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#44087 10-26-2004 09:31 AM
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Nicki Offline OP
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Alleluia! We made our last daily trip to UVA yesterday and feel like we have been sprung from jail! Tom is incredibly weak and gray-looking, but happy to be home. Those long drives took a lot out of him.

We are to let him 'cool' for about 2 weeks before a scan, and our appt with the surgeon is on NOv. 11th. The radiation doc said we'd be discussing surgery or the 'wait and see' option (!?)....didn't think we'd have an option from all I've read from all of you!

You would not believe the 'welcome home' we received! Our driveway is about 1/2 mile long.....Tom's company (he owns a landscape contracting co.) came out and put up a huge "FINISH" line, complete with an arch of balloons towards the end of the drive, and then lined the rest of the drive up to the garage with signs and balloons......awesome and overwhelming...! There were huge balloons and "We Love and Miss You" signs in the house..and one of our Mexican laborers planted a big ol' boot with fall plants...really neat. An arch of balloons was above the mantle, even had a huge bouquet of balloons in the bedroom!

What an emotional homecoming. Could hardly take it all in, but the love was wonderful!

I'm off now to take him to the LOCAL doctor for his blood problems. this, as least, is an easy ride!
Love to all of you, and thank you for your terrific support and the wealth of information you have provided. I'll keep you posted on what happens next......
Nicki


Nicki, wife of Thomas
dx July 2004, SCC, Stage 4 Tonsil. Tx begun 8/4/04. Cisplatin/Xeloda x 4; IMRT 7 wks, 8/7 - 10/25/04 Modified Radical Dissection (right), Selective Dissection (Left) 12/10/04.
#44088 10-26-2004 09:55 AM
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Congratulations Nicki and Tom!
You must be a great couple to have so many people care about you so much.
Onward and Upward guys.
Take care
Marica


Caregiver to husband Pete, Dx 4/03 SCC Base of Tongue Stage IV. Chemo /Rad no surgery. Treatment finished 8/03. Doing great!
#44089 10-26-2004 10:01 AM
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Nicki,

Congratulations to you and Tom! Even though it's been years, I still remember that "sprung from jail" feeling.

As some of the others here have said, the recovery process can be slow and sometimes frustrating after the radiation stops, but hopefully it won't be too long before he starts to see some improvement. At least you now have some respite from those long daily drives!

Cathy


Tongue SCC (T2M0N0), poorly differentiated, diagnosed 3/89, partial glossectomy and neck dissection 4/89, radiation from early June to late August 1989
#44090 10-26-2004 10:10 AM
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Congratulations on making it to the finish line. What a marvelous surprise from his employees. Must have lit up both of your days. Certainly lit up mine.

I remember that marvelous feeling - NO MORE MASK - on the last day of treatment and I only had to drive 5 minutes to get to my treatments. They will never get something over my face again.

Again, congatulations and enjoy
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
#44091 10-26-2004 11:10 AM
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Congratulations Nicki and Tom

What a joyful welcome home. I felt very proud of myself when I completed radiation and now know that it was worth it. My clinic tends to the 'wait and see' approach.

Love and light from Helen cool


RHTonsil SCC Stage IV tx completed May 03
#44092 10-26-2004 11:27 AM
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Nicki, I'm so pleased for both of you. Please keep in mind that the next 2-3 weeks will be a little difficult, but you are almost out of the tunnel at the end of which is a light. It sounded like your welcome home was very emotional, that's a good thing. One thing about this disease is it sure brings out the emotions in people. As far as the surgery goes, I recommend Tom have it done as it is very simple compared to rad and removes any chance of this cancer coming back. After all, if it is surgically removed, it can't come back. A different one may develop, but this same one will be in the pathologists trash after he tests it. I get great images of mine in the trash and then being thrown into the furnace for an appropriate ending. At any rate, I have been waiting for this posting since your first post a few months ago, congrats to you both.


Regards, Kirk Georgia
Stage IV, T1N2aM0, right tonsil primary, Tonsilectomy 11/03, 35 rad/3cisplatin chemo, right neck dissection 1/04 - 5/04.
#44093 10-26-2004 12:56 PM
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Nicki (Tom, too),

I was smiling, sobbing and cheering as I read your post. Tom is surely the type of person I would like to work for based on the wonderful celebration at the finish line! It was so much fun to travel this journey with you and I am honored that you kept us all informed along the way.

I had the "wait and see" treatment, too. The scans have shown no signs of cancer for over a year but for some silly reason, I am still second guessing the decision to not have surgery. If I knew what I know now about this dreaded disease, I believe I would have opted for the surgery after radiation. Just my two cents worth.

