| Joined: Oct 2012 Posts: 17 Member | OP Member Joined: Oct 2012 Posts: 17 | I am concerned that it is taking quite a bit of time to get a full diagnosis and worry about the time that it is taking to begin treatment. I found a lump in my neck in mid August. I just thought it was an inflamed node and let it be for a week. After 7-10 days I went to see my GP and he got me in to an ENT 7 to 10 days later. The ENT biopsied the node then I'll fast forward to last Thursday when I was diagnosed with SCC, HPV+. This has taken 2 months - now I need a PET scan and then oncology hopefully this week. The cancer has been here since mid August! Is this normal? Am I concerned about nothing? Thanks. Ray
Ray
SCC Right Pharangeal wall Stage IV HPV+ T1-2N2bMO Dx 10/12/2012 Father for the second time to 2nd beautiful boy 11/2/12 Port Implanted 11/20/12 - no feeding tube Tx - 11/26/12 35 IMRT Rads 5X/week Weekly Cisplatin Last treatment 1/15/13 "Grind it out, I will be cured as I have too much to live for"
| | | | Joined: Jun 2007 Posts: 10,507 Likes: 7 Administrator, Director of Patient Support Services Patient Advocate (old timer, 2000 posts) | Administrator, Director of Patient Support Services Patient Advocate (old timer, 2000 posts) Joined: Jun 2007 Posts: 10,507 Likes: 7 | Since you did not go to the ENT first, it took several weeks before you saw the right professional. This is normal for just being diagnosed and you are now right on track. A PET is necessary to determine if cancer is anywhere else and how advanced it is.
Relax and soon the flurry of appointments settle down and you will have a treatment plan.
Last edited by ChristineB; 10-21-2012 09:11 PM. Reason: clarified
ChristineSCC 6/15/07 L chk & by L molar both Stag I, age44 2x cispltn-35 IMRT end 9/27/07 -65 lbs in 2 mo, no caregvr Clear PET 1/08 4/4/08 recur L chk Stag I surg 4/16/08 clr marg 215 HBO dives 3/09 teeth out, trismus 7/2/09 recur, Stg IV 8/24/09 trach, ND, mandiblctmy 3wks medicly inducd coma 2 mo xtended hospital stay, ICU & burn unit PICC line IV antibx 8 mo 10/4/10, 2/14/11 reconst surg OC 3x in 3 years very happy to be alive | | | | Joined: Dec 2010 Posts: 5,264 Likes: 4 "OCF Canuck" Patient Advocate (old timer, 2000 posts) | "OCF Canuck" Patient Advocate (old timer, 2000 posts) Joined: Dec 2010 Posts: 5,264 Likes: 4 | Wait sorry I disagree. You should have had your results two weeks post biopsy, at that point your dr. Should have made an appointment for a pet (right away) you should have had it by mid September, is is too long to wait if your not being seen by a ccc get to one speed is important when dealing with cancer. Also you will need to visit a dental concologist (for trays and removal of any teeth that might be an issue (if they are in the path of radiation) ) and a hearing test - all this will take time. The amount of time between dx and surgery for me was 6 weeks. Had radiation been needed instead of surgery (dependant on cancer type and location) it would have been maybe a week less as it was I had to wait to be scheduled for surgery. Dx'd dec 20 surgery feb 4. (this included christmas slow down) That's normal. 2 -3 months is not - and you haven't even gone for mask making etc.. Push - make noise. This is your health. Good luck - ps pet results are usually available withing 24 hrs max - do not wait a week for results. And try to get them to schedule the other things as well.
