oh yes-the last 8 years since successfully treating I have had no quality of life due to fatigue pain and cognitive issues.Ritalin is very difficult to get a prescription for in the uk so /I don't have even a few hours to get things done-feels like I'm still waiting for life to start again post treatment.
You'll find lot of folk here suffer with chronic fatigue from hcv or treatment.
Dear Can't TakeAnymore
I wish I could offer you more than sympathies. Almost to the letter, my post-Pegasus experience duplicates yours. I had a liver transplant in 2004 owing to HCV. Within three weeks the virus has returned. This was expected. I lived with it without too much trouble. My gastroenterologist called my wife I to meet with him and the hospital's pharmacist. They explain that my HCV was replicating far to quickly and they gave us a $0.25 explanation with the pharmacist stating, "If you don't take the Pegasus treatment I would be committing suicide"! (I nearly hit the floor at such a statement) Nevertheless I enrolled and complete the full 52 weeks of treatment. Each Friday night I would inject myself with interferon. I literally could not get our of bed until the following Tuesday afternoon. Now, this very deep fatigue, lack of vitality & malaise has resulted in the need to take 100 mg of Ritalin daily just for a few fleeting hours during which I can attend to my life's "stuff." I'll close for now but not before asking if anyone else in this community suffered with mean, black, evil fatigue.
Once a week I sleep for about 16+ hours. It helps my brain, improves my energy. I do the flu shot every years, but still get colds that take forever to go away.
put Adolph's meet tenderizer on the area. same as a jelly fish sting.