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#139927 09-13-2011 09:57 AM
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Please offer opinions if you have the time.
I am scheduled to have most of my jaw removed and replaced with one of the fibula from my leg. Dr. Carlson & Dr. Herbig at the University of Tenn. will be performing the operation. They seem competent. I will undergo 10 more Hyperbaric dives after the surgery.

Do any of you have experience with this procedure?
What should I expect?

Thanks for any comments.
Mark


11/1999 SCC tongue - surgery
1/2000 Met(s) in lymph nodes - modRND
2/2000-4/2000 RT ~6 weeks
end of 2006 SCC tongue - surgery
1/2008 SCC BOT - surgery / PEG installed
2/2008 chemo & RT
4/2008 last time I consumed solid food by mouth
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Hi there - there are a few people here who've been through the same surgery. They will chime in I'm sure. I know its not an easy surgery since I've heard that from others. But if your surgeons are good, and the fact that they are using your own bone really helps then hopefully all will go well. The HBO is supposed to be great for healing! Just wanted to wish you luck and will turn you over to the experts! ;o) take care.


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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hello it looks likes you have already been through alot.
with jaw replacement you should be prepared not to be
able to walk for 2 months i was in very good physical
shape before surgery and i was very suprised of all the
strength it took to walk 50 feet with the aid of two nurses.
but now 2 years later my fibulia free leg is at 90%.
Ihope you fair as well Joe.


dx 5/15/09 stage 4 scc no positive nodes partial maxillectomy composit mandibulectomy fibular free flapleft neck dissection.
66gy all teeth removed surgery 7/8/09 peg placed 10/5/09 2 pets all clear 12/20/10.stage stage 2 melanoma 3/15/00
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Mark, I am very sorry to hear you have to go thru a mandibulectomy. Dont worry, you have come to the right place to get info about it. I have had it done, twice. The operation is a long and involved one. Before I get into the info, always remember everyone is different and will respond in their own way to surgeries, medications and procedures. You can not rush your recovery, take it day by day or if necessary, hour by hour.

Expect to be in the hospital for 2 - 4 weeks. It could be even longer so be prepared for anything. most patients are there for about 2 weeks. Ask your docs for a POSSEY MUIR valve trach. That will enable you to talk easily with it in. It helped me alot! If you dont ask you wont get so speak up. Take a dry erase board just in case. Make sure you have someone stay close to you during your hospital stay so they can advocate for you. Dont be surprised if you are kept sedated for a couple days immediately after the surgery. Its a good thing to let your body rest.

The surgery is a rough one to recover from. Since you are going thru HBO, it will make your healing much faster. Try to prepare for a recovery of at least 3 months. It will take that long before you begin to feel better. Dont worry, your docs can give you pain meds to ease any discomfort. You will need physical therapy and possibly speech therapy. Dont put these things off or it will be harder to return to your regular self. Expect to wait for one full year before any reconstructive surgery can be done. It will take that long for the swelling to completely go away and for new tiny blood vessels to grow on their own. Not all mandibulectomy patients need to have reconstructive surgery.

Im a huge believer in positive thinking. I feel it helps you to recover faster. Try your best to keep a positive outlook. Think of this surgery as another step in becoming cancer free. Please fee free to ask any questions you may have about this. I will do my best to help guide you thru. Good luck!!!!!


Last edited by ChristineB; 09-13-2011 02:55 PM. Reason: wrong name

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
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christine b i am not sure how to address messages (re.air kitty)


dx 5/15/09 stage 4 scc no positive nodes partial maxillectomy composit mandibulectomy fibular free flapleft neck dissection.
66gy all teeth removed surgery 7/8/09 peg placed 10/5/09 2 pets all clear 12/20/10.stage stage 2 melanoma 3/15/00
Joined: Jun 2007
Posts: 10,507
Likes: 7
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If you want to respond to this thread by airkitty, just type in the white box and click submit. If you want to contact them privately that is called a private message or PM. Click on the person's name and a drop down menu will appear, click on private message and type away. That is only between you and that person, it is not anything anyone on the forum can see.


