Re: helo

[Guest guest]

Hi Jan I'm Terry. If you have insurance you should be able to get treatment any time you need, as long as the aprove it & most will. Glad to have you in here. Terryihop2jan <ihop2jan@...> wrote: i dont know if i am using this right, as i have never used a chat orsimilar before. (ancient me). i have had hep c for over twenty years now, no treatment or support, iam an ex addict. (nearly 16 years ago) Two weeks ago, my ex partner also hep c, died, overdose i assume, thechildren,3, and i feel in limbo, and i feel frustrated.i dont want to get sick. i want to live. live a long and happy lifefor my children. My strain is 1 something, and i know from a viz tothe dr. last year that "i am not at the early stages, not at theworst, but

inbetween." Not that that is telling me a lot.What treat ment is there?My neice is 32, in australia, and about to start interferon, as thegovernment says they no longer have to wait for cirrossis (cant spell,sorry). i am pleased for her, but a bit envious too.i dont want to wait till i get really ill to have a chance for a cure.is there anything i can do or take to help myself get a better chance?i am in contact with no other person with hep c on a one to one. ifeel ignorant of my illness and isolated. Anyone got suggestions? Iam 44.Jan

[Guest guest]

Hello and welcome. I was in about your place a few years ago. I had type 1b, probably about 18 years. I used some Milk Thistle, before I started treatment and it brought my alt/ast counts down. I had no cirrhosis either, and I started the interferon combo (with ribavarin) treatment. I have been undetectable for the virus since then. I did 48 weeks of treatment and when tested at 6 mos. I was undetectable, but still completed the course. Good luck, with whatever you choose. -dz-ihop2jan <ihop2jan@...> wrote: i dont know if i am using this right, as i have never used a chat orsimilar before. (ancient me). i have had hep c for over twenty years now, no treatment or support, iam an ex addict. (nearly 16 years ago) Two weeks ago, my ex partner also hep c, died, overdose i assume, thechildren,3, and i feel

in limbo, and i feel frustrated.i dont want to get sick. i want to live. live a long and happy lifefor my children. My strain is 1 something, and i know from a viz tothe dr. last year that "i am not at the early stages, not at theworst, but inbetween." Not that that is telling me a lot.What treat ment is there?My neice is 32, in australia, and about to start interferon, as thegovernment says they no longer have to wait for cirrossis (cant spell,sorry). i am pleased for her, but a bit envious too.i dont want to wait till i get really ill to have a chance for a cure.is there anything i can do or take to help myself get a better chance?i am in contact with no other person with hep c on a one to one. ifeel ignorant of my illness and isolated. Anyone got suggestions? Iam 44.Jan

[Guest guest]

helo dave,thankyou for replying to me. i will use some milkthistle too, then. i do not know what alt ast counts are. i am not science minded, and i think it all sound all so complicated.i do have some symptoms of the virus, mostly feeling sick and real fatigue. it is heartenning to hear that you had success with your treatment. will you stay undetected, or will it come back, i hope it doesnt. please excuse punctuation, shift keys not working on keyboard.all the best, jan. Re:

[ ] helo Hello and welcome. I was in about your place a few years ago. I had type 1b, probably about 18 years. I used some Milk Thistle, before I started treatment and it brought my alt/ast counts down. I had no cirrhosis either, and I started the interferon combo (with ribavarin) treatment. I have been undetectable for the virus since then. I did 48 weeks of treatment and when tested at 6 mos. I was undetectable, but still completed the course. Good luck, with whatever you choose. -dz-ihop2jan <ihop2jan@...> wrote: i dont know if i am using this right, as i have never used a chat orsimilar before. (ancient me). i have had hep c for over twenty years now, no treatment or support, iam an ex addict. (nearly 16 years ago) Two weeks ago, my ex partner also hep c, died,

overdose i assume, thechildren,3, and i feel in limbo, and i feel frustrated.i dont want to get sick. i want to live. live a long and happy lifefor my children. My strain is 1 something, and i know from a viz tothe dr. last year that "i am not at the early stages, not at theworst, but inbetween." Not that that is telling me a lot.What treat ment is there?My neice is 32, in australia, and about to start interferon, as thegovernment says they no longer have to wait for cirrossis (cant spell,sorry). i am pleased for her, but a bit envious too.i dont want to wait till i get really ill to have a chance for a cure.is there anything i can do or take to help myself get a better chance?i am in contact with no other person with hep c on a one to one. ifeel ignorant of my illness and isolated. Anyone got suggestions? Iam 44.Jan

