Hi group....my Mercola letter....

[Guest guest]

Hi group,

Ok, first I thought...*gulp*...I was not volunteering to write to Dr.

Mercola but rather thought that if several did so, I'd be up for going to

physically visit with him, seeing that my close proximity to him was a plus.

I'm never all that secure in the fact that my letter writing abilities are

all that great..*s*. Anyway, I thought I'd give it a shot and e-mailed him

today at his www.mercola.com site. This is the letter in it's entirety and

that is followed by the response that I received. I do heartily recommend

that others write to him as well, might make it more convinceable? Ok, here

is my letter...

Hi..this message is for Dr. Mercola. I have been subcribing to your news

letter for some time now and have come to really respect your ideas and

philosophies. That is why I have decided to write to you to inform you of

something that may seem quite remarkable and indeed it is. I am part of a

group of thousands of MS and other auto-immune disorder patients. We

are all part of this group because we are all lucky enough to own a computer

and after doing some research online we all miracluously found a therapy

that Dr. Bihari in New York has been experimenting with for maybe some 15

years now. It is called Low Dose Naltrexone and I have been taking a low

dose of 4.5mg of this drug for 3 years now for my MS. I am here to tell you

that it has halted any further progress of my MS, which is, by all accounts

secondary progressive and I really don't have any MS issues to speak of

other then some permanent damage from the pre LDN days. Many in the group

feel the way I do, that you are a wonderful person to contact as many of us

get the newsletter and feel that you would be receptive to such information.

I live about 25 miles north of Chicago so I volunteered to write and told

the group that I'd even be willing to meet with you if you would be

interested. I am part of the patient panel for the first ever LDN Conference

that is being held in New York this June 11th. There is so much to tell

regarding this remarkable therapy and I don't want to make this a long

message but please write to me and I will explain to you the urgency of

getting this information out to the public at large. It is amazing just how

many people would stand to gain by such information about a tiny dose of a

very harmless drug. ALS, Parkinsons, Rheumatoid Arthritis, Lupus, HIV and

some cancers to name just a few. You see, we are up against the huge

pharmaceuticals. This medication has been in use some 20 years now so

therefore there is no hope for a patent for it. I'm sure you know where I'm

going with this. There are thousands of us just using it for our MS. If you

go to www.remedyfind.com you will see what actual patients say about what

they use and LDN/Revia is rated #1 right now. Sad thing is that if you are

an MS patient you will not even hear of this remarkable treatment. Is that

fair to the typical MS patient I ask? You can find info about the LDN at

www.ldninfo.org that is run by the son of a childhood friend of Dr. Bihari.

As a doctor yourself, surely you realize just how much one lone doctor can

do in this world of big business pharmaceuticals. Well thankfully the

internet has helped greatly. What we need now is more influencial people on

our side to get this therapy right where it needs to be, in the hands of

deserving patients. Thanks so much for listening Dr. Mercola and keep up the

good work. Please write to me and let me know if you'd like for me to pay a

visit to your office. I will be attending the conference because my passion

these days is LDN and what it has to offer so so many people. I say, huge

pharmaceutals be damned...we the people will prevail. Joyce

****************************** (full name, address and phone number deleted

from original letter to protect the innocent..lol) (sorry for the length of

this message but we really do need someone to champion this for us, please

don't let us down).

Here is their quick response. Not exactly the response that I was expecting:

" Dear Subscriber,

We thank you very much for the feedback. We will make sure this information

is looked into and perhaps Dr. Mercola will address your question in a

future newsletter article. Please note that we cannot respond to individual

health and product questions.

The Mercola.com Staff "

[Guest guest]

WELL DONE, Joyce, for giving it a go, and best of success in getting a positive response from him shortly. Well put!

Rae

From: low dose naltrexone [mailto:low dose naltrexone ] On Behalf Of Joyce F.Sent: Saturday, April 30, 2005 3:21 PMlow dose naltrexone Subject: [low dose naltrexone] Hi group....my Mercola letter....

