Re: LDN Neuro in Long Island?

[Guest guest]

--- In low dose naltrexone , " jennemcleavy " <jennemcleavy@y...>

wrote:

> Hello, everyone,

>

> I have tried appealing to both my GP and my neuro about the benefits

> of

> LDN for MSers. I was on Copaxone for 3 years and Avonex for about 6

> weeks- I swear to you, that poison was really doing more harm than

> good. I gave both doctors packets stuffed with LDN information and

> resources. Of course, they both said, flat-out no. My neuro even said

> that he doesn't recommend anything but the CRABs, so it wouldn't have

> mattered anyway.

>

> I would really love to work with a supportive neuro who would

> prescribe

> LDN and monitor my progress. However, if that's not an option, I'm

> ordering from Mexico and I'll be asking for guidance on how to make

> my

> own dosages- God help me. :-)

>

> Prayers and good thoughts and hope to everyone,

>

> Jenne

=========

See Dr. Enlander's info. and website on my list of LDN prescribing docs. Click

link below...Dr. Enlander is the second doctor listed.

Low Dose Naltrexone Forum - List of LDN docs

http://ldn.proboards3.com/index.cgi?board=doctors & action=display & thread=10791588\

56

[Guest guest]

You will do fine! We are all here for you and it is safe. Be at peace and know you are doing one of the most positive things for your ms. You may halt progression or see symptomatic improvement in a short time. Good Luck and Keep the Faith. Kathy

[low dose naltrexone] LDN Neuro in Long Island?

Hello, everyone,I have tried appealing to both my GP and my neuro about the benefitsof LDN for MSers. I was on Copaxone for 3 years and Avonex for about 6 weeks- I swear to you, that poison was really doing more harm than good. I gave both doctors packets stuffed with LDN information and resources. Of course, they both said, flat-out no. My neuro even said that he doesn't recommend anything but the CRABs, so it wouldn't have mattered anyway. I would really love to work with a supportive neuro who wouldprescribe LDN and monitor my progress. However, if that's not an option, I'm ordering from Mexico and I'll be asking for guidance on how to makemy own dosages- God help me. :-)Prayers and good thoughts and hope to everyone,Jenne

[Guest guest]

> > Hello, everyone,

> >

> > I have tried appealing to both my GP and my neuro about the

benefits

> > of

> > LDN for MSers. I was on Copaxone for 3 years and Avonex for about

6

> > weeks- I swear to you, that poison was really doing more harm

than

> > good. I gave both doctors packets stuffed with LDN information

and

> > resources. Of course, they both said, flat-out no. My neuro even

said

> > that he doesn't recommend anything but the CRABs, so it wouldn't

have

> > mattered anyway.

> >

> > I would really love to work with a supportive neuro who would

> > prescribe

> > LDN and monitor my progress. However, if that's not an option,

I'm

> > ordering from Mexico and I'll be asking for guidance on how to

make

> > my

> > own dosages- God help me. :-)

> >

> > Prayers and good thoughts and hope to everyone,

> >

> > Jenne

> =========

>

> See Dr. Enlander's info. and website on my list of LDN prescribing

docs. Click link below...Dr. Enlander is the second doctor listed.

>

> Low Dose Naltrexone Forum - List of LDN docs

> http://ldn.proboards3.com/index.cgi?

board=doctors & action=display & thread=1079158856

>

>

, I am sitting in my office in tears. Thank you for the glimmer

of hope!

[Guest guest]

> > > Hello, everyone,

> > >

> > > I have tried appealing to both my GP and my neuro about the

> benefits

> > > of

> > > LDN for MSers. I was on Copaxone for 3 years and Avonex for

about

> 6

> > > weeks- I swear to you, that poison was really doing more harm

> than

> > > good. I gave both doctors packets stuffed with LDN information

> and

> > > resources. Of course, they both said, flat-out no. My neuro

even

> said

> > > that he doesn't recommend anything but the CRABs, so it

wouldn't

> have

> > > mattered anyway.

> > >

> > > I would really love to work with a supportive neuro who would

> > > prescribe

> > > LDN and monitor my progress. However, if that's not an option,

> I'm

> > > ordering from Mexico and I'll be asking for guidance on how to

> make

> > > my

> > > own dosages- God help me. :-)

> > >

> > > Prayers and good thoughts and hope to everyone,

> > >

> > > Jenne

> > =========

> >

> > See Dr. Enlander's info. and website on my list of LDN

prescribing

> docs. Click link below...Dr. Enlander is the second doctor listed.

> >

> > Low Dose Naltrexone Forum - List of LDN docs

> > http://ldn.proboards3.com/index.cgi?

> board=doctors & action=display & thread=1079158856

> >

> >

>

> , I am sitting in my office in tears. Thank you for the

glimmer

> of hope!

just let me tell you about my wifes ms, she has it for about 23 years

and soon after Betaseron came out i started to give her the

injections every other day and at that time she was still walking

very good without any help.

into about the 7th year of taking Betaseron she started to have

exacerbations that made her use a cane for walking then later a

walker and then a wheelchair, along with that came the incontinence,

it got that bad that she wouldn't go anywhere anymore and she wore

the poise pads 24/7 and we had a porta potty beside her bed.

a few years ago i started to read about the LDN here on the

computer and we asked our neuro about it and he never heard of it.

Some one emailed me and told me of a few doctors that you could call

on the phone and get a prescription for it and this is what we did.