[Guest guest]

hi terry,thankyou for replying to me. no, i do not have health insurance, as you have to declare it, dont you, so i believed that most insurance companies do not want hcv pos. people. or, those that do, have extreme high premiums. .... or do you know an insurance company that is otherwise. please excuse punctuation, shift keys not working....hope to talk to you again,jan. Re: [ ] helo Hi Jan I'm Terry. If you have insurance you should be able to get treatment any time you

need, as long as the aprove it & most will. Glad to have you in here. Terryihop2jan <ihop2jan@...> wrote: i dont know if i am using this right, as i have never used a chat orsimilar before. (ancient me). i have had hep c for over twenty years now, no treatment or support, iam an ex addict. (nearly 16 years ago) Two weeks ago, my ex partner also hep c, died, overdose i assume, thechildren,3, and i feel in limbo, and i feel frustrated.i dont want to get sick. i want to live. live a long and happy lifefor my children. My strain is 1 something, and i know from a viz tothe dr. last year that "i am not at the early stages, not at theworst, but inbetween." Not that that is telling me a lot.What treat ment is there?My neice is 32, in

australia, and about to start interferon, as thegovernment says they no longer have to wait for cirrossis (cant spell,sorry). i am pleased for her, but a bit envious too.i dont want to wait till i get really ill to have a chance for a cure.is there anything i can do or take to help myself get a better chance?i am in contact with no other person with hep c on a one to one. ifeel ignorant of my illness and isolated. Anyone got suggestions? Iam 44.Jan

[Guest guest]

Most often they will make you wait one year after covering befor they would cover treatment. But these days all health insurance is costly. Untill my health insurance kicks in on my new job, we are paying $250 a month hor me & $175 a month for a secondary insurance for my wife. TerryJanet Myers <ihop2jan@...> wrote: hi terry,thankyou for replying to me. no, i do not have health insurance, as you have to declare it, dont you, so i believed that most insurance companies do not want hcv pos. people. or, those that do, have extreme high premiums. .... or do you

know an insurance company that is otherwise. please excuse punctuation, shift keys not working....hope to talk to you again,jan. Re: [ ] helo Hi Jan I'm Terry. If you have insurance you should be able to get treatment any time you need, as long as the aprove it & most will. Glad to have you in here. Terryihop2jan <ihop2jan@...> wrote: i dont know if i am using this right, as i have never used a chat orsimilar before. (ancient me). i have had hep c for over twenty years now, no treatment or support, iam an ex addict. (nearly 16 years ago) Two weeks ago, my

ex partner also hep c, died, overdose i assume, thechildren,3, and i feel in limbo, and i feel frustrated.i dont want to get sick. i want to live. live a long and happy lifefor my children. My strain is 1 something, and i know from a viz tothe dr. last year that "i am not at the early stages, not at theworst, but inbetween." Not that that is telling me a lot.What treat ment is there?My neice is 32, in australia, and about to start interferon, as thegovernment says they no longer have to wait for cirrossis (cant spell,sorry). i am pleased for her, but a bit envious too.i dont want to wait till i get really ill to have a chance for a cure.is there anything i can do or take to help myself get a better chance?i am in contact with no other person with hep c on a one to one. ifeel ignorant of my illness and isolated. Anyone got suggestions? Iam

44.Jan

[Guest guest]

Hi there,I am in London, i did not realise that this was and american site. but you have certainly given me something to think about. Has your wife got it too hep c, i mean. I am a full time mum, so i do not work and have the benefit of job insurance, but i am pleased for you that it has worked out so well.jan Re: [ ] helo Hi Jan I'm Terry. If you have insurance you should be able to get treatment any time you need, as long as the aprove it & most will. Glad to have you in here. Terryihop2jan <ihop2jan@...> wrote: i dont know if i am using this right, as i have never used a chat orsimilar before. (ancient me). i have had hep c for over twenty years now, no treatment or support, iam an ex addict. (nearly 16 years ago) Two weeks ago, my ex partner also hep c, died, overdose i assume, thechildren,3, and i feel in limbo, and i feel frustrated.i dont want to get sick.

