live in? If you're in the northeast, e-mail me privately

and I'll give you the name of my son's dr. I've been very happy with him.

Sharon in PA

Steinbach wrote:

> Hi, Randi!

>

> Both Diflucan and chelation are hard on the kidneys. Perhaps if you stop

demanding so much of his kidneys for a while, he may improve. Have you had any

tests for kidney and liver function recently? Either one of these may be part

of the problem. Just a thought.

>

>

> [ ] Help Please

>

> We have a 2.9 year old celating for 6 months in the last month he has

> gone backward big time. I know it is yeast and I have had a

> dysbiosis done on him, per Dr. Cave. he was high in P-Hydroxybenzoate

> (Bacterial/Protozal) and Citramalate & B-Ketoglutarate(yeat/Fungal)

> Dr. cave has given him Dilucan(which is really bad on) and when

> finished with that a homaphathic Candidia 200c. What has everyone

> else have been on when Dysbiosis is like this. I need my child back.

> Fill like I have gone back so long. Don't want to celate untill I have

> this under control. Andy if you out there please help. If anyone know

> a doctor in Penn. that would be great. He has been on pro-gold and

> culturelle on the ON days and Diflucan. Is Diflucan the best way to go

> and how long is the die off. I have been on Diflucan for 21/2 weeks

> and it is not fun. THe child only poops once a day and I have to help

> him go poop 4 days out of week.

>

> Any information would be great thank you all

>

> Randi Bell

> email @...

>

>

[Guest guest]

Randi,

I am interested in how much Diflucan he is taking in? Some doctors

tend to overdose our little ones. My doc prescribed 3mls of the 40mg

Diflucan for my 3.4 year old 40lb son. He had us start with 1ml and

work our way up. We had his diet yeast-free for a month before we

started this and are still going strong. We thought we were seeing

some die-off after 10 days but it ended up being a virus. Others

have suggested preparing the body with probiotics first before using

the Diflucan. I think both of those ideas are good ones. Supposedly

Diflucan really inhibits new growth of yeast more than it causes die-

off. It does have floride in it as someone mentioned and he could be

responding to that.

Theresa,

SA, TX

--- In @y..., " Steinbach " <tsteinbach4@h...>

wrote:

> Hi, Randi!

>

> Both Diflucan and chelation are hard on the kidneys. Perhaps if

you stop demanding so much of his kidneys for a while, he may

improve. Have you had any tests for kidney and liver function

recently? Either one of these may be part of the problem. Just a

thought.

>

>

> [ ] Help Please

>

>

> We have a 2.9 year old celating for 6 months in the last month he

has

> gone backward big time. I know it is yeast and I have had a

> dysbiosis done on him, per Dr. Cave. he was high in P-

Hydroxybenzoate

> (Bacterial/Protozal) and Citramalate & B-Ketoglutarate

(yeat/Fungal)

> Dr. cave has given him Dilucan(which is really bad on) and when

> finished with that a homaphathic Candidia 200c. What has

everyone

> else have been on when Dysbiosis is like this. I need my child

back.

> Fill like I have gone back so long. Don't want to celate untill I

have

> this under control. Andy if you out there please help. If anyone

know

> a doctor in Penn. that would be great. He has been on pro-gold

and

> culturelle on the ON days and Diflucan. Is Diflucan the best way

to go

> and how long is the die off. I have been on Diflucan for 21/2

weeks

> and it is not fun. THe child only poops once a day and I have to

help

> him go poop 4 days out of week.

>

> Any information would be great thank you all

>

> Randi Bell

> email @p...

>

>

>

>

[Guest guest]

> She doesn't get any calcium thought this would be a good source. I also

thought that this would take care of certain things that she needed that I

wasn't supplementing. Bad idea?

No

> Also, that's all the magnesium she takes? 20mg?

> yes, does she need more?

If you're chelating, yes. A lot more. My son was taking at the beginning of

chelation more than 300mg per day. Now he takes 50mg but we are not chelating

anymore.

Andy says that a good way to see how much magnesium you need is to up the dose

more and more until you have diarrhea and then go back a little.

Also, remember to give it in small doses, many times a day (3-4 times), just

like the water soluble vitamins.

> What kind of selenium is in that multivit.?

> It says Amino Acid Chelate - is this bad?

I don't know... sorry

We use selenomethionine. We also used in the past selenium yeast. Both worked

for us.

> Well, how much zinc is she taking now?

> I had moved out the 30mg 2 x day - I'm thinking that I need to put that back!!

