Hepatitis C Support Group
Hepatitis C is a blood-borne viral disease which can cause liver inflammation, fibrosis, cirrhosis and liver cancer. The hepatitis C virus (HCV) is spread by blood-to-blood contact with an infected person's blood. Many people with HCV infection have no symptoms and are unaware of the need to seek treatment. Hepatitis C infects an estimated 150-200 million people worldwide.
Been there, done that. Walked into the bathroom one day to take my meds, got distracted and walked out 20 minutes later not knowing if I'd taken them or not. Damn brain fog! LOL.
Anyways, the next day I went to the drugstore and purchased a pill organizer like this one. Save my ass. I fill it up every Saturday. When I finish treatment I will ceremoniously set it on fire in the back yard.
http://www.forgettingthepill.com/products/push-button-4xday-weekly-pill-organizer
Good luck,
Bob
i'm still trying understand the effects.... because it is evident things get foggy.. but i don't know if i am overanalyzing...
You definately should get the pill organizer that MrO mentioned. mine was provided to me 1st time I did treatment 3 yrs ago. I also take other meds. Two I keep by my bed, one btwn 1 & 3am and the other one around 6am. The hcv meds, bloodpresser, & pm pantaprazole were in the organizer. Mine had am & pm. Don't rely on memory.... and you can set your cell phone alarm to help too.
Also pill alarms on ur phone or watch are essential. I had 3-4 alarms going off daily. Yes it's maddening -- the whole experience was a bit maddening.
Victrelis seems to worsen anemia but the sides appear less than Incivek from what I've read in my almost 1 year here. I only did peg/riba for 32 and can't believe I just wrote "only." It was not pleasant by any means.
The HCV meds will not be forever. It just feels like that for a long time. Hope it goes relatively smooth for you.
When all this is gone it will have been worth it.
If I can help,let me know!
Bill
Allow yourself to rest, sleep, lay on the couch as much as you need to.
Your body is in a major battle right now. Since I did tx before, going into it this time I pre-warned my friends not to expect much socializing from me, and I told myself that this year was more or less a write off in alot of ways, but the future would be a different story. I knew I would be depressed, tired, & feel like crap. Knowing it seems to help. Keep saying, 'this too shall pass'.
I year ago tomorrow I finished 40 weeks of triple with Vic. Successfully finished, and am SVR
Over the previous decade I failed twice with INF and Riba, so the Vic was the super ingredient. However, the first two times I didn't get anemia, but this time i most definitely did
People say its the Inf or Riba that makes you anemic, but for me it was the Vic. But it's also what cured me
The protocol for Vic is very different from Incivek. For Vic you take 4 weeks of Inf + Riba, then add Vic for the duration of the treatment, 36-48 weeks depending on your history
So it's a pain in the ass (in my case literally) taking so many pills every day, but unlike Incivek you don't get the major body rash side effect Also Incivek requires 20g of fat with each dose, Vic just needs a snack
Get the pill box, and also set the alarm on your phone for the mid day Vic pills. They need to be taken every 8 hrs, with very little leeway.
No one does tx for fun, curing hcv, with today's technology, requires some ugly drugs. Pretty soon thatll change, but in the meantime drink a lot of water and don't plan on any marathons