Previous Thread
Next Thread
Print Thread
Page 2 of 5 1 2 3 4 5
davidcpa #97870 06-22-2009 11:26 AM
Joined: Feb 2007
Posts: 1,940
"OCF across the pond"
Patient Advocate (1000+ posts)
Offline
"OCF across the pond"
Patient Advocate (1000+ posts)

Joined: Feb 2007
Posts: 1,940
Funny how opinions differ David.having a neck dissection makes perfect sense to me ,but i expect thats because rob had one and so do most patients in the uk.It seems fairly logical that the lymph glands should be thoroughly examined and sent for pathology if the primary is quite advanced,and really the neck dissection was a breeze compared to everything else,three days in hospital and back at work after ten.I do however worry about surgery on irradiated skin the healing process is so much harder with fragile tissue.Still i suppose its horses for courses,and as rob already had a massive secondary in his parotid gland a neck dissection was a no brainer.I wonder perhaps if we all tend to lend our opinion to the treatment we chose,especially if it worked!!

liz


Liz in the UK

Husband Robin aged 44 years Dx 8th Dec 2006 poorly differentiated SCC tongue with met to neck T1N2cM0 Surgery and Radiation.Finished TX April 2007
Recurrence June/07 died July 29th/07.

Never take your eye off the ball, it may just smack you in the mouth.
davidcpa #97881 06-22-2009 02:15 PM
Joined: Jan 2009
Posts: 1,844
Patient Advocate (1000+ posts)
Offline
Patient Advocate (1000+ posts)

Joined: Jan 2009
Posts: 1,844
I had to laugh at the neck dissection being a breeze comment and beg to differ. Experience one neck cramp and get back to me on that one, ok? Or the loss of movement of the lower lip, feeling and movement to one side of your tongue...all of these can be side effects (of which I suffer from them all) and are in no way a "breeze". They are in fact life altering.

I was however glad to have one done as they did find a few nodes with signs of cancer even after going through chemo and radx.

Elizabeth, I was 33 at time of diagnosis and have gone through much of what you are about to experience, although I don't have your type of cancer. I think you made a good choice with MD Anderson, 2nd opinions are smart, but you can't get better care really. Don't let this stuff scare you, you can do this! I've had the whole right side of my jaw replace, neck dissection...the works, if you have any questions don't hesitate to ask. I'm also on facebook, www.facebook.com/eric.statler, I love facebook! and recommend it to help keep people updated.

Good luck and keep breathing!

Eric


Young Frack, SCC T4N2M0, Cisplatin,35+ rads,ND, RT Mandiblectomy w fibular free flap, facial paralysis, "He who has a "why" to live can bear with almost any "how"." -Nietzche "WARNING" PG-13 due to Sarcasm & WAY too much attitude, interact at your own risk.
EricS #97887 06-22-2009 02:50 PM
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
Liz,

I'm sure everyone promotes the type of treatment they rec'd especially when it works but I also have read hundreds and hundreds of negative posts re ND's dealing with post surgery complications some posting years after their surgery about neck cramps, stiffness and life altering complications. So when I'm told by Moffitt, one of the top 10 CCC's in the U.S. and by one of the county's leading RO's that (in my case) he recommends the concurrent radiation/chemo first and no ND knowing that 3 doctors before him did recommend a ND and he tells me that Moffitt's experience has shown that the patient fares better with this approach and couple that with all the negative posts of people that did have one, I try to tell people my story and suggest they should get a 2nd opinion by a CCC. In Elizabeth's case she had already had multiple opinions and has been seen by a CCC but I still felt I needed to share my thoughts.


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 #97899 06-22-2009 03:58 PM
Joined: Dec 2008
Posts: 1,004
Patient Advocate (1000+ posts)
Offline
Patient Advocate (1000+ posts)

Joined: Dec 2008
Posts: 1,004
Hi Elizabeth and welcome. Wow....an oncology nurse? That just shows you never know what's going to happen. I bet it's nice to really have an understanding of what the docs are saying to you and understanding those darn pathology reports!!!

I'm sure you have knowledge, we will provide the support. I'm 29 also, minus the 3 kids:) I just have the husband.

How are you doing with the chemo?


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:)
suzanne98 #97907 06-22-2009 06:16 PM
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
Liz,, whatever I agree with you on this one too. I had it and it wasn't all that bad compared to everything else I have had. Yep, it was a breeze compared. Try an aneurysm guys and see what the real stuff can be like. They cut your stomache muscles and when you try to sit up or something that moves the stomache. you think you might end up in 2 pieces. But I can handle that too. LOL with tears at times.


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
suzanne98 #97908 06-22-2009 06:18 PM
Joined: Mar 2008
Posts: 404
Likes: 2
"OCF Down Under"
Platinum Member (300+ posts)
Offline
"OCF Down Under"
Platinum Member (300+ posts)

Joined: Mar 2008
Posts: 404
Likes: 2
IMO, David's posts recommending getting several opinions from CCCs, if someone hasn't already, for anyone starting on this crappy journey are probably one of the best pieces of advice anyone could get.

