Hi New Here

[Guest guest]

Hi, .<br>I just wanted to welcome you, and

let you know of another site where you'll find

another message board and tons of support from a great

group of people. I myself have had 4 surgeries on my

lumbar spine, and am on the mend now. Anyway, here is

the

site:<br><a href=http://www.spinedisorders.org/index.html

target=new>http://www.spinedisorders.org/index.html</a><br>I hope to see you

there.<br>Beth

[Guest guest]

Hi ,

Good to see you here - I am JulesA on AiA. Have you done

anything else different in the last few weeks that you can think of ,I know

we spoke about washing powders etc., or has he been eating anything

different ?

I'm not really knowledgeable enough to give much advice but there are many

who can.

Have you looked at Dana's site ? http://www.danasview.net/index.htm there

are also lots of files in the files section of this list which might help.

Hope someone gets back to you soon.

Julea )

The first step towards success is taken when you refuse to be a captive of

the environment in which you first found yourself.

[Guest guest]

Hi ,

Good to see you here - I am JulesA on AiA. Have you

done anything else different in the last few weeks that you can

think of ,I know we spoke about washing powders etc., or has he been

eating anything different ?

I'm not really knowledgeable enough to give much advice but there

are many who can.

Have you looked at Dana's site ? http://www.danasview.net/index.htm

there are also lots of files in the files section of this list which

might help.

Hope someone gets back to you soon.

Julea )

The first step towards success is taken when you refuse to be a

captive of the environment in which you first found yourself.

> Hi everyone,

>

> Well I say I am new here but I was a member about a year ago but

left and now

> I am hoping to be accepted bac as I am not aplling on disappearing

unless

> people would prefer me to go. I have just found the last few

years very hard as

> I am sure other have.

>

> My son Mikey will be five now in a couple of weeks. He has been

on and off a

> GFCF diet and enzymes for about three years now with varying

results. We

> have finally decided to try him with a GFCF diet and also

enzymes.

>

> My question is I have Pepitzyde, HM Zyme and No Fenol enzymes.

What do I

> use? How many? And is it OK to give in a rice dessert.

>

> So far I have been giving Mikey 1/2 a capsule of each twice a day

in a

> dessert together with the GFCF diet. No improvement at all for

over three weeks

> now. He is soya free as well. He has been getting a very red

tongue, could the

> enzymes be burning him?

>

> I am tearing my hair out now because I am not sure which way to go

from here.

> Any advice would be greatly appreciated.

>

> Best wishes

> Thank you

> Michele

>

>

>

[Guest guest]

> have finally decided to try him with a GFCF diet and also enzymes.

>

> My question is I have Pepitzyde, HM Zyme and No Fenol enzymes. What

do I

> use? How many?

The Peptizyde would be for cross contamination and infractions of g/c,

plus soy and other proteins. You can start with any of the three,

because they address different foods. I would start at 1/2 capsule

and work up to 1 capsule per meal if required.

>>And is it OK to give in a rice dessert.

Yes, but they will begin to digest the food, so be sure he eats it

quickly.

>

> So far I have been giving Mikey 1/2 a capsule of each twice a day in

a

> dessert together with the GFCF diet. No improvement at all for over

three weeks

> now. He is soya free as well. He has been getting a very red

tongue, could the

> enzymes be burning him?

Give them 3x per day, to see if it is the 3rd meal which is causing

him problems.

He also might not tolerate certain foods and/or supplements, even with

enzymes.

Dana

[Guest guest]

Give them every time the child snacks or eats or drinks. Use a straw to avoid

the red lips and tongue. I'd stick to 1/2 cap until you've adjusted to using

them with every meal, drink and snack. My son has to drink his enzymes mixed

with water or juice through a straw prior to eating anything. Good luck. We too

are GFCF and using enzymes. Use the enzymes appropriate to the food/drink, you

don't want to waste them.

HI NEW HERE

Hi everyone,

Well I say I am new here but I was a member about a year ago but left and now

I am hoping to be accepted bac as I am not aplling on disappearing unless

people would prefer me to go. I have just found the last few years very hard

as

I am sure other have.

My son Mikey will be five now in a couple of weeks. He has been on and off a

GFCF diet and enzymes for about three years now with varying results. We

have finally decided to try him with a GFCF diet and also enzymes.

