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Joined: Feb 2011
Posts: 45
hurlock Offline OP
Contributing Member (25+ posts)
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Contributing Member (25+ posts)

Joined: Feb 2011
Posts: 45
I just finished 6 weeks Tomo radiation cancer of the larynx. I was doing great through 5 weeks but the last week really got to me. I can't believe 347 seconds of daily radiation can make me this tired. After 2 hours doing anything I feel like I need a nap. I had vocal cord webbing from past surgeries before the radiation and my voice was pretty compromised then, Now it is worse...
Doctors said I should feel better in two weeks but from what I am reading and feeling I can't imagine much improvementSimilar symptoms of coughing up large white mucus, sore throat (BUT I CAN SWALLOW) as most experience.I am wondering now if I did the right thing. An article I read said that killing the cancer and preserving the larynx should be primary but if the larynx becomes non-functional then I should seek alternatives.
Should I just wait? Should I try to seek speech therapy at this early date? I really can't wait 2 years to see if voice will return with some clearity. Sorry for the downer mood but I need some good advice. Thanks Steve Hurlock


SCC of larynx,2/1/2011 surgery 16 times to remove papilloma on vocal cords,started TOMO rad treatment 4/11.2011 T2N0M0 possible invasion onto cartilage tissue Cancer back 6/2012. Polyp removed Came back spindle cell carcenoma 6/22/12
Joined: Nov 2010
Posts: 167
Senior Member (100+ posts)
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Senior Member (100+ posts)

Joined: Nov 2010
Posts: 167
Hi Steve - I know you probably don't feel in a congratulatory mood but I'm going to congratulate you anyways for getting through treatment. It is a huge accomplishment! I can appreciate your question "Now what?" I felt the same way. The fatigue is normal, the voice issues are normal. That being said, the sooner you begin working with a speech therapist, the better. It's WAAAAAY to soon to even think about your larynx being non-functional!
So my answer to your question is: do things that feel good, even if it is for short periods of time and begin voice rehab!
Take care!


Jennifer (39)
02/10 SCCa Tongue & Base, HPV-
03/10 Partial Glossectomy & ND 11/10 Revision due to additional nodes 12/20-2/2/11 IMRT & concommitant chemo 2/11 PEG in 3/11 PEG out
Back at work and feeling good 03/24/11!
12/20/11 - 9 month f/u PET/CT - all clear!
Joined: Nov 2006
Posts: 2,671
Patient Advocate (old timer, 2000 posts)
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Patient Advocate (old timer, 2000 posts)

Joined: Nov 2006
Posts: 2,671
Steve - that "Now what?" stage happens to many of us right after Tx ends and you have to get used to a new unfamiliar routine and away from the old routine that you kind of got used to. As a caregiver, I definitely got that unnerving "What Now?" feeling, too - but another couple or three weeks and things should definitely look up. Being really tired is part of it. My son slept most of the time and so much so, that at times I would go into his room and hold a mirror to his mouth just to make sure he was still breathing! You have just completed an important milestone in your recovery and that is certainly something to feel good about. You can look forward to better days ahead!


Anne-Marie
CG to son, Paul (age 33, non-smoker) SCC Stage 2, Surgery 9/21/06, 1/6 tongue Rt.side removed, +48 lymph nodes neck. IMRTx28 completed 12/19/06. CT scan 7/8/10 Cancer-free! ("spot" on lung from scar tissue related to Pneumonia.)



Joined: May 2002
Posts: 2,152
Patient Advocate (old timer, 2000 posts)
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Patient Advocate (old timer, 2000 posts)

Joined: May 2002
Posts: 2,152
We all had trouble talking after radiation for a few weeks and ours wasn't directed AT the larynx. Give your voice a break for a couple of weeks and give it time to heal.

Also fatigue is common. You've been through a lot. Take those naps but also try to get outside in the fresh air and take some walks or do a little gardening. Light execise helps the fatigue.

I think you are doing great and wish I had had the chance to save my larnynx. I'm sure you will be too.

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: Jan 2011
Posts: 168
Senior Member (100+ posts)
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Senior Member (100+ posts)

Joined: Jan 2011
Posts: 168
Hi Steve: I am just a little ahead of you, (nine weeks post-treatment). I think I understand what you are going through. People on this site told me to be patient, that I will get better, stronger after treatment, but that it takes time. I didn't believe them; I felt so awful, but they were right. You will improve, too, slowly. One woman told me she stayed in bed practically the first month. I used to think of that comment when I felt so tired I couldn't lift my head off the pillow. For me, recovery was worse than any part of my journey: worse than surgery, worse than the actual radiation, and even worse than chemo. I kept thinking I should feel better and I wanted my regular life back so much. You will get through this. We all do; I am still in recovery, still using the feeding tube and not working full time, but each week brings progress. That's another thing someone told me: count progress by the weeks, not the days. Stay in touch. You can do this. We are here for you. -Michelle


SCC left tonsil, stage IV, HPV+, metastatic to one lymph node. Biopsy 12/23/10; tonsillectomy 1/13/11; DX 1/25/11; Peg in 1/28/11. Peg out 6/29. TX 1/31/11-3/21/11: 35 IMRT plus 3 Cisplatin. Pet-Scan 6/20/11 = CLEAR! Three years out, learning to live with the long-term side effects of radiation while reminding myself to feel blessed.

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