Re: diagnosed with ms

[Guest guest]

Read this before seeing your neurologist:

How To Talk to Your Doctor about LDN

http://www.gazorpa.com/PatientGuide.html

If he says no, come back here asap, we have other ways/ideas to

get you on LDN.

Good luck.

-Art

>

> Hello Everyone:

>

> About 5 years ago I was diagnosed with MS. Before that it was

Lupus.

> Upon seeing the MS Specialist he made a final diagnosis of MS,

based

> on MRI findings. His course of treatment was the ABC drugs (

Avonex,

> Rebif). I was in denial and so decided not to proceed with his

> recommendations. I also stopped going to him as I found him to be

> very arrogant and a uncompasionate Dr. I have since seen 2 other

> Neurologists plus have had another MRI , this last was showed

disease

> progression, but the neurologist I went to seemed to think because

I

> showed no visible signs of disability, there was no reason to treat

> me, it would be a let's wait and see what happens. Well, in last

last

> 3 months I have had 2 Flares, the 2nd one was a major one, and the

> residual effects have been difficult, MY feet are always numb, and

> spastic the tightness is also unbearable, I have also experience

> numbness in my legs and waist that extends to my torso. This has

been

> very frightening. 2 weeks ago as I was getting ready to go sawy for

a

> few days, I got out of my car to take the shuttle bus to the

AIrport

> and I could not stand my legs felt like jello. I am very scared

that

> this disease has taken hold of my body and I am only going to get

> worse over time. I have since learnt about Naltrexone and have

> mentioned it to my family doctor, because this is a drug that

hasn't

> been approved by the MS society or recognized by them or by the

> medical communtiy nobody seems to want to get involved. Now I am

> seeing my Neuroligist again tomorrow in the hope that he will

> consider putting me on the drug.

>

> I would appreciated any feedback that you would care to offer me on

> this subject.

>

> I look forward to hearing from those who have shared similiar

> experiences. Or have suggestions on how I can get myself on this

drug

> if my doctor refuses to offer it to me.

>

> Thanks,

>

>

>

[Guest guest]

Hello Art:

A Million Thank-yous. How Wonderful that you have

provided me with this information before my

appointment today. I am now prepared to present my

Doctor with all the information you have kindly made

available to me. I only hope that he agrees and writes

the prescription for Naltrexone. I will let you know

the outcome later.

Thanks for all your help.

--- Art Hansen <rtee54@...> wrote:

>

> Read this before seeing your neurologist:

>

> How To Talk to Your Doctor about LDN

>

> http://www.gazorpa.com/PatientGuide.html

>

> If he says no, come back here asap, we have other

> ways/ideas to

> get you on LDN.

>

> Good luck.

>

> -Art

>

>

> >

> > Hello Everyone:

> >

> > About 5 years ago I was diagnosed with MS. Before

> that it was

> Lupus.

> > Upon seeing the MS Specialist he made a final

> diagnosis of MS,

> based

> > on MRI findings. His course of treatment was the

> ABC drugs (

> Avonex,

> > Rebif). I was in denial and so decided not to

> proceed with his

> > recommendations. I also stopped going to him as I

> found him to be

> > very arrogant and a uncompasionate Dr. I have

> since seen 2 other

> > Neurologists plus have had another MRI , this last

> was showed

> disease

> > progression, but the neurologist I went to seemed

> to think because

> I

> > showed no visible signs of disability, there was

> no reason to treat

> > me, it would be a let's wait and see what happens.

> Well, in last

> last

> > 3 months I have had 2 Flares, the 2nd one was a

> major one, and the

> > residual effects have been difficult, MY feet are

> always numb, and

> > spastic the tightness is also unbearable, I have

> also experience

> > numbness in my legs and waist that extends to my

> torso. This has

> been

> > very frightening. 2 weeks ago as I was getting

> ready to go sawy for

> a

> > few days, I got out of my car to take the shuttle

> bus to the

> AIrport

> > and I could not stand my legs felt like jello. I

> am very scared

> that

> > this disease has taken hold of my body and I am

> only going to get

> > worse over time. I have since learnt about

> Naltrexone and have

> > mentioned it to my family doctor, because this is

> a drug that

> hasn't

> > been approved by the MS society or recognized by

> them or by the

> > medical communtiy nobody seems to want to get

> involved. Now I am

> > seeing my Neuroligist again tomorrow in the hope

> that he will

> > consider putting me on the drug.

> >

> > I would appreciated any feedback that you would

> care to offer me on

> > this subject.

> >

> > I look forward to hearing from those who have

> shared similiar

> > experiences. Or have suggestions on how I can get

> myself on this

> drug

> > if my doctor refuses to offer it to me.

> >

> > Thanks,

> >

> >

> >

>

>

>

________________________________________________________________________________\

____

Check out the hottest 2008 models today at Autos.

http://autos./new_cars.html

[Guest guest]

Hello Again:

Well I am back to squsre one. I presented my

Neurologist with all the information you suggested I

take with to my apppointment, he casually looked at

it, and said to me he was aware of the drug, but

claims there are not many using it. Please keep in

mind I live in Canada, I don't know if this is true,or

not as I know there are alot of people here in this

group using LDN but am unsure where they are located.

I think he was giving me an excuse not to prescribe.

He asked me if I would be interested in entering a

clinical Trial I told him yes, so now it is " I

willget back to you and let you know " situation, and

in the interim I am getting worse. I am at the point

where standing on my feet for any length of time is a

problem. I want to go on the Naltrexone immediately, I

just p\ut in a call to my family doctor and I am

hoping with some persistence she will agree to put me

on this drug. I have also put in a call to a friend of

mine who happens to be a pharmacist to see if maybe he

can help me. I am really at my wits end with this. I

want to act now. If you have any suggestions I would

certainly very much appreciate hearing back from you.

Thanks.

--- Art Hansen <rtee54@...> wrote:

>

> Read this before seeing your neurologist:

>

> How To Talk to Your Doctor about LDN

>

> http://www.gazorpa.com/PatientGuide.html

>

> If he says no, come back here asap, we have other

> ways/ideas to

> get you on LDN.

>

> Good luck.

>

> -Art

>

>

> >

> > Hello Everyone:

> >

> > About 5 years ago I was diagnosed with MS. Before

> that it was

> Lupus.

> > Upon seeing the MS Specialist he made a final

> diagnosis of MS,

> based

> > on MRI findings. His course of treatment was the

> ABC drugs (

> Avonex,

> > Rebif). I was in denial and so decided not to

> proceed with his

> > recommendations. I also stopped going to him as I

> found him to be

> > very arrogant and a uncompasionate Dr. I have

> since seen 2 other

> > Neurologists plus have had another MRI , this last

> was showed

> disease

> > progression, but the neurologist I went to seemed

> to think because

> I

> > showed no visible signs of disability, there was

> no reason to treat

> > me, it would be a let's wait and see what happens.

> Well, in last

> last

> > 3 months I have had 2 Flares, the 2nd one was a

> major one, and the

> > residual effects have been difficult, MY feet are

> always numb, and

> > spastic the tightness is also unbearable, I have

> also experience

> > numbness in my legs and waist that extends to my

> torso. This has

> been

> > very frightening. 2 weeks ago as I was getting

> ready to go sawy for

> a

> > few days, I got out of my car to take the shuttle

> bus to the

> AIrport

> > and I could not stand my legs felt like jello. I

> am very scared

> that

> > this disease has taken hold of my body and I am

> only going to get

> > worse over time. I have since learnt about

> Naltrexone and have

> > mentioned it to my family doctor, because this is

> a drug that

> hasn't

> > been approved by the MS society or recognized by

> them or by the

> > medical communtiy nobody seems to want to get

> involved. Now I am

> > seeing my Neuroligist again tomorrow in the hope

> that he will

> > consider putting me on the drug.

> >

> > I would appreciated any feedback that you would

> care to offer me on

> > this subject.

> >

> > I look forward to hearing from those who have

> shared similiar

> > experiences. Or have suggestions on how I can get

> myself on this

> drug

> > if my doctor refuses to offer it to me.

> >

> > Thanks,

> >

> >

> >

>

>

>

________________________________________________________________________________\

____

Check out the hottest 2008 models today at Autos.

http://autos./new_cars.html

[Guest guest]

Not sure if he will help you due to you living outside the USA, but

this doctor does telephone consulations and prescribes LDN:

G. Ayre, M.D.

Contemporary Medicine

322 Burr Ridge Parkway

Burr Ridge, IL 60527

630.321.9010

http://www.contemporarymedicine.net/index.htm

If he's of no help, you can purchase Naltrexone online:

https://www.riverpharmacy.com/

and make your own homemade LDN:

Liquid LDN (Easiest): Acquire some ml measuring equipment from the

baby section of a Drug Store and a small bottle with a screw-on cap.