I sure wish I had of got more than 2.

Best wishes Elizabeth with all your appointments.

Karen

Last edited by Karen Rose; 06-22-2009 07:36 PM.

46 yrs:
Apr 07-SCC 80% entire tongue removed,T4N1M0
Neck/D,Jaw Split, Trache 2 ops,PEG 3.5yrs
30 x rad,6 x Cisplatin,
30 x HBO
Apr'08- flap Recon + ORN Mandibulectomy
(hip bone to reconstruct jaw)
Oct'08 1 Plate out-jaw
Mar'09 Debulk flap
Sep'09/Jan&Nov'10/Feb&Jun'11/Jan&Jul'12/Oct'13/April'14-More surgery
EzJim #97909 06-22-2009 06:20 PM
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
The Nissen fundiplication on your esophagus is no walk in the park either. In fact it might be worse. They wrap 1/3 of your stomache around your esophagus and believe me, I still feel that thing and this surgery was done in 1996. A lifetime of Zantac and Mylanta for me.


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
davidcpa #97914 06-22-2009 06:38 PM
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
Elizabeth, I had so many opinions they confused each other, The Oncologist I saw 1st at A Hospital in Wheeling , WVa was the one that had it right from the get go.After him I was sent to West Virginia University Hospital, then I was went to Ohio State James Comp. Cancer center. I had a couple of surgeries there but was told I didn't need chemo or rads because OSU got it all. The Oncologist from Wheeling Hosp, would call OSU and argue wuth him to give me the rads and chemo. Finally OSU said I had Cancer back and operated on me 2 more times then told me I need rads and chemo. LOL The Dr at OSU dsaid I suppose you want that Dr from wheeling to do what else you need. Hell yes I did, I had to have my teeth removed , I had a fortune in thise babies, and then after that I had the rads and chemo and was treated agressivley. I had Rad seed implants in my tongue or what is left of it. I was supposed to be in LaLa land for 3 days which turned into 7 days.Was readied for a rest home to die until I woke up the day before transfer. Dr was sitting by my bed when I opened my eyes and he siad, Jim, you are my mis=racle patient and have been his and the surgeons buddy since. Tell me to shut up will ya? I got carried away,, sorry Elizabeth. My daughter is the charge nurse in ouy heart unit and I have a couple more nurses in the family
too.


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
ESikon #97923 06-22-2009 07:10 PM
Joined: Jan 2009
Posts: 253
Gold Member (200+ posts)
Offline
Gold Member (200+ posts)

Joined: Jan 2009
Posts: 253
Dear Elizabeth:
I'm sorry you have to join our support group, but members on this site will do their best to help you on your journey to get well.
I am hesitant to mention this as I don't want to scare you, but since you're being treated by one of the best (Anderson, Texas) and you'r a nurse, I feel more comfortable relating this to you.
Last month at our Support Group, a gentlemen was there that had cancer in his Salivary Gland. He was treated at Georgetown Hospital, DC and Cyberknife. His left side of his face was paralyzed, and he was deaf in left ear. He was extremely bitter, so no one engaged him in conversation too much. I'm mentioning this as to warn you to ask as many questions as possible about what COULD go wrong with the operation.

Wishing you the best.
Sandyst



Sandy 56, BOT SCC Biopsy 1/21/09 Stage 3, T3NXM0.
Finished 3 cycle induction chemotherapy 4/7/09. (Chisplatin, 5-fu and Texotere). Re-staged 4/20/09,(very successful.) Will start Carboplatin/radiation 2 Gy/5 days/7 weeks (Tomotherapy) starting May 4th. Finished 6/22/09.
OCF member/supporter

EricS #97924 06-22-2009 07:16 PM
Joined: Feb 2007
Posts: 1,940
"OCF across the pond"
Patient Advocate (1000+ posts)
Offline
"OCF across the pond"
Patient Advocate (1000+ posts)

Joined: Feb 2007
Posts: 1,940
[quote]A breeze COMPARED TO EVERYTHING ELSE [/quote]


Liz in the UK

Husband Robin aged 44 years Dx 8th Dec 2006 poorly differentiated SCC tongue with met to neck T1N2cM0 Surgery and Radiation.Finished TX April 2007
Recurrence June/07 died July 29th/07.

Never take your eye off the ball, it may just smack you in the mouth.
Page 2 of 5 1 2 3 4 5

Link Copied to Clipboard
Top Posters
ChristineB 10,507
davidcpa 8,311
Cheryld 5,264
EzJim 5,260
Brian Hill 4,918
Newest Members
duchess, Firoze, jllawilsns01, TS75, makkie
13,316 Registered Users
Forum Statistics
Forums23
Topics18,246
Posts197,130
Members13,317
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