As I slept, and this is a first, I broke out in the sweats. Not one of those sweaty forehead deals, but more like puddles of sweat in your belly button kind of nights. I assume the chemo (pegasus/ribaviron) therapy took a turn. My itches on my hands and legs have "really" started to get really itchy as well. The soreness in my joints seems to focus on different parts of my body...ignoring the others until due process. Legs a bit sore..but nothing like the effects from the first set of pills.
I never told the wife about the sweats, we have a king sized bed and rarely touch each other as it is... I wonder what she'd have thought if she looked over last night and saw me squirting infected juice out of all my pores? These thoughts shouldn't be here for another 7 or so weeks...so I'll just blow them off for now.
I need a better morning start plan. Winter is coming, so I might just be naturally inclined to park the motorcycle instead of riding every day. Winter is coming and I'm all for babying myself during the treatment... I'm excited to start my Monday!!!
Reflecting on my life recently, I've come to terms with the fact that...I'm not lazy, but given a chance, I will fall into a deep sleep for hours. Not sure of the exact reason, but I need to do some research to determine if this is a result of the rise of HEP C viral loads in my system. If that is the case, WATCH OUT WORLD...I'm in treatment and will be hunting you down again..like I did in my 30's.
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