My question is I have Pepitzyde, HM Zyme and No Fenol enzymes. What do I

use? How many? And is it OK to give in a rice dessert.

So far I have been giving Mikey 1/2 a capsule of each twice a day in a

dessert together with the GFCF diet. No improvement at all for over three

weeks

now. He is soya free as well. He has been getting a very red tongue, could

the

enzymes be burning him?

I am tearing my hair out now because I am not sure which way to go from here.

Any advice would be greatly appreciated.

Best wishes

Thank you

Michele

[Guest guest]

That's what we did, gave the enzymes every single time food went in.

Are you giving the right enzymes for the right food, like

asked?

Also, 's book (and in this group she's also mentioned it)

discusses somewhere that some kids who don't benefit from the gfcf

diet do really well with the Specific Carbohydrate Diet. Have you

tried that or other diets? Is there a tough yeast or bacterial

problem? How about viral? Just trying to brainstorm why it seems

diet/enzymes aren't working for your son...

> Give them every time the child snacks or eats or drinks. Use a

straw to avoid the red lips and tongue. I'd stick to 1/2 cap until

you've adjusted to using them with every meal, drink and snack. My

son has to drink his enzymes mixed with water or juice through a

straw prior to eating anything. Good luck. We too are GFCF and using

enzymes. Use the enzymes appropriate to the food/drink, you don't

want to waste them.

> HI NEW HERE

>

>

> Hi everyone,

>

> Well I say I am new here but I was a member about a year ago but

left and now

> I am hoping to be accepted bac as I am not aplling on

disappearing unless

> people would prefer me to go. I have just found the last few

years very hard as

> I am sure other have.

>

> My son Mikey will be five now in a couple of weeks. He has been

on and off a

> GFCF diet and enzymes for about three years now with varying

results. We

> have finally decided to try him with a GFCF diet and also

enzymes.

>

> My question is I have Pepitzyde, HM Zyme and No Fenol enzymes.

What do I

> use? How many? And is it OK to give in a rice dessert.

>

> So far I have been giving Mikey 1/2 a capsule of each twice a day

in a

> dessert together with the GFCF diet. No improvement at all for

over three weeks

> now. He is soya free as well. He has been getting a very red

tongue, could the

> enzymes be burning him?

>

> I am tearing my hair out now because I am not sure which way to

go from here.

> Any advice would be greatly appreciated.

>

> Best wishes

> Thank you

> Michele

>

>

>

[Guest guest]

Greetings

Well you have come to the right place for help.

Did you look at the section for those who are new?

" A great place to start.. "

I suggest that all of you new folks do that. It helps

so much the information in there, these folks are

great at telling their stories!!!

I am type 2 and I am getting better as the time goes

on as long as I do not go crazy and have a huge chesse

burger and a non beer beer..(yeast you know!!!

What kind of cream did you get by the way???

Well again welcome to you and all the new people.

FYI:

We get on the average 4 people new a day!!!

Remember your posts are moderated for a while and then

free of that restriction.

Good health to all and the means to maintain it.

nieema

--- djlopez7914 <djlopez7914@...> wrote:

HI

> I HAVE BEEN SUFFERING FROM THIS FOR SOMETIME AND IM

> GOING CRAZY (THE

> ITCHING DRIVES ME CRAZY AT NIGHT)...I HAVE BEEN TO

> THE DOCTOR AND

> ALL I WAS TOLD ITS JUST A COMMON YEAST INFECTION

> HERES SOME CREAM TO

> CURE IT....I HAD TO SURF THE NET AND I FINALLY FOUND

> SOME WEBSITES

> ABOUT CANDIDA AND I WAS READING ALL THE SYMPTOMS AND

> I HAVE LIKE THE

> MAJORITY OF THE SYMPTOMS....I AM A DIABETIC AND I

> GUESS THAT MAKES

> IT WORST?....CAN SOMEONE PLEASE TELL ME HOW I CAN

> GET STARTED TO RID

> MY SELF OF THIS?....IS THERE A CURE?....IS THIS

> REALLY SERIOUS IF IT

> GOES UNTREATED?...

>

=====

I hope this message finds you and yours in the

best of Health and Spirit.

