#48832     09-14-2007 05:17 AM      |       Joined:  May 2002  Posts: 2,152    Patient Advocate (old timer, 2000 posts)   |           Patient Advocate (old timer, 2000 posts)    Joined:  May 2002  Posts: 2,152  |    Helen, Apple juice was one the FIRST things I could drink even when everything else burned my tongue. Shows just how different everyone is, unless they make it differently down under. I did take Zinc Sulphate after radiation recommended by dietician to help heal and improve taste. 
  Take care, Eileen        
---------------------- Aug 1997 unknown primary, Stage III mets to 1 lymph node in neck; rt ND, 36 XRT rad  Aug 2001 tiny tumor on larynx, Stage I total laryngectomy; left ND June 5, 2010 dx early stage breast cancer  June 9, 2011 SCC 1.5 cm hypo pharynx, 70% P-16 positive, no mets, Stage I     
  |      |       |                      
#48833     09-14-2007 05:41 AM      |       Joined:  Jul 2005  Posts: 207    Platinum Member (200+ posts)   |           Platinum Member (200+ posts)    Joined:  Jul 2005  Posts: 207  |    Hi,
  Not sure of the extent of his radiation, but it was 7 weeks after my treatment before I could eat.  Taste comes back slowly.  Sweets came first.  I esp. like brown sugar on oatmeal.  NO CARBONATED BEVERAGES for a while as they will burn.
  Give it some time.  I think it will slowly get back to normal.        
SCC, base of tongue, 2 lymph nodes, stage 3/4.  35 X's IMRT radiation, chemo: Cisplatin x 2, 5FU x2, &  Taxol x2.    Hooray, after 3 years I'm in still in remission.
  |      |       |                      
#48834     09-14-2007 01:45 PM      |       Joined:  Nov 2002  Posts: 541    "Above & Beyond" Member (500+ posts)   |           "Above & Beyond" Member (500+ posts)    Joined:  Nov 2002  Posts: 541  |    Hi,  My experience is more or less like Helen with my taste getting better gradually but not 100% as how I felt before treatment. Now that I have reached my 6th anniversary, the mouth sore is still with me and I can never eat anything spicy or take any carbonated beverages. Not a big deal as I still have a lot of food for my choice.
  Karen        
Karen stage 4B (T3N3M0)tonsil cancer diagnosed in 9/2001.Concurrent chemo-radiation treatment ( XRT x 48 /Cisplatin x 4) ended in 12/01. Have been in remission ever since.
  |      |       |                      
#48835     09-14-2007 02:46 PM      |       Joined:  Aug 2006  Posts: 294    Gold Member (200+ posts)   |           Gold Member (200+ posts)    Joined:  Aug 2006  Posts: 294  |    Steve,
  I had forgotten about brown sugar on oatmeal.  I must have eaten a ton of it while in Tx and several times daily in the first few weeks post Tx.  It was great and is still a fond memory.
  Bill D.        
Dx 4/27/06, SCC, BOT, Stage III/IV, Tx 5/25/06 through 7/12/06 - 33 IMRT and 4 chemo, radical right side neck dissection 9/20/06.
  |      |       |                      
#48836     09-15-2007 03:38 PM      |       Joined:  Jun 2007  Posts: 214    Gold Member (200+ posts)   |           Gold Member (200+ posts)    Joined:  Jun 2007  Posts: 214  |    I am 3 months out from treatment, taste started back at 2 weeks post tx, improving at two week intervals. I now have 85% of my taste back, if not more. I literally willed my taste back, smelling my food, then imagining that I actually tasted it even if I really couldn't. Call it 'taste training'.        
Left tonsil SCC, HPV+. T2N0M0. Tonsillectomy 3-07, bilateral radiation, cisplatin 3x, Tx completed 6-06. Clear PET 4-01-2008. Thyroidectomy 5-9-08, resulting in permanent surgically-induced hypoparathyroidism and adrenal problems. Bummer.    |      |       |                      
#48837     09-15-2007 06:26 PM      |       Joined:  Sep 2007  Posts: 11    Member   |      OP      Member    Joined:  Sep 2007  Posts: 11  |    Thanks to all of you who responded on taste loss.  VERY best wishes to you, Steve J.  Hang in there! Joe is forcing himself to eat, even if he can't taste it.  Started working out a little and that seem to improve his spirit.  We were lucky to have several cases of Boost left from his feeding tube days.  That has been a litteral lifesaver.  He didn't have the feeding tube for the cancer, but the day after his tumor surgery was hit with a neuro-muscular disease that, within 5 days, paralyzed him totally and put him in ICU, on vent and feed tube for 3 months, THEN, he could address the cancer issue.  He's had a long haul, but looks like dalight soon, thank God!      |      |       |                      
#48838     09-16-2007 03:52 PM      |       Joined:  Apr 2005  Posts: 2,676    Patient Advocate (old timer, 2000 posts)   |           Patient Advocate (old timer, 2000 posts)    Joined:  Apr 2005  Posts: 2,676  |    Glad to hear youall are seeing some daylight! Way to go Joe! It would be neat if youwould expand your signature to let us know what has gone on with him so we could be better informed. Amy in the Ozarks        
CGtoJohn:SCC Flr of Mouth.Dx 3\05. Surg.4\05.T3NOMO.IMRTx30. Recur  Dx 1\06.Surg 2\06. Chemo: 4 Cycles of Carbo\Taxol:on Erbitux for 7 mo. Lost our battle 2-23-07- But not the will to fight this disease
  :
  |      |       |                      
#48839     09-16-2007 05:23 PM      |       Joined:  May 2006  Posts: 137    Senior Member (100+ posts)   |           Senior Member (100+ posts)    Joined:  May 2006  Posts: 137  |    Welcome to the new normal.        
dx 2/13/06.  modified radical neck dissection 3/9/06  multiple biopsies of upper airway and direct laryngoscopy. 1 of 47 lymph nodes positive for metastatic undifferentiated carcinoma (lymphoepithelioma). Unknown primary. Finished radiation 5/24/06.
  |      |       |                      
#48840     09-17-2007 01:17 PM      |       Joined:  Aug 2007  Posts: 580    "Above & Beyond" Member (500+ posts)   |           "Above & Beyond" Member (500+ posts)    Joined:  Aug 2007  Posts: 580  |    Hi, Just thought I'd give you all a good site with info on this topic.  http://www.meei.harvard.edu/patient/taste.php Hope this is usefull to some of you. Cheers, Mike         
Dentist since 1995, 12 year Cancer Survivor, Father, Husband, Thankful to so many who supported me on my journey so far, and more than happy to comfort a friend.   Live, Laugh, Love & Learn.
  |      |       |                      
#48841     09-20-2007 11:08 AM      |       Joined:  Jun 2007  Posts: 5,260    Patient Advocate (old timer, 2000 posts)   |           Patient Advocate (old timer, 2000 posts)    Joined:  Jun 2007  Posts: 5,260  |    I have no taste on the right side , but on the left side where they did the surgery , I have good taste. I also have the burning tongue from anything sweet. Everything else is fine. Have  great day all.  Jim        
     Since posting this. UPMC, Pittsburgh, Oct 2011 until Jan.  I averaged  about 2 to 3 surgeries a week there.  w  Can't have jaw made as bone is deteroriating steaily that is left in jaw. Mersa is to blame. Feeding tube .  Had trach for 4mos. Got it out April. --- Passed away 5/14/14, will be greatly missed by everyone here
  |      |       |                
            |   Forums23  Topics18,280  Posts197,206  Members13,413   |  |   Most Online2,371 Sep 11th, 2025   |       |         |      |