i want to live. live a long and happy lifefor my children. My strain is 1 something, and i know from a viz tothe dr. last year that "i am not at the early stages, not at theworst, but inbetween." Not that that is telling me a lot.What treat ment is there?My neice is 32, in australia, and about to start interferon, as thegovernment says they no longer have to wait for cirrossis (cant spell,sorry). i am pleased for her, but a bit envious too.i dont want to wait till i get really ill to have a chance for a cure.is there anything i can do or take to help myself get a better chance?i am in contact with no other person with hep c on a one to one. ifeel ignorant of my illness and isolated. Anyone got suggestions? Iam 44.Jan

[Guest guest]

No she doesn't have it, she was tested after discovering that I had it in 2001. I spent 48 weeks in 2002 & have tested free seance 24 weeks into treatment. TerryJanet Myers <ihop2jan@...> wrote: Hi there,I am in London, i did not realise that this was and american site. but you have certainly given me something to think about. Has your wife got it too hep c, i mean. I am a full time mum, so i do not work and have the benefit of job insurance, but i am pleased for you that it has worked out so well.jan Re: [ ] helo Hi Jan I'm Terry. If you have insurance you should be able to get treatment any time you need, as long as the aprove it & most will. Glad to have you in here. Terryihop2jan <ihop2jan@...> wrote: i dont know if i am using this right, as i have never used a chat

orsimilar before. (ancient me). i have had hep c for over twenty years now, no treatment or support, iam an ex addict. (nearly 16 years ago) Two weeks ago, my ex partner also hep c, died, overdose i assume, thechildren,3, and i feel in limbo, and i feel frustrated.i dont want to get sick. i want to live. live a long and happy lifefor my children. My strain is 1 something, and i know from a viz tothe dr. last year that "i am not at the early stages, not at theworst, but inbetween." Not that that is telling me a lot.What treat ment is there?My neice is 32, in australia, and about to start interferon, as thegovernment says they no longer have to wait for cirrossis (cant spell,sorry). i am pleased for her, but a bit envious too.i dont want to wait till i get really ill to have a chance for a cure.is there anything i can do or take to help myself get a better chance?i am in contact

with no other person with hep c on a one to one. ifeel ignorant of my illness and isolated. Anyone got suggestions? Iam 44.Jan

[Guest guest]

--- ihop2jan <ihop2jan@...> wrote:

> My GP does not have the time of day to look into

> drug companies and

> sponsership, here, i get sent for blood tests once

> or twice a year and

> see the hospital specialist once a year. unless

> some one has liver

> function problems, there is no treatment. they say

> my past tests have

> been ok, so no need for treatment.

> except, i had a 'yellow day', my younger son said i

> looked like bart

> simpson.! freaked me a bit, it was just one day. i

> saw the doctor two

> days ago, she was not concerned.

> can i find sponsorship myself? How?

> jan,london.

>

>

>

>

In my last post, I placed a link to a web site. It is

for the site in the USA, but has a clickable link to

the UK web site.

Cyndi

__________________________________________________

[Guest guest]

Hey Jan,

My name is and i am on the treatments right

now. I am so very lucky i have a great GP. He found

this place for me. The phone number is

1-800-521-7157.It is called comit to care. They may be

able to help you too. I hope so and good luck!! Please

let me know what they say or if they can help. I hope

so. If an address will help i will find it for you.

--- Cyndi Wertman <ceejay540@...> wrote:

>

>

> --- ihop2jan <ihop2jan@...> wrote:

>

> > My GP does not have the time of day to look into

> > drug companies and

> > sponsership, here, i get sent for blood tests once

> > or twice a year and

> > see the hospital specialist once a year. unless

> > some one has liver

> > function problems, there is no treatment. they say

> > my past tests have

> > been ok, so no need for treatment.

> > except, i had a 'yellow day', my younger son said

> i

> > looked like bart

> > simpson.! freaked me a bit, it was just one day.

> i

> > saw the doctor two

> > days ago, she was not concerned.

> > can i find sponsorship myself? How?

> > jan,london.

> >

> >

> >

> >

> In my last post, I placed a link to a web site. It

> is

> for the site in the USA, but has a clickable link to

> the UK web site.

