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#55816 11-16-2004 09:43 AM
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Terry K Offline OP
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Since completing my radiation and chemo for SQC cancer at the base of my tongue 3 weeks ago, I have recently noticed that I have a continuous humming sound in my ears. The Doctor called it Tinnitus and said it is a possible side effect of the chemo. I had a hearing test done and seem to have also lost my high pitch hearing as well. Unfortunately he said there is nothing that can be done for the humming sound, but they say the high pitch hearing problem may be corrected by a hearing aid. Have any of you experienced this problem and if so did it go away or what did you do about it? Thanks for your comments.


Terry
#55817 11-17-2004 12:20 AM
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Hi Terry,

I also have constant humming in my ears and my ENT said the same thing, that it is a possible side effect of the chemo (cisplatin) that I had. He, too, said that there is nothing that can be done. I just hit my 1 year mark since completing treatments and the humming is still there. I've sort of gotten use to it except those times when it's really loud. I just wish it would start playing a different tune!

Take care,

Nancy


Stage IV oral cancer (tongue), T3N2, total glossectomy with right and left modified neck dissection 7/03, rad /chemo ended 11/03
#55818 11-17-2004 12:41 AM
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I had my last radation April 28, 2003 and no chemo but I have very hard wax in my ears. They said it is from the radation and I have to go every two to three months to get it cleaned out.
Mary Lee

#55819 11-17-2004 01:30 AM
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Hello everyone, this to is happening to me. I have to go about every 4 months to have my ears FLUSHED. It doesn't really hurt hurt. The side I hade the surgery on hurts the worst. The stuff he gets out is hard dried up blood. It feels good for about 4 days, then it is slowly closing back up. Doc says it may always be this way. Mine is due to the radiation and the fact that my mouth was held open for so long during surgery. Who would have ever thought. It is all these things that no one tells us about. Live and live with it.....you thought I was going to say LEARN. LOL......There is only living with all this.........Always Miss Vicki

#55820 11-17-2004 02:43 AM
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I STILL have the hard wax problem to some extent -- from time to time I can feel the pressure building up and over-the-counter ear drops can't entirely solve the problem. The people at my eye/ear clinic have said I'll just have to keep having it flushed out when it reaches that stage.

Cathy


Tongue SCC (T2M0N0), poorly differentiated, diagnosed 3/89, partial glossectomy and neck dissection 4/89, radiation from early June to late August 1989
#55821 11-17-2004 06:51 AM
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I still have tinnitus to some degree but it's probably from years of being a musician. It was worse after the chemo - especially if you had Cisplatin. It should get better over time. In subsequent hearing tests, my high freqency response actually improved. Ear wax will cut down the HF response.

I saw a cartoon one time that said if you have a constant humming then they will put you in touch with a compulsive toe tapper.


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)
#55822 11-18-2004 11:51 AM
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I notice the ringing in my ears mostly when I can not get to sleep and when I want it really quiet...it just gets louder and louder. It reminds me of locusts when I was growing up in Kansas.

I read once that a standard question asked of people in psychiatric therapy is if they hear a ringing in their ears. Now, I don't know if it is from the Cisplatin or before treatment. What a dilemma. It's one of those things I just keep quiet about when the doctor is asking questions eek

Ed


SCC Stage IV, BOT, T2N2bM0
Cisplatin/5FU x 3, 40 days radiation
Diagnosis 07/21/03 tx completed 10/08/03
Post Radiation Lower Motor Neuron Syndrome 3/08.
Cervical Spinal Stenosis 01/11
Cervical Myelitis 09/12
Thoracic Paraplegia 10/12
Dysautonomia 11/12
Hospice care 09/12-01/13.
COPD 01/14
Intermittent CHF 6/15
Feeding tube NPO 03/16
VFI 12/2016
ORN 12/2017
Cardiac Event 06/2018
Bilateral VFI 01/2021
Thoracotomy Bilobectomy 01/2022
Bilateral VFI 05/2022
Total Laryngectomy 01/2023
#55823 11-18-2004 04:07 PM
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Hi Terry, The tinnitus I have had was for the year prior to my glossectomy and for about 3-4 months afterward, not having had Chemo or Rad I was told that it was from referred pain from tongue base and YES it does get better! I have noticed recurrences but then that may be because there is more cancer in my thyroid?
LOL Ed I dont mention the little people making noises anymore either laugh


01/04 SCC of tongue base, T1N0M0
03/04 Partial glossectomy
04/04 Rad
12/04 Throidectomy(follicular cancer)
#55824 11-21-2004 03:47 PM
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Terry, I have the buzzing also. Had cisplatin and the oncologist said it was due to that. Went to a hearing specialist and was tested and the high end is gone for me as well. The doctor said it was permanent as the ciplatin destoys the functionality of the hair-like things in the ear that enable us to hear. Oh well, part of the "new normal".


Regards, Kirk Georgia
Stage IV, T1N2aM0, right tonsil primary, Tonsilectomy 11/03, 35 rad/3cisplatin chemo, right neck dissection 1/04 - 5/04.
#55825 11-22-2004 01:29 PM
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Terry and Kirk,

My doctor is involved in a study regenerating cochlear hair. Here's hoping all goes well and it can make a difference for those needing it in their new normal. I don't have specifics about the study, but it is listed in his vitae.

Sincerely,
Lisa


Lisa
SCC of Tongue Stage 1 (T1,N0,M0)
partial glossectomy,modified neck dissection 4/14/03
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