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#145086 01-27-2012 06:03 AM
Joined: Jul 2009
Posts: 280
CMMoore Offline OP
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Posts: 280
PET and CT were yesterday, we get results later today.
We got a good impression of the doc when we met her last week, but she didn't know what to do next really, and said that it seems the previous team threw everything medically available at the cancer already.
We have watched documentaries of the Gerson therapy and natural cures, which seem to be the core of CTCA programs. That may be all that Matt has left to try.
I haven't slept much in the past few days. Speculation of what might be coming today is enough to make me crazy (er)....
Neither of us are ready for the news we fear will come.

I know... positive thinking, etc. I am grateful that this forum is here.


CG to my husband, Matt. Dx June 2009 Stage IV Oropharengeal SCC right tonsil primary with distant metastases. Rad to neck- Surgeries to lungs- Every avail chemo - ran out of options Jan 2012, called for hospice help Feb 2012, at rest March 19, 2012.
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"OCF Canuck"
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No clinical trials? Someone here is looking into personalized chemo, they require a fresh biopsy sampl an a an checks it to see specifically what it responds to... Check the post about personalized care. Good luck!


Cheryl : Irritation - 2004 BX: 6/2008 : Inflam. BX: 12/10, DX: 12/10 : SCC - LS tongue well dif. T2N1M0. 2/11 hemigloss + recon. : PND - 40 nodes - 39 clear. 3/11 - 5/11 IMRT 33 + cis x2, PEG 3/28/11 - 5/19/11 3 head, 2 chest scans - clear(fingers crossed) HPV-, No smoke, drink, or drugs, Vegan
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I cant even begin to image what you and your husband are going thru. It must be pure torture waiting to hear the results. Try your best to keep busy to help pass the time. I will keep you both in my prayers.


Christine
SCC 6/15/07 L chk & by L molar both Stag I, age44
2x cispltn-35 IMRT end 9/27/07
-65 lbs in 2 mo, no caregvr
Clear PET 1/08
4/4/08 recur L chk Stag I
surg 4/16/08 clr marg
215 HBO dives
3/09 teeth out, trismus
7/2/09 recur, Stg IV
8/24/09 trach, ND, mandiblctmy
3wks medicly inducd coma
2 mo xtended hospital stay, ICU & burn unit
PICC line IV antibx 8 mo
10/4/10, 2/14/11 reconst surg
OC 3x in 3 years
very happy to be alive smile
Joined: Jul 2010
Posts: 531
"Above & Beyond" Member (500+ posts)
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Posts: 531
So good to hear from you Christine and prayers going to you and your hubby! Hope to hear good things.


CG to Ron
Out of Pain 4/3/13
4/12-lung and under chin growth no treatment
1/13/12 lung biopsy
6/11 recur 6/30 resection #2 Clear margins
Clear 12/10
Surg 5/13/10 neck dis/nodes part gloss/flap R thigh all teeth out
RAD 30 8/10
DX 4/2/10 "Oral Cavity" T3NOMO
12/28/07 Non Hodg Lymph remission 7/08
passed away 4.3.15, RIP Ron, you are greatly missed
SUEZ #145420 02-03-2012 10:12 AM
Joined: Jun 2011
Posts: 188
Senior Member (100+ posts)
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Posts: 188
The personalized chemo testing nut 'tis me. Initially my Dad's MO, as well as every MO we've spoken with, dismissed this type of testing as unnecessary, not proven, etc. You do NEED your MO to at least consider the findings of this type of testing, and we were pleasantly surprised to learn that he changed his mind and his tumor sample is being reviewed as of now.

In reality, we do not anticipate a miracle and suspect the results will recommend similar Rx to what's on his agenda now. But I HAD TO LOOK FURTHER.

My Dad's mets sound similar to Matts. He is currently on this trial http://clinicaltrials.gov/ct2/show/NCT01044433 and as of now his mets have shrunk. To be clear, his MO is pleased but all MOs still confirm this is palliative care.


Caco
CG to Dad. Biopsy 5/11 non-op, SCC stage IV poorly dif at base of tongue with nodes, quit smoking in '85, ChemoRad began 8/2/11 ended 9/22/11 with NED. Distant mets 11/11, clinical trials. War raging on!

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