Hi group,Ok, first I thought...*gulp*...I was not volunteering to write to Dr. Mercola but rather thought that if several did so, I'd be up for going to physically visit with him, seeing that my close proximity to him was a plus. I'm never all that secure in the fact that my letter writing abilities are all that great..*s*. Anyway, I thought I'd give it a shot and e-mailed him today at his www.mercola.com site. This is the letter in it's entirety and that is followed by the response that I received. I do heartily recommend that others write to him as well, might make it more convinceable? Ok, here is my letter...Hi..this message is for Dr. Mercola. I have been subcribing to your news letter for some time now and have come to really respect your ideas and philosophies. That is why I have decided to write to you to inform you of something that may seem quite remarkable and indeed it is. I am part of a group of thousands of MS and other auto-immune disorder patients. We are all part of this group because we are all lucky enough to own a computer and after doing some research online we all miracluously found a therapy that Dr. Bihari in New York has been experimenting with for maybe some 15 years now. It is called Low Dose Naltrexone and I have been taking a low dose of 4.5mg of this drug for 3 years now for my MS. I am here to tell you that it has halted any further progress of my MS, which is, by all accounts secondary progressive and I really don't have any MS issues to speak of other then some permanent damage from the pre LDN days. Many in the group feel the way I do, that you are a wonderful person to contact as many of us get the newsletter and feel that you would be receptive to such information. I live about 25 miles north of Chicago so I volunteered to write and told the group that I'd even be willing to meet with you if you would be interested. I am part of the patient panel for the first ever LDN Conference that is being held in New York this June 11th. There is so much to tell regarding this remarkable therapy and I don't want to make this a long message but please write to me and I will explain to you the urgency of getting this information out to the public at large. It is amazing just how many people would stand to gain by such information about a tiny dose of a very harmless drug. ALS, Parkinsons, Rheumatoid Arthritis, Lupus, HIV and some cancers to name just a few. You see, we are up against the huge pharmaceuticals. This medication has been in use some 20 years now so therefore there is no hope for a patent for it. I'm sure you know where I'm going with this. There are thousands of us just using it for our MS. If you go to www.remedyfind.com you will see what actual patients say about what they use and LDN/Revia is rated #1 right now. Sad thing is that if you are an MS patient you will not even hear of this remarkable treatment. Is that fair to the typical MS patient I ask? You can find info about the LDN at www.ldninfo.org that is run by the son of a childhood friend of Dr. Bihari. As a doctor yourself, surely you realize just how much one lone doctor can do in this world of big business pharmaceuticals. Well thankfully the internet has helped greatly. What we need now is more influencial people on our side to get this therapy right where it needs to be, in the hands of deserving patients. Thanks so much for listening Dr. Mercola and keep up the good work. Please write to me and let me know if you'd like for me to pay a visit to your office. I will be attending the conference because my passion these days is LDN and what it has to offer so so many people. I say, huge pharmaceutals be damned...we the people will prevail. Joyce ****************************** (full name, address and phone number deleted from original letter to protect the innocent..lol) (sorry for the length of this message but we really do need someone to champion this for us, please don't let us down).Here is their quick response. Not exactly the response that I was expecting:"Dear Subscriber,We thank you very much for the feedback. We will make sure this informationis looked into and perhaps Dr. Mercola will address your question in afuture newsletter article. Please note that we cannot respond to individualhealth and product questions.The Mercola.com Staff"

[Guest guest]

Hi Joyce! This retired/disabled English

teacher/librarian gives your response to Mercola's

staff an A plus for composition and clarity. Will try

to follow up with your request for publicity. Am

giving the LDN website address to everyone with

writing materials. Somewhere I read/heard " Those who

are supposed to get the message will receive it. Those

who are not supposed to get it won't. I've taught

first and second grades. Some children were eager to

learn; some children were bored with new ideas.

Failing the grade means " I'll see you next year! " You

did a superior job in writing to Dr. Mercola. shylotz

--- " Joyce F. " <joyce445@...> wrote:

> Hi group,

> Ok, first I thought...*gulp*...I was not

> volunteering to write to Dr.

> Mercola but rather thought that if several did so,

> I'd be up for going to

> physically visit with him, seeing that my close

> proximity to him was a plus.

