Re: (unknown)

[Guest guest]

Dear Shweta,

Here is a good one liner on this one ===>

I'm not a vegetarian because I love animals, I'm one because I hate plants!

:-D

Ravin '82

> Dear sir,Thanks for not being offended by it and having an open

mind....This is something I feel very strongly bout...It's not like I was

always a vegetarian,I did eat nonveg till a few yrs back...n then it just

struck me one day that what I was doin was wrong and I decided to leave it

for good.....also I've always had pets n seemed a lil hypocritical for me to

love one animal so much that I would cry when they were sick or in pain n

then on the other hand to b eating another animal..

> Please I'm not trying to b preachy or anything....Hope nobody is offended

by this...

>

> P.S- Was spelling ur name as ASOKA intentional or just a typo error ?

>

> Shweta'96

[Guest guest]

Dear Shweta,

Here is a good one liner on this one ===>

I'm not a vegetarian because I love animals, I'm one because I hate plants!

:-D

Ravin '82

> Dear sir,Thanks for not being offended by it and having an open

mind....This is something I feel very strongly bout...It's not like I was

always a vegetarian,I did eat nonveg till a few yrs back...n then it just

struck me one day that what I was doin was wrong and I decided to leave it

for good.....also I've always had pets n seemed a lil hypocritical for me to

love one animal so much that I would cry when they were sick or in pain n

then on the other hand to b eating another animal..

> Please I'm not trying to b preachy or anything....Hope nobody is offended

by this...

>

> P.S- Was spelling ur name as ASOKA intentional or just a typo error ?

>

> Shweta'96

[Guest guest]

Hi again Bev,

We are always so sad to hear of children that suffer. I don't have ideas to

answer your questions but please keep posting and we shall try and help as much

as we can. A big hug for you and . My nickname is Melt so you know I'm

strange but lovable. Smiles, Melt

----- Original Message -----

From: beverley francis

Hi my name is Bev i am the mother of Francis who suffers from stills,

he is 5 and has been suffering since he was 2 his birth date is 2nd September

1999 we live in Clayton, U.K

[Guest guest]

welcome to the group my name is janie this is very wonderful family group so it nice to meet you

(unknown)

Hello everyone!!!! !!!!!!!! I'm new to this group. I am currently an non-responder waiting to try a clinical trial in March or april.

Looking for last minute shopping deals? Find them fast with Yahoo! Search.

Looking for last minute shopping deals? Find them fast with Yahoo! Search.

[Guest guest]

Hi Joyce I am D. welcome Joyce wrote: Hello everyone!!!!!!!!!!!! I'm new to this group. I am currently an non-responder waiting to try a clinical trial in March or april. Looking for last minute shopping deals? Find them fast with Yahoo! Search.

Looking for last minute shopping deals? Find them fast with Yahoo! Search.

[Guest guest]

Hi Joyce & welcome..Im pat, aka pattypooh, pooh and a few other names...

Did you do the old treatment?..Our mama Gail did the old tx(treatment)...it was very agrressive...

Im from san antonio texas, widowed and have 4 grown kids and one granddaughter..two silly dogs and 2 finch..

Im geno 1, stage 1, grade2 and have been undetectable for 3 yrs

welcome aboard

PatMc

(unknown)

Hello everyone!!!!!!!!!!!! I'm new to this group. I am currently an non-responder waiting to try a clinical trial in March or april.

Looking for last minute shopping deals? Find them fast with Yahoo! Search.

No virus found in this incoming message.Checked by AVG Free Edition. Version: 7.5.516 / Virus Database: 269.17.11/1200 - Release Date: 12/27/2007 1:34 PM

[Guest guest]

Hi Joyce Welcome...I'm a caregiver in the group. My boyfriend is in his 6th week... This group is great!!! Lots of character. They are wonderful w/ info. I would be lost w/ out them. Happy New Year GJoyce wrote: Hello everyone!!!!!!!!!!!! I'm new to this group. I am currently an non-responder waiting to try a clinical trial in March or april. Looking for last minute shopping deals? Find them fast with Yahoo! Search.

