Previous Thread
Next Thread
Print Thread
Page 1 of 2 1 2
Joined: Jun 2008
Posts: 3
JudyC Offline OP
Member
OP Offline
Member

Joined: Jun 2008
Posts: 3
Does anyone out there have severe sore throat issues still lingering after radical neck dissection and radiation and feel like they are swallowing a lump all the time ---pain constant inside of throat and pain exterior from lower ear to mid jaw line to shoulder--inside and outside of throat? He is hoarse when he wakes up and throat hurts more and more throughout the day. Docs have done camera scans, swallowing tests, Xrays but it shows nothing. The severe pain is compromising his life but still he does do not wish to take any pain meds as they compromise life too.
Does anyone else experience this and have you found any relief? He has just undergone accupuncture for 4 weeks but no help. The more pain he feels, the more he gets scared.
Any and all suggestions are appreciated!
Anyone use lidocaine patches? Neurontin? Judy

Joined: Jun 2005
Posts: 349
Likes: 2
Platinum Member (300+ posts)
Offline
Platinum Member (300+ posts)

Joined: Jun 2005
Posts: 349
Likes: 2
I can tell you from personal experience that the fear can be crippling, even though he IS 4 years out! (congrats on that by the way).

Pain of any kind is miserable, but chronic, ongoing, invisible pain can be especially troublesome.

Does he followup with his surgeon who may shed some light on the muscular makeup of his throat, etc and offer some suggestions?

I've used both the patches and the Neurontin. Both make me feel "cotton head" and I don't like the sensation.

Plus, medication is rarely a long term pain management solution. The acupuncture idea is a great start. He may need to see a different acupuncture specialist, or change the routine, sequence, etc.

Guided meditation and/or some light hypnotherapy is well worth trying too (in my opinion).

I also think herbal remedies are worth considering, and an herbalist/naturopath may be able to make some good suggestions.

I too have "constant" pain in some areas, and I notice it's worse when I am stressed and fatigued.

Maybe reducing stress and exhaustion are good ideas anyway?

I think the fear component is likely compounding an already painful situation, so being vigilant with Dr followup and being pro-active with the Drs may help somewhat.

I can recommend a topical product called Topricin. It has been a miracle for me and many of my spa guests with pain that is not too far into the body. Seems like superficial muscle and joint pains can be significantly impacted by this product, especially arthritic type pains. Might be worth a shot. Most health food stores carry this, and a quick google search will produce lots of results.

One other anecdotal item, I noticed my pains decreased considerably after getting a wireless headset for my office phone.

I was having SEVERE pain and discomfort in my Scapula area the first several months to a year + after tx. I started using a cordless headset which seems to help.

:-)


Michael | 53 | SCC | Right Tonsil | Dx'd: 06-10-05 | STAGE IV, T3N2bM0 | 3 Nodes R Side | MRND & Tonsillectomy 06/29/05 Dr Fee/Stanford | 8 wks Rad/Chemo startd August 15th @ MSKCC, NY | Tx Ended: 09-27-05 | Cancer free at 16+ Yrs | After-Effects of Tx: Thyroid function is 0, ok salivary function, tinnitus, some scars, neck/face asymmetry, gastric reflux. 2017 dysphagia, L Carotid stent / 2019, R Carotid occluded not eligible for stent.2022 dental issues, possible ORN, memory/recall challenges.
Joined: Jun 2005
Posts: 349
Likes: 2
Platinum Member (300+ posts)
Offline
Platinum Member (300+ posts)

Joined: Jun 2005
Posts: 349
Likes: 2
PS: Also, I noticed that my throat hurts more (inside), the more dehydrated I let myself get, so constant rehydration might be a good idea too.

sorry if my comments down play the severity by suggesting such seemingly insignificant ideas...I just wanted to throw out some non-conventional ideas since you'll have plenty of the conventional kind.


