#54308 01-28-2004 10:15 AM | Joined: Jun 2003 Posts: 41 Contributing Member (25+ posts) | Contributing Member (25+ posts) Joined: Jun 2003 Posts: 41 | Hi Dan, Just wanted to add my own note of support for you. I know that here in NJ the cold has been giving me a bit of troulbe with new aches and stifffness and the like so I can only imagine what it is like further north. I decided a short time ago that I was going to tell my ENT anything that seemed out of the ordinary and not worry about it until he told me to worry about it. For awhile I was anxious about every odd feeling etc. Now I just keep plugging along. I like the term the "new normal." We will not return to what we were like before this journey began but thats ok. I think there is a lot going for the "new normal." Many of us will agree that the way we approach life is different, and the difference is better. I still have everyone in my prayers. Let us know when the docs tell you that there was nothing to worry aobut Peace, Fr. Mike
Fr. Mike SCC on the base of tongue, right side. T2 N1 M0. July 25, 2003 partial (40%) glossectomy, forearm flap reconstruction, right side neck disection.
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#54309 01-28-2004 02:17 PM | Joined: Nov 2002 Posts: 3,552 Patient Advocate (old timer, 2000 posts) | Patient Advocate (old timer, 2000 posts) Joined: Nov 2002 Posts: 3,552 | Hi Dan, It was exactly one year ago today that I started treatment and I am happy to tell you that life can be damn close to what it used to be. In many ways it's even better. And "new normal" to me just means making minor adjustments to the changes in physiology from pre treatment. Some of these things might have occured as a part of the natural aging process anyway. I too, like probably most of us, suffered depression post Tx and lived through that also. It's just part of the process - it'll pass too...
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)
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#54310 01-28-2004 02:31 PM | Joined: Nov 2002 Posts: 458 Platinum Member (300+ posts) | Platinum Member (300+ posts) Joined: Nov 2002 Posts: 458 | Hey Dan,
Just wanted to fire off a note of encouragemet. Seems I've been out of contact, my e-mail service provider took a "vacation" during Chinese New Year, and they should be back in business sometime today or tomorrow. (maybe)
I didn't have to deal with PEG and such, but man, the post treatment depression was something to deal with. At least from chatting with some folks from the board here I knew what it was and was able to cope. Yep, the feeling that "somethings's up" will stay for a while too, last scan I was still as nervous as the first one post treatment.
Guess these feelings of pre-scan fear lessen with time, maybe even the physical post treatment side effects too!! What doesn't help is the cold winter weather. Anyway you would be surprised what activities can cause sore neck muscles, especially if they are on the opposite side of surrgery as we over compensate because of the weakened muscles on the surgery side.
It gets better, really it does. Take care Bob
SCC Tongue, stage IV diagnosed Sept, 2002, 1st radical neck dissection left side in Sept, followed by RAD/Chemo. Discovered spread to right side nodes March 2003, second radical neck dissection April, followed by more RAD/Chemo.
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#54311 01-28-2004 03:25 PM | Joined: Nov 2002 Posts: 541 "Above & Beyond" Member (500+ posts) | "Above & Beyond" Member (500+ posts) Joined: Nov 2002 Posts: 541 | Hi Dan , Bob is right: things can really get better. I choose not to respond to your post earlier because I know very well that with such a wonderful family standing by your side, I am very sure you can overcome your depression with ease. As cancer survivors, we tend to be too greedy if we expect ourselves to resume to the normal life we used to have before cancer.Not realistic! I had been summoned to serve as juror here for three times before I had cancer and I was summoned again three weeks ago. It hurt when I knew very well that I was unfit to be one and so, with my oncologist's certification, I asked for permanent exemption. Something that I could do with ease in the past can no longer be done today. But to look at life from another perspective, there are still a lot of things I can do. I learn to count my blessing every day, which makes myself a lot happier. We are not fighting with a cold but a severe illness called CANCER. To be able to live is already the biggest blessing. One more thing, don't be too lazy when you eat. If you can eat by mouth, forget the PEG tube!
Karen stage 4 tonsil cancer diagnosed in 9/01.
Karen stage 4B (T3N3M0)tonsil cancer diagnosed in 9/2001.Concurrent chemo-radiation treatment ( XRT x 48 /Cisplatin x 4) ended in 12/01. Have been in remission ever since.
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#54312 01-28-2004 09:00 PM | Joined: Mar 2003 Posts: 189 Gold Member (100+ posts) | Gold Member (100+ posts) Joined: Mar 2003 Posts: 189 | Hey Danny Boy,
We've been through a lot together.
You've been one of my strongest supporters.
I'm just the caregiver, but you've picked me off the floor more than once.
Now it's my turn.
This phase of recovery is very hard. During treatment you are "fighting" the devil. Once treatment ends, at least in our experience, you feel so freakin' vulnerable. No longer does the disease have a face, but the shadow of a "lurking" enemy. Dennis had the worst time during this phase, but I promise that it gets better.
Nothing is easy about this fight. I'm not about to tell you otherwise, but I'm a firm believer in faith. Whatever shape, form,.....doesn't matter. Just a belief in your own strength is enough to fight this coward. And, I KNOW you are strong, and able to give it an extraordinary run for its' money.
Love you Babe, Mandi
Husband diagnosed with stage III tonsil and floor of mouth cancer in August 2002. Three rounds of chemo/42 RAD treatments. Upper right lung lobectomy in March 2003. (Benign)
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#54313 01-30-2004 11:22 AM | Joined: Jan 2004 Posts: 64 Supporting Member (50+ posts) | Supporting Member (50+ posts) Joined: Jan 2004 Posts: 64 | Hi Dan, I just joined this forum today and have seen your name quite a few times in my reading. I didnt realize you were so recent out of treatment. If you read my introduction, you'll realize that I'm knee deep in self pity, that sometimes I dont realize that there are a lot of people out there in the same predicament. I just want to say that it does get better. I was diagnosed with stage 4 tonsil cancer, had modified radical neck disection, 33 radiation treatments and 3 cycles of cisplatin. It was a nightmare. But each day it gets better. Keep a positive attitude and know that depression goes with the territory. I was on antidepressants for 6 months and my doc suggests I go back on them. I suppose I'm just not allowed to cry in front on anyone anymore. Well, except for you guys. Hang in there, you'll enjoy food again, once the thrush is gone and you are able to taste. I do think cold weather affects me adversely, so I can understand your frustration. But get out there and shovel that snow, it'll get your blood pumping.
Keep your chin up,
Kelley
SCC tonsil(left) with contralateral mets. Modified right neck disection August, 2002. 33 rads(62 gy)both sides of neck and 3 cycles cisplatin completed October 25, 2002. 34 yo at time of diagnosis
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