Our Health is Our Responsibility

http://www.a-healing-village.com

nieema

[Guest guest]

In a message dated 11/5/04 8:01:21 AM Eastern Standard Time,

artfulcah@... writes:

> Is that why it feels like I'm being totally ignored? I've asked

> several questions over a 4 day period and had not one response. A couple of

> times I tried visiting " chat " rooms and this has felt just the same. Or am I

> invisible?

> :) :) ?

> Carol

Hi, Carol. I just read this group occasionally, but today I do see all of

your posts. So they do show up

If you go to the group's website at and search for a post from me about

a month ago (it includes the word " lithiasis " ) then you'll see what I

discovered on my own when I researched whether liver stones exist. (Searching at

involves repeated pressing of the " Next " key.)

But be careful of any advice that you read on an internet discussion group,

naturally. This one specifically is not a scientific group. One person in

particular goes around topic to topic, saying that his understanding of science

is

far above the rest of the world (everyone else is always " misinformed " ), yet

he continually gives out faulty info garnered from pop websites and books. You

can find threads where he is proven wrong again and again, and then

immediately people will ask him for more advice. The group owner(s) should thank

people

for exposing his nonsense, but instead discourages that. So go figure. I'd

think the list should be more about getting to the truth than about everybody

just getting along.

As regards liver flushes, it sounds zany but I've read reports from people

that say it does make them feel better. OTOH, there are some now on the yeast-L

list who report bad or neutral results. My guess is that the cholesterol

stones might be formed from the flushing process itself - and to my knowledge no

one knows factually where they reside before being expelled. The whole thing

would and should require lots of reading. Be wary of self-styled gurus and their

cheerleaders, which I think you would do anyway. Good luck

[Guest guest]

<<Remember your posts are moderated for a while and then free of that

restriction.>>

Is that why it feels like I'm being totally ignored? I've asked

several questions over a 4 day period and had not one response. A couple of

times I tried visiting " chat " rooms and this has felt just the same. Or am I

invisible?

:) :) ?

Carol

nieema <nieema0@...> wrote:

Greetings

Well you have come to the right place for help.

Did you look at the section for those who are new?

" A great place to start.. "

I suggest that all of you new folks do that. It helps

so much the information in there, these folks are

great at telling their stories!!!

I am type 2 and I am getting better as the time goes

on as long as I do not go crazy and have a huge chesse

burger and a non beer beer..(yeast you know!!!

What kind of cream did you get by the way???

Well again welcome to you and all the new people.

FYI:

We get on the average 4 people new a day!!!

Remember your posts are moderated for a while and then

free of that restriction.

Good health to all and the means to maintain it.

nieema

--- djlopez7914 wrote:

HI

> I HAVE BEEN SUFFERING FROM THIS FOR SOMETIME AND IM

> GOING CRAZY (THE

> ITCHING DRIVES ME CRAZY AT NIGHT)...I HAVE BEEN TO

> THE DOCTOR AND

> ALL I WAS TOLD ITS JUST A COMMON YEAST INFECTION

> HERES SOME CREAM TO

> CURE IT....I HAD TO SURF THE NET AND I FINALLY FOUND

> SOME WEBSITES

> ABOUT CANDIDA AND I WAS READING ALL THE SYMPTOMS AND

> I HAVE LIKE THE

> MAJORITY OF THE SYMPTOMS....I AM A DIABETIC AND I

> GUESS THAT MAKES

> IT WORST?....CAN SOMEONE PLEASE TELL ME HOW I CAN

> GET STARTED TO RID

> MY SELF OF THIS?....IS THERE A CURE?....IS THIS

> REALLY SERIOUS IF IT

> GOES UNTREATED?...

>

=====

I hope this message finds you and yours in the

best of Health and Spirit.

Our Health is Our Responsibility

http://www.a-healing-village.com

nieema

[Guest guest]

Carol, You are definitely not invisible. I think it just gets a little

frustrating to type the same sort of replies over and over again. I know that I

will occasionally see a welcome message pop up when someone identifies themself

as new. They are instructed to look at the archives and the " new members "

information to get started. That is what I would advise for you. It could just

be that people have answered the same question as your many times before. They

don't want to type it over again.

This group is very supportive and kind. Please check out the archives and stick

around.

Rhonda

Re: HI NEW HERE

<<Remember your posts are moderated for a while and then free of that

restriction.>>

Is that why it feels like I'm being totally ignored? I've

asked several questions over a 4 day period and had not one response. A couple

of times I tried visiting " chat " rooms and this has felt just the same. Or am I

invisible?

