Previous Thread
Next Thread
Print Thread
Page 1 of 5 1 2 3 4 5
#106746 11-09-2009 08:42 PM
Joined: Nov 2009
Posts: 76
Supporting Member (50+ posts)
OP Offline
Supporting Member (50+ posts)

Joined: Nov 2009
Posts: 76
Hi all,

I am doing some research to help with my coping and understanding of a recent diagnosis to my future father in law.

my future father in law (ive been engaged about 2 and a half months) has been diagnosed with a cancerous tumor that resides near his left jaw bone. He�s been going to a bunch of specialists for a while to try to pinpoint the cause of the pain he�s been feeling for the past 6-9 months, and they�ve finally found the tumor. He has surgery scheduled for Wednesday to remove it (along with some of the surrounding bone, tissue, and muscle), which will then be followed by rounds of radiation/chemotherapy as appropriate and then reconstructive surgery when the area is cancer-free. They have also seen some "bumps" on his neck so they will open the neck during the surgery and check that out/clean it out as well if necessary. I�ve been told that the surgery will be tricky, most likely an all day affair, but that they are optimistic about it and the chances are good that the cancer is localized to only this area. He will be in the intensive care unit of the hospital for about a week and then either return home or go to general care based on how things go.

I am trying to remain optimistic but get very scared when i read about the survival rates and everything that he will be going through in the upcoming months.
- does anyone have similar experiences- with tumors near jaw bone? this happened to my future father in law in the past and they did surgery to remove it. the current tumor is behind his scar tissue.
- what is he allowed to eat/drink, what can i bring him that will help?

feeling very overwhelmed, scared, nervous. but it has helped now that i have found this website to talk to others. thanks in advance for your help.


*KATIE*
future FIL dx with s4 SCC in jaw11/09 15 hour surg/trach/PEG in. 7 weeks of cisplatin/rads. 6/10- cancerous lung nodule- 1 wk of radiation. 8/13 pneumonia. 8/24 pulmonary embolism, on ventillator. 9/3/10 died peacefully w/o pain with family. 9/17/10 my wedding
palmtree27 #106749 11-09-2009 09:14 PM
Joined: Apr 2005
Posts: 2,219
Patient Advocate (old timer, 2000 posts)
Offline
Patient Advocate (old timer, 2000 posts)

Joined: Apr 2005
Posts: 2,219
Does your future FIL also live in NJ? If so,he has access to several excellent CCC's Comprehensive Cancer Centers and I hope that is where he is being treated. What is the name of the hospital?

There are many members that will be giving you some feedback, but it would good to know some things about his diagnosis and treatment, such as staging and the name of the chemo. This information can be put into your signature section so you don't have to keep writing. Take a look at some of th signatures so that you will have an idea of what should be there, then go to your profile and add the info at the bottom.


Jerry

Retired Dentist, 59 years old at diagnosis. SCC of the left lateral border of the tongue (Stage I). Partial glossectomy and 30 nodes removed, 4/6/05. Nodes all clear. No chemo no radiation 18 year survivor.

"Whatever doesn't kill me, makes me stronger"
wilckdds #106754 11-10-2009 01:41 AM
Joined: Jun 2007
Posts: 10,507
Likes: 7
Administrator, Director of Patient Support Services
Patient Advocate (old timer, 2000 posts)
Offline
Administrator, Director of Patient Support Services
Patient Advocate (old timer, 2000 posts)

Joined: Jun 2007
Posts: 10,507
Likes: 7
Palmtree, welcome to OCF. You will find lots of support here and help with your concerns. An important thing to remember, everyone here is different. We all heal and respond to treatments/meds in our own way. Please add a signature line when you are able to. There are several members from NJ/PA.

Ive just gone thru a similar operation. My lower L jaw was removed and replaced with a steel jaw. It sounds like my surgery was more involved than what you described. My cheek was removed, thats where my cancer was the cheek and it invaded my jawbone. I was in ICU for a few weeks, then a few weeks in other parts of the hospital. Radiation/chemo I had during my first round of cancer so I didnt have them. Thats also why it took me a long time in the hospital. Skin that has had radiation doesnt heal as well.

Let your FIL eat/drink anything he can. Currently, I use a feeding tube and eat only very soft foods like yogurt, soup broth and pudding. This is only temporary, things will improve.

Your FIL will have whats called a neck dissection. It takes a few lymph nodes from his neck and checks them for cancer. It will be done while he has his other surgery. My surgery was about 11 hours with 5 surgeons. You will see the neck dissection abbreviated as ND.

There are a few of us here who have gone thru this type of treatment. Best of luck with everything. Let me know if I can be of further assistance.


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
ChristineB #106766 11-10-2009 09:15 AM
Joined: Nov 2009
Posts: 76
Supporting Member (50+ posts)
OP Offline
Supporting Member (50+ posts)

Joined: Nov 2009
Posts: 76
Hi christine, im glad you have been through a similar experience. i think he'll be having the same surgery you did, but will have chemo/radiation after he heals. he is supposed to heal for 4-6 weeks before that part starts.

i will update my signature, once i know more details- i honestly dont know much ive only been told 2nd hand info from my fiance.

my future fil lives in syracuse, i know he is having the surgery done by an ENT but i dont think its a CCC.


*KATIE*
future FIL dx with s4 SCC in jaw11/09 15 hour surg/trach/PEG in. 7 weeks of cisplatin/rads. 6/10- cancerous lung nodule- 1 wk of radiation. 8/13 pneumonia. 8/24 pulmonary embolism, on ventillator. 9/3/10 died peacefully w/o pain with family. 9/17/10 my wedding
palmtree27 #106768 11-10-2009 10:50 AM
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
See if you can get him to visit this site. It will be invaluable to him.