ALA tends to impair the excretion of copper, so you might want to think again

about the zinc. Zinc reduces copper.

> Well, apparently with all the hand flapping and talking to her hands and not

paying attention and visual stims - I think she might need it. What do you

think?

I would put the vit.A back.

I know a lot of people are very afraid of vit. A and maybe they are right. But

for my son vit.A did really really great things. I really like that vitamin

> Yep that one, I was wondering if I should do this because of using DMSA, ya

know cysteine levels and stuff - I don't know what hers are....

It's a very informative test in my opinion. You find out a lot of things.

But it feels kind of bad to give to your kid all those Tylenols

> It's just weird she did so well when we did nothing but ALA. With DMSA she's

just not doing so great.

Maybe the Comp. Detox. Profile will tell you something...

I remember my son wasn't very happy either when we started DMSA. But he got

better...

> I had someone tell me that I may be chelating for the wrong things if I didn't

do the hair test? AM I SCREWING UP HERE!!!!!!?????

No I don't think you do. But if it would make you feel safer, you can order

it anytime... I didn't have a hair test when we chelated, but I ordered one now,

when I'm done

Why do you say you're worried? Because you don't have a hair test?

Valentina

[Guest guest]

It's just weird she did so well when we did nothing but ALA. With DMSA she's

just not doing so great. I had someone tell me that I may be chelating for the

wrong things if I didn't do the hair test? AM I SCREWING UP HERE!!!!!!?????

If you are refering to my answer to you, I didn't mean you were chelating for

the wrong things (if she is getting better you must be doing something right). I

just thought if there was lead as well, you might want to know, because you need

the DMSA then. It is just what happened with my daughter, I was using ALA only,

until I did a hair test and found the lead. The other issue is, if there is lead

or other heavy metals, you might be able to remove the sources and if there was

lead exposure and you are using DMSA, might there be a risk of moving the lead

into the body, rather than out of it? Please tell me, if you don't want me to

comment. My idea is not to make you feel bad.

Dagmar.

[Guest guest]

> No this was something someone had just posted awhile back, possibly not

even to me, I tend to read everything and use what I find most comfy for me.

It's a good thing to have different opinions. Trust me I wasn't pointing any

nubby fingers at anyone.

However, on that note she tested at 51 1-100 range in lead. I've since found

that we have lead in our water!!! So I probably do need to do the DMSA for

things like this.

Karyn

> From: " Dagmar " <dagmarjahr@...>

> Date: 2003/02/18 Tue AM 02:28:08 EST

> < >

> Subject: Re: [ ] Help please

>

>

[Guest guest]

I'd bet it was the strawberries given her reaction. Unfortunately, the

after-effects of some allergic reactions can last as long as several weeks,

though we've found they're usually over within four days or so.

Gaylen

[Guest guest]

Shona,

It is my understanding that it can take SSRIs up to 6 weeks to be

fully in your system (or however you say it). I don't know if takes

that long for the side effects to work themselves out, though. Seems

like it might. I know for adults Psychiatrists (at least the

cautious ones) want to give an SSRI dosage that much time to see what

the final effect will be.

timary

> Hi everyone! I need your help, please. My daughter, almost 5

years

> old now, has been taking paxil for 11 days. We haven't seen any

> positive changes in her so far. Friday night she had a huge

> allergice reaction to some strawberries that she ate. We had

company

> over for supper and I made a strawberry pie. She broke out in red

> whelps and cried for a while. We gave her benadryl for the

reaction

> and she seemed much better the next day. However, since that time,

> she has not had as much expressive language, and has not been

> interested in playing at all with other kids. What do you think?

Is

> it the paxil, or lingering effects from the reaction? How long

does

> it take for paxil to get in their systems and be effective? A lot

> of questions here, I know, but I'm so frustrated and really mad at

> myself for having the strawberries around. Thanks for any input.

>

> Shona

[Guest guest]

Thanks everyone for your posts. You all are such a wonderful support for me. I

was really down when I posted the last message. We've been with Dr. G since

December and have had all the tests run. Even though she didn't show up as

allergic to strawberries in the food panel, she is definitely allergic to them.

There is a statement in the do's and don'ts of diet about all berries. I just

overlooked it somehow. :-( She has been a little better today, not quite as

anxious, upset, etc. and the expressive language is slowly coming back. It's

amazing what an allergic reaction can do to them.

> Thanks again.

