Previous Thread
Next Thread
Print Thread
#99286 07-11-2009 11:42 PM
Joined: Jul 2009
Posts: 453
WendyG Offline OP
"OCF Down Under"
Platinum Member (300+ posts)
OP Offline
"OCF Down Under"
Platinum Member (300+ posts)

Joined: Jul 2009
Posts: 453
Hi everyone. I've searched everywhere for answers to these questions but can't seem to find them so thought you may all be able to help. Steve is complaining of head and neck ache on and off but he believes it's because he's tense. I'm not so sure. He is also getting massive amounts of mucous which is starting to make him have trouble swallowing. This is why he believes he is tense. I have no idea what to think. I know mucous is common with treatment but Steve's treatment doesn't begin until tomorrow so we can't blame the radiation for it. He's had the mucous for months now but up until today it's never been an issue. Normally he could swallow it but now it just seems to be getting know where. He said he swallows but not all of it goes. Any help please?


Wife to Steve 43. DX 5 May 09. T4N2MO SCC tongue, floor of mouth, lymph nodes & jaw bone
No surgery
Teeth removed 06/07/2009
radiation 13/07/2009 x 7wks
chemo 15/07/2009 x 3 Cisplatin
last TX 28/08/2009
25/11/2009 PET-lymph node activity.
08/01/2010 CT Scan-ALL CLEAR
03/03/2010-Peg removed
01/2013 left side of Jaw removed and replaced with pectoral flap.
23/12/2020 scan show lesion in tongue
01/2021 SCC stage 3 base of tongue diagnosed
01/03/2021 chemotherapy started.
WendyG #99288 07-12-2009 04:22 AM
Joined: Jun 2009
Posts: 24
Member
Offline
Member

Joined: Jun 2009
Posts: 24
I've had that same issue since before I finished radiation on March 27 of this year. The thick mucus had just parked at the top of my throat. This has been the biggest obstacle to my eating recently because it blocks me from being able to swallow. In fact, today was my very first 24 hour period with no PEG food since finishing tx! (Yipee!) Like Steve, I'd swallow, but it wouldn't move. Couldn't swallow it, couldn't cough it up, couldn't swallow past it. Finally, today, I was able to go a full day without that feeling and I could eat real food. I know it's different for everybody, but for me, it seems to finally be going away. Good luck to Steve tomorrow! Truth is, it'll get worse before it gets better, but it WILL get better, and we will all be here to help both of you through as best we can.


Dana, Male, Age 52, DX 11/08
SCC right tonsil, Stage 3. RND, tonsilectomy, and PEG install done collectively 12/26/08, Cisplatin x3, IMRT x35. Post-TX PET clear 9/09, PEG removed 9/09, PEG stoma surgical repair 9/17/09. Dx renal cell carcinoma 11/09. Partial nephrectomy 01/10.
DanaOx #99290 07-12-2009 04:40 AM
Joined: Jul 2009
Posts: 453
WendyG Offline OP
"OCF Down Under"
Platinum Member (300+ posts)
OP Offline
"OCF Down Under"
Platinum Member (300+ posts)

Joined: Jul 2009
Posts: 453
thanks Dana. Sounds like it's going to be a truly trying time. It's hard already and I expect it will get harder before getting easier as you've said. We will hang in there. I just expected the mucous to start after radiation had begun, not before. So my well planned things to expect list went out the window and I panicked. Just wondering also, does the pain from the tumour reduce as radiation progresses or does he have to deal with that pain as well as the side effects? Thanks again for your help.


Wife to Steve 43. DX 5 May 09. T4N2MO SCC tongue, floor of mouth, lymph nodes & jaw bone
No surgery
Teeth removed 06/07/2009
radiation 13/07/2009 x 7wks
chemo 15/07/2009 x 3 Cisplatin
last TX 28/08/2009
25/11/2009 PET-lymph node activity.
08/01/2010 CT Scan-ALL CLEAR
03/03/2010-Peg removed
01/2013 left side of Jaw removed and replaced with pectoral flap.
23/12/2020 scan show lesion in tongue
01/2021 SCC stage 3 base of tongue diagnosed
01/03/2021 chemotherapy started.
WendyG #99292 07-12-2009 05:28 AM
Joined: Sep 2006
Posts: 8,311
Senior Patient Advocate
Patient Advocate (old timer, 2000 posts)
Offline
Senior Patient Advocate
Patient Advocate (old timer, 2000 posts)

Joined: Sep 2006
Posts: 8,311
Obviously the mucus is not related to the rad that hasn't started so I would talk to his primary care doctor or the dentist that removed his teeth. Dairy products, like milk can cause excessive mucus but surely if this problem has just come on the scene, there must be a logical explanation. That said, I think he needs to get this resolved soon because the rad will cause him enough problems in this dept.

Re his H & N pain. Again talk to his doctors as it may have something to do with his teeth removal and also consider the stress that he's undergoing right now. IMO not enough focus is put on the mental aspect of this or any cancer.


