Previous Thread
Next Thread
Print Thread
Page 2 of 2 1 2
Joined: Feb 2008
Posts: 19
Pookie Offline OP
Member
OP Offline
Member

Joined: Feb 2008
Posts: 19
Tom, I think that we talked on here the first time I posted, I'm the one born in Massillon, GO TIGERS! Yes I'd appreciate a name of a Doc at UH, but I'm confused as to what kind I should see, an oncologist (and oh by the way, do they all treat all forms of cancer, probably a stupid question) or a RO?

This is a mess to me and any guidance would help immensely.

Thanks,

Paua


51 yr old female...dx 12/28/07, partial gloss 1/23/08, nd 3/5/08. Opened the neck AGAIN, 5/21/08. Non smoker, occasional drinker. Additional node pos. 6/26/09, Starting rads and chemo (5-fu, Cisplatin) 7/13/09 T1N2MO. Almost 2yrs out of treatment and feeling great....
Joined: Sep 2007
Posts: 98
Senior Member (75+ posts)
Offline
Senior Member (75+ posts)

Joined: Sep 2007
Posts: 98
Hi Paula,
I remember you now because you went to Massillon HS and my wife went to McKinley HS. Big high school football rivalry.

My ENT doctor at UH is Dr Pierre Lavertu. He chose my course of treatment of radiation and chemo. Phone - (216) 844-4773.

I actually saw Dr. Lavertu today and he said he just graduated me from 2 month visits to 3 month visits as of today.

My Radiation Oncologist is Dr. Kunos.

My Medical Oncologist is Dr Savvides.

All these doctors work as a team at the UH Ireland Cancer Center.

Lavertu is a Head and Neck doctor. I think Kunos and Savvides treat all types of cancers.

I hope this helps. Let me know if you need any other info.


Tom
SCC T4N1M0 left side tongue & 1 node
Dx 05/21/07 42 yrs old
40 Tx IMRT @ 70 Gy started 06/25/07
Cysplatin & 5fu 1st & 4th wks
treatment ended 08/23/07
Joined: Jun 2007
Posts: 5,260
Patient Advocate (old timer, 2000 posts)
Offline
Patient Advocate (old timer, 2000 posts)

Joined: Jun 2007
Posts: 5,260
How about that, Pookie with the Tigers, Tom's wife with McKinley and I'm with Steubenville Big Red. LOL Now those used to some big game for all 3 schools. WE all played each other then.


Since posting this. UPMC, Pittsburgh, Oct 2011 until Jan. I averaged about 2 to 3 surgeries a week there. w Can't have jaw made as bone is deteroriating steaily that is left in jaw. Mersa is to blame. Feeding tube . Had trach for 4mos. Got it out April.
--- Passed away 5/14/14, will be greatly missed by everyone here
Joined: May 2007
Posts: 132
"OCF Down Under"
Senior Member (100+ posts)
Offline
"OCF Down Under"
Senior Member (100+ posts)

Joined: May 2007
Posts: 132
Hi Paula,
I agree with the other posters that you should get a second opinion but would also like to offer a word of warning about biopsies. I had 3 surgeries last year for two cancers in my mouth with clear margins (the last surgery was a partial mandibulectomy in September). No rad or chemo was deemed necessary by my ENT and his cohorts on the tumour board (which he chairs) and all looked good until March when a lump appeared under my chin just two weeks after a 'clear' check up. I went back to the ENT and was sent for a CT scan which confirmed an enlarged 'suspicious' 1.8 cm node.

I then had a PET/CT scan and a fine needle biopsy which both were 'negative' for cancer. No uptake in the node and no cancer was found in the samples from the needle aspiration. Due to the results of the original CT scan my surgeon wanted to remove the node anyway so I had surgery on the 12th May. The node was removed and a frozen section taken and sent to pathology while I was still under. It was almost 3cm in size and there was extracapsular spread. It was cancerous so a selective neck dissection was done and 48 further nodes removed (all were found to be free of cancer). I am now having chemo and radiation.

I guess the moral to my story is get as many tests done as possible and don't make any decisions based solely on biopsy results - they are just a sample and the cancer could be potentialy be missed.

Good Luck!

Sue



55 y/o
SCC LL Tongue 3/27/07
Part. mandibulectomy 9/2/07
Left ND 5/12/08
RT/Chemo
Rec LL Tongue 07/09
Part gloss 8/5 & 8/25
Surg 10/28/09 re mets to R neck & L jaw
RT & Chemo finished 12/22/09
PEG fitted 05/06/10
L buccal SCC 10/10
freeflap (forearm)surgery 2/28/11 L buccal and gingiva
Joined: Sep 2006
Posts: 8,311
Senior Patient Advocate
Patient Advocate (old timer, 2000 posts)
Offline
Senior Patient Advocate
Patient Advocate (old timer, 2000 posts)

Joined: Sep 2006
Posts: 8,311
True the downside to a FNA is that the cells can only be tested from the fluid withdrawn and if that misses the cancer in whatever they stick then the cancer would be overlooked. I know that my FNA involved 2 separate sticks and a considerable amount of fluid and even so I feel fortunate that they were able to Dx my cancer.


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.
Page 2 of 2 1 2

Link Copied to Clipboard
Top Posters
ChristineB 10,507
davidcpa 8,311
Cheryld 5,264
EzJim 5,260
Brian Hill 4,918
Newest Members
Firoze, jllawilsns01, TS75, makkie, richv0001
13,315 Registered Users
Forum Statistics
Forums23
Topics18,245
Posts197,129
Members13,316
Most Online1,788
Jan 23rd, 2025
OCF Awards

Great Nonprofit OCF 2023 Charity Navigator OCF Guidestar Charity OCF

Powered by UBB.threads™ PHP Forum Software 7.7.5