Re: Got the word 3 days ago

[Guest guest]

hello Tallin.I'm Jack<br>The unknown is always a

little scary,big words and alot of doctors doesn't

help<br>But be brave don't let them scare you,just ask your

medical people(docs,nurses,the ones who do the paqper

work,lab techs) any question that comes to mind,,,write

yourself notes so you will remember what you want to ask

them....this diease is controlable but it's up to you to do

the leg work,be nosey take active part in wanting to

know things(I can even tell when they take extra blood

in labs now...I always ask why)..lots of good stuff

and support to be found here,as alway question what

you read,only silly question is the one that isn't

asked

[Guest guest]

hello Tallin.I'm Jack<br>The unknown is always a

little scary,big words and alot of doctors doesn't

help<br>But be brave don't let them scare you,just ask your

medical people(docs,nurses,the ones who do the paqper

work,lab techs) any question that comes to mind,,,write

yourself notes so you will remember what you want to ask

them....this diease is controlable but it's up to you to do

the leg work,be nosey take active part in wanting to

know things(I can even tell when they take extra blood

in labs now...I always ask why)..lots of good stuff

and support to be found here,as alway question what

you read,only silly question is the one that isn't

asked

[Guest guest]

Hi Tallin001it is o.k. to be scared. but u can

read alot about hep and it will make u feelbetter. I

have had hep for 30 yrs and now it is that I have know

alot about it. andI have beeh scared to . so go at it

and read . and u will have your ups and down.but it

is o.k. u have to be a fighter.u have a friend here.

if u want u can E- mail me. god bless and be a

fighter o.k. smile

[Guest guest]

Hi Tallin001it is o.k. to be scared. but u can

read alot about hep and it will make u feelbetter. I

have had hep for 30 yrs and now it is that I have know

alot about it. andI have beeh scared to . so go at it

and read . and u will have your ups and down.but it

is o.k. u have to be a fighter.u have a friend here.

if u want u can E- mail me. god bless and be a

fighter o.k. smile

[Guest guest]

tallin - its okay to be scared, especially upon

initial diagnosis - having a computer will help so much

for gathering information --the elevated something or

other was either your liver panel or viral load, i am

guessing- they may suggest a biopsy to see what damage, if

any, has been done - you may have caught this early -

i too was recently diagnosed in august with biopsy

showing damage and i still have positive attitude, but

believe me - i was one scared puppy when told - anytime u

want to talk - email me rpt@...

[Guest guest]

tallin - its okay to be scared, especially upon

initial diagnosis - having a computer will help so much

for gathering information --the elevated something or

other was either your liver panel or viral load, i am

guessing- they may suggest a biopsy to see what damage, if

any, has been done - you may have caught this early -

i too was recently diagnosed in august with biopsy

showing damage and i still have positive attitude, but

believe me - i was one scared puppy when told - anytime u

want to talk - email me rpt@...

[Guest guest]

Hello Tallin...i just want to let you know that

you are not alone and since you have a comp..well you

will not only be able to research this disease...but

make some awsome online friends at the same time if

you wish to...my husband bought me my pc when i was

dx last year and i dont know what i would have done

without it...ive been off tx for 5 wks and did 8 months

of the interferon/ribivirn combo am waiting to start

the peg intron..in 2 wks...so i will never clain to

be an exspert about this but i can certianly be here

for you as a friend and help you in anyway i can with

questions....feelings...and maybe give you some maoral support....my email

addy ison my profile feel free to use it if you

wish....you too rpt@... forward to getting to

know you both....feel privilegde...many cant or dont

get help...your on your way on a journey that will

not only change your life...but i found i learned so

much about who i really am...in light & HOpe &

Peace...Felisha...take the best of care.....god bless you

[Guest guest]

Hello Tallin...i just want to let you know that

you are not alone and since you have a comp..well you

will not only be able to research this disease...but

make some awsome online friends at the same time if

you wish to...my husband bought me my pc when i was

dx last year and i dont know what i would have done

without it...ive been off tx for 5 wks and did 8 months

of the interferon/ribivirn combo am waiting to start

the peg intron..in 2 wks...so i will never clain to

be an exspert about this but i can certianly be here

for you as a friend and help you in anyway i can with

questions....feelings...and maybe give you some maoral support....my email

addy ison my profile feel free to use it if you

wish....you too rpt@... forward to getting to

know you both....feel privilegde...many cant or dont

get help...your on your way on a journey that will

not only change your life...but i found i learned so

much about who i really am...in light & HOpe &

Peace...Felisha...take the best of care.....god bless you