Re: MMR Research Interviews

[Guest guest]

> I just called the MMR Research phone number mentioned by Claudine,

> to participate in their survey (for $50), but I did not qualify.

> They are looking for people who are either 1) treatment naive,

I hate to be so naive...... but what does naive mean? :-)

Someone who has never had any treatment?

Elin

BTW, my husband's appt. with the doc to hear the results of the biopsy

are later this afternoon.

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[Guest guest]

> I just called the MMR Research phone number mentioned by Claudine,

> to participate in their survey (for $50), but I did not qualify.

> They are looking for people who are either 1) treatment naive,

I hate to be so naive...... but what does naive mean? :-)

Someone who has never had any treatment?

Elin

BTW, my husband's appt. with the doc to hear the results of the biopsy

are later this afternoon.

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[Guest guest]

> I just called the MMR Research phone number mentioned by Claudine,

> to participate in their survey (for $50), but I did not qualify.

> They are looking for people who are either 1) treatment naive,

I hate to be so naive...... but what does naive mean? :-)

Someone who has never had any treatment?

Elin

BTW, my husband's appt. with the doc to hear the results of the biopsy

are later this afternoon.

________________________________________________________________

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[Guest guest]

> I just called the MMR Research phone number mentioned by Claudine,

> to participate in their survey (for $50), but I did not qualify.

> They are looking for people who are either 1) treatment naive,

I hate to be so naive...... but what does naive mean? :-)

Someone who has never had any treatment?

Elin

BTW, my husband's appt. with the doc to hear the results of the biopsy

are later this afternoon.

________________________________________________________________

YOU'RE PAYING TOO MUCH FOR THE INTERNET!

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[Guest guest]

--- Elin L Criswell <texswede@...> wrote:

>

> I hate to be so naive...... but what does naive

> mean? :-)

>

> Someone who has never had any treatment?

Treatment naive means 'never been treated'.

__________________________________________________

[Guest guest]

--- Elin L Criswell <texswede@...> wrote:

>

> I hate to be so naive...... but what does naive

> mean? :-)

>

> Someone who has never had any treatment?

Treatment naive means 'never been treated'.

__________________________________________________

[Guest guest]

--- Elin L Criswell <texswede@...> wrote:

>

> I hate to be so naive...... but what does naive

> mean? :-)

>

> Someone who has never had any treatment?

Treatment naive means 'never been treated'.

__________________________________________________

[Guest guest]

--- Elin L Criswell <texswede@...> wrote:

>

> I hate to be so naive...... but what does naive

> mean? :-)

>

> Someone who has never had any treatment?

Treatment naive means 'never been treated'.

__________________________________________________

[Guest guest]

>Hi Elin..

Just read yur e-mail about the MMM research. since I am a naive hcv patient

I would be interested in participating. do you stilll have their number or

e-mail address? Could you send it to me? thanks...and Happy Thanksgiving!

Glenna

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[Guest guest]

>Hi Elin..

Just read yur e-mail about the MMM research. since I am a naive hcv patient

I would be interested in participating. do you stilll have their number or

e-mail address? Could you send it to me? thanks...and Happy Thanksgiving!

Glenna

_________________________________________________________________________

Get Your Private, Free E-mail from MSN Hotmail at http://www.hotmail.com.

Share information about yourself, create your own public profile at

http://profiles.msn.com.

[Guest guest]

>Hi Elin..

Just read yur e-mail about the MMM research. since I am a naive hcv patient

I would be interested in participating. do you stilll have their number or

e-mail address? Could you send it to me? thanks...and Happy Thanksgiving!

Glenna

_________________________________________________________________________

Get Your Private, Free E-mail from MSN Hotmail at http://www.hotmail.com.

Share information about yourself, create your own public profile at

http://profiles.msn.com.

[Guest guest]

>Hi Elin..

Just read yur e-mail about the MMM research. since I am a naive hcv patient

I would be interested in participating. do you stilll have their number or

e-mail address? Could you send it to me? thanks...and Happy Thanksgiving!

Glenna

_________________________________________________________________________

Get Your Private, Free E-mail from MSN Hotmail at http://www.hotmail.com.

