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#34866 01-15-2007 04:53 PM
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Hi Kerry,

Believe me when I tell you that you nor your husband will move on until both of you face the fact that your old lives are NEVER coming back. The toughest stage of recovery for me was accepting that. I would be overwhelmed with feelings of homesickness, that was the only word I could think of to describe how I felt. I missed my old self and my old life so desperately. It made it impossible for me to learn to love my new self and my new life. And that is truly what we all have to do, in particular the ones of us that suffer more severe side effects that are permanent.

Say goodbye to your old life and help Stephen to say goodbye to his old self and THEN the clouds will lift............I promise you this will happen. It's amazing what the human body and mind can adjust to and accept. I still have moments of missing some of my favorite foods, but it's not that bone deep feeling I used to get that would stay with me for hours after. And my healthier body helps me accept it also!

He's only 8 months out, he's still battling the depression of it all and so are you. Get him to talk about "missing" himself. Once I started sharing my feelings it made me feel so much better.


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.
#34867 01-16-2007 02:13 AM
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Minniea you are a perfect example of facing not only the fear of cancer but the physical aspects of this horrible disease. You have been a good example to many and I'm prouder of people like you who strive to keep moving forward emotionally under such unstable times.
P.S. Minnie my 12 yr. old got a rebound off the other teams Free Throw and put it up for 2 points in the wrong basket yesterday. My wife is the only one who jumped up and cheered.


Mark D. Stage 3 Nasopharynx dx10/99 T2N3M0 40xrad 2x Cisplatin 5FU. acute leuk 1998.
#34868 01-16-2007 02:48 AM
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Minnea. I think you just hit the nail on the head. I needed to be told that because somrwhere inside I've been fooling myself in thinking things could be the same "if this" or "if that". But there are no ifs about this and thank you for putting that down on paper for me so that I can see things more clearly. Sometimes you need, or at least I need, someone to spell things out that maybe deep down you know but hearing someone say it helps me to know that this is how it has to be. And we need to repair our marraige so that I can help Stephen accept his new normal. We have not been there for each other and I know he still needs my support to continue his recovery. We both need some individual therapy as well as marital counseling but you just laid out our goal.... Leave the past behind and try to start anew...
With sincerest thanks...


Kerry/wife of stephenm
StageIV - Base of Tongue T4N0M0
XRT x42 / Taxol and Carboplatin x4
Tx. Finished 5/08/06
#34869 01-16-2007 02:57 AM
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Kerry,

You've gotten lots of great advice about some of the positive aspects of "moving on" to the rest of your life (which I totally agree with). Also, even though it may feel like a lot of time has passed since your husband's treatment, and he may think he should be fully recovered, I can tell you it took me much longer than that to get where I could really enjoy eating again, and a very long time to heal to the point where I could get some additional saliva back. (I also had XRT and there was nothing available at the time to preserve saliva glands, so for me it's been a slow process with a combination of medication, careful dental hygiene, some extra fluids, and Biotene rinses.)

Then, as I was starting to feel more fully recovered, my husband went through a serious health crisis of his own with an extended hospital stay and several weeks more of recovery at home, and we had a role reversal for awhile.

Like many other people, I found that this kind of experience shook up my approach to my career, as well as several other aspects of my life, and it was uncomfortable for awhile as I tried to figure out what I could do and what I thought I SHOULD do. I actually came to see that there were parts of the "old life" that weren't as great as I once thought and that this was a chance to do some things very differently. I've said it here before and I'll say it again -- if someone told me now that I could go back 18 years and erase the whole cancer experience and then just continue on with the "old life", I'd say "no thanks". I've had too many great opportunities that have opened up that I never would have been in a position to see or follow up on if I had just kept on with the old routine and what I was accustomed to in the "old life".

