I had the same message on my phone this morning about good news. Called back and to my surprise the nurse said the virus was undetectable at 12 weeks. That news makes it much easier to think of the weeks ahead. At least we know we are getting results and hopefully it will last.
I am wondering if anyone who has relapsed or gone off of therapy still experiences joint ache? I finished therapy in Aug. and felt incredibly well for about 3 weeks and then the aches & soreness are back. I am beginning to wonder if these are not a symptom of Hep C? I will be starting therapy again in May, this time treating with Infergen/Ribavarin. Has anyone been on this combo. My Hepatatis Specialist has had more success with this treatment for relapsers. For those AD questions, I started before therapy, cutting back on the dosage gradually at the end & had no problems. I feel they helped me get through the 1st. round. I will definitely continue with the 2nd. round of treatment.
I am wondering what therapy Dr. Johnson has prescribed for you and how you are doing? If you want you can e-mail me at ***@****
Bill, good news.........let us know when you verify! I also will "assume" that congratulations are in order. I hope that once all your insurance woes are solved, that the stress will be less and your rage will subside.
Petey 7, That sweet news should sure help you keep moving forward! Good for you! Congrats!
ambush :)
eagerly awating the week of feb 16th thats when i finaly start the run to clear.
i realy hate that ya'll are haveing trouble with your dr's nurses,(try leaving a box of candy one day for no reason).
i guess i'm lucky in that the nurse i will be seeing is the
same one i get chemo for leukeamia from so she and i are old friends(i always bring home made goodies to the chemo room).
also the oncologist i use is a dr. i worked with for about 10 years so good to go there.
beating the dragon has to be the first thing and most important thing in our lives.
if your getting grief from treatment team have you tried talking to your dr. ?
i cant hurt and might help.
best of luck to ya'll see ya on the train around the 16th.
2 more work nights then vacation starts heading to micky world next week for a blow out before treatment. will think of ya'll when screaming my head off on a roller coaster.
The only thing that worries me is if you quit w/out your Dr. permission. Insurance companies are sometimes very picky. "If you can't follow yourDr. on this, how do you expect to get well?" If you didn't have your Dr.s permission,see if you can have him add permission to your file and explain to him why. I'm glad you're doing better and keep heading that way!! Joni
Howdy Bill thats great news about the getting off AD's, so what's going on with your Tx are you still doing the Interferon + Riba, have you missed any because of their stupidity ...
My personal opinion about the AD drugs is they should be used for the right reason ... for me I think way too many people start on them like you did Bill on their say so, they say ok you start Tx I want you to start AD's 2 weeks before just like some kind of routine safety net ... well not everyone experiences depression in fact I think its under 50% that don't ... sometimes everyone gets a bit down feeling & thats "Not" clynical depresion .... I think that those AD drugs can create even more problems for people who are not needing them ... I did 26 weeks without anything in that class 2 weeks left to finish line, No I don't want a medal LOL & I realise some truly need these drugs
hahaha ok I'll get off my soap box now heppers, surely there are others that agree with me .... addiction to any Benzodiazapines is a horrible thing, previous experience, I was taking them for 6 weeks in hospital years ago but when I got out of hospital & never took them anymore I had all sorts of major problems & didn't know until weeks later why I was so freaked out & thought I'd dropped a few marbles <b>.....Steve.....</b>
Steve', I agree w/you that AD's are not the panacea for everyone. And many people don't get depressed on tx, esp if depression and anxiety are handled w/exercise, nutrition, herbs and meditation/prayer.
I wanted CURE so badly and was so grateful to have patched together a no cost treatment plan, I never dreaded, or hesitated, at each pill and each injection (3Xwk). Only the past depressed me, not the future or the present.
Petey7: I cl'ed @18 days. The rest of the time zipped by, b/c I had the prize in hand and was only insuring that prize by moping up any lingering hep c virus hangin' around.
DhBill, I pray that the answer will will be SVR for you!!!!! Hang in there...if the rage gets worse...get some Zyprexa. It helped me! Many Prayers for you tonite! Cindee
Petey7, WOW GREAT NEWS!!!!!!! Hope you continue in the SVR direction!!!! prayers to you and all, Cindee
I guess some of you have Not been reading or listening. The first 6 to 8 weeks of tx went good I lived with whatever but when I complained about insomnia he reluctently gave me trazadone wich I had a reaction to. I asked for Ambian as I had heard such good things he said he had never presribed that before so he reluctently gave me 15-5 mg tabs for occasional use. I asked for mail order so wouldn't have to hastle with this every month cause I have been told to call each month after blood draw to make sure my peg/copeg are on time the pharmacy has always had to fax additional reminder to get it on time. Every month this goes down to the wire. I have been told the last several times that I always have the option of stopping tx as my liver isn't that bad off.
AS to effexor that is his drug of choice no other. I firmly believe if I told him I wanted to stop effexor he would say my only choice would be to stop tx. He refuses to do mail order cause he says he needs to see me eyeball to eyeball each month to make sure I'm not depressed. I'm not depressed, a drug addict or alcohlic. All of my tests have been very good he said I was in the top 10% of responders The head HVC nurse just resigned last Wednesday would not say why. She did tell me she didn't aways agree with doc. The end of every meeting with him if I disagree or question is "you can always stop tx" I had a lot of faith in him from others in medical profession he was suppose to be the Golden Boy from Berkeley Calif. I will talk to him again next week but very carefully as he could opt to stop tx even though all my stats are good and appear to be still clear at 24 wks.