I trusted my otolaryngologist since he had the experience and mine was already stage IV with 2 lymph node involvement.

I know today was in important milestone and you should stop and enjoy the moment. All I really remember from this period of treatment was running to the toilet because when I looked in the bathroom mirror, the image I saw scared me a little. My wife nicknamed me Jarjar Binks because I just darted across the mirror.

May God continue to shower His blessings on you and Tom.

Ed


SCC Stage IV, BOT, T2N2bM0
Cisplatin/5FU x 3, 40 days radiation
Diagnosis 07/21/03 tx completed 10/08/03
Post Radiation Lower Motor Neuron Syndrome 3/08.
Cervical Spinal Stenosis 01/11
Cervical Myelitis 09/12
Thoracic Paraplegia 10/12
Dysautonomia 11/12
Hospice care 09/12-01/13.
COPD 01/14
Intermittent CHF 6/15
Feeding tube NPO 03/16
VFI 12/2016
ORN 12/2017
Cardiac Event 06/2018
Bilateral VFI 01/2021
Thoracotomy Bilobectomy 01/2022
Bilateral VFI 05/2022
Total Laryngectomy 01/2023
#44094 10-26-2004 01:59 PM
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Welcome home,
i expect the couch will be well used for a few weeks. Naps are so nice after radiation.

relax and enjoy,
cu,
larryb

#44095 10-26-2004 02:27 PM
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Nicki and Tom,
Excellent news to hear that radiation is complete. You guys got a well deserved homecoming. Keep us posted on how things are coming along.
D


Mom's caregvr. DDS failed to dx 01/03. Dx Stg IV SCC 05/03. Induct. chemo, IMRT, 5FU, H, Iressa, Neck disect, radiation. Dad's caregvr. Dx 01/04 Ext. Stg SCLC. Mets to liver/bone 08/04. Died 11/12/04. Mom tongue CA dx 06/13, hemiglossectomy (80% removed) 08/13. Clean margins and nodes, but PNI. 6/15/15: Tongue CA at base of remnant tongue. Declined further tx; hospice.
Died 10/13/15. What a long and difficult journey.
#44096 10-26-2004 03:19 PM
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Nicki,
Congrats on getting Tom home. I was so happy on my last day of radiation at MDACC when I threw that mask in the trash, rang the bell, and went home. Little did I know that the hard part had just begun. Something about seeing those people everyday and even twice a day and being proactive about getting treated, energizes us. But once treatment ended, I got very depressed for the first time and thought...at 8 AM, " what do I have to look forward to...my noon tube feeding?" I say this not to make you sad, but to prepare you, as others have done, by mentioning that the first few weeks after radiation can be very difficult.

The good new is that once I started taking a walk every day, made sure that a friend or two visited every day, ran a couple of simple errands, and even got some counseling, things rapidly improved.
Best of luck and take care...of both of you.

Danny G.


Stage IV Base of Tongue SCC
Diagnosed July 1, 2002, chemo and radiation treatments completed beginning of Sept/02.
#44097 10-26-2004 04:26 PM
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Nicki,
Danny G. voiced exactly what I was going to post. I hit a severe depression when I finished radiation. I felt like I was sitting there doing nothing but waiting for "it" to come back. I cried all the time and held myself away from my family. It only took me a few weeks to snap out of the worst of it but the feelings of fear were still very strong for months and months. Cancer dominated my every waking thought. That does pass and gets better until we all find our own ways of dealing with it all while enjoying life.
Boy do I remember my last day of radiation.......it was the one and only time my husband and younger children came with me......and I rang the heck out of that bell. I threw the mask away (couldn't believe they asked me if I wanted to keep it) and walked out of there near tears.
I hope it goes well for Tom and be sure to keep an eye on him for depression.
Take care,
Minnie


SCC Left Mandible. Jaw replaced with bone from leg. Neck disection, 37 radiation treatments. Recurrence 8-28-07, stage 2, tongue. One third of tongue removed 10-4-07. 5-23-08 chemo started for tumor behind swallowing passage, Our good friend and much loved OCF member Minnie has been lost to the disease (RIP 10-29-08). We will all miss her greatly.
#44098 10-26-2004 05:45 PM
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Nicki and Tom,
Praise be to God! Get thru the next few weeks slowly with lots of naps and slow walking and things will get better!!! I am so happy for you both and may God give you strength as recovery begins!
Deb


