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Hi Debbie - Although it has probably been 30 years since I contracted Hepc

(college was a lot of fun), I only was diagnosed this past October. A

friend bugged me to be tested because I have been a little tired for about 4

years now, which I thought, and which still may be, due to menopause. Both

my doctor & I definitely thought we were indulging her. Not! My biopsy is

scheduled for Jan. 31 at Beth Israel, to be done by Dr. Chopra. However,

unless I am in more advanced stages of chirrosis or fibrosis, I won't be

doing interferon right away. Any information you can give me on herbs &

vitamins would be very much appreciated. I am trying to find out about

thymic therapy. The notion that to beat Hepc you must beef up your immune

system until the immune system can overcome it makes sense to me.

I hope your husband continues to be well.

Thank you

Pam

>From: NCA2JMOM@...

>Reply-Hepatitis Conelist

>Hepatitis Conelist

>Subject: combo treatment

>Date: Tue, 11 Jan 2000 07:26:45 EST

>

>Hi all,

>

>My husband tested positive for Hep C in 1994, but we think he contracted it

>in 1989 while undergoing surgery for a badly broken ankle. He tried the

>Intron A treatments for about 8 months in '97-'98, but was a non-responder.

>The sides almost killed him, including a horrible depression that neither

>of

>us really understood until he was off the Interferon and his head cleared.

>After that, we investigated and researched the herbal route and came up

>with

>a plan of about 5 herbs and a good multi vitamin for him to try. He started

>on those and then in August of '99 he began the combo treatment of

>Interferon

>and Ribavirin. Before he started those treatments, his liver enzyme levels

>had gone done some and they have continued to go down. His viral load is

>now

>less than 1 million and his other levels are all within normal limits and

>have been for several months. He feels BETTER than he has in years -- the

>only real side effect he has had to live with is losing some hair. He is

>convinced that the herbs have helped his body not only fight the Hep C but

>also to deal with the Interferon and Ribavirin. Please E-mail me privately

>if

>you'd like more information as I don't want to bog down the mailboxes of

>those who are not interested. I am so glad this list is going and I know it

>will be a valuable resource for all of us who deal with this insidious

>disease.

>

>Blessings,

>Debbie

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Hi all,

My husband tested positive for Hep C in 1994, but we think he contracted it

in 1989 while undergoing surgery for a badly broken ankle. He tried the

Intron A treatments for about 8 months in '97-'98, but was a non-responder.

The sides almost killed him, including a horrible depression that neither of

us really understood until he was off the Interferon and his head cleared.

After that, we investigated and researched the herbal route and came up with

a plan of about 5 herbs and a good multi vitamin for him to try. He started

on those and then in August of '99 he began the combo treatment of Interferon

and Ribavirin. Before he started those treatments, his liver enzyme levels

had gone done some and they have continued to go down. His viral load is now

less than 1 million and his other levels are all within normal limits and

have been for several months. He feels BETTER than he has in years -- the

only real side effect he has had to live with is losing some hair. He is

convinced that the herbs have helped his body not only fight the Hep C but

also to deal with the Interferon and Ribavirin. Please E-mail me privately if

you'd like more information as I don't want to bog down the mailboxes of

those who are not interested. I am so glad this list is going and I know it

will be a valuable resource for all of us who deal with this insidious

disease.

Blessings,

Debbie

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I have been through Acupuncture and use Chinese

Herbs, the first six months brought an encouraging response when comparing

my blood work from the previous six months, so being such the dedicated

individual I am I slowly stopped the herbs and my current blood work

reflects its impact. So I am back to taking them regularly!

I take " Long Dan (Xie Gan Wan) " for the dry skin and

it worked great, notice the difference in the first week, the remaining

five to six herbs I will have to lookup how to write them and I'll let you

all know tomorrow their names.

History for me - I was diagnosed Oct. of 98, after

my husband had been screen through the VA and tested positive. First

thought - finally they know why I am feeling so lousy, I can manage the

symptoms and get my life back. The medical world offered very little as

you all know to making my life better. My first doctor gave me a death

sentence and his entire staff was " afraid " of me every time I walked into

the building. Found a new doctor he is wonderful, his approach is one of

management for health and overall well-being. He explained that

" traditional " medicine lacked in being able to provide relief from the

symptoms, and encouraged me to see my Acupuncturist, he has had very good

results with defeating Hep C as well as making life bearable, Quality of

life is worth a lot. So I underwent the five months of treatments and herb

therapy, the results were there, I was feeling better getting my energy back

and my life. Then I stopped the herbs, let the diet go - got lazy, in

Nov.99 I got a cold - flu. I am still fighting it, my blood work shows my

Viral Load is down 50% but the Liver functions tests have tripled. Back to

the diet back to the herbs

Lesson - Don't give up and don't quit what is

working 'til your are ALL better.

