Starting day three slow

I start and end each day slowly and peak a little in the middle. Nothing really hurts, but I am incredibly tired at the beginning and end of the day. Yesterday, I got a little work done over email and phone. Bob was here for a little while, and a friend, Matt, who is doing a fellowship here came be for a nice visit and chat. That made the afternoon go by faster. That is the problem. The days are so long. I have 7.5 hours for drug and then there is another hour or so of getting ready so
I am usually here from 8:45 to about 5:15pm. I feel asleep in the care on the way home with Loree and went straight to bed. Bob even feed me in bed. I rallied about 8pm and Gloria came over and played Backgammon with me till 10:30. Neither of us had played in about 20 years so we kept having to call Syd to remember how to set up the board. I think we have the hang up of it now. And now Syd and I can play each other on the internet or when she comes over on Friday.

For at least a few days, I DO NOT HAVE THE WOUND VAC. They are trying to get rid of that slough stuff with some gel solution so I will probably not have it though the weekend. No plugs during the weekend (except I will probably need some home IV's for a couple of hours each day). Nurse Kathy says its possible by then the wound could be small enough that I won't need the wound vac anymore but she till not committ to that. I will take the weekend and be happy with that................so far. I do have to take some chemo home with me tonight but it does not have an electrical plug-- just plugged into me. But after tonight no all night apparatisus for a few days.

Day three moving was a little harder than I remembered but I am bouncing back mid morning.
I 'd like to do a few work email and sleep the day away but it doesn't quite work that way. It is just a very long lonely day. But is it day 3 of the last!