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Dear ,

There is light at the end of this tunnel. I too cannot tolerate treatment. I

am on permanent disability now and have to deal with permanent brain fog and

fatigue. But I am free to write all the bad poetry I can now (which is

considerable) and I am most at peace with myself. The " last wife " sounds like a

pit

bull but I don't want to sound too unkind

Bob Drury

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Hey there !

Welcome to our happt little family! If you need any advice, someone to talk

to, or just a swift kick in the backside I'm here for ya!

I'm only on my fourth shot now, but I know what you mean about the lack of

appetite. If the Doc hadn't told me to take my co-peg with food, I don't think

I would eat anything all day. As it is, I only eat twice, and then just to

take my meds. My liquid intake has skyrocketed, however! I'm thirsty all the

time, and I can go through a gallon of Sweet Tea or Kool-Aid in an afternoon,

and thats cutting it with Gator-aid and/or water to temper the sugar intake!

Anyways, welcome! May your journey with us be full of insight, fun,

friendships, and strength.

Peace,

D

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Ive been lurking for a long while, only post so far was back a good

long time ago. Things have changed as is wont to happen.

Found out I had hepc in 96 or so, was married to my 3rd wife and

things really changed at that point. We had been going down hill

since then.

I tried IF only several years ago and was non responsive after 3

months so I gave it up. I didnt feel all that bad, tired mostly.

Talked to my GE dr and told him I watned to have a quality of life

that the meds didnt provide so I just went on with my life, no

alcohol of course. Had the biopsy done and it was very difficult

mentally, while physically it was a trial.

I work for a big software company in WA state as a network engineer

and worked hard. As an engineer I had to work late nights at times

and all night at other times when issues arose. The work is very

challenging and a mistake can be catastrophic.

My original GE retired and I was assigned to another GE through

Group Health. He wanted to talk to me about the hep a few months

ago and wanted me to have another biopsy which I did about 6 months

ago. I had some scarring and we discussed the new IF/ribavirin

treatment.

After much soul searching I relented and said I would like to try

the treatment as Im 55 and wanted to give it a chance. I agreed to

start in April this year. However my " last wife " as she called

herself decided that after Id made this big decision she wanted a

divorce. This coupled with the high anxiety workplace was a serious

blow to me.

I finally started the treatment in April and my work performance

went into the toilet and I had to take a medical leave of which I am

so fortunate and glad was possible.

I am on shot 11 now and wondering if I can ever feel like I can work

again.

Ive been a depressive person in the past which caused me great

consertation about taking the drugs so I went on prozac prior to the

initial treatment. Just upped the dose as I feel its working for me

but I still have episodes of worthlessness, crying etc as I am sure

all here can relate.

Ive got congestion in the head and chest that drive me crazy so I am

taking an antihistemine to help with that. I have back probelems

that get worse Saturday to Wednesday and then it tapers off till the

next shot. I hate the nauseous feeling and the lack of appetite, I

am tired of toast and cereal so I have to have someone make me eat

stuff. IVe become more of a vegeterian now also.

I just wanted to take this opportunity to say hello and join this

community online.

Jah provides.

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,keep the faith brother. This too shall pass.

I take shot two tonight and see dr. Friday for some

anti deppressants. Positive attitude and prayer and

well all get through this. GOOD LUCK AND GOD BLESS

ALAN

---

hideogumperjr wrote: > Ive been

lurking for a long while, only post so far

> was back a good

> long time ago. Things have changed as is wont to

> happen.

>

> Found out I had hepc in 96 or so, was married to my

> 3rd wife and

> things really changed at that point. We had been

> going down hill

> since then.

>

> I tried IF only several years ago and was non

> responsive after 3

> months so I gave it up. I didnt feel all that bad,

> tired mostly.

> Talked to my GE dr and told him I watned to have a

> quality of life

> that the meds didnt provide so I just went on with

> my life, no

> alcohol of course. Had the biopsy done and it was

> very difficult

> mentally, while physically it was a trial.

>

> I work for a big software company in WA state as a

> network engineer

> and worked hard. As an engineer I had to work late

> nights at times

> and all night at other times when issues arose. The

> work is very

> challenging and a mistake can be catastrophic.

>

> My original GE retired and I was assigned to another

> GE through

> Group Health. He wanted to talk to me about the hep

> a few months

> ago and wanted me to have another biopsy which I did

> about 6 months

> ago. I had some scarring and we discussed the new

> IF/ribavirin

> treatment.

>

> After much soul searching I relented and said I

> would like to try

> the treatment as Im 55 and wanted to give it a

> chance. I agreed to

> start in April this year. However my " last wife " as

> she called

> herself decided that after Id made this big decision

> she wanted a

> divorce. This coupled with the high anxiety

> workplace was a serious

> blow to me.

>

> I finally started the treatment in April and my work

> performance

> went into the toilet and I had to take a medical

> leave of which I am

> so fortunate and glad was possible.

>

> I am on shot 11 now and wondering if I can ever feel

> like I can work

> again.

>

> Ive been a depressive person in the past which

> caused me great

> consertation about taking the drugs so I went on

> prozac prior to the

> initial treatment. Just upped the dose as I feel

> its working for me

> but I still have episodes of worthlessness, crying

> etc as I am sure

> all here can relate.

>

> Ive got congestion in the head and chest that drive

> me crazy so I am

> taking an antihistemine to help with that. I have

> back probelems

> that get worse Saturday to Wednesday and then it

> tapers off till the

> next shot. I hate the nauseous feeling and the lack

> of appetite, I

> am tired of toast and cereal so I have to have

> someone make me eat

> stuff. IVe become more of a vegeterian now also.

>

> I just wanted to take this opportunity to say hello

> and join this

> community online.

>

> Jah provides.

>

>

>

>

>

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