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#54181 12-20-2003 01:25 PM
Joined: Jun 2003
Posts: 41
fr mike Offline OP
Contributing Member (25+ posts)
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Contributing Member (25+ posts)

Joined: Jun 2003
Posts: 41
Hi everyone,

Just read some of the posts about follow-up exams. My ENT also prefers the physical/visual exam approach to things. While talking to my brother earlier today he raised a question that I might get a good answer to here.

Would there be any benefits to periodic blood tests? I'm not looking to be stuck with needles anytime soon; well anytime for that matter, but I'll endure whatever it takes. Should I ask the ENT at my next follow up visit about it? Does anyone know if it is worth it?

Peace,

Fr. Mike


Fr. Mike
SCC on the base of tongue, right side. T2 N1 M0. July 25, 2003 partial (40%) glossectomy, forearm flap reconstruction, right side neck disection.
#54182 12-20-2003 02:31 PM
Joined: Nov 2002
Posts: 541
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Posts: 541
Fr Mike,I am not sure my case is similar to yours. I had blood test every time I visited the oncologist who said it was important. I don't know exactly what the test reflects but one thing for sure is the tumor marker. He told me that when I was diagnosed with cancer, the reading was much higher than normal and kept rising until I completed my treatment. Then the figure started going down and now it is back to the normal level. Every time I had my medical appointment, I asked about the blood result.When my oncologist said'normal", I was relieved. About piercing a needle into my arm, I don't have much feeling with it after going through so many pains in these 2 years.This is just a piece of cake.

Karen stage 4 tonsil cancer diagnosed in 9/01.


Karen stage 4B (T3N3M0)tonsil cancer diagnosed in 9/2001.Concurrent chemo-radiation treatment ( XRT x 48 /Cisplatin x 4) ended in 12/01. Have been in remission ever since.
#54183 12-20-2003 07:01 PM
Joined: Nov 2002
Posts: 3,552
Patient Advocate (old timer, 2000 posts)
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Patient Advocate (old timer, 2000 posts)

Joined: Nov 2002
Posts: 3,552
Fr. Mike,
I have have to admit that as time went on I resented the blood tests more and more. I have calluses on my veins from being poked so often. I don't know anything about tumor markers -if they were looking at that I wasn't aware of it. The radiation oncologist and oncologist were really interested in the results of the bloodwork and required a draw prior to every visit for up to about 2 -3 months post Tx. The oncologist was monitoring my white and red blood cell counts and creatinine (kidneys), probably looking for potential damage from the chemo and or radiation or infection maybe. Certainly I was immuno supressed for a long time. It appeared that they were all standard blood chemistry stuff. Finally I told him I had had enough needles and he said that it was cool to back off. I haven't had a blood test for months now and I don't miss it.


Gary Allsebrook
***********************************
Dx 11/22/02, SCC, 6 x 3 cm Polypoid tumor, rt tonsil, Stage III/IVA, T3N0M0 G1/2
Tx 1/28/03 - 3/19/03, Cisplatin ct x2, IMRT, bilateral, with boost, x35(69.96Gy)
________________________________________________________
"You are a mist that appears for a little while and then vanishes" (James 4:14 NIV)
#54184 12-21-2003 12:39 PM
Joined: Nov 2002
Posts: 458
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Posts: 458
Fr. Mike, I can empathise with your dislike of needles. I cringe when anyone goes near me with one. Made worse by the fact that half the people drawing blood don't have the faintest idea what they're doing.

Only time I usually get blood test is during the 6 month PET/CT follow ups, when they're going to access the veins anyway. Then mostl to check general red/white count, thyroid, etc. That coupled with my once a year visit to the local hospital for my China residence visa check up is plenty for me, and they check the same things plus HIV, Hep A,B,C, etc.

Take care
Bob


SCC Tongue, stage IV diagnosed Sept, 2002, 1st radical neck dissection left side in Sept, followed by RAD/Chemo. Discovered spread to right side nodes March 2003, second radical neck dissection April, followed by more RAD/Chemo.

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