This past May she has been taking 4.5 mg for two years. Soon after

taking it she bacame stronger and happier and her incontinence went

away so she stopped using the poise pads and we put the porta potty

down in the basement and now she can transfer herself from her

recliner to the wheel chair and go to the bathroom without any

problems.

LDN has changed our life , it was like a miracle for us.

We didn't see our neuro since taking the LDN because we feel like we

don't have to see him. She didn't have any exacerbations since taking

the LDN so we think every thing is going just fine. We do walk her

down the hall in our house every few days , it doesn't go too good

but at least she walks with me holding on to her and her walker.

Very few doctors will prescribe LDN because it isn't a money making

drug for them.

Read Trudues book " What they don't tell you about natural

cures " and you will understand why doctors don't want you to take

this inexpensive drug, it's all about money for these doctors pusing

all the crab medicine.

My wife will never take those injectables meds again because they

just poison your body, and that's a fact.

[Guest guest]

> > > > Hello, everyone,

> > > >

> > > > I have tried appealing to both my GP and my neuro about the

> > benefits

> > > > of

> > > > LDN for MSers. I was on Copaxone for 3 years and Avonex for

> about

> > 6

> > > > weeks- I swear to you, that poison was really doing more harm

> > than

> > > > good. I gave both doctors packets stuffed with LDN

information

> > and

> > > > resources. Of course, they both said, flat-out no. My neuro

> even

> > said

> > > > that he doesn't recommend anything but the CRABs, so it

> wouldn't

> > have

> > > > mattered anyway.

> > > >

> > > > I would really love to work with a supportive neuro who would

> > > > prescribe

> > > > LDN and monitor my progress. However, if that's not an

option,

> > I'm

> > > > ordering from Mexico and I'll be asking for guidance on how

to

> > make

> > > > my

> > > > own dosages- God help me. :-)

> > > >

> > > > Prayers and good thoughts and hope to everyone,

> > > >

> > > > Jenne

> > > =========

> > >

> > > See Dr. Enlander's info. and website on my list of LDN

> prescribing

> > docs. Click link below...Dr. Enlander is the second doctor

listed.

> > >

> > > Low Dose Naltrexone Forum - List of LDN docs

> > > http://ldn.proboards3.com/index.cgi?

> > board=doctors & action=display & thread=1079158856

> > >

> > >

> >

> > , I am sitting in my office in tears. Thank you for the

> glimmer

> > of hope!

>

> just let me tell you about my wifes ms, she has it for about 23

years

> and soon after Betaseron came out i started to give her the

> injections every other day and at that time she was still walking

> very good without any help.

> into about the 7th year of taking Betaseron she started to have

> exacerbations that made her use a cane for walking then later a

> walker and then a wheelchair, along with that came the

incontinence,

> it got that bad that she wouldn't go anywhere anymore and she wore

> the poise pads 24/7 and we had a porta potty beside her bed.

> a few years ago i started to read about the LDN here on the

> computer and we asked our neuro about it and he never heard of it.

> Some one emailed me and told me of a few doctors that you could

call

> on the phone and get a prescription for it and this is what we

did.

> This past May she has been taking 4.5 mg for two years. Soon

after

> taking it she bacame stronger and happier and her incontinence went

> away so she stopped using the poise pads and we put the porta potty

> down in the basement and now she can transfer herself from her

> recliner to the wheel chair and go to the bathroom without any

> problems.

> LDN has changed our life , it was like a miracle for us.

> We didn't see our neuro since taking the LDN because we feel like

we

> don't have to see him. She didn't have any exacerbations since

taking

> the LDN so we think every thing is going just fine. We do walk her

> down the hall in our house every few days , it doesn't go too good

> but at least she walks with me holding on to her and her walker.

> Very few doctors will prescribe LDN because it isn't a money

making

> drug for them.

> Read Trudues book " What they don't tell you about natural

> cures " and you will understand why doctors don't want you to take

> this inexpensive drug, it's all about money for these doctors

pusing

> all the crab medicine.

> My wife will never take those injectables meds again because they

> just poison your body, and that's a fact.

I see today 7/16/05 that people are asking if LDN halted the ms and

i must say it did for my wife, she didn't have an exacerbation for

over two years.

[Guest guest]

God be with you. Best Luck to you.

--- Bren <TwisterAlley2@...> wrote:

>

> > Hello, everyone,

> >

> > I have tried appealing to both my GP and my neuro

> about the benefits

> > of

> > LDN for MSers. I was on Copaxone for 3 years and

> Avonex for about 6

> > weeks- I swear to you, that poison was really

> doing more harm than

> > good. I gave both doctors packets stuffed with LDN

> information and

> > resources. Of course, they both said, flat-out no.

> My neuro even said

> > that he doesn't recommend anything but the CRABs,

> so it wouldn't have

> > mattered anyway.

> >

> > I would really love to work with a supportive

> neuro who would

> > prescribe

> > LDN and monitor my progress. However, if that's

> not an option, I'm

> > ordering from Mexico and I'll be asking for

> guidance on how to make

> > my

> > own dosages- God help me. :-)

> >

> > Prayers and good thoughts and hope to everyone,

> >

> > Jenne

> =========

>

> See Dr. Enlander's info. and website on my list of

> LDN prescribing docs. Click link below...Dr.

> Enlander is the second doctor listed.

>

> Low Dose Naltrexone Forum - List of LDN docs

>

http://ldn.proboards3.com/index.cgi?board=doctors & action=display & thread=10791588\

56

>

>

>

>

>

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