Put 50ml of water (distilled is best) and one 50mg " ReVia " Naltrexone

tablet in the small bottle and let it dissolve with a little time and

shaking. Now each ml of water in that small bottle contains 1 mg of

Naltrexone. At bedtime shake the bottle, take a desired dose (no more

than 4.5ml), chase it down with some water and store the small bottle

in the refrigerator. Some people have reported splitting the tablet

in half and dissolving it in 25ml of water to assure freshness every

week.

http://goodshape.net/HomemadeLDN.html

Art

--

>

> Hello Again:

>

> Well I am back to squsre one. I presented my

> Neurologist with all the information you suggested I

> take with to my apppointment, he casually looked at

> it, and said to me he was aware of the drug, but

> claims there are not many using it. Please keep in

> mind I live in Canada, I don't know if this is true,or

> not as I know there are alot of people here in this

> group using LDN but am unsure where they are located.

> I think he was giving me an excuse not to prescribe.

> He asked me if I would be interested in entering a

> clinical Trial I told him yes, so now it is " I

> willget back to you and let you know " situation, and

> in the interim I am getting worse. I am at the point

> where standing on my feet for any length of time is a

> problem. I want to go on the Naltrexone immediately, I

> just p\ut in a call to my family doctor and I am

> hoping with some persistence she will agree to put me

> on this drug. I have also put in a call to a friend of

> mine who happens to be a pharmacist to see if maybe he

> can help me. I am really at my wits end with this. I

> want to act now. If you have any suggestions I would

> certainly very much appreciate hearing back from you.

>

> Thanks.

>

>

>

[Guest guest]

,

Leave your neuro, he doesn't care about your suffering. He casually looked at what you brought in. That's your first clue and he bargained with you to maybe go into a trial. You need it now. There are doctors that will give you a phone appointment and fax the subscription to a compounding pharmacy. I was hanging by a thread and after trying 3 doctors went the phone appointment route. I pay only $20 a month for 3.0 mg of low dose naltrexone.

How can he make a statement that not many people are taking it. I don't know the numbers but I'm sure someone on this group does. You are not a lab rat, you are a human being that deserves to get ldn now.

Be Strong......

email me privately if you need more info

From: low dose naltrexone [mailto:low dose naltrexone ] On Behalf Of Suzzie BSent: Thursday, September 27, 2007 12:58 PMlow dose naltrexone Subject: Re: [low dose naltrexone] Re: Diagnosed with MS

Hello Again:Well I am back to squsre one. I presented myNeurologist with all the information you suggested Itake with to my apppointment, he casually looked atit, and said to me he was aware of the drug, butclaims there are not many using it. Please keep inmind I live in Canada, I don't know if this is true,ornot as I know there are alot of people here in thisgroup using LDN but am unsure where they are located.I think he was giving me an excuse not to prescribe.He asked me if I would be interested in entering aclinical Trial I told him yes, so now it is " Iwillget back to you and let you know " situation, andin the interim I am getting worse. I am at the pointwhere standing on my feet for any length of time is aproblem. I want to go on the Naltrexone immediately, Ijust p\ut in a call to my family doctor and I amhoping with some persistence she will agree to put meon this drug. I have also put in a call to a friend ofmine who happens to be a pharmacist to see if maybe hecan help me. I am really at my wits end with this. Iwant to act now. If you have any suggestions I wouldcertainly very much appreciate hearing back from you.Thanks.--- Art Hansen <rtee54 > wrote:> > Read this before seeing your neurologist:> > How To Talk to Your Doctor about LDN> > http://www.gazorpa.com/PatientGuide.html> > If he says no, come back here asap, we have other> ways/ideas to > get you on LDN.> > Good luck.> > -Art> > > >> > Hello Everyone:> > > > About 5 years ago I was diagnosed with MS. Before> that it was > Lupus. > > Upon seeing the MS Specialist he made a final> diagnosis of MS, > based > > on MRI findings. His course of treatment was the> ABC drugs ( > Avonex, > > Rebif). I was in denial and so decided not to> proceed with his > > recommendations. I also stopped going to him as I> found him to be > > very arrogant and a uncompasionate Dr. I have> since seen 2 other > > Neurologists plus have had another MRI , this last> was showed > disease > > progression, but the neurologist I went to seemed> to think because > I > > showed no visible signs of disability, there was> no reason to treat > > me, it would be a let's wait and see what happens.> Well, in last > last > > 3 months I have had 2 Flares, the 2nd one was a> major one, and the > > residual effects have been difficult, MY feet are> always numb, and > > spastic the tightness is also unbearable, I have> also experience > > numbness in my legs and waist that extends to my> torso. This has > been > > very frightening. 2 weeks ago as I was getting> ready to go sawy for > a > > few days, I got out of my car to take the shuttle> bus to the > AIrport > > and I could not stand my legs felt like jello. I> am very scared > that > > this disease has taken hold of my body and I am> only going to get > > worse over time. I have since learnt about> Naltrexone and have > > mentioned it to my family doctor, because this is> a drug that > hasn't > > been approved by the MS society or recognized by> them or by the > > medical communtiy nobody seems to want to get> involved. Now I am > > seeing my Neuroligist again tomorrow in the hope> that he will > > consider putting me on the drug. > > > > I would appreciated any feedback that you would> care to offer me on > > this subject.> > > > I look forward to hearing from those who have> shared similiar > > experiences. Or have suggestions on how I can get> myself on this > drug > > if my doctor refuses to offer it to me.> > > > Thanks,> > > > > >> > > __________________________________________________________Check out the hottest 2008 models today at Autos.http://autos./new_cars.html

[Guest guest]

Hi ,

I am also from Canada, recently diagnosised with MS, not on drup therapy yet, but very interested in LDN as well. I have an appointment with my family doctor next week - going to ask for a prescription of LDN, if no go I am waiting for an appointment with the Calgary MS clinic - will then ask them. Hopefully either will work - although I am still looking for a pharmacy that dispences it. If you have some success before that, please let me know. thanks Kristie

P.S. Or if anyone else on this site knows of a DR. that prescribes in AB, or an AB pharmacy that dispenses, please let me know. thanks

Re: [low dose naltrexone] Re: Diagnosed with MS

Hello Again:Well I am back to squsre one. I presented myNeurologist with all the information you suggested Itake with to my apppointment, he casually looked atit, and said to me he was aware of the drug, butclaims there are not many using it. Please keep inmind I live in Canada, I don't know if this is true,ornot as I know there are alot of people here in thisgroup using LDN but am unsure where they are located.I think he was giving me an excuse not to prescribe.He asked me if I would be interested in entering aclinical Trial I told him yes, so now it is " Iwillget back to you and let you know " situation, andin the interim I am getting worse. I am at the pointwhere standing on my feet for any length of time is aproblem. I want to go on the Naltrexone immediately, Ijust p\ut in a call to my family doctor and I amhoping with some persistence she will agree to put meon this drug. I have also put in a call to a friend ofmine who happens to be a pharmacist to see if maybe hecan help me. I am really at my wits end with this. Iwant to act now. If you have any suggestions I wouldcertainly very much appreciate hearing back from you.Thanks.--- Art Hansen <rtee54 > wrote:> > Read this before seeing your neurologist:> > How To Talk to Your Doctor about LDN> > http://www.gazorpa.com/PatientGuide.html> > If he says no, come back here asap, we have other> ways/ideas to > get you on LDN.> > Good luck.> > -Art> > > >> > Hello Everyone:> > > > About 5 years ago I was diagnosed with MS. Before> that it was > Lupus. > > Upon seeing the MS Specialist he made a final> diagnosis of MS, > based > > on MRI findings. His course of treatment was the> ABC drugs ( > Avonex, > > Rebif). I was in denial and so decided not to> proceed with his > > recommendations. I also stopped going to him as I> found him to be > > very arrogant and a uncompasionate Dr. I have> since seen 2 other > > Neurologists plus have had another MRI , this last> was showed > disease > > progression, but the neurologist I went to seemed> to think because > I > > showed no visible signs of disability, there was> no reason to treat > > me, it would be a let's wait and see what happens.> Well, in last > last > > 3 months I have had 2 Flares, the 2nd one was a> major one, and the > > residual effects have been difficult, MY feet are> always numb, and > > spastic the tightness is also unbearable, I have> also experience > > numbness in my legs and waist that extends to my> torso. This has > been > > very frightening. 2 weeks ago as I was getting> ready to go sawy for > a > > few days, I got out of my car to take the shuttle> bus to the > AIrport > > and I could not stand my legs felt like jello. I> am very scared > that > > this disease has taken hold of my body and I am> only going to get > > worse over time. I have since learnt about> Naltrexone and have > > mentioned it to my family doctor, because this is> a drug that > hasn't > > been approved by the MS society or recognized by> them or by the > > medical communtiy nobody seems to want to get> involved. Now I am > > seeing my Neuroligist again tomorrow in the hope> that he will > > consider putting me on the drug. > > > > I would appreciated any feedback that you would> care to offer me on > > this subject.> > > > I look forward to hearing from those who have> shared similiar > > experiences. Or have suggestions on how I can get> myself on this > drug > > if my doctor refuses to offer it to me.> > > > Thanks,> > > > > >> > > __________________________________________________________Check out the hottest 2008 models today at Autos.http://autos./new_cars.html

Internal Virus Database is out-of-date.Checked by AVG.Version: 7.5.430 / Virus Database: 268.14.6/536 - Release Date: 11/16/2006 3:51 PM

[Guest guest]

Hi Caroline,

A gal named Crystal maintains a list by location of physicians who

prescribe LDN and of pharmacies that compound it. You can contact her at

crystalangel6771@...