:) :) ?

Carol

nieema <nieema0@...> wrote:

Greetings

Well you have come to the right place for help.

Did you look at the section for those who are new?

" A great place to start.. "

I suggest that all of you new folks do that. It helps

so much the information in there, these folks are

great at telling their stories!!!

I am type 2 and I am getting better as the time goes

on as long as I do not go crazy and have a huge chesse

burger and a non beer beer..(yeast you know!!!

What kind of cream did you get by the way???

Well again welcome to you and all the new people.

FYI:

We get on the average 4 people new a day!!!

Remember your posts are moderated for a while and then

free of that restriction.

Good health to all and the means to maintain it.

nieema

--- djlopez7914 wrote:

HI

> I HAVE BEEN SUFFERING FROM THIS FOR SOMETIME AND IM

> GOING CRAZY (THE

> ITCHING DRIVES ME CRAZY AT NIGHT)...I HAVE BEEN TO

> THE DOCTOR AND

> ALL I WAS TOLD ITS JUST A COMMON YEAST INFECTION

> HERES SOME CREAM TO

> CURE IT....I HAD TO SURF THE NET AND I FINALLY FOUND

> SOME WEBSITES

> ABOUT CANDIDA AND I WAS READING ALL THE SYMPTOMS AND

> I HAVE LIKE THE

> MAJORITY OF THE SYMPTOMS....I AM A DIABETIC AND I

> GUESS THAT MAKES

> IT WORST?....CAN SOMEONE PLEASE TELL ME HOW I CAN

> GET STARTED TO RID

> MY SELF OF THIS?....IS THERE A CURE?....IS THIS

> REALLY SERIOUS IF IT

> GOES UNTREATED?...

>

=====

I hope this message finds you and yours in the

best of Health and Spirit.

Our Health is Our Responsibility

http://www.a-healing-village.com

nieema

[Guest guest]

Hi Carol,

For sure no one is ignoring you... we just get so much email

sometimes that it's hard to sort through all of them. If you're

asking a new question but inside an email that's a reply to someone

else's mail, it's best to put in a new subject line (not everyone is

reading every single mail).

Do you mind repeating your questions again?

I think in one of the emails you asked about the liver flush.. the

idea is that gallstones accumulate in the liver and cause all sorts

of problems because the liver isn't function as well as it should.

The procedure calls for drinking epsom salts (to cleanse the bowels)

and a mixture of olive oil/grapefruit juice (to push the stones

out). Once you clean out the stones in the liver, then your health

may improve considerably. If you look at the files there is a book

you can download (only for the next couple of days), or go to

www.curezone.com and click on the Liver flush link - there is lots of

information there on how to do, what to expect, etc. You can also

post messages there.

Regards,

asli

> <<Remember your posts are moderated for a while and then free of

that restriction.>>

>

> Is that why it feels like I'm being totally

ignored? I've asked several questions over a 4 day period and had

not one response. A couple of times I tried visiting " chat " rooms

and this has felt just the same. Or am I invisible?

>

:) :) ?

>

Carol

[Guest guest]

Dear ,

Welcome to our group! You'll be very happy you found us.

>

> Hi,

> New to group.Looks pretty good with so much information.

> Battling CFS and fibromyalgia. Is their anything I should know not to

> eat. How long does this diet take to get a handle on candida. Do many

> people see results. Seems overwhelming, so much to read.

> has so many groups, just fell in here.

==>All of the information can be overwhelming for sure. Take your

time, it's your future that is at stake and education is the first step

to regaining your health. Read my main article first " How to

Successfully Overcome Candida " and after that take one step at a time -

don't rush - starting on the diet and supplements correctly and

gradually is key!

Hugs, Bee

>

[Guest guest]

Hi karen welcome to the group. It sounds like you are really on top

of things and are catching everything very early. Are you from the

UK? If so I think that there is a Plagiocephaly UK group which may be

of more assitance to you. I am not positive about this but maybe

someone else here will be able to confirm this. Good luck at your

appointment, let us know how things go.

Haylee

mom to Andre 21 months/tort/doc band #1 22/11/05 doc band #2 coming

soon & Lesly 21 months

>

> Hi all im karen, mummy to 4, Tori - Lee is 5 months old and has been

> having therapy for torti collis since she was about 5 weeks old, her

> head shape now is really noticeable and her eye and ear are out of

> line, i am researching about helmets/ starbands and also trying to

get

> it funded, she has an appointment tomorow with the ped. I have a lot

> of info to take with me and her therapist is also coming with me to

> back me up as she feels the band would really help Tori - Lee.