Cheryl : Irritation - 2004 BX: 6/2008 : Inflam. BX: 12/10, DX: 12/10 : SCC - LS tongue well dif. T2N1M0. 2/11 hemigloss + recon. : PND - 40 nodes - 39 clear. 3/11 - 5/11 IMRT 33 + cis x2, PEG 3/28/11 - 5/19/11 3 head, 2 chest scans - clear(fingers crossed) HPV-, No smoke, drink, or drugs, Vegan
| | | | Joined: Jun 2007 Posts: 10,507 Likes: 7 Administrator, Director of Patient Support Services Patient Advocate (old timer, 2000 posts) | Administrator, Director of Patient Support Services Patient Advocate (old timer, 2000 posts) Joined: Jun 2007 Posts: 10,507 Likes: 7 | The best place to go for treatment is a NCI cancer center. Here is the link. NCI Cancer Centers ChristineSCC 6/15/07 L chk & by L molar both Stag I, age44 2x cispltn-35 IMRT end 9/27/07 -65 lbs in 2 mo, no caregvr Clear PET 1/08 4/4/08 recur L chk Stag I surg 4/16/08 clr marg 215 HBO dives 3/09 teeth out, trismus 7/2/09 recur, Stg IV 8/24/09 trach, ND, mandiblctmy 3wks medicly inducd coma 2 mo xtended hospital stay, ICU & burn unit PICC line IV antibx 8 mo 10/4/10, 2/14/11 reconst surg OC 3x in 3 years very happy to be alive | | | | Joined: Oct 2011 Posts: 805 "Above & Beyond" Member (500+ posts) | "Above & Beyond" Member (500+ posts) Joined: Oct 2011 Posts: 805 | I agree with Cheryl, but unfortunately your story is all too familiar. Kevin found the lump in April and was diagnosed in mid July! We started induction chemo on July 25th. By then it was stage IV. Just had our 1 year PET though and he's clear so far!! Hang in there, but you are thinking correctly in my opinion. You have to advocate for yourself and try to get things going. Kathy
Kathy wife/caregiver to: Kevin age:53 Dx 7/15/11 HPV16+ SCC Stage IV BOT/R Non smoker, casual drinker 7/27/11 Cistplatin, taxotere,5FU 2/3week sessions, followed by IMRT 125cgy x 60 (2x daily) w/Erbitux weekly. Last rad 10/26/11. Last Erbitux 10/27/11 PEG placed 9/1/11 Removed 11/8/11 Clear PET 10/12 and 10/13 and ct in 6/14 | | | | Joined: Sep 2006 Posts: 1,357 Likes: 5 "OCF Canuck" Patient Advocate (1000+ posts) | "OCF Canuck" Patient Advocate (1000+ posts) Joined: Sep 2006 Posts: 1,357 Likes: 5 | My first worry was a sore spot on my tongue - Feb of 2002 - firm diagnosis Feb 19, 2003, surgery April 2003. With My recurrance my first thought that it was back was in March of 2004, firm diagnosis Sept 24, 2004, surgery Oct 2004. Sometimes it is misdiagnosed and even when it is suspected, sometimes it can be difficult to diagnose.
It sounds to me like things are moving along at a very good pace for you. It is so hard to be patient. I remember wanting this cancer OUT - not NOW - but RIGHT NOW!!!
Keep us posted and good luck with everything.
Donna
Donna,69, SCC L Tongue T2N1MO Stg IV 4/04 w/partial gloss;32 radtx; T2N2M0 Stg IV; R tongue-2nd partial gloss w/graft 10/07; 30 radtx/2 cispl 2/08. 3rd Oral Cancer surgery 1/22 - Stage 1. 2022 surgery eliminated swallowing and bottom left jaw. Now a “Tubie for Life”.no food envy - Thank God! Surviving isn't easy!!!! .Proudly Canadian - YES, UNIVERSAL HEALTH CARE IS WONDERFUL! (Not perfect but definitely WONDERFUL)
| | | | Joined: Oct 2012 Posts: 17 Member | OP Member Joined: Oct 2012 Posts: 17 | Well it has been a while, but here is the update. I went to Beth Israel to see Dr. Lou Harrison for a second opinion as well as the folks at MSK. Both concurred with my local RO opinion for a treatment plan. After some thought, we opted for local treatment. Harrison and my RO are close colleagues and Dr. Smiths care has been exemplary. Thanks to the folks here for the help getting this far. I am finishing week 2 of treatment and my throat is starting to dry out a bit. Other than that - no complaints. I feel pretty fortunate so far. Treatment plan is 35 IMRT treatments 5 times per week for 7 weeks, cisplatin once a week for 7 weeks. The doc at MSK gave my wife and I a great deal of hope. He said that someone at my age and HPV+ with no tobacco use should be very very curable. Upwards of 95%. Granted, this is not 100%, but we like the odds.
