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--- Dee Dee <deetaylor76@...> wrote:

> Hi All,

> My test results came back as Grade 2, stage 1. Also

my daughter

> came back NEG!!!!!!!!!!!! What a relief. Now to

> have my other 2 daughters

> tested.

Dear Dee Dee,

That is great news, both about your biopsy and

your daughter. The Grade is the amount of

inflammation, the Stage is the amount of fibrosis. So

at this point you have very little damage!

Congratulations!

I'm sure your other daughters will come back

negative also. So I assume from what you've been

saying that your family is taking the news pretty

well?

Take care,

Claudine

=====

Claudine

claudinecrews@...

__________________________________________________

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--- Dee Dee <deetaylor76@...> wrote:

> Hi All,

> My test results came back as Grade 2, stage 1. Also

my daughter

> came back NEG!!!!!!!!!!!! What a relief. Now to

> have my other 2 daughters

> tested.

Dear Dee Dee,

That is great news, both about your biopsy and

your daughter. The Grade is the amount of

inflammation, the Stage is the amount of fibrosis. So

at this point you have very little damage!

Congratulations!

I'm sure your other daughters will come back

negative also. So I assume from what you've been

saying that your family is taking the news pretty

well?

Take care,

Claudine

=====

Claudine

claudinecrews@...

__________________________________________________

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--- Dee Dee <deetaylor76@...> wrote:

> Hi All,

> My test results came back as Grade 2, stage 1. Also

my daughter

> came back NEG!!!!!!!!!!!! What a relief. Now to

> have my other 2 daughters

> tested.

Dear Dee Dee,

That is great news, both about your biopsy and

your daughter. The Grade is the amount of

inflammation, the Stage is the amount of fibrosis. So

at this point you have very little damage!

Congratulations!

I'm sure your other daughters will come back

negative also. So I assume from what you've been

saying that your family is taking the news pretty

well?

Take care,

Claudine

=====

Claudine

claudinecrews@...

__________________________________________________

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Share on other sites

--- Dee Dee <deetaylor76@...> wrote:

> Hi All,

> My test results came back as Grade 2, stage 1. Also

my daughter

> came back NEG!!!!!!!!!!!! What a relief. Now to

> have my other 2 daughters

> tested.

Dear Dee Dee,

That is great news, both about your biopsy and

your daughter. The Grade is the amount of

inflammation, the Stage is the amount of fibrosis. So

at this point you have very little damage!

Congratulations!

I'm sure your other daughters will come back

negative also. So I assume from what you've been

saying that your family is taking the news pretty

well?

Take care,

Claudine

=====

Claudine

claudinecrews@...

__________________________________________________

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Claudine,

Sorry for the delayed reply. Yes, the familly has taken it fine. My oldest

daughter knew. I guess I left a letter from the Dr. office laying around

which she read. I even told them I probablly got it back some 30 years ago

when I was their age and did something very stupid. Experimented with IV

drugs. Of course my 15 year old...... " and you said you never even smoked

pot " Hopefully this will be a good lesson for them.

I've been keeping up with my messages. I'm reading with interest the

progress with you . Hope you are feeling ok. Also Pat. 0-kill! Man,

I'm not sure if I'll be able to handle this. I start treatment on the 6th

of Sept. Good thing I didn't start last Monday. Hubby brings home 3 cases

of tomatoes and 2 cases of peaches for me to can after work. Lately I've

been feeling increased flu-like symptoms. Nausia, diareha,

tired......irritable. Time for treatment. BYW....something said about

stoping treatment once started is not a good thing. What if you can't

tolorate the sides? Well, gotta go......Dee Dee

>From: claudine intexas <claudineintexas@...>

>Reply-Hepatitis Cegroups

>Hepatitis Cegroups

>Subject: Re: biopsy results

>Date: Thu, 17 Aug 2000 08:42:12 -0700 (PDT)

>

>

>--- Dee Dee <deetaylor76@...> wrote:

> > Hi All,

> > My test results came back as Grade 2, stage 1. Also

>my daughter

> > came back NEG!!!!!!!!!!!! What a relief. Now to

> > have my other 2 daughters

> > tested.