> I'm never all that secure in the fact that my letter

> writing abilities are

> all that great..*s*. Anyway, I thought I'd give it a

> shot and e-mailed him

> today at his www.mercola.com site. This is the

> letter in it's entirety and

> that is followed by the response that I received. I

> do heartily recommend

> that others write to him as well, might make it more

> convinceable? Ok, here

> is my letter...

>

> Hi..this message is for Dr. Mercola. I have been

> subcribing to your news

> letter for some time now and have come to really

> respect your ideas and

> philosophies. That is why I have decided to write to

> you to inform you of

> something that may seem quite remarkable and indeed

> it is. I am part of a

> group of thousands of MS and other auto-immune

> disorder patients. We

> are all part of this group because we are all lucky

> enough to own a computer

> and after doing some research online we all

> miracluously found a therapy

> that Dr. Bihari in New York has been experimenting

> with for maybe some 15

> years now. It is called Low Dose Naltrexone and I

> have been taking a low

> dose of 4.5mg of this drug for 3 years now for my

> MS. I am here to tell you

> that it has halted any further progress of my MS,

> which is, by all accounts

> secondary progressive and I really don't have any MS

> issues to speak of

> other then some permanent damage from the pre LDN

> days. Many in the group

> feel the way I do, that you are a wonderful person

> to contact as many of us

> get the newsletter and feel that you would be

> receptive to such information.

> I live about 25 miles north of Chicago so I

> volunteered to write and told

> the group that I'd even be willing to meet with you

> if you would be

> interested. I am part of the patient panel for the

> first ever LDN Conference

> that is being held in New York this June 11th. There

> is so much to tell

> regarding this remarkable therapy and I don't want

> to make this a long

> message but please write to me and I will explain to

> you the urgency of

> getting this information out to the public at large.

> It is amazing just how

> many people would stand to gain by such information

> about a tiny dose of a

> very harmless drug. ALS, Parkinsons, Rheumatoid

> Arthritis, Lupus, HIV and

> some cancers to name just a few. You see, we are up

> against the huge

> pharmaceuticals. This medication has been in use

> some 20 years now so

> therefore there is no hope for a patent for it. I'm

> sure you know where I'm

> going with this. There are thousands of us just

> using it for our MS. If you

> go to www.remedyfind.com you will see what actual

> patients say about what

> they use and LDN/Revia is rated #1 right now. Sad

> thing is that if you are

> an MS patient you will not even hear of this

> remarkable treatment. Is that

> fair to the typical MS patient I ask? You can find

> info about the LDN at

> www.ldninfo.org that is run by the son of a

> childhood friend of Dr. Bihari.

> As a doctor yourself, surely you realize just how

> much one lone doctor can

> do in this world of big business pharmaceuticals.

> Well thankfully the

> internet has helped greatly. What we need now is

> more influencial people on

> our side to get this therapy right where it needs to

> be, in the hands of

> deserving patients. Thanks so much for listening Dr.

> Mercola and keep up the

> good work. Please write to me and let me know if

> you'd like for me to pay a

> visit to your office. I will be attending the

> conference because my passion

> these days is LDN and what it has to offer so so

> many people. I say, huge

> pharmaceutals be damned...we the people will

> prevail. Joyce

> ****************************** (full name, address

> and phone number deleted

> from original letter to protect the innocent..lol)

> (sorry for the length of

> this message but we really do need someone to

> champion this for us, please

> don't let us down).

>

> Here is their quick response. Not exactly the

> response that I was expecting:

>

> " Dear Subscriber,

>

> We thank you very much for the feedback. We will

> make sure this information

> is looked into and perhaps Dr. Mercola will address

> your question in a

> future newsletter article. Please note that we

> cannot respond to individual

> health and product questions.

>

> The Mercola.com Staff "

>

>

>

__________________________________________________

[Guest guest]

Good job, Joyce. I've been subscribing to the Mercola newsletter for

about a year now and never thought of writing to him. Thank you.