Debbie - Caregiver for husband, Dan, diagnosed with tongue cancer 7/03. Partial gloss., mod. neck dissections, graft. Recurrence neck tumor 12/03. Radical left neck dissection 12/24/03-unable to get all the tumor. 8 weeks chemo/rad beginning 1/12/04.
#44099 10-26-2004 10:43 PM
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Dear Nicki and Tom,

Congrats on such a significant milestone!! I'm about 5 months post-radiation now, and even though I'm a dentist, and even though my CA center told me what a rough road it would likely be, it still was more difficult than I ever imagined. My recovery has been slower than I would like, but I am getting better. Plus, we're all different, and recover at different rates. I wish for Tom a speedy recovery! God bless you both.


David


Stage 1 lateral border of tongue in 1986 requiring L neck dissection, three surgeries later in Feb 2004 invasive SCC (poorly differentiated) L radical neck dissection followed by 37 treatments XRT
#44100 10-27-2004 02:05 AM
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Nicki Offline OP
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Good morning, All my wonderful friends smile

I'm going to stay home with him today...he's asked me to, and I could use it, anyway. You all are so right in saying that feeling of 'doing nothing' kind of hits you. And, believe it or not, we had become attached to the health care team, and miss them!!! And this after one day???!! Of course, I WAS baking things for them all the time, and that was the only cooking exercises I'd been doing for a long time, so that might be my reason for feeling like I'm 'doing nothing!'

We have to go out today for more blood work, but that won't be a big deal. Yesterday afternoon, about 7 people from his work came by and we had a short business meeting....brought Tom up to speed on several projects, the forecast for the next quarter, etc, etc. I did most of Tom's talking; he's getting good at sign language, however! smile It was a GREAT meeting and surely did a lot to lift Tom's outlook. Thankfully, even without Tom at work (or perhaps BECAUSE he wasn't there! smile ), this looks to be the best year the company has ever had.....God is good!

Tom and I BOTH agree, Ed and Kirk, that we will listen to the surgeon, but that the removal of the offending tissue seems like the right thing to do.........

I'm already anxious about the scan and I don't even know the date!!

Love you
Nicki


Nicki, wife of Thomas
dx July 2004, SCC, Stage 4 Tonsil. Tx begun 8/4/04. Cisplatin/Xeloda x 4; IMRT 7 wks, 8/7 - 10/25/04 Modified Radical Dissection (right), Selective Dissection (Left) 12/10/04.
#44101 10-28-2004 10:07 AM
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Nicki,

If you feel you need to keep baking to maintain your routine, I can always give you an address to send them to. I am only offering this as you slowly wean yourself from this routine you have become accustomed to. laugh

Ed


SCC Stage IV, BOT, T2N2bM0
Cisplatin/5FU x 3, 40 days radiation
Diagnosis 07/21/03 tx completed 10/08/03
Post Radiation Lower Motor Neuron Syndrome 3/08.
Cervical Spinal Stenosis 01/11
Cervical Myelitis 09/12
Thoracic Paraplegia 10/12
Dysautonomia 11/12
Hospice care 09/12-01/13.
COPD 01/14
Intermittent CHF 6/15
Feeding tube NPO 03/16
VFI 12/2016
ORN 12/2017
Cardiac Event 06/2018
Bilateral VFI 01/2021
Thoracotomy Bilobectomy 01/2022
Bilateral VFI 05/2022
Total Laryngectomy 01/2023
#44102 10-28-2004 12:34 PM
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Nicki Offline OP
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Ed, I would be honored to bake something for you. Cooking is one of my passions - and you can imagine how bored I've become with having anyone to eat dinner with me frown

I think you all could qualify as a health-care clinic! Everything you've said has come true....I'm the one becoming depressed....Tom at this point is just BORED....... I'm SO missing hugs, kisses and cuddles (I'm a real 'feeler,' personality-wise) and all I want is to have MY TOM back the way he was, so we can be back the way WE were! I know it is selfish, but I can't keep back the 'sad.'

Guess I'll go scramble an egg. How exciting...
Hope everyone has a great night (or DAY, as the case may be!)
XO
Nicki


Nicki, wife of Thomas
dx July 2004, SCC, Stage 4 Tonsil. Tx begun 8/4/04. Cisplatin/Xeloda x 4; IMRT 7 wks, 8/7 - 10/25/04 Modified Radical Dissection (right), Selective Dissection (Left) 12/10/04.
#44103 11-04-2004 08:09 AM
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Congrats Tom and Nicki!!!! Glad you guys are across that finish line!!! Keep up the good work...

