Previous Thread
Next Thread
Print Thread
Page 2 of 4 1 2 3 4
Joined: Jan 2009
Posts: 1,844
Patient Advocate (1000+ posts)
Patient Advocate (1000+ posts)

Joined: Jan 2009
Posts: 1,844
Debbie,

You are right...statistics don't apply to a case of one, for the good and the bad. There have been examples of stage 1 SCC (90% 5year)patients here that have died a year after being diagnosed.

"I have been referred to a local doctor and I am told I will be put in with all his other new patients and taken as he feels
necessary. I have been told it may be weeks before I can see him for even a consult."

This is the information you provided dear...to me if I was told this I would immediately look for care elsewhere. MD Anderson is a wonderful program, the Houston facility is well regarded and top rated. You can wait around and see if you are one of the "special" few this obviously overworked Dr picks to work with and see how that works out for you.

I didn't say you were being casual...but the information you gave showed examples of your medical professional being that way and the MD Anderson response is at best dissappointing. I doubt you would get the same response from a Cancer Care Center or from the sounds of things Moffit.

I also depended on my looks and speaking abilities for my profession and even being treated at one of the top programs in the US for cancer (6th) and otolaryngology (12th) I ended up disfigured and severely affected speech, unable to return to my work. My point was Debbie, you want a team as passionate about YOUR cancer as you are and your initial information painted a different picture.


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.
Joined: Sep 2006
Posts: 8,311
Senior Patient Advocate
Patient Advocate (old timer, 2000 posts)
Senior Patient Advocate
Patient Advocate (old timer, 2000 posts)

Joined: Sep 2006
Posts: 8,311
Debbie,

Sorry for the news. This may help you:

www.oralcancerfoundation.org/facts/rare/mc/index.htm

Either MDA or Moffitt would be a good choice so lets see what MDA says.

Good luck.


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.
Joined: Nov 2009
Posts: 396
Platinum Member (300+ posts)
Platinum Member (300+ posts)

Joined: Nov 2009
Posts: 396
seda bug,
search mucoepidermoid in the search box. it will take u to older post of others with this cancer.
finding the right team can be aggravating...but u will KNOW the right team when u find them.
good luck in ur search and keep us posted.


Teresa
-----------
CG to ANDY. Nasopharyngeal Carcinoma (NPC)
T2N2cMxG4 stage 4. 43 @ dx 8/31/09
tx 9/21/09-11/06/09 cispatin/docetaxel/5-FU X3
PORT 9/9/09, PEG 12/07/09
35 IMRT-1/wk carbo 11/30/09-2/3/10
tx stopped due to complications
IMRT BOOST 3/08-3/12/10
PET 4/12/10 CLEAR!
PEG out 4/14/10
Joined: Jan 2010
Posts: 142
Senior Member (100+ posts)
Senior Member (100+ posts)

Joined: Jan 2010
Posts: 142
I thank all of you for your assistance. Thanks to this board I have spoken with one Doctor from Knoxville and I have an appointment in the AM with local Doctor.
I had a suprising moment the other night when after spending HOURS reserching this and reading your posts and searching your site I came across the page showing the size of a cm it took me a couple of minutes to understand that 4 cm is larger than 4 mm.
I am not entirely stupid I just didn't grow up with metric I don't think in metric and there is only one little letter change didn't seem that big a difference.
The good news is that mine was only 4 mm Not 4 cm which means a different route for me. I will know tomorrow but the one conversation I had with the specialists was that this is very early to find it.
No EricS I won't let down my guard.
I want to thank you for being so blunt the other day I know I was defensive and confused. I have been on so many roller coasters since Monday I can't ever remember quite so many highs and lows in such a short time. But the list helped me there because I read that is normal.
So I will update and ask for advice after the meeting tomorrow.
Thanks again!


55 12/17/09 High Grade Muceopidermoid Carcinoma Alerted by Largo my Mini Schnauzer
1/18/10 Clr PET
1/27/10 Surgery found Perineural invasion
3/22/10 Began Rad
05/05/10 34 rads
8/19/10 Clr Pet Scan
12/13/10 Clr Ultra sound/biopsy
5/4/11 MRI Clear
8/2/11 All Clear
5/25/12 All Clear
6/3/2016 All Clear
5/25/2025 All Clear
Joined: Jan 2009
Posts: 1,844
Patient Advocate (1000+ posts)
Patient Advocate (1000+ posts)

Joined: Jan 2009
Posts: 1,844
Debbie,

No worries, I'm an acquired taste really which is why I generally apologize before I post. My heart is usually in the right place however at heart I'm a jerk with too much attitude and it oozes into everyhing I seem to write.