> Has anybody had them funded from the nhs and if so what area do you

> live in, we are in halton,cheshire

>

[Guest guest]

The link to the UK group is

http://www.plagiocephaly.org.uk

Jen

(22 mo), tort resolved, Hanger Band Grad

(4 years)

> >

> > Hi all im karen, mummy to 4, Tori - Lee is 5 months old and has

been

> > having therapy for torti collis since she was about 5 weeks old,

her

> > head shape now is really noticeable and her eye and ear are out

of

> > line, i am researching about helmets/ starbands and also trying

to

> get

> > it funded, she has an appointment tomorow with the ped. I have a

lot

> > of info to take with me and her therapist is also coming with me

to

> > back me up as she feels the band would really help Tori - Lee.

> > Has anybody had them funded from the nhs and if so what area do

you

> > live in, we are in halton,cheshire

> >

>

[Guest guest]

> - Are there any negative long-term side effects of using enzymes?

I am unaware of negative *long term* effects. I know that if the

child does not tolerate the enzyme, usually removing it will eliminate

any problems.

> - Is excessive sweating, especially when sleeping, a sign of mercury

> poisoning or something else?

It is a sign that the body is attempting to detox from something it

encountered during the day that it did not tolerate [foods,

environmental issues, etc]. Mercury toxicity can cause this.

Dana

[Guest guest]

Hi Lolly,

Someone here recently recommended using an amber-colored jar to store the

LDN. I guess even the light that reaches it in the refrigerator can degrade

it.

My understanding is to stick with the 1.5 dose until you're sleeping well

(maybe a month), and then work up to either 3 or 4.5 mg. Hopefully you will

have some improvement in your eye disease promptly. And who knows, it may

help your body convert the T4 better.

Best,

B., Graves' disease and cold-stage thyroid eye disease

________________________________

From: low dose naltrexone

[mailto:low dose naltrexone ] On Behalf Of lollyjolly58

Sent: Tuesday, February 12, 2008 6:16 PM

low dose naltrexone

Subject: [low dose naltrexone] Hi new here

Hi all,

I am new to this site, I have been reading up on LDN and ordered some

a

couple of weeks ago from River Pharmacy in Canada.

They arrived sooner than I expected, shipping arrival date was

between 16th-23rd Feb they arrived on the 11th

I live in the UK.

I have Graves Disease with Thyroid Eye Disease.

I had a Total Thyroidectomy last year, but since then have had a

rollercoaster ride,at one point they thought I just wasn't absorbing

Levothyroxine my current dose is 200mcg's.

I wanted to try LDN to see if it would help with the eye disease as

that have flared up since my surgery.

I've been having some help,by other graves disease suffers regarding

LDN.

My question is...

I was reading about River Pharmacy's,the Tablets I

received (looks like mine came from India), generic name is Revia

50mgs X30 tabs, I opened one to see if it is, how you described them

on one of the posts here,tablet is light orange colour, scored,round

no writing on it at all, expiry date 2010.

Came in 10 tab blister packets

with Nordic and Naltrexone Hydrochloride,there were no inserts with

it or leaflets explaining the medication, although I know to make up

my own with distilled water, I will be doing only 25mg's at a time

have a pill cutter and keeping it refrigerated starting on 1.5mg's

the first week, increasing to 2.5mgs's the second and going up to

3mg's, not sure if I should be going any higher than this,so any

input wtll be appreciated.

I haven't started them yet as I am waiting on lab results,Thyroid,

Liver panel, and full blood count I had labs on Monday, plus I have a

stinking cold.

Thank you

Lolly

[Guest guest]

Hi ,

I already have some amber coloured pots ready for storage, glass ones

have a synringe and dropper, just have to get some distilled water.

Yes I will do as you advice and stay on 1.5mgs for a month and then

increase.

I don't sleep that well anyway so it won't be anything new.

Thank you for all your help aswell I hope it helps my eyes too and my

levels.

Best Wishes

Lolly

>

> Hi Lolly,

>

> Someone here recently recommended using an amber-colored jar to

store the

> LDN. I guess even the light that reaches it in the refrigerator can

degrade

> it.

