Wednesday, November 23, 2011
The "New Normal"
So....this is stage one of the hair alteration. At first I thought I was going to be all tough and "Hard-Core" and just go ahead and shave my head completely without so much as a bat of the eyelash. Somewhere over the course of the last couple of weeks I decided to go in stages and that, in fact, the whole baldness thing will probably affect me more that I originally thought. (I'm losing my freaking hair for God's Sakes!!!!!!!!). Thus the "short" before the "bald". A friend came over and kindly did the deed! As many of you know I've sported the short thing in my life before. It's kind of nice to have the short back...but, of course, I'm trying not to get to attached. :)
It feels as if months have passed since my last entry. My concept of time right now has definitely gone out the window as each day is brand new, and there is not a lot of my "old" life left right now to give me some kind of anchor. So I am adjusting to a whole new routine. This new routine consists mainly of pill taking, doctors, oncologists, naturopath, counsellor etc appointments, daily walks, making sure I am eating properly, keeping up with correspondence, visiting with friends. Yesterday I actually slept the entire day!
Thankfully, so far, the effects of my first chemotherapy treatment haven't been as bad as I thought they would be. I have had some discomfort, nausea and fatigue, but all things considered, things could be WAY worse. I do have a sense of foreign chemicals being in my body, which is strange, and my body has never craved fresh food more in all of my life!!
I figure that is a good thing.
I had a great few days of tender loving care courtesy of Mom - I realize that sometimes, no matter how old you are, you just need your mother! We went on a hat shopping spree which was fun (and thank you Aunt Jean - your gift to me went straight into come of the coolest hats ever!). We also took care of a lot of details. I think I may now be one of the most organized cancer patients you've ever met!
My next treatment is on Friday December 2. Next week I have been warned by my oncologist to steer clear of big crowds or anyone who is sick, as my white blood cell count will be at it's very lowest and I am a greater risk of infection (and treatment delay). So it will be a quiet week here.
Again - I want to thank EVERYONE for EVERYTHING. I am just now trying to get a bit on top of my correspondence but please know if I don't get back to you right away, its just that there is a lot. Every bit of encouragement means so much.
Thanks from the bottom of my heart.