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Re: ray&doug

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hi names nancy brothers got ms progressed like yours Always getting worse

never a remission. He started on betaseron then avonex then copaxone now

hes not on anything but will go on LDN soon. Copaxone what can i say about

it. Nothing it did nothing helped nothing if anything we believe this

interfered with his vitamin /nutrient/herb regamin and if anything he

progressed even faster.When he was at his worst a few yrs ago doctor got him

off muscle relaxers and avonex and within few weeks he was doing much

better.diagnosed 12 yrs ago he cannot transfer himself at all.

have you asked anyone if they dropped their copaxone after starting LDN?

By the way we have surplus copaxone still in frig if you want it,So

expensive cant bring myself to throw away :)

>From: " Rae & Doug Bower " <radbower@...>

>Reply-low dose naltrexone

><low dose naltrexone >

>Subject: RE: [low dose naltrexone] question

>Date: Fri, 26 May 2006 09:38:00 -0400

>

>

>

>

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I concur about copaxone. I believe it did nothing at all for my wife.

She's relapsing remitting and had more exacerbations while on copaxone

than at any other time during her 10 year battle with MS. Not to say

that copaxone caused them, but it didn't prevent them, either. She

stopped copaxone at the same time as starting LDN. The skin lesions

from it were horrible.

I, too, couldn't bring myself to throw away the left over copaxone,

knowing we would never use it. Threw it away after it expired. Strange

the attachments we develop.

nancy millar wrote:

>hi names nancy brothers got ms progressed like yours Always getting worse

>never a remission. He started on betaseron then avonex then copaxone now

>hes not on anything but will go on LDN soon. Copaxone what can i say about

>it. Nothing it did nothing helped nothing if anything we believe this

>interfered with his vitamin /nutrient/herb regamin and if anything he

>progressed even faster.When he was at his worst a few yrs ago doctor got him

>off muscle relaxers and avonex and within few weeks he was doing much

>better.diagnosed 12 yrs ago he cannot transfer himself at all.

>have you asked anyone if they dropped their copaxone after starting LDN?

>By the way we have surplus copaxone still in frig if you want it,So

>expensive cant bring myself to throw away :)

>

>

>

>

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I also concur about copaxone. I am rrms and started Copaxone and LDN at the same time 3.5 years ago. I quit Copaxone 3 months ago -am still doing fine. I also have kept some in the refrigerator "just in case".

Take care

Dianna

(Toronto, ON)

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yes well brother came home to live with me from hospital in warm springs ga

at this time was only on mentioned alternative meds but docs took him off

all alternatives and when he arrived here he had a catheter that was clogged

which bought on his first seizure and severe uti,we spent 6 months trying to

get right seizure meds for him and tried to get him back on alternative meds

but this seizure made his memory worse and the meds did not work he had 2

more seizures and then docs changed his seizure meds to valporic acid and

put him on copaxone.During these 2 yrs he has been in hospital 4 times in 04

and 8 times in 05 5 times in 06 so far before the copaxone and the uti

from clogged up cath he would get sick 1-2 times a year needing hospital.

the more he went in the hospital the worse he came home,proven fact.

our copaxone has a while yet before we throw it out. yes strange

attachments lol

>From: Wesley <inspirfe@...>

>Reply-low dose naltrexone

>low dose naltrexone

>Subject: Re: [low dose naltrexone] ray & doug

>Date: Fri, 26 May 2006 13:12:16 -0500

>

>

>

>

>I concur about copaxone.  I believe it did nothing at all for my wife. 

>

>She's relapsing remitting and had more exacerbations while on copaxone

>

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Many people have dropped their copaxine after starting LDN. It is nice

however that someone could take the two together so they don't feel scared

about being without something while starting out with LDN.

, you are a wonderful sister to be there for your brother.

Aletha

RE: [low dose naltrexone] question

>>Date: Fri, 26 May 2006 09:38:00 -0400

>>

>>

>>

>>

>

> _________________________________________________________________

> Express yourself instantly with MSN Messenger! Download today - it's FREE!

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Hi all. I was going to reply to privately, then thought several LDN

users out there might have leftover Copaxone out there, and might appreciate

this advice...

Thanks for offering your surplus Copaxone. If you don't have the

packaging anymore, it's not worth trying to ship it to me. Instead, why

don't you give it to your local MS Support Group, where you'll likely find a

local user for it in your area. If you do have the packaging, I'm in St

sburg, FL, and you can reach me privately on raebower@....

Best regards, Rae

Re: [low dose naltrexone] ray & doug

>Date: Fri, 26 May 2006 13:12:16 -0500

>

>

>

>

>I concur about copaxone.  I believe it did nothing at all for my wife.

>

>She's relapsing remitting and had more exacerbations while on copaxone

>

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hi i wonder 3 1/2 yrs with both meds cant help but wonder if you had not

been taking the copaxone how would you be right now. most people i read

about are very new to ldn makes one wonder what if?

>From: evilangl22@...

>Reply-low dose naltrexone

>low dose naltrexone

>Subject: [low dose naltrexone] Re: ray & doug

>Date: Fri, 26 May 2006 18:39:56 EDT

>

>I also concur about copaxone. I am rrms and started Copaxone and LDN at

>the

>same time 3.5 years ago. I quit Copaxone 3 months ago -am still doing

>fine.

>I also have kept some in the refrigerator " just in case " .

>

>Take care

>

>Dianna

>(Toronto, ON)

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