Re: Not waiting any longer

[Guest guest]

Hey Dave thanks - don't have any Copaxone - never took any ABCR drugs and don't believe I ever will. Will be happy to smash yours thought!!!

Take care - ann

[Guest guest]

GO GO KERRY....WE ARE WITH YOU ALL THE WAY...WE WILL HAVE A REBIFF

BURNING PARTY..LOL. ALL THE LUCK IN THE WORLD WITH LDN,

HUGS, SALLY

> Hi Everyone,

> I made a decision today....I'm not going to wait until my

appointment

> with my neuro for my prescription of ldn. I have an appointment

with

> him on the 21st of this month. I have mailed him all kinds of

> information (I'm 2 hours away from him) on ldn, and told him that

I

> wanted him to read it, and that we would discuss it when I seen

him

> on the 21st. I've only seen this man once before, so I have no

idea

> of what his views are going to be on ldn, and from what I've read

in

> here there are very few neuros that are open minded enough to let

> people try it.

>

> I sat here this morning looking at my rebif needle, thinking how

much

> I did NOT want to take it..... and I didn't take it, it's still

> sitting here on my desk. I called and made an appointment with my

GP

> for Monday morning. I have given him the information already, but

I

> doubt that he has read it. I'm going to give him a week to look

into

> it, and then I'm going to go back and see him again. He has been

> very open minded to everything else I have suggested in the

past...so

> hopefully he will be open minded about ldn as well.

>

> Even if my GP does give me the ldn, I'm not going to tell my

neuro.

> I just really want to see what he will say about it..and if he

says

> no, then I'll say ha ha..I'm already taking it (hopefully) The

thing

> is that I would really like to go through my neuro, as he has way

> more potential of reaching others with MS, but in the meantime I

have

> to look after myself and just get on the stuff. Cross your

fingers

> for me k? Take care....Kerry

[Guest guest]

Everyone in the world is invited to my place in South Carthage. Maine for a Copaxone smashing party on Labor day! Bring your own everything!

----- Original Message -----

From: Sally

low dose naltrexone

Sent: Wednesday, July 09, 2003 5:47 PM

Subject: [low dose naltrexone] Re: Not waiting any longer

GO GO KERRY....WE ARE WITH YOU ALL THE WAY...WE WILL HAVE A REBIFF BURNING PARTY..LOL. ALL THE LUCK IN THE WORLD WITH LDN,HUGS, SALLY> Hi Everyone,> I made a decision today....I'm not going to wait until my appointment > with my neuro for my prescription of ldn. I have an appointment with > him on the 21st of this month. I have mailed him all kinds of > information (I'm 2 hours away from him) on ldn, and told him that I > wanted him to read it, and that we would discuss it when I seen him > on the 21st. I've only seen this man once before, so I have no idea > of what his views are going to be on ldn, and from what I've read in > here there are very few neuros that are open minded enough to let > people try it. > > I sat here this morning looking at my rebif needle, thinking how much > I did NOT want to take it..... and I didn't take it, it's still > sitting here on my desk. I called and made an appointment with my GP > for Monday morning. I have given him the information already, but I > doubt that he has read it. I'm going to give him a week to look into > it, and then I'm going to go back and see him again. He has been > very open minded to everything else I have suggested in the past...so > hopefully he will be open minded about ldn as well. > > Even if my GP does give me the ldn, I'm not going to tell my neuro. > I just really want to see what he will say about it..and if he says > no, then I'll say ha ha..I'm already taking it (hopefully) The thing > is that I would really like to go through my neuro, as he has way > more potential of reaching others with MS, but in the meantime I have > to look after myself and just get on the stuff. Cross your fingers > for me k? Take care....Kerry

[Guest guest]

Go for it, Kerry, and we wish you the best.

Noland

----- Original Message -----

From: " Kerry " <r.s@...>

<low dose naltrexone >

Sent: Wednesday, July 09, 2003 3:27 PM

Subject: [low dose naltrexone] Not waiting any longer

> Hi Everyone,

> I made a decision today....I'm not going to wait until my appointment

> with my neuro for my prescription of ldn. I have an appointment with

> him on the 21st of this month. I have mailed him all kinds of

> information (I'm 2 hours away from him) on ldn, and told him that I

> wanted him to read it, and that we would discuss it when I seen him

> on the 21st. I've only seen this man once before, so I have no idea

> of what his views are going to be on ldn, and from what I've read in

> here there are very few neuros that are open minded enough to let

> people try it.

