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Joined: Jun 2007
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Christine is my hero too. For sure she is a one of a kind lady that knows how to fight. Christine doesn't talk about herself much, but likes to boost others into being positive.


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
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Hi and welcome Jeanna,
As you have discovered this is the best place to find information and support for OC.
I myself am a nearly 3 year survivor but from what you have described you and WendyG are travelling a very similar and difficult path at the moment.
The Lyn that Jim has mentioned is also in Melbourne and posts here under the name LynfromOz as well as Karen Rose and Sue G.
Wendy and I are both from NSW as are some friends who post under the name of Tizz and Aussieh.
There are also a few others who post from time to time.
Even though there are a few of us from Downunder the disease is international and even though we are all from different countries we all consider ourselves to be part of a family.
Some of us including Liz, Christine and Jim are also friends on facebook where you can see a little more about us and what we look like.
http://www.facebook.com/oralcancerfoundation .
Am at work writing this and just wanted to say hello for now and as Christine wrote we want to let you know that you are not alone.
Welcome {{{{{hug}}}}}Gabriele


History Leukoplakia bx 8/2006 SCC floor mouth T3N0M0- Verrucous Carcinoma.
14 hour 0p SCC-Right ND/excision/marginal mandibulectomy 9/2006, 4 teeth removed, flap from wrist, trach-ng 6 days- no chemo/rad.
6 ops and debulking (flap/tongue join) + bx's 2006-2012.
bx Jan 2012 Hyperkeratosis-Epithelial Dysplasia
24cm GIST tumour removed 8/2013. Indefinite Oral Chemo.

1/31/16 passed away peacefully surrounded by family

Joined: May 2009
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Hi and Welcome Jeanna. I am glad you found this site. There are a lot of wonderful people on here. This is my "family." As the people here know what we go through and the emotions that can hit us when we least expect it. Keep us updated on Ron's progress.


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
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Thank you all so much for the support you have already shown me & my other. I like it that you all still manage to have a laugh - that is really important. I had to laugh at the person who woke from some sort of surgery & started hallucinating...Rod did the same after his peg was inserted, can't quite remember but something about a wheelbarrow on the ceiling...he told me he had everyone in recovery laughing but was a bit embarrased when he found out what he was like. I went to my chiro this morning & was telling him about this site. I said I felt so much better mentally after coming across this support.

Rod had 4 weetbix this morning for breakfast, I said if he ate it all he only had to have 1 x formular via the peg. He did good. He said he will try & eat something else at lunchtime, I would assume it's very hard for anyone with no teeth. Eating anything is a good thing. His next follow up is on Tuesday next week. I'll be decreasing the MS Contin again tomorrow.

Question - I would have expected the small lymph node to go by now but it hasn't. The large one has decreased in height more than size - is that normal for 3 weeks post Tx?



Jeanna
Wife/Carer of Rod, 56, Dx 5/3/09, SCC Oropharnyx T4 N2, End Tx 28th 07/09, 7wks Rad, 3 Cisplatin, primary tonsil, 4cm Lymph right of neck, 1cm left, in jaw & soft palate & base of tongue. Peg 06/09. CT & PET scans 02/11 - NED. Dentures 20/09/11, PEG out 28/10/11.
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that's great news Jeanna that Rod had weetbix. Every little bit counts. Steve had 1 today plus 4 glasses of icecream so I'm happy with that. Plus he's on 5 cans of 2cal via his peg and his weight is slowly climbing back up. I'll be interested to see what answers you get to your question. Steve also has 2 tumours still showing and we are nearly at the end of treatment. I'm concerned as well but figure treatment continues to work for a bit after it ends so I'm hopeful they will continue to shrink. I will be thinking about you and Rod and wishing you all the luck in the world.


Wife to Steve 43. DX 5 May 09. T4N2MO SCC tongue, floor of mouth, lymph nodes & jaw bone
No surgery
Teeth removed 06/07/2009
radiation 13/07/2009 x 7wks
chemo 15/07/2009 x 3 Cisplatin
last TX 28/08/2009
25/11/2009 PET-lymph node activity.
08/01/2010 CT Scan-ALL CLEAR
03/03/2010-Peg removed
01/2013 left side of Jaw removed and replaced with pectoral flap.
23/12/2020 scan show lesion in tongue
01/2021 SCC stage 3 base of tongue diagnosed
01/03/2021 chemotherapy started.
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About no tetth. LOL If it can't be gummed to death, trash it. I have been trying to eat for 20 months without chompers. It just doesn't work so great. It's a lot like a Bear trying to not empty out in the woods. LOL hard to do.


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: Aug 2009
Posts: 207
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LOL Jim, but all he wants for Xmas is a full set of teeth & an eye fillet steak!! Are you going to eventually invest in some chompers yourself? I've heard a lot from my mum about people gumming to death & being fine with it. Rod hates it, think he wishes now he'd looked after his before gtting them all out!!

Thanks for your ET's email add, once I get used to this site, I'll write to her.

J


Jeanna
Wife/Carer of Rod, 56, Dx 5/3/09, SCC Oropharnyx T4 N2, End Tx 28th 07/09, 7wks Rad, 3 Cisplatin, primary tonsil, 4cm Lymph right of neck, 1cm left, in jaw & soft palate & base of tongue. Peg 06/09. CT & PET scans 02/11 - NED. Dentures 20/09/11, PEG out 28/10/11.
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LOL Jim, but all he wants for Xmas is a full set of teeth & an eye fillet steak!! Are you going to eventually invest in some chompers yourself? I've heard a lot from my mum about people gumming to death & being fine with it. Rod hates it, think he wishes now he'd looked after his before gtting them all out!!

Thanks for your ET's email add, once I get used to this site, I'll write to her.

J


Jeanna
Wife/Carer of Rod, 56, Dx 5/3/09, SCC Oropharnyx T4 N2, End Tx 28th 07/09, 7wks Rad, 3 Cisplatin, primary tonsil, 4cm Lymph right of neck, 1cm left, in jaw & soft palate & base of tongue. Peg 06/09. CT & PET scans 02/11 - NED. Dentures 20/09/11, PEG out 28/10/11.
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Oops...well, just in case you wanted to read that twice!! smile Note; if I don't laugh once a day, I'll cry inside all day.....you guys rock.....


Jeanna
Wife/Carer of Rod, 56, Dx 5/3/09, SCC Oropharnyx T4 N2, End Tx 28th 07/09, 7wks Rad, 3 Cisplatin, primary tonsil, 4cm Lymph right of neck, 1cm left, in jaw & soft palate & base of tongue. Peg 06/09. CT & PET scans 02/11 - NED. Dentures 20/09/11, PEG out 28/10/11.
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