Ray
SCC Right Pharangeal wall Stage IV HPV+ T1-2N2bMO Dx 10/12/2012 Father for the second time to 2nd beautiful boy 11/2/12 Port Implanted 11/20/12 - no feeding tube Tx - 11/26/12 35 IMRT Rads 5X/week Weekly Cisplatin Last treatment 1/15/13 "Grind it out, I will be cured as I have too much to live for"
| | | | Joined: Sep 2006 Posts: 8,311 Senior Patient Advocate Patient Advocate (old timer, 2000 posts) | Senior Patient Advocate Patient Advocate (old timer, 2000 posts) Joined: Sep 2006 Posts: 8,311 |
David
Age 58 at Dx, HPV16+ SCC, Stage IV BOT+2 nodes, non smoker, casual drinker, exercise nut, Cisplatin x 3 & concurrent IMRT x 35,(70 Gy), no surgery, no Peg, Tx at Moffitt over Aug 06. Jun 07, back to riding my bike 100 miles a wk. Now doing 12 Spin classes and 60 outdoor miles per wk. Nov 13 completed Hilly Century ride for Cancer, 104 miles, 1st Place in my age group. Apr 2014 & 15, Spun for 9 straight hrs to raise $$ for YMCA's Livestrong Program. Certified Spin Instructor Jun 2014.
| | | | Joined: Nov 2009 Posts: 493 Platinum Member (300+ posts) | Platinum Member (300+ posts) Joined: Nov 2009 Posts: 493 | Wow. I guess I was lucky. I had a biopsy on a Monday, got my diagnosis a week later, and saw the ENT the next day. I had a PET scan during the same week, and surgery the following week. Saw my dentist prior to my treatments starting where I was fitted for fluoride trays. I also got a PEG and a port prior to starting my treatments. They really didn't mess around with me. Glad that you are now on track!
Female, nonsmoker, 70, diag. 5/09 after tongue biopsy: stage IV. Left hemi-gloss. and left selec. neck disec. 30 lymph nodes removed May 20. Over 7 weeks daily rads. with three chemo. PEG removed 12/4/09 Am eating mostly soft foods. Back to work 11/09 Retired 4/1/11. 7 clear scans! Port out 9/11. 2/13. It's back: base of tongue, very invasive surgery involving lifestyle changes. 2/14: Now speaking w/Passey-Muir valve. Considering a swallow study. Grateful to be alive.
| | | | Joined: Dec 2010 Posts: 5,264 Likes: 4 "OCF Canuck" Patient Advocate (old timer, 2000 posts) | "OCF Canuck" Patient Advocate (old timer, 2000 posts) Joined: Dec 2010 Posts: 5,264 Likes: 4 | Awesome so glad you are getting through it.
Cheryl : Irritation - 2004 BX: 6/2008 : Inflam. BX: 12/10, DX: 12/10 : SCC - LS tongue well dif. T2N1M0. 2/11 hemigloss + recon. : PND - 40 nodes - 39 clear. 3/11 - 5/11 IMRT 33 + cis x2, PEG 3/28/11 - 5/19/11 3 head, 2 chest scans - clear(fingers crossed) HPV-, No smoke, drink, or drugs, Vegan
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