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#39581 01-18-2006 08:17 AM
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Hey all,

I just got back from my visit with a team of doctors at UPMC Presbyterian Hospital in Pittsburgh. I may start HBO therapy as soon as Monday.

The doctors feel that this therapy will heal the fistula that I developed. I asked about the success rate. I was told that it falls somewhere between 75% to 80%. If it works I can avoid surgery to correct the problem.

I was allowed to take a test run in one of the tubes. I may have to be under a mild sedative for the therapy sessions, as I discovered that I'm a bit claustrophobic. The sessions will last for 2 hours, 5 days a week for 6 weeks.

This really goes a long way in relieving my fears of ORN.

I'll keep posting throughout this process.

I'd love to hear from anyone else who may have gone through this.

John


SCC base of tongue. Diagnosed as stage IV, Sept. '04. Partial glossectomy, Radical neck dissection left side, 37 Radiation sessions, Chemo x 7 weeks. Finished treatments January '05. Cancer surivor!
#39582 01-18-2006 11:59 AM
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Good luck with the treatment John, I would need more than a "mild sedative" to get in one of those contraptions. We have a friend who is getting ready to start a course and are really hopeful it will help him.
Take care
Marica


Caregiver to husband Pete, Dx 4/03 SCC Base of Tongue Stage IV. Chemo /Rad no surgery. Treatment finished 8/03. Doing great!
#39583 01-18-2006 02:56 PM
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Marica,

I was hoping that the tube would be somewhat larger. I know when the opening is shut and locked behind me that it will be a problem. I first notice the claustrophobia when I had my mask made for the radiation.

I'll make it through. I'll have to be sedated and someone else will have to drive me home.

Let me know how things turn out for your friend.

John


SCC base of tongue. Diagnosed as stage IV, Sept. '04. Partial glossectomy, Radical neck dissection left side, 37 Radiation sessions, Chemo x 7 weeks. Finished treatments January '05. Cancer surivor!
#39584 01-18-2006 04:27 PM
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Hi John,
I did 30 "dives" of HBO treatment and did well with it. I was also fearful and claustrophobic of the mask for radiation but soon adapted to it. You'll find yourself doing the same with this chamber. Bring a movie to watch and that will help keep your mind off the closeness of the tube. I did find that I was tired after the treatments, which I think was simply from being still for so long, not from the treatment itself. The biggest change I had from the treatment was a change in my eyesight. I could see better! The improvement only lasted approx. 6 weeks though.
Good luck with it.
Minnie


SCC Left Mandible. Jaw replaced with bone from leg. Neck disection, 37 radiation treatments. Recurrence 8-28-07, stage 2, tongue. One third of tongue removed 10-4-07. 5-23-08 chemo started for tumor behind swallowing passage, Our good friend and much loved OCF member Minnie has been lost to the disease (RIP 10-29-08). We will all miss her greatly.
#39585 01-19-2006 07:19 AM
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Minnie,

The doctor did tell me that one of the side effects would be a change in my vision. He told me not to get a prescription changed if I had one.

I know I'll have to have something to calm my nerves. I just don't do well in tight, confined spaces.

The treatments sound promising and I'm looking forward to it.

John


SCC base of tongue. Diagnosed as stage IV, Sept. '04. Partial glossectomy, Radical neck dissection left side, 37 Radiation sessions, Chemo x 7 weeks. Finished treatments January '05. Cancer surivor!
#39586 01-19-2006 07:45 AM
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John, it really does get to be familiar and non-scary after the first or second dive. If I was not watching movies, I slept. Here is a tip. Take an antihistamine pill 30 min. before each treatment. This will help with pressure in your ears. Also, my vision improved dramatically and three years later is STILL good. Wore glasses to read and use compute for years and do not need them now. So you may get a big bonus if you wear glasses. I know you will do fine. It does feel strange in the beginning, but the speaker system lets you talk to the attendants at any time. They will never, ever leave you alone. Just concentrate on the good it is doing for you.

#39587 01-19-2006 08:53 AM
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Thanks for the support guys. I just don't want to get in the tube and have a panic attack. I know I was told that I could be out in as little as 45 seconds. But with that being said, I'd rather have something in me to calm the nerves before I start.

John


SCC base of tongue. Diagnosed as stage IV, Sept. '04. Partial glossectomy, Radical neck dissection left side, 37 Radiation sessions, Chemo x 7 weeks. Finished treatments January '05. Cancer surivor!
#39588 01-19-2006 03:38 PM
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John
They had discussed doing that treatment with my dad. He is so claustraphobic, let me put it this way, he can barley wash his hair under the shower claustraphobic. Imagine when he had to do Pet scans as well. That was his only fear. Not cancer, not radiation. I think if you just discovered it you'll be fine. Ask for Adavant. Works really good. The day I took him for his PET he thought we were in my car the entire trip instead of his. Breathe deeply, relax, and good luck.


P.Silveira
***************
Caregiver to Dad SCC Stage III T2N1M0 left hard & soft palate, left Node Dx 8/17/05, Neck Dissection 9/6/05 clear margins, Rx 30 ended 11/9/05, Still not cancer free. + path, agressive, upcoming chemo
#39589 01-20-2006 04:22 AM
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Zanax or Valium work well also. I saw a picture of a new model HBO unit in the paper the other day which was clear plexiglass. They also have big HBO chambers that hold 6 people.


Gary Allsebrook
***********************************
Dx 11/22/02, SCC, 6 x 3 cm Polypoid tumor, rt tonsil, Stage III/IVA, T3N0M0 G1/2
Tx 1/28/03 - 3/19/03, Cisplatin ct x2, IMRT, bilateral, with boost, x35(69.96Gy)
________________________________________________________
"You are a mist that appears for a little while and then vanishes" (James 4:14 NIV)
#39590 01-20-2006 05:43 AM
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The unit that I'll be in is clear acrylic. I can see all around the room. It's just the confinement that has me nervous. I have no problem with the PET scans or Ct scans. This is different. I'm hoping to hear something today, so that I can start this on Monday.

Thanks for the support guys!

John


SCC base of tongue. Diagnosed as stage IV, Sept. '04. Partial glossectomy, Radical neck dissection left side, 37 Radiation sessions, Chemo x 7 weeks. Finished treatments January '05. Cancer surivor!
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