May 13, 2015
Health Update
Since last update on
April 3,2015
Generally these last 2month
have kicked me in the “Arse” as the British say.
The side effects for a few
days after treatment have been challenging. Different since changed
to Camptosar for last three infusions. Very poor energy level after
Camptosar for last three infusions. Burning hands. Very dry nasal
passages, neuropathy, poor appetite.
Then life got interesting.
April 24th To ER
2 am as was jaundiced, had temp of
100.5, and white blood count and associated numbers down. Bilirubin
count up. Admitted and placed on antibiotics of course. Diagnosed
with neutropenic fever.
April 24- Had planned to go
to Knoxville, Tennessee today to visit Joyce's cousin, Joan and her family—didn't
happen. Very disappointing.
April 26th
Released noon from hospital
Of
course, chemo postponed.
May
7, Thurs Met with Dr. Reid to prepare for liver duct exam. “Endoscopic retrograde
cholangiopancreatography” ERCP. When at the office visit, had me
do blood work. My blood was thin. Also did a ultrasound of both legs
to check about the blood clot.
May
8th-Friday postponed chemo
May
9th. Scheduled ERCP on Saturday AM. Checked my blood, still too thin.
Dr. Reid admitted me to the hospital to supervise getting blood less
thin. Got 5 units of plasma, plus antibiotics
Decided
it would be less risky if I had a venous umbrella screen to prevent
any blood clot moving.
May
10th. Sunday AM Dr. Yanneta installed the screen. I didn't help Joyce much to celebrate Mother's Day.
May
11th. Monday, Dr. Reid performed ERCP, placed a stent in my liver
duct to help drain bile. Decided to learn more of the words to the song They Call me Mellow Yellow by Donavan 1966
May
12th Tuesday- off and on severe abdominal pain. Drowsy
May
13 Still in hospital....liver functions slightly improved Dr. Reid
wants to stay in hospital for a few days with better Bilirubin scores. Feeling much better.
May get out Friday, unless
Dr. Reid decides to put in tube to liver to drain to outside of body
(percutaneous transhepatic biliary drainage)
No
chemo his week.
I may write some blogs of a brief nature, or post some photos, rather than send an email.
http://itwonthappenthatway.blogspot.com/
The support and encouragement for not only me but Joyce, too, has been impressive. If you see her, don't ask how John is doing. Ask how she is doing.
As
usual feel free to share with others. Hopefully I encourage others to
not hide or be ashamed of cancer. I often enjoy helping someone. If
you hide your problems, you are denying others the opportunity to feel
good about helping someone.
John E. Swank
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