Welcome, Lindy. This forum is keeping me sane and hopefully will do the same for you. I was dx'd in late July and am currently going through the steps leading to treatment. Yes, I had some symptoms, mainly an autoimmune skin thing and fatigue which I had attributed to advancing years. And no, I don't fit into any of the risk factor categories either. There are many of us who have no idea how we got this thing - maybe some hunches, but no IVDU or transfusions. The source really doesn't matter; the main thing is to take care of yourself. Best of luck, and stay in touch.
Yes, a lot of people have it who aren't in the "high risk" group. Yes, it could be possible all this time you had Hep C, people are often diagnosed incorrectly and fibro is a popular misdiagnosis. Hep C can be a very sneaky disease and difficult to diagnose. You are not in a high risk group so your doctor might never have put the two together. I was midiagnosed too, it's common.
The waiting is hard but it gives you time to gather information.What are all your symptoms? ou might try typing "extra hepatic manifestations" into a search engine. You might find some of your issues there.
Thank you both! I already feel better. My symptoms started suddenly...first with a very bad headache for two weeks, then I woke up one morning shortly after with muscle pain everywhere that has never gone away, then fatigue set in - which has never gone away, low grade fever almost everyday, and now since I have stopped taking Lortabs for the muscle pain I am naseous most of the time along with all of the above mentioned symptoms as well.
I just hate thinking that I have been taking anywhere from 30 to 50 mgs of Lortab for the past year and a half in order to function if all along it has been Hep C!
Since I can't function so well right now, I am taking a medical leave of absence from work until I see the specialist and find out what's going on. I hold a key position in my organization and I can tell you my boss is none too happy about it but I have to look out for my health. Also I am a single mother with an 11 yr old at home to look out for - gotta make choices you don't like sometimes, I guess.
You are right about that. Sometimes you have to put yourself first and it sounds like you have a lot of symptoms you are coping with. try not to be too hard on yourself about the Lortabs. My doctor misdiagnosed me and also was treating me for a back disorder and the treatment was injections of steroids every few months and that is really bad with Hep C, steroids that often and injected no less. What's done is done, all we can do is move on from here and be grateful we found out when we did. Once you talk with the specialist and learn all about the condition of your liver you can begin to think about what you will do about it.
Thanks for the boost! Gosh I already felt so isolated when I thought I had fibro. I have felt even more isolated since the Hep C dx. Sometimes I would just wish someone could be in my body for one day so they would understand. I am soooo glad I found you all!!
We are a very diverse group of people here but we all have HCV in common. Glad you found us, HV can make you feel vry isolated and alone at times so a forum like this can be so helpful. Lots of good info here too, browe the archives there is a ton of info there too.