Home › Forums › Main Forum › Patient Stories › New to Forum › Day 1… here we go
- This topic has 85 replies, 27 voices, and was last updated 7 years ago by erica.
-
AuthorPosts
-
18 August 2017 at 12:03 pm #26781
Fantastic news Edge.
G3a since ’78 – Dx ’12 – F4 (2xHCC)
24wk Tx – PEG/Riba/Dac 2013 relapsed
24wk Tx – Generic Sof/Dac/Riba 2015/16 relapsed
16wk Tx – 12/01/17 -> 03/05/17 NS3/NS5a + Generic Sof
SVR7 – 22/06/17 UND
SRV12 – 27/07/17 UND
SVR24 – 26/10/17 UND
18 August 2017 at 6:38 pm #26782coral wrote:There are so many different side effects that you may not be hit with the insomnia stick.
I was thinking about this thread during the night as I lay awake yet again from about 2am to 4am. I had forgotten we were discussing insomnia! For the past few weeks I’ve been racking my brain about why I’m not sleeping. Hopefully it wears off soon! I’m about 16 weeks post EOT now.
Genotype 1B
SVR 24 (10/17/17): VL UND / ALT 25 / AST 17
SVR 12 (7/25/17): VL UND / ALT 21 / AST 14
SVR 4 (5/31/17): VL UND / ALT 21 / AST 19
EOT (5/1/17): VL UND / ALT 32 / AST 22
T+19w (3/27/17): VL UND / ALT 23 / AST 20
T+4w (12/12/16): VL UND / ALT 31 / AST 24
T+0w (11/19/16): VL 343,484 / ALT 36 / AST 28Previous treatment in 2012: 48 weeks peg-interferon/riba, relapsed at some point in the 24 weeks post treatment (around 2014). Found redemption trials and applied in Aug 2016.
19 August 2017 at 10:10 am #26783Hi Edge,
Delighted to hear your news.
All the best,
RSF
G3a. Probably infected 40 years ago.
Diagnosed July 2015
7/7/2015: ALP 69, ALT 209, WBC 5.8, VL 40,000. Fibroscan 9.5 Kpa.
Commenced treatment Sof/Dac (Natco Pharma) 24 wks in Feb 16
VL UND @ 4 wks, 12 wksEOT 6/7/16
SVR 12
SVR 24PHEW! Thank you so much Dr James, Monkmeds and all at Fixhepc
19 August 2017 at 1:34 pm #26788Hi Edge
great reading your posts. Sounds like you are nearly there, just a short step away. That insomnia stick has a long reach doesn’t it? !!!
love Nadia
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!20 August 2017 at 3:11 am #26789Hi Edge,
Hoping your insomnia resolves soon, mine has improved considerably since I completed treatment. I linked this before but here is Dr Freeman’s blog again about it which you and others may find helpful.
http://gp2u.blogspot.com.au/2015/02/how-do-i-fix-my-insomnia.html
G3a since ’78 – Dx ’12 – F4 (2xHCC)
24wk Tx – PEG/Riba/Dac 2013 relapsed
24wk Tx – Generic Sof/Dac/Riba 2015/16 relapsed
16wk Tx – 12/01/17 -> 03/05/17 NS3/NS5a + Generic Sof
SVR7 – 22/06/17 UND
SRV12 – 27/07/17 UND
SVR24 – 26/10/17 UND
20 August 2017 at 3:01 pm #26794Hi everyone
I Want to thank you for this forum as it really helped me when I was diagnosed in April. I was in total shock as I didnt know what hep c was. I was ready to join redemption trials but thankfully in Ireland they had just opened up DAA for everyone. They stopped new people getting approved in August as the budget was used up so I was very lucky I was diagnosed when I was. this forum kept me sane and helped me take a positive outlook on the situation. I am starting week 8 of my 12 weeks and all is going well. Main side effect has been fatigue but thankfully no insomnia or stomach problems. Good luck to all who are starting treatment the time goes by very quickly.
Diagnosed 1a April 17
Started viekirax exvirra &Ribavarin July 17
VL 2m ALT 180 fibroscan 4.75
2 weeks VL 48 ALT 3022 August 2017 at 9:44 am #26800Hi Edge,
Congratulations – that’s fantastic news.