My Doc started me on AD's before tx because lots of people on this forum had told me I should get on them, so I did and been on them, my question is what if you are on them but actually don't need them them. How will your sytstem react to them, will they make you feel better than you should or just not do anything, I'm on paxil, not really knowing if I need them or not- I'll probably be on them a year- will it be hard to come off of paxil, and how long- and if I'm on paxil and really don't need them, is it going to harm my system or what type of sides should I be looking for. You get so many sides from the riba and interf., how and the heck would you know what sides are coming from what med.-- HD
PS- I have a question- I've been lucky with side, not much to talk about, your usauall fatigue, that is probably everyones biggest side, I do have one side that bothers me and it is my tongue burning when I eat or drink, it actually just tastes like the food or drink is overspiced but it's not- does anyone else have this and is there something I can do?- Thank's -- HD
I started pegysus and copegus on January 8th. So far so good. My symptoms have been minor annoyances compared to what I was expecting. The nausea has been the most disturbing. I was given a script for phenergen but it makes me sleepy. Is there something "nautral" or herbal that works?
Also I am having some achy feelings in the area of my liver. My enzymes are still normal (they have always been). Is this from the irritaion - so to speack - from the meds?
I had a time w/ my mouth when I was on tx. My doc prescribed Majic Mouth. It worked so good, tastes nasty, but it's worth it in the long run. Good luck, Cindee
Morning everyone, I have won a battle with the insurance company(HMO)My first visit to a GI was an aweful experience, he was very "pessimistic" regarding everything he said to me. I searched and found a Hepatology dr of MY CHOICE who happens to be the Director of Hepatology at Cedars-Sinai, I found out they would take my insurance, and...are willing to see me! I DID the footwork cuz I definately wanted to get away from the 1st GI. They were caught in a lie to my primary care dr about submitting for a biopsy which was NEVER done. I will still have to wait a week for an appt to the New Dr but...I'm fine with this for now. I was able to"draft" a letter to the insurance co using a form letter from a good site...patientsarepowerful.org I was able to be my own advocate to get what I need for myself.
Sorry I used this to ramble on about myself but...I am just so darn happy to be able to see a Hepatologist that specializes in HepC! I've learned, you need to be your own best advocate and keep going forward to get what you need, even if you think the odds are against ya! Positive thoughts your way, Annette
Sorry to barge in here, but just saw this. Wouldn't it be great if we could get this in the U.S.?
Details of Hepatitis C Ex-Gratia Payment Scheme Announced
London, GNN
DEPARTMENT OF HEALTH News Release (2004/0025) issued by the Government News Network on 23 January 2004
Health Secretary John Reid today announced a scheme by which, people infected with Hepatitis C from NHS blood or blood products will be eligible to receive ex-gratia payments from the Department of Health.
Every person in the UK who was alive on the 29 August 2003 and whose Hepatitis C infection is found to be attributable to NHS treatment with blood or blood products before September 1991 will be eligible for the payments.
The ex-gratia payment scheme means that:
How did you all cope when getting close to the end of Tx?
I have 2 shots to go and my family are all very excited, but not me.
I am so sick,sick,sick of feeling completley **** I don't know how to get through each day.
I know that alot of you are going through exactly the same thing and I know deep down that I am extremely lucky that I am undetectable and close to the end,but I can't get rid of the thoughts that I just want to stop now.
Every day is either bad, extremely bad or worse, never good or even reasonable.
Sorry to be so down but I just feel the need to ' stamp my feet' today.
Best wishes
Joanna ( also known as Baldy)
I know what you mean. I'm heading towards the finish line w 9 weeks to go to my 45th week. I have mixed emotions right now with it all. I can't figure out if the first 24 or the last 24 are more painful and difficult.
I'm getting myself a little worked up as my GI will probably want me to do and extension of 6 - 8 on the meds, further to my 48 weeks.
Hang in there - nothing about this treatment and meds are/were easy, to say the least.
I meant 9 weeks to go to my 48th week.
You sound alot like me. I finished Pegasus in October, I start Infergen and Ribavirin on Sunday. I felt the same way with joint pain, it went away for about a month after treatment, and now it is back. Mostly in my knees and elbows. I just think all of this treament does wierd things to our bodies that nobody will really know about until years from now. I try to get a massage every six weeks and that really helps. I'll let you know how the Infergen does. Kat
I think were at about same shot. I do #27 tonight and I do experience the mouth thing, sometime feels raw it took my wife a while to understand it's not her cooking it's me. I think it is getting better.
I'm 3 weeks thru stopping the effexor the last week was ROUGH when I totally stopped had very bad ringing in ears, something called brain shivers which srared me until I read it was normal. My biggest concern was my blood pressure. Before I started tx I got EVERYTHING checked out and my heart had some problems. Heart doc said it would be ok if I kept it down to 110-120 which is normal for me. As soon as I started AD it went to over 140. Brought letter from heart doc to to hep doc and he handed it back to me holding it from the corner by his index finger and thumb like it was dirty and said I always have the option of stopping tx. Thats when I first said to my self HOUSTON WE HAVE A PROBLEM. This guy has a cookie cutter aprouch he will no deviate from.
Wish some of the old timers would step in here about stopping AD's. I think it would helped to have valium or some pot to help along.
My bp is under 110, feel less fatigued and my ambition and manlihood is comming back : ) NO DEPRESSION OR BAD THOUGHTS I'm just pissed at this doc and will just try to get thru to end.
#
Sorry about that space, also ment bp is under 120
YaHoooooo!!!
This is wonderful news. I know I haven't been up for awhile. I'm so happy for you. I know when I got the news it made the rest of the travels easier. You will make it. Keep up with the meds. and you will be fine. <b>CONGRATULASTIONS!!!</B>.
People have been fighting for this for a long time to bring the compensation into line with that given to HIV infected patients. The problem is that most of us in the UK did not get this from transfusions etc and are not haemophiliacs. It is a way of separating the sheep from the goats, if you see what I mean!