Thanks! It is a good feeling. All along I have been worried that my VL would go up, but it hasn't! Just a worry wart, I guess. Now that I am past 22 weeks and UND, I feel more confident I will make it through 48 weeks UND too. On my way to SVR!!!
I Almost Missed This...
A Great Big CONGRATULATIONS To You!!!!!!
Way To Go!!!!!!
:)
Ugggh. Sorry to hear you are feeling so badly. I know how bad the sx's can be. I have heard others that the end of tx is the worst. What kind of sx's are you having now? My beginning was bad, now I can do a few things, but I am not going to keep my expectations that all will continue like this.
Seven more shots! You are almost there! I have 27 more to go.
I think that you will go through a honeymoon period, , I think it was around 34weeks when things stsrted to get ugly for me , but thats after i had been anemic for a while , now its better with the procrit for sure, and now its like this last7 shots im having to take one day at a time just to get through this...
Thanks for nice words. I am almost half way there! YEAH! I also feel like I am aclimating to the meds. My sx's aren't as bad now. Of course we know that this could change any moment, but I will enjoy the good moments when I can.
Wow, that is some story. Well, discounts my theory.
Can't get over your story....How are you now? That was a long time to have elevated enzymes. Are you doing okay? Have you tx?
i guesse if it was 70 copies you would still have to tx for 48 weeks so it is irrelevant???
i recommend 4 week pcr to all to really get an idea of progress. a large percent at 4 wks clear.
bobby
Despite not having the most sensitive test available an undetectable result is cause for celebration. We've got to keep things in perspective which isn't always easy and it is clear that you are responding. I would probably research and bring copies of articles discussing the benefits of sensitive testing as well as the potential pitfalls with less sensitive testing. The guy might just learn something and you might end up getting a better test next time. But by all means do not dispair or agonize over what's been done. It's still great news. Congratulations again! Mike
I think I could beat you in being a pain in the neck, girl! LOL This stuff is a pain in the neck and worrying about everything just exasperates it. Sometimes I wish I were really stupid (no comments about that please!!) and just could cruise on through, but my head does double time thinking about all this stuff. As does yours!! LOL
Thanks for the congrats! It does feel good to be UND. I was worried and now I am more worried...LOL The dr. says he was the first to do PCR's. Well maybe they are more reliable now. He worked in NYC with HIV patients back in the day. While I do think the sensitive tests are more reliable, it is interesting that the same sample can change in an hour! The what if's are driving me nutz!
I can't wait until you start tx and become a REAL pain in the neck! I am gonna get you then! LOL
i had it 37 years and knew it ...they kept saying i had CRONIC hep before they knew about hep c. married 32 yrs and she is neg and i am sure will stay that way. it does't hide they just did not understand it. good theory though...keep thinking.
she just was refused to give blood again.
I am really one of the hard core 4 week PCR people. It is CRUCIAL to my overly obsessive HCV mind.
I was 411 at 4 weeks. 3 log drop. Yippee right?
But at week 12 I was 419. 3 log drop. Yippee?
If I had not had the 4 week PCR I would have mistakenly thought I'd been going down, down down the entire time but as it was...
Of course in the end it really made no difference because I extend anyway due to the positive at week 12. But I really believe that having more frequent PCRs gives you a clearer indication of what is going on.
I asked Dr. J about this and he said that they always do monthly PCRs during treatment but it was more to satisfy curiosity than anything.
So I guess really ... its very subjective and depends on how much you want to know or not. Some people unlike us in here just treat and never ask ONE question - don't know what geno they are except "the bad one" etc.
of course..........we need to know EVERYTHING ;)
I know I am responding and am very happy about that. I really feel for those that don't even respond to the drugs. This has to be heartbreaking! So yeah, I won't look back, but as NY says, who knows if I was REALLY UND at 12 weeks, since my test was to 75IU. As an obsessive treater that obsesses about all of it, it's hard not to think about all of this!
You know, I go through the I wish I'd had a 4 week PCR, I wish I had a biopsy, I wish I had txed 5 years ago etc, etc. Just a real worry wart I am!
In the end it is the luck of the draw. Some of us will relapse, that is just the fact of it all, especially us 1's. We all know we are against the odds going in. Those that are Geno 2 and 3, now have to worry about txing time with all the relapses.
Congrats! Sounds good to me!
Your doctor may just have a different perspective about this, but doesn't mean he is correct. None of the doctors have it all, because this disease is still a mystery in many ways.
Plus, he didn't really want to push for cat scan either?? I know insurance reasons and stuff, but i don't know,,,,,,
Don't let anything the doc said discourage you...you are on the road to SVR!!!!! Congrats!
Another subject....one thing I have been thinking of is...they say alot of us have been carrying this 35 years,as I was told to be carrying 35 years,,, how come there are people who are in their 20's who are getting it and some even saying they know they contracted it 5 years ago, such as niceguy (I think he said that)
Why doesn't it stay dormant for 35 years in their system? And if it does stay dormant 35 years, maybe our spouses have it and it is undectable until 35 years after being exposed. If you know your spouse only 10 years and he is negative..maybe in 25 years it will be positive? God forbid.
Whose to say that it doesn't hide when first exposed ...occult beginning, test neg, then replication begins,,detectable in blood,,,,tx,,,UND,,,but possible occult,,,,then relapse.
