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I'm on #19,only 29 to go after tomorrow. Yeah it's

not as bad as I expected but I'll be glad when it's

over. I'm a genotype 2b so I have a good chance to

respond. I'm in a clinical study so I'm on it for a

full year if my body can take it. So far the bloodwork

is holding it's own, so I'm doing good. Plus I have a

real positive attitude about it.

Sharon

--- Terry Long <pawpawto3@...> wrote:

>

> Sharon your shot night is Thursday, mine is

> Friday. This Friday will be my 9th shot. So far they

> haven't been to bad.

> Terry

> Sharon Zeis <szeis_1@...> wrote: Things are

> going good. Thursday is shot night and

> then I can start the cycle over.

>

> Sharon

> --- Terry Long <pawpawto3@...> wrote:

> >

> > Sharon, I did need up taking the night off

> last

> > night. I feel a little better this morning. So I

> > will go into work tonight. I hope things are going

> > well with you.

> > Terry

> > Sharon Zeis <szeis_1@...> wrote: I hope

> your

> > feeling better today. I know it's hard

> > for me to stop when I feel good and then I pay for

> > it.

> > Take it easy and listen to your body.

> >

> > Sharon

> > --- Terry Long <pawpawto3@...> wrote:

> > >

> > > Good morning everyone. I thank I over did it

> > this

> > > last weekend. I didn't thank I was at the time,

> I

> > > didn't do that much " Saturday late morning &

> early

> > > afternoon I washed both cars, went out with

> > friends

> > > Saturday night & Sunday went to church for the

> > first

> > > time in four weeks " . But I'm dead tired now, had

> > to

> > > come home from work early last night. I slept

> > around

> > > nine & half hours last night & I'm still dead

> > tired.

> > > I'm debatting about calling in sick tonight.

> > >

> > > Terry

> > >

> > >

> > >

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

> > >

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Terry tx does take alot out of you..I hope you will beable to handle both work and tx..It is hard and I understand as I'm sure everyone else in the group do..Isn't your guy Jeff Gordon?? I am hoping to get back on line like I use too now that Floyd is working again..Wish me luck on that one..He is suppose to be home at about 3:00pm..YUCK too early for me..Has anyone heard from Diane yet??I haven't..Well without naming names I want to tell everyone hello this morning..Hope all is doing well..See I don't want to name anyone cause I know I'll forget someone again..LOL...I have CRS bad latley...Being my liver DOES NOT HURT I am having a ultrasound on it Friday to see where the pain is coming from..I'll get the results on the 27th..

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thanks so much Kathy

--- UrthMan <outerspace@...> wrote:

> We are always here for you .

>

> Kathy

> (unknown)

>

>

>

> It's been one year since my brother was kicked out

> of

> the house. I personally want to thank you for

> asking

> how things are, comforting me, and trully

> listening to

> me when I was having troubled times. When he lived

> with us- he caused abuse to my parents and myself.

> He

> took an inside piece of me- something that I'll

> never

> get back.

>

> Sincerely,

>

>

> __________________________________________________

>

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Well isn't it high time we liven things up a bit?? Now Arlene help me since Diane is no where to be found ok??

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Hopefully not Terry..I have told them time and again there is nothing in there for them..LOL..It's bad enough that they have to be in there for the surgery!!

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I didn't like Jeff last year cause he was always winnin and my guy is Dale Jr.. but this year I find myself lookin for Jeff too...I'm gettin better at remembering who everyone is..I never watched racing until last year so i'm new at this..When Floyd would say he wanted to go to a race I'd say I hope there's a mall close but now I'm asking where is the best place to sit!!

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LOL...!!! See I didn't forget ya and do you know I was almost thinking the exact same thing when I said that!! I knew I'd get ya!! I couldn't be missed regardless if I ducked or not!!!

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boy cindy, the incidents are a little different but sure sounds like me !!!!

kathy in il welcome and i hope you continue to feel better!!!!

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It was a slow day, wasn't it? I only had one message

when I got up. We haven't heard from Diane for a while

and Jan's been off and on too. Has anybody heard from

Diane? -dz-

--- Terry Long <pawpawto3@...> wrote:

>

> Where is everyone today, are you out there lurking

> around or did you all fall off of the face of the

> earth.