If that doesn't work out, you can buy 50 mg Naltrexone without a

prescription tablets here:

http://tinyurl.com/2vfdw5

and convert them to LDN using the instructions here:

http://tinyurl.com/3alm3y

For more information about LDN, visit

http://tinyurl.com/2boot2

With best wishes,

Dudley Delany

dudley_delany

[Guest guest]

Hi Caroline:

Not sure why you email didn't come through. Should not

of been a problem. I am at a road block right now,

nobody wants to prescrible this drug for me. If you

wouldn't mind sending that information once again I

would appreciate it. I hope your doctor listens and

prescribes what you need. I in the interim am seeing

another Neuroligist in November, so we'll see, my

family doctor told me if I should find a patient who

is on this drug and would be prepared to give me their

doctors name then she would be willing to speak to

their doctor and go from there. Anyways, good luck and

all the best.

--- Caroline Remax <remaxcaroline@...> wrote:

> Hi ,

> I am also from Canada, recently diagnosised with

> MS, not on drup therapy yet, but very interested in

> LDN as well. I have an appointment with my family

> doctor next week - going to ask for a prescription

> of LDN, if no go I am waiting for an appointment

> with the Calgary MS clinic - will then ask them.

> Hopefully either will work - although I am still

> looking for a pharmacy that dispences it. If you

> have some success before that, please let me know.

> thanks Kristie

> P.S. Or if anyone else on this site knows of a

> DR. that prescribes in AB, or an AB pharmacy that

> dispenses, please let me know. thanks

> Re: [low dose naltrexone] Re: Diagnosed

> with MS

>

>

> Hello Again:

>

> Well I am back to squsre one. I presented my

> Neurologist with all the information you suggested

> I

> take with to my apppointment, he casually looked

> at

> it, and said to me he was aware of the drug, but

> claims there are not many using it. Please keep in

> mind I live in Canada, I don't know if this is

> true,or

> not as I know there are alot of people here in

> this

> group using LDN but am unsure where they are

> located.

> I think he was giving me an excuse not to

> prescribe.

> He asked me if I would be interested in entering a

> clinical Trial I told him yes, so now it is " I

> willget back to you and let you know " situation,

> and

> in the interim I am getting worse. I am at the

> point

> where standing on my feet for any length of time

> is a

> problem. I want to go on the Naltrexone

> immediately, I

> just p\ut in a call to my family doctor and I am

> hoping with some persistence she will agree to put

> me

> on this drug. I have also put in a call to a

> friend of

> mine who happens to be a pharmacist to see if

> maybe he

> can help me. I am really at my wits end with this.

> I

> want to act now. If you have any suggestions I

> would

> certainly very much appreciate hearing back from

> you.

>

> Thanks.

>

>

> --- Art Hansen <rtee54@...> wrote:

>

> >

> > Read this before seeing your neurologist:

> >

> > How To Talk to Your Doctor about LDN

> >

> > http://www.gazorpa.com/PatientGuide.html

> >

> > If he says no, come back here asap, we have

> other

> > ways/ideas to

> > get you on LDN.

> >

> > Good luck.

> >

> > -Art

> >

> >

> > >

> > > Hello Everyone:

> > >

> > > About 5 years ago I was diagnosed with MS.

> Before

> > that it was

> > Lupus.

> > > Upon seeing the MS Specialist he made a final

> > diagnosis of MS,

> > based

> > > on MRI findings. His course of treatment was

> the

> > ABC drugs (

> > Avonex,

> > > Rebif). I was in denial and so decided not to

> > proceed with his

> > > recommendations. I also stopped going to him

> as I

> > found him to be

> > > very arrogant and a uncompasionate Dr. I have

> > since seen 2 other

> > > Neurologists plus have had another MRI , this

> last

> > was showed

> > disease

> > > progression, but the neurologist I went to

> seemed

> > to think because

> > I

> > > showed no visible signs of disability, there

> was

> > no reason to treat

> > > me, it would be a let's wait and see what

> happens.

> > Well, in last

> > last

> > > 3 months I have had 2 Flares, the 2nd one was

> a

> > major one, and the

> > > residual effects have been difficult, MY feet

> are

> > always numb, and

> > > spastic the tightness is also unbearable, I

> have

> > also experience

> > > numbness in my legs and waist that extends to

> my

> > torso. This has

> > been

> > > very frightening. 2 weeks ago as I was getting

> > ready to go sawy for

> > a

> > > few days, I got out of my car to take the

> shuttle

> > bus to the

> > AIrport

> > > and I could not stand my legs felt like jello.

> I

> > am very scared

> > that

> > > this disease has taken hold of my body and I

> am

> > only going to get

> > > worse over time. I have since learnt about

> > Naltrexone and have

> > > mentioned it to my family doctor, because this

> is

> > a drug that

> > hasn't

> > > been approved by the MS society or recognized

> by

> > them or by the

> > > medical communtiy nobody seems to want to get

> > involved. Now I am

> > > seeing my Neuroligist again tomorrow in the

> hope

> > that he will

> > > consider putting me on the drug.

> > >

> > > I would appreciated any feedback that you

> would

> > care to offer me on

> > > this subject.

> > >

> > > I look forward to hearing from those who have

> > shared similiar

> > > experiences. Or have suggestions on how I can

> get

> > myself on this

> > drug

> > > if my doctor refuses to offer it to me.

> > >

> > > Thanks,

> > >

> > >

> > >

> >

> >

> >

>

>

>

__________________________________________________________

> Check out the hottest 2008 models today at

> Autos.

> http://autos./new_cars.html

>

>

>

>

>

>

------------------------------------------------------------------------------

>

>

> Internal Virus Database is out-of-date.

> Checked by AVG.

> Version: 7.5.430 / Virus Database: 268.14.6/536 -

> Release

=== message truncated ===

________________________________________________________________________________\

____

Fussy? Opinionated? Impossible to please? Perfect. Join 's user panel and

lay it on us. http://surveylink./gmrs/_panel_invite.asp?a=7

[Guest guest]

Hi ,

Here is my direct address remaxcaroline@... where I work.. You can e-mail me there.. I will let you know how my appointment goes. Where do you live? I take it you have tried numerous doctors in your area and have had no luck. Kristie

Re: [low dose naltrexone] Re: Diagnosed> with MS> > > Hello Again:> > Well I am back to squsre one. I presented my> Neurologist with all the information you suggested> I> take with to my apppointment, he casually looked> at> it, and said to me he was aware of the drug, but> claims there are not many using it. Please keep in> mind I live in Canada, I don't know if this is> true,or> not as I know there are alot of people here in> this> group using LDN but am unsure where they are> located.> I think he was giving me an excuse not to> prescribe.> He asked me if I would be interested in entering a> clinical Trial I told him yes, so now it is " I> willget back to you and let you know " situation,> and> in the interim I am getting worse. I am at the> point> where standing on my feet for any length of time> is a> problem. I want to go on the Naltrexone> immediately, I> just p\ut in a call to my family doctor and I am> hoping with some persistence she will agree to put> me> on this drug. I have also put in a call to a> friend of> mine who happens to be a pharmacist to see if> maybe he> can help me. I am really at my wits end with this.> I> want to act now. If you have any suggestions I> would> certainly very much appreciate hearing back from> you.> > Thanks.> > > --- Art Hansen <rtee54 > wrote:> > > > > Read this before seeing your neurologist:> > > > How To Talk to Your Doctor about LDN> > > > http://www.gazorpa.com/PatientGuide.html> > > > If he says no, come back here asap, we have> other> > ways/ideas to > > get you on LDN.> > > > Good luck.> > > > -Art> > > > > > >> > > Hello Everyone:> > > > > > About 5 years ago I was diagnosed with MS.> Before> > that it was > > Lupus. > > > Upon seeing the MS Specialist he made a final> > diagnosis of MS, > > based > > > on MRI findings. His course of treatment was> the> > ABC drugs ( > > Avonex, > > > Rebif). I was in denial and so decided not to> > proceed with his > > > recommendations. I also stopped going to him> as I> > found him to be > > > very arrogant and a uncompasionate Dr. I have> > since seen 2 other > > > Neurologists plus have had another MRI , this> last> > was showed > > disease > > > progression, but the neurologist I went to> seemed> > to think because > > I > > > showed no visible signs of disability, there> was> > no reason to treat > > > me, it would be a let's wait and see what> happens.> > Well, in last > > last > > > 3 months I have had 2 Flares, the 2nd one was> a> > major one, and the > > > residual effects have been difficult, MY feet> are> > always numb, and > > > spastic the tightness is also unbearable, I> have> > also experience > > > numbness in my legs and waist that extends to> my> > torso. This has > > been > > > very frightening. 2 weeks ago as I was getting> > ready to go sawy for > > a > > > few days, I got out of my car to take the> shuttle> > bus to the > > AIrport > > > and I could not stand my legs felt like jello.> I> > am very scared > > that > > > this disease has taken hold of my body and I> am> > only going to get > > > worse over time. I have since learnt about> > Naltrexone and have > > > mentioned it to my family doctor, because this> is> > a drug that > > hasn't > > > been approved by the MS society or recognized> by> > them or by the > > > medical communtiy nobody seems to want to get> > involved. Now I am > > > seeing my Neuroligist again tomorrow in the> hope> > that he will > > > consider putting me on the drug. > > > > > > I would appreciated any feedback that you> would> > care to offer me on > > > this subject.> > > > > > I look forward to hearing from those who have> > shared similiar > > > experiences. Or have suggestions on how I can> get> > myself on this > > drug > > > if my doctor refuses to offer it to me.> > > > > > Thanks,> > > > > > > > >> > > > > > > > >__________________________________________________________> Check out the hottest 2008 models today at > Autos.> http://autos./new_cars.html> > > > > >----------------------------------------------------------> > > Internal Virus Database is out-of-date.> Checked by AVG.> Version: 7.5.430 / Virus Database: 268.14.6/536 -> Release === message truncated ===__________________________________________________________Fussy? Opinionated? Impossible to please? Perfect. Join 's user panel and lay it on us. http://surveylink./gmrs/_panel_invite.asp?a=7

