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.
I'm in the same boat as Jenandroses. I was diagnosed in 98 probably had it since early 70's. Was ADAMENTLY opposed to tx. But I felt GOOD then! A little fatigue from time to time was my only sx. So I didn't do alcohol, tylenol or anything I knew of that would stress my liver, except, I must admit ciggies and pushing myself far too hard in a very stressful profession. All was GREAT until about 2005/06. Then the Cryoglobulemia started hitting. EVERYTHING you described about the way you feel now, is what I feel now and I've never had tx! My quality of life sucks!! I fought hard to keep working, put up w/ a lot of crap at work because I sick, finally I pretty much forced by these above me to go out on disability a little over a year ago. I loved my work and now Am on disability, struggling every day just to get out of bed, cook a little something and wash dishes. A trip to any of the Docs., or going out anywhere is usually a trip to HELL. I'm usually down and in bed for 1-2 days afterward. I can't be a wife to my husband, I no can no longer enjoy the many things I loved before, the joys that make life worth living are gone! Tx. is my ONLY hope and I'm praying that I get excepting in the Clinical trial my Doc has refered me for. I'm 59 yrs old. If my quality of life had remained close to what it was 6 or 7 yrs. ago, I'd prob. wait for tx., new meds, or just keep trying to take good care of myself. But as it is now, I have no quality of life. I pray that I do well and come out of this clinical trial (if I even get in) in better shape. I know that I may not happen. Even though I'm a 1a,Stage 2 I'm fortunate to have the CC genetic marker which predicts good outcomes as far as clearing the Hep. As far as "clearing the sides" I guess its just a crapshoot. The only chance I have for a better life, actually for life at all because I can't go on like this much longer, is to ROLL THE DICE!
everyday hang on to that 1 thing that makes u see beauty even if its looking at a flower or being grateful 4 wrinkles cause they don't hurt :)
cultivate loving kindness
I have now been on radical antibiotics since Thanksgiving. I am hoping they will help
I still take the stance I WOULDN"T DO IT AGAIN. I know there are very few with life long side effects and I hope Im not one of them. But so far things have been bad.
I do miss all my friends who were so much help and support.
Be well
Tom
Wishing the beary best for you in the future:):)
As far as being hypothyroid after treatment, I do too but my daily thyroid pill controls that issue. I hope it does the trick for you too.
Taking heavy duty antibiotics are surely adding to your feeling of ill health but I hope they fix the problem.
Please keep us posted!
I ended up with terrible rage about what I considered terrible injustices and of course the rage just fed the virus and made me really sick. I just heard about a book called Power vs Force, by David Hawkins. He graphed emotions according to scores measured by machines. I would say I spent way too much time in the lower energies since about a year before my diagnosis. Anger, fear, apathy, guilt, grief and shame and all it took was anything critical, or even perceived as critical when it wasn't, from my spouse. The dragon took over and I could not find myself until something shifted, generally he shifted, but I learned to do the shifting, it was hard, but I did it.
I've broken a lot of things......but this spring something happened, and I have not been so angry anymore. I've let go. And when I let go, I got better. I started being able to do more and hurt less. Sunday I hiked my first hike of the year, to the overlook of Grandeur Peak. I developed sore muscles the following afternoon, and fever blisters from too much sun, but hey, anyone can have that happen on their first hike of the year.
Might I offer that you check in with your thoughts and feelings? Are you getting up every morning and saying Thank you? I find that really helps. When I feel grateful, it boosts my immune system and helps me feel better. I got my garden all planted too! It's pretty big. Hubby tilled it and then I shoveled it into 3 long raised beds. Planted tomatoes, melons, broccoli, cabbage, cauliflower, potatoes, beans, peas, carrots, beets, onions, and mixed salad greens. The garden is about 35 by 20. not as big as before I got sick, but bigger than last year.
What I did was just accept that I wasn't able to do things, but I wasn't sick enough to get SSI, or just couldn't find a doctor willing to help me without making me do Tx. So I just decided to do what I could and quit being hard on myself. I'm finally in the mood to clean up after myself and get the dishes done before I go to bed, instead of 3 or 4 days later! LOL
I'm happy. I feel that if a person is willing to eat a damn near perfect diet of veggies and fruits, whole nuts, seeds and grains, no refined foods, no junk foods, and very little animal if any, that that will take a load off the liver so it can handle the virus. I may not live to be 100, but who knows, maybe I will!
I have created a news article about recovering from Tx, but I can see now it is not complete. I would love to make it better, so that people struggling to detox from Tx can have hope. Maybe you can help me with some feed back.
http://www.dailystrength.org/groups/alternative-treatments-for-hep-c/news/view/1713412