#9750 02-26-2007 08:24 AM | Joined: Feb 2007 Posts: 7 Member | OP Member Joined: Feb 2007 Posts: 7 | Hello everyone, I am Rob, and I am new.My Wife was Diagnosed stage 3 hard palate SCC in mid Jan. She has been receiving chemo and radiation 5 times a week. Today they told her that it has progressed to stage 4A and it is now in her left side Lymph nodes and sinuses. I will be talking to the doctor Wednesday, and was wondering if any of you had any advice as to the most important questions to ask at this stage.
Rob
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#9751 02-26-2007 11:39 AM | Joined: Sep 2006 Posts: 8,311 Senior Patient Advocate Patient Advocate (old timer, 2000 posts) | Senior Patient Advocate Patient Advocate (old timer, 2000 posts) Joined: Sep 2006 Posts: 8,311 | Rob,
Please limit your similar questions to one board so we can concentrate our responses. Since you posted the same question to Introduce Yourself, that's where I posted my response.
You will find this site to be of tremendous value.
David
Age 58 at Dx, HPV16+ SCC, Stage IV BOT+2 nodes, non smoker, casual drinker, exercise nut, Cisplatin x 3 & concurrent IMRT x 35,(70 Gy), no surgery, no Peg, Tx at Moffitt over Aug 06. Jun 07, back to riding my bike 100 miles a wk. Now doing 12 Spin classes and 60 outdoor miles per wk. Nov 13 completed Hilly Century ride for Cancer, 104 miles, 1st Place in my age group. Apr 2014 & 15, Spun for 9 straight hrs to raise $$ for YMCA's Livestrong Program. Certified Spin Instructor Jun 2014.
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#9752 02-26-2007 06:24 PM | Joined: Apr 2006 Posts: 794 "Above & Beyond" Member (500+ posts) | "Above & Beyond" Member (500+ posts) Joined: Apr 2006 Posts: 794 | Hi, Rob. I am sorry that you and your wife have to go through this experience. I, too, had SCC on the hard palate as well as the right maxilla. My details and treatment were different from yours, but still I feel a kinship. There are not many people on the forum with SCC of the palate.
I see that you are in Knoxville. One of our contributors, Raymond Cupp, lives in Knoxville and had surgery for SCC of the palate at UT on this past Friday. Not surprisingly, he has not posted since then, but I expect him to post again as soon as he feels better. He might be a good source of information about UT.
I wish you the best. Please keep us posted, and ask anything you wish of anyone on this forum. It is a wonderful place to get information you can't get anywhere else. And it is a place where people understand what you are going through.
Colleen--T-2N0M0 SCC dx'd 12/28/05...Hemi-maxillectomy, partial palatectomy, neck dissection 1/4/06....clear margins, neg. nodes....no radiation, no chemo....Cancer-free at 4 years!
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#9753 02-27-2007 01:18 AM | Joined: Feb 2007 Posts: 7 Member | OP Member Joined: Feb 2007 Posts: 7 | I thought two worms would catch more fish. Sorry for the multiple posting. My wife, Pat, was diagnosed by an Oncologist at Thompson Cancer Center. They have been treating her twice a day. Chemo in the morning and radiation in the afternoon 5 days a week. I am hopefull. The fact that it is now in her lymph nodes scares both of us. They did a blood test to determine if it has spread to her liver yesterday. Results today or tomorrow.
Rob
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