After making the previous post I was asked, "What is T'ai Chi Chih?"
Here is a website: http://www.taichichih.org/index.htm.
T'ai Chi Chih was developed from T'ai Chi Chuan, a martial arts form also known as "meditation in motion." There is extensive peer-reviewed research demonstrating a broad range of health benefits available through the practice of T'ai Chi Chuan. Benefits include improved balance, with a reduced risk of falls and fractures, improved bone strength and improved immune function, among others.
T'ai Chi Chih was developed as a simpler, non-violent form. (Frankly, I never found any violence in t'ai chi chuan, which I studied when I lived in Phoenix.) It is easy to learn and easy to do, yet it engages the entire body.
"Balancing the chi" is simply a paradigm upon which the form was developed. It is not necessary to believe in chi for the practice to yield benefits.
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
-
▼
2007
(70)
-
▼
August
(18)
- Lunar Eclipse
- I'm tired.
- The aftermath...
- They just don't make 'em like they used to.
- You can't always get what you want.
- Decisions, decisions...
- This is a test.
- T'ai Chi Chih
- Follow up: The Wellness Community, Central AZ
- Divine Intervention
- It's Working!
- Success!
- On the other hand....
- Well. THAT was fun. (Not!)
- Starting out on the right foot
- Retreat
- CT Scan, part 2
- CT Scan, part 1
-
▼
August
(18)
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