Karie

PS. I'll write about the diet and the other Chinese

Herbs tomorrow.

Stay well - stay happy

combo

treatment

>Date: Tue, 11 Jan 2000 07:26:45 EST

>

>Hi all,

>

>My husband tested positive for Hep C in

1994, but we think he contracted it

>in 1989 while undergoing surgery for a

badly broken ankle. He tried the

>Intron A treatments for about 8 months in

'97-'98, but was a non-responder.

>The sides almost killed him, including a

horrible depression that neither

>of

>us really understood until he was off the

Interferon and his head cleared.

>After that, we investigated and researched

the herbal route and came up

>with

>a plan of about 5 herbs and a good multi

vitamin for him to try. He started

>on those and then in August of '99 he began

the combo treatment of

>Interferon

>and Ribavirin. Before he started those

treatments, his liver enzyme levels

>had gone done some and they have continued

to go down. His viral load is

>now

>less than 1 million and his other levels

are all within normal limits and

>have been for several months. He feels

BETTER than he has in years -- the

>only real side effect he has had to live

with is losing some hair. He is

>convinced that the herbs have helped his

body not only fight the Hep C but

>also to deal with the Interferon and

Ribavirin. Please E-mail me privately

>if

>you'd like more information as I don't want

to bog down the mailboxes of

>those who are not interested. I am so glad

this list is going and I know it

>will be a valuable resource for all of us

who deal with this insidious

>disease.

>

>Blessings,

>Debbie

______________________________________________________

Get Your Private, Free Email at

http://www.hotmail.com

---------------------------

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I'd be very interested in your info on herbal stuff - I put Big Boy on Milk

Thistle with dandelion but the last Dr poopooed that. I definitely understand

the depression angle =. while I'm trying as hard as I can it's really difficult

to make allowances sometimes for what I call the UGLIES.

Regards,

Michnevitz.

NCA2JMOM@... wrote:

> From: NCA2JMOM@...

>

> Hi all,

>

> My husband tested positive for Hep C in 1994, but we think he contracted it

> in 1989 while undergoing surgery for a badly broken ankle. He tried the

> Intron A treatments for about 8 months in '97-'98, but was a non-responder.

> The sides almost killed him, including a horrible depression that neither of

> us really understood until he was off the Interferon and his head cleared.

> After that, we investigated and researched the herbal route and came up with

> a plan of about 5 herbs and a good multi vitamin for him to try. He started

> on those and then in August of '99 he began the combo treatment of Interferon

> and Ribavirin. Before he started those treatments, his liver enzyme levels

> had gone done some and they have continued to go down. His viral load is now

> less than 1 million and his other levels are all within normal limits and

> have been for several months. He feels BETTER than he has in years -- the

> only real side effect he has had to live with is losing some hair. He is

> convinced that the herbs have helped his body not only fight the Hep C but

> also to deal with the Interferon and Ribavirin. Please E-mail me privately if

> you'd like more information as I don't want to bog down the mailboxes of

> those who are not interested. I am so glad this list is going and I know it

> will be a valuable resource for all of us who deal with this insidious

> disease.

>

> Blessings,

> Debbie

>

> ---------------------------

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I'd be very interested in your info on herbal stuff - I put Big Boy on Milk

Thistle with dandelion but the last Dr poopooed that. I definitely understand

the depression angle =. while I'm trying as hard as I can it's really difficult

to make allowances sometimes for what I call the UGLIES.

Regards,

Michnevitz.

NCA2JMOM@... wrote:

> From: NCA2JMOM@...

>

> Hi all,

>

> My husband tested positive for Hep C in 1994, but we think he contracted it

> in 1989 while undergoing surgery for a badly broken ankle. He tried the

> Intron A treatments for about 8 months in '97-'98, but was a non-responder.

> The sides almost killed him, including a horrible depression that neither of

> us really understood until he was off the Interferon and his head cleared.

> After that, we investigated and researched the herbal route and came up with

> a plan of about 5 herbs and a good multi vitamin for him to try. He started

> on those and then in August of '99 he began the combo treatment of Interferon

> and Ribavirin. Before he started those treatments, his liver enzyme levels

> had gone done some and they have continued to go down. His viral load is now

> less than 1 million and his other levels are all within normal limits and

> have been for several months. He feels BETTER than he has in years -- the

> only real side effect he has had to live with is losing some hair. He is

> convinced that the herbs have helped his body not only fight the Hep C but

> also to deal with the Interferon and Ribavirin. Please E-mail me privately if

> you'd like more information as I don't want to bog down the mailboxes of

> those who are not interested. I am so glad this list is going and I know it

> will be a valuable resource for all of us who deal with this insidious

> disease.