Share information about yourself, create your own public profile at

http://profiles.msn.com.

[Guest guest]

Glenna:

That phone number is 1-800-204-7346, refer to the Hep C study, or

study#00-054.

Claudine:

When my hubby did that phone interview, he told me that it sounded like

there may be yet another new treatment coming out, six months after the

pegas (sp?) comes out. Do you know anything about that?

And for everyone else............. :-)

I haven't posted this to the group, but we did recently meet with our

gastro doctor. The results of the biopsy was .... " moderate activity

with mild inflammation. "

The doc want my husband to wait until the beginning of the year when the

pegas interferon comes out before starting treatment.

So we were excited about that. And hoping that as further treatment

options come along, that they'll only get better.

Elin

On Mon, 20 Nov 2000 12:59:48 GMT " glenna gebauer "

<gebauer719@...> writes:

>

>

>

> >Hi Elin..

> Just read yur e-mail about the MMM research. since I am a naive hcv

> patient

> I would be interested in participating. do you stilll have their

> number or

> e-mail address? Could you send it to me? thanks...and Happy

> Thanksgiving!

> Glenna

>

_________________________________________________________________________

> Get Your Private, Free E-mail from MSN Hotmail at

> http://www.hotmail.com.

>

> Share information about yourself, create your own public profile at

> http://profiles.msn.com.

>

>

> -------------------------- eGroups Sponsor

>

>

[Guest guest]

Glenna:

That phone number is 1-800-204-7346, refer to the Hep C study, or

study#00-054.

Claudine:

When my hubby did that phone interview, he told me that it sounded like

there may be yet another new treatment coming out, six months after the

pegas (sp?) comes out. Do you know anything about that?

And for everyone else............. :-)

I haven't posted this to the group, but we did recently meet with our

gastro doctor. The results of the biopsy was .... " moderate activity

with mild inflammation. "

The doc want my husband to wait until the beginning of the year when the

pegas interferon comes out before starting treatment.

So we were excited about that. And hoping that as further treatment

options come along, that they'll only get better.

Elin

On Mon, 20 Nov 2000 12:59:48 GMT " glenna gebauer "

<gebauer719@...> writes:

>

>

>

> >Hi Elin..

> Just read yur e-mail about the MMM research. since I am a naive hcv

> patient

> I would be interested in participating. do you stilll have their

> number or

> e-mail address? Could you send it to me? thanks...and Happy

> Thanksgiving!

> Glenna

>

_________________________________________________________________________

> Get Your Private, Free E-mail from MSN Hotmail at

> http://www.hotmail.com.

>

> Share information about yourself, create your own public profile at

> http://profiles.msn.com.

>

>

> -------------------------- eGroups Sponsor

>

>

[Guest guest]

could that be heptazyme? love sylv

Re: MMR Research Interviews

> Glenna:

>

> That phone number is 1-800-204-7346, refer to the Hep C study, or

> study#00-054.

>

>

>

> Claudine:

>

> When my hubby did that phone interview, he told me that it sounded like

> there may be yet another new treatment coming out, six months after the

> pegas (sp?) comes out. Do you know anything about that?

>

>

> And for everyone else............. :-)

>

> I haven't posted this to the group, but we did recently meet with our

> gastro doctor. The results of the biopsy was .... " moderate activity

> with mild inflammation. "

>

> The doc want my husband to wait until the beginning of the year when the

> pegas interferon comes out before starting treatment.

>

> So we were excited about that. And hoping that as further treatment

> options come along, that they'll only get better.

>

>

> Elin

>

>

>

>

>

>

> On Mon, 20 Nov 2000 12:59:48 GMT " glenna gebauer "

> <gebauer719@...> writes:

> >

> >

> >

> > >Hi Elin..

> > Just read yur e-mail about the MMM research. since I am a naive hcv

> > patient

> > I would be interested in participating. do you stilll have their

> > number or

> > e-mail address? Could you send it to me? thanks...and Happy

> > Thanksgiving!

> > Glenna

> >

> _________________________________________________________________________

> > Get Your Private, Free E-mail from MSN Hotmail at

> > http://www.hotmail.com.

