Posted By: DeepSeaDan eating during rads? - 08-24-2017 12:45 PM
G'Day All,

Here's my questions: is it possible to consume nourishment orally during RT treatment? Can this preclude the necessity of a feeding tube ( if Chemo isn't part of the treatment plan )? Are swallowing exercises necessary if you are consuming Vitamixed foods and tolerable liquids on a daily basis?

Thank you!

Regards,
Dan
Posted By: gmcraft Re: eating during rads? - 08-24-2017 01:50 PM
Hi Dan,

You may not have a choice with PMH when it comes to the tube. John was told he had to have it and that was it. Do you know how much radiation you will be getting -- how many grays? John had 70 grays over 35 days and that was the lifetime maximum for that area of the body. By the middle of week 3, he could no longer swallow because it was so painful, not even a sip of water.

If you are able to swallow consistently, then the swallowing exercise may not be necessary. The exercises help mitigate the effects of the swallowing muscles becoming atrophied.
Posted By: DeepSeaDan Re: eating during rads? - 08-24-2017 03:34 PM
Hey GMC,

The RO said the tube was mandatory if Chemo was used, and optional if it isn't. They want to get it in before the chemo affects the bloodstream, and fighting infection gets harder. Not sure how many "grays" I'm getting, as the Tx. schedule is as yet not determined.

What is a "Gray?" A unit of radiation dose perhaps?
Posted By: gmcraft Re: eating during rads? - 08-24-2017 03:51 PM
A gray is a unit of radiation.
Posted By: ChristineB Re: eating during rads? - 08-24-2017 07:31 PM
Dan, Ive sent you a private message (PM). Click on the tiny flashing envelope next to your "My Stuff" to get your messages. When you have time please follow the direction included in the link to add your signature.

Thank you smile
Posted By: David2 Re: eating during rads? - 08-28-2017 07:18 PM
Dan - welcome to our family. You're one of us now.

I had something like 31 trips on the ride, as I called the radiation setup, after a neck dissection and chose not to get the tube. My RO had told me that the treatment would be tough but that I could do it if I applied myself. It helped that I hadn't needed chemo.

All of that said, if I had it to do over again I would have gone with the PEG. After a few weeks, even with swishing viscous lidocaine around my mouth for ten minutes prior, taking the several glasses of liquid nutrition by mouth at each feeding was incredibly painful. Of course each of us is different, each radiation plan is different, and you may have an experience that's much less taxing. My advice would be to discuss the pros and cons thoroughly with members of your medical team. The oncology nurses are amazing - the one I had was of enormous help with these maintenance issues. Couldn't have done it without her.

Perhaps others here will weigh in with their experiences. I turned down the PEG because I knew it was another surgery, and my neck dissection had a major complication that nearly killed me and was possibly related to the anesthetic. So you can understand I was reluctant to go under again so quickly. But again, your experience will be different.

Best of luck. You will definitely get through this, and we're all here to help you.
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