| Joined: Feb 2011 Posts: 45 Contributing Member (25+ posts) | OP Contributing Member (25+ posts) Joined: Feb 2011 Posts: 45 | It is almost 4 weeks since I finished radiation 2nd time and chemo. I expected to start to feel better but I don't. The truth is I probably feel worse today then I did two weeks ago. I've had 130 GY total so I know thats a lot...but I did expect some relief. I keep getting bouts of thrush and need to take liquid oxy to keep my throat under control. Scheduled for PET and CT the end of Feb. This is getting old quick. Steve Hurlock
SCC of larynx,2/1/2011 surgery 16 times to remove papilloma on vocal cords,started TOMO rad treatment 4/11.2011 T2N0M0 possible invasion onto cartilage tissue Cancer back 6/2012. Polyp removed Came back spindle cell carcenoma 6/22/12
| | | | Joined: Jul 2012 Posts: 3,267 Likes: 4 Patient Advocate (old timer, 2000 posts) | Patient Advocate (old timer, 2000 posts) Joined: Jul 2012 Posts: 3,267 Likes: 4 | As you probably know, it takes time even for a veteran. The chemo and radiation wears you down physically, including your immune system, which is probably why you keep getting thrush, a fungal infection. The Oxy pain meds can also make you tired, and has side effects of its own. I assume you are doing the salt water, baking soda, and other oral rinses? Diflucan, flocomizole, is often prescribed for effective treatment of Thrush, and I often say to change your toothbrush to keep from reinfecting yourself. Thrush, basucally a yeast infection, feeds on sugar, alcohol, yeast and processed foods, so you may want to look into that too. Good luck with your PET. Mine is 2/19.
You might want to ask the doctor for a full blood work up besides the usual CBC to include a the TSH, Vit D, testosterone, and A1c to see if there are any deficiencies.
Last edited by PaulB; 02-05-2013 02:50 PM. Reason: blood work
10/09 T1N2bM0 Tonsil 11/09 Taxo Cisp 5-FU, 6 Months Hosp 01/11 35 IMRT 70Gy 7 Wks 06/11 30 HBO 08/11 RND PNI 06/12 SND PNI LVI 08/12 RND Pec Flap IORT 12 Gy 10/12 25 IMRT 50Gy 6 Wks Taxo Erbitux 10/13 SND 10/13 TBO/Angiograph 10/13 RND Carotid Remove IORT 10Gy PNI 12/13 25 Protons 50Gy 6 Wks Carbo 11/14 All Teeth Extract 30 HBO 03/15 Sequestromy Buccal Flap ORN 09/16 Mandibulectomy Fib Flap Sternotomy 04/17 Regraft hypergranulation Donor Site 06/17 Heart Attack Stent 02/19 Finally Cancer Free Took 10 yrs
| | | | 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 | Steve, sorry you arent feeling better!
Hows your nutrition? Are you still pushing the calories and hydration? For at least the first year you will need to continue the minimum of 2500 calories daily and 48 oz of water. If you are getting that much every single day then try to boost it and take in extra for a few days and see if that makes a difference. I would suggest going for 3500 calories and 60 oz of water every day for 5 days and see if you feel any different. Even with taking in that much you probably wont gain an ounce as your body is struggling right now to rebuild itself so its burning up calories like crazy.
Thats just my suggestion. Maybe it will help. I know you want to be well so badly and its very frustrating not making more progress. Time will heal you and soon you will be feeling a little better. Recovery isnt like one day you wake up and you are well again, its a very slow go of it with small improvements along with set backs. Hope you feel better soon. 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 | Hi Steve, It sucks...We know. Vent away on here, then vent some more as you wait it out. Please try to be patient with yourself though. I feel like anything else I would say would just be blah, blah...so, hang in there. ;o) Cheers, 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: Mar 2011 Posts: 1,024 "OCF Kiwi Down Under" Patient Advocate (1000+ posts) | "OCF Kiwi Down Under" Patient Advocate (1000+ posts) Joined: Mar 2011 Posts: 1,024 | Time. It all takes time. Hang in there Steve. Tammy
Caregiver/advocate to Husband Kris age 59@ diagnosis DX Dec '10 SCC BOT T4aN2bM0 HPV+ve.Cisplatin x3 35 IMRT. PET 6/11 clear. R) level 2-4 neck dissection 8/1/11 to remove residual node - necrotic with NED Feb '12 Ca back.. 3/8/12 total glossectomy/laryngectomy/bilat neck dissection/partial pharyngectomy etc. clear margins. All nodes negative for disease. PEG in. March 2017 - 5 years disease free. Woohoo!
| | | | Joined: Jul 2009 Posts: 1,409 Patient Advocate (1000+ posts) | Patient Advocate (1000+ posts) Joined: Jul 2009 Posts: 1,409 | Steve, we're all pulling with you on this. Keep up the good fight, buddy.