Be a better friend, newshound, and know-it-all with Yahoo! Mobile. Try it now.

[Guest guest]

They call me Mama Gail cause I'm the oldest girl here and been undetectable for 9yrs this coming March 11the.Theres a great bunch of people here that are at different stages of treatment,different disease levels.They can pretty much cover all your questions and if they can't they will find an answer.

Gail

-----Original Message-----From: HepatitisCSupportGroupForDummies [mailto:HepatitisCSupportGroupForDummies ]On Behalf Of DoyleSent: December 27, 2007 7:30 PMTo: HepatitisCSupportGroupForDummies Subject: Re: (unknown)

Hi Joyce I am D. welcome

Joyce wrote:

Hello everyone!!!!!!!!!!!! I'm new to this group. I am currently an non-responder waiting to try a clinical trial in March or april.

Looking for last minute shopping deals? Find them fast with Yahoo! Search.

Looking for last minute shopping deals? Find them fast with Yahoo! Search.

[Guest guest]

My treatment was a trial in 98-99.They will let you know exactly what you can or can't take.They want the trials to be as true as possible so they might not allow help with your red and white blood count if it gets to low.Usually if you white count gets extremely low they use Epogen and Procrit to increase the red blood count.Ask them about that.

Gail

-----Original Message-----From: HepatitisCSupportGroupForDummies [mailto:HepatitisCSupportGroupForDummies ]On Behalf Of JoyceSent: December 27, 2007 4:36 PMTo: HepatitisCSupportGroupForDummies Subject: (unknown)Hello everyone!!!!!!!!!!!! I'm new to this group. I am currently an non-responder waiting to try a clinical trial in March or april.

Looking for last minute shopping deals? Find them fast with Yahoo! Search.

[Guest guest]

hello joyce sounds like we are in the same boat i'm also the caregiver

well anyway the one that makes sure he knows about appointments and

takes meds, shots and gets all tlc. he is in his 3rd week of treatment.

the first 2 wasn't bad but this past he hasn't felt so good i think he

is fighting a cold its hard to tell if its the side effects or fighting

a cold. hope to hear from you

Holly

> Hello everyone!!!!!!!!!!!! I'm new to this group. I am currently an

non-responder waiting to try a clinical trial in March or april.

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

> Looking for last minute shopping deals? Find them fast with Yahoo!

Search.

>

>

>

>

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

> Be a better friend, newshound, and know-it-all with Yahoo! Mobile. Try

it now.

>

[Guest guest]

HI Kathy I am D. I have had hep for about 4 years and am waiting to do treatment. Hope all goes well at the drs.KATHY LITTLE wrote: Hi Everyone My name is Kathy and I have had Hep C for 9 or 10 years now. I have done 2 rounds of treatment with no response. I also have diabetes which I got from taking the treatment. I don't have ins. so I am

going thru the county of LA, Calif. Tomorrow I will see a liver spec, and I have a list of questions for them. I have alot of problems from both conditions and I am worried. I will try and post tomorrow what they say. Hopefully it will be very good. Take Care All KATHY Never miss a thing. Make Yahoo your homepage.

Be a better friend, newshound, and know-it-all with Yahoo! Mobile. Try it now.

[Guest guest]

Welcome to the group Kathy.The drug companies also have programs that if you can't afford treatment they will provide the drugs.You just have to fill out a form stating income,and photocopies of all your expenses each month.I sent everything in and my drugs were free.I live in Canada,but they have the same thing in USA.Take someone with you tomorrow become sometimes the information is so much to take in and a friend or family member will remember what you don't.Get copies of all lab work or tests they do each time,so you will have a copy for yourself.I have had three specialists leave town and their files go with them and you have to go through the whole thing all over again.Keep a paper trail for yourself and there secretary can photocopy the info and give you back your copy.Start getting used to drinking extra water and make sure you do not go on a treatment that you have already had.Each time you have treatment the virus becomes ammune to that treatment.Take care and good luck and please tell us what the doctor says and ask for a copy of your lab work off him.

