Hi Pat1 that is one beautiful post thank you. I am just over 1 week into treatment and feeling somewhat shattered today so reading your SVR news is super emotional and has given me such a lift. It is certainly one huge rollercoaster we are all on not quite knowing where we are heading but hoping its the same end stop
The loneliness you mention in your post is so the reason we all need one another on here. I have come onto the website each day when I get a moment to read a little of everyones posts past and present, as it is quite a bit to take in! There are so many great stories, questions?????? ideas

and so so much more particularly loving the music

I find it hard to concentrate on writing too much but reading your post today just had to come and say a big THANK YOU Pat1 for sharing your words and your rainbow

I hope you do stick around for a good while.
much love and hugs
Nadia xxx
Diagnosed Hep C genotype 1b early 1990's. Treated 1998 peg Interferon/Riba non responder

( Meds stopped after 4 or 5 months.
Fibroscan April 2013- 7.3kPa repeated May 2015- 5.8kPa mild scaring
May 2015 ALT 59 AST 56
21/7/2016 ALT 36 AST 44 BIL14
VL 939000
thanks FixhepC +Monkmed started Sof/Led 16/8/2016.

)
OCT 3 AST33 VL UND
OCT 11 ALT 29 AST 36 VL UND
NOV 10 ALT 27 AST 37 VL UND
JAN 30 2017 ALT 23 AST 29 VL UND
SVR12 ALT 23 AST 27 VL UND!!
SVR 24 UND!!!TY EVERYONE!