Be Happy

Be Happy
Watercolor by Renee Locks, from Brush Dance
Showing posts with label ribivarin. Show all posts
Showing posts with label ribivarin. Show all posts

Saturday, January 17, 2009

At Peace Tonight

It's Friday again. I've taken my Peg-Intron shot and ribivarin capsules.

I've been in bed most of the week, with a few short walks, mostly to the grocery store. Today I read and enjoyed several articles in WIRED Magazine. What a relief to be able to think and take in information and ideas. Most likely this will not be possible again for several days, but it's comforting. It helps me believe there may one day be an end, or at least a significant amelioration, of my fogginess and low energy.

Did I tell you about the inflamed, red, itchy rash on the upper torso? Don't ask!

The second viral load test again showed significant decrease in the virus, meaning it is worth while to continue the treatment. The goal is "no detectable virus" at the end of treatment, and again six month later. Alevai - from your lips to God's ears.

Wednesday, November 12, 2008

And More Patience

Ribivarin depletes iron quickly. I'm taking the iron supplement again. In another week I'll get the results from the viral load test. Now and then I'm strong enough to do errands, and go for tests. Yesterday I saw the sky colors at sunset.

Saturday, November 8, 2008

Patience

The ribivarin is educating the interferon, which is alerting T-cells that the Hep C is a virus and needs to be killed. I hope.

My forehead is always hot, my arms flush red at times, I'm achy and lethargic. So, it does resemble a mild flu. I address symptoms and try to get lots of rest.

Next week the lab tests will include assessing viral load. That may give us an early clue to how well the treatment is working.

Patience and hope.

Monday, August 18, 2008

Countdown to Treatment

On September 16th I plan to start treatment with PEG-Intron (Interferon)and ribivarin at Kaiser Permanente. I'm scared and elated. People have reacted to these chemicals with flu-like symptoms, anywhere from mild to severe. Many endure this on the weekends, then go to work on Monday. The treatments last 48 weeks, with a weekly shot of interferon and daily tablet of ribivarin. Blood tests every two weeks will show whether the amount of virus is being reduced. If there isn't much effect by three months, the treatment will be stopped. Of those who complete the 48 weeks of treatment, 50% can be expected to be clear of virus and stay clear at least six months.

Several people have told me they took the same treatment and have been clear of the Hep C virus, one for four years, another for eight years. They've encouraged me to try.

It may not work, but I'll take the 50-50 odds gladly.