Re: Does Betaferon (Betaseron) was really effective for you ?

[Guest guest]

Hi. I am on Rebif, which is one of the forms of the interferons on the market.

At this time, I have a build up of antibodies which cancels the action of the

interferon. This means it is not working. I am going to be going to a

Homeopath in the near future to see what she can do to help me. Good luck if

you decide to try one of the interferons. I've heard it works really well for

most people.

nimaoy wrote:

Hello dear friends, I want to know Does Betaferon (Betaseron) was

really effective for you ? if yes why and if not why ? what was

different of number and severity of attack before and after use of

Betaferon (Betaseron)?

thank you

[Guest guest]

I'm considering trying Rebif BUT upon further research, LDN seems to be the way

to go. My husband and I spent all weekend researching it and wow... i cannot

believe how effective it has been for most.

I've heard many people's experiences with it and am extremely optimistic about

it. I think I'd like to try LDN before Rebif. Perhaps , this might help you

too.

I hear the only side effects in only 2% of people taking it is difficulty

sleeping.

Can anyone who is on LDN eleborate more about it?

cathy carsten wrote:

Hi. I am on Rebif, which is one of the forms of the interferons on the

market. At this time, I have a build up of antibodies which cancels the action

of the interferon. This means it is not working.

[Guest guest]

Please check out Direct IV ozone therapy for treating MS. Go to

www.ozoneuniversity.com and for scientific articles go to www.pubmed.gov and

type " intravenous ozone therapy " in 'search' for M.D. and P.H.D. research

articles from around the world. It may not be available legally in your state,

but it works when all else has failed.

cathy carsten wrote: Hi. I am on Rebif, which

is one of the forms of the interferons on the market. At this time, I have a

build up of antibodies which cancels the action of the interferon. This means it

is not working. I am going to be going to a Homeopath in the near future to see

what she can do to help me. Good luck if you decide to try one of the

interferons. I've heard it works really well for most people.

nimaoy wrote:

Hello dear friends, I want to know Does Betaferon (Betaseron) was

really effective for you ? if yes why and if not why ? what was

different of number and severity of attack before and after use of

Betaferon (Betaseron)?

thank you

[Guest guest]

hi, my homeopath gave me MS remedy by Chappel and Lathyrus.

I am on it now for months.

It seems to strenghten me a little.

Benka

Re: Does Betaferon (Betaseron) was really effective for you ?

Please check out Direct IV ozone therapy for treating MS. Go to

www.ozoneuniversity .com and for scientific articles go to www.pubmed.gov and

type " intravenous ozone therapy " in 'search' for M.D. and P.H.D. research

articles from around the world. It may not be available legally in your state,

but it works when all else has failed.

cathy carsten <ccarsten2001@ yahoo.com> wrote: Hi. I am on Rebif, which

is one of the forms of the interferons on the market. At this time, I have a

build up of antibodies which cancels the action of the interferon. This means it

is not working. I am going to be going to a Homeopath in the near future to see

what she can do to help me. Good luck if you decide to try one of the

interferons. I've heard it works really well for most people.

nimaoy <nimaoyyahoo (DOT) com> wrote:

Hello dear friends, I want to know Does Betaferon (Betaseron) was

really effective for you ? if yes why and if not why ? what was

different of number and severity of attack before and after use of

Betaferon (Betaseron)?

thank you

[Guest guest]

>

> I was on Rebif for about 1 1/2 years and it did

> nothing for me. I am on Copaxone now; I go toa new

> neuro on the 22 and I'm gonna ask about LDN. I hear

> so much good things about it.

>

I've done Rebif, Copaxone, Raki, faith healers, and now naltrexone.

The low dose naltrexone website has lots of information that can be

given to docs. Maybe print some the nlatrexone info out and take it

along and see if they listen?? The naltrexone is FDA approved at

50mg/day. The low dose is 3 to 4.5mg per day. The naltrexone does

not require blood tests for liver functiion and does not cause

suicidal ideation. So I think the safety aspect is covered.

The concensus on the LDN message board is that Rebif and LDN cancel

each other out. There is also talk that LDN and Copaxone get along

well.

[Guest guest]

I have printed up numerous things about LDN to take to

the doctor when I go; so he can read. I can't wait

until I go to the neuro on the 22nd.

So you don't take the naltrexone with anything? Is

that the way it works?

--- alrightguy123 wrote:

>

> >

> > I was on Rebif for about 1 1/2 years and it did

> > nothing for me. I am on Copaxone now; I go toa

> new

> > neuro on the 22 and I'm gonna ask about LDN. I

> hear

> > so much good things about it.

> >

> I've done Rebif, Copaxone, Raki, faith healers, and

> now naltrexone.

> The low dose naltrexone website has lots of

> information that can be

> given to docs. Maybe print some the nlatrexone info

> out and take it

> along and see if they listen?? The naltrexone is

> FDA approved at

> 50mg/day. The low dose is 3 to 4.5mg per day. The

> naltrexone does

> not require blood tests for liver functiion and does

> not cause

> suicidal ideation. So I think the safety aspect is

> covered.

>

> The concensus on the LDN message board is that Rebif

> and LDN cancel

> each other out. There is also talk that LDN and

> Copaxone get along

> well.

>

>

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[Guest guest]

I hope he is open-minded also. I don't know much

about him; this is my first time seeing him. He was

given to me by the MS Society. We will see what

happens.

Hi Colleen,

You have to understand Neuro's work for the drug companies, they are paid to

prescribe drugs, the MS society are sponsored by the drug companies. This is

why they want you on drugs not alternative therapies.

.

[Guest guest]

>I hope he is open-minded also. I don't know much

> about him; this is my first time seeing him. He was

> given to me by the MS Society. We will see what

> happens.

>

> Hi Colleen,

>

You have to understand Neuro's work for the drug companies, they are paid

to prescribe drugs, the MS society are sponsored by the drug companies.

This is why they want you on drugs not alternative therapies.

.