Hepatitis C Support Group
Hepatitis C is a blood-borne viral disease which can cause liver inflammation, fibrosis, cirrhosis and liver cancer. The hepatitis C virus (HCV) is spread by blood-to-blood contact with an infected person's blood. Many people with HCV infection have no symptoms and are unaware of the need to seek treatment. Hepatitis C infects an estimated 150-200 million people worldwide.
You should make your Dr sit down and answer all your ?'s-make a list! If he is a good doc he should be able to explain...if not and you aren't comfortable w/him now it will only get worse w/tx---need someone you can trust-I had to change drs and I'm VERY glad.
On the mental health issue-you didn't say what type problem it was (& I respect your privacy). I have Bipolar Disorder. 1st dr didn't even want to do bx or consider tx until I saw pshy 3 mos and maybe not at all just monitor blood work every 6 mos-old pschy said I was ok (been seeing 4 yrs) and my new phys I saw once said I was ok; key is that you see pschy regularly so that he can monitor you and adjust meds if needed-also provide counseling if you need it. (he should also be willing to work w/you Dr) I was see pschy every 6 mos now every 6 wks for now. Depending on your actual mental issue it may make a difference-your dr is right that you should see you pschy 1st (but at least you have your bx already) It is hard to guess which will be worse-mental health or HepC which can progress to a horrid end! Only you along w/doc & pschy's advice can make this important life critical decision. You need to know what grade/stage before seeing pschy so you can talk intellegienly to him about his opinion on taking tx!
I'm so sorry that you are confused-you came to the right site-you are very welcome here-lots of loving, caring, supportive and information people at all stages of HepC all here for ?'s and advise. Please let us know how this all plays out as I'm here for ya anytime...if you take tx same time as me maybe we can help each other w/tx and mental issues!
One more bit of advice: I use this site everyday; however there is another great site - google it "Be In Charge" - a 'real' live Practioner Nurse will call you ever other week to answer ?'s-give advise-work w/your Dr if needed, etc. they are available 24x7 and will follow you through entire journel! Might want to give it a try!! Also I've found that writing a daily journal here helps me alot..personal choice (can set up where only you read, just your friends or everyone!)
You think you were a bit lengthy (ha) everyone here on this site is aware that my answers and JI's are all mini-books and they haven't kicked me out (yet!!!).
I'm a genotype 1a with severe liver damage (Stage 3, Grade 3 on a scale of 4). I did 48 weeks of treatment and cleared the virus 12 weeks into treatment. I remained clear throughout the rest of my treatement and have my 6 month PCR coming up in 11 days. I'm positive I'm still going to be virus free.
I'm a genotype 1 that is a good example of "yes it can be done".
I fortunately did not have the mental health issues to work around but I know others have and can offer you great advice.
Mouse
Genotype 1a, Stage 3, Grade 3
Finished 48 weeks of tx on 4/13/07
Hoping for SVR on 9/20/07
(11 days and counting!)
Modified hepatic activity index (HAI) is the name.
A couple of the ones for fibrosis stage could be the Knodell 1 up to 6, and Metavir 1 up to 4.
On my biopsy, I was considered mild.
HAI 3/18, Knodell 2/6, and Metavir 1/4
As for tx working for you, you really can't tell ahead of time, but it's best to try tx while you are young and your general health is good. The mental health issue you can discuss with your drs; it is possible to do tx if you work closely with your dr to monitor how you react to tx.
As for tx being worth it, I say yes. The virus progressively damages your liver. If you do tx, and you clear the virus, even for a short while, you are giving your liver a chance to do some healing.
And any amount of healing can't be a bad thing, right?