Internal Virus Database is out-of-date.Checked by AVG.Version: 7.5.430 / Virus Database: 268.14.6/536 - Release Date: 11/16/2006 3:51 PM

[Guest guest]

Hi Caroline:

I am in Toronto. That's what I seem to be dealing

with. That is pretty bad and you don't even live here.

I am feeling as though nobody cares in the medical

community. At least though my family doctor is willing

to speak to another doctor that has prescribed the

drug. Have you had any experience with Kawalla. I am

thinking of trying that as well.

Take care.

--- Caroline Remax <remaxcaroline@...> wrote:

> Hi ,

> Here is my direct address

> remaxcaroline@... where I work.. You can

> e-mail me there.. I will let you know how my

> appointment goes. Where do you live? I take it you

> have tried numerous doctors in your area and have

> had no luck. Kristie

> Re: [low dose naltrexone] Re: Diagnosed

> > with MS

> >

> >

> > Hello Again:

> >

> > Well I am back to squsre one. I presented my

> > Neurologist with all the information you

> suggested

> > I

> > take with to my apppointment, he casually looked

> > at

> > it, and said to me he was aware of the drug, but

> > claims there are not many using it. Please keep

> in

> > mind I live in Canada, I don't know if this is

> > true,or

> > not as I know there are alot of people here in

> > this

> > group using LDN but am unsure where they are

> > located.

> > I think he was giving me an excuse not to

> > prescribe.

> > He asked me if I would be interested in entering

> a

> > clinical Trial I told him yes, so now it is " I

> > willget back to you and let you know "

> situation,

> > and

> > in the interim I am getting worse. I am at the

> > point

> > where standing on my feet for any length of time

> > is a

> > problem. I want to go on the Naltrexone

> > immediately, I

> > just p\ut in a call to my family doctor and I am

> > hoping with some persistence she will agree to

> put

> > me

> > on this drug. I have also put in a call to a

> > friend of

> > mine who happens to be a pharmacist to see if

> > maybe he

> > can help me. I am really at my wits end with

> this.

> > I

> > want to act now. If you have any suggestions I

> > would

> > certainly very much appreciate hearing back from

> > you.

> >

> > Thanks.

> >

> >

> > --- Art Hansen <rtee54@...> wrote:

> >

> > >

> > > Read this before seeing your neurologist:

> > >

> > > How To Talk to Your Doctor about LDN

> > >

> > > http://www.gazorpa.com/PatientGuide.html

> > >

> > > If he says no, come back here asap, we have

> > other

> > > ways/ideas to

> > > get you on LDN.

> > >

> > > Good luck.

> > >

> > > -Art

> > >

> > >

> > > >

> > > > Hello Everyone:

> > > >

> > > > About 5 years ago I was diagnosed with MS.

> > Before

> > > that it was

> > > Lupus.

> > > > Upon seeing the MS Specialist he made a

> final

> > > diagnosis of MS,

> > > based

> > > > on MRI findings. His course of treatment was

> > the

> > > ABC drugs (

> > > Avonex,

> > > > Rebif). I was in denial and so decided not

> to

> > > proceed with his

> > > > recommendations. I also stopped going to him

> > as I

> > > found him to be

> > > > very arrogant and a uncompasionate Dr. I

> have

> > > since seen 2 other

> > > > Neurologists plus have had another MRI ,

> this

> > last

> > > was showed

> > > disease

> > > > progression, but the neurologist I went to

> > seemed

> > > to think because

> > > I

> > > > showed no visible signs of disability, there

> > was

> > > no reason to treat

> > > > me, it would be a let's wait and see what

> > happens.

> > > Well, in last

> > > last

> > > > 3 months I have had 2 Flares, the 2nd one

> was

> > a

> > > major one, and the

> > > > residual effects have been difficult, MY

> feet

> > are

> > > always numb, and

> > > > spastic the tightness is also unbearable, I

> > have

> > > also experience

> > > > numbness in my legs and waist that extends

> to

> > my

> > > torso. This has

> > > been

> > > > very frightening. 2 weeks ago as I was

> getting

> > > ready to go sawy for

> > > a

> > > > few days, I got out of my car to take the

> > shuttle

>

=== message truncated ===

________________________________________________________________________________\

____

Need a vacation? Get great deals

to amazing places on Travel.

http://travel./

[Guest guest]

Hi Caroline:

I am in Toronto. That's what I seem to be dealing

with. That is pretty bad and you don't even live here.

I am feeling as though nobody cares in the medical

community. At least though my family doctor is willing

to speak to another doctor that has prescribed the

drug. Have you had any experience with Kawalla. I am

thinking of trying that as well.

Take care.

--- Caroline Remax <remaxcaroline@...> wrote:

> Hi ,

> Here is my direct address

> remaxcaroline@... where I work.. You can

> e-mail me there.. I will let you know how my

> appointment goes. Where do you live? I take it you

> have tried numerous doctors in your area and have

> had no luck. Kristie

> Re: [low dose naltrexone] Re: Diagnosed

> > with MS

> >

> >

> > Hello Again:

> >

> > Well I am back to squsre one. I presented my

> > Neurologist with all the information you

> suggested

> > I

> > take with to my apppointment, he casually looked

> > at

> > it, and said to me he was aware of the drug, but

> > claims there are not many using it. Please keep

> in

> > mind I live in Canada, I don't know if this is

> > true,or

> > not as I know there are alot of people here in

> > this

> > group using LDN but am unsure where they are

> > located.

> > I think he was giving me an excuse not to

> > prescribe.

> > He asked me if I would be interested in entering

> a

> > clinical Trial I told him yes, so now it is " I

> > willget back to you and let you know "

> situation,

> > and

> > in the interim I am getting worse. I am at the

> > point

> > where standing on my feet for any length of time

> > is a

> > problem. I want to go on the Naltrexone

> > immediately, I

> > just p\ut in a call to my family doctor and I am

> > hoping with some persistence she will agree to

> put

> > me

> > on this drug. I have also put in a call to a

> > friend of

> > mine who happens to be a pharmacist to see if

> > maybe he

> > can help me. I am really at my wits end with

> this.

> > I

> > want to act now. If you have any suggestions I

> > would

> > certainly very much appreciate hearing back from

> > you.

> >

> > Thanks.

> >

> >

> > --- Art Hansen <rtee54@...> wrote:

> >

> > >

> > > Read this before seeing your neurologist:

> > >

> > > How To Talk to Your Doctor about LDN

> > >

> > > http://www.gazorpa.com/PatientGuide.html

> > >

> > > If he says no, come back here asap, we have

> > other

> > > ways/ideas to

> > > get you on LDN.

> > >

> > > Good luck.

> > >

> > > -Art

> > >

> > >

> > > >

> > > > Hello Everyone:

> > > >

> > > > About 5 years ago I was diagnosed with MS.

> > Before

> > > that it was

> > > Lupus.

> > > > Upon seeing the MS Specialist he made a

> final

> > > diagnosis of MS,

> > > based

> > > > on MRI findings. His course of treatment was

> > the

> > > ABC drugs (

> > > Avonex,

> > > > Rebif). I was in denial and so decided not

> to

> > > proceed with his

> > > > recommendations. I also stopped going to him

> > as I

> > > found him to be

> > > > very arrogant and a uncompasionate Dr. I

> have

> > > since seen 2 other

> > > > Neurologists plus have had another MRI ,

> this

> > last

> > > was showed

> > > disease

> > > > progression, but the neurologist I went to

> > seemed

> > > to think because

> > > I

> > > > showed no visible signs of disability, there

> > was

> > > no reason to treat

> > > > me, it would be a let's wait and see what

> > happens.