David 2 SCC of occult origin 1/09 (age 55)| Stage III TXN1M0 | HPV 16+, non-smoker, moderate drinker | Modified radical neck dissection 3/09 | 31 days IMRT finished 6/09 | Hit 15 years all clear in 6/24 | Radiation Fibrosis Syndrome kicked in a few years after treatment and has been progressing since | Prostate cancer diagnosis 10/18
| | | | Joined: May 2007 Posts: 666 "Above & Beyond" Member (500+ posts) | "Above & Beyond" Member (500+ posts) Joined: May 2007 Posts: 666 | Steve 130 GY ... you are sure you are not turning green? (Hulk) That is a hell of an overall dose. Hang in there! A >6 Gy (whole body dose) is nearly 100% fatal. You have a right to feel crappy!!
Best !
Partial glossectomy (25%) anterior tongue. 4/6/07/. IMRT start @5/24/07 (3x) Erbitux start/end@ 5/24/07. IMRT wider field (30x) start 6/5/07. Weekly cisplatin (2x30mg/m2), then weekly carbo- (5x180mg/m2). End of Tx 19 July 07.
| | | | 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 | You WILL feel better and the sun will shine again for you, but as the others have said you are expecting far too much from your medically abused body. The problem is that the improvement will happen in such minute stages that you won't notice them until, say two weeks have passed and you notice that you can be active for 10 minutes longer than you were. Real challenge here is to try to keep depression from getting a firm hold.. How can you be mentally healthy when you don't feel well?
And while babies grow while they sleep, we adults hear when we sleep. If you need help getting a sound sleep - talk to your doctor. Great nutrition and good sleep will help. Hang in there.
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: Mar 2008 Posts: 3,082 Patient Advocate (old timer, 2000 posts) | Patient Advocate (old timer, 2000 posts) Joined: Mar 2008 Posts: 3,082 | Steve
You don't feel better because you are perfectly normal for those of us in the over 130 GY club (Kelly -190, me - 137, Paul B 135.) It's unrealistic to think that our recovery will be similar to the standard 70 - 77 GY TX that some radiologist still think is the maximum. Markus' post makes the point with subtle humor that our doses are extremely toxic. My RO said the way to look at it is that while the damage is so bad, it's not as bad as what the cancer would have done without it. I foolishly thought this last round would be easier after so much . Instead the recovery is slower. At 4 months after radiation and chemo over, I did not expect to suddenly develop radiation induced COPD that lead to my emergency hospitalization this week. Suddenly, I'm on a nebulizer every four hours and steroids just to keep my airways open. My RO did put me back on the Fentanyl patch which is much better consistent relief. I could not have said it better [quote]This is getting old quick[/quote] . Unfortunately, only tincture of time is going to work here. Hang in there brother. Charm
Last edited by Charm2017; 02-09-2013 07:47 AM. Reason: added GYs
65 yr Old Frack Stage IV BOT T3N2M0 HPV 16+ 2007:72GY IMRT(40) 8 ERBITUX No PEG 2008:CANCER BACK Salvage Surgery 25GY-CyberKnife(5) 3 Carboplatin Apaghia /G button 2012: CANCER BACK -left tonsilar fossa 40GY-CyberKnife(5) 3 Carboplatin Passed away 4-29-13
| | | | Joined: Feb 2011 Posts: 45 Contributing Member (25+ posts) | OP Contributing Member (25+ posts) Joined: Feb 2011 Posts: 45 | Thanks guys for the upbeat...and Charm I hope this does not get any worse. I have some good days and then wham!!!! (where did those good days go). Today if feels like my throat is half closed. Doctors never tell you about the long term possible side affects...I don't think they really know what to expect from their patients. The first go around was a piece of cake to this. I may have to go back on the patch also. I cut down less than 25mg but it does not seem to help...much more makes me spacey. Thanks Steve HurlocK
SCC of larynx,2/1/2011 surgery 16 times to remove papilloma on vocal cords,started TOMO rad treatment 4/11.2011 T2N0M0 possible invasion onto cartilage tissue Cancer back 6/2012. Polyp removed Came back spindle cell carcenoma 6/22/12
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