Cathy


Tongue SCC (T2M0N0), poorly differentiated, diagnosed 3/89, partial glossectomy and neck dissection 4/89, radiation from early June to late August 1989
#34870 01-16-2007 04:46 AM
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Cathy makes some great points about what we learn from the experience of cancer. I thought it sounded so cliche when I was a "newbie", but now I see the depth of that statement. We DO learn and take from cancer IF WE CHOOSE TO. We can also make the choice to let it define us and let it steal more then our health. In my opinion, we all go through a stage where the cancer and the fear of the cancer overshadow any logical thoughts we might have, and we give into the fear. Then, when we realize that we just might survive this cancer, we are left with all the changes in our lives to deal with. That is when the REAL work begins! There is no preparation for this type of life event,such as we have for puberty, childbirth, etc.,...........so we have to muddle through it. Now that I'm far enough into recovery and in a frame of mind that allows me to look back and see myself more clearly, it amazes me how powerful the human mind is. When we are in the early stages of recovery we don't understand until much later just how strong we really WERE during those tough times. We don't give ourselves enough credit for what we endured.

Kerry, you are on a true roller coaster right now. The emotions you are feeling and the ones Stephen is feeling are so overwhelming that it makes you just want to crawl in bed and sleep for years and years. At one stage for me, just about the point of recovery your husband is in right now, I had a difficult time spending meaningful time with my girls. Anytime they seemed happy, it made me sad, because I was so fearful of dying and missing that with them, of leaving them to live without me. I pulled away from them and pushed my husband into a more hands on role. Three years later, that stage in recovery turned into a blessing for us, as now my husband will tell the world how much closer he is to his daughters because of the cancer experience. When our youngest, who is now 12, started her period about 6 months ago............she had no problems telling her father, lol. I love it.
In the short span of three and a half years, I went from worrying about living another year, never thinking past a week or so...............to feeling natural while making plans with my family for trips a year from now and talking to my 16 year old about which colleges we want to visit next year. But that all takes time and growth on our parts. Time is one of the most important words in cancer recovery, in particular a cancer that has such lasting effects as oral cancer. It's a tough lesson for impatient people such as myself, but at the same time, it has made me slow down and ENJOY the things that seemed small and and didn't warrant as much attention from me before I had my life threatened. The joy of stopping in the middle of something I'm doing to sit on the bottom step while my 2 year old grandaughter sings her ABC's is still new to me, leaving the dinner dishes on the table to go take a walk or bike ride with my 14 year old is still a new feeling for me..............all the new things in my "new" life. In my old life I would have said, "we'll do it later" and I would have kept walking down the stairs past my grandaughter and I would have cleaned all the dinner mess until my kitchen was shining........and it was to dark outside to take a bike ride. Boy, the things I missed in my old life!
I have eating issues that my family has had to incorporate into their lives to a point and I also wear my cancer on my face, something else that my husband and children have had to adjust to as have I. We go out to eat all the time now, but the first thing my husband and girls do (which always makes me grin) is they will check out the menu and give me suggestions on what I can probably eat. I continue my coaching at the school and have found a world for myself that knows my cancer story and is aware of why my bottom lip droops, understands my surgeries, etc. But this acceptance of myself didn't come overnight, it came in stages and I suspect there are more stages for me to go through. It's tougher on us oral cancer patients, in my opinion. It's impossible for me to "forget" about the cancer as I always physically feel the effects of it, and forever will. My girlfriend of 10 years had breast cancer 6 years ago. Mastectomy, chemo, all of it. She tells me that she goes weeks without thinking of her cancer. But she doesn't wear it on her face, it doesn't affect her eating or her speech, etc. We do have a tougher road.

Stephen will reach his stages in good time, and he'll get through them. Having young children is a bonus for him, they are like a natural healing power. You will also, if you approach this with the right frame of mind, come out of this cloud with a depth to your marriage that a "non-cancer" couple cannot possibly achieve. The connection I feel with my husband is something I'm blessed to have. I'm also aware that it wouldn't be as powerful if we hadn't shared this experience together.
Please keep us posted on how he's doing, and how you're doing. You are such a key player in his recovery and in how your children will incorporate cancer into their lives. 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.
#34871 01-16-2007 05:12 AM
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Hey Mark,

Can I tell you how much I LOVED the story about your 12 year old and the wrong basket? My 14 year old daughter (she's now reached 5ft 8) plays ball and it's such a fantastic sport. I'm like your wife, I love to cheer loudly and proudly! I even stand and holler when the kids on the other teams make a great play.......boy does THAT get me some strange looks from our home crowd, lol.