[Guest guest]

I don't know if this will help or not... I have been on Methotrexate

since I was diagnosed at age 24ish ( I am 33 now) In addition to

Methotrexate, I take Relafen and folic acid. I have tried many

medications to get my RA under control and it wasn't until I started

Remicade and had that every 6 weeks for over 2 years that I stopped

having major flare-ups. My nsaid has been changed over and over

through the years and Relafen seems to work the best for me. I don't

see the difference in the way I feel when I miss taking my

methotrexate ( and believe me I have missed taking it a lot over the

past ten years)I have never used any pain medication because my

rheumatologist believes in solving the problem not masking it. I

took prednisone for along time up until I started the Remicade and

then I weened myself off that. Today I rarely have flare-ups.. I

believe that the Remicade was the best thing for me. I know a lot of

people can't afford/or insurance won't pay for it though. I would

still be on it now if my insurance hadn't changed and now it is a

900.00 dollar coinsurance for me to have it. There are so many side

effects with any of the drugs that you take, you just have to weigh

out the pro's and con's and see what is best for you. I hope this

helps you in some way and answers a couple of your questions...

>

> I don't post much and I have probably asked someone this before

but

> I need advice. I have RA and take 12.5 mg Methotrexate once a

> week. It doesn't seem to be working. Have been on it since

> February. They tried increasing my dose but it made my anxiety go

> through the roof and my heart was racing. Rheumy had put me from

> 12.5 mg to 20 mg.

>

> My question is I am having to take prescription strength Aleve

> lately every 12 hours and even a percocet during the day. Is it

> safe and/or normal to take Nsaids with methotrexate? Also is it

> normal to have them start you right on Methotrexate right from

> diagnosis?

>

> I am really feeling lost that things seem to be getting worse

rather

> than better. I see a new rhuemy and a naturopath doc on the

28th.

> Anyone had any experience with the naturopaths? Sorry for so many

> questions but I could just cry right now. It is so hard taking

care

> of the kids when you hurt. I was on zoloft but had to stop taking

> it because it was making my hair fall out believe it or not. I

> always seem to have the weird side affects.

>

> Any help would be great.

>

>

[Guest guest]

, Hi I read your email and I don't know how to post.I tried once but I

reckon I did something wrong.I have RA as well and when I got diagnosed my

doctor put me on Methotrexate 12.5 and predisone 80 mg. daily, plus

pain pills, percocet, morphine, all kinds and the only one that touched the

pain was endocet. I just recently started Enbrel, I will take my third

injection on tuesday.My Doctor told me to quit taking my Aleve when I

started the MTX, and predisone. If it worries you so much just talk to your

Dr. and he can explain whether it would be safe to mix Aleve or other

insaids with the others you are taking. If you need a friend I am here.

Rhonda

[ ] Help please;

>I don't post much and I have probably asked someone this before but

> I need advice. I have RA and take 12.5 mg Methotrexate once a

> week. It doesn't seem to be working. Have been on it since

> February. They tried increasing my dose but it made my anxiety go

> through the roof and my heart was racing. Rheumy had put me from

> 12.5 mg to 20 mg.

>

> My question is I am having to take prescription strength Aleve

> lately every 12 hours and even a percocet during the day. Is it

> safe and/or normal to take Nsaids with methotrexate? Also is it

> normal to have them start you right on Methotrexate right from

> diagnosis?

>

> I am really feeling lost that things seem to be getting worse rather

> than better. I see a new rhuemy and a naturopath doc on the 28th.

> Anyone had any experience with the naturopaths? Sorry for so many

> questions but I could just cry right now. It is so hard taking care

> of the kids when you hurt. I was on zoloft but had to stop taking

> it because it was making my hair fall out believe it or not. I

> always seem to have the weird side affects.

>

> Any help would be great.

>

>

>

>

>

>

>

>

>

[Guest guest]

Thank you Rhonda and for your replies. I am going to have

to talk to my new doc when i see him on the 28th.

>

> , Hi I read your email and I don't know how to post.I tried

once but I

> reckon I did something wrong.I have RA as well and when I got

diagnosed my

> doctor put me on Methotrexate 12.5 and predisone 80 mg. daily, plus

> pain pills, percocet, morphine, all kinds and the only one that

touched the

> pain was endocet. I just recently started Enbrel, I will take my

third

> injection on tuesday.My Doctor told me to quit taking my Aleve

when I

> started the MTX, and predisone. If it worries you so much just

talk to your

> Dr. and he can explain whether it would be safe to mix Aleve or

other

> insaids with the others you are taking. If you need a friend I am

here.