Michael | 53 | SCC | Right Tonsil | Dx'd: 06-10-05 | STAGE IV, T3N2bM0 | 3 Nodes R Side | MRND & Tonsillectomy 06/29/05 Dr Fee/Stanford | 8 wks Rad/Chemo startd August 15th @ MSKCC, NY | Tx Ended: 09-27-05 | Cancer free at 16+ Yrs | After-Effects of Tx: Thyroid function is 0, ok salivary function, tinnitus, some scars, neck/face asymmetry, gastric reflux. 2017 dysphagia, L Carotid stent / 2019, R Carotid occluded not eligible for stent.2022 dental issues, possible ORN, memory/recall challenges.
Joined: Jun 2007
Posts: 10,507
Likes: 7
Administrator, Director of Patient Support Services
Patient Advocate (old timer, 2000 posts)
Offline
Administrator, Director of Patient Support Services
Patient Advocate (old timer, 2000 posts)

Joined: Jun 2007
Posts: 10,507
Likes: 7

Judy

Welcome to OCF and congrats on your husbands 4 year mark!!!!!

Many OC survivors have late effect side effects from rad/chemo/surgery. Its just part of the whole cancer experience, some have it others dont. While I do not have first hand experience with the procedures that your husband has encountered, I do know about the long lasting side effects which can carry on for years. When in doubt, check with the doctor. Sorry I wasnt more helpful.


Christine
SCC 6/15/07 L chk & by L molar both Stag I, age44
2x cispltn-35 IMRT end 9/27/07
-65 lbs in 2 mo, no caregvr
Clear PET 1/08
4/4/08 recur L chk Stag I
surg 4/16/08 clr marg
215 HBO dives
3/09 teeth out, trismus
7/2/09 recur, Stg IV
8/24/09 trach, ND, mandiblctmy
3wks medicly inducd coma
2 mo xtended hospital stay, ICU & burn unit
PICC line IV antibx 8 mo
10/4/10, 2/14/11 reconst surg
OC 3x in 3 years
very happy to be alive smile
Joined: Sep 2007
Posts: 20
Member
Offline
Member

Joined: Sep 2007
Posts: 20
I am 18 months post treatment and still suffer from throat pain which seems to worsen as the day goes on. The pain actually seems to radiate into my head/ears from my throat when I do a lot of talking. My MO says that the effects of Radiation and Chemo can take years before some people reach maximum improvement. I have just completed having a MRI of the brain and another Pet Scan of my body, both of which were totally normal. The brain scan was done due to my complaining about having dull headaches which were really beginning to stress me out as I had convinced myself that I was suffering from brain cancer. I think all of the stress associated with worrying about my symtoms further causes and contributes to my having headaches. So, its kinda like trying to figure out which came first...the chicken or the egg? My ENT Surgeon who I think is really very smart and knowledgeable had told me months ago when I complained to her about all my side effects and I asked if she had "any suggestions of what I could do?" said "yes, I have a suggestion for you, stop your whinning and suck it up!" So, maybe this is the price some of us have to pay to be cancer free. I think its just hard to accept that life ain't what it use to be after treatment.


SCC Base of Tongue
Stage IV T2N2bM0
IMRTx32, Cisplatin x3
Diagnosed 1/25/07
Treatment Completed 4/20/07
Scans all good as of October,2011
Joined: Jun 2008
Posts: 3
JudyC Offline OP
Member
OP Offline
Member

Joined: Jun 2008
Posts: 3
Thank you all--please everyone keep your suggestions and thoughts coming. It helps him to read that others experience some of his same symptoms---not good for all of you but he doesn't feel he is so alone and psychosomatic with pain. Judy

Joined: Sep 2008
Posts: 250
Platinum Member (200+ posts)
Offline
Platinum Member (200+ posts)

Joined: Sep 2008
Posts: 250
Judy,

Nothing psychosomatic about all this, as you know! Who needs pretend when you've got the real thing. I know how he feels, though. Until I found this site last month I had the same thoughts.

You know, years ago my husband said that I had a low threshhold for pain. I actually believed him. After all, he knows everything. Then, while he was writhing in pain from something I considered fairly small, it occurred to me that he couldn't possibly have any way to judge my level of pain. He has never mentioned it again - especially since my battle with OC began 3 years ago.

