I wrote a couple of months back about trying to find a doctor without insurance. Just want to share this with you all. After trying to find a private doctor several times, I came across Health Services of North Texas quite by accident. They do sliding scale. For viral load, genotyping, abdominal (liver) ultrasound, chest x-ray and about ten other blood tests including Hbsag and AFP, my cost was $257.00. My doctor is compassionate, very knowledgeable about HCV, and knows the ins and outs of working with the drug companies. My blood work has not come back, however, my liver US and PA/lateral chest x-ray are normal. No masses or hydronephrosis, Liver is not fatty nor enlarged nor cirrhotic. Blood flow is visible through portal veins. Basically, Normal US/abdominal/liver and normal chest x-ray. It's kind of hard to believe my liver is not in worse condition since I have developed so many symptoms over the last two years, mainly "liver itch," psoriasis, eczema, petechiae on a lower extremity, and my CBC and CMP have more abnormal values than normal values.
Waiting for the blood work to come back and hopefully there are no tumor markers. Then, we will go from there with my doctor and Gilead Support Path.
What I want to say is that there is hope for treatment if you're uninsured. Gilead will pay for the new drugs, Solvaldi, Olysio combos and Harvoni (I think that has been available since 10/10/2014-not sure). Harvoni is specifically for genotype 1. If you are uninsured, have been turned down for affordable healthcare, are not on Medicaid, Medicare or have VA health benefits, you could qualify for Gilead's help. I started with Gilead Support Path and worked backwards. I did find a great doctor. It was a strange synchronicity.
If you don't have insurance, look at every available option and don't give up. There are services for us. The drugs out there are good and more are coming from Abviee.
I really want to come back and see that everyone who has been treated has attained SVR. There are more and more. Someone has kind of a chain with a template in the forum and it shows so many people reaching SVR.
It's never really a good time to have hep C, but I see hope now and in the future.
My thoughts are with all of you struggling with this. I was diagnosed in 1997. It turned my world upside down and nothing has been the same since. I think of my life in terms of pre-hep C diagnosis and post-hep C diagnosis. There was still an innocence and hope before 1997. It didn't help that I was diagnosed by a physician who told me I had hep C and 5 years to live. My son was in school and I was the sole provider. I actually believed this doctor until I saw someone who knew what they were talking about.
Don't give up! I almost did.