> > > Well, in last

> > > last

> > > > 3 months I have had 2 Flares, the 2nd one

> was

> > a

> > > major one, and the

> > > > residual effects have been difficult, MY

> feet

> > are

> > > always numb, and

> > > > spastic the tightness is also unbearable, I

> > have

> > > also experience

> > > > numbness in my legs and waist that extends

> to

> > my

> > > torso. This has

> > > been

> > > > very frightening. 2 weeks ago as I was

> getting

> > > ready to go sawy for

> > > a

> > > > few days, I got out of my car to take the

> > shuttle

>

=== message truncated ===

________________________________________________________________________________\

____

Building a website is a piece of cake. Small Business gives you all the

tools to get online.

http://smallbusiness./webhosting

[Guest guest]

Hi , No I have no experience with Kawalla but it does sound interesting. I have found a lady thru www.joolysjoint.com with the handle miz.mel - she is from Toronto as well & she is on LDN. Perhaps you can go to that site, go in the chatroom & talk to her. Kristie

Re: [low dose naltrexone] Re: Diagnosed> > with MS> > > > > > Hello Again:> > > > Well I am back to squsre one. I presented my> > Neurologist with all the information you> suggested> > I> > take with to my apppointment, he casually looked> > at> > it, and said to me he was aware of the drug, but> > claims there are not many using it. Please keep> in> > mind I live in Canada, I don't know if this is> > true,or> > not as I know there are alot of people here in> > this> > group using LDN but am unsure where they are> > located.> > I think he was giving me an excuse not to> > prescribe.> > He asked me if I would be interested in entering> a> > clinical Trial I told him yes, so now it is " I> > willget back to you and let you know "> situation,> > and> > in the interim I am getting worse. I am at the> > point> > where standing on my feet for any length of time> > is a> > problem. I want to go on the Naltrexone> > immediately, I> > just p\ut in a call to my family doctor and I am> > hoping with some persistence she will agree to> put> > me> > on this drug. I have also put in a call to a> > friend of> > mine who happens to be a pharmacist to see if> > maybe he> > can help me. I am really at my wits end with> this.> > I> > want to act now. If you have any suggestions I> > would> > certainly very much appreciate hearing back from> > you.> > > > Thanks.> > > > > > --- Art Hansen <rtee54 > wrote:> > > > > > > > Read this before seeing your neurologist:> > > > > > How To Talk to Your Doctor about LDN> > > > > > http://www.gazorpa.com/PatientGuide.html> > > > > > If he says no, come back here asap, we have> > other> > > ways/ideas to > > > get you on LDN.> > > > > > Good luck.> > > > > > -Art> > > > > > > > > >> > > > Hello Everyone:> > > > > > > > About 5 years ago I was diagnosed with MS.> > Before> > > that it was > > > Lupus. > > > > Upon seeing the MS Specialist he made a> final> > > diagnosis of MS, > > > based > > > > on MRI findings. His course of treatment was> > the> > > ABC drugs ( > > > Avonex, > > > > Rebif). I was in denial and so decided not> to> > > proceed with his > > > > recommendations. I also stopped going to him> > as I> > > found him to be > > > > very arrogant and a uncompasionate Dr. I> have> > > since seen 2 other > > > > Neurologists plus have had another MRI ,> this> > last> > > was showed > > > disease > > > > progression, but the neurologist I went to> > seemed> > > to think because > > > I > > > > showed no visible signs of disability, there> > was> > > no reason to treat > > > > me, it would be a let's wait and see what> > happens.> > > Well, in last > > > last > > > > 3 months I have had 2 Flares, the 2nd one> was> > a> > > major one, and the > > > > residual effects have been difficult, MY> feet> > are> > > always numb, and > > > > spastic the tightness is also unbearable, I> > have> > > also experience > > > > numbness in my legs and waist that extends> to> > my> > > torso. This has > > > been > > > > very frightening. 2 weeks ago as I was> getting> > > ready to go sawy for > > > a > > > > few days, I got out of my car to take the> > shuttle> === message truncated ===__________________________________________________________Need a vacation? Get great dealsto amazing places on Travel.http://travel./

Internal Virus Database is out-of-date.Checked by AVG.Version: 7.5.430 / Virus Database: 268.14.6/536 - Release Date: 11/16/2006 3:51 PM

[Guest guest]

Hi Krisie:

I went to joolysjoint and did met miz.mel she was very

helpful for me, and so I thank-you for informing me

about the chat room I will continue to use it.

Thanks,

--- Caroline Remax <remaxcaroline@...> wrote:

> Hi , No I have no experience with Kawalla but

> it does sound interesting. I have found a lady thru

> www.joolysjoint.com with the handle miz.mel - she

> is from Toronto as well & she is on LDN. Perhaps

> you can go to that site, go in the chatroom & talk

> to her. Kristie

> Re: [low dose naltrexone] Re: Diagnosed

> > > with MS

> > >

> > >

> > > Hello Again:

> > >

> > > Well I am back to squsre one. I presented my

> > > Neurologist with all the information you

> > suggested

> > > I

> > > take with to my apppointment, he casually

> looked

> > > at

> > > it, and said to me he was aware of the drug,

> but

> > > claims there are not many using it. Please

> keep

> > in

> > > mind I live in Canada, I don't know if this is

> > > true,or

> > > not as I know there are alot of people here in

> > > this

> > > group using LDN but am unsure where they are

> > > located.

> > > I think he was giving me an excuse not to

> > > prescribe.

> > > He asked me if I would be interested in

> entering

> > a

> > > clinical Trial I told him yes, so now it is "

> I

> > > willget back to you and let you know "

> > situation,

> > > and

> > > in the interim I am getting worse. I am at the

> > > point

> > > where standing on my feet for any length of

> time

> > > is a

> > > problem. I want to go on the Naltrexone

> > > immediately, I

> > > just p\ut in a call to my family doctor and I

> am

> > > hoping with some persistence she will agree to

> > put

> > > me

> > > on this drug. I have also put in a call to a

> > > friend of

> > > mine who happens to be a pharmacist to see if

> > > maybe he

> > > can help me. I am really at my wits end with

> > this.

> > > I

> > > want to act now. If you have any suggestions I

> > > would

> > > certainly very much appreciate hearing back

> from

> > > you.

> > >

> > > Thanks.

> > >

> > >

> > > --- Art Hansen <rtee54@...> wrote:

> > >

> > > >

> > > > Read this before seeing your neurologist:

> > > >

> > > > How To Talk to Your Doctor about LDN

> > > >

> > > > http://www.gazorpa.com/PatientGuide.html

> > > >

> > > > If he says no, come back here asap, we have

> > > other

> > > > ways/ideas to

> > > > get you on LDN.

> > > >

> > > > Good luck.

> > > >

> > > > -Art

> > > >

> > > >

> > > > >

> > > > > Hello Everyone:

> > > > >

> > > > > About 5 years ago I was diagnosed with MS.

> > > Before

> > > > that it was

> > > > Lupus.

>

=== message truncated ===

________________________________________________________________________________\

____

Tonight's top picks. What will you watch tonight? Preview the hottest shows on

TV.

http://tv./

[Guest guest]

Hi ,

Were you able to get your doctor to prescribe LDN? I had an excellent experience with my appointment yesterday. Had a bunch of info, but she did not need convincing. Already has another ms patient of LDN. I am getting my LDN today will start taking it tonight. I hope you are having better results than before. Kristie

Re: [low dose naltrexone] Re: Diagnosed> > with MS> > > > > > Hello Again:> > > > Well I am back to squsre one. I presented my> > Neurologist with all the information you> suggested> > I> > take with to my apppointment, he casually looked> > at> > it, and said to me he was aware of the drug, but> > claims there are not many using it. Please keep> in> > mind I live in Canada, I don't know if this is> > true,or> > not as I know there are alot of people here in> > this> > group using LDN but am unsure where they are> > located.> > I think he was giving me an excuse not to> > prescribe.> > He asked me if I would be interested in entering> a> > clinical Trial I told him yes, so now it is " I> > willget back to you and let you know "> situation,> > and> > in the interim I am getting worse. I am at the> > point> > where standing on my feet for any length of time> > is a> > problem. I want to go on the Naltrexone> > immediately, I> > just p\ut in a call to my family doctor and I am> > hoping with some persistence she will agree to> put> > me> > on this drug. I have also put in a call to a> > friend of> > mine who happens to be a pharmacist to see if> > maybe he> > can help me. I am really at my wits end with> this.> > I> > want to act now. If you have any suggestions I> > would> > certainly very much appreciate hearing back from> > you.> > > > Thanks.> > > > > > --- Art Hansen <rtee54 > wrote:> > > > > > > > Read this before seeing your neurologist:> > > > > > How To Talk to Your Doctor about LDN> > > > > > http://www.gazorpa.com/PatientGuide.html> > > > > > If he says no, come back here asap, we have> > other> > > ways/ideas to > > > get you on LDN.> > > > > > Good luck.> > > > > > -Art> > > > > > > > > >> > > > Hello Everyone:> > > > > > > > About 5 years ago I was diagnosed with MS.> > Before> > > that it was > > > Lupus. > > > > Upon seeing the MS Specialist he made a> final> > > diagnosis of MS, > > > based > > > > on MRI findings. His course of treatment was> > the> > > ABC drugs ( > > > Avonex, > > > > Rebif). I was in denial and so decided not> to> > > proceed with his > > > > recommendations. I also stopped going to him> > as I> > > found him to be > > > > very arrogant and a uncompasionate Dr. I> have> > > since seen 2 other > > > > Neurologists plus have had another MRI ,> this> > last> > > was showed > > > disease > > > > progression, but the neurologist I went to> > seemed> > > to think because > > > I > > > > showed no visible signs of disability, there> > was> > > no reason to treat > > > > me, it would be a let's wait and see what> > happens.> > > Well, in last > > > last > > > > 3 months I have had 2 Flares, the 2nd one> was> > a> > > major one, and the > > > > residual effects have been difficult, MY> feet> > are> > > always numb, and > > > > spastic the tightness is also unbearable, I> > have> > > also experience > > > > numbness in my legs and waist that extends> to> > my> > > torso. This has > > > been > > > > very frightening. 2 weeks ago as I was> getting> > > ready to go sawy for > > > a > > > > few days, I got out of my car to take the> > shuttle> === message truncated ===__________________________________________________________Need a vacation? Get great dealsto amazing places on Travel.http://travel./

