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Saturday, April 6, 2013
This article appeared in my pilots’ union newspaper.
Friday, April 5, 2013
Chemo 9 (Round 8)
Talking about Highs and Lows…….. I have just retuned from the most wonderful trip to Zimbabwe to my reality of chemo therapy here in Baltimore. Though I shouldn’t moan too much about the Lows of chemo because that’s what is allowing me these wonderful opportunities to experience the true Highs in life.
If you are going to visit a few continents in your lifetime then visit Africa twice !
Carpe Diem
If you are going to visit a few continents in your lifetime then visit Africa twice !
Carpe Diem
Sunday, March 17, 2013
Thursday, March 14, 2013
The Zimkids Center
On Saturday March 23rd (from 2:30 until 4:00pm) there will be a dedication plaque unveiling for me at the Adrian Suskin Center for Zimkids in Pumula. It will be followed by a brief celebration.
I cannot begin to tell you how honored and flattered I am about this dedication.
I am unbelievably proud of Zimkids and could not be happier working with the likes of Dennis Gaboury, Tinashe Basa and all the other talented and dedicated individuals that organize and run the program.
Thank you and……
Carpe Diem.
P.S. Yes, I will be there :-)
Wednesday, March 13, 2013
Tuesday, March 5, 2013
5 years and counting
March 5th, 2008 I was diagnosed with Stage IV non-small cell adenocarcinoma of the right lung. I am way beyond my “best before” date but still going. I am grateful to my family, friends and doctors for all they have done for me to date.
Carpe Diem.
Carpe Diem.
Monday, March 4, 2013
Happy birthday to my favorite son.
Well…….. my only son. I hope you have a great and enjoyable day. It’s been amazing and wonderful having you in my life all these years. I love you, Dadrian.
Carpe Diem.
P.S. This picture was taken in 2003 :-)
P.S. This picture was taken in 2003 :-)
Thursday, February 21, 2013
A visit with Bobba The Bear
I spent a good couple of days with my mom in Boca. As always, I had an enjoyable time with her. We even visited my dad. He didn’t really say much :-)
I almost missed my return flight to Baltimore. I thought I was leaving Friday and it turns out I was leaving Thursday. Oops. Never done that before !
Carpe Diem.
Friday, February 15, 2013
Cause and effect
Post chemo this is my usual run down. I’ll start with day 1 and go through to day 21.
1. Chemo day is usually fine.
2. Still feel ok but get flushed. Looks like I have a tan.
3. Still a bit flushed and vision gets a bit blurry. Nothing glasses can't fix.
4. Fatigue sets in and mild nausea starts. Lots of rest and meds to help with the nausea.
5. Same as day 4.
6. Same as day 4 but getting milder.
7. For the most part, generally feeling better.
8. One of the chemo drugs causes some pretty bad constipation. Nothing meds, an ice cream stick and some TNT can't cure.
9. Ok.
10. Ok but slight fatigue.
11 −21. Generally ok.
So in summation, if I have 5 out of 21 days that are not great at least I have 16 days that are more or less OK. I’m also very relieved and happy that the maintenance therapy that I’m on is doing it’s job. Stable and no spread. The only pain in the arse is scheduling all my travel between chemos :-)
Carpe Diem.
Blow by blow for chemo day
I usually don't sleep well before chemo day. Maybe it's because I have to take Dexamethasone (steroid) tablets the day before chemo, the day of chemo and the day after chemo. I prep my port with a numbing agent and then off the Infusion Center (hospital). I live about 5 minutes from the hospital and no, I didn't plan it that way.
I check in and get my wrist bracelets so they don't confuse me with Mrs. Mittleschmatz (fictitious name :-)). I then get my vital signs taken. Weight, blood pressure etc and then proceed to my assigned chemo chair. I usually work with the same nurse but sometimes they change it up to keep me on my toes. Yea, right. Medical questions are asked (yada yada) and then I'm hooked up to a saline drip. They draw my blood and send it off to a dedicated lab for chemo and infusion patients. The results usually come back after about 45 minutes. I also have to give them a urine sample so they can check for protein in the urine. The Alimta can sometimes mess with your kidneys.
When the blood work comes back and all looks good then Dr. Schraeder orders the premeds and the chemo. The premeds are given before the chemo. I get more Dexamethasone tablets, Pepcid via IV (for heart burn) and then Aloxi via IV (for nausea). Then I get the the Alimta and the Avastin. The Avastin takes about 30 minutes to administer via IV and the Alimta takes about 10 minutes. When that is all done I get a 5 minute saline IV flush and I'm off. The whole process takes about 3 hours. Not too bad. I can walk around with the IV pole and go bother the nurses and staff so it's not too terrible. In the past I have had treatments that lasted as long as 8 hours !
Carpe Diem.
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