I'm back living in North Carolina by the way... Glad to be back east

Eric


Tongue cancer (SCC), diagnosed Oct. 2003 (T2 N0 M0). Surgery to remove tumor. IMRT Radiation 30x in Dec 2003 - Jan. 2004. Recurrence lymph node - radical neck dissection June 2004. Second round of rad/chemo treatments ended Sept. 2004.
#44104 11-04-2004 09:58 AM
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Hi, Eric - and the rest of my favorite team!

It is a dreary wet day here in Virginia - wish I could have stayed home. Tom is doing much better smile , however, so I'm a little less apprehensive about leaving him home alone. He does want me around all the time, and I do believe that is a sign of him still being very much 'on-edge' about the outcome of this thing.

He is taking in generally 6 cans of Jevity a day, along with his coumadin and the laxative stuff they prescribed. He's on 75 mcg of the Duragesic patch and except for occasional break-through, he's doing fine with that. I don't like that it makes him 'twitch' all day long, asleep or awake.

Heavy sigh......instant gratification is not part of this program, I can surely see. Right now I can't even look at pictures of him 'B.C.'
I get too sad. The radiation seems to have done a number on the hair at the nape of his neck as well as his beard. Don't know quite how we'll be able to work around that later on...........

Eric, we are going to Emerald Isle, NC for a week coming up soon. Are you anywhere near I95?

Everyone - please take care of yourselves. Don't know if I mentioned this, but I had a scare with a recall mammogram last week. Thankfully, I've been given a clean bill! God is good.

Love,
Nicki


Nicki, wife of Thomas
dx July 2004, SCC, Stage 4 Tonsil. Tx begun 8/4/04. Cisplatin/Xeloda x 4; IMRT 7 wks, 8/7 - 10/25/04 Modified Radical Dissection (right), Selective Dissection (Left) 12/10/04.
#44105 11-04-2004 05:30 PM
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Nicki,

I have a picture of my mom with my baby girl on my desk right before she started radiation and chemo and I would love to see her look like that again...I look at that picture everyday and its hard to believe that it was less than a year ago that she looked like that. I think it just takes time. Its one of the hardest things for me. I keep expecting her to look like her old self but gaining weight seems to be difficult for her and she just doesn't look as healthy as before. I'm sure it gets better. Tom will start to feel better gradually and soon you won't even remember how hard this time has been for you both.

My prayers are with you!
Dani


Originally joined OCF on 12/12/03 as DaniO or Danijams
Dani-Mom SCC BOT & floor of mouth surgery-recur then surgery/rads & chemo completed 3/04
surgery 11/06 to remove dead bone & replace jaw w/ leg bone & titanium plate
#44106 11-05-2004 03:08 AM
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Hi Guys, just wanted to chime in, I think Oral Cancer is one of the cruelest in so much as it takes away from your physical appearance and leaves you with scars that EVERYONE can see! Just had my 8 week with oral surgeon, he said he will do a revision of my trach scar and possibly something with the scar on my neck. That one bothers me the most cuz it looks like a chunk of my neck is missing. I have gained back all of my weight and some, SMILE!! I don't want to sound vain cuz I am truly grateful to be alive and I know that God still has a plan for my life, but I do wish I looked my old self again...Take Care and Have a great day everbody!! Love, Carol


Diagnosed May 2002 with Stage IV tongue cancer, two lymph nodes positive. Surgery to remove 1/2 tongue, neck dissection, 35 radiation treatments. 11/2007, diagnosed with cancer of soft palate, surgery 12/14/07, jaw split. 3/24/10, cancer on tongue behind flap, need petscan, surgery scheduled 4/16/10
---update passed away 8-27-11---
#44107 11-05-2004 03:13 AM
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Sorry, I posted that reply too quickly. Anyway, on a positive note, I am able to do pretty much everything I did pre surgery and radiation and for that I am unbelievably grateful!!! God Bless!!


Diagnosed May 2002 with Stage IV tongue cancer, two lymph nodes positive. Surgery to remove 1/2 tongue, neck dissection, 35 radiation treatments. 11/2007, diagnosed with cancer of soft palate, surgery 12/14/07, jaw split. 3/24/10, cancer on tongue behind flap, need petscan, surgery scheduled 4/16/10
---update passed away 8-27-11---
#44108 11-05-2004 04:27 AM
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Nicki,

The hair and beard stuff will most likely return to normal. I had not cut my hair this year because the radiated area in conjuntion with the chemo created a little swatch of curls. Being asian descent, I have never had even a slight curl in my hair. I wanted to trim it up a bit for a job interview and the cutest of the curls are gone confused . Of all the things, I wanted this one thing to not go back to the way it was before cancer. God certainly has a sense of humor!