>

> Cyndi

>

>

>

>

> __________________________________________________

>

[Guest guest]

hi brenda,

cheers. is that an american no? i am in uk.

jan

Re: [ ] helo

Hey Jan,

My name is and i am on the treatments right

now. I am so very lucky i have a great GP. He found

this place for me. The phone number is

1-800-521-7157.It is called comit to care. They may be

able to help you too. I hope so and good luck!! Please

let me know what they say or if they can help. I hope

so. If an address will help i will find it for you.

--- Cyndi Wertman <ceejay540@...> wrote:

>

>

> --- ihop2jan <ihop2jan@...> wrote:

>

> > My GP does not have the time of day to look into

> > drug companies and

> > sponsership, here, i get sent for blood tests once

> > or twice a year and

> > see the hospital specialist once a year. unless

> > some one has liver

> > function problems, there is no treatment. they say

> > my past tests have

> > been ok, so no need for treatment.

> > except, i had a 'yellow day', my younger son said

> i

> > looked like bart

> > simpson.! freaked me a bit, it was just one day.

> i

> > saw the doctor two

> > days ago, she was not concerned.

> > can i find sponsorship myself? How?

> > jan,london.

> >

> >

> >

> >

> In my last post, I placed a link to a web site. It

> is

> for the site in the USA, but has a clickable link to

> the UK web site.

>

> Cyndi

>

>

>

>

> __________________________________________________

>

[Guest guest]

Jan,

Cheers is good LOL. I will be here if you have any

questions. I have had Hep C for a long time too. It

took me a long time to decide to do the treatments. I

too want to live.But what it took for me to decide

that was this wonderful man to come into my life.He

made me realize what i had to live for.I have 6 kids

and 8 grandbabies and one on the way. I have lost 50

lbs and i was sick for a long time ,but i think i have

got through the bad part. Just keep in touch with this

group, they are awesome!!

It has been very nice to meet some one from the UK.I

have never been there ,but maybe one day i will!!

Please keep in touch.

--- Janet Myers <ihop2jan@...> wrote:

> hi brenda,

> cheers. is that an american no? i am in uk.

> jan

>

> Re: [ ] helo

>

> Hey Jan,

> My name is and i am on the treatments right

> now. I am so very lucky i have a great GP. He found

> this place for me. The phone number is

> 1-800-521-7157.It is called comit to care. They may

> be

> able to help you too. I hope so and good luck!!

> Please

> let me know what they say or if they can help. I

> hope

> so. If an address will help i will find it for you.

>

> --- Cyndi Wertman <ceejay540@...> wrote:

>

> >

> >

> > --- ihop2jan <ihop2jan@...> wrote:

> >

> > > My GP does not have the time of day to look into

> > > drug companies and

> > > sponsership, here, i get sent for blood tests

> once

> > > or twice a year and

> > > see the hospital specialist once a year. unless

> > > some one has liver

> > > function problems, there is no treatment. they

> say

> > > my past tests have

> > > been ok, so no need for treatment.

> > > except, i had a 'yellow day', my younger son

> said

> > i

> > > looked like bart

> > > simpson.! freaked me a bit, it was just one day.

>

> > i

> > > saw the doctor two

> > > days ago, she was not concerned.

> > > can i find sponsorship myself? How?

> > > jan,london.

> > >

> > >

> > >

> > >

> > In my last post, I placed a link to a web site. It

> > is

> > for the site in the USA, but has a clickable link

> to

> > the UK web site.

> >

> > Cyndi

> >

> >

> >

> >

> > __________________________________________________

> >

[Guest guest]

I know I ran into the same problem with my gp. I switched gp's and the new one, while he wasn't all that familiar with hepc, he referred me to a specialist. It may depend on your insurance, but I think under most you have the right to be referred to a specialist. At the very least I would ask the gp for a referral. There are doctors specializing in hepatitis, which are called hepatologists, we didn't have any in Green Bay, but a gastro-enterologist, has the expertise, at least of the liver. I found mine very knowledgeable. On your bloodwork, I would ask the doctor for copies of your results and pay close attention to the AST/ALT counts. Also the bilirubin, that has to do with the yellow juandice. -dz-ihop2jan <ihop2jan@...> wrote: My GP does not have the time of day to look into drug companies andsponsership, here, i

get sent for blood tests once or twice a year andsee the hospital specialist once a year. unless some one has liverfunction problems, there is no treatment. they say my past tests havebeen ok, so no need for treatment.except, i had a 'yellow day', my younger son said i looked like bartsimpson.! freaked me a bit, it was just one day. i saw the doctor twodays ago, she was not concerned. can i find sponsorship myself? How? jan,london.