Just possible theory running through my head. But it comes down to this....we have to hope for the best....You are a very upbeat, positive person, continue to be that way, don't let a doctor who may be completely wrong discourage you.. Not saying you shouldn't have posted this and asked this.
There are many knowing people on board that help in sorting things out, I'm not in that position yet, but we all have a role in helping, whatever mine may be,besides being a pain in the neck lol
But anyhow, congrats SFBaygirl!!!
I have been thinking a lot about the PCR also-what does it really mean. Undetected to <5iu which is about less than 10 copies per mil. This is very good but even if there is only 1 copy per mil there still can be a lot there. In a pint of blood there is about 500 mil so if only 1 virus per mil is in the blood that that
Hi bobby,
when you say 37 years ago,,,,did they "test" you 37 years ago and find hep or are they assuming it was from 37 years ago without test? I know they didn't call it hep c, just wanted to clarify, don't know if I misunderstood you.
also you said...
"she just was refused to give blood again." How come they are refusing her to give blood if she is neg? That would lean towards my theory of the occult beginning stage....or was it a typo and you meant to say your wife doesn't give blood, just to play it safe, so to speak?
Where are you as far as stats? are you tx or finished? Hope all is well with you.
I developed acute hep symptoms around 30 years ago. Was diagnosed and treated for Hep A. At the time, there were only two hep types identified - A [infectious], and B [serum]. A little later, a third type called non-A, non-B was identified but it was some years before hep C was described and classified. In any case, the symptoms subsided and I was declared cured.
Clock forward 30+ years, and a positive diagnosis of HCV with an initial VL of 27.5 million IU/ml. Antibody and surface antigen tests for hep A and B were negative, meaning I had never had hep A. The diagnosis was the result of a terrific [and rare] Dr who saw elevated ALTs and was determined to prove why they were high. My ALTs had been elevated for 20+ years, but ignored by every Dr who had seen them over that time!!
No question that I was symptomatic, particularly over the last 10 years - reduced energy, v low tolerance for alcohol, etc. My wife was not infected.
lol yeah you guys will have your hands full when I start tx. Please be kind and gentle, I'm sensitive.lol
I was going to ask for volunteers to man the forum on the graveyard shift, just to make sure there was always someone on forum in the middle of the night to hold my hand.lol
a new symptom today,,,feels like the virus is walking around in my head lol,,,but really does. Oh so tired of feeling like my body is not my own anymore, like some alien has invaded.
Everyday some new weird feeling in our bodies,,,,can really get on your last nerve...
see ya later......... again ..............CONGRATS!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!
------------------------------------------------------------------
Paris, where are you??? are you okay?
I have been thinking a lot about the PCR also-what does it really mean. Undetected to <5iu which is about less than 10 copies per mil. This is very good but even if there is only 1 copy per mil there still can be a lot there. In a pint of blood there is about 500 mil so if only 1 virus per mil is in the blood that that
Its a saga, that's for sure:-)
BX showed S3 fibrosis, so I was getting close to cirrosis. The little buggers had been munching away at my liver and doing some serious damage.
Timing is a wonderful thing. I'm at week 9 of the VX950 clinical trial. ALT and AST returned to low normal within 4 weeks of starting tx. HGB is down to 10.4 and both WBC and PLT are marginal at around 1/2 of my basline levels. SX are almost tolerable, but I'm in awe of anyone who stands up for a second or third round of soc!! Still, the enzymes are suggesting that something good is happening. We will know for sure at week 20.
Well, good to hear you are tx and doing well.
Please keep us all informed as you continue. Good talking to you. And.....I will be starting tx hopefully real soon, next month some time...please jump in any of my posts to offer advice....don't be shy lol I need all the help i can get.
wishing you the best!!!!
There are other VX'ers who post here. I though that thy 'unblind' you at week 12 and give you some viral load info. No?
The VX950 trial protocol comprises four arms. Of these, arm D is dosed for 12 weeks with the combined SOC + VX-950. It is my understanding that the Arm D subjects will be unblinded at week 10, and that Arm A, B, & C subects will be unblinded at week 20.
Welcome to the forum. You aren't alone - there are plenty of us in here who had no idea we had this disease for 25 years or more. Personally I'm a stage 3 too - never had any symptoms that I am aware of.
I consider it lucky that we finally found out we had it so we could smash it into oblivion with meds. :)
I'm on week 53 of 72 so I'll be around here still for quite a while. The guys in here are the best and are always willing to hand hold.
It's great so see another VXer in here so we can see how it goes! It's exciting stuff!
(I am on regular old Peg/Riba just so I dont make it sound like I am another VXer by mistake).
Great luck to you!
"Why doesn't it stay dormant for 35 years in their system? And if it does stay dormant 35 years, maybe our spouses have it and it is undectable until 35 years after being exposed. If you know your spouse only 10 years and he is negative..maybe in 25 years it will be positive? God forbid."
the way it works so far, is that those that just found out at age 20, that they are positive, just lucked out that the drs are now testing for hep c. it has nothing to do with 'dormancy' since there is no such thing with hep c. The infection is chronic, your body is reacting to it, whether you notice it or not, whether your enzymes are normal or not. Those that say they had it for 35 yrs and now know about it, it is just that they recently were tested. If they would have had a hep c test 35 yrs ago, it would have been positive. It is about testing, not dormancy.