So, I've been out a bit. My PC use is about 30 minutes every 2 hours, after that it's back to laying down or at least putting my feet up on the couch.. Energy is really low. Hard to eat, one of the anti-rejection drugs makes everything taste bad for the first 4 months... like all food tastes like vomit. Most drinks too. :/ Losing weight fast... but I didn't need to.
Trouble staying hydrated too, stomach shrank from 25 days not/barely eating in ICU... and the taste isn't helping either. It's hard for me to get 4 cups of water a day, apparently I need 11 a day because of the transplant, not 8 anymore... It's rough.