Internal Virus Database is out-of-date.Checked by AVG.Version: 7.5.430 / Virus Database: 268.14.6/536 - Release Date: 11/16/2006 3:51 PM

[Guest guest]

Hi Kristie:

I just keep hitting road blocks. I asked my family

doctor to prescribe, the excuse was she is not a MS

Dr. and could lose her license. BS is what I say. My

Neurologist took a serious look at the literature that

was written about the drug and wants me to go back and

discuss it with the MS Specialist who is head of

Neurology and the MS clinic here in toronto. So at

this point I am back to square one. I haven't given up

though and am more determined then ever now to find

someone to prescribe it for me, someone in joolysjoint

suggested I go for a colonoscopy and speak to the

doctor there and ask them to prescribe. they thought

it might be an easier method. Wonderful news for you,

you must be so pleased.Let me know how your feeling

now that your on the drug. Are you also dealing with

MS and are you symptomatic?

Please keep in touch.

All the very best.

--- Caroline Remax <remaxcaroline@...> wrote:

> Hi ,

> Were you able to get your doctor to prescribe

> LDN? I had an excellent experience with my

> appointment yesterday. Had a bunch of info, but she

> did not need convincing. Already has another ms

> patient of LDN. I am getting my LDN today will

> start taking it tonight. I hope you are having

> better results than before. Kristie

> Re: [low dose naltrexone] Re: Diagnosed

> > > with MS

> > >

> > >

> > > Hello Again:

> > >

> > > Well I am back to squsre one. I presented my

> > > Neurologist with all the information you

> > suggested

> > > I

> > > take with to my apppointment, he casually

> looked

> > > at

> > > it, and said to me he was aware of the drug,

> but

> > > claims there are not many using it. Please

> keep

> > in

> > > mind I live in Canada, I don't know if this is

> > > true,or

> > > not as I know there are alot of people here in

> > > this

> > > group using LDN but am unsure where they are

> > > located.

> > > I think he was giving me an excuse not to

> > > prescribe.

> > > He asked me if I would be interested in

> entering

> > a

> > > clinical Trial I told him yes, so now it is "

> I

> > > willget back to you and let you know "

> > situation,

> > > and

> > > in the interim I am getting worse. I am at the

> > > point

> > > where standing on my feet for any length of

> time

> > > is a

> > > problem. I want to go on the Naltrexone

> > > immediately, I

> > > just p\ut in a call to my family doctor and I

> am

> > > hoping with some persistence she will agree to

> > put

> > > me

> > > on this drug. I have also put in a call to a

> > > friend of

> > > mine who happens to be a pharmacist to see if

> > > maybe he

> > > can help me. I am really at my wits end with

> > this.

> > > I

> > > want to act now. If you have any suggestions I

> > > would

> > > certainly very much appreciate hearing back

> from

> > > you.

> > >

> > > Thanks.

> > >

> > >

> > > --- Art Hansen <rtee54@...> wrote:

> > >

> > > >

> > > > Read this before seeing your neurologist:

> > > >

> > > > How To Talk to Your Doctor about LDN

> > > >

> > > > http://www.gazorpa.com/PatientGuide.html

> > > >

> > > > If he says no, come back here asap, we have

> > > other

> > > > ways/ideas to

> > > > get you on LDN.

> > > >

> > > > Good luck.

> > > >

> > > > -Art

> > > >

> > > >

> > > > >

> > > > > Hello Everyone:

> > > > >

> > > > > About 5 years ago I was diagnosed with MS.

> > > Before

>

=== message truncated ===

________________________________________________________________________________\

____

Moody friends. Drama queens. Your life? Nope! - their life, your story. Play

Sims Stories at Games.

http://sims./

[Guest guest]

Dearest ,

Listed below are the names of doctors that have in the past been reported to prescribe LDN. We save these names and numbers in order to help those that are having a difficult time finding doctors in their area that know about LDN. I cannot guarantee that these doctors will prescribe or what their overall feelings about LDN are. I only know that at least once they have prescribed it to someone. We don't necessarily have permission from these doctors to share their names and information, so please tread lightly. I would not share these numbers with anyone unless you have asked the doctors if they are OK with telling others. At least it is a start and they have at one time known about and prescribed LDN.

Please let me know how it goes.

All my best, Aletha (see below for list of doctors in Canada)

a Canada

Markham

Dr. Gannage

(905) 294-2335

300 Main Street

a Canada

Markham

Dr. Ko

????

**

www.musclepainrelief.ca

a Canada

Edmondton Alberta

Dr. Tris Trethart -Holistic doctor who takes LDN himself

(780) 433-7401

10303 65th avenue

a Canada

Toronto

Dr. Jaconelle

(416) 463-2911

a Canada

Toronto

Dr. Burton/ Dr. Connor

St. Mikes

a Canada

Toronto (con't)

Dr's based at St. 's

(416) 864-5830

a Canada

Ottawa

e-mail at whisper@...

Re: [low dose naltrexone] Re: Diagnosed> > > with MS> > > > > > > > > Hello Again:> > > > > > Well I am back to squsre one. I presented my> > > Neurologist with all the information you> > suggested> > > I> > > take with to my apppointment, he casually> looked> > > at> > > it, and said to me he was aware of the drug,> but> > > claims there are not many using it. Please> keep> > in> > > mind I live in Canada, I don't know if this is> > > true,or> > > not as I know there are alot of people here in> > > this> > > group using LDN but am unsure where they are> > > located.> > > I think he was giving me an excuse not to> > > prescribe.> > > He asked me if I would be interested in> entering> > a> > > clinical Trial I told him yes, so now it is "> I> > > willget back to you and let you know "> > situation,> > > and> > > in the interim I am getting worse. I am at the> > > point> > > where standing on my feet for any length of> time> > > is a> > > problem. I want to go on the Naltrexone> > > immediately, I> > > just p\ut in a call to my family doctor and I> am> > > hoping with some persistence she will agree to> > put> > > me> > > on this drug. I have also put in a call to a> > > friend of> > > mine who happens to be a pharmacist to see if> > > maybe he> > > can help me. I am really at my wits end with> > this.> > > I> > > want to act now. If you have any suggestions I> > > would> > > certainly very much appreciate hearing back> from> > > you.> > > > > > Thanks.> > > > > > > > > --- Art Hansen <rtee54 > wrote:> > > > > > > > > > > Read this before seeing your neurologist:> > > > > > > > How To Talk to Your Doctor about LDN> > > > > > > > http://www.gazorpa.com/PatientGuide.html> > > > > > > > If he says no, come back here asap, we have> > > other> > > > ways/ideas to > > > > get you on LDN.> > > > > > > > Good luck.> > > > > > > > -Art> > > > > > > > > > > > >> > > > > Hello Everyone:> > > > > > > > > > About 5 years ago I was diagnosed with MS.> > > Before> === message truncated ===__________________________________________________________Moody friends. Drama queens. Your life? Nope! - their life, your story. Play Sims Stories at Games.http://sims./

[Guest guest]

Opps, sorry everyone that last e-mail was supposed to go to 's e-mail, not to go out to the whole group. Please disregard it.

