Sorry I guess I misunderstood you. I guess you are going in for labs. And I am glad you don't have it because it sux! lol
Have a great day!!
Jules
no thank god,that don,t sound good.
Thank you I will start drinking more water.
You said you had to get up and go give blood. Do you have hemocromatosis also? Just curious
Have a great day!
Jules
How are your HGB's? Are you anemic at all? Are you on AD's?
Even at it's easiest this treatment can wear on people, but it looks like you are over half way through, so you are on the down hill slide.
When did become Undetected?
which treatment are you doing?
Are you keeping communications open with your doctor about how you are feeling?
Hello and welcome to the forum.
I don't know what to tell you because I don't really have much information. There is little on your profile page. However, I did notice that you seem to be drinking only 40 ounces of water per day. That is really not enough water. My doctor told me to drink a gallon of water per day. 1 gallon of water is 128 ounces so you can see that 40 ounces is only 5 cups of fluid. (I did drink a gallon a day and still am. ) You may be somewhat dehydrated which will make you feel miserable. More water might help with the itching. It might also help with weakness and fatigue, although those are pretty common side effects.
Best of luck to you.
I,m on hep c treatment,maybe if my platletes was up I,d feel like doing more with the family.I been on treatment 8 months and have to june to go.
Tonite I get that my shot,and then get up and go give blood.My pain managment doc said he wants to check my plateltes.If low he said he can,t do anything.I need a neoropathy.
We know what you are going through.This site saved me from quitting.They answer my questions,help with side effects and caring advice.Welcome.
what type of Hep C do you have?
what was your Biopsy results?
Which treatment are you on?