Welcome, Guest. Please login or register.
July 16, 2019, 02:21:36 pm

Login with username, password and session length


Members
  • Total Members: 6109
  • Latest: Kchi23
Stats
  • Total Posts: 54224
  • Total Topics: 4581
  • Online Today: 71
  • Online Ever: 1314
  • (June 22, 2016, 05:23:42 am)
Users Online
Users: 0
Guests: 43
Total: 43

Welcome

Welcome to the Hep Forums, a round-the-clock discussion area for people who have Hepatitis B, C or a co-infection, their friends and family and others with questions about hepatitis and liver health. Check in frequently to read what others have to say, post your comments, and hopefully learn more about how you can reach your own health goals.

Privacy Warning: Please realize that these forums are open to all, and are fully searchable via Google and other search engines. If this concerns you, then do not use a username or avatar that are self-identifying in any way. We do not allow the deletion of anything you post in these forums, so think before you post.
  • The information shared in these forums, by moderators and members, is designed to complement, not replace, the relationship between an individual and his/her own physician.
  • All members of these forums are, by default, not considered to be licensed medical providers. If otherwise, users must clearly define themselves as such.
  • Product advertisement (including links); banners; and clinical trial, study or survey participation—is strictly prohibited by forums members unless permission has been secured from the Hep Forum Moderators.
Finished Reading This? You can collapse this or any other box on this page by clicking the symbol in each box.

Author Topic: Taking the plunge  (Read 2479 times)

0 Members and 1 Guest are viewing this topic.

Offline cementjungle

  • Member
  • Posts: 11
Taking the plunge
« on: April 08, 2017, 01:21:52 am »
Hi all... brand new here, and glad I found this forum!

I was dx back around 2002 (Geno 1A). Probably had Hep C for 29-30 years prior. I was a heavy drinker probably for 25 years prior to dx, but stopped cold turkey the day I learned I had Hep C (and had a really rough week in the process). For years after diagnoses I went for regular checkups with a top Hep doc at UCLA who kept telling me to wait for a cure to come out of the pipeline. He said l would probably die from something other than the Hep C (as long as I didn't drink), so I should wait rather than do the brutal Interferon type treatments.

Now we have these new drugs, so I've been waiting for the pricing to come down... Harvoni is still $94K for a 12 week course. Ouch.

I went to a gastro doc who claims her office can get good deals and I should give it a shot... so I did the liver sonogram and just today did all the blood tests/drug test.

I have no idea what kind of cost reduction I can expect or hope for... I certainly can't afford $94K... something like $20-30K *might* be doable, put painful... especially if it doesn't work.

Do most folks here get decent/affordable reductions in costs through their insurance, or should I assume that I'm going to be looking at $50K or more no matter what?

Also, if the treatment fails to cure, then can my situation (other than financial) actually be worse as a result? Can it make the HEP C get angry and do more damage/faster?

As it stands now, my liver functions are only slightly out of whack and the sonogram came back "fine" whatever that means. I don't think I have any ill-effects from the Hep C, but I don't have the energy I did when I was younger... I'm 61 now... so maybe age is more a factor than anything.
1978 (or thereabouts) contracted
2001 Discovered HepC (quit drinking immediately) Genotype 1a

Jan 2017 Viral load 22,800,000 7.36 H
Jan 2017 AST 36 ALT 65
Jan 2017 Fibrosis score 0.78 (F4)

July 2017 start tx (12 week course)

3 weeks into tx: not detected
AST 17 ALT 19

7 weeks into tx: not detected
AST 18 ALT 21

3 months post treatment: not detected

Offline Lynn K

  • Global Moderator
  • Member
  • Posts: 4,263
  • Get tested, get treated, get cured, fight Hep c!
Re: Taking the plunge
« Reply #1 on: April 08, 2017, 03:03:38 am »
Do you have insurance?  Insurers are getting better about paying for treatment than they were when these medicine first came out. With assistance from Giliead and their copay coupon my copay was $5 per refill.

https://www.harvoni.com/support-and-savings/co-pay-coupon-registration?gclid=CjwKEAjw8ZzHBRCUwrrV59XinXUSJADSTE5kfclCurwBtlkIbqpo9rkorSyfF55JW-Eq8lVxk0RZeRoCDWPw_wcB

If you don't have insurance there have been some here who got generic meds from overseas I think maybe $1000 per refill maybe less but that should be a back up plan not plan "A" in my thinking.

Hep c is a silent illness with most people reporting few symptoms the most common is tiredness which is why the CDC is wanting baby boomers get tested for hep c as most people have no idea they are infected. Really the first symptom I noticed was some lower leg swelling (edema) caused by my cirrhosis which I developed after being infected for 30 years. My liver function tests were always just slightly above normal. There is no relationship between extent of liver damage and liver function tests or even viral load.

Cure rates are better than 98% and you can't make hep c angry if it does comeback. Worst case at least you gave your liver a 12 week break from being attacked. We have had a couple of people who failed initial treatment but were successfully retreated and cured later.

If you look at my signature you can see I was a 3 time treatment null responder to interferon based treatments. I also relapsed after treating with Sovaldi and Olysio. I also had cirrhosis for 7 years before my final treatment with Harvoni for 24 weeks and 15 weeks of ribavirin.

I am cured you will be too.
« Last Edit: April 08, 2017, 03:07:57 am by Lynn K »
Genotype 1a
1978 contracted, 1990 Dx
1995 Intron A failed
2001 Interferon Riba null response
2003 Pegintron Riba trial med null response
2008 F4 Cirrhosis Bx
2014 12 week Sov/Oly relapse
10/14 fibroscan 27 PLT 96
2014 24 weeks Harvoni 15 weeks Riba
5/4/15 EOT not detected, ALT 21, AST 20
4 week post not detected, ALT 26, AST 28
12 week post NOT DETECTED (07/27/15)
ALT 29, AST 27 PLT 92
24 week post NOT DETECTED! (10/19/15)
44 weeks (3/11/16)  fibroscan 33, PLT 111, HCV NOT DETECTED!
I AM FREE!

 


© 2019 Smart + Strong. All Rights Reserved.   terms of use and your privacy
Smart + Strong® is a registered trademark of CDM Publishing, LLC.