> Rhonda

> [ ] Help please;

>

>

> >I don't post much and I have probably asked someone this before

but

> > I need advice. I have RA and take 12.5 mg Methotrexate once a

> > week. It doesn't seem to be working. Have been on it since

> > February. They tried increasing my dose but it made my anxiety

go

> > through the roof and my heart was racing. Rheumy had put me from

> > 12.5 mg to 20 mg.

> >

> > My question is I am having to take prescription strength Aleve

> > lately every 12 hours and even a percocet during the day. Is it

> > safe and/or normal to take Nsaids with methotrexate? Also is it

> > normal to have them start you right on Methotrexate right from

> > diagnosis?

> >

> > I am really feeling lost that things seem to be getting worse

rather

> > than better. I see a new rhuemy and a naturopath doc on the

28th.

> > Anyone had any experience with the naturopaths? Sorry for so

many

> > questions but I could just cry right now. It is so hard taking

care

> > of the kids when you hurt. I was on zoloft but had to stop

taking

> > it because it was making my hair fall out believe it or not. I

> > always seem to have the weird side affects.

> >

> > Any help would be great.

> >

> >

> >

> >

> >

> >

> >

> >

> >

[Guest guest]

You are welcome Rhonda and Good luck with your new doctor. I hope he

can get you feeling better.

> >

> > , Hi I read your email and I don't know how to post.I tried

> once but I

> > reckon I did something wrong.I have RA as well and when I got

> diagnosed my

> > doctor put me on Methotrexate 12.5 and predisone 80 mg. daily,

plus

> > pain pills, percocet, morphine, all kinds and the only one that

> touched the

> > pain was endocet. I just recently started Enbrel, I will take my

> third

> > injection on tuesday.My Doctor told me to quit taking my Aleve

> when I

> > started the MTX, and predisone. If it worries you so much just

> talk to your

> > Dr. and he can explain whether it would be safe to mix Aleve or

> other

> > insaids with the others you are taking. If you need a friend I

am

> here.

> > Rhonda

> > [ ] Help please;

> >

> >

> > >I don't post much and I have probably asked someone this before

> but

> > > I need advice. I have RA and take 12.5 mg Methotrexate once a

> > > week. It doesn't seem to be working. Have been on it since

> > > February. They tried increasing my dose but it made my

anxiety

> go

> > > through the roof and my heart was racing. Rheumy had put me

from

> > > 12.5 mg to 20 mg.

> > >

> > > My question is I am having to take prescription strength Aleve

> > > lately every 12 hours and even a percocet during the day. Is

it

> > > safe and/or normal to take Nsaids with methotrexate? Also is

it

> > > normal to have them start you right on Methotrexate right from

> > > diagnosis?

> > >

> > > I am really feeling lost that things seem to be getting worse

> rather

> > > than better. I see a new rhuemy and a naturopath doc on the

> 28th.

> > > Anyone had any experience with the naturopaths? Sorry for so

> many

> > > questions but I could just cry right now. It is so hard

taking

> care

> > > of the kids when you hurt. I was on zoloft but had to stop

> taking

> > > it because it was making my hair fall out believe it or not. I

> > > always seem to have the weird side affects.

> > >

> > > Any help would be great.

> > >

> > >

> > >

> > >

> > >

> > >

> > >

> > >

> > >

[Guest guest]

Oops I meant katie..sorry..lol long day

> >

> > , Hi I read your email and I don't know how to post.I tried

> once but I

> > reckon I did something wrong.I have RA as well and when I got

> diagnosed my

> > doctor put me on Methotrexate 12.5 and predisone 80 mg. daily,

plus

> > pain pills, percocet, morphine, all kinds and the only one that

> touched the

> > pain was endocet. I just recently started Enbrel, I will take my

> third

> > injection on tuesday.My Doctor told me to quit taking my Aleve

> when I

> > started the MTX, and predisone. If it worries you so much just

> talk to your

> > Dr. and he can explain whether it would be safe to mix Aleve or

> other

> > insaids with the others you are taking. If you need a friend I

am

> here.

> > Rhonda

> > [ ] Help please;

> >

> >

> > >I don't post much and I have probably asked someone this before

> but

> > > I need advice. I have RA and take 12.5 mg Methotrexate once a

> > > week. It doesn't seem to be working. Have been on it since

> > > February. They tried increasing my dose but it made my

anxiety

> go

> > > through the roof and my heart was racing. Rheumy had put me

from

> > > 12.5 mg to 20 mg.