Our old friend insomnia and why is it always 2am to 4am?!! I had it for years on and off which was probably due to the virus. Then it ramped up quite a lot with the Ribavirin but I have to say that sleeping is much easier for me post treatment. Hoping it will ease for you too soon.22 August 2017 at 9:58 am #26803Hi Kate,
Good to see you are at Week 8 – not long to go now. Hang on a little longer and that fatigue will disappear
22 August 2017 at 6:14 pm #26806Hi Kate – good luck with your treatment. You are nearly there!
Genotype 1B
SVR 24 (10/17/17): VL UND / ALT 25 / AST 17
SVR 12 (7/25/17): VL UND / ALT 21 / AST 14
SVR 4 (5/31/17): VL UND / ALT 21 / AST 19
EOT (5/1/17): VL UND / ALT 32 / AST 22
T+19w (3/27/17): VL UND / ALT 23 / AST 20
T+4w (12/12/16): VL UND / ALT 31 / AST 24
T+0w (11/19/16): VL 343,484 / ALT 36 / AST 28Previous treatment in 2012: 48 weeks peg-interferon/riba, relapsed at some point in the 24 weeks post treatment (around 2014). Found redemption trials and applied in Aug 2016.
24 August 2017 at 3:16 am #26807Congratulations Edge on SVR 12! Next stop is SVR 24!
29 August 2017 at 8:49 pm #26808Can’t come soon enough, Greedfighter!!!
Genotype 1B
SVR 24 (10/17/17): VL UND / ALT 25 / AST 17
SVR 12 (7/25/17): VL UND / ALT 21 / AST 14
SVR 4 (5/31/17): VL UND / ALT 21 / AST 19
EOT (5/1/17): VL UND / ALT 32 / AST 22
T+19w (3/27/17): VL UND / ALT 23 / AST 20
T+4w (12/12/16): VL UND / ALT 31 / AST 24
T+0w (11/19/16): VL 343,484 / ALT 36 / AST 28Previous treatment in 2012: 48 weeks peg-interferon/riba, relapsed at some point in the 24 weeks post treatment (around 2014). Found redemption trials and applied in Aug 2016.
30 October 2017 at 8:24 pm #26964SVR 24!!
To all on the forum, and especially Dr Freeman and Dr Devsam, thank you for your support and for making this possible.
My only question now is what happens next?? Do I take it that achieving SVR24 is a cure? Do I need to get tested again regularly? Just so relieved that this seems to be over.
Genotype 1B
SVR 24 (10/17/17): VL UND / ALT 25 / AST 17
SVR 12 (7/25/17): VL UND / ALT 21 / AST 14
SVR 4 (5/31/17): VL UND / ALT 21 / AST 19
EOT (5/1/17): VL UND / ALT 32 / AST 22
T+19w (3/27/17): VL UND / ALT 23 / AST 20
T+4w (12/12/16): VL UND / ALT 31 / AST 24
T+0w (11/19/16): VL 343,484 / ALT 36 / AST 28Previous treatment in 2012: 48 weeks peg-interferon/riba, relapsed at some point in the 24 weeks post treatment (around 2014). Found redemption trials and applied in Aug 2016.
31 October 2017 at 1:51 am #26965Hi Edge, wonderful news!
You are officially cured. If the virus was still present it has had 24 weeks to grow back and during 23 or so of those weeks you have had no useful levels of medication in your system so there has been nothing to stop it.
It has not come back because it is gone… for good.
You can still catch it again, but short of that it is officially over.
Well done and thanks for your faith in us!
YMMV
31 October 2017 at 3:10 am #26966Congratulations Edge on SVR 24!
Cured baby!
31 October 2017 at 4:58 am #26967Awesome to you!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!
Genotype 3
VL 4,100,000
ALT 101 AST 71
Treatment Naive
Started Sof/Dac Jan 12, 2016
VL= <15 4 weeks in. AST/ALT normal.
VL=UNDETECTED 8 weeks in.
SVR4= Virus back. 3,300,000Started generic Epclusa Sep. 23, 2017
4 weeks in <15 *Detected.
12 weeks in <15 *Not Detected.
16 weeks in <15 *Not Detected.
Finished 24 weeks treatment 3-17-18
SVR5 <15 Not Detected.
SVR 20 <15 Not Detected.
SVR 44 <15 Not Detected.Thank you Jesus.
Thank you Dr. James -
AuthorPosts
- You must be logged in to reply to this topic.