>

>Dear Dee Dee,

> That is great news, both about your biopsy and

>your daughter. The Grade is the amount of

>inflammation, the Stage is the amount of fibrosis. So

>at this point you have very little damage!

>Congratulations!

> I'm sure your other daughters will come back

>negative also. So I assume from what you've been

>saying that your family is taking the news pretty

>well?

>Take care,

>Claudine

>

>

>=====

>Claudine

>claudinecrews@...

>

>__________________________________________________

>

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Claudine,

Sorry for the delayed reply. Yes, the familly has taken it fine. My oldest

daughter knew. I guess I left a letter from the Dr. office laying around

which she read. I even told them I probablly got it back some 30 years ago

when I was their age and did something very stupid. Experimented with IV

drugs. Of course my 15 year old...... " and you said you never even smoked

pot " Hopefully this will be a good lesson for them.

I've been keeping up with my messages. I'm reading with interest the

progress with you . Hope you are feeling ok. Also Pat. 0-kill! Man,

I'm not sure if I'll be able to handle this. I start treatment on the 6th

of Sept. Good thing I didn't start last Monday. Hubby brings home 3 cases

of tomatoes and 2 cases of peaches for me to can after work. Lately I've

been feeling increased flu-like symptoms. Nausia, diareha,

tired......irritable. Time for treatment. BYW....something said about

stoping treatment once started is not a good thing. What if you can't

tolorate the sides? Well, gotta go......Dee Dee

>From: claudine intexas <claudineintexas@...>

>Reply-Hepatitis Cegroups

>Hepatitis Cegroups

>Subject: Re: biopsy results

>Date: Thu, 17 Aug 2000 08:42:12 -0700 (PDT)

>

>

>--- Dee Dee <deetaylor76@...> wrote:

> > Hi All,

> > My test results came back as Grade 2, stage 1. Also

>my daughter

> > came back NEG!!!!!!!!!!!! What a relief. Now to

> > have my other 2 daughters

> > tested.

>

>Dear Dee Dee,

> That is great news, both about your biopsy and

>your daughter. The Grade is the amount of

>inflammation, the Stage is the amount of fibrosis. So

>at this point you have very little damage!

>Congratulations!

> I'm sure your other daughters will come back

>negative also. So I assume from what you've been

>saying that your family is taking the news pretty

>well?

>Take care,

>Claudine

>

>

>=====

>Claudine

>claudinecrews@...

>

>__________________________________________________

>

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Share on other sites

Claudine,

Sorry for the delayed reply. Yes, the familly has taken it fine. My oldest

daughter knew. I guess I left a letter from the Dr. office laying around

which she read. I even told them I probablly got it back some 30 years ago

when I was their age and did something very stupid. Experimented with IV

drugs. Of course my 15 year old...... " and you said you never even smoked

pot " Hopefully this will be a good lesson for them.

I've been keeping up with my messages. I'm reading with interest the

progress with you . Hope you are feeling ok. Also Pat. 0-kill! Man,

I'm not sure if I'll be able to handle this. I start treatment on the 6th

of Sept. Good thing I didn't start last Monday. Hubby brings home 3 cases

of tomatoes and 2 cases of peaches for me to can after work. Lately I've

been feeling increased flu-like symptoms. Nausia, diareha,

tired......irritable. Time for treatment. BYW....something said about

stoping treatment once started is not a good thing. What if you can't

tolorate the sides? Well, gotta go......Dee Dee

>From: claudine intexas <claudineintexas@...>

>Reply-Hepatitis Cegroups

>Hepatitis Cegroups

>Subject: Re: biopsy results

>Date: Thu, 17 Aug 2000 08:42:12 -0700 (PDT)

>

>

>--- Dee Dee <deetaylor76@...> wrote:

> > Hi All,

> > My test results came back as Grade 2, stage 1. Also

>my daughter

> > came back NEG!!!!!!!!!!!! What a relief. Now to

> > have my other 2 daughters

> > tested.

>

>Dear Dee Dee,

> That is great news, both about your biopsy and

>your daughter. The Grade is the amount of

>inflammation, the Stage is the amount of fibrosis. So

>at this point you have very little damage!