[Guest guest]

JOYCE, YOU REALLYDID RELAY THE INFO IN A VERY ARTICULATE MANNER AND I'M SURE YOU SPENT A GREAT DEAL OF TIME ON IT. THANKS FROM ALL OF US. I THINK SEVERAL OF US SHOULD DO A FOLLOW UP WITH HIM AND WHEN I DO WILL BE SURE TO STRESS THE NON TOXIC EFFECTS OF THE THERAPY. THIS SHOULD CARRY ALOT OF MERIT SINCE HE IS A NATURALIST.I WANT TO MAKE SURE HE KNOWS HOW LOW, LOW DOSE NALTREXONE REALLY IS! GOD BLESS AND THANKS FOR ALL YOUR EFFORTS. KATHY

[low dose naltrexone] Hi group....my Mercola letter....

Hi group,Ok, first I thought...*gulp*...I was not volunteering to write to Dr. Mercola but rather thought that if several did so, I'd be up for going to physically visit with him, seeing that my close proximity to him was a plus. I'm never all that secure in the fact that my letter writing abilities are all that great..*s*. Anyway, I thought I'd give it a shot and e-mailed him today at his www.mercola.com site. This is the letter in it's entirety and that is followed by the response that I received. I do heartily recommend that others write to him as well, might make it more convinceable? Ok, here is my letter...Hi..this message is for Dr. Mercola. I have been subcribing to your news letter for some time now and have come to really respect your ideas and philosophies. That is why I have decided to write to you to inform you of something that may seem quite remarkable and indeed it is. I am part of a group of thousands of MS and other auto-immune disorder patients. We are all part of this group because we are all lucky enough to own a computer and after doing some research online we all miracluously found a therapy that Dr. Bihari in New York has been experimenting with for maybe some 15 years now. It is called Low Dose Naltrexone and I have been taking a low dose of 4.5mg of this drug for 3 years now for my MS. I am here to tell you that it has halted any further progress of my MS, which is, by all accounts secondary progressive and I really don't have any MS issues to speak of other then some permanent damage from the pre LDN days. Many in the group feel the way I do, that you are a wonderful person to contact as many of us get the newsletter and feel that you would be receptive to such information. I live about 25 miles north of Chicago so I volunteered to write and told the group that I'd even be willing to meet with you if you would be interested. I am part of the patient panel for the first ever LDN Conference that is being held in New York this June 11th. There is so much to tell regarding this remarkable therapy and I don't want to make this a long message but please write to me and I will explain to you the urgency of getting this information out to the public at large. It is amazing just how many people would stand to gain by such information about a tiny dose of a very harmless drug. ALS, Parkinsons, Rheumatoid Arthritis, Lupus, HIV and some cancers to name just a few. You see, we are up against the huge pharmaceuticals. This medication has been in use some 20 years now so therefore there is no hope for a patent for it. I'm sure you know where I'm going with this. There are thousands of us just using it for our MS. If you go to www.remedyfind.com you will see what actual patients say about what they use and LDN/Revia is rated #1 right now. Sad thing is that if you are an MS patient you will not even hear of this remarkable treatment. Is that fair to the typical MS patient I ask? You can find info about the LDN at www.ldninfo.org that is run by the son of a childhood friend of Dr. Bihari. As a doctor yourself, surely you realize just how much one lone doctor can do in this world of big business pharmaceuticals. Well thankfully the internet has helped greatly. What we need now is more influencial people on our side to get this therapy right where it needs to be, in the hands of deserving patients. Thanks so much for listening Dr. Mercola and keep up the good work. Please write to me and let me know if you'd like for me to pay a visit to your office. I will be attending the conference because my passion these days is LDN and what it has to offer so so many people. I say, huge pharmaceutals be damned...we the people will prevail. Joyce ****************************** (full name, address and phone number deleted from original letter to protect the innocent..lol) (sorry for the length of this message but we really do need someone to champion this for us, please don't let us down).Here is their quick response. Not exactly the response that I was expecting:"Dear Subscriber,We thank you very much for the feedback. We will make sure this informationis looked into and perhaps Dr. Mercola will address your question in afuture newsletter article. Please note that we cannot respond to individualhealth and product questions.The Mercola.com Staff"