>

> I sat here this morning looking at my rebif needle, thinking how much

> I did NOT want to take it..... and I didn't take it, it's still

> sitting here on my desk. I called and made an appointment with my GP

> for Monday morning. I have given him the information already, but I

> doubt that he has read it. I'm going to give him a week to look into

> it, and then I'm going to go back and see him again. He has been

> very open minded to everything else I have suggested in the past...so

> hopefully he will be open minded about ldn as well.

>

> Even if my GP does give me the ldn, I'm not going to tell my neuro.

> I just really want to see what he will say about it..and if he says

> no, then I'll say ha ha..I'm already taking it (hopefully) The thing

> is that I would really like to go through my neuro, as he has way

> more potential of reaching others with MS, but in the meantime I have

> to look after myself and just get on the stuff. Cross your fingers

> for me k? Take care....Kerry

>

>

>

>

[Guest guest]

Way to go. I hope that you get your LDN. But if you don't, don't give up.

There are other ways. We all went through this. I just wish that I didn't

waste so much time waiting to see all those doctors that I went to. Like I

said it was a waste of time. I could have been on the LDN for a lot longer

than I am. I have been on it a month and doing good. Please let us know

how you make out We care.

Marie

----- Original Message -----

From: " Kerry " <r.s@...>

<low dose naltrexone >

Sent: Wednesday, July 09, 2003 5:27 PM

Subject: [low dose naltrexone] Not waiting any longer

> Hi Everyone,

> I made a decision today....I'm not going to wait until my appointment

> with my neuro for my prescription of ldn. I have an appointment with

> him on the 21st of this month. I have mailed him all kinds of

> information (I'm 2 hours away from him) on ldn, and told him that I

> wanted him to read it, and that we would discuss it when I seen him

> on the 21st. I've only seen this man once before, so I have no idea

> of what his views are going to be on ldn, and from what I've read in

> here there are very few neuros that are open minded enough to let

> people try it.

>

> I sat here this morning looking at my rebif needle, thinking how much

> I did NOT want to take it..... and I didn't take it, it's still

> sitting here on my desk. I called and made an appointment with my GP

> for Monday morning. I have given him the information already, but I

> doubt that he has read it. I'm going to give him a week to look into

> it, and then I'm going to go back and see him again. He has been

> very open minded to everything else I have suggested in the past...so

> hopefully he will be open minded about ldn as well.

>

> Even if my GP does give me the ldn, I'm not going to tell my neuro.

> I just really want to see what he will say about it..and if he says

> no, then I'll say ha ha..I'm already taking it (hopefully) The thing

> is that I would really like to go through my neuro, as he has way

> more potential of reaching others with MS, but in the meantime I have

> to look after myself and just get on the stuff. Cross your fingers

> for me k? Take care....Kerry

>

>

>

>

[Guest guest]

WELL IT'S TOO LATE DAVE...I THREW OUT $1000 WORTH OF COPAXONE FOR A

BOTTLE OF $20. LDN...LOL...SALLY

> Hey Dave thanks - don't have any Copaxone - never took any ABCR

drugs and

> don't believe I ever will. Will be happy to smash yours thought!!!

>

> Take care - ann

[Guest guest]

You go girl. Oh I just wanted to mention that I read somewhere that Dr.

Bihari will never refuse a call from another doctor who calls wanting info

about the LDN so if your doc is wondering, have him call? Joyce.

From: " Kerry "

low dose naltrexone

Subject: [low dose naltrexone] Not waiting any longer

Date: Wed, 09 Jul 2003 21:27:11 -0000

Hi Everyone,

I made a decision today....I'm not going to wait until my appointment

with my neuro for my prescription of ldn. I have an appointment with

him on the 21st of this month. I have mailed him all kinds of

information (I'm 2 hours away from him) on ldn, and told him that I

wanted him to read it, and that we would discuss it when I seen him

on the 21st. I've only seen this man once before, so I have no idea

of what his views are going to be on ldn, and from what I've read in

here there are very few neuros that are open minded enough to let

people try it.

I sat here this morning looking at my rebif needle, thinking how much

I did NOT want to take it..... and I didn't take it, it's still

sitting here on my desk. I called and made an appointment with my GP

for Monday morning. I have given him the information already, but I

doubt that he has read it. I'm going to give him a week to look into

it, and then I'm going to go back and see him again. He has been

very open minded to everything else I have suggested in the past...so

hopefully he will be open minded about ldn as well.

Even if my GP does give me the ldn, I'm not going to tell my neuro.

I just really want to see what he will say about it..and if he says

no, then I'll say ha ha..I'm already taking it (hopefully) The thing

is that I would really like to go through my neuro, as he has way

more potential of reaching others with MS, but in the meantime I have

to look after myself and just get on the stuff. Cross your fingers

for me k? Take care....Kerry

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