Aletha

Re: [low dose naltrexone] Re: Diagnosed> > > with MS> > > > > > > > > Hello Again:> > > > > > Well I am back to squsre one. I presented my> > > Neurologist with all the information you> > suggested> > > I> > > take with to my apppointment, he casually> looked> > > at> > > it, and said to me he was aware of the drug,> but> > > claims there are not many using it. Please> keep> > in> > > mind I live in Canada, I don't know if this is> > > true,or> > > not as I know there are alot of people here in> > > this> > > group using LDN but am unsure where they are> > > located.> > > I think he was giving me an excuse not to> > > prescribe.> > > He asked me if I would be interested in> entering> > a> > > clinical Trial I told him yes, so now it is "> I> > > willget back to you and let you know "> > situation,> > > and> > > in the interim I am getting worse. I am at the> > > point> > > where standing on my feet for any length of> time> > > is a> > > problem. I want to go on the Naltrexone> > > immediately, I> > > just p\ut in a call to my family doctor and I> am> > > hoping with some persistence she will agree to> > put> > > me> > > on this drug. I have also put in a call to a> > > friend of> > > mine who happens to be a pharmacist to see if> > > maybe he> > > can help me. I am really at my wits end with> > this.> > > I> > > want to act now. If you have any suggestions I> > > would> > > certainly very much appreciate hearing back> from> > > you.> > > > > > Thanks.> > > > > > > > > --- Art Hansen <rtee54 > wrote:> > > > > > > > > > > Read this before seeing your neurologist:> > > > > > > > How To Talk to Your Doctor about LDN> > > > > > > > http://www.gazorpa.com/PatientGuide.html> > > > > > > > If he says no, come back here asap, we have> > > other> > > > ways/ideas to > > > > get you on LDN.> > > > > > > > Good luck.> > > > > > > > -Art> > > > > > > > > > > > >> > > > > Hello Everyone:> > > > > > > > > > About 5 years ago I was diagnosed with MS.> > > Before> === message truncated ===__________________________________________________________Moody friends. Drama queens. Your life? Nope! - their life, your story. Play Sims Stories at Games.http://sims./

[Guest guest]

,

Have you tried the Doctors on the LDN website?.That is where I found mine. I hear that some you can call and they will prescribe the LDN for a consulation fee. I saw a doctor that lived four hours Massachusetts. He lives in New Jersey where I used to live. In fact, if he was not so far I would love to have him for a Nuero.My name is also so I will sign off B.

Best of luck,

B from Cape Cod

Re: [low dose naltrexone] Re: Diagnosed> > > with MS> > > > > > > > > Hello Again:> > > > > > Well I am back to squsre one. I presented my> > > Neurologist with all the information you> > suggested> > > I> > > take with to my apppointment, he casually> looked> > > at> > > it, and said to me he was aware of the drug,> but> > > claims there are not many using it. Please> keep> > in> > > mind I live in Canada, I don't know if this is> > > true,or> > > not as I know there are alot of people here in> > > this> > > group using LDN but am unsure where they are> > > located.> > > I think he was giving me an excuse not to> > > prescribe.> > > He asked me if I would be interested in> entering> > a> > > clinical Trial I told him yes, so now it is "> I> > > willget back to you and let you know "> > situation,> > > and> > > in the interim I am getting worse. I am at the> > > point> > > where standing on my feet for any length of> time> > > is a> > > problem. I want to go on the Naltrexone> > > immediately, I> > > just p\ut in a call to my family doctor and I> am> > > hoping with some persistence she will agree to> > put> > > me> > > on this drug. I have also put in a call to a> > > friend of> > > mine who happens to be a pharmacist to see if> > > maybe he> > > can help me. I am really at my wits end with> > this.> > > I> > > want to act now. If you have any suggestions I> > > would> > > certainly very much appreciate hearing back> from> > > you.> > > > > > Thanks.> > > > > > > > > --- Art Hansen <rtee54 > wrote:> > > > > > > > > > > Read this before seeing your neurologist:> > > > > > > > How To Talk to Your Doctor about LDN> > > > > > > > http://www.gazorpa.com/PatientGuide.html> > > > > > > > If he says no, come back here asap, we have> > > other> > > > ways/ideas to > > > > get you on LDN.> > > > > > > > Good luck.> > > > > > > > -Art> > > > > > > > > > > > >> > > > > Hello Everyone:> > > > > > > > > > About 5 years ago I was diagnosed with MS.> > > Before> === message truncated ===__________________________________________________________Moody friends. Drama queens. Your life? Nope! - their life, your story. Play Sims Stories at Games.http://sims./

[Guest guest]

Hi ,

Ya, that excuse that your doctor can't prescribe because not an ms doctor is BS - my family dr prescribed for me. Try a different dr. I have been diagnosised with MS approx 3 wks ago. Only been on LDN now for 4 days - not noticing any immediate change. First got symptoms on July 29 but they disappeared 5 days later only to appear again 2 wks later. But this time they subsided but haven't gone away.. I have vision issues - my left eye is only about 50% vision, right eye 100% - but that makes it hard to see right. Also have balance problems - not too bad & pins & needles all over. The pins & needles bothered me the most to start with but its my vision that I wish would straighten up.

How about you, how long have you had ms? Kristie

Re: [low dose naltrexone] Re: Diagnosed> > > with MS> > > > > > > > > Hello Again:> > > > > > Well I am back to squsre one. I presented my> > > Neurologist with all the information you> > suggested> > > I> > > take with to my apppointment, he casually> looked> > > at> > > it, and said to me he was aware of the drug,> but> > > claims there are not many using it. Please> keep> > in> > > mind I live in Canada, I don't know if this is> > > true,or> > > not as I know there are alot of people here in> > > this> > > group using LDN but am unsure where they are> > > located.> > > I think he was giving me an excuse not to> > > prescribe.> > > He asked me if I would be interested in> entering> > a> > > clinical Trial I told him yes, so now it is "> I> > > willget back to you and let you know "> > situation,> > > and> > > in the interim I am getting worse. I am at the> > > point> > > where standing on my feet for any length of> time> > > is a> > > problem. I want to go on the Naltrexone> > > immediately, I> > > just p\ut in a call to my family doctor and I> am> > > hoping with some persistence she will agree to> > put> > > me> > > on this drug. I have also put in a call to a> > > friend of> > > mine who happens to be a pharmacist to see if> > > maybe he> > > can help me. I am really at my wits end with> > this.> > > I> > > want to act now. If you have any suggestions I> > > would> > > certainly very much appreciate hearing back> from> > > you.> > > > > > Thanks.> > > > > > > > > --- Art Hansen <rtee54 > wrote:> > > > > > > > > > > Read this before seeing your neurologist:> > > > > > > > How To Talk to Your Doctor about LDN> > > > > > > > http://www.gazorpa.com/PatientGuide.html> > > > > > > > If he says no, come back here asap, we have> > > other> > > > ways/ideas to > > > > get you on LDN.> > > > > > > > Good luck.> > > > > > > > -Art> > > > > > > > > > > > >> > > > > Hello Everyone:> > > > > > > > > > About 5 years ago I was diagnosed with MS.> > > Before> === message truncated ===__________________________________________________________Moody friends. Drama queens. Your life? Nope! - their life, your story. Play Sims Stories at Games.http://sims./

Internal Virus Database is out-of-date.Checked by AVG.Version: 7.5.430 / Virus Database: 268.14.6/536 - Release Date: 11/16/2006 3:51 PM

[Guest guest]

Hi Caroline, I live in California, so I'm unfamiliar with Canada laws. My doctor does to phone consults and appointments, and he's WONDERFUL and open to lots of different things....he prescribed LDN for me. He works at Whitaker Wellness Center, which you can research on the internet. I just called them, and the first visit needs to be in person, and then all other visits can be via phone. Any chance of coming here to arrange that and take a vacation at the same time....maybe Disneyland?! He also works with a compounding pharmacy, out of NY, but I called them, and they only ship within the US. I'm sure he has contacts in Canada, though....people come from ALL OVER to visit this place. If you want to call and leave a message for his nurse, here's the # (949) 851-1550. Let me know what you find out, and good luck! I just started LDN, myself, so no change yet. Take care, Caroline Remax <remaxcaroline@...> wrote: Hi , Ya, that excuse that your doctor can't prescribe because not an ms doctor is BS - my family dr prescribed for me. Try a different dr. I have been diagnosised with MS approx 3 wks ago. Only been on LDN now for 4 days - not noticing any immediate change. First got symptoms on July 29 but they disappeared 5

days later only to appear again 2 wks later. But this time they subsided but haven't gone away.. I have vision issues - my left eye is only about 50% vision, right eye 100% - but that makes it hard to see right. Also have balance problems - not too bad & pins & needles all over. The pins & needles bothered me the most to start with but its my vision that I wish would straighten up. How about you, how long have you had ms? Kristie Re: [low dose naltrexone] Re: Diagnosed> > > with MS> > > > > > > > > Hello Again:> > > > > > Well I am back to squsre one. I presented my> > > Neurologist with all the information you> > suggested> > > I> > > take with to my apppointment, he casually> looked> > > at> > > it, and said to me he was aware of the drug,> but> > > claims there are not many using it. Please> keep> > in> > > mind I live in Canada, I don't know if this is> > > true,or> > > not as I know there are alot of people here in> > > this> > > group using LDN but am

unsure where they are> > > located.> > > I think he was giving me an excuse not to> > > prescribe.> > > He asked me if I would be interested in> entering> > a> > > clinical Trial I told him yes, so now it is "> I> > > willget back to you and let you know "> > situation,> > > and> > > in the interim I am getting worse. I am at the> > > point> > > where standing on my feet for any length of> time> > > is a> > > problem. I want to go on the Naltrexone> > > immediately, I> > > just p\ut in a call to my family doctor and I> am> > > hoping with some persistence she will agree to> > put> > > me> > > on this drug. I have also put in a call to a> > > friend of> > > mine who happens

to be a pharmacist to see if> > > maybe he> > > can help me. I am really at my wits end with> > this.> > > I> > > want to act now. If you have any suggestions I> > > would> > > certainly very much appreciate hearing back> from> > > you.> > > > > > Thanks.> > > > > > > > > --- Art Hansen <rtee54 > wrote:> > > > > > > > > > > Read this before seeing your neurologist:> > > > > > > > How To Talk to Your Doctor about LDN> > > > > > > > http://www.gazorpa.com/PatientGuide.html> > > > > > > > If he says no, come back here asap, we have>

> > other> > > > ways/ideas to > > > > get you on LDN.> > > > > > > > Good luck.> > > > > > > > -Art> > > > > > > > > > > > >> > > > > Hello Everyone:> > > > > > > > > > About 5 years ago I was diagnosed with MS.> > > Before> === message truncated ===__________________________________________________________Moody friends. Drama queens. Your life? Nope! - their life, your story. Play Sims Stories at Games.http://sims./ Internal Virus Database is out-of-date.Checked by AVG.Version: 7.5.430 / Virus Database: 268.14.6/536 - Release Date: 11/16/2006 3:51

PM

Tonight's top picks. What will you watch tonight? Preview the hottest shows on TV.