[Guest guest]

I found this number for UK It says 'national rates will be charged' for the call. I'm not sure what that means. uk hepatitis hotline: TELEPH0NE HELPLINE - 0870 200 1 200 more info here:http://www.hepcuk.info/data/UserContentRoot/Home/Janet Myers <ihop2jan@...> wrote: hi brenda, cheers. is that an american no? i am in uk.jan Re: [ ] heloHey Jan, My name is and i am on the treatments rightnow. I am so very lucky i have a great GP. He foundthis place for me.

The phone number is1-800-521-7157.It is called comit to care. They may beable to help you too. I hope so and good luck!! Pleaselet me know what they say or if they can help. I hopeso. If an address will help i will find it for you. --- Cyndi Wertman <ceejay540@...> wrote:> > > --- ihop2jan <ihop2jan@...> wrote:> > > My GP does not have the time of day to look into> > drug companies and> > sponsership, here, i get sent for blood tests once> > or twice a year and> > see the hospital specialist once a year. unless> > some one has liver> > function problems, there is no treatment. they say> > my past tests have> > been ok, so no need for treatment.> > except, i had a 'yellow day', my younger son said> i>

> looked like bart> > simpson.! freaked me a bit, it was just one day. > i> > saw the doctor two> > days ago, she was not concerned. > > can i find sponsorship myself? How? > > jan,london.> > > > > > > > > In my last post, I placed a link to a web site. It> is> for the site in the USA, but has a clickable link to> the UK web site. > > Cyndi> > > > > __________________________________________________>

[Guest guest]

Hello,

Enzymedica is a great brand. They make the number one selling

Digestive enzyme called DigestGold. If you would like me to mail you

information and samples, just let me know. You can give your child

enzymes even at the age of 3. Feel free to ask me any questions!

Alessandra

Enzymedica's Education Department

enzymedica.com

>

> i still new here, i am indonesian,

> my child is autis begins 1 year old,

> now 3 year old, there is no progress.

>

> is there side effects from valtrex for age 3 year?

> enzyme what yg used?

> where do i buy?what brand?

>

> thank, sory my grammar is ugly.

>

[Guest guest]

> i still new here, i am indonesian,

> my child is autis begins 1 year old,

> now 3 year old, there is no progress.

> is there side effects from valtrex for age 3 year?

I don't know about a child so young [i used other anti-virals], but I

do know that addressing viruses does tend to cause a lot of yeast

overgrowth, so watch for that.

> enzyme what yg used?

I used HNI with much success

http://www.houstonni.com/

Dana

[Guest guest]

On Wed, 10 Dec 2008 00:35:46 +0800, Alessandra <milagros205@...>

wrote:

> Hello,

> Enzymedica is a great brand. They make the number one selling

> Digestive enzyme called DigestGold. If you would like me to mail you

> information and samples, just let me know. You can give your child

yes I need information, I still doubt whether the goods can be sent to

indonesia or can't?

thanks

[Guest guest]

Hello again. Yes we can send it to Indonesia. We can't gaurantee that you will

receive the samples but we do send them out. Just email me your address..

 

Alessandra

> Hello,

> Enzymedica is a great brand. They make the number one selling

> Digestive enzyme called DigestGold. If you would like me to mail you

> information and samples, just let me know. You can give your child

yes I need information, I still doubt whether the goods can be sent to

indonesia or can't?

thanks

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

[Guest guest]

>

> > Hello,

> > Enzymedica is a great brand. They make the number one selling

> > Digestive enzyme called DigestGold. If you would like me to mail

you

> > information and samples, just let me know. You can give your child

>

> yes I need information, I still doubt whether the goods can be sent

to

> indonesia or can't?

>

> thanks

>

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

>

>

[Guest guest]

We did Valtrex. Yes, there are many side effects. Buying it is not possible,

must be prescribed here in the U.S. because it is a serious pharmaceutical

drug. We had no success with Valtrex.

helo

>i still new here, i am indonesian,

> my child is autis begins 1 year old,

> now 3 year old, there is no progress.

>

> is there side effects from valtrex for age 3 year?

> enzyme what yg used?

> where do i buy?what brand?

>

> thank, sory my grammar is ugly.

>

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

>

>