>

> Blessings,

> Debbie

>

> ---------------------------

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Amy,

I believe you are called a " relapser " , not a " non-responder " . As for

what now, only you can decide that! Talk with your doctor and do lots of

research. There are a lot of new treatments on the horizon to consider.

Infergen is available now, but not with the ribavirin. Pegylated interferon

is just down the road, and there are a lot of really promising sounding

treatments being researched that I've barely had time to look at! No one can

tell you the one best thing for you to do. How do you FEEL? What extent

of liver damage do you have? What in your genotype? Your viral count is

low, and you say LFT's are normal, so that is good. I say just consider all

factors before you decide. Not much help, I know!! Good luck!

Claudine

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Amy,

I believe you are called a " relapser " , not a " non-responder " . As for

what now, only you can decide that! Talk with your doctor and do lots of

research. There are a lot of new treatments on the horizon to consider.

Infergen is available now, but not with the ribavirin. Pegylated interferon

is just down the road, and there are a lot of really promising sounding

treatments being researched that I've barely had time to look at! No one can

tell you the one best thing for you to do. How do you FEEL? What extent

of liver damage do you have? What in your genotype? Your viral count is

low, and you say LFT's are normal, so that is good. I say just consider all

factors before you decide. Not much help, I know!! Good luck!

Claudine

______________________________________________________

Get Your Private, Free Email at http://www.hotmail.com

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Amy,

I believe you are called a " relapser " , not a " non-responder " . As for

what now, only you can decide that! Talk with your doctor and do lots of

research. There are a lot of new treatments on the horizon to consider.

Infergen is available now, but not with the ribavirin. Pegylated interferon

is just down the road, and there are a lot of really promising sounding

treatments being researched that I've barely had time to look at! No one can

tell you the one best thing for you to do. How do you FEEL? What extent

of liver damage do you have? What in your genotype? Your viral count is

low, and you say LFT's are normal, so that is good. I say just consider all

factors before you decide. Not much help, I know!! Good luck!

Claudine

______________________________________________________

Get Your Private, Free Email at http://www.hotmail.com

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Amy,

I believe you are called a " relapser " , not a " non-responder " . As for

what now, only you can decide that! Talk with your doctor and do lots of

research. There are a lot of new treatments on the horizon to consider.

Infergen is available now, but not with the ribavirin. Pegylated interferon

is just down the road, and there are a lot of really promising sounding

treatments being researched that I've barely had time to look at! No one can

tell you the one best thing for you to do. How do you FEEL? What extent

of liver damage do you have? What in your genotype? Your viral count is

low, and you say LFT's are normal, so that is good. I say just consider all

factors before you decide. Not much help, I know!! Good luck!

Claudine

______________________________________________________

Get Your Private, Free Email at http://www.hotmail.com

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I got my RNA levels back.....its 141,000. At the end of the cobo treatment

they were undetectable. It has now been 6 months. So does this mean I am a

" non-responder " ? And what now from here? I did the monotherapy a year and a

half ago and did not have a sustained response. My LFT's are within normal

limits. Any comments/ideas?

Amy

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I got my RNA levels back.....its 141,000. At the end of the cobo treatment

they were undetectable. It has now been 6 months. So does this mean I am a

" non-responder " ? And what now from here? I did the monotherapy a year and a

half ago and did not have a sustained response. My LFT's are within normal

limits. Any comments/ideas?

Amy

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I got my RNA levels back.....its 141,000. At the end of the cobo treatment

they were undetectable. It has now been 6 months. So does this mean I am a

" non-responder " ? And what now from here? I did the monotherapy a year and a

half ago and did not have a sustained response. My LFT's are within normal

limits. Any comments/ideas?

Amy

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Share on other sites

I got my RNA levels back.....its 141,000. At the end of the cobo treatment

they were undetectable. It has now been 6 months. So does this mean I am a

" non-responder " ? And what now from here? I did the monotherapy a year and a

half ago and did not have a sustained response. My LFT's are within normal

limits. Any comments/ideas?

Amy

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Yes, you are in the relapse stage but not yet a candidate for therapy as

your enzymes are normal. I suggest you have a liver biopsy to decide if

you need combo treatment.

Dr S C Misra

Re: Combo Treatment

From: McCoyAngel@...