>Congratulations!

> I'm sure your other daughters will come back

>negative also. So I assume from what you've been

>saying that your family is taking the news pretty

>well?

>Take care,

>Claudine

>

>

>=====

>Claudine

>claudinecrews@...

>

>__________________________________________________

>

Link to comment
Share on other sites

Claudine,

Sorry for the delayed reply. Yes, the familly has taken it fine. My oldest

daughter knew. I guess I left a letter from the Dr. office laying around

which she read. I even told them I probablly got it back some 30 years ago

when I was their age and did something very stupid. Experimented with IV

drugs. Of course my 15 year old...... " and you said you never even smoked

pot " Hopefully this will be a good lesson for them.

I've been keeping up with my messages. I'm reading with interest the

progress with you . Hope you are feeling ok. Also Pat. 0-kill! Man,

I'm not sure if I'll be able to handle this. I start treatment on the 6th

of Sept. Good thing I didn't start last Monday. Hubby brings home 3 cases

of tomatoes and 2 cases of peaches for me to can after work. Lately I've

been feeling increased flu-like symptoms. Nausia, diareha,

tired......irritable. Time for treatment. BYW....something said about

stoping treatment once started is not a good thing. What if you can't

tolorate the sides? Well, gotta go......Dee Dee

>From: claudine intexas <claudineintexas@...>

>Reply-Hepatitis Cegroups

>Hepatitis Cegroups

>Subject: Re: biopsy results

>Date: Thu, 17 Aug 2000 08:42:12 -0700 (PDT)

>

>

>--- Dee Dee <deetaylor76@...> wrote:

> > Hi All,

> > My test results came back as Grade 2, stage 1. Also

>my daughter

> > came back NEG!!!!!!!!!!!! What a relief. Now to

> > have my other 2 daughters

> > tested.

>

>Dear Dee Dee,

> That is great news, both about your biopsy and

>your daughter. The Grade is the amount of

>inflammation, the Stage is the amount of fibrosis. So

>at this point you have very little damage!

>Congratulations!

> I'm sure your other daughters will come back

>negative also. So I assume from what you've been

>saying that your family is taking the news pretty

>well?

>Take care,

>Claudine

>

>

>=====

>Claudine

>claudinecrews@...

>

>__________________________________________________

>

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  • 2 months later...

Dear Jenn,

That is great news! Yes, definitely wait for a

pegylated with ribavirin or other 'helper' drug. The

sides are supposed to be so much easier, and the

success rate is so much better. By the time you have

your blood work rechecked in 6 months the new pegs

should be available, and hopefully with ribavirin too.

You certainly don't need to rush into anything!

Congratulations!

Claudine

__________________________________________________

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Dear Jenn,

That is great news! Yes, definitely wait for a

pegylated with ribavirin or other 'helper' drug. The

sides are supposed to be so much easier, and the

success rate is so much better. By the time you have

your blood work rechecked in 6 months the new pegs

should be available, and hopefully with ribavirin too.

You certainly don't need to rush into anything!

Congratulations!

Claudine

__________________________________________________

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Share on other sites

Dear Jenn,

That is great news! Yes, definitely wait for a

pegylated with ribavirin or other 'helper' drug. The

sides are supposed to be so much easier, and the

success rate is so much better. By the time you have

your blood work rechecked in 6 months the new pegs

should be available, and hopefully with ribavirin too.

You certainly don't need to rush into anything!

Congratulations!

Claudine

__________________________________________________

Link to comment
Share on other sites

Dear Jenn,

That is great news! Yes, definitely wait for a

pegylated with ribavirin or other 'helper' drug. The

sides are supposed to be so much easier, and the

success rate is so much better. By the time you have

your blood work rechecked in 6 months the new pegs

should be available, and hopefully with ribavirin too.

You certainly don't need to rush into anything!

Congratulations!

Claudine

__________________________________________________

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Share on other sites

Jenn great news!

