Hi Caravan1990,
It's good to hear that you are on the pathway to seeking treatment. Keep pushing forward with the aim of getting the medication and curing yourself of Hep C.
Brain fog is very common for those of us that had/have Hep C. You will see from my profile that I had the virus for a long time and have been cured for a few years now, through Dr James and this site.
Caravan 1990 we know exactly how you are feeling. I have experienced all that you have with the brain fog. In the few years before I finally found the treatment through fixHepc my ability to focus decreased along with my confidence in my own abilities and intellect. I had quite a high level and demanding job and found that everything, especially decision making, was starting to take longer. The fog became heavier with fatigue and what I now recognise as some depression. I hid it all pretty well but it was certainly there and it was very frustrating and confusing.
I can guarantee that when you cure yourself of Hep C the fog will gradually start to lift and your clarity of thought will return. You can start to feel benefits as the medication kicks in but for me the improvements were gradual but continual until I finally felt like my "old self". Or rather a "new old self" with a greater appreciation for my good fortune and my health.
We're with you on this so let us know how you are travelling. Looking forward to reading that you are starting your treatment.
Coral
G1a probably early 1980's, Biopsy F1(2010), F2-F3(2015). VL 5+mill; 2+mill (2014) Tx naive. Accessed Sof/Led through Dr Freeman at GP2U and Buyers Club (lifesavers!!!)
Commenced tx 12/11/15. 9 wk: VL <15 Detected but LFT = Normal 12 week results: UND (Yay!) Due to slow response commenced Sof/Dac 4 Feb for 12 weeks. EOT @ 24 weeks 27 April 2016. (With thanks to Dr Freeman et al). SVR11 result: VL 1,950,000. It's back!
New tx 030916 (Viekira Pak, Solvadi, Ribavirin UND @ 111116. EOT 170217.
SVR12 and SVR 24