Hi Jennifer,
I'm sorry you had to discontinue treatment due to the awful side effects you had. I wish I could think of something more encouraging to say, but all I can think of is to repeat what your doc said: new drugs will soon become available that are easier to tolerate and have higher cure rates. So, don't give up hope, and take good care of yourself.
Sue
I went to c my specialist today and she advised me to give up the treatment as I was not coping at all. She said about all these new drugs coming from America/Canada. I cried my eyes out as I was so determined to complete it. I havent been coping. Iv not been eating and those panic attacks were do horrendous that my specialist was worried I'd end up in psychiatric hospital. So iv come off it.
I went to c my specialist today and she advised me to give up the treatment as I was not coping at all. She said about all these new drugs coming from America/Canada. I cried my eyes out as I was so determined to complete it. I havent been coping. Iv not been eating and those panic attacks were do horrendous that my specialist was worried I'd end up in psychiatric hospital. So iv come off it.
Hi I am a 65 year old femAle diagnosed with hep c genotype 1a last year and started triple therapy in Oct of this year. I have probably had hep c for 40+ years. I was previously married to a iv drug user in the late 60s early ,70s. in the early days I.often went to the tp complaining if tiredness but they never knew much about hep c then so they used to give,ne iron tablets or tell me yo rest etc. They only found out last year cos of my raised liver function test. I am having interferon injection once a week and boceptivir and ribavirin. I have been feeling like nothing on earth. My nurse had to reduce the ribavirin once as my bloods went from 14.to 9.6. I can cope Roth all this but now I hav started hsbomg panic attacks which I can't seem to control. I had three yesterday and today. iv had paramedics out about 3/4 timed. I dont know what to do. It makes it all worse as it's Christmas week anf I know I dont get the support I need over the holidays. Is anyone else suffering like this, if so tell me how to cope. I feel I'm.going mad
i was working as a butcher, 48 hrs a week for the 1st 2 times i treated with int/riba. tylenol or motrin(if numbers are good) took my focus off side effects in the 1st 4 months. thats when my hemoglobin dropped to levels that caused shortness of breath and fatigue. i never thought of quitting. good luck with this tx barry
Thinking of you, praying for you dear Bo
Love
Dee
Ok, thanks for the information. The doctor told me that it effects everyone differently. they say my overall numbers are actually pretty good considering. But I am a Truck Driver and am nervous about it, I love my job. But like I said the outcome is better than the other outcome, thanks for the input.
Just started my second week of Interferon with Ribavirin and Incivek. Thus far I am tired, but have suffered no other ill effects. The Interferon is taken on Friday and it does slow me down. If it doesn't get worse I can do my six months.
Hello there! Everyone is different so hard to say how you will feel.
I treated back in 2008, I was able to work though not full time.
I took my shot on Friday as soon as I got home from work hoping I would feel well enough to go to work on Monday. Sometimes it worked others I had to take the day.
Saying that I did have cirrhosis and that would have entered in to how I felt. Others have worked with little problem, they might come home and go to bed but they made it to work :)
My best to you!
Dee
Oh everyone is nervous to start, that is normal
I will be taking the interferon and the ribavirun for genotype 3 for 6 months.
Are you taking just the Interferon and the Ribaviran (for genotype 2,3 &4) or the Triple Treatment, for Genotype 1's, because that one includes many more pills,of either Victrelis, or Incivek~