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#24021 08-12-2007 05:31 AM
Joined: Aug 2007
Posts: 7
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Joined: Aug 2007
Posts: 7
A couple of days ago I introduced myself on the ACOR reflector . It was suggested to me that my story might help others on this board, so here I am!

My name is Bob. I was diagnosed on Nov. 30, 2006 with stage 3 SCC (T2 N1 M0) with a left tonsil primary. The mass was ~ 3.5cm at its widest, and the cancer had spread to the adjacent lymph node (thus the stage 3 diagnosis). I should note that I am the youngest of 3 boys, and that every male member of my family has had cancer. I had three rounds of chemo (5 drugs) for a total of 9 weeks. I then had 5 weeks "off" while I took care of dental issues... had a tooth with cracked filling capped, had all four wisdom teeth extracted (they were expected to be in the radiation field and cause problems later), and a complete dental cleaning, etc. Radiation was 35 IMRT treatments with concurrent additional (though milder) chemo. Four days out of five, I would get IV hydration and an Amifostine injection... then hike across the street to the Cancer Center for radiation. On the 5th day (I picked Thursday) I got Carboplatin and Erbitux (but no Amifostine), then the IMRT.

Yesterday (AUG 10) was the 3 month anniversary since ending treatments, and next Wednesday (AUG 15) is my first follow-up visit (5 weeks) with my oncologist since being declared CANCER FREE.

I joined a telephone support group for HNC patients, and so far have counseled one guy with almost the exact same diagnosis.

I'll read the postings here with great interest. If I can offer something constructive, I will. Otherwise, I'll just lurk. wink If anyone has questions of me, dont hesitate to ask (in the forum or via PM, as appropriate).

-Bob


Stage 3 SCC survivor, left tonsil primary (T2 N1 M0)
Joined: May 2007
Posts: 622
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Joined: May 2007
Posts: 622
Hi Bob

Glad to have ya here

Welcome!

Kevin


18 YEAR SURVIVOR
SCC Tongue (T3N0M0) diag 06/2006.
No evidence of disease 2010
Another PET 12-2014 pre-HBO, still N.E.D.


�Remember to look up at the stars and not down at your feet. It matters that you don't just give up.�
Stephen Hawking
Joined: Jun 2007
Posts: 510
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Wow, Bob! What an inspiration you are! You give all of us something to look forward to. I'm sure there are many here who will keep you busy answering their questions.
Welcome to OCF...I look forward to reading your responses! Lois & Buzz in NC


CG to 77 y/o hubby;SCC Alveolar Ridge; Wake Forest Baptist Hosp surgery: 07/19/07; bi mod radical resection/jaw replacement;
T2 N2-B M0 Stage IV-A
28 IMRT +
6 Paclitaxel/Carboplatin
Getting stronger every day!
Joined: Apr 2006
Posts: 583
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Posts: 583
Hi Bob,

Welcome... and Congratulations on making it through...

Hope your first visit back for check up will be OK. I am sure it will, but it is still nice to hear.

Take care,
Diane..


2004 SCC R.tip 1/4 tongue Oct. 2005 R. Neck SCC cancer/Chemo Cisplatin 2x/8wks. Rad. Removed Jugular vein, Lymph gland & some neck muscle. TX finished 1/20/06... B.Cancer 3/29/07 Finished 6/07 Bi-op 7/15/09 SCC in-situ, laser surgery removed from 1st. sight. Right jaw replacement 11/3/14. 9 yrs cancer free as of Jan. 2015
Joined: Feb 2007
Posts: 1,940
"OCF across the pond"
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"OCF across the pond"
Patient Advocate (1000+ posts)

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Posts: 1,940
Welcome Bob

nice to see a sucess story i am sure your experience will provide valuable support for all the other "newbies " who join us every day.

Liz


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.

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