>

> Terry

>

>

>

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

>

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there you are! It's been pretty quiet around here..

-dz-

--- Jannewilms42@... wrote:

> I'm still here but was busy today..HUBY GOT A NEW

> JOB!!!!!!!!!!!! Now I can

> have my house back...YEAH!!!!!!

>

__________________________________________________

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Teah, I think you get used to being tired after

awhile. It's only when I try to do as much as I did

before treatment that I realize I can't any more. My

worst side effect is the headaches but I don't get

them as often any more. I think the peg-interferon is

more user-friendly than the old interferon. I feel

lucky I wasn't diagnosed until it was available. Of

course I would have been luckier not to have this.

Sharon

__________________________________________________

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Thanks.

Sharon

--- Jannewilms42@... wrote:

> Sharon I wish ya the best with the tx..It's nice to

> see you today

>

__________________________________________________

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I'm so glad to hear that you and Terry are doing so

well. It gives me greater hope if I have to re-do the

program. I was on the 3 shot a week combo and it was

pretty trying. They didn't have the peg available yet.

Of course I'm still hoping I never have to take it

again, but the results weren't as good for the old

combo. It was only about a 30% shot at a long term

response. Now that I have achieved at least the short

term response, my odds are increased to 50% that I

will remain in remission. -dz-

--- Sharon Zeis <szeis_1@...> wrote:

> I'm on #19,only 29 to go after tomorrow. Yeah it's

> not as bad as I expected but I'll be glad when it's

> over. I'm a genotype 2b so I have a good chance to

> respond. I'm in a clinical study so I'm on it for a

> full year if my body can take it. So far the

> bloodwork

> is holding it's own, so I'm doing good. Plus I have

> a

> real positive attitude about it.

>

> Sharon

__________________________________________________

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Good luck with the ultrasound. Is it a pelvic

ultrasoud? I had one of those once. Yuk.

Sharon

--- Jannewilms42@... wrote:

> Terry tx does take alot out of you..I hope you will

> beable to handle both

> work and tx..It is hard and I understand as I'm sure

> everyone else in the

> group do..Isn't your guy Jeff Gordon?? I am hoping

> to get back on line like I

> use too now that Floyd is working again..Wish me

> luck on that one..He is

> suppose to be home at about 3:00pm..YUCK too early

> for me..Has anyone heard

> from Diane yet??I haven't..Well without naming names

> I want to tell everyone

> hello this morning..Hope all is doing well..See I

> don't want to name anyone

> cause I know I'll forget someone again..LOL...I have

> CRS bad latley...Being

> my liver DOES NOT HURT I am having a ultrasound on

> it Friday to see where the

> pain is coming from..I'll get the results on the

> 27th..

>

__________________________________________________

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Surprising he never told you that. Most of us are type

1, either 1a or 1b, which are the more difficult ones

to treat. I guess type 2 and type 3 have better

response rates. -dz-

--- Terry Long <pawpawto3@...> wrote:

>

> Sharon, My Doctor never told me my genotype, But

> did tell me that mine was one of the ones that

> responded best to treatment. He said that the

> treatment would last a year, if my body can take it.

> So far my blood work has come back good. My side

> affects haven't been bad at all. My biggest thing is

> always being tired. It hasn't been to bad at work up

> unto now, my current job asignment has not been very

> physical in my department. But they are switching

> our asignments on Monday " they switch us every 3 to

> 4 months " and I will be asighned to a somewhat

> physcal asignment for the next 4 to 5 months. We

> will see how I'm doing next week. If I get overly

> tired I'm sure my boss & coworkers will give me a

> hand. My immedat boss & our department head has been

> very understanding & willing to work with me so far.

> Our department haed is battling major health

> problems of his own & has an idea what I'm going

> through. Thank god I went into Salary 17 months ago.

> Now I have sick time, when I was hourly I didn't &

> was working a very physcal job. I don't know if I

> could of handled it while on Tx.

