Previous Thread
Next Thread
Print Thread
#29323 09-03-2007 05:20 AM
Joined: Feb 2007
Posts: 20
Member
OP Offline
Member

Joined: Feb 2007
Posts: 20
Hi. My husband had his first (5 months) post IMRT CAT scan. We haven't actually seen the report yet, but the feedback his primary care physician was able to get over the phone was something like: not positive, but follow up is recommended. The report is still on its way to his ENT/oncologist. I know we just need to do the follow up, and it could take a week or two. I also know that "inconclusive" spans anything from scar tissue to a recurrence. Any words of encouragement to get thru the next 2 weeks?


2006 tongue T2/N1; hemiglossectamy + MRND +32X IMRT
2010 "cured"
6/ 2016 recurrence right tongue T1/N0 perineural invasion 9/2016 3X carboplatin/taxotere
#29324 09-03-2007 07:12 PM
Joined: Jul 2007
Posts: 9
Member
Offline
Member

Joined: Jul 2007
Posts: 9
Hi, Never think the worse, always try to be positive. I know that is difficult, waiting is actually the worse time I know. I also learned that positive thoughts do help.
I keep you in my prayers

#29325 09-06-2007 03:45 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
My first years worth of MRI's sucked so don't expect a clean MRI for a while. They will exhaustively check every detail. Scans are only a small part of the diagnostic follow up.


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)
#29326 09-06-2007 07:21 PM
Joined: Feb 2007
Posts: 1,940
"OCF across the pond"
Patient Advocate (1000+ posts)
Offline
"OCF across the pond"
Patient Advocate (1000+ posts)

Joined: Feb 2007
Posts: 1,940
I often wondered why after his treatment had finished that all Robin had in the way of follow up was a cursuory physical exam by the head and neck clinic ,that consisited of physical examination of his neck scar,four weeks later.
This was then followed by another four week check up lasting a few minutes and ending with the words " so far so good"
The thought that all that time the tumour in his jaw and mouth was still growing at an alarming rate and had not been eradicated by the aggressive radiation treatment is horrifying.but how would they know without scans or x- rays?These were not even considered an option until after the tumour had burst through his face by which time it wasnt necessary as you could see the damn thing with the naked eye.
Too late.

Surely a false positive or a few days worry about inconclusive results is better than blissful ignorance and then the devestation of terminal recurrance that has been overlooked or just plain missed.


Liz in the UK

Husband Robin aged 44 years Dx 8th Dec 2006 poorly differentiated SCC tongue with met to neck T1N2cM0 Surgery and Radiation.Finished TX April 2007
Recurrence June/07 died July 29th/07.

Never take your eye off the ball, it may just smack you in the mouth.
#29327 09-07-2007 03:26 AM
Joined: Jul 2007
Posts: 939
"Above & Beyond" Member (500+ posts)
Offline
"Above & Beyond" Member (500+ posts)

Joined: Jul 2007
Posts: 939
Liz,

I know that this is haunting you and I am so sorry. I live every day with the worry that we aren't doing enough or making the right treatment decisions. I can't imagine, when you have a negative outcome like Robins, what your demons are, but I say a little prayer that you can find peace at some level.

I do know that you can fight this with what you are doing...posting your experiences will help us all make better decision and be more militant in our quest for a cure. You can only do what you know to do. When you gain knowledge, you gain power!

Sending you a hug today, Deb


Deb..caregiver to husband, age 63 at diagnosis, former smoker who quit in 1997.
DIAGNOSIS: 6/26/07 SCC right tonsil/BOT T4N0M0
TREATMENT START: 8/9/07 cisplatin/taxol X 7..IMRT twice daily X 31.5.
TREATMENT END: 10/1/07
PEG OUT: 1/08
PORT OUT: 4/09
FOLLOWUP: Now only annual exams. ALL CLEAR!

Passed away 1/7/17 RIP Bill
#29328 09-08-2007 12:54 PM
Joined: Feb 2007
Posts: 20
Member
OP Offline
Member

Joined: Feb 2007
Posts: 20
Thanks to all for your support. Greg personally retrieved the report and Fed-Exed it to his oncologist last Wed. Our (uneducated) reading of the report makes us think it is just scar tissue on his tongue. His neck, which is what we were most worried about, was completely clear. We should hear from the oncologist this week.


2006 tongue T2/N1; hemiglossectamy + MRND +32X IMRT
2010 "cured"
6/ 2016 recurrence right tongue T1/N0 perineural invasion 9/2016 3X carboplatin/taxotere

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
iMarc845, amndcllns01, Jina, VintageMel, rahul320
13,105 Registered Users
Forum Statistics
Forums23
Topics18,170
Posts196,933
Members13,105
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