From Shadow CPTN:
Hey there folks, hope this post finds you all well.
Having a liver biopsy next week, need some kidney work done (haha) for a stone removal & eval of a cyst. After all that, I will begin the 3-drug, 48-week treatment for hcv 1a.
I feel like s*|t. Like I have the flu all of the time. Tired isn't the word & the tenderness of my swollen liver sux. My mood and 'tude are fantastic though!
Lots of prayers have been blatently answered and I'm positive that I will get through treatment just fine. In my spare time, I've been scripting in prep for my core courses for my comp sci degree. Am tossing around the idea of putting a dent into obtaining said degree during the treatment. Refocus is golden. smile :)
Hoping that you all are doing well. Am mostly posting to see how y'all fine folks, who helped support me when I was newly diagnosed, have been doing twith your own hcv? Anything new going on?
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(S-cap) -- I copied your post in to a new thread as this is an important topic and we are already on 3rd page of your old thread.
Folks with Hep C are VERY anxious to hear about your journey and will want you to post here.
(Moderator) -- Can one of you lock the old thread, please.
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My partner, Mike, is a year post transplant and has a liver biopsy next month. They are talking about treatemtn again for him (2 drug combo 2003 failed for his Hep C 1a that he has had since at least 1970).
He, and likely others, will be interested to hear how you are doing symptom wise, mental status wise, and, of course will be holding their breath to hear the magic words: CLEAR! And then finally, SVR, Sustained Viral Response.
You have a very positive mental attitude going in, so that will work in your favor. Some have the Hep C fog (or treatment fog) and would not have your mental energy to do computer science classes.
We all hope you are successful...with treatment, with school, with SVR!
Best,
Carol