> >

> > Share information about yourself, create your own public profile at

> > http://profiles.msn.com.

> >

> >

> > -------------------------- eGroups Sponsor

> >

> >

[Guest guest]

could that be heptazyme? love sylv

Re: MMR Research Interviews

> Glenna:

>

> That phone number is 1-800-204-7346, refer to the Hep C study, or

> study#00-054.

>

>

>

> Claudine:

>

> When my hubby did that phone interview, he told me that it sounded like

> there may be yet another new treatment coming out, six months after the

> pegas (sp?) comes out. Do you know anything about that?

>

>

> And for everyone else............. :-)

>

> I haven't posted this to the group, but we did recently meet with our

> gastro doctor. The results of the biopsy was .... " moderate activity

> with mild inflammation. "

>

> The doc want my husband to wait until the beginning of the year when the

> pegas interferon comes out before starting treatment.

>

> So we were excited about that. And hoping that as further treatment

> options come along, that they'll only get better.

>

>

> Elin

>

>

>

>

>

>

> On Mon, 20 Nov 2000 12:59:48 GMT " glenna gebauer "

> <gebauer719@...> writes:

> >

> >

> >

> > >Hi Elin..

> > Just read yur e-mail about the MMM research. since I am a naive hcv

> > patient

> > I would be interested in participating. do you stilll have their

> > number or

> > e-mail address? Could you send it to me? thanks...and Happy

> > Thanksgiving!

> > Glenna

> >

> _________________________________________________________________________

> > Get Your Private, Free E-mail from MSN Hotmail at

> > http://www.hotmail.com.

> >

> > Share information about yourself, create your own public profile at

> > http://profiles.msn.com.

> >

> >

> > -------------------------- eGroups Sponsor

> >

> >

[Guest guest]

could that be heptazyme? love sylv

Re: MMR Research Interviews

> Glenna:

>

> That phone number is 1-800-204-7346, refer to the Hep C study, or

> study#00-054.

>

>

>

> Claudine:

>

> When my hubby did that phone interview, he told me that it sounded like

> there may be yet another new treatment coming out, six months after the

> pegas (sp?) comes out. Do you know anything about that?

>

>

> And for everyone else............. :-)

>

> I haven't posted this to the group, but we did recently meet with our

> gastro doctor. The results of the biopsy was .... " moderate activity

> with mild inflammation. "

>

> The doc want my husband to wait until the beginning of the year when the

> pegas interferon comes out before starting treatment.

>

> So we were excited about that. And hoping that as further treatment

> options come along, that they'll only get better.

>

>

> Elin

>

>

>

>

>

>

> On Mon, 20 Nov 2000 12:59:48 GMT " glenna gebauer "

> <gebauer719@...> writes:

> >

> >

> >

> > >Hi Elin..

> > Just read yur e-mail about the MMM research. since I am a naive hcv

> > patient

> > I would be interested in participating. do you stilll have their

> > number or

> > e-mail address? Could you send it to me? thanks...and Happy

> > Thanksgiving!

> > Glenna

> >

> _________________________________________________________________________

> > Get Your Private, Free E-mail from MSN Hotmail at

> > http://www.hotmail.com.

> >

> > Share information about yourself, create your own public profile at

> > http://profiles.msn.com.

> >

> >

> > -------------------------- eGroups Sponsor

> >

> >

[Guest guest]

could that be heptazyme? love sylv

Re: MMR Research Interviews

> Glenna:

>

> That phone number is 1-800-204-7346, refer to the Hep C study, or

> study#00-054.

>

>

>

> Claudine:

>

> When my hubby did that phone interview, he told me that it sounded like

> there may be yet another new treatment coming out, six months after the

> pegas (sp?) comes out. Do you know anything about that?

>

>

> And for everyone else............. :-)

>

> I haven't posted this to the group, but we did recently meet with our

> gastro doctor. The results of the biopsy was .... " moderate activity

> with mild inflammation. "

>

> The doc want my husband to wait until the beginning of the year when the

> pegas interferon comes out before starting treatment.

>

> So we were excited about that. And hoping that as further treatment

> options come along, that they'll only get better.

