And cranky.
I've been fighting a sinus infection since last week. The last two days I've felt sufficiently un-well that I sucked on zinc lozenges and got extra rest. Apparently that wasn't enough. I woke up this morning feeling distinctly ill, with a stuffy head, body aches, earaches and a spot on my pharynx that was red, swollen and sore.
Unfortunately, my office is still torn up, I have a mystery shop due today and the clean dishes have been in the dishwasher for days.
But...I am still thrilled with having my home theater accessible, and I can now watch TV and use the Internet at the same time. (I had to add a cable outlet.)
I've been drowning my symptoms in fruit juice. My throat feels better. My materials are printed for the mystery shop this afternoon.
I am going to start a stack of CDs playing and go back to bed.
skip to main |
skip to sidebar
I started this blog to share my medical status and progress with my friends, but it has grown to include much more. Want just the medical updates? Use the label index, bottom right, to select "CLL." Want details of my recent hospitalization and return home? Check out the new blogs, to the right.
AzLady2's Blog List
Eating crow.... (1/20/09)
How quickly things change! In the three weeks -- to the day! -- since announcing that I was not ready for chemo, I have become very, very sick, been admitted, received chemo, had all sorts of new experiences and am now in the process of getting ready to return home.
When my oncologist told me that I would need to receive my first treatment as an inpatient, she estimated a four to five day stay. When I was admitted she estimated a week. Her senior partner said if I were his patient to expect a month. It has now been eleven days. While the end is not in sight, things are looking much better, and I've begun physical and other therapy that will make the transition easier.
My internet access is made possible by http://www.theblf.org/, a foundation which has made computers available for the use of patients with long term stays. These lightweight notebooks use the hospital wi-fi network. The security is preset, which would not be possible if each patient connected individually. I can keep this with me until I am released or until another patient needs it. (There are three units; they are rotated among the long term patients.) Getting online this afternoon has made a huge difference in my outlook. I am indeed grateful for the opportunity.
Also, it is far easier for me to type than to either speak or write, so I will be using this blog or email for most of my communication.
-------------------------------------
Most of you reaching this page know that I was diagnosed with Chronic Lymphocytic Leukemia in June 2007. After six months of relatively stable lab results my numbers started climbing rapidly.
As of 12/30/08 the increase is still accelerating. My doctor seems to believe that one day I'll wake up very, very sick, and treatment will become urgent.
She would have been happy if I started chemo months ago. Not yet.
When my oncologist told me that I would need to receive my first treatment as an inpatient, she estimated a four to five day stay. When I was admitted she estimated a week. Her senior partner said if I were his patient to expect a month. It has now been eleven days. While the end is not in sight, things are looking much better, and I've begun physical and other therapy that will make the transition easier.
My internet access is made possible by http://www.theblf.org/, a foundation which has made computers available for the use of patients with long term stays. These lightweight notebooks use the hospital wi-fi network. The security is preset, which would not be possible if each patient connected individually. I can keep this with me until I am released or until another patient needs it. (There are three units; they are rotated among the long term patients.) Getting online this afternoon has made a huge difference in my outlook. I am indeed grateful for the opportunity.
Also, it is far easier for me to type than to either speak or write, so I will be using this blog or email for most of my communication.
-------------------------------------
Most of you reaching this page know that I was diagnosed with Chronic Lymphocytic Leukemia in June 2007. After six months of relatively stable lab results my numbers started climbing rapidly.
As of 12/30/08 the increase is still accelerating. My doctor seems to believe that one day I'll wake up very, very sick, and treatment will become urgent.
She would have been happy if I started chemo months ago. Not yet.
About Me
Blog Archive
-
▼
2008
(82)
-
▼
May
(14)
- By the way... (inconsistent Internet access)
- Momentum challenge!
- Yes, I'm in New York.
- It's not broken...
- Nick, pt. 2 (fan)
- Nearly Headless Nick does not make a good fan.
- Google Docs and my new leukemia album
- Knowing where I'm going... (housing)
- The end result...
- I'm sick. Part 2
- I'm sick.
- Clearing up the confusion
- All in all, a good day's work.
- Back online!
-
▼
May
(14)
Labels
- Cancer Project (1)
- celebration (1)
- CLL (41)
- computers (4)
- confidence (2)
- cooking (4)
- discharge (3)
- family (1)
- Food for Life (1)
- home stuff (11)
- infrastructure (3)
- Inpatient (11)
- Life and Times (4)
- lifestyle (1)
- non CLL (2)
- NY (1)
- photos (1)
- Priorities (1)
- scrapbooking (3)
- status (28)
- supplemental (1)
- this blog (7)
- treatment (9)
- whining (6)
- wish list (1)
Posts
No comments:
Post a Comment