Lastly, if you want to begin your own new post, click on the topic along the left your post fits under. then towards the top right click on New Topic. Type away and click submit.

If you need any other info, please send me a PM.


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: Nov 2006
Posts: 2,671
Patient Advocate (old timer, 2000 posts)
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Posts: 2,671
Hi Mark - Dr Eric Carlson was my son's maxillofacial surgeon and I can tell you that he is very aggressive and is one of the very best. You are in good hands! That was five years ago and my son is doing just great now. He did not have your particular experience but I'm glad to see that others here have responded with experience similar to what you will be having. You will find lots of support and information from very experienced and compassionate people. If you need local info on the area or the UT Med Ctr, just send me a PM.


Anne-Marie
CG to son, Paul (age 33, non-smoker) SCC Stage 2, Surgery 9/21/06, 1/6 tongue Rt.side removed, +48 lymph nodes neck. IMRTx28 completed 12/19/06. CT scan 7/8/10 Cancer-free! ("spot" on lung from scar tissue related to Pneumonia.)



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Thanks for the insights and encouragements. Christine - thank you for all of the good info. I will contact Dr. Carlson and request the special trach. I am scheduled to leave the hospital and go straight into an assisted living/rehab where PT & Speech Therapy are available. I have experience there with speech therapy. I learned to always have an advocate that is not medicated. My Wife and Mom will be with me to keep the staff in line. I remember as a young diabetic in a local hospital the nurses wanted to feed me then check my blood glucose then give me insulin. That order of events could have been very dangerous. Advocates if you want to live through a hospital visit. Joe - thanks for the support. Your time frames are what I am hoping for now. If I can ride my bicycle in two years then this procedure will be a success in my book. How did you sleep after the surgery (sitting up, on your back, etc...)? Did you have hyperbaric treatments?


11/1999 SCC tongue - surgery
1/2000 Met(s) in lymph nodes - modRND
2/2000-4/2000 RT ~6 weeks
end of 2006 SCC tongue - surgery
1/2008 SCC BOT - surgery / PEG installed
2/2008 chemo & RT
4/2008 last time I consumed solid food by mouth
Joined: Jan 2009
Posts: 1,844
Patient Advocate (1000+ posts)
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Posts: 1,844
Mark,

Ive had the procedure as well, what I will say is that everyone is going to be different and there are so many factors involved. I'm 3 years out and I'm very active but my leg is nowhere near 90%. Bike riding is doable and I even run bleachers, sprints and lift weights but that's been a long road.

A white board and advocates are wonderful suggestions as is the trach, I didn't have one set and should've looking back. I slept mostly sitting up or inclined. You sound like you're in good hands so keep a great attitude and I wish you the best of luck.

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.
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Hi, Mark,

My husband had the same procedure 11/09. He didn't need a trach but at the time was still on a PEG. That helped him keep up his nutrition requirements which are so important for healing. It's no picnic but was essential. His leg was very sore for months. He used a walker for a few weeks at home.

He has done well except for some post surgery infections. Everyone is different and you may not have that complication. He eventually had the titanium hardware removed because of infection.

There is some residual numbness around his mouth but he seems to managing that very well. Today, my husband and I are playing golf 4 times a week. We use a cart but there is still a lot of walking around.

My very best to you--
Anita



Anita (68)
CG to husband, Clark, 79,
DX SCC 11/07, T4N0Mx, PEG 1/08, RAD, post rad infection 3/08,
HBOT 40 dives, ORN, Surg 11/09 mandibulectomy w/fibular graft.
Plastic Surg 4/10, 12/10, 3/11, 10/11, 4/12, 10/12. All PETS clear,
PEG out 1/11. 6/11 non union jaw fracture
Fractured jaw w/surgery 7/14
Aspiration pneumonia 7/21, 10/22
PEG 7/21
Botox injections
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