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Hep C Discussion Forum -> Post Treatment -> more great news to add to Judy & Tim!!
Post Info TOPIC: more great news to add to Judy & Tim!!
krowdog


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RE: more great news to add to Judy & Tim!!
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Perfect!!!



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(Geno 1a, Incivek Triple Tx, 6 month post TX - 9/20/2012 = SVR!!!)
iggle


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Tremendous news biggrin



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Judy S


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Wonderful news, Meghan!!!  This makes me so happy.  Yeah guys, we ARE making this virus look bad!  This just made my weekend!



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Geno 1a; VL 4.7 million in Feb 2012. Started PegIntron & Ribavirin 3-9-12. Added Victrelis 4-6-12. UND since Week 8. Stopped tx Wk 23. UND 4 Wks post-tx. Relapsed 12-weeks-post.

52 y/o F, started Epclusa 11-10-19, F0/F1.  EOT 2-1-2020. UND. All liver function tests normal.
Shep


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Yea Meghan!! Great, great news!!


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Diagnosed 1996 genotype 1b VL alot tx starting 12/23/11 Victrelis UND week 8!!! 28 weeks of tx

Completed tx 7/6/12--still UND!!!!
jrc


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congrats meghan like the others said if und at 3 months post tx the odds are 99% SVRsmile



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Geno 1 A Started Tx w/ Victrelis  8-3-11, Viral Load  21.2 Million,  Und Weeks 4 Through 28 ,End Of Tx 2-15-2012 !SVR
hrsetrdr


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LanaiSurferGirl wrote:

Welll, it is a great day on this forum!

I just got the results from my blood test last week which was 5 weeks post treatment.  I tested negative for Hep C and for the first time since I can remember in 1998 my liver enzymes were within normal limits!!  :)  My hemoglobin is at 12 and my doctor said "no wonder you have so much more energy...you used to be at half of this"!! :) Platelets were still low but much higher than I have ever seen them (I have portal vein hypertesion and an enlarged spleen that keeps the platelets from fully enerting my circulating blood).  He has suggested too that the new SVR tests are done at 3 months post treatment but we agreed to re-test in December.  I will wait til the end of December to test and want to test again after that anyway to put my mind at ease.

 

Have a great weekend everyone,

Meghan

 Meghan,

Phenomenal news,  I KNOW that you will have a really great weekend with having received such exciting news!     burnout.gif



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"hrsetrdr"=Tim

Treatment halted on Aug.8,2012 due to vision problem.  6 month post tx labs

Aug.2013 SVR

Be strong when you are weak, brave when you are scared, and humble when you are victorious.
- Unknown

 

 
Mary Jane


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LanaiSurferGirl wrote:

Welll, it is a great day on this forum!

I just got the results from my blood test last week which was 5 weeks post treatment.  I tested negative for Hep C and for the first time since I can remember in 1998 my liver enzymes were within normal limits!!  :)  My hemoglobin is at 12 and my doctor said "no wonder you have so much more energy...you used to be at half of this"!! :) Platelets were still low but much higher than I have ever seen them (I have portal vein hypertesion and an enlarged spleen that keeps the platelets from fully enerting my circulating blood).  He has suggested too that the new SVR tests are done at 3 months post treatment but we agreed to re-test in December.  I will wait til the end of December to test and want to test again after that anyway to put my mind at ease.

 

Have a great weekend everyone,

Meghan

 Awesome... It tis great news all a buzz in Dragon land... headbang.gif I am so happy for you...Meghan Surfergirl.. peace and love all the best.. MJ



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Do not go where the path may lead, go instead where there is no path and leave a trail.Ralph Waldo Emerson

1a - VL 22 million  F2- IL28B- CT / Inck-Riba- Peg triple therapy 9/15/12 UND 4/8/14  8 wks BT ..3/1/2013 done! 3wks Post UND
news


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Way to go, Meghan. Like Malcolm said, we are making that virus look bad. We 36-week vets have to keep track until we are all SVR. I have not heard anything from my doc or CRNP about a three month SVR, but I know jrc's doctor graduated him at three months post. I have a feeling my guys will make me wait till six monts. Alan

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Geno 1A  Started Pegasys/Ribavirin/Incivek Nov. 20, 2011 .  Completed July 28, 2012 (36 weeks). For a treatment history, see:  https://jshare.johnshopkins.edu/xythoswfs/webview/_xy-9921874_1

SVR on January 14, 2013!!
alohaKim


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Congrats Meghan!! Awesome news!


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Genotype 1a, non responder to Peg/Riba in 2005. Started triple therapy 1-27-12 with Victrelis.  UNDETECTABLE as of 8wk labs (after 4 weeks of Victrelis) 4-3-12. UND at week 8, 12, 16 & 20 of tx. Completed triple therapy Oct 2012. relapsed 10/2012
JIme


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Congrats Meghan!!!!!!  Fantastic!



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jim

GT1a, St2 Lv2 last biopsy 2002, VL  11.4m,  start triple tx 9/30/11

VL 470 @4wks.....VL 22,000 @8wks  stopped tx

Round 2-  Started 3/16/12   PSI-7977, BMS-790052, Riba Undetectable day 14

Did 24 weeks Still UND 12 weeks post tx, SVR24!!!!!!! 2/14/13

 

 

 

 

 
Cinnamon Girl


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That`s fantastic Meghan, more excellent news!  Very well done, congrats! w00t.gif

Great to hear your energy is coming back - hoping you go from strength to strength!  smile 

Love from Jill xxx



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Jill 

(71 yo, lives in UK)

Was Gen 3a, 

24wks Peg Ifn/Riba, Sep 2010 - Mch 2011

UND @ Wk.4, UND @ EOT, 

SVR Nov 2011 --> Still UND @ EOT + 4 yrs.

 

 
mallani


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Meghan, what fantastic news! It's a bad time for the virus with Alan, Judy, Tim and now you showing it can be done. Congrats!!biggrin



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Geno 1b, IL28B CT,  x3 prior relapser,  ex-cirrhotic, 75 yo, did 48 weeks with Victrelis/Peg./Riba.  VL 1.28m at start, UNDET. at 8 ,12 ,16 ,24 ,30  and 48 weeks.  EOT 15 Feb 2013 , UNDET. at EOT + 28 weeks. SVR!  Still Undet. at EOT +5 years

Malcolm
LanaiSurferGirl


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Welll, it is a great day on this forum!

I just got the results from my blood test last week which was 5 weeks post treatment.  I tested negative for Hep C and for the first time since I can remember in 1998 my liver enzymes were within normal limits!!  :)  My hemoglobin is at 12 and my doctor said "no wonder you have so much more energy...you used to be at half of this"!! :) Platelets were still low but much higher than I have ever seen them (I have portal vein hypertesion and an enlarged spleen that keeps the platelets from fully enerting my circulating blood).  He has suggested too that the new SVR tests are done at 3 months post treatment but we agreed to re-test in December.  I will wait til the end of December to test and want to test again after that anyway to put my mind at ease.

 

Have a great weekend everyone,

Meghan



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geno 1a, mother & brother also hep c +...mom got a blood transfusion and passed it along.  Started tx with incivik 11/23/11 and brother started 2/8/2012.  Both of us und. at 4,8,12 and me at 24.  I am going 36 wks and brother is going 48 weeks.
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