Hello. I am 47 years old and I'm assuming I contracted HEP C from a blood
transfusionExchange transfusion
Exchange transfusion - series
Transfusion reaction in 1978 due to a
miscarriage. So I would have had HEP C for 27 years without any symptoms that I am aware of. I found out about 6 months ago from a
routineRoutine sputum culture blood test. Needless to say, I went through all the emotions, of course,
firstFirst progesterone mc10
First progesterone mc5
First-progesterone vgs 100
First-progesterone vgs 200
First-progesterone vgs 25
First-progesterone vgs 400
First-progesterone vgs 50
First-testosterone
First-testosterone mc which was denial,
fearFears and phobias,
angerIslets of langerhans
Ovarian cancer dangers
Pancreatic islet cell tumor, etc. Now I'm ready to really try and figure out what I need to do. I had all tests so far, EXCEPT biopsy which I'm trying to decide if I should.
I am genotype 1b with viral load over 2 million IU or 5.4 million copies/ml; which on some charts is medium and some charts is high, which is it medium or high? My blood tests are all normal from ALT 28, AST 24 to CBC w/white blood cell count, billirubin, alkaline phosphate, AFP, etc. Also had ultrasound of liver, kidneys, spleen, aorta (ultrasound of abodomen) which is also unremarkable (meaning no abnormalities from what they can see from ultrasound anyway). Can they see if I have cirrohsis? Fibrosis? Can you tell from ultrasound and/or blood tests?
Since all blood tests, ultrasound, etc are normal, do I need a biopsy YET? And if I do have a biopsy w/zero to mild damage do I treat? And if I have ALOT of damage should I treat and what are chances of responding to treatment w/my genotype and viral load? and which treatment is best?
Also, anyone w/1b genotype and high viral load...can you tell me about response, what treatment you did, sides, and results? I'm 1b w/viral load, which I got two ways 5.4 million copies or 2.2 million IU's. Thanks in advance for your information.