| Joined: Oct 2005 Posts: 47 Contributing Member (25+ posts) | OP Contributing Member (25+ posts) Joined: Oct 2005 Posts: 47 | I don't post really, i just come hear and read when i need to feel not so alone with this cancer. I found out thursday it has come back for the third time. for the second time on my right inside cheek. I find out on Monday when i have surgery. I have Dr. Tufano at Johns Hopkins, i really trust him and he is a great doctor. The good thing is they caught it way early and according to my doc he will be removing a smaller piece then last time (Oct 2007 it came back) and putting on a smaller graft.
I don't know how to shake the fear that has knocked my on my butt. i am not afraid of procedures, but how do i find the courage to keep fighting without crying all the time? and who but the people here can understand how i feel? i go about my day and go to work and try to be "normal" as best i can. but inside i am screaming.
thanks for listening... Gina
scc 4/2004 r side tongue, flr of mouth. neck disection,4 lymph nodes 34x rad,3X chemo 10/2007 r cheek. remove w/graft. 40 HBO dives. 01/2010 r cheek. surgery w/graft 04/2010,surgery remove lower right jaw, reconstruct. 4x chemo 25x rad. clear margins. pet 8/2010 clear July 2012 right side bot cancer. surgery to remove, clear margins 4/2013 Surgery to remove cancer in lymph node near thyroid, clear margins 6/2013 start of rad 25X Chemo 7X
| | | | Joined: Sep 2009 Posts: 618 "Above & Beyond" Member (500+ posts) | "Above & Beyond" Member (500+ posts) Joined: Sep 2009 Posts: 618 | FunnyGirl.
Screaming inside is what we all do and it's all we can do some days. On others we scream on the outside (just ask the care givers) The important thing is that you are a fighter. I am always sadned when I see a post from a care giver that a loved one has given up and won't fight.
You have great care at LH and it looks like you will have a painfull procedure but you have made it through worse.
Come here any time and vent. Your in great company.
Kelly
Kelly Male 48, SCC (Soft Palet) Rt., Stage 1, T3n0m0, Dx, 8-09, Start IMRT 35 9-2-09 end 10-21-09 04-20-10 NED 8-11 recurrence, node rt. neck N2b 10-11 33 IMRT w/chemo wkly 3-12-12 PET - residual cancer 4-12 5 treatments with Cyberknife & Erbitux 6-19-12 Pet scan CLEAR 12-3-12 PET - CLEAR
| | | | Joined: Dec 2008 Posts: 1,004 Patient Advocate (1000+ posts) | Patient Advocate (1000+ posts) Joined: Dec 2008 Posts: 1,004 | Hi Gina,
The important thing is you know you are not alone. That has helped me more than anything. Anyone in your shoes would feel like screaming...and I think you should scream if you want to. You have the courage in you...I know you do. It's hard and you may not always feel like you can do it. When you feel that way come here...talk to us...vent to us and let us help you.
Please take care of yourself and come here when you need to.
Suzanne *********** T1 SCC on right side of tongue Age 31...27 when diagnosed 4 partial glossectomies No chemo or radiation Biopsy on 2/2/10-Clear Surgery needed again...no later than April 2011 Loving life and just became a mother on 11/25/10 It's not what we CAN'T do..it's what we CAN do:)
| | | | Joined: Sep 2009 Posts: 148 Likes: 1 Senior Member (100+ posts) | Senior Member (100+ posts) Joined: Sep 2009 Posts: 148 Likes: 1 | Hi Gina, How I wish this could all be behind you. How we just hate cancer, it's so damm evil and every other nasty thing we could say. I fell apart when I had a scare, so when you talk about crying...I hear that. In the end, what other choices are there, but to continue along the required path to wellness? Without this site...I would be so dumb! At least we have each other to cheer us on, encourage & learn from and lean on! Keep us posted, because we really, really care! DianneMH
BOT T3N2M0 No surgery, 38radiation treatments,4 chemo rounds, peg removed 11/08, still have a port. Treatments ended 6/20/08. So far, so Good ! "I know God won't give me anything I can't handle. I just wish He didn't trust me so much !"
*** Admin update --- Dianne has passed away on August 25, 2015 ***
| | | | Joined: Oct 2005 Posts: 47 Contributing Member (25+ posts) | OP Contributing Member (25+ posts) Joined: Oct 2005 Posts: 47 | Thanks for the posts, they help so much. I go to Johns Hopkins this friday, surgery is at 3 pm. right now i am just trying to keep my regular schedule and not fall apart too much. I alway feel better when i come here. only the people on this site know exactly how i feel. i will never give up and i am not necessarily afraid of pain. If only i knew going through all of this would mean victory for me in the end. but then we all feel that way.
it's like fighting round after round without an end in sight. But then i guess that's why i go to the gym 5 days a week!