>

> My understanding is to stick with the 1.5 dose until you're

sleeping well

> (maybe a month), and then work up to either 3 or 4.5 mg. Hopefully

you will

> have some improvement in your eye disease promptly. And who knows,

it may

> help your body convert the T4 better.

>

> Best,

> B., Graves' disease and cold-stage thyroid eye disease

> ________________________________

>

> From: low dose naltrexone

> [mailto:low dose naltrexone ] On Behalf Of lollyjolly58

> Sent: Tuesday, February 12, 2008 6:16 PM

> low dose naltrexone

> Subject: [low dose naltrexone] Hi new here

>

> Hi all,

>

> I am new to this site, I have been reading up on LDN and ordered

some

> a

> couple of weeks ago from River Pharmacy in Canada.

> They arrived sooner than I expected, shipping arrival date was

> between 16th-23rd Feb they arrived on the 11th

> I live in the UK.

> I have Graves Disease with Thyroid Eye Disease.

> I had a Total Thyroidectomy last year, but since then have had a

> rollercoaster ride,at one point they thought I just wasn't

absorbing

> Levothyroxine my current dose is 200mcg's.

>

> I wanted to try LDN to see if it would help with the eye disease as

> that have flared up since my surgery.

> I've been having some help,by other graves disease suffers

regarding

> LDN.

> My question is...

> I was reading about River Pharmacy's,the Tablets I

> received (looks like mine came from India), generic name is Revia

> 50mgs X30 tabs, I opened one to see if it is, how you described

them

> on one of the posts here,tablet is light orange colour,

scored,round

> no writing on it at all, expiry date 2010.

> Came in 10 tab blister packets

> with Nordic and Naltrexone Hydrochloride,there were no inserts with

> it or leaflets explaining the medication, although I know to make

up

> my own with distilled water, I will be doing only 25mg's at a time

> have a pill cutter and keeping it refrigerated starting on 1.5mg's

> the first week, increasing to 2.5mgs's the second and going up to

> 3mg's, not sure if I should be going any higher than this,so any

> input wtll be appreciated.

> I haven't started them yet as I am waiting on lab results,Thyroid,

> Liver panel, and full blood count I had labs on Monday, plus I have

a

> stinking cold.

>

> Thank you

>

> Lolly

>

[Guest guest]

If you tolerate 3.0mgs without problems, you can try 4.5mgs. This is

the optimal adult dosage. If you experience problems, then drop back

down. See how you feel. Simple.

Art

--

>

> Hi all,

>

> I am new to this site, I have been reading up on LDN and ordered

some

> a

> couple of weeks ago from River Pharmacy in Canada.

> They arrived sooner than I expected, shipping arrival date was

> between 16th-23rd Feb they arrived on the 11th

> I live in the UK.

> I have Graves Disease with Thyroid Eye Disease.

> I had a Total Thyroidectomy last year, but since then have had a

> rollercoaster ride,at one point they thought I just wasn't

absorbing

> Levothyroxine my current dose is 200mcg's.

>

> I wanted to try LDN to see if it would help with the eye disease as

> that have flared up since my surgery.

> I've been having some help,by other graves disease suffers

regarding

> LDN.

> My question is...

> I was reading about River Pharmacy's,the Tablets I

> received (looks like mine came from India), generic name is Revia

> 50mgs X30 tabs, I opened one to see if it is, how you described

them

> on one of the posts here,tablet is light orange colour,

scored,round

> no writing on it at all, expiry date 2010.

> Came in 10 tab blister packets

> with Nordic and Naltrexone Hydrochloride,there were no inserts with

> it or leaflets explaining the medication, although I know to make

up

> my own with distilled water, I will be doing only 25mg's at a time

> have a pill cutter and keeping it refrigerated starting on 1.5mg's

> the first week, increasing to 2.5mgs's the second and going up to

> 3mg's, not sure if I should be going any higher than this,so any

> input wtll be appreciated.

> I haven't started them yet as I am waiting on lab results,Thyroid,

> Liver panel, and full blood count I had labs on Monday, plus I have

a

> stinking cold.

>

> Thank you

>

> Lolly

>

[Guest guest]

> >

> > Hi all,

> >

> > I am new to this site, I have been reading up on LDN and ordered

> some

> > a

> > couple of weeks ago from River Pharmacy in Canada.