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.
#34872 01-16-2007 05:58 AM
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Just finished reading all the posts. So much good and oh so true information. I still have goosebumps from reading Minnie's. You are so right. This beast has caused me to not work for the past 10 mos, but I have spent so much time with family and friends. My grandchildren got to stay with me a few times over the holiday vacation, my son was in from Ohio for a week, I've made it to my nieces basketball games. Things I couldn't find time for before. Now I know I'll find that time. I was looking and waiting impatiently for the "normal" to be back. But the past isn't the norm anymore, it's the present.


Dx3/20/06 SCC,BOT,1N Tx:5cycles Carbo/Taxol, Rad:35x, brachytherapy:6x, completed 7/24/06
#34873 01-16-2007 08:22 AM
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Kerry,
As the primary food lover and provider for our family I have to tell you that not being able to cook was just as rough on me as not being able to eat. I remember the horrifying look on their faces one particular meal when I asked how everything tasted. eek It was honestly all just cardboard to me. I missed the taste of coffee for almost 2 years and also green tea off and on. The first time in my life I pickled some jalapenos and they happened to be the hottest I remember in my life. I had to reach for the miracle mouthwash to ease the pain...but I smiled through it all because I could really taste how great they were. To digress a bit, I happened to have severely whittled down on the list of "first time" things in my life over the past 3 years especially. Make that list of everything you BOTH want to do in life and pick them out in the right order and GIT UR DONE, girl.

I enjoy all foods now and really started putting back the weight about 18 months after treatment ended. Yesterday and today I spent 1 to 1/2 hours in a refrigerated manufacturing plant and even spent some time in 10 below zero in the freezer. I almost panicked a couple of weeks ago when I realized this will be the farthest from my water bottle (it is not allowed in manufacturing areas). My lips were chapped for days last time and I imagine what they will be like tomorrow but guess what...I DID IT!!! cool cool

Life is different now but so much deeper, if I can use that term. Someone on the board long ago mentioned "don't sweat the little things and all things in life are really little things" or something like that. I gave up worrying for the most part.

However, the fear comes back like yesterday when I had a voice mail from the nurse asking me to please call so we could review the results of my annual chest xray last week. I was almost planning my funeral by the time I got in touch only to hear everything was "normal again" on the other end. I had convinced myself that she would have left those two words in the message if everything was fine. WTF...do they ever think things through when they leave messages? I guess they didn't want the wrong person by accident to hear everything is fine???

Anyway, hang in there things will progress slowly and then suddenly a huge amount of time passes and you find yourself offering the same words of encouragement to someone exactly where you were at one point. The advice freely offered from everyong is spot on.

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
#34874 01-16-2007 09:30 AM
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You really said it all ed. I keep thinking what a baby I am to worry over my husbands after treatment symptoms and tests. It takes so little to shake up our world and yet you are right- the little things who didn't call, cancelled plans, billing error nothing like that even registers on the radar. My husband doing a dance step in the kitchen or playing with our golden retiver or just a hug for no reason makes me smile.
Kerry - Hold on to all the love in your family.


caregiver to Gil dx SCC 11/05 T2N2M0
finished tx 3/10/06 stage 4 rt tonsil,BOT,2 lymphnodes,35IRMT,6 chemo
#34875 01-16-2007 03:58 PM
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I'm starting my 2nd anger management group on the 28th. Churches and many hospitals and HMO's, etc., offer them. Steve has a lot to look forward to - it took me almost 2 years to get back to about 98%.

Life can definitely get better. His expectations may be a little high for 8 months post Tx.


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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