Gail

-----Original Message-----From: HepatitisCSupportGroupForDummies [mailto:HepatitisCSupportGroupForDummies ]On Behalf Of KATHY LITTLESent: March 9, 2008 5:10 PMTo: HepatitisCSupportGroupForDummies Subject: (unknown)

Hi Everyone

My name is Kathy and I have had Hep C for 9 or 10 years now. I have done 2 rounds of treatment with no response. I also have diabetes which I got from taking the treatment. I don't have ins. so I am going thru the county of LA, Calif. Tomorrow I will see a liver spec, and I have a list of questions for them. I have alot of problems from both conditions and I am worried. I will try and post tomorrow what they say. Hopefully it will be very good.

Take Care All

KATHY

Never miss a thing. Make Yahoo your homepage.

[Guest guest]

Kathy, welcome to our group. I hope the news is going to be good for you tomorrow. Hugs, VickieG

(unknown)

Hi Everyone

My name is Kathy and I have had Hep C for 9 or 10 years now. I have done 2 rounds of treatment with no response. I also have diabetes which I got from taking the treatment. I don't have ins. so I am going thru the county of LA, Calif. Tomorrow I will see a liver spec, and I have a list of questions for them. I have alot of problems from both conditions and I am worried. I will try and post tomorrow what they say. Hopefully it will be very good.

Take Care All

KATHY

Never miss a thing. Make Yahoo your homepage.

Be a better friend, newshound, and know-it-all with Yahoo! Mobile. Try it now.

[Guest guest]

Welcome to our group and you are right where we all have been at one time.You are no longer alone with this disease and we can understand what and how you are feeling.There is a lot of info in the file section to help educate yourself.Ask anything and we will try to help you.

Gail

-----Original Message-----From: HepatitisCSupportGroupForDummies [mailto:HepatitisCSupportGroupForDummies ]On Behalf Of reneeSent: June 6, 2008 1:41 PMTo: HepatitisCSupportGroupForDummies Subject: (unknown)

hi i just joined because i found out yesterday that i am going to start tx. Ive had hcv since 1990 when i contracted it after a short period of craziness which included iv drug use.i still have to have an ultrasound, biopsy, and see a therapist because of mental issues in my past, then i start. i am so worried and feel like i have no clue what it will be like.thanks

reneeI'm not superstitious, but I am a little stitious. www.myspace.com/arbeez

[Guest guest]

Some of us here used to use, but it is past us now and does not matter here.

Here how we got HEP C is not an issue. Taking the best care of us and our liver

is the issue. So happy to have you both.

D

Hoku Lani wrote:

> Hi ,

> I am new also.  Same as you too, IV back in the early 80's.  I still haven't

gotten a liver biopsy.  Hope my liver is OK, yours too!  Keep us posted on your

progress

> Hoku

> [HepatitisCSupportG roupForDummies] (unknown)

> hi i just joined because i found out yesterday that i am going to start tx. 

Ive had hcv since 1990 when i contracted it after a short period of craziness

which included iv drug use. i still have to have an ultrasound, biopsy, and see

a therapist because of mental issues in my past, then i start.  i am so worried

and feel like i have no clue what it will be like. thanks

>  

> renee I'm not superstitious, but I am a little stitious. www.myspace.

com/arbeez

>

[Guest guest]

Here ya go... and welcome to the group!

Letter to People Without Hepatitis & Liver Disease

Authored by Bek Oberin

Having Hepatitis means many things

change, and a lot of them are invisible. Unlike having cancer or being hurt

in an accident, most people do not understand even a little about HCV and its

effects, and of those that think they know, many are actually mis-informed.

In the spirit of informing those who wish to understand ... These are the

things that I would like you to understand about me before you judge me...