We had a family portrait done just before everything started and it is prominently displayed where we all see it as soon as we leave our bedrooms. I may still look a bit "undernourished" compared to the picture but I planted some winter rye that will look like a golf course all winter and get cut 1-2 times a week and a bit over a hundred flowers in the front flower beds. I missed that the past two winters with various illnesses. (I sneaked a peak at the flowers twice already this morning laugh .)

I am glad to hear the mammogram was good!

Ed


SCC Stage IV, BOT, T2N2bM0
Cisplatin/5FU x 3, 40 days radiation
Diagnosis 07/21/03 tx completed 10/08/03
Post Radiation Lower Motor Neuron Syndrome 3/08.
Cervical Spinal Stenosis 01/11
Cervical Myelitis 09/12
Thoracic Paraplegia 10/12
Dysautonomia 11/12
Hospice care 09/12-01/13.
COPD 01/14
Intermittent CHF 6/15
Feeding tube NPO 03/16
VFI 12/2016
ORN 12/2017
Cardiac Event 06/2018
Bilateral VFI 01/2021
Thoracotomy Bilobectomy 01/2022
Bilateral VFI 05/2022
Total Laryngectomy 01/2023
#44109 11-05-2004 05:31 AM
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Boy aren't you the optimist! I have "holes" in my beard where the main beam entry points were and the hair from the bottom of my chin to the top of my shoulders is permanently gone (except for a few very annoying hairs on my adams apple -but maybe that bodes well for the thyroid).

Many of the hair follicles fell out. It also killed all the skin tags and I don't snore anymore. Better living through mad science :p


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)
#44110 11-05-2004 07:00 AM
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Nicki, about the hair at the back of Tom's neck, I, too, had what the techs referred to as the "radiation hairline" but it all returned to normal. I wear my hair up most of the time so the hairline is exposed to all and I would never do that if it were as crazy looking as it was. Yet another thing that just takes time.

#44111 11-05-2004 09:31 AM
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Nicki,
Hair follicles lost to radiation don't grow back. Like Brian, I could grow a goatee, but the part of my beard on my lower jaws will never grow back. (not that I mind...it leaves less area to shave, and the skin is as smooth as a baby's).

It took a while, but even with my limited diet, I have gained back as much weight as I want...the waist in some of my pants has gotten tight. I feel like I am strong and still play a lot of golf, and can hit the ball as far as I ever could...subject only to my less than perfect golf swing!

Yes, the boredom is one of the worst things about the recovery period after radiation treatment ends. I read a lot, took a daily walk, napped a lot, and even got to where I liked the rap music T.V. shows that came on in the afternoon that my teen-aged son turned me on to. Go figure.

Anyway, things will no doubt improve for Tom, and for you as well in time. The good news is that interest in intimacy returns as well.

Take care,
Danny G.


Stage IV Base of Tongue SCC
Diagnosed July 1, 2002, chemo and radiation treatments completed beginning of Sept/02.
#44112 11-05-2004 11:37 AM
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Hi, All..
Tom's first 'day out' didn't go as well as we'd hoped. A friend came by to visit, and ended up driving Tom to a party being held at Tom's office. Tom's been asleep since I got home, but the friend called to tell me that Tom got sick on the way in - - but insisted on getting to the office. From what I understand, he was able to stay around there for about one hour, and a co-worker brought him home. Guess he's been asleep since.
I'm glad he got out - he hasn't seen some of his employees since September - and hope the episode of vomiting doesn't deter him from venturing out again. A very good friend is testing for 6th degree black-belt tomorrow night, and I know he wants to be there. I'm not so certain I want him in a poorly-ventilated dojo with a lot of people, some of whom you KNOW will be carrying something!

QUESTION - Is a CTscan a definitive test, or would another PETscan be needed to see if there are still 'hot spots?'

Talk to you all soon. This is a big ol' lonely house with just me rolling around in it.....having him up and about will be a good thing! smile
Nicki


Nicki, wife of Thomas
dx July 2004, SCC, Stage 4 Tonsil. Tx begun 8/4/04. Cisplatin/Xeloda x 4; IMRT 7 wks, 8/7 - 10/25/04 Modified Radical Dissection (right), Selective Dissection (Left) 12/10/04.
#44113 11-05-2004 12:22 PM
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No scan is definitive. It is only a piece of the data and subject to interpretation. The visual and palpation exam are equally as important.