> > >

> > > My question is I am having to take prescription strength Aleve

> > > lately every 12 hours and even a percocet during the day. Is

it

> > > safe and/or normal to take Nsaids with methotrexate? Also is

it

> > > normal to have them start you right on Methotrexate right from

> > > diagnosis?

> > >

> > > I am really feeling lost that things seem to be getting worse

> rather

> > > than better. I see a new rhuemy and a naturopath doc on the

> 28th.

> > > Anyone had any experience with the naturopaths? Sorry for so

> many

> > > questions but I could just cry right now. It is so hard

taking

> care

> > > of the kids when you hurt. I was on zoloft but had to stop

> taking

> > > it because it was making my hair fall out believe it or not. I

> > > always seem to have the weird side affects.

> > >

> > > Any help would be great.

> > >

> > >

> > >

> > >

> > >

> > >

> > >

> > >

> > >

[Guest guest]

Sorry you are having pain -- I too have 2 kids (4 & 11) and it is very hard to

keep up with the pace when all you want to do is lay down! My Rhuemy started me

on MTX at diagnoses -- I have been on it now for 2 years -- I have added Minocin

(AP therapy) and it is working -- my sed rate is down for the first time in

years -- it takes time with all these meds to start working enough for you to

feel the difference -- don't give up! I too was on Oxycodone and Hydrocodone

for months -- now have moved down to Darvocet -- I take MTX, Minocin, folic

acid, (and for Fibro) Lyrica, Provigil, Requip and Darvocet -- I at least can

function with a daily routine (most days) -- I would ask for better pain meds to

get through the hump! Keep your chin up!

DON, HOLLYE, BRIANNA, AND JESS

MALVERN, AR

[Guest guest]

Yes, you'll have to see him personally for your initial appointment

and then you can do phone consults and labs locally. There are only

3 places to get the protocol and Dr. G is not affiliated with

the other two, NNY Autism Clinic in NY and they have an office in TX.

DAN will focus more heavily on metabolic issues and natural methods.

Dr. G will not being doing a ton of supps with you. He won't be

chelating, he won't be Rxing MB12, telling you to get HBOT, etc. So

it's very different from DAN. He would also prefer you start the

diet. You can get a lot more info on what he does and how he

does it on his website.

www.neuroimmunedr.com and www.nids.net.

Let us know if you have any more questions after that!

cheryl

On Mar 16, 2008, at 5:07 PM, yorkm25 wrote:

> Do we have to travel to Dr. Goldberg to have my sons issues address

> this way or are their experienced Dr.s in different states. I read one

> of the doc. articles and i couldn't stop jumping up and down yelling

> there it is, there it is. His opinions hit home with me. We are about

> to go see our first Dan and I don't know how they are different. Any

> info would be great.

> m

>

>

>

[Guest guest]

Cheryl,

We are also new to . We live in Northern California and are

interested in bringing our daughter to him. I looked on the websites

and had a hard time finding a way to contact them. I found an email

address but no phone number. I am sure I just missed something but I

have looked a couple times on both sites. What is the best way to

contact his office??

Cheryl Lowrance wrote:

> Yes, you'll have to see him personally for your initial appointment

> and then you can do phone consults and labs locally. There are only

> 3 places to get the protocol and Dr. G is not affiliated with

> the other two, NNY Autism Clinic in NY and they have an office in TX.

>

> DAN will focus more heavily on metabolic issues and natural methods.

> Dr. G will not being doing a ton of supps with you. He won't be

> chelating, he won't be Rxing MB12, telling you to get HBOT, etc. So

> it's very different from DAN. He would also prefer you start the

> diet. You can get a lot more info on what he does and how he

> does it on his website.

>

> www.neuroimmunedr.com and www.nids.net.

>

> Let us know if you have any more questions after that!

>

> cheryl

>

> On Mar 16, 2008, at 5:07 PM, yorkm25 wrote:

>

> > Do we have to travel to Dr. Goldberg to have my sons issues address

> > this way or are their experienced Dr.s in different states. I read one

> > of the doc. articles and i couldn't stop jumping up and down yelling

> > there it is, there it is. His opinions hit home with me. We are about

> > to go see our first Dan and I don't know how they are different. Any

> > info would be great.