Please understand that being sick doesn't mean I'm not still a human being. I

have to spend most of my day in considerable pain and exhaustion, and if you

visit I probably don't seem like much fun to be with, but I'm still me stuck

inside this body. I still worry about life and work and my family and

friends, and most of the time I'd still like to hear you talk about yours

too.

Please understand the difference between

"happy" and "healthy". When you've got the flu you

probably feel miserable with it, but I've been sick for years. I can't be

miserable all the time, in fact I work hard at not being miserable. So if

you're talking to me and I sound happy, it means I'm happy. That's all. It

doesn't mean that I'm not in a lot of pain, or extremely tired, or that I'm

getting better, or any of those things. Please, don't say, "Oh, you're

sounding better!". I am not sounding better, I am sounding happy. If you

want to comment on that, you're welcome.

Please understand that being able to stand up for

ten minutes, doesn't necessarily mean that I can stand up for twenty minutes,

or an hour. And, just because I managed to stand up for thirty minutes

yesterday doesn't mean that I can do the same today. With a lot of diseases

you're either paralyzed, or you can move. With this one it gets more

confusing.

Please repeat the above paragraph substituting,

"sitting", "walking", "thinking", "being

sociable" and so on ... it applies to everything. That's what Hepatitis

does to you. Please understand that HCV or HBV is variable. It's quite

possible (for me, it's common) that one day I am able to walk to the park and

back, while the next day I'll have trouble getting to the kitchen. Please

don't attack me when I'm ill by saying, "But you did it before!",

if you want me to do something then ask if I can. In a similar vein, I may

need to cancel an invitation at the last minute, if this happens please do

not take it personally. Please understand that "getting out and doing

things" does not make me feel better. Telling me that I need a

treadmill, or that I just need to loose (or gain)weight, get this exercise

machine, join this gym, try these classes... may frustrate me to tears, and

is not correct... if I was capable of doing these things, don't you know that

I would? I am working with my doctor and physical therapist and am already

doing the excercise and diet that I am suppose to do. Another statement that

hurts is, "You just need to push yourself more, exercise harder..."

Obviously HCV deals directly with muscles, and because our muscles don't

repair themselves the way your muscles do, this does far more damage than

good and could result in recovery time in days or weeks or months from a

single activity. Also, Hepatitis may cause secondary depression (wouldn't you

get depressed if you were hurting and exhausted for years on end!?) but it is

not created by depression. Please understand that if I say I have to sit

down/lie down/take these pills now, that I do have to do it right now - it

can't be put off or forgotten just because I'm out for the day (or whatever).

Hepatitis does not forgive.

If you want to suggest a cure to me, don't. It's not

because I don't appreciate the thought, and it's not because I don't want to

get well. It's because I have had almost every single one of my friends

suggest one at one point or another. At first I tried them all, but then I

realized that I was using up so much energy trying things that I was making

myself sicker, not better. If there was something that cured, or even helped,

all people with Hepatitis then we'd know about it. This is not a drug-company

conspiracy, there is worldwide networking (both on and off the Internet)

between people with Hepatitis if something worked we would KNOW.

If after reading that, you still want to suggest a

cure, then do it, but don't expect me to rush out and try it. I'll take what

you said and discuss it with my doctor.

In many ways I depend on you - people who are not

sick - I need you to visit me when I am too sick to go out... Sometimes I

need you help me with the shopping, cooking or cleaning. I may need you to

take me to the doctor, or to the physical therapist. I need you on a

different level too ... you're my link to the outsideworld... if you don't

come to visit me, then I might not get to see you... and, as much as it's

possible, I need you to understand me.

Signed Tiredly with Love,

All Us Heppers

JackieSubject: (unknown)To: Hepatitis_C_Central Date: Saturday, August 2, 2008, 2:59 PM

Dear Friends,

I have a question about a short letter that I stumbled onto about 7 or 8 years ago that was titled, " To someone who doesn't have Hep-C " I have been trying to find it for a long time. It describes to someone who has no knowledge of the pain and suffering that we go through with Hep-C. I hope someone might know of it. This is my first post as a new member of this group. This pic is from when I was strong and full of life. I'm not on the pity-pot

Love and peace,

Dennis

[Guest guest]

Great pic of you Dennis,Welcome to the group.

