Previous Thread
Next Thread
Print Thread
#38374 04-05-2005 06:12 AM
Joined: Sep 2002
Posts: 642
"Above & Beyond" Member (500+ posts)
OP Offline
"Above & Beyond" Member (500+ posts)

Joined: Sep 2002
Posts: 642
Friends,
As I wrote earlier, my most recent CT scan showed a very small node (8mm) under my chin that had changed size slightly since the previous CT scan. MDACC recommened that I return in 3 months for another CT scan. Having been in this "game" now for almost 3 years, and having learned a long time ago to be my own advocate, I was not willing to sit around for 3 months wondering if I had a recurrance.
The doctors at MDACC recommended doing nothing for 3 months or having an ultrasound, which, I and my radiologist friends believed, would reveal nothing. Fortunately my cousin, a radiologist, operates an imaging clinic and recommended a PET scan. For some reason the head and neck doctors at MDACC do not believe that PET scans are good diagnostic tools for recurrances of H&N cancer. Others disagree, including my cousin, who has been a radiologist at at major hospital, specializing in neuro-radiology for 30 years. So yesterday I had the PET scan along with a CT scan.
Fortunately, both scans showed no recurrance, so I am very relieved.
One realizes, after a while, that medicine is as much an art as a science, and different doctors and hospitals are attached to their own protocols, which can be inflexible.
This is not to say that the doctors at MD Anderson are wrong, but I personally feel a lot better now that I have explored other avenues.

Danny G.


Stage IV Base of Tongue SCC
Diagnosed July 1, 2002, chemo and radiation treatments completed beginning of Sept/02.
#38375 04-05-2005 07:22 AM
Joined: Aug 2002
Posts: 76
Supporting Member (50+ posts)
Offline
Supporting Member (50+ posts)

Joined: Aug 2002
Posts: 76
Hi, My husbands Doctors in Detroit, he went to one of the hospitals on the list do not like using the PET scan either. Dan may insist this month because he cannot have an MRI due to metal in his jaw during reconstructive surgery. His Team of Docs say the PET has way too many false positives.
I have heard from friends that have gone to other hospitals, for other reasons that alot of Docs don't like to use them either.


Sherrie wife to Dan, Tonsil cancer survivor, Stage IV diagnosed July/2001
#38376 04-05-2005 08:36 AM
Joined: Mar 2003
Posts: 1,384
Likes: 1
Patient Advocate (1000+ posts)
Offline
Patient Advocate (1000+ posts)

Joined: Mar 2003
Posts: 1,384
Likes: 1
Thank you Danny for the update. I had been reading your posts and was wondering.

It is funny in a way, that the dr.s suggesting you wait for three months would also have also been right. BUT then they don't have to live with the wait do they!

Good news, I appreciate hearing it.


Mark, 21 Year survivor, SCC right tonsil, 3 nodes positive, one with extra-capsular spread. I never asked what stage (would have scared me anyway) Right side tonsillectomy, radical neck dissection right side, maximum radiation to both sides, no chemo, no PEG, age 40 when diagnosed.
#38377 04-05-2005 01:33 PM
Joined: Jul 2003
Posts: 1,163
Patient Advocate (1000+ posts)
Offline
Patient Advocate (1000+ posts)

Joined: Jul 2003
Posts: 1,163
Thanks for sharing the good news Danny. Different strokes for different folks!!! True in the medical world also. Glad you followed up and have the peace of mind knowing there is no reoccurrance.
Buying a golf pass this year. Have alot of rounds to play. Get that handicapp down to 8 or 9. (hoping) Best part is to be golfing with my buddies again. There is life after and during cancer treatment!!!

Best Wishes, Danny Boy


Daniel Bogan DX 7/16/03 Right tonsil,SCC T4NOMO. right side neck disection, IMRT Radiation x 33.

Recurrance in June 05 in right tonsil area. Now receiving palliative chemo (Erbitux) starting 3/9/06

Our good friend and loved member of the forum has passed away RIP Dannyboy 7-16-2006
#38378 04-06-2005 11:50 PM
Joined: Nov 2002
Posts: 458
Platinum Member (300+ posts)
Offline
Platinum Member (300+ posts)

Joined: Nov 2002
Posts: 458
Danny (Texas) glad to hear the good news, have the same deal, rather rock hard node under my chin, was going to have it needle biopsied, but after PET/CT and ultrasound they figured out it was just a hard node of some sort and said no bother. That was about a year ago and two more PET/CT's ago, still no change.

Danny Boy, glad to hear you're back playing golf. My sticks are sitting in my office, nice and conventient for that trip to the driving range after work now that my shoulder can move again. Maybe I'll get my handicap back down to 20-25 or so. Never was much of a golfer, enjoyed the heck out of it though.
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.
#38379 04-07-2005 01:12 PM
Joined: Nov 2002
Posts: 3,552
Patient Advocate (old timer, 2000 posts)
Offline
Patient Advocate (old timer, 2000 posts)

Joined: Nov 2002
Posts: 3,552
Hey I'm learning how to play golf too! The CEO is a golfer and we went to the course yesterday and played nine holes. Maybe we can do a golf event at the next reunion. There is definitely life after cancer.

Bob - it looks like I'm going to be in China for two weeks toward the end of May.


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)
#38380 04-08-2005 01:24 PM
Joined: Sep 2002
Posts: 642
"Above & Beyond" Member (500+ posts)
OP Offline
"Above & Beyond" Member (500+ posts)

Joined: Sep 2002
Posts: 642
Guys,
I wrote Danny privately to let him know how happy and proud I was that he is back playing golf. I played today in nice Texas weather. I told my doctor friend that I have played with for 10 years...."let's face it, we will always suck at this game". He said, " yeah, but I will always enjoy it." It is a maddening game, so exasperating, but very addictive and the occasional great shot makes you feel like a million bucks. I am very happy to be back at it again. I just throw 3 or 4 bottles of chocolate Boost in my bag in case I get hungry, keep a lot of bottles or cups of water on hand, and I am almost as good ( or bad ) as pre-cancer.

Take care,
Danny G.


Stage IV Base of Tongue SCC
Diagnosed July 1, 2002, chemo and radiation treatments completed beginning of Sept/02.

Moderated by  Brian Hill 

Link Copied to Clipboard
Top Posters
ChristineB 10,507
davidcpa 8,311
Cheryld 5,260
EzJim 5,260
Brian Hill 4,912
Newest Members
Jina, VintageMel, rahul320, Sean916, Megm37
13,103 Registered Users
Forum Statistics
Forums23
Topics18,168
Posts196,924
Members13,103
Most Online458
Jan 16th, 2020
OCF Awards

Great Nonprofit OCF 2023 Charity Navigator OCF Guidestar Charity OCF

Powered by UBB.threads™ PHP Forum Software 7.7.5