Hi Linda,
You sound good....yes, it's good to stay busy.
I've been finding that out lately. My med's are helping, but I still have to give myself that little "kick" to get going. I can "veg-out" real easy, if I allow myself.
Today, I'm determined to get the laundry caught-up and try to clean the attic.
Your house sounds lovely. I think the older homes have such charm. I have a smaller house, but everyone always comments on how much space there is, once inside. Since I was on the road for so long, I let a lot of things go---I'm trying to catch up, now...but, it's going to take some time. I'm still not up-to-par.
Right before I was dx, I had trouble with my arms falling asleep. I think it was because of my growing lymph node...now, I'm having trouble again, but I think it's caused by my treatment (at least I'm praying). I think it's "neuropathy." I'd search it on the internet, but everytime I do, I regret it. I think I'll call my chemo nurses tomorrow to see it there's anything I can to alleviate it. I wake up every half hour or so, and have to rearrange myself, because something has fallen asleep---usually my arms. I'm trying not to obsess....of course, I'm worrying there's another lymph node swelling somewhere.
When does this all subside? Weeks? Months?
In the meantime, I'm pushing on....thank God I've found something to take, that's working somewhat to ease my nerves.
I'm glad you dad is coming to stay with you over Xmas. That will be nice to have him with your family.
Marn, I "feel" for you. It's always the "not knowing" that drives you nutso.
That's why I'm trying to stay busy. I can sink real deep, if I allow myself. There's always a new symptom on the horizon.... I know it's hard, but staying busy....reading, cleaning, visiting, shopping,...whatever, anything... helps.
CC...hope you're doing better today.
When you can, post and let us know how you're doing.
I'm glad you have someone helping you out. Is it a visiting nurse?
I hope you're on the mend today. I know how hard ABVD was, and I can only imagine how difficult this must be for you. You're always in my prayers....Linda, too...Marn, you also.
Well...off I go.
I've been sleeping a lot on these med's. I guess I need it. But, my days are starting later and later... That's o.k., though. We all need sleep. My chemo nurses have stressed that to me over & over.
Have a lovely Sunday. I'm so glad I have my friends here.

love, S.