Just found out today that I am a CT. My doc suggested that I wait until the new drugs come out to treat. Which is a good thing because prior to me shoving the Labcorp test in front of him, he didn't know much about it, but he is actively researching. I like that he is open to the info I give him and is accepting that I intend to be an active participant in my care. He called me "tenacious" on my last visit, I think he meant that as a compliment...lol.
I've got to admit, I'm kind of bummed out. It's not easy to always embrace the positives. I feel agitated and impulsive, my 1st reaction was to look at clinical trials, not sure why, most of the information I read may as well be in another language. There is a lot going on in the Philly area, which is where I live, I just don't understand any of it, they use a lot of numbers and codes for drugs, or maybe the drugs don't have names yet. Any clarification on that would be awesome. I don't mean to be a downer, I knew I only had a 37% chance so it wasn't a surprise and as I've been seeing lately postings about higher viral loads being consistent with the CC allele, I knew that my last 3 viral load tests have been all under 200,000. I was wondering how much having chronic allergies and colds play into my immune system constantly being in overdrive...just curious. Even though I am not a CC, I'm glad I did the test. I haven't had any treatment yet, and my hope is to do this once, and even better, hopefully a shorter duration. I guess it's all a gamble.....trouble is, I've never been lucky at gambling :)