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#50853 08-17-2004 04:14 AM
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sbk Offline OP
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Hello all,

It so good to be able to read and hear how people are going. Things have been so busy, I haven't even had time to check in here...John finished radiation about 6 weeks ago and has had the trach out for 3 weeks and hopefully will be able to get the G-Tube out soon. I feel like I should be thrilled, jumping for joy, etc...etc...But mostly, I feel exhausted. John is really amazing he is working almost full time and sleeping when he gets home, our 3 1/2 year old is really coping well (Last evening she said, "I think this cheese is soft enough for you to eat...what to try some Daddy?"...We both thought we would cry...she's a real doll!!!) My work has been so supportive even though I've been really, really slow at getting anything accomplished...So really everything is going well, but I feel exhausted...I already did the Paxil thing...so I don't feel depressed really...just, well, exhausted...and I have the easy job..poor John is doing rehab, working to swallow, managing all the spasms...and I'm the one who wants a vacation...can someone please talk some sense into me... :-)....

Thanks and lots of love,
Sara


Wife of John, 40yo, SCC R Tonsil (3/10/04), s/p resection and rad neck, forarm falp, taxolx3 pre rad, rad (30 txmnts) & taxol/carbo. Now he is 49 and doing well!!!
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Sara,
I don't think you need any "sense talked into you." You have every right to feel like you need a vacation after what you have been through. Hope you are at least getting some "mini vacations" - moments to take time out for yourself. I know that I felt exhausted from helping my husband through treatment, and I didn't have a 3 1/2 year od to think about, as well. Though I suspect that little girl also gives you and your husband the spark to keep going.

It is great that John is back to work so soon. Good for him. My husband was still sleeping most of the day away at 6 weeks post treatment.

Best wishes to you...things will get better and better.
Anita


Husband Dx 12/02 Stage 4 Tonsil Cancer T1N2bM0; surgery, radiation, chemo 1/03 - 4/03.
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Sara-
My husband (of two months!) dangled a Hawaiian vacation in front of me as an added incentive to make it through chemo! I couldn't see myself there until I got rid of the PEG tube though. So we put if off until our first anniversary. Any vacation time you can arrange just to get away from it for a while??? The treatments and the stress of the diagnosis is very draining for the whole family. Celebrate surviving treatment and head out of town for a long weekend! Those little ones can sure bring a smile to your face! - Kris


SCC Stage IV left tonsil neck disection 3/02 radiation finished 6/02 chemo finished 9/02
Stage 2A left breast cancer 3/09, chemo and radiation, finished treatment 2/7/10 -Stage 2 right beast cancer 10/14 chemo and radiation
Every day is still a gift :-)
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Hello Sara,

I think it's just as diffucult being the caregiver as the cancer victim. There is a special place in heaven for caregivers. It's normal to feel overwhelmed at times. Please take some time for yourself. You certainley earned it Sara! This is quite a rollarcoaster ride on your emotions though.

Hoping you feel better soon,

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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Hey Sara,
I sure know the feeling as a caregiver. It's just an exhausting...wish I could do more to help my husband feeling. I had to use Xanax and Ambien and some Lexapro to make it thru. You guys are doing great. My Dan is just back to work 5 months post treatment. I got layed off three weeks into Dan's treatment which turned out to be quite a blessing. I couldn't have worked full time during all the treatment days. And Dan wasn't sleeping much at nite and many nites I didn't sleep at all...too much to think about. Anyway, I sure know where you are coming from. As he feels better, so will you, or at least that is how it has been with me.
Take care and God bless,
Debbie


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.
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Sara, I've been on both sides of the fence now, both as cancer patient and caregiver to someone with cancer, and it ain't no picnic no matter what side of the fence you're on. Garegiver's just as hard as patient, if not almost more so.

Don't feel guilty, and remember to schedule some "me" time. You would be surprised how one night a week out with the girls, one afternoon a week just doing what you want to do can recharge the batteries.

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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Sara, It is not just OK for you to have time away, I believe it is mandatory!

Get with some friends and have a weekend (or longer) at least 100 miles away. If your husband can't take care of the little one yet find a good place for her to stay seperately (grandma etc.)
Don't call in and don't worry. You need this and your family will benefit from the "new you" when you return.

This ordeal IS really hard on caregivers and loved ones alike. It is really important for you to get a real break from it.


Mark, 21 Year survivor, SCC right tonsil, 3 nodes positive, one with extra-capsular spread. I never asked what stage (would have scared me anyway) Right side tonsillectomy, radical neck dissection right side, maximum radiation to both sides, no chemo, no PEG, age 40 when diagnosed.
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computer glitch!

Suddenly there were three posts of the same thing. eek


Mark, 21 Year survivor, SCC right tonsil, 3 nodes positive, one with extra-capsular spread. I never asked what stage (would have scared me anyway) Right side tonsillectomy, radical neck dissection right side, maximum radiation to both sides, no chemo, no PEG, age 40 when diagnosed.
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Mark, an old time poster like you knows that the last little icon next to your name with the paper and pencil allows you to edit or delete your own posts. I have done this for you. Only the poster can edit or delete a post of their own, unless you are the webmaster or the forum moderator, i.e....... me.


Brian, stage 4 oral cancer survivor. OCF Founder and Director. The first responsibility of a leader is to define reality. The last is to say thank you. In between, the leader is a servant.
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Indeed! Today was post number 600, and I am old enough to claim senility with regard to DELETE (I always knew about the edit) shocked


Mark, 21 Year survivor, SCC right tonsil, 3 nodes positive, one with extra-capsular spread. I never asked what stage (would have scared me anyway) Right side tonsillectomy, radical neck dissection right side, maximum radiation to both sides, no chemo, no PEG, age 40 when diagnosed.
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