I am really struggling to piece together what is going on with me. I am seeing a gastoenterologist, and he is rather stumped, I have six months of monthly blood panels to track what is going on but typically, if you get HEP A, you get sick (which I did, I almost had to have a liver transplant) but then your liver repairs itself and you get better. By the time I was cleared to go back to work my ALT/AST was down to normal ranges. In February they spiked up into the hundreds, they have come down, but however in the 60/70 range. I struggle with nausea sometimes and fatigue.
I have researched everywhere and have seen nothing about HEP A and long term effects, so I'm wondering what is going on?