I got my RNA levels back.....its 141,000. At the end of the cobo

treatment

they were undetectable. It has now been 6 months. So does this mean

I am a

" non-responder " ? And what now from here? I did the monotherapy a

year and a

half ago and did not have a sustained response. My LFT's are within

normal

limits. Any comments/ideas?

Amy

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Yes, you are in the relapse stage but not yet a candidate for therapy as

your enzymes are normal. I suggest you have a liver biopsy to decide if

you need combo treatment.

Dr S C Misra

Re: Combo Treatment

From: McCoyAngel@...

I got my RNA levels back.....its 141,000. At the end of the cobo

treatment

they were undetectable. It has now been 6 months. So does this mean

I am a

" non-responder " ? And what now from here? I did the monotherapy a

year and a

half ago and did not have a sustained response. My LFT's are within

normal

limits. Any comments/ideas?

Amy

------------------------------------------------------------------------

------

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------

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Yes, you are in the relapse stage but not yet a candidate for therapy as

your enzymes are normal. I suggest you have a liver biopsy to decide if

you need combo treatment.

Dr S C Misra

Re: Combo Treatment

From: McCoyAngel@...

I got my RNA levels back.....its 141,000. At the end of the cobo

treatment

they were undetectable. It has now been 6 months. So does this mean

I am a

" non-responder " ? And what now from here? I did the monotherapy a

year and a

half ago and did not have a sustained response. My LFT's are within

normal

limits. Any comments/ideas?

Amy

------------------------------------------------------------------------

------

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------------------------------------------------------------------------

------

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Yes, you are in the relapse stage but not yet a candidate for therapy as

your enzymes are normal. I suggest you have a liver biopsy to decide if

you need combo treatment.

Dr S C Misra

Re: Combo Treatment

From: McCoyAngel@...

I got my RNA levels back.....its 141,000. At the end of the cobo

treatment

they were undetectable. It has now been 6 months. So does this mean

I am a

" non-responder " ? And what now from here? I did the monotherapy a

year and a

half ago and did not have a sustained response. My LFT's are within

normal

limits. Any comments/ideas?

Amy

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------

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Hope you don't mind me writing to you. I'm new to the hepc thing. I've had

it since 86, i think. my doc tells me my liver tests are fine. i asked for

a virual load and she acted as if i was wasting the hospital $. she gave in

cause i insisted but she said they showed nothing harmful. what does it take

to find out if someone needs treatment and what kind of tests should i ask

for. also should i get a GI Dr. like all of you refer too??

thanks

thomas

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Hope you don't mind me writing to you. I'm new to the hepc thing. I've had

it since 86, i think. my doc tells me my liver tests are fine. i asked for

a virual load and she acted as if i was wasting the hospital $. she gave in

cause i insisted but she said they showed nothing harmful. what does it take

to find out if someone needs treatment and what kind of tests should i ask

for. also should i get a GI Dr. like all of you refer too??

thanks

thomas

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Share on other sites

Hope you don't mind me writing to you. I'm new to the hepc thing. I've had

it since 86, i think. my doc tells me my liver tests are fine. i asked for

a virual load and she acted as if i was wasting the hospital $. she gave in

cause i insisted but she said they showed nothing harmful. what does it take

to find out if someone needs treatment and what kind of tests should i ask

for. also should i get a GI Dr. like all of you refer too??

thanks

thomas

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Share on other sites

Hope you don't mind me writing to you. I'm new to the hepc thing. I've had

it since 86, i think. my doc tells me my liver tests are fine. i asked for

a virual load and she acted as if i was wasting the hospital $. she gave in

cause i insisted but she said they showed nothing harmful. what does it take

to find out if someone needs treatment and what kind of tests should i ask

for. also should i get a GI Dr. like all of you refer too??

thanks

thomas

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Claudine, My name is and I believe I've had Hep C since 86 when I got

very sick and the Dr's.had no idea what I had. Later about 8 yrs, my doc

told me I have Hep c. she always tell me my liver tests are fine. I asked

for a viral count or load and she acted as if it cost too much. I insisted

and the results came back OK (from her). Could you let me know what I need

to ask for so I can track the progress of this disease and should I get a

different Dr. maybe a GI?

if you have time I'd appreciate a reply

thanks

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Claudine, My name is and I believe I've had Hep C since 86 when I got

very sick and the Dr's.had no idea what I had. Later about 8 yrs, my doc

told me I have Hep c. she always tell me my liver tests are fine. I asked

for a viral count or load and she acted as if it cost too much. I insisted

and the results came back OK (from her). Could you let me know what I need

to ask for so I can track the progress of this disease and should I get a

different Dr. maybe a GI?

if you have time I'd appreciate a reply

thanks

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