-
Recent Posts
Archives
- April 2013
- February 2013
- January 2013
- December 2012
- November 2012
- October 2012
- September 2012
- August 2012
- July 2012
- June 2012
- May 2012
- April 2012
- March 2012
- February 2012
- January 2012
- December 2011
- November 2011
- October 2011
- September 2011
- August 2011
- July 2011
- June 2011
- May 2011
- April 2011
- March 2011
- February 2011
Categories
- Acute GVHD
- Back pain & fractures
- Bad reactions to Meds
- Chronic GVHD
- Going Home
- Healing Process
- Home Challenges
- Hospitalization
- Immunocompromised Issues
- Mobility Issues
- New Normal
- Possibility of dying
- Post-Transplant Issues
- Post-Transplant Updates
- Pre-Transplant Updates
- Relapse issues
- Side effects of long term steroids
- Tips & Tricks
- Transplant Updates
- Updates
Tag Archives: sleep deprivation
My Daily Routine – 21 April 2012
Being bed-ridden makes me a sitting duck. I seem to have very little control over how my time is allotted throughout the day. I think people assume I just sit in bed and have nothing to do. Not so much! … Continue reading →
Posted in Acute GVHD, Bad reactions to Meds, Chronic GVHD, Healing Process, Possibility of dying, Post-Transplant Issues, Relapse issues, Side effects of long term steroids
|
Tagged Acute GVHD, bad-pans, basic needs, being told you will die, bilirubin, blood work, care-givers, chronic GVHD, cll, dry eyes GVHD, dry mout GVHD, eating, emotional turmoil, energy sucking, fatigue, friends, GI Tract issues, going home, hallucinations, healing, human error, interruptions, leukemia, life threatening, life threatening infections, liver, long-term steroids effects, Lung Infection, lymphoma, Marie-Chantal Marchand, mariechantalmarchand, meals, meds, mobility issues, napping, not a vacation, not lounging around, occupational therapy, on-going Chronic GVHD, physical challenges, physio therapy, pills, relying on nurses, relying on people for basic needs, resting, Richter's Transformation, self-conscious, sleep deprivation, sleepless nights, SLL, specialists, steroids, time, TP53 with 17p Deletion, visiting, visiting friends
|
1 Comment
Hallucinations – 29 March 2012
Note: This is an extremely long blog as it covers 8 days. Eight days of constant hallucinations. Check it out. Grab a coffee, put your feet up, I think it reads like a cheesy paperback bad fictional drama story line. So, I basically … Continue reading →
Posted in Bad reactions to Meds, Chronic GVHD, Healing Process
|
Tagged bad reaction to meds, catheter, clarity, confusion, dying, falling, fantasy, fear of dying, hallucinations, miscontrued reality, no cognitive power, no focus, no spatial sense, reality, sanity, sleep deprivation, unreal
|
3 Comments
