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#38556 05-18-2005 06:30 PM
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Dad starts IMRT on Wednesday (tongue tumor removed 4/27) and saw the dentist day before yesterday. He had 1 cavity filled and a second old filling w/new cavity drilled out with a temporary cap placed on it. Anybody know if it's really a good idea to start rad w/ a temp on or if it's better to wait till tooth is permanently fixed? From all I've read about the importance of healthy mouth, I wonder, but, then again, I wonder about everything lately.


Daughter of 75-yr-old Dad with tongue cancer (T3NOMO) surgery and rt neck dissec 4/27/05; completed 27 X IMRT on 7/01/05; recurrance w/ surgical removal of another SCC tumor on 10/7 (he's also nonHodgkins lymphoma survivor since 1/94)
#38557 05-18-2005 09:37 PM
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It's good that your dad is getting the maintenance done now. I can't really answer the question about the cap however. When does he get the permanent one put on? Have you run this by the radiation oncologist? I take it that he had a dental assessment? Was he fitted for dental trays to do the at home flouride treatments he will need to do?

The radiation effects will start to appear at about 3 weeks - sooner for some.


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)
#38558 05-19-2005 03:40 AM
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Dentist sez he can put the permanent cap on during radiation period if Dad feels well enough, or they can wait until he's done. He sees the RO for the final run through on Tuesday, so we can ask him about his thoughts on it then. He was fitted for the flouride trays Monday and should get them today. His RO said by week three things likely would get rough. It's the same RO who did rad on a non-Hodgkin's tumor on the head in 2001 and another on the back in 2003. Dad just finished chemo (w/Retuxan)in January for non-H tumor in stomach. He was supposed to get his next Retuxan-only treatment in June, but oncologist sez it can wait till he'd done w/ rad for oral. Wondering if all this prior treatment for non-H will make it more likely he'll have problems with rad for the oral cancer. Seems like the hits just keep on coming.


Daughter of 75-yr-old Dad with tongue cancer (T3NOMO) surgery and rt neck dissec 4/27/05; completed 27 X IMRT on 7/01/05; recurrance w/ surgical removal of another SCC tumor on 10/7 (he's also nonHodgkins lymphoma survivor since 1/94)
#38559 05-19-2005 08:31 AM
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I had two temporary caps put on one week before I started my radiation and I had no problems with it at all. Believe it or not, I still have the temp caps on.
Minnie


SCC Left Mandible. Jaw replaced with bone from leg. Neck disection, 37 radiation treatments. Recurrence 8-28-07, stage 2, tongue. One third of tongue removed 10-4-07. 5-23-08 chemo started for tumor behind swallowing passage, Our good friend and much loved OCF member Minnie has been lost to the disease (RIP 10-29-08). We will all miss her greatly.
#38560 05-19-2005 06:37 PM
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I would think that as long as the dental work does not involve bone or blood (as in extractions or work below the gum line) then it will not be a problem getting temporary work done.

As for the effects of radiation, everyone has a personal reaction. Some of us had relatively lower side effects and I have yet to see a common reason for those lower side effects. A stubborn positive attitude helps, as does a strong support system.

Your father will have to brace himself and pace himself. It is a slow and grinding process until he gets his last radiation treatment. Use humor and humility liberally. He can do this.


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.
#38561 05-20-2005 02:37 AM
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Gary, thanks for replying. Wow, Minnie, you know how to make temporary last! The input is good. Helps me to stop fussing about the little things. I'm heading back to Chicago on Sunday and plan to be there for most of the next 8 weeks. Mom's been hanging in there, but needs to get to some medical appointments herself.

Mark, good factual info as always. And poetry, too. Brace and pace. Humor and humility.
I like that. Thanks everybody for being there.
Tina


Daughter of 75-yr-old Dad with tongue cancer (T3NOMO) surgery and rt neck dissec 4/27/05; completed 27 X IMRT on 7/01/05; recurrance w/ surgical removal of another SCC tumor on 10/7 (he's also nonHodgkins lymphoma survivor since 1/94)

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