Tom's doing pretty good - I didn't go out in public places at all until June (my treatment was concluded in March). He's taking a small risk with a compromised immune system.


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)
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"You are a mist that appears for a little while and then vanishes" (James 4:14 NIV)
#44114 11-05-2004 01:13 PM
Joined: May 2003
Posts: 928
"Above & Beyond" Member (500+ posts)
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"Above & Beyond" Member (500+ posts)

Joined: May 2003
Posts: 928
One day at a time Nicki
Thats the way it goes.
Sending good wishes and positive thoughts your way.
Marica


Caregiver to husband Pete, Dx 4/03 SCC Base of Tongue Stage IV. Chemo /Rad no surgery. Treatment finished 8/03. Doing great!
#44115 11-05-2004 01:32 PM
Joined: Nov 2002
Posts: 541
"Above & Beyond" Member (500+ posts)
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"Above & Beyond" Member (500+ posts)

Joined: Nov 2002
Posts: 541
Talking about hair loss as a result of radiation, I consider myself really very very lucky that I not only kept all my hair but it grew even stronger and healthier after radiation. I was prepared to lose most of my hair during treatment as I was already warned by my doctors that the possibility was high due to my intensive treatment of both chemo and radiation. So before my treatment started, I spent a lot of money getting a wig for myself. Really expensive because it was made from genuine human hair. I am that kind of woman who dosen't want to appear different and get people's sympathy. Surprisingly, apart from normal hair fall off after washing, nothing changed on my head. That's why when I returned to my work after a few months, some naughty colleagues came to pull my hair to see it was a wig!They were 'disappointed' laugh So the wig is still lying in my closet and hopefully it will be there forever and that I won't need it for the rest of my life. My friend who received radiation only to his neck area did lose hair at the back and a letter M appeared. It took quite some time for the hair to grow back in that area. Since he is a man, he doesn't care too much and just tells people with amazing looks that it is the latest hair style for mature guys. eek Sometimes a sense of humor can be a good medicine.Be patient Tom,things will get better.

Karen


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.
#44116 11-07-2004 10:26 AM
Joined: Dec 2003
Posts: 2,606
Likes: 2
Patient Advocate (old timer, 2000 posts)
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Patient Advocate (old timer, 2000 posts)

Joined: Dec 2003
Posts: 2,606
Likes: 2
Nicki,

I went back to work a couple of weeks after radiation and actually worked for about 2 1/2 months before the fatigue kicked my butt. Of all the things that I remembered, one day I was heading back just before Christmas (work was 400 miles away). I had not planned on coming back so I asked someone for a ride to the airport 2 1/2 hours away. As we were getting ready to go, I threw up violently and was so embarassed. This guy that worked for me was so nonchalant about it but it still bothered me. He is still the only person in my life that has seen me throw up at work. Lucky him, he got to see it several times.

Tom is really doing well and you are so awesome!

Ed


SCC Stage IV, BOT, T2N2bM0
Cisplatin/5FU x 3, 40 days radiation
Diagnosis 07/21/03 tx completed 10/08/03
Post Radiation Lower Motor Neuron Syndrome 3/08.
Cervical Spinal Stenosis 01/11
Cervical Myelitis 09/12
Thoracic Paraplegia 10/12
Dysautonomia 11/12
Hospice care 09/12-01/13.
COPD 01/14
Intermittent CHF 6/15
Feeding tube NPO 03/16
VFI 12/2016
ORN 12/2017
Cardiac Event 06/2018
Bilateral VFI 01/2021
Thoracotomy Bilobectomy 01/2022
Bilateral VFI 05/2022
Total Laryngectomy 01/2023
#44117 11-07-2004 01:35 PM
Joined: Jul 2003
Posts: 1,163
Patient Advocate (1000+ posts)
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Patient Advocate (1000+ posts)

Joined: Jul 2003
Posts: 1,163
Hang in there Nicki,

There will be lots of time for you and Tom. Tell him to take it easy. Don't want to see him picking up a bug. Time to heal. Be selfish.

Danny Boy


Daniel Bogan DX 7/16/03 Right tonsil,SCC T4NOMO. right side neck disection, IMRT Radiation x 33.

Recurrance in June 05 in right tonsil area. Now receiving palliative chemo (Erbitux) starting 3/9/06

Our good friend and loved member of the forum has passed away RIP Dannyboy 7-16-2006
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