Love

Janet

"There are souls in this world that have the gift of finding joy everywhere and of leaving it behind them when they go"

Frederick Faber

Subject: (unknown)To: Hepatitis_C_Central Date: Saturday, August 2, 2008, 4:59 PM

Dear Friends,

I have a question about a short letter that I stumbled onto about 7 or 8 years ago that was titled, " To someone who doesn't have Hep-C " I have been trying to find it for a long time. It describes to someone who has no knowledge of the pain and suffering that we go through with Hep-C. I hope someone might know of it. This is my first post as a new member of this group. This pic is from when I was strong and full of life. I'm not on the pity-pot

Love and peace,

Dennis

[Guest guest]

How was your father hurt ? What was his online nickname I need more information before I can help you out

(unknown)

This is a foward that I posted about my dad. I realize you can't come but I just wanted to let you know.

I'm sad to say that my dad passed away today in a Columbus Hospital. His body just gave out. I wanted to thank all of you who emailed me well wishes, thoughts and prayers for him. He was a good man and a lot of people loved him. I want to also than everyone in the community who has supported him and been his friend. My dad has been happiest since he moved "back home". I just wanted to address the people who did this and say that not only did you hurt my father, well you also hurt many many friends, a fiance, family, neighbors, and basically a community. There are also several young grandchildren who want answers that I don't have. So please i am still begging anyone for information. you can email me, heck if you want to email me, I can give you my number and we can talk on the phone. At this point I will do anything to find out. Thanks so much for reading and sending my your thoughts, and prayers. King-StaceyIf interested, arrangements for my dad (Leroy King), will be Sat. at Mc Funeral home. Calling hours will be at 2:30 and the funeral at 3:00 with burial to follow in Coalton Cemetary. Afterwards, there will be a Celebration of life at Havey's on 2nd street in Wellston, Ohio. Please join us to celebrate my dad's life and to pay last respects.thanks Kingyou can email me if you need directions or information

[Guest guest]

Sorry for the loss of your father hon.

Gentle hugs***

Love

Janet

"There are souls in this world that have the gift of finding joy everywhere and of leaving it behind them when they go"

Frederick Faber

Subject: (unknown)To: "Junemoms 1999" <JuneMoms1999 >, may99 Date: Thursday, August 28, 2008, 4:13 PM

This is a foward that I posted about my dad. I realize you can't come but I just wanted to let you know.

I'm sad to say that my dad passed away today in a Columbus Hospital. His body just gave out. I wanted to thank all of you who emailed me well wishes, thoughts and prayers for him. He was a good man and a lot of people loved him. I want to also than everyone in the community who has supported him and been his friend. My dad has been happiest since he moved "back home". I just wanted to address the people who did this and say that not only did you hurt my father, well you also hurt many many friends, a fiance, family, neighbors, and basically a community. There are also several young grandchildren who want answers that I don't have. So please i am still begging anyone for information. you can email me, heck if you want to email me, I can give you my number and we can talk on the phone. At this point I will do anything to find out. Thanks so much for reading and sending my your thoughts, and prayers. King-StaceyIf interested,

arrangements for my dad (Leroy King), will be Sat. at Mc Funeral home. Calling hours will be at 2:30 and the funeral at 3:00 with burial to follow in Coalton Cemetary. Afterwards, there will be a Celebration of life at Havey's on 2nd street in Wellston, Ohio. Please join us to celebrate my dad's life and to pay last respects.thanks Kingyou can email me if you need directions or information

[Guest guest]

