Sorry it's been a while since I've been here. Hope you all are doing well. We have been busy with complications from surgery (fistula that lead to going back on a feeding tube for 2 weeks). Last week my husband finished his first course of chemo and this week marked his second week of radiation treatments. He is beginning to complain about food tasting just awful to him. I would greatly appreciate it if you all could tell me what helped you through this time. Food choices, recipes, anything you found helpful to keep your nutrition intake and weight up or any other information and or ideas that kept you going.
Thanks in advance and many happy thoughts to you all.
Jingle Bell

Hi Jingle Bell, good to see you back. Everyone undergoing radiotherapy will have aversion to food at some point of time because of loss of taste buds, saliva and other oral changes.

Try moist and soft food as long as he can eat however boost his calorie intake by giving him drinks like Ensure, Prosure etc. You'll see more suggestions for others in the forum shortly.

Hi there unfortunately the taste thing is common... Try vegetable opus and blend them - no spices really except maybe salt and bouillon - I usually make a fresh veg soup, toss it into a blender and then slurp it! Yes for the ensures etc, egg isn't too bad if it's soft with cheese - Mac and cheese fresh - no craft dinner) they ar bland easier on the mouth, puddings, too it ,ay not help with the taste but if its bland it won be too shocking! To his mouth. No pop ( that's gross) I still cant drink pop! I found natural food tasted the most normal. - they still do. good luck! It may get harder but it will improve!

Here is a list of easy to eat foods. His sense of taste will slowly decrease as time goes by. Its only an unpleasant temporary problem. Ive noticed that texture plays a huge role in what a patient can eat.

http://oralcancersupport.org/forums/ubbthreads.php?ubb=showflat&Number=94621#Post94621

Hi, Jinglebell,
want works seems to vary by the individual. My husband could not tolerate anything bitter when the rads ramped up. Greens peppers were a particular annoyance. He could eat cooked carrots, canned green peas, and macaroni and cheese pretty late into the treatment. Since his taste may vary day by day, do not take if personally if your carefully crafted meals include the occaisional catestrophic failure. Good luck to you both!

I am 5 weeks out and all I eat are two eggs a day I have a peg tube for feedings at night. I have no appetite and no desire to eat. My doctor says that eating right now should be looked at as a therapy to exercise my mouth and tongue. I do eat canned beans with lots of butter. I'm going to try canned mushrooms again with lots of butter. Ive lost 50 lbs through this. Lots of luck Pat

If nothing else try to drink your meals if you can it helps with the swallowing reflex. So if you have ensure try half a bottle see how that goes - or make your own protein shake!

Thank you all for the great suggestions! I am happy to report that with all your advice, hubby has gained a pound! The chemo and radiation folks are thrilled. Mashed potatoes, mashed veggies, grits, scrambled eggs, and Ensure have been our saving grace. He still can't taste much and what he does eat tastes awful but at least he has found some things he can tolerate. Thank you all again, and keep the advice coming!

awesome!!! glad he's doing better - tell him to think about it like he's on xfactor- he may have to eat a lot of stuff that tastes like crap ( no offense to the cook) but there's a payoff at the end!!

I'm halfway through 6 weeks of radio/chemo and food and drink to me tastes absolutely terrible.The metallic taste is overwhelming.I've fortunatley had a PEG fitted and am now completely reliant on this as all food makes me wretch.I still drink water to keep my swallowing in shape and have found that it's easier to take with a little lemon juice in each glass.I've also tried miracle fruit/berry tablets but found these only gave me a fairly temporary taste change.