> > They arrived sooner than I expected, shipping arrival date was

> > between 16th-23rd Feb they arrived on the 11th

> > I live in the UK.

> > I have Graves Disease with Thyroid Eye Disease.

> > I had a Total Thyroidectomy last year, but since then have had a

> > rollercoaster ride,at one point they thought I just wasn't

> absorbing

> > Levothyroxine my current dose is 200mcg's.

> >

> > I wanted to try LDN to see if it would help with the eye disease

as

> > that have flared up since my surgery.

> > I've been having some help,by other graves disease suffers

> regarding

> > LDN.

> > My question is...

> > I was reading about River Pharmacy's,the Tablets I

> > received (looks like mine came from India), generic name is

Revia

> > 50mgs X30 tabs, I opened one to see if it is, how you described

> them

> > on one of the posts here,tablet is light orange colour,

> scored,round

> > no writing on it at all, expiry date 2010.

> > Came in 10 tab blister packets

> > with Nordic and Naltrexone Hydrochloride,there were no inserts

with

> > it or leaflets explaining the medication, although I know to

make

> up

> > my own with distilled water, I will be doing only 25mg's at a

time

> > have a pill cutter and keeping it refrigerated starting on

1.5mg's

> > the first week, increasing to 2.5mgs's the second and going up

to

> > 3mg's, not sure if I should be going any higher than this,so any

> > input wtll be appreciated.

> > I haven't started them yet as I am waiting on lab

results,Thyroid,

> > Liver panel, and full blood count I had labs on Monday, plus I

have

> a

> > stinking cold.

> >

> > Thank you

> >

> > Lolly

> >

>

[Guest guest]

I am at 3 mg and was thinking of raising to 4.5. However last night

I had a REALLY scary dream. Has anyone noticed an increase in bad

dreams with upping the dosage?

> >

> > Hi all,

> >

> > I am new to this site, I have been reading up on LDN and ordered

> some

> > a

> > couple of weeks ago from River Pharmacy in Canada.

> > They arrived sooner than I expected, shipping arrival date was

> > between 16th-23rd Feb they arrived on the 11th

> > I live in the UK.

> > I have Graves Disease with Thyroid Eye Disease.

> > I had a Total Thyroidectomy last year, but since then have had a

> > rollercoaster ride,at one point they thought I just wasn't

> absorbing

> > Levothyroxine my current dose is 200mcg's.

> >

> > I wanted to try LDN to see if it would help with the eye disease

as

> > that have flared up since my surgery.

> > I've been having some help,by other graves disease suffers

> regarding

> > LDN.

> > My question is...

> > I was reading about River Pharmacy's,the Tablets I

> > received (looks like mine came from India), generic name is

Revia

> > 50mgs X30 tabs, I opened one to see if it is, how you described

> them

> > on one of the posts here,tablet is light orange colour,

> scored,round

> > no writing on it at all, expiry date 2010.

> > Came in 10 tab blister packets

> > with Nordic and Naltrexone Hydrochloride,there were no inserts

with

> > it or leaflets explaining the medication, although I know to

make

> up

> > my own with distilled water, I will be doing only 25mg's at a

time

> > have a pill cutter and keeping it refrigerated starting on

1.5mg's

> > the first week, increasing to 2.5mgs's the second and going up

to

> > 3mg's, not sure if I should be going any higher than this,so any

> > input wtll be appreciated.

> > I haven't started them yet as I am waiting on lab

results,Thyroid,

> > Liver panel, and full blood count I had labs on Monday, plus I

have

> a

> > stinking cold.

> >

> > Thank you

> >

> > Lolly

> >

>

[Guest guest]

Hi Lolly,I suggest increasing the dosage at a slower rate until you see how LDN affects you. Also, you may need to adjust the dosage of your medication to compensate for the influence of LDN on your system.For more information about LDN, visithttp://tinyurl.com/2boot2Best regards,Dudley Delany

dudley_delanyFrom: lollyjolly58

Sent: Tuesday, February 12, 2008 6:15 PM

low dose naltrexone

Subject: [low dose naltrexone] Hi new here

Hi all,

I am new to this site, I have been reading up on LDN and ordered some

a

couple of weeks ago from River Pharmacy in Canada.