Thank you Rochelle for keeping us updated as we do care about all our members and their families.. I know exactly how you are feeling, I lost my father almost a year ago,, it will be one year on Sept 8.. I miss him terribly but I know he was so suffering so badly at the end that Im glad he is no longer suffering.. Each day it gets easier.. IM here if you need to talk,,

hugs,Jackie

Subject: (unknown)To: ftackett@...Date: Sunday, August 31, 2008, 8:31 AM

For those of you who didn't make it I just wanted to let friends and acquaintences know that the service was beautiful and he truly would have been satisfied with it. His Granddaughter Lyndsey Channell, and Grandson Lucas Norman (my children) both wrote letters to their papaw. Lyndsey read hers but lucas is only 9 and I had to read his. It was so heartbreaking to see all these children saying goodbye to there papaw. I myself wanted to say that I miss my father so much already and I just can't believe he's gone. I love you daddy and will never forget all of our good times. RIP Daddy

[Guest guest]

That's cute Amber....what is normal anyway. My shrink says I'm normal and I find that scarey LOL. I am going to a stationary store to see if I can find a "note pad on a rope" that I can wear around my neck. Its gotten so bad now that I will think of something to tell hubby walk over to where he is and totally forget in 2 min what I was going to say. I always remember eventually (I think) but I think the note on the rope is what I need to do to stay sane and stop crying in frustration so much. I have a tape recorder for Doctor visits and that's been invaluable in getting important things like med changes or diet changes correctly AND I don't have to drag my poor hubby to every visit either

I'll wear it inside my shirt. Its just going to take some repetition to remember to write stuff down on it

Subject: (unknown)To: "Hepatitis _C_Central" <Hepatitis_C_Central >Date: Tuesday, October 14, 2008, 9:14 PM

I've decided I need a necklace of post it notes. In the 6wks of tx I cannot believe what I forget. I or my kid's can write where/what I am doing. I'm at a conf and got lost finding my hotel room. Scary for 47. I have to say I appreciate "normal" here although I've raised my kid's to know that is only a setting on the dryer. AmberSent via BlackBerry by AT & T

[Guest guest]

My ? is, what's the problem causing the "turn out"-is it the carpus or the elbow?

has there been a diagnosis?

(unknown)

Hi All,I have a Bernese Mountain Dog (show dog) who is turned out in the carpus(valgus). Are there any exercises I can give the owners to do that will bring him back into the proper position? The only thing I can think of is digging. It's Friday and my mind's not working today :-)Thanks in advance,Kim

[Guest guest]

That Rodger guy is obviously a liar. Have you seen his new profile picture? I think there is something deeply wrong with that man. At the very least, he is extremely immature.

Shari

 

That link is not even funny.  Did you read it?  I don't see where anyone with a right mind would find it remotely funny.  I would be very very upset if one of those photos were one of my children.  I do think we need to be proactive when we stumble upon this stuff.  Remember anyone can be anyone on the internet.  I don't know why any of my family members would use my son's picture as their signature picture.  I would question the gester.

Sherry Mom to Evan(8), Olivia(7), and (4)*

" Anyone who has never made a mistake has never tried anything new. " --Albert Einstein

[Guest guest]

OMG i am sorry about that i am not sure what happened there. have to reset the passwordKASSIAwife,mother,student,kettlebellehttp://ldysolana.blogspot.comSubject: (unknown)To: dippelpop2@..., jay_jay08742@..., ash@..., exercisevideos , secretsdream@..., hkatndog@..., Mayo_K1@..., w.tulecki@..., marta_weis@...Date: Thursday, June 16,

2011, 11:15 AMhttp://tis-systems.com/find11.html------------------------------------

[Guest guest]

Thanks, Sydney! And, I'm already getting DOMS in my legs/butt from today's workout. I figure it is pretty well balanced with enough "therapy" workouts like Pilates & Yoga to keep injuries, aches and pains at bay. My abs are getting a tad sore, too.

Yay -

Donna

Subject: (unknown)To: "exercisevideos " <exercisevideos >Date: Sunday, August 28, 2011, 4:03 PM

Donna, your rotation sounds wonderful!!Sydney"The most important persuasion tool you have in your entire arsenal is integrity " Zig Ziglar