ROLL CALL 2015 (ENROLLMENT, CHECKING-IN, STATUS UPDATE) CLOSED 8-15-15
Comments
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JThornsbury -- Living Large in the Lone Star State
Diagnosised on Jan 2013 with SSC of RTonsil after tonsilectomy. offical diagnosis Tx(2) N2b M0. Completed 32 radiation treatements at MD Anderson in Houston Texas. Frist all clear May 2013 two months after my 50th birthday. All Clear with upcoming 2 year and two month scan on July 20th...litte dry mouth. most taste is back. ran and completed my first 13.1 half in March right before my 52th birthday and planning to run the next one in November! Plan is to run two 13.1 a year till I'm 100! I am living each day grateful and thankful!
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checking inNJShore said:NJShore
NJShore - Kari & Dan
October, 2012
T2N2bM0 stage IV A left tonsicular squamous cell carcinoma (Dan)
it's not an easy road, but a road worth traveling -- and we were fortunate to find this awesome place and incredible people to guide us through.
Kari & Dam,
What a great looking couple (and fur baby too).
Great to see you!
Matt
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work in progressmeaganb said:meaganb
Sorry double post
Andrew. New Zealand. Diagnosed Sept 2014. Invasive SCC nasal septum extending into maxilla. Incomplete excision Oct 2014. Radio and chemo for 35 days. PET scan April 2015- NED. Facial reconstruction surgery with fibula free flap June 2015. Recovering prior to tidy up surgeries.
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Cureitall66
Cureitall66, Michigan- 54 yr old male (Loved one, Kreg)
Joined Forum Aug 2012
Dx Aug 2012 Stage IV, SCC BOT, 2 lymph nodes, HPV16+
Tx ended Nov 2012 No surgery, Chemo (Carboplatin & Paclitaxel) once wk for 7 wks, Radiation 5 days wk for 7 wks
Latest check up 07/16/2015 - NED
Back to Golfing and riding his Harley! Enjoying Life!
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3rd time tx?Hondo said:Wow what a wonderful way to remember Johnny:
Tim “Hondo”
Lafayette Louisiana
2002: First treatment for NPC Did just radiation 180 rad once a day
2004: Recurring NPC in the same place Did 120 rad twice a day and Chemo
2006: Recurring NPC again same area, was giving 6 to 12 mounts to live
2015: Still alive no sign of recurring NPC, living with some very bad radiation side effects and Norcoses to the soft palate, but still alive and thanking God for everyday one day at a time.
On Vacation in the tropical Island of Utila Honduras
Hondo,
Your story is a miracle... Did you do any tx for 3rd time diagnosis... ?
Kat
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KB56 - Keith
Diagnosed 4/1/2013 (April Fool's Day) and completed 34 Radiation treatments and 7 Erbitux.
T2N2M0, primary right tonsil and multiple lymph nodes on the right side of the neck.
Last CT SCAN and Doctor visit was June 2015 and all NED!
Home state is Texas right outside of Dallas.
a new grandfather (the first for us) and a very proud grandfather to my new granddaughter.
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Lots of friends hereKB56 said:KB56 - Keith
Diagnosed 4/1/2013 (April Fool's Day) and completed 34 Radiation treatments and 7 Erbitux.
T2N2M0, primary right tonsil and multiple lymph nodes on the right side of the neck.
Last CT SCAN and Doctor visit was June 2015 and all NED!
Home state is Texas right outside of Dallas.
a new grandfather (the first for us) and a very proud grandfather to my new granddaughter.
Ratface
Chicago
Diagnosed 2009
Still here!
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roll callElaineh said:Roll call
Hey Matt. I want to enroll but am not sure how??
Elaineh,
you just did.
Feel free to say where you are from, a little bit about yourself, if you’re undergoing treatment how’s it going, if you’re finished how are your side effects?
We are very informal here at the H&N forum. Say whatever you feel like saying, cancer is the common thread here, but possibly not the most important.
Matt
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Four Years Out
Nick finished his treatment 4 years ago at the end of June, 2011. He had been diagnosed in March of that years with BOT SCC Stage IV, HPV +. After a consultation with Dr. Urken at Beth Israel (NYC) and a trip to Johns Hopkins, he went with treatment here at the Jersey Shore. It was the standard 35 doses of radiation via IMRT and three cisplatin. All things considered, the cisplatin was the worst of it, but Atavin was a life saver. He never got a PEG and ate--with great difficulty and perseverance--throughout. Taste came back in stages though he tells me even now apples don't taste as wonderful as they once did. Some hearing disability from the cisplatin--he did have the dose reduced for the 2nd and 3rd treatments. The big residual is his failing thyroid that we can't quite get ahead of.
I always read the board and am so happy to see so many get successfully to the other side of this challenging treatment--as our medical oncologist told us, outside of some leukemias, this is about the worst of the cancer treatments. Especially glad to see my spirit guides Skiffin and Hondo still here giving with such generosity.
Nancy
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Caregiver to husband...
Husband was diagnosed August 2013 – SCC of epiglottis with 2 lymph nodes, Stage 4b - HPV negative. Completed treatment end of November 2013 – 35 rads, weekly cisplatin (6 total), no surgery.
Did our research and 3 consults before treatment. Walter Reed suggested surgery to remove epiglottis along with the tumor and put in a temporary trach tube, then chemo and rads. Was told that the rads would destroy epiglottis and that is why they would remove it. Local ENT suggested chemo and rads, no surgery. Local radiologist was furious that we were told rads would destroy epiglottis; said they were trying to save it, not destroy it. Went with local ENT, radiologist and oncologist. Were shocked with the differing opinions of treatment!
Here we are, almost 2 years later, NED. Second PET scan will be in November. Issues with dry mouth and taste, some swallowing/slight choking issues, occasional flair ups of the radiation site.
Every day is a gift.
From Fredericksburg, Virginia
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Awww Shucks..Redbanker said:Four Years Out
Nick finished his treatment 4 years ago at the end of June, 2011. He had been diagnosed in March of that years with BOT SCC Stage IV, HPV +. After a consultation with Dr. Urken at Beth Israel (NYC) and a trip to Johns Hopkins, he went with treatment here at the Jersey Shore. It was the standard 35 doses of radiation via IMRT and three cisplatin. All things considered, the cisplatin was the worst of it, but Atavin was a life saver. He never got a PEG and ate--with great difficulty and perseverance--throughout. Taste came back in stages though he tells me even now apples don't taste as wonderful as they once did. Some hearing disability from the cisplatin--he did have the dose reduced for the 2nd and 3rd treatments. The big residual is his failing thyroid that we can't quite get ahead of.
I always read the board and am so happy to see so many get successfully to the other side of this challenging treatment--as our medical oncologist told us, outside of some leukemias, this is about the worst of the cancer treatments. Especially glad to see my spirit guides Skiffin and Hondo still here giving with such generosity.
Nancy
Glad to see you here and doing well...
John
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Debbie
Debbie
larynx
8/2009 had 35 rad tx
2/2012 recurrence and had total laryngectomy
Ohio
It is a very rough road but its a fight you can win!! Hang tough!
0
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