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#128574 01-26-2011 01:24 PM
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suzee Offline OP
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Hi everyone. I'm Suzee. My father,77, was diagnosed with tonsil cancer just before Christmas. He had just gone to Las Vegas for the winter when he had a huge lump coming out the side of his neck. The Dr he saw in LV gave him a scrip for antibiotics and said he could be scheduled for a CT scan right after the holidays. My sister took him to the ER the next day, where a CT showed the tumor.

We have moved him and his wife to Houston and MDAnderson for the duration of his treatment. My brother and SIL live in Houston and my SIL is an ER doc so we were able to fast track him through the referral process.

The inter-disciplinary team decided on 7 weeks of Erbitux and 30 radiation treatments. Originally it was to be on the right tonsil but last week they decided to radiate on both sides, which made my father sad.

He had his first Erbitux infusion on Monday. He ran a fever for 12 hours and had a severe headache for 24. I think he has progressed to just dizziness.

My father and his wife are Korean and she speaks little english. I will be down in Houston every weekend throughout treatment, and the other 4 are taking turns being in Houston during the weeks.

We are all scared. I have been lurking on this board for several weeks and it really has helped me process what treatment will be like and how to be best prepared. You could never realize the great comfort you've brought to us kids already. Thank you!


Daughter and weekend care-giver/cheer-er up-er person for my Daddy - 77
12/10 diagnosed SCC right tonsil, T2N2bM0, HPV+
Being treated at MD Anderson
Cituximab started 1/24/11 33xIMRT started 1/31/11
suzee #128575 01-26-2011 01:33 PM
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Suz,

Welcome to the group!

It sounds as though your Dad is in good hands and is very lucky to have such a proactive group of family members.

Yes, lurking and reading the boards is a great way to learn what you are dealing with. It gives you ammunition to ask the questions that are so pertinent to your father's case.

This is a place of comfort for sure!

Deb


Deb..caregiver to husband, age 63 at diagnosis, former smoker who quit in 1997.
DIAGNOSIS: 6/26/07 SCC right tonsil/BOT T4N0M0
TREATMENT START: 8/9/07 cisplatin/taxol X 7..IMRT twice daily X 31.5.
TREATMENT END: 10/1/07
PEG OUT: 1/08
PORT OUT: 4/09
FOLLOWUP: Now only annual exams. ALL CLEAR!

Passed away 1/7/17 RIP Bill
debandbill #128576 01-26-2011 01:42 PM
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Was he a tobacco user?

Have they mentioned HPV?

MD Anderson is a top notch facility.


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.
davidcpa #128579 01-26-2011 01:51 PM
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suzee Offline OP
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Thank you Deb!

David, My father was not a tobacco user. He was a drinker, and he has tested HPV+. We have all been asked by MDA to give blood for research testing and all but one of us did.


Daughter and weekend care-giver/cheer-er up-er person for my Daddy - 77
12/10 diagnosed SCC right tonsil, T2N2bM0, HPV+
Being treated at MD Anderson
Cituximab started 1/24/11 33xIMRT started 1/31/11
suzee #128580 01-26-2011 01:58 PM
Joined: Dec 2008
Posts: 1,004
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Hi Suzee and welcome to OCF. I'm happy that you joined our group here. You will find the surrport you need and answers to all of your questions.

I wish your father, you and your family strength during this hard time.


Suzanne
***********
T1 SCC on right side of tongue
Age 31...27 when diagnosed
4 partial glossectomies
No chemo or radiation
Biopsy on 2/2/10-Clear
Surgery needed again...no later than April 2011
Loving life and just became a mother on 11/25/10
It's not what we CAN'T do..it's what we CAN do:)
suzee #128581 01-26-2011 02:02 PM
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Posts: 8,311
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You will hear us say "we all can respond to the same or similar treatment differently" and that's because it's true. Some breeze through, some have a horrible time from day one but most of us start to feel the effects of concurrent chemo/rad around the 4th week and we get progressively worst until the 3rd week POST Tx with the few weeks post Tx our worse. Make sure he gets plenty of water daily (minimum 48ozs), consumes 2500+ calories each and every day and stays on top of his pain. Keep after his cancer team and make them aware of everything. Also ask us any question or vent 24/7. That's what we are really good at because between the patients and the caregivers we have assembled on this site at any one point, we have probably been there done it.

As you have probably been told an HPV+ Dx is a good thing.


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.
davidcpa #128614 01-26-2011 11:55 PM
Joined: May 2010
Posts: 224
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Sorry to hear but the support you all are giving him will definately help him through this!


25/female at diagnosis
Dx;stage 3 SCC tongue 03/25/2010
Surgery 04/13/2010
Trach,ng tube, peg feeding tube
Hemiglossectomy, right side neck dissection, 40 lymph nodes removed. Free-Flap transplant to tongue.
30 rounds IMRT ended July 15,2010

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