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.
davidcpa #99324 07-13-2009 01:25 AM
Joined: Jul 2009
Posts: 453
WendyG Offline OP
"OCF Down Under"
Platinum Member (300+ posts)
OP Offline
"OCF Down Under"
Platinum Member (300+ posts)

Joined: Jul 2009
Posts: 453
Thanks David. We changed him from oxydone to ordine today and the mucous appears to have disappeared or at least lessened. He went on the oxydone when his teeth came out and the excess mucous really seemed to get full on from that day. So not sure if it is the oxydone or the teeth. We have an appt with dentist tomorrow and then again with our specialist on wednesday. I have a huge list of questions to take with me thanks to everything I'm learning from all of you. It's nice to not feel so alone anymore.


Wife to Steve 43. DX 5 May 09. T4N2MO SCC tongue, floor of mouth, lymph nodes & jaw bone
No surgery
Teeth removed 06/07/2009
radiation 13/07/2009 x 7wks
chemo 15/07/2009 x 3 Cisplatin
last TX 28/08/2009
25/11/2009 PET-lymph node activity.
08/01/2010 CT Scan-ALL CLEAR
03/03/2010-Peg removed
01/2013 left side of Jaw removed and replaced with pectoral flap.
23/12/2020 scan show lesion in tongue
01/2021 SCC stage 3 base of tongue diagnosed
01/03/2021 chemotherapy started.
WendyG #99328 07-13-2009 05:20 AM
Joined: Sep 2006
Posts: 8,311
Senior Patient Advocate
Patient Advocate (old timer, 2000 posts)
Offline
Senior Patient Advocate
Patient Advocate (old timer, 2000 posts)

Joined: Sep 2006
Posts: 8,311

I bet there are quite a few doctors that wish their patients had never come to this site and got an education on this cancer.

Power to the people!! lol


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.
davidcpa #99346 07-13-2009 07:31 AM
Joined: Jul 2007
Posts: 939
"Above & Beyond" Member (500+ posts)
Offline
"Above & Beyond" Member (500+ posts)

Joined: Jul 2007
Posts: 939
Power to the people indeed:

KNOWLEDGE IS POWER...that is why this board/website is so valuable.


Deb..caregiver to husband, age 63 at diagnosis, former smoker who quit in 1997.
DIAGNOSIS: 6/26/07 SCC right tonsil/BOT T4N0M0
TREATMENT START: 8/9/07 cisplatin/taxol X 7..IMRT twice daily X 31.5.
TREATMENT END: 10/1/07
PEG OUT: 1/08
PORT OUT: 4/09
FOLLOWUP: Now only annual exams. ALL CLEAR!

Passed away 1/7/17 RIP Bill
debandbill #99368 07-13-2009 02:21 PM
Joined: Jan 2009
Posts: 1,844
Patient Advocate (1000+ posts)
Offline
Patient Advocate (1000+ posts)

Joined: Jan 2009
Posts: 1,844
lol...my ENT has told me to stay the "f" off the internet before...but at the time I was convinced I had seen leukoplakia on the other side of my mouth and was obsessed. My new PCP worries about that as well with me.


Young Frack, SCC T4N2M0, Cisplatin,35+ rads,ND, RT Mandiblectomy w fibular free flap, facial paralysis, "He who has a "why" to live can bear with almost any "how"." -Nietzche "WARNING" PG-13 due to Sarcasm & WAY too much attitude, interact at your own risk.
EricS #99379 07-13-2009 03:42 PM
Joined: Mar 2002
Posts: 4,918
Likes: 67
OCF Founder
Patient Advocate (old timer, 2000 posts)
Offline
OCF Founder
Patient Advocate (old timer, 2000 posts)

Joined: Mar 2002
Posts: 4,918
Likes: 67
There are some surprisingly bad bits of info about oral cancer on the web. Besides those sites that want you to take some herb or something else, THE NCI AND THE CDC actually have some outdated information on their site about OC, and the ADA, oh my God, they would have you believe that a biopsy brush (sold by someone that gave them 9 million dollars) will prevent you from ever getting oral cancer.

The web is wonderful and dangerous place at the same time depending on what site you are on.....




Brian, stage 4 oral cancer survivor. OCF Founder and Director. The first responsibility of a leader is to define reality. The last is to say thank you. In between, the leader is a servant.

Link Copied to Clipboard
Top Posters
ChristineB 10,507
davidcpa 8,311
Cheryld 5,264
EzJim 5,260
Brian Hill 4,918
Newest Members
Kpwin, Boost iV Miami, dcrowman, Yuka, monkeytoes
13,361 Registered Users
Forum Statistics
Forums23
Topics18,265
Posts197,179
Members13,362
Most Online1,788
Jan 23rd, 2025
OCF Awards

Great Nonprofit OCF 2023 Charity Navigator OCF Guidestar Charity OCF

Powered by UBB.threads™ PHP Forum Software 7.7.5