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 #106788 11-10-2009 06:28 PM
Joined: Nov 2009
Posts: 76
Supporting Member (50+ posts)
OP Offline
Supporting Member (50+ posts)

Joined: Nov 2009
Posts: 76
i definitely will... he'll be in the hospital for up to a week and then home recovering- once hes at that point and has a lot of "time on his hands" so to speak, ill suggest this place for him. thank you!!!


*KATIE*
future FIL dx with s4 SCC in jaw11/09 15 hour surg/trach/PEG in. 7 weeks of cisplatin/rads. 6/10- cancerous lung nodule- 1 wk of radiation. 8/13 pneumonia. 8/24 pulmonary embolism, on ventillator. 9/3/10 died peacefully w/o pain with family. 9/17/10 my wedding
palmtree27 #106963 11-13-2009 01:20 AM
Joined: Jan 2009
Posts: 1,844
Patient Advocate (1000+ posts)
Offline
Patient Advocate (1000+ posts)

Joined: Jan 2009
Posts: 1,844
Palm,

I too have had a similar surgery. My primary tumor was on my right side, in my molar area. It was a large tumor that destroyed my jaw and took up nearly the whole side of my face. I also had 3 lymph nodes that were cancerous.

My medical team needed to shrink the tumors before surgery so my radiation and chemo was before surgery. The surgery was done at UWMC in Seattle and was a 17 hour fun fest. Due to the size of the tumor there were complications, during the surgery my facial nerve was compromised, paralyzing the right side of my face.

My jaw was removed and replaced with my fibula and my inner cheek tissue was removed and my mouth was lined with tissue from my fibula area (fibular free flap). I had a ND removing 40 some odd nodes during this surgery.

Christine (my hero) is completely right in having your FIL eat whatever he wants as he can. A PEG tube may be inserted and be fed by that or if he can eat orally he may only be able to get down liquids. Have your FIL sign up to this sight so that he can get support from those of us that have walked down this path. It will be important for advice, support and just to vent.

Your FIL may only get 1 chance at beating this beast so be sure to get the best care available...Cancer Care Centers are a great option there. Good luck if I can be of any help I'd be happy to help, although ChristineB is my hero (among others on this forum) and I believe so valuable in the info department.

Good luck


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 #107110 11-15-2009 07:06 PM
Joined: Nov 2009
Posts: 76
Supporting Member (50+ posts)
OP Offline
Supporting Member (50+ posts)

Joined: Nov 2009
Posts: 76
hi thank you for your story and advice eric S!
future FIL went into surgery on wednesday. the tumor was removed and the doctors are fairly certain and optimistic they got it all out. the flap was taken of his chest/side area and inserted- apparently during the surgery they were at first not going to insert the flap, and leave it open, but then decided to.
i am not sure if there was a full neck dissection or not.
he was in the ICU wednesday through sunday and then today he was moved into regular surgical inpatient! they said hes been healing well and is no longer considered "urgent care".
thank you for your advice so far and ill continue to keep you updated/ask questions.


*KATIE*
future FIL dx with s4 SCC in jaw11/09 15 hour surg/trach/PEG in. 7 weeks of cisplatin/rads. 6/10- cancerous lung nodule- 1 wk of radiation. 8/13 pneumonia. 8/24 pulmonary embolism, on ventillator. 9/3/10 died peacefully w/o pain with family. 9/17/10 my wedding
palmtree27 #107111 11-15-2009 07:07 PM
Joined: Nov 2009
Posts: 76
Supporting Member (50+ posts)
OP Offline
Supporting Member (50+ posts)

Joined: Nov 2009
Posts: 76
forgot to mention- he did have his whole side of the jaw removed/teeth included, steel jaw was insertd. facial reconstruction will happen down the road. right now he has trach and peg tubes in. will he be getting fake teeth inserted during reconstructive surgery? thanks!


*KATIE*
future FIL dx with s4 SCC in jaw11/09 15 hour surg/trach/PEG in. 7 weeks of cisplatin/rads. 6/10- cancerous lung nodule- 1 wk of radiation. 8/13 pneumonia. 8/24 pulmonary embolism, on ventillator. 9/3/10 died peacefully w/o pain with family. 9/17/10 my wedding
palmtree27 #107114 11-15-2009 07:20 PM
Joined: Jun 2007
Posts: 10,507
Likes: 7
Administrator, Director of Patient Support Services
Patient Advocate (old timer, 2000 posts)
Offline
Administrator, Director of Patient Support Services
Patient Advocate (old timer, 2000 posts)

Joined: Jun 2007
Posts: 10,507
Likes: 7

Sounds like your FIL is doing very well. Thats great news. I have a jaw made of steel too. The teeth would be done by a specialized dentist or oral surgeon familar with prosthodontics. Sometimes teeth are put in immediately during surgery.


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
Page 1 of 5 1 2 3 4 5

Link Copied to Clipboard
Top Posters
ChristineB 10,507
davidcpa 8,311
Cheryld 5,260
EzJim 5,260
Brian Hill 4,912
Newest Members
Jina, VintageMel, rahul320, Sean916, Megm37
13,103 Registered Users
Forum Statistics
Forums23
Topics18,168
Posts196,925
Members13,103
Most Online458
Jan 16th, 2020
OCF Awards

Great Nonprofit OCF 2023 Charity Navigator OCF Guidestar Charity OCF

Powered by UBB.threads™ PHP Forum Software 7.7.5