Gina
scc 4/2004 r side tongue, flr of mouth. neck disection,4 lymph nodes 34x rad,3X chemo 10/2007 r cheek. remove w/graft. 40 HBO dives. 01/2010 r cheek. surgery w/graft 04/2010,surgery remove lower right jaw, reconstruct. 4x chemo 25x rad. clear margins. pet 8/2010 clear July 2012 right side bot cancer. surgery to remove, clear margins 4/2013 Surgery to remove cancer in lymph node near thyroid, clear margins 6/2013 start of rad 25X Chemo 7X
| | | | Joined: Nov 2009 Posts: 644 Likes: 1 "OCF Down Under, Kiwi" "Above & Beyond" Member (500+ posts) | "OCF Down Under, Kiwi" "Above & Beyond" Member (500+ posts) Joined: Nov 2009 Posts: 644 Likes: 1 | I know what you mean about the fear. Antidepressants help when it all becomes too much. I hope writing it down helped too. Sometimes I think riding the fear helps a bit. Acknowledge you're afraid and tell people - which you have just done - but others will understand too. You sound very brave about the surgical procedures and your outlook sounds good. It's so tough and unfair to get cancer over and over and I know from personal experience that when people acknowledge this and understand it, I feel a bit better. So much of the time we try to be brave and no-one but fellow patients know the turmoil inside. I wish you the very best for your surgery and hope you get a bit of time to relax after it!
1996, ovarian cancer surgery + cisplatin and taxol. September, 2007, SCC of left lateral tongue. Excision. October, 2009 recurrence in scar tissue, T1NOMO. Free flap surgery from left wrist - neck dissection. 63 year old New Zealander. No chemo, no RT. February, 2014. New primary in left buccal mucosa. Marginal mandibulectomy, neck dissection, right arm free forearm flap. T1N0M0 but third occurrence and some areas of concern: RT started 8 April and finished 19 May.
| | | | Joined: Dec 2008 Posts: 1,004 Patient Advocate (1000+ posts) | Patient Advocate (1000+ posts) Joined: Dec 2008 Posts: 1,004 | I feel the same way...I wouldn't mind the surgery if I thought it was end....good luck tomorrow. Hope to hear from you when your home:) Remember, we are all here for you.
Suzanne *********** T1 SCC on right side of tongue Age 31...27 when diagnosed 4 partial glossectomies No chemo or radiation Biopsy on 2/2/10-Clear Surgery needed again...no later than April 2011 Loving life and just became a mother on 11/25/10 It's not what we CAN'T do..it's what we CAN do:)
| | | | Joined: Apr 2009 Posts: 104 Senior Member (100+ posts) | Senior Member (100+ posts) Joined: Apr 2009 Posts: 104 | Best thoughts to you, Gina.
GM, for John who has SCC Rt tonsil with 3+ nodes, Stage T1 N2b MX; surgery 04/09; Rad X 33 completed 7/14/09...f/u imaging and scopes looking good as of Feb 2011
| | | | Joined: Oct 2005 Posts: 47 Contributing Member (25+ posts) | OP Contributing Member (25+ posts) Joined: Oct 2005 Posts: 47 | Hello Everyone,
I made it through surgery well. i was home about 3 weeks and i went back to work after presidents day. i got the pathlogy back from surgery and it was 3 millimeters. the margins were clean and my surgeon is very happy. my surgeon actually took a second biopsy because i have a spot from 2007 that didn't heal well and he was concerned it was in my jaw bone. that came back negative as well that god. is it just a matter of time before it reaches my jaw?
i am dealing with the trimus issues, i can only open my mouth 22 millimeters, but hopefully using the thereabite device will help. depression has been lingering and my doctor gave me a name of someone at johns hopkins i can talk to.
i haven't called yet, cuz i just don't know what someone can say that will stop my worrying about cancer coming back over and over again?
i am getting better everyday, i am just not sure i will ever be the same.
thanks for listening.
gina
scc 4/2004 r side tongue, flr of mouth. neck disection,4 lymph nodes 34x rad,3X chemo 10/2007 r cheek. remove w/graft. 40 HBO dives. 01/2010 r cheek. surgery w/graft 04/2010,surgery remove lower right jaw, reconstruct. 4x chemo 25x rad. clear margins. pet 8/2010 clear July 2012 right side bot cancer. surgery to remove, clear margins 4/2013 Surgery to remove cancer in lymph node near thyroid, clear margins 6/2013 start of rad 25X Chemo 7X
| | | | Joined: Feb 2010 Posts: 235 Gold Member (200+ posts) | Gold Member (200+ posts) Joined: Feb 2010 Posts: 235 | Gina. glad to hear the surgery went well. I hope when you are ready you do pick up the phone and call for help with your depression. I understand what you are saying about there not being any magic words to make it go away. But there are techniques and/or meds that can help.
Also, I think sometimes it's helpful to be able to speak to someone where you don't have to worry about their reaction, or their emotions. To have an hour or so a week where you can focus your thoughts, say whatever you want, break down if you need to and get some additional support.
I've been a therapist for over 25 years so if I can answer any questions, please feel free to PM me. Happy to help if I can...
CG to Spouse BOT, Chemo and radiation started on March 29,2010 Ended on May 14,2010. LET THE HEALING BEGIN!!!
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