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#10917 06-12-2007 10:08 AM
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Great News today. My husband has finished his treatment. After 35 radiation and 2 chemo he has completed his treatment plan. The doctor was so excited about the size of his tumour now and what is was like when he first seen it. Prior to treatment the doctor told us it was the largest tumor he had ever seen. (20 + years experience) and he explained this to the other doctor present at the time and who was removing my husbands trach. He felt it was a great accomplishment and he wanted to tell his colleague about his achievement. Follow up in two weeks with the radiation and chemo doctors.
I would like to thank all of you for sharing with me your experiences. I cant begin to tell you all
what this forum has meant to me. It gave me a positive outlook on my husbands illness and an insight in what to expect as we took this incredible horrible devastating treatment. There were times when I could not get home fast enough from visiting my husband at the hospital to ask questions regarding my husbands symptoms. I hope I have helped some of you in trying to answer your questions. Perhaps my only experience will be that of a caregiver. I felt I can share my emotional side of this disease. Thank you all for your prayers. Thank you all for sharing your thoughts and experiences with me. I find this forum and it members go beyond, almost reaching out and saying its OK....We have been there and we know...
what pain both emotionally and physically you will have to endure...Thank you again....Carol..


Carol CG to Husband age 60 Stage IV SCC right tonsil T4AN2B tx rad x 35 chemo x 2 Currently after treatment no sign of cancer in throat. (all clear to date)
#10918 06-12-2007 10:57 AM
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Carol, I am SO PLEASED for you both. It's an incredible stuggle, and there is still a ways to go for you both. Just remember, we're still here. If you hurt, or need...call out!
Wayne


SCC left mandible TIVN0M0 40% of jaw removed, rebuilt using fibula, titanium and tissue from forearm.June 06. 30 IMRT Aug.-Oct. 06
#10919 06-12-2007 11:29 AM
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Carol-

Congrats to you BOTH, you have both made it thru a huge storm. As Wayne said, there is still a ways to go. The pain, depression, etc actually kicked in AFTER therapy was done. Remember, the rad stays in the body for approx 6 weeks after tx. I am not trying to rain on your parade AT ALL--I just wanted to let you know. The good part is, now he can sleep & you 2 can be together (I'm assuming) and you know there is light at the end. Great job-I hope all stays well!


SCC-tongueT3N0M0- IMRT 35times-1/07-3/07; along with one cycle of Cisplat & one cycle of Carboplat; weekly erbitux.finished all tx.3/07-supposedly gone. Recurrence 6/07. Age 31-non-smoker/social drinker. Devastated it's back.
#10920 06-12-2007 12:15 PM
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Jordan, my husband is having a terrible time sleeping. He cant sleep in his bed. He sleeps on a loveseat sitting up. He saids he has to wake up every hour because of the dry mouth and spitting up mucous. The pain is quite severe. He has lots of medication, ointment etc. for pain and dry mouth. He has a feed tube but as stated he had the trach removed today. Thank you for your reply... hope all is well with you.
Carol Ann.


Carol CG to Husband age 60 Stage IV SCC right tonsil T4AN2B tx rad x 35 chemo x 2 Currently after treatment no sign of cancer in throat. (all clear to date)
#10921 06-12-2007 01:07 PM
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Glad your treatments are over. Ditto to all the above. My husband is still not sleeping in bed cause we have a water bed and he said is to hard for him to get out of cause of his peg tube and laying flat is just not comfortable. He has been in his recliner or on the couch. You are correct in saying this forum is a God send. Please know I am praying for you both.


CG to husband 53,39 rads. 3 rds cisplastin ended 6/2/07 Tonsils removed 1.10.07 11 of 20 nodes positive- lump removed on rt. side of neck 1/26/07 cancer of nasal pharnyx TXN2MX 2nd rd. of chemo- carbo/taxol on 6/11/07
#10922 06-12-2007 05:08 PM
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Carol Ann-

Does your husband take anything for sleep? I wasn't too troubled with mucous at night but I had pain that would keep me awake. I started on Ambien and it has been a huge help. This is so hard to go thru and even harder when we're tired. So, look into that. Ambien lasts about 5-6 hours and Ambien CR lasts 7-8 hours. Hope it works for him as it did for me. That can make for long nights.


SCC-tongueT3N0M0- IMRT 35times-1/07-3/07; along with one cycle of Cisplat & one cycle of Carboplat; weekly erbitux.finished all tx.3/07-supposedly gone. Recurrence 6/07. Age 31-non-smoker/social drinker. Devastated it's back.
#10923 06-12-2007 08:48 PM
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Hi Carol

well thats the first major struggle done with and the daily hospital and treatment routine is over.Like Jordan i just want to whisper a little word of caution because the euphoria of finishing often has a sting in its tail so dont get caught unawares.
Congratulations and all the very best to you both.


Liz in the UK

Husband Robin aged 44 years Dx 8th Dec 2006 poorly differentiated SCC tongue with met to neck T1N2cM0 Surgery and Radiation.Finished TX April 2007
Recurrence June/07 died July 29th/07.

Never take your eye off the ball, it may just smack you in the mouth.
#10924 06-13-2007 03:27 AM
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Carol,

Finishing the rad Txs is definitely a milestone to celebrate but if he's like many of us the next 2 to 3 weeks will be his worst so tell him to stay on top of the water and food and he'll finally walk out of that tunnel in no time.


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.
#10925 06-13-2007 08:07 AM
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Not even started treatments yet, but have had loads of pain and sleep problems with tumour pressing on nerve and following biopsy.
When in CA at Easter I discovered AdvilPM which has helped enormously with my sleeping and docs here say it's okay! Probably milder than your hubby needs, but believe me, they've worked for me when been in SERIOUS pain!
Brenda


Brenda in UK--Diagnosis 30/5/07--undifferentiated carcinoma in right jawbone and muscles. Stage 4
6/7/07--new diagnosis primary is in lung. Finished 4cycles of palliative carboplatin/gemcitabine
therapy September 07
Now dying to live!
#10926 06-13-2007 12:25 PM
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Hi Carol

That is Great News! I am so happy for you two. I am wishing you continued progress and will keep you in my prayers.

I feel that you are a part of this forum. A caregiver is 1/2 the equation. You have so much valuable knowledge now.

Always check in now and then after this is a non-issue for you. You could be that one voice that will give hope and inspiration to a person just starting or at any point of their journey.

Wishing you the Best. Petey smile


DX 3-21-07 L tongue,SCC Stage IV (T3N2MO) TX Slash/Burn/Poison Method.
***Rapid Aggressive Recurrence 8-4-07 with same DX/TX. Life does not cease to be funny when people die any more than it ceases to be serious when people laugh. Never Give Up! ****UPDATE**** Our dear friend Petey passed away, RIP 9-2-07
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