>

>

> Elin

>

>

>

>

>

>

> On Mon, 20 Nov 2000 12:59:48 GMT " glenna gebauer "

> <gebauer719@...> writes:

> >

> >

> >

> > >Hi Elin..

> > Just read yur e-mail about the MMM research. since I am a naive hcv

> > patient

> > I would be interested in participating. do you stilll have their

> > number or

> > e-mail address? Could you send it to me? thanks...and Happy

> > Thanksgiving!

> > Glenna

> >

> _________________________________________________________________________

> > Get Your Private, Free E-mail from MSN Hotmail at

> > http://www.hotmail.com.

> >

> > Share information about yourself, create your own public profile at

> > http://profiles.msn.com.

> >

> >

> > -------------------------- eGroups Sponsor

> >

> >

[Guest guest]

--- " Elin L. Criswell " <texswede@...> wrote:

> When my hubby did that phone interview, he told me

> that it sounded like

> there may be yet another new treatment coming out,

> six months after the

> pegas (sp?) comes out. Do you know anything about

> that?

Elin,

When I did the interview I got the distinct impression

that this is a La Roche sponsored survey, about

Pegasys. So I would guess that the new drug would be

Maxamine, since Maxim and Roche signed an agreement to

test the use of their drugs together, in the same way

that Intron-A is now used with ribavirin. However, if

it is Maxamine I'm sure this combo will only be

available in trials for quite a while. Don't let that

discourage you though, since there is a fair chance

that some doctor in your area will be participating in

the trials. And with your husbands really good biopsy

results (tell him congratulations!) he really does

have that option to wait if he wants. What is his

genotype?

Claudine

__________________________________________________

[Guest guest]

--- " Elin L. Criswell " <texswede@...> wrote:

> When my hubby did that phone interview, he told me

> that it sounded like

> there may be yet another new treatment coming out,

> six months after the

> pegas (sp?) comes out. Do you know anything about

> that?

Elin,

When I did the interview I got the distinct impression

that this is a La Roche sponsored survey, about

Pegasys. So I would guess that the new drug would be

Maxamine, since Maxim and Roche signed an agreement to

test the use of their drugs together, in the same way

that Intron-A is now used with ribavirin. However, if

it is Maxamine I'm sure this combo will only be

available in trials for quite a while. Don't let that

discourage you though, since there is a fair chance

that some doctor in your area will be participating in

the trials. And with your husbands really good biopsy

results (tell him congratulations!) he really does

have that option to wait if he wants. What is his

genotype?

Claudine

__________________________________________________

[Guest guest]

> What is his

> genotype?

Claudine:

Danny's genotype is 1a.

Elin

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[Guest guest]

> What is his

> genotype?

Claudine:

Danny's genotype is 1a.

Elin

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[Guest guest]

Edie,

The interviewer talked to me for a few minutes

afterwards. It is Roche and is about

Pegasys......Connie

--- Gil & Edie <erodrig1@...> wrote:

> I did the research interview the other day. It took

> about 40 minutes and I

> really enjoyed it. The person was really nice and

> said I would get my money

> in about 30 days.

>

> Yes, it does sound like some company is coming out

> with a newer Peg version

> some 5 or 6 months after the first one is supposed

> to come out.

>

> Thanks for the tip, as I would have never got a

> chance to do this if it

> wasn't for this list.

>

> Edie in San Diego

>

>

__________________________________________________

[Guest guest]

Edie,

The interviewer talked to me for a few minutes

afterwards. It is Roche and is about

Pegasys......Connie

--- Gil & Edie <erodrig1@...> wrote:

> I did the research interview the other day. It took

> about 40 minutes and I

> really enjoyed it. The person was really nice and

> said I would get my money

> in about 30 days.

>

> Yes, it does sound like some company is coming out

> with a newer Peg version

> some 5 or 6 months after the first one is supposed

> to come out.

>

> Thanks for the tip, as I would have never got a

> chance to do this if it

> wasn't for this list.

>

> Edie in San Diego

>

>

__________________________________________________

[Guest guest]

I did the research interview last Thursday. I agree, they were very nice and

asked intelligent questions..............like maybe someone had clued them in

on what they were asking about. Thanks for the heads up. Anne