They arrived sooner than I expected, shipping arrival date was

between 16th-23rd Feb they arrived on the 11th

I live in the UK.

I have Graves Disease with Thyroid Eye Disease.

I had a Total Thyroidectomy last year, but since then have had a

rollercoaster ride,at one point they thought I just wasn't absorbing

Levothyroxine my current dose is 200mcg's.

I wanted to try LDN to see if it would help with the eye disease as

that have flared up since my surgery.

I've been having some help,by other graves disease suffers regarding

LDN.

My question is...

I was reading about River Pharmacy's,the Tablets I

received (looks like mine came from India), generic name is Revia

50mgs X30 tabs, I opened one to see if it is, how you described them

on one of the posts here,tablet is light orange colour, scored,round

no writing on it at all, expiry date 2010.

Came in 10 tab blister packets

with Nordic and Naltrexone Hydrochloride,there were no inserts with

it or leaflets explaining the medication, although I know to make up

my own with distilled water, I will be doing only 25mg's at a time

have a pill cutter and keeping it refrigerated starting on 1.5mg's

the first week, increasing to 2.5mgs's the second and going up to

3mg's, not sure if I should be going any higher than this,so any

input wtll be appreciated.

I haven't started them yet as I am waiting on lab results,Thyroid,

Liver panel, and full blood count I had labs on Monday, plus I have a

stinking cold.

Thank you

Lolly

[Guest guest]

Don't know about " bad " dreams, but the imagination is active while

sleeping when using LDN. My dreams are quite memorable.

Perhaps you were watching one of the presidential candidates on TV

right before bed? They alone give me nightmares.

Art

--

>

> I am at 3 mg and was thinking of raising to 4.5. However last night

> I had a REALLY scary dream. Has anyone noticed an increase in bad

> dreams with upping the dosage?

[Guest guest]

HAAH! No actually it was an Andy Griffith rerun on TVLand.

> >

> > I am at 3 mg and was thinking of raising to 4.5. However last

night

> > I had a REALLY scary dream. Has anyone noticed an increase in

bad

> > dreams with upping the dosage?

>

[Guest guest]

Hi Art

Are you saying to start with 3.0mg or start at 1.5mg's?

Lolly

> >

> > Hi all,

> >

> > I am new to this site, I have been reading up on LDN and ordered

> some

> > a

> > couple of weeks ago from River Pharmacy in Canada.

> > They arrived sooner than I expected, shipping arrival date was

> > between 16th-23rd Feb they arrived on the 11th

> > I live in the UK.

> > I have Graves Disease with Thyroid Eye Disease.

> > I had a Total Thyroidectomy last year, but since then have had a

> > rollercoaster ride,at one point they thought I just wasn't

> absorbing

> > Levothyroxine my current dose is 200mcg's.

> >

> > I wanted to try LDN to see if it would help with the eye disease

as

> > that have flared up since my surgery.

> > I've been having some help,by other graves disease suffers

> regarding

> > LDN.

> > My question is...

> > I was reading about River Pharmacy's,the Tablets I

> > received (looks like mine came from India), generic name is Revia

> > 50mgs X30 tabs, I opened one to see if it is, how you described

> them

> > on one of the posts here,tablet is light orange colour,

> scored,round

> > no writing on it at all, expiry date 2010.

> > Came in 10 tab blister packets

> > with Nordic and Naltrexone Hydrochloride,there were no inserts

with

> > it or leaflets explaining the medication, although I know to make

> up

> > my own with distilled water, I will be doing only 25mg's at a

time

> > have a pill cutter and keeping it refrigerated starting on

1.5mg's

> > the first week, increasing to 2.5mgs's the second and going up to

> > 3mg's, not sure if I should be going any higher than this,so any

> > input wtll be appreciated.

> > I haven't started them yet as I am waiting on lab

results,Thyroid,

> > Liver panel, and full blood count I had labs on Monday, plus I

have

> a

> > stinking cold.

> >

> > Thank you

> >

> > Lolly

> >

>

[Guest guest]

The advised conservative formula is to start at 1.5mgs, then after one

month go up to 3.0mgs and one month later try 4.5mgs, which is the

optimal adult dosage. I started at 3.0mgs and went to 4.5 one month

later and have been there since April 2005.

Art

--

>

>

> Hi Art

> Are you saying to start with 3.0mg or start at 1.5mg's?

>

> Lolly

>