#5560 06-19-2005 09:15 PM | Joined: Oct 2003 Posts: 18 Member | | Member Joined: Oct 2003 Posts: 18 | im 2 and a half years out of treatment and my spit glands seem to be trying to work again, there is actually days i can spit, i know that sounds groce but to me im excited about it, has any one else experienced this going from a mouth so dry u could pull dust balls out to actually being able to spit, there is times it is thick but they seem to be trying to come back, every thing i have read and have been told once you loose them there gone, is this just a temp. thing or can they come back? | | |
#5561 06-20-2005 02:46 AM | Joined: Jan 2005 Posts: 108 Gold Member (100+ posts) | | Gold Member (100+ posts) Joined: Jan 2005 Posts: 108 | It's one year since I began my rads and for the most part I am still dry...but not as bone dry as it was six months ago. On a recent trip to the dentist, she said she could actually see a lttle saliva pooling in the bottom of my mouth (very little!) but I'll take what I can get. If at 2 1/2 years there is continuing progress I am delighted to hear it. I am also delighted to hear of a 2 1/2 year survival. I'd say you're hitting on all eight cylinders Coop..congratulations. Fran B
SCC Base of tongue diag. April 04 Stage IV, mets to rt. neck multiple nodes 35 rads+8 boosts First recurrence Jan05. Rt.rad neck dissection Feb02/05. Recurred with bone mets in neck July 05. Committed to survival with dignity.
| | |
#5562 06-20-2005 02:52 AM | Joined: Mar 2002 Posts: 1,140 Likes: 1 Patient Advocate (1000+ posts) | | Patient Advocate (1000+ posts) Joined: Mar 2002 Posts: 1,140 Likes: 1 | Nothing gross about it. Coop. Going in, I told the rad people to do their best, and all I wanted when it was finished was to be able to spit. Strangely, the side which received the most rad, where they told me I would lose the salivary glads, is now back on line. I am 3-1/2 years out and the saliva function just keeps increasing to where I must be 95% of normal. Hang in there! | | |
#5563 06-20-2005 09:47 AM | Joined: Jul 2003 Posts: 1,163 Patient Advocate (1000+ posts) | | Patient Advocate (1000+ posts) Joined: Jul 2003 Posts: 1,163 | I had IMRT radiation and i lost about half of my saliva function. I am two years out from surgery on July 31st. I can't spit due to the surgical procedure. Congratulations on being two & 1/2 years out. Sounds like you are doing well.
Hope it continues to improve for you.
Best Wishes, Danny Boy
Daniel Bogan DX 7/16/03 Right tonsil,SCC T4NOMO. right side neck disection, IMRT Radiation x 33.
Recurrance in June 05 in right tonsil area. Now receiving palliative chemo (Erbitux) starting 3/9/06
Our good friend and loved member of the forum has passed away RIP Dannyboy 7-16-2006
| | |
#5564 06-20-2005 12:59 PM | Joined: May 2003 Posts: 928 "Above & Beyond" Member (500+ posts) | | "Above & Beyond" Member (500+ posts) Joined: May 2003 Posts: 928 | Just you spit away Coop...lol thats great , congratulations. Marica
Caregiver to husband Pete, Dx 4/03 SCC Base of Tongue Stage IV. Chemo /Rad no surgery. Treatment finished 8/03. Doing great!
| | |
#5565 06-20-2005 05:25 PM | Joined: Feb 2004 Posts: 261 Gold Member (200+ posts) | | Gold Member (200+ posts) Joined: Feb 2004 Posts: 261 | We need to have a spitting contest!! I've found in the last few weeks if I focus a little in the morning before I get out of bed & run for a drink of water that spit will start to flow sometimes. I've actually woke up a couple different times & was excited that I had drooled a little bit. Maybe I'm dreaming of food or something! A round of spit for all who need it, on me!!! Ah, the simple things! Erik
dx 2/11/04 scca bot T3 IU 2B MO poorly differentiated, margins ok, 3/16 modest, jaw split, over half of tongue removed, free flap from left forearm - finished chemo & rad treatment 5/20/04
| | |
#5566 06-20-2005 10:11 PM | Joined: Nov 2002 Posts: 3,552 Patient Advocate (old timer, 2000 posts) | | Patient Advocate (old timer, 2000 posts) Joined: Nov 2002 Posts: 3,552 | Like Joanna, my salivary function has slowly improved over time. It can take 18 months or longer. Sometimes I even forget my water bottle now.
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)
| | |
#5567 06-21-2005 12:38 AM | Joined: Apr 2004 Posts: 837 "Above & Beyond" Member (300+ posts) | | "Above & Beyond" Member (300+ posts) Joined: Apr 2004 Posts: 837 | Like some of the others here, I saw some improvement within a year or two after my treatment ended. What surprises me is that even now -- after 16 years -- I'm STILL noticing incremental improvements over a year or two ago.
Spit happens! :p
Cathy
Tongue SCC (T2M0N0), poorly differentiated, diagnosed 3/89, partial glossectomy and neck dissection 4/89, radiation from early June to late August 1989
| | |
#5568 06-22-2005 07:56 PM | Joined: Oct 2003 Posts: 18 Member | | Member Joined: Oct 2003 Posts: 18 | thanks yall, i was told once there gone there gone my ent told me he had never seen anyone as dry as i was but now it does seem to be getting so much better and yes i forget my water alot but i reckon it is the panic thing when i notice it isnt with me i stop and get a bottle lol, now if i could just get on some more weight, but what the heck i eat all i want and it makes other people sick to see i can do that so i guess it has its good sides to | | |
#5569 06-23-2005 05:22 AM | Joined: May 2005 Posts: 497 "Above & Beyond" Member (300+ posts) | | "Above & Beyond" Member (300+ posts) Joined: May 2005 Posts: 497 | Happiness at cha buddy. I hope they continue to improve each and every day. Bless you, Barbara~
[i]"The artist, a traveler on this earth, leaves behind imperishable traces of his being." -Fran
| | |
| Forums23 Topics18,286 Posts197,241 Members13,435 | | Most Online2,386 Nov 19th, 2025 | | |
This is another custom island. This one could be used for ads. This spot is one of the best places for ads on your site to be placed. This can be enabled/disabled on a per forum basis.
| | | |