I try and steer clear of new posters and the caregiver forums as I feel I don't relate well in those areas...I know the last thing you need is to feel attacked on a "support" forum.

Good luck Debbie, I hope all goes well.

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.
Joined: Jul 2008
Posts: 507
"Above & Beyond" Member (500+ posts)
"Above & Beyond" Member (500+ posts)

Joined: Jul 2008
Posts: 507
Debbie,
I would agree with Kelly. You are quite fortunate to have a MDA Cancer Center in Orlando (affiliate of the renown UT MDA Houston CCC) and Moffit in Tampa.

I have seen some of the TomoTherapy presentations from the Orlando MDA and their work with Tomo in Head & Neck cancer has been pioneering. MDA's Tomo protocols seems to set a benchmark for many other Tomo centers (but I don't know is Tomo will be their recommended approach for Mucoepidermoid Carcinoma).

With a second opinion from Moffit you should be in good hands.


Don
TXN2bM0 Stage IVa SCC-Occult Primary
FNA 6/6/08-SCC in node<2cm
PET/CT 6/19/08-SCC in 2nd node<1cm
HiRes CT 6/21/08
Exploratory,Tonsillectomy(benign),Right SND 6/23/08
PEG 7/3/08-11/6/08
35 TomoTherapy 7/16/08-9/04/08 No Chemo
Clear PET/CT 11/15/08, 5/15/09, 5/28/10, 7/8/11

Joined: May 2009
Posts: 1,413
Likes: 1
Patient Advocate (1000+ posts)
Patient Advocate (1000+ posts)

Joined: May 2009
Posts: 1,413
Likes: 1
Debbie, so sorry about the news. You will be in my prayers.


Angelia
31 at Dx.
DX: 4/30/09, 10/21/09 SCC on floor of mouth,
T1NOMO, T2N1M0
TX: 39 IMRT, 8 cisplatin 11/30/09
PET/CT: 11/03/09: Lymph node involvement
PEG/PORT: 11/09
TX end: 02/01/10
PET Scan: 04/05/10 clear
PEG Out: 06/21/10
Biopsy: 12/23/10: fibrosis
HBO: 01/04/11 - ORN
Baby girl born 11-30-12
Joined: Sep 2008
Posts: 711
"Above & Beyond" Member (500+ posts)
"Above & Beyond" Member (500+ posts)

Joined: Sep 2008
Posts: 711
Debbie, 1 question. Do you have someone to accompany you to your appointments? It's a very good thing to have someone to take notes and ask questions you may not think of. A lot of info is going to be coming at you and you may feel overwhelmed by it all. I hope you have people to support you through this.


David R. 65 yr old male non-smoker, light drinker, stage 3 or 4, depending on which doc you ask, scc rt. tonsil, 2 nodes, 7 weeks radiation and chemo. No surgery. Teatment ended 3/20/08. PET scan 8/08 showed no cancer.
And now, as of oct, 2010, caregiver to wife, Linda, with breast cancer.
May, 2013, Linda diagnosed with stage 3 ovarian cancer. Enuf already.
Joined: Jun 2007
Posts: 5,260
Patient Advocate (old timer, 2000 posts)
Patient Advocate (old timer, 2000 posts)

Joined: Jun 2007
Posts: 5,260
If you have a recorder , take it in with you and record what is said. Good luck with your visit .


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: Sep 2009
Posts: 148
Likes: 1
Senior Member (100+ posts)
Senior Member (100+ posts)

Joined: Sep 2009
Posts: 148
Likes: 1
Hi Debbie, Sorry to have you as a new member here. You have already found out for yourself how helpful & wonderful a site this is, so you are already making smart choices in your care! It stinks going to the doctor on a Friday...makes for a very long weekend! Don't worry, great care is on its way & I'm sure your going to be just fine.


BOT T3N2M0 No surgery, 38radiation treatments,4 chemo rounds, peg removed 11/08, still have a port. Treatments ended 6/20/08. So far, so Good ! "I know God won't give me anything I can't handle. I just wish He didn't trust me so much !"

*** Admin update --- Dianne has passed away on August 25, 2015 ***
Page 2 of 4 1 2 3 4

Link Copied to Clipboard
Top Posters
ChristineB 10,507
davidcpa 8,311
Cheryld 5,264
EzJim 5,260
Brian Hill 4,918
Newest Members
Red Chicken, Teach, Harry B, Snowdrop123, Aurora1369
13,503 Registered Users
Forum Statistics
Forums23
Topics18,305
Posts197,297
Members13,504
Most Online7,516
Mar 21st, 2026
Powered by UBB.threads™ PHP Forum Software 8.0.1