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Joined: May 2002
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That's one dentist's opinion. I don't think anyone on this board uses them all night or much longer than 30 minutes.

Take care,
Eileen


----------------------
Aug 1997 unknown primary, Stage III
mets to 1 lymph node in neck; rt ND, 36 XRT rad
Aug 2001 tiny tumor on larynx, Stage I total laryngectomy; left ND
June 5, 2010 dx early stage breast cancer
June 9, 2011 SCC 1.5 cm hypo pharynx, 70% P-16 positive, no mets, Stage I
Joined: Jul 2008
Posts: 507
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I can't keep mine in more than about 10 minutes. They make me gag (tray nausea)!



Don
TXN2bM0 Stage IVa SCC-Occult Primary
FNA 6/6/08-SCC in node<2cm
PET/CT 6/19/08-SCC in 2nd node<1cm
HiRes CT 6/21/08
Exploratory,Tonsillectomy(benign),Right SND 6/23/08
PEG 7/3/08-11/6/08
35 TomoTherapy 7/16/08-9/04/08 No Chemo
Clear PET/CT 11/15/08, 5/15/09, 5/28/10, 7/8/11

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Like David, I put them in for a full half hour. I've tried leaving them in all night, but I wound up ingesting most of the fluoride, which is not good. If I am grinding my teeth (Happens occasionally), then I wear them all night *after* rinsing them out.


Age 67 1/2
Ventral Tongue SCC T2N0M0G1 10/05
Anterior Tongue SCC T2N0M0G2 6/08
Base of Tongue SCC T2N0M0G2 12/08
Three partial glossectomy (10/05,11/05,6/08), PEG, 37 XRT 66.6 Gy 1/06
Neck dissection, trach, PEG & forearm free flap (6/08)
Total glossectomy, trach, PEG & thigh free flap (12/08)
On August 21, 2010 at 9:20 am, Pete went off to play with the ratties in the sky.
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No one has really talked about how often to use the trays.

My dentist (oncology patient specialist) has advised they need to be used twice per day. This is consistent with other information I have found on the internet that suggests that the flouride is more effective if used twice per day.

Anyway, that nothwithstanding, I usually just leave mine in for 1/2 hour, although I was advised I only need to keep them in for 5 minutes then leave the flouride alone (no water) for the next 25 minutes.

Best wishes,

Chris


SCC left tonsil, 2 lymph nodes, modified radical neck dissection, IMRT (both sides) completed 10/25/06, Erbitux and Cisplatin weekly, Ethyol daily
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That's the same instructions that my husband was given. He has his trays but is not using them until after he is done with treatments and his mouth heals up.
Pat


Crgvr to Husband 55-yrs, surgery to remove cyst-diagnosed as SCC, 4/3/09 CT & Pet Scan showed more cancer in left lymph node and primary at the base of the tongue.TX Radiation 7 weeks 5 days a week last day is 6/25/09
Chemo completed 6/19/09
Peg Tube 5/22/09
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Pat,

Encourage him to listen to what his Doctors say, not what he thinks his best for him.


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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I wish my husband could wear his trays. His mouth is so full of sores. He hates magic mouthwash says it makes him sick. Aney other ideas? I beg him to eat yogurt. Got 4 teaspoons in him today. Any ideas or brand names of Yogurt for a non eating yogurt eater?


dx 04/09 BOT Stage 4b, scc, met to leison 6th cervical spine, May 15th, 2009, 12 rounds rt to spine. no relief for pain, top of back and right arm. started 38 rounds of rt and Carboplatin and Erbitux June 2 once a week at least while receiving RT, RT daily. Port and peg.
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I found during radiation that inserting and removing the trays was making me gag, so I just brushed with the paste/gel. Better than nothing, if he can handle that.


Age 67 1/2
Ventral Tongue SCC T2N0M0G1 10/05
Anterior Tongue SCC T2N0M0G2 6/08
Base of Tongue SCC T2N0M0G2 12/08
Three partial glossectomy (10/05,11/05,6/08), PEG, 37 XRT 66.6 Gy 1/06
Neck dissection, trach, PEG & forearm free flap (6/08)
Total glossectomy, trach, PEG & thigh free flap (12/08)
On August 21, 2010 at 9:20 am, Pete went off to play with the ratties in the sky.
Joined: Jun 2007
Posts: 718
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I feel like my husband is the only one who didn't get flouride trays...should that worry me?

His dentist told him to brush daily with flouride instead of toothpaste and he does. For those of you who are through treatment...do you still use your trays?


Margaret
----------
C/G: Husband, 48 (at time of dx)
Dx 5/18/07 SCC, BOT, lymph node involvement. T1N2BM0. (Stage 4a, G2/3)
Tx 6/18 - 8/3/07, IMRT x 33 Cisplatin x3 (stopped after 1st dose due to hearing issues). Weekly Erbitux started 6/27/07 completed 8/6/07.
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He can also put some on his finger and just swipe his teeth. I can't tell by your signature line, but is he having rad presently? I started wearing my trays one month pre Tx and there were a few days during Tx that I couldn't so I didn't. No big deal according to my docs. Almost 3 years now and still wearing them.

Also Agent Orange has never been associated with SCC.


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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