My biopsy was very mild inflamation, but like you I had awful hep symptoms -

joint pain, achy muscles, insomnia, major fatigue - and so decided to do

treatment knowing that if it was too much for me, I could quit without

serious consequences. I'm a 1b so if my 6th mo pcr is negative I go another

6 months (I'm waiting on those results now). After my first interferon shot,

I felt great! It took away my joint pain and muscles aches. I'm still tired,

and at my 5th mo I had to increase my anti depressant, but I didn't realize

how much I really did hurt from the hep till I started treatment and got

some relief. I was scared to death to do combo, but now I'm glad I did. Goes

to show you, just never know how the combo will treat you :)

alley/

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Jenn great news!

My biopsy was very mild inflamation, but like you I had awful hep symptoms -

joint pain, achy muscles, insomnia, major fatigue - and so decided to do

treatment knowing that if it was too much for me, I could quit without

serious consequences. I'm a 1b so if my 6th mo pcr is negative I go another

6 months (I'm waiting on those results now). After my first interferon shot,

I felt great! It took away my joint pain and muscles aches. I'm still tired,

and at my 5th mo I had to increase my anti depressant, but I didn't realize

how much I really did hurt from the hep till I started treatment and got

some relief. I was scared to death to do combo, but now I'm glad I did. Goes

to show you, just never know how the combo will treat you :)

alley/

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Hi All, well I guess I have turned in to a skinny no hair hepper. I

don't like what I look like but all this will change. I have been

feeling very well lately. But I have been drinking lots of water and

getting lots and lots rest.

Does anyone else get wired when they take the shot?Boy I do

Love Jessie

EZ-DOES IT

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Hi All, well I guess I have turned in to a skinny no hair hepper. I

don't like what I look like but all this will change. I have been

feeling very well lately. But I have been drinking lots of water and

getting lots and lots rest.

Does anyone else get wired when they take the shot?Boy I do

Love Jessie

EZ-DOES IT

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Share on other sites

Hi All, well I guess I have turned in to a skinny no hair hepper. I

don't like what I look like but all this will change. I have been

feeling very well lately. But I have been drinking lots of water and

getting lots and lots rest.

Does anyone else get wired when they take the shot?Boy I do

Love Jessie

EZ-DOES IT

Link to comment
Share on other sites

Hi All, well I guess I have turned in to a skinny no hair hepper. I

don't like what I look like but all this will change. I have been

feeling very well lately. But I have been drinking lots of water and

getting lots and lots rest.

Does anyone else get wired when they take the shot?Boy I do

Love Jessie

EZ-DOES IT

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I would wait for something better. There was an interesting post at

Hep-Central a while ago-it was titled " A New Treatment For Hep C' (or

something along that line) and it was totally blank.

gail

----------

>From: " jenn fisher " <jenniboop2@...>

>Hepatitis Cegroups

>Subject: biopsy results

>Date: Wed, Nov 8, 2000, 5:46 PM

>

> Hello All,

> Im so excited right now I just got off the phone with my Dr. and my

> biopsy score was like between 0-1 so she said I have time to wait. I do have

> anoying hcv symptoms like achey joints and fatigue and chills , but they

> seem to be getting better,...so do i realy want to go through 6 months (im

> type 3) of hell (from what i hear)

> or at least i have time to wait for the peg to be approved , any thoughts on

> what you might do? I'm gonna have my blood work checked in 6 months

> jumping for joy,

> jenn

> _________________________________________________________________________

> 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.

>

>

>

>

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I would wait for something better. There was an interesting post at

Hep-Central a while ago-it was titled " A New Treatment For Hep C' (or

something along that line) and it was totally blank.

gail

----------

>From: " jenn fisher " <jenniboop2@...>

>Hepatitis Cegroups

>Subject: biopsy results

>Date: Wed, Nov 8, 2000, 5:46 PM

>

> Hello All,

> Im so excited right now I just got off the phone with my Dr. and my

> biopsy score was like between 0-1 so she said I have time to wait. I do have

> anoying hcv symptoms like achey joints and fatigue and chills , but they

> seem to be getting better,...so do i realy want to go through 6 months (im

> type 3) of hell (from what i hear)

> or at least i have time to wait for the peg to be approved , any thoughts on

> what you might do? I'm gonna have my blood work checked in 6 months

> jumping for joy,

> jenn

> _________________________________________________________________________

> 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.

>

>

>

>

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