Lani



SCC part glossectomy 3/06, recur 8/06 glossectomy, floor of mouth, part of jaw removed, RT/chemo thru 10/12/06, PET clear 7/08
"A bend in the road is not the end of the road, unless you fail to make the turn"
Passed away 12/14/08
Joined: Oct 2007
Posts: 71
Supporting Member (50+ posts)
Offline
Supporting Member (50+ posts)

Joined: Oct 2007
Posts: 71
I would suggest a second opinion if you haven't already done so. Everyone is so different but 4 yrs seems like along time to have severe pain. I am 1 yr out of surgery and have moderate jaw pain. My ENT tells me that everyone is different so time will tell what is instore for me. I hope that he will some comfort.

Steven, I can so relate to what your ENT said. My ENT also told me to suck it up and get on with your life. I guess people live with pain everyday from different situations. But it is nice to have this site to refer to and get support. We all somewhat understand what one another is going through.


Tammy 43 yr non smoker- Dx-10/11/07 Stage 4 Tongue Cancer Surg.10/17/07, 1/4 Tongue and 14 Lymph nodes 5 positive, Peg tube/Chemo port,Chemo 3 wks/Radiation 6 wks begins 11/07 end 02/08.Teeth removed prior to radiation. PetScan 05/08 CLEAR 09/09. 2011 diag. w/osteoradionecrosis.100 HBO's
Joined: Jun 2007
Posts: 10,507
Likes: 7
Administrator, Director of Patient Support Services
Patient Advocate (old timer, 2000 posts)
Offline
Administrator, Director of Patient Support Services
Patient Advocate (old timer, 2000 posts)

Joined: Jun 2007
Posts: 10,507
Likes: 7

One thing that helped me to heal and eliminated my jaw pain was hyperbaric oxygen treatments (HBO). After about 3 visists, my jaw pain which had been constant and severe started to get better. By the time I had done 10, the jaw pain was completely gone and has not come back. If you do a search about HBO then you will find some lengthy posts about it here and also articles about it on the main OCF site. I think the post is under After treatment issues.


Christine
SCC 6/15/07 L chk & by L molar both Stag I, age44
2x cispltn-35 IMRT end 9/27/07
-65 lbs in 2 mo, no caregvr
Clear PET 1/08
4/4/08 recur L chk Stag I
surg 4/16/08 clr marg
215 HBO dives
3/09 teeth out, trismus
7/2/09 recur, Stg IV
8/24/09 trach, ND, mandiblctmy
3wks medicly inducd coma
2 mo xtended hospital stay, ICU & burn unit
PICC line IV antibx 8 mo
10/4/10, 2/14/11 reconst surg
OC 3x in 3 years
very happy to be alive smile
Joined: Jun 2008
Posts: 3
JudyC Offline OP
Member
OP Offline
Member

Joined: Jun 2008
Posts: 3
Hey everyone-------- We went to an Orthopaedic Dr. about Lou's pain in shoulder from all the surgery of the neck dissection-he put Lou on Lyrica-------and he went from a 9 pain level 24/7 and is at a 2. Miracle! Please tell everyone how well this has worked for him. We discussed Neurontin and it has more side affects than this one. So far, we have no side affects other than PAIN RELIEF!
Judy

Page 1 of 2 1 2

Moderated by  Eva Grayzel 

Link Copied to Clipboard
Top Posters
ChristineB 10,507
davidcpa 8,311
Cheryld 5,260
EzJim 5,260
Brian Hill 4,912
Newest Members
amndcllns01, Jina, VintageMel, rahul320, Sean916
13,104 Registered Users
Forum Statistics
Forums23
Topics18,168
Posts196,927
Members13,104
Most Online458
Jan 16th, 2020
OCF Awards

Great Nonprofit OCF 2023 Charity Navigator OCF Guidestar Charity OCF

Powered by UBB.threads™ PHP Forum Software 7.7.5