[Guest guest]

Hi Caroline, I forgot to give you my doctor's name......Dr. Farrier. Just tell him you were referred by me - .Caroline Remax <remaxcaroline@...> wrote: Hi , Ya, that excuse that your doctor can't prescribe because not an ms doctor is BS - my family dr prescribed for me. Try a different dr. I have been diagnosised with MS approx 3 wks ago. Only been on

LDN now for 4 days - not noticing any immediate change. First got symptoms on July 29 but they disappeared 5 days later only to appear again 2 wks later. But this time they subsided but haven't gone away.. I have vision issues - my left eye is only about 50% vision, right eye 100% - but that makes it hard to see right. Also have balance problems - not too bad & pins & needles all over. The pins & needles bothered me the most to start with but its my vision that I wish would straighten up. How about you, how long have you had ms? Kristie Re: [low dose naltrexone] Re: Diagnosed> > > with MS> > > > > > > > > Hello Again:> > > > > > Well I am back to squsre one. I presented my> > > Neurologist with all the information you> > suggested> > > I> > > take with to my apppointment, he casually> looked> > > at> > > it, and said to me he was aware of the drug,> but> > > claims there are not many using it. Please> keep> > in> > > mind I live in Canada, I don't know if this is> > > true,or> > > not as I know there are alot of people here in> > > this> > > group using LDN but am

unsure where they are> > > located.> > > I think he was giving me an excuse not to> > > prescribe.> > > He asked me if I would be interested in> entering> > a> > > clinical Trial I told him yes, so now it is "> I> > > willget back to you and let you know "> > situation,> > > and> > > in the interim I am getting worse. I am at the> > > point> > > where standing on my feet for any length of> time> > > is a> > > problem. I want to go on the Naltrexone> > > immediately, I> > > just p\ut in a call to my family doctor and I> am> > > hoping with some persistence she will agree to> > put> > > me> > > on this drug. I have also put in a call to a> > > friend of> > > mine who happens

to be a pharmacist to see if> > > maybe he> > > can help me. I am really at my wits end with> > this.> > > I> > > want to act now. If you have any suggestions I> > > would> > > certainly very much appreciate hearing back> from> > > you.> > > > > > Thanks.> > > > > > > > > --- Art Hansen <rtee54 > wrote:> > > > > > > > > > > Read this before seeing your neurologist:> > > > > > > > How To Talk to Your Doctor about LDN> > > > > > > > http://www.gazorpa.com/PatientGuide.html> > > > > > > > If he says no, come back here asap, we have>

> > other> > > > ways/ideas to > > > > get you on LDN.> > > > > > > > Good luck.> > > > > > > > -Art> > > > > > > > > > > > >> > > > > Hello Everyone:> > > > > > > > > > About 5 years ago I was diagnosed with MS.> > > Before> === message truncated ===__________________________________________________________Moody friends. Drama queens. Your life? Nope! - their life, your story. Play Sims Stories at Games.http://sims./ Internal Virus Database is out-of-date.Checked by AVG.Version: 7.5.430 / Virus Database: 268.14.6/536 - Release Date: 11/16/2006 3:51

PM

Take the Internet to Go: Go puts the Internet in your pocket: mail, news, photos more.

[Guest guest]

Hi :

Is this doctor in Toronto? if so could you please tell

me where and what his phone number is so that I can

call him. Is he a Neurologist or a MD.

Thanks,

--- Missie - <melissa4tse@...> wrote:

> Hi Caroline,

>

> I forgot to give you my doctor's name......Dr.

> Farrier. Just tell him you were referred by

> me - .

>

> Caroline Remax <remaxcaroline@...> wrote:

> Hi ,

> Ya, that excuse that your doctor can't

> prescribe because not an ms doctor is BS - my family

> dr prescribed for me. Try a different dr. I have

> been diagnosised with MS approx 3 wks ago. Only

> been on LDN now for 4 days - not noticing any

> immediate change. First got symptoms on July 29 but

> they disappeared 5 days later only to appear again 2

> wks later. But this time they subsided but haven't

> gone away.. I have vision issues - my left eye is

> only about 50% vision, right eye 100% - but that

> makes it hard to see right. Also have balance

> problems - not too bad & pins & needles all over.

> The pins & needles bothered me the most to start

> with but its my vision that I wish would straighten

> up.

> How about you, how long have you had ms?

> Kristie

> Re: [low dose naltrexone] Re: Diagnosed

> > > > with MS

> > > >

> > > >

> > > > Hello Again:

> > > >

> > > > Well I am back to squsre one. I presented my

> > > > Neurologist with all the information you

> > > suggested

> > > > I

> > > > take with to my apppointment, he casually

> > looked

> > > > at

> > > > it, and said to me he was aware of the drug,

> > but

> > > > claims there are not many using it. Please

> > keep

> > > in

> > > > mind I live in Canada, I don't know if this is

>

=== message truncated ===

________________________________________________________________________________\

____

Be a better Heartthrob. Get better relationship answers from someone who knows.

Answers - Check it out.

http://answers./dir/?link=list & sid=396545433

[Guest guest]

I understand that www.skipspharmacy.com ship LDN just about anywhere in the world.

mjh

He also works with a compounding pharmacy, out of NY, but I called them, and they only ship within the US. I'm sure he has contacts in Canada, though....people come from ALL OVER to visit this place.See what's new at AOL.com and Make AOL Your Homepage.

[Guest guest]

Hi ,

is from California - so I don't think her dr can help you. Did miz.mel from Toronto not help you out with the name & # of her dr that prescribed LDN or did she get it off the internet? You can order it without a prescription - you just have to dilute it because they send you 50 mg. Have you tried the list that Crystal has of dr's that prescribe? Kristie

Re: [low dose naltrexone] Re: Diagnosed> > > > with MS> > > > > > > > > > > > Hello Again:> > > > > > > > Well I am back to squsre one. I presented my> > > > Neurologist with all the information you> > > suggested> > > > I> > > > take with to my apppointment, he casually> > looked> > > > at> > > > it, and said to me he was aware of the drug,> > but> > > > claims there are not many using it. Please> > keep> > > in> > > > mind I live in Canada, I don't know if this is> === message truncated ===__________________________________________________________Be a better Heartthrob. Get better relationship answers from someone who knows. Answers - Check it out. http://answers./dir/?link=list & sid=396545433

Internal Virus Database is out-of-date.Checked by AVG.Version: 7.5.430 / Virus Database: 268.14.6/536 - Release Date: 11/16/2006 3:51 PM

[Guest guest]

Hi Barb,

I am new to this group and I hope everthing works out for you. I

thought I would pass along some information to you that I found in

Heinerman's Encyclopedia of Healing Juices, p46. Black and Red

Currant berrys produce GLA, and prostaglandin PGE-1. Which is

essential for muscle locamotion and nerve transmission, in diseases

such as multiple sclerosis is of considerable benefit.

Good Luck,

Craig

>

> while ususally just a lurker, I feel like i know so many of you

> personslly after all these years.

>

> The middle of June I started to have weird symtoms. My balance and

my

> handwriting. I made a doc's appt. but since I was a new patient

they

> would not see me until July 23rd (havent been to a doc in years).

The

> end of June my symtoms were a lot worse. My husband begged me to go

> to the er which I finally did July 1. At first they thought it was

a

> stroke (which I didnt believe since I'm only 41 and eat healthy and

> Im fairly active and a nonsmoker)only to be diagnosed with MS. They

> did a CAT scan, blood tests, 2 ultra sounds, 3 MRI's (the last one

> lasting 90 minutes) and a spinal tap.

>

> I lost a lot on my right side (this was actally after I was

adnmitted

> and they were giving me steroids) now walking with a walker and

very

> limited use of my arm and hand (I am getting occupasional and

> physical therapy). in fact typing this is very slow with only my

left

> hand.

>

> I will be seeing a specialist on Tues expecting to get on meds.

>

> Any advice or experience would be appreciated.

>

> Barb

>