> > m

> >

> >

> >

>

>

[Guest guest]

818-343-1010

Cheryl

On Mar 16, 2008, at 8:30 PM, Caroline wrote:

> Cheryl,

>

> We are also new to . We live in Northern California and are

> interested in bringing our daughter to him. I looked on the websites

> and had a hard time finding a way to contact them. I found an email

> address but no phone number. I am sure I just missed something but I

> have looked a couple times on both sites. What is the best way to

> contact his office??

>

>

>

> Cheryl Lowrance wrote:

>

> > Yes, you'll have to see him personally for your initial appointment

> > and then you can do phone consults and labs locally. There are only

> > 3 places to get the protocol and Dr. G is not affiliated with

> > the other two, NNY Autism Clinic in NY and they have an office in

> TX.

> >

> > DAN will focus more heavily on metabolic issues and natural methods.

> > Dr. G will not being doing a ton of supps with you. He won't be

> > chelating, he won't be Rxing MB12, telling you to get HBOT, etc. So

> > it's very different from DAN. He would also prefer you start the

> > diet. You can get a lot more info on what he does and how he

> > does it on his website.

> >

> > www.neuroimmunedr.com and www.nids.net.

> >

> > Let us know if you have any more questions after that!

> >

> > cheryl

> >

> > On Mar 16, 2008, at 5:07 PM, yorkm25 wrote:

> >

> > > Do we have to travel to Dr. Goldberg to have my sons issues

> address

> > > this way or are their experienced Dr.s in different states. I

> read one

> > > of the doc. articles and i couldn't stop jumping up and down

> yelling

> > > there it is, there it is. His opinions hit home with me. We are

> about

> > > to go see our first Dan and I don't know how they are

> different. Any

> > > info would be great.

> > > m

> > >

> > >

> > >

> >

> >

[Guest guest]

Sorry for chiming in so late, but I was wondering if these phone

consults are covered by insurance?

ville, Florida

>

> > Do we have to travel to Dr. Goldberg to have my sons issues

address

> > this way or are their experienced Dr.s in different states. I

read one

> > of the doc. articles and i couldn't stop jumping up and down

yelling

> > there it is, there it is. His opinions hit home with me. We are

about

> > to go see our first Dan and I don't know how they are different.

Any

> > info would be great.

> > m

> >

> >

> >

>

>

>

>

[Guest guest]

No, I don't know of any insurance company that covers phone consults.

cheryl

On Mar 19, 2008, at 1:01 PM, lil1cutie101 wrote:

> Sorry for chiming in so late, but I was wondering if these phone

> consults are covered by insurance?

>

> ville, Florida

>

>

> >

> > > Do we have to travel to Dr. Goldberg to have my sons issues

> address

> > > this way or are their experienced Dr.s in different states. I

> read one

> > > of the doc. articles and i couldn't stop jumping up and down

> yelling

> > > there it is, there it is. His opinions hit home with me. We are

> about

> > > to go see our first Dan and I don't know how they are different.

> Any

> > > info would be great.

> > > m

> > >

> > >

> > >

> >

> >

> >

> >

[Guest guest]

I have never heard of them being covered. Sheri

lil1cutie101 <gmontg@...> wrote: Sorry for chiming in so late,

but I was wondering if these phone

consults are covered by insurance?

ville, Florida

>

> > Do we have to travel to Dr. Goldberg to have my sons issues

address

> > this way or are their experienced Dr.s in different states. I

read one

> > of the doc. articles and i couldn't stop jumping up and down

yelling

> > there it is, there it is. His opinions hit home with me. We are

about

> > to go see our first Dan and I don't know how they are different.

Any

> > info would be great.

> > m

> >

> >

> >

>

>

>

>

[Guest guest]

Hi Sheri

Thank you so much for taking the time to speak with me today. I know I asked

alot of questions. I am going to have blood drawn tomorrow. I will call you in

the am so that we can confirm all the details.

Vicki Eisen

Sheri <eszbi5@...> wrote:

I have never heard of them being covered. Sheri

lil1cutie101 <gmontg@...> wrote: Sorry for chiming in so late, but I was

wondering if these phone

consults are covered by insurance?

ville, Florida

>

> > Do we have to travel to Dr. Goldberg to have my sons issues

address

> > this way or are their experienced Dr.s in different states. I

read one

> > of the doc. articles and i couldn't stop jumping up and down

yelling

> > there it is, there it is. His opinions hit home with me. We are

about

> > to go see our first Dan and I don't know how they are different.

Any

> > info would be great.

> > m

> >

> >

> >

>

>

>

>