>

> Terry

>

>

>

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

>

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Don't feel bad, I'm afraid I could never remember all

the names if I tried that, so I just wish the best to

all. (which I am doing now :) -dz-

--- Jannewilms42@... wrote:

> I want to tell everyone

> hello this morning..Hope all is doing well..See I

> don't want to name anyone

> cause I know I'll forget someone again..LOL...I have

> CRS bad latley...Being

> my liver DOES NOT HURT I am having a ultrasound on

> it Friday to see where the

> pain is coming from..I'll get the results on the

> 27th..

>

__________________________________________________

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It's good to hear something positive about the

treatment. I like to hear when people respond. The

best thing about the peg is being once a week ,I start

feeling really good by Tuesday and great by Thursday.

Of course then you have to start the cycle again but

at least you have some good days.

Sharon

--- imaganeer <imaganeer@...> wrote:

> I'm so glad to hear that you and Terry are doing so

> well. It gives me greater hope if I have to re-do

> the

> program. I was on the 3 shot a week combo and it was

> pretty trying. They didn't have the peg available

> yet.

> Of course I'm still hoping I never have to take it

> again, but the results weren't as good for the old

> combo. It was only about a 30% shot at a long term

> response. Now that I have achieved at least the

> short

> term response, my odds are increased to 50% that I

> will remain in remission. -dz-

__________________________________________________

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Jan, yes my driver is Jeff Gordon. He's not doing well so far this year. I thank the new one motor per race weekend rule is hurting them. Before they had a practice motor, a qualifying motor, a race motor they even a back up race motor. They just haven't figured out how to do it all in one motor. But they are not the only teem with that problem, their are several teams having the same problem.

I have faith in god, that he is going to give me what I need to handle Tx & my work load.

Terry

Jannewilms42@... wrote: Terry tx does take alot out of you..I hope you will beable to handle both work and tx..It is hard and I understand as I'm sure everyone else in the group do..Isn't your guy Jeff Gordon?? I am hoping to get back on line like I use too now that Floyd is working again..Wish me luck on that one..He is suppose to be home at about 3:00pm..YUCK too early for me..Has anyone heard from Diane yet??I haven't..Well without naming names I want to tell everyone hello this morning..Hope all is doing well..See I don't want to name anyone cause I know I'll forget someone again..LOL...I have CRS bad latley...Being my liver DOES NOT HURT I am having a ultrasound on it Friday to see where the pain is coming from..I'll get the results on the 27th..

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I was wondering if Diane got bumped off the list again. Does anyone have her E-Mail address. I thought I would send her an E-mail but lost the address.

Terry

imaganeer <imaganeer@...> wrote: It was a slow day, wasn't it? I only had one messagewhen I got up. We haven't heard from Diane for a whileand Jan's been off and on too. Has anybody heard fromDiane? -dz---- Terry Long <pawpawto3@...> wrote:> > Where is everyone today, are you out there lurking> around or did you all fall off of the face of the> earth.> > Terry> > > > --------------------------------->

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Sharon I agree if we were all lucky none of us would have this. But like you I wasn't diagnosed until we had the peg-intron was available. I haven't had any bad headaches so far.

Terry

Sharon Zeis <szeis_1@...> wrote: Teah, I think you get used to being tired afterawhile. It's only when I try to do as much as I didbefore treatment that I realize I can't any more. Myworst side effect is the headaches but I don't getthem as often any more. I think the peg-interferon ismore user-friendly than the old interferon. I feellucky I wasn't diagnosed until it was available. Ofcourse I would have been luckier not to have this. Sharon__________________________________________________

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Hi its me from the back row. Short and Fluffy.... One of those no names. ROTFLMHO K Re: [ ] (unknown) Terry tx does take alot out of you..I hope you will beable to handle both work and tx..It is hard and I understand as I'm sure everyone else in the group do..Isn't your guy Jeff Gordon?? I am hoping to get back on line like I use too now that Floyd is working again..Wish me luck on that one..He is suppose to be home at about 3:00pm..YUCK too early for me..Has anyone heard from Diane yet??I haven't..Well without naming names I want to tell everyone hello this morning..Hope all is doing well..See I don't want to name anyone cause I know I'll forget someone again..LOL...I have CRS bad latley...Being my liver DOES NOT HURT I am having a ultrasound on it Friday to see where the pain is coming from..I'll get the results on the 27th..

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