Cannot swallow

Hello everyone, another question. I can hardley swallow water now, and when I do it goes down the wrong pipe, so I end up coughing up most of the water. And whenever I do drink it comes out my nose. It seemed like it happened all of the sudden, I have not been able to swallow that well at all since my partial neck disection but about two weeks ago my swallowing function has just about stoped. I need to get into the doctor, but the ENT doctor I see at the Reno VA doesnt care and has never helped me and I really don't want to go down to San Francisco until after the holidays, they never have given me good news of any kind. The one thing that I am hoping is we are in the process of moving to Idaho and I will start to use the VA in Salt Lake City and I am praying that that doctor will care and have something to say. Any way I don't have any real pain when I swallow it like I am fighting muscles on the left side of my neck to get my esophagus to open. Food gets stuck really bad, I mean if I eat like corn or nuts, when I could swallow, a few days later I would hack up some of that food. My wife thinks that this is the problem to my bad odor, food sticking in my throught and rotting. Any way thanks and Merry Christmas to all.

Brad

Comments

  • Hondo
    Hondo Member Posts: 6,636 Member
    Hi Brad
    I get this too something it is called aspiration where the food goes into the lungs. With me it is caused by the damage nerve on the side of my face, I can’t remember the name of the nerve. But it has a lot to do with my swallowing and numbness in the left side of my face as well. Sometimes it also comes up and out of my nose when it gets hung up and can’t go down. Then a day or so later when I rinse out my nose there is some stuff I ate a few days before.

    I can’t find a doctor either that really cares enough to give me any help. What they say is you should be glad just to be alive, I am so sick of hearing that. I tell them I can’t be the only person in the world with these problems, what can be done to help, that is about all I get from them.

    My wife has been making me some soft food and I try to eat only when I feel the throat and swallowing is working as best as it can. I eat very slow and little bites at a time, I also found that putting my head down in a 45 degree angle helps in swallowing.

    I am sorry to hear you have to live like this too, I am looking at getting a PEG tube put in to avoid having to eat.

    Another guy on CSN Denny has the same problem and that is what he done and it is working well with him.

    If you do find a doctor to help please remember me and let me know what he gives you to do.
    Hondo
  • MarineE5
    MarineE5 Member Posts: 1,034 Member
    Neck Disection
    Brad,

    I am sorry to hear that you are going thru this, and I really don't know your history, but you mentioned a neck disection and problems swallowing. I too had sudden problems eating after my treatments once I got to the point that I could eat again. All of a sudden, I was having trouble swallowing items like corn as you mentioned. I realized that my neck and face were swelling as well.

    Are you having this issue as well, swelling of the face and neck. I ask because if you are, then the neck disection has caused some Lymphadema which in turn can cause your throat to narrow and result in problems swallowing. Do you sleep laying flat and not elevated? if so, try sleeping in an incline for a bit.

    If the Lymphadema is an issue, please read in the SUPER Thread that Sweetblood keeps on this front page, look under tips for stretching exercises and gentle massage that is posted there so you may get some relief from any swelling. You can ask to see a massage therapist as well.

    Here it is----- http://csn.cancer.org/node/196680

    My Best to You and Everyone Here
  • longtermsurvivor
    longtermsurvivor Member Posts: 1,842 Member
    Several important things have been mentioned
    First, I've had lots of swallowing problems for the last year, though I think your exceed mine by quite a bit. Hondo mentioned the angle he has to acchieve to facilitate swallowing. So do I. I've completely re-learned how to swallow, or fluids absolutely pour out of my nose. I do mean this, I literally flood my shirt, the plate, everything. But if I'm careful and swallow properly, I don't leak at all.

    Lymphedema was mentioned as a possible cause. That's a good thought to. You need a proper evaluation to determine some of these contributions to the mechanism. A swallowing study would be very helpful. I had one, done by a very determined, helpful speech pathologist years ago. It was most helpful, as were the exercises she worked with me on.

    Lastly, you talked about eating some things I have learned I can simply not eat, or else I pay a high price. Anything solid that chews down to particles. Not for me. I aspirate the pieces, and I just don't need the aggravation.

    I'm sure some of this relates to your odor. And odor is never a good thing. Sorry for rambling a bit. If you aren't getting help from your local guy, but it will be awhile to find a new doctor, how about asking the current one for a referral for a swallowing study/ speech pathologist?

    Happy holidays.

    Pat
  • sweetblood22
    sweetblood22 Member Posts: 3,228

    Several important things have been mentioned
    First, I've had lots of swallowing problems for the last year, though I think your exceed mine by quite a bit. Hondo mentioned the angle he has to acchieve to facilitate swallowing. So do I. I've completely re-learned how to swallow, or fluids absolutely pour out of my nose. I do mean this, I literally flood my shirt, the plate, everything. But if I'm careful and swallow properly, I don't leak at all.

    Lymphedema was mentioned as a possible cause. That's a good thought to. You need a proper evaluation to determine some of these contributions to the mechanism. A swallowing study would be very helpful. I had one, done by a very determined, helpful speech pathologist years ago. It was most helpful, as were the exercises she worked with me on.

    Lastly, you talked about eating some things I have learned I can simply not eat, or else I pay a high price. Anything solid that chews down to particles. Not for me. I aspirate the pieces, and I just don't need the aggravation.

    I'm sure some of this relates to your odor. And odor is never a good thing. Sorry for rambling a bit. If you aren't getting help from your local guy, but it will be awhile to find a new doctor, how about asking the current one for a referral for a swallowing study/ speech pathologist?

    Happy holidays.

    Pat

    I agree about there being
    I agree about there being just some things that are just too hard to swallow, or impossible to swallow. I have a long list. Corn and nuts are on there. I may sometimes get away with almonds, but I put them through the mini chopper first. They don't work whole or in big pieces. Coconut flakes or shred is an impossibility.

    You definitely need a swallow study with a good speech pathologist. Sorry you are having issues with docs right now.
  • rmkbrad
    rmkbrad Member Posts: 176

    I agree about there being
    I agree about there being just some things that are just too hard to swallow, or impossible to swallow. I have a long list. Corn and nuts are on there. I may sometimes get away with almonds, but I put them through the mini chopper first. They don't work whole or in big pieces. Coconut flakes or shred is an impossibility.

    You definitely need a swallow study with a good speech pathologist. Sorry you are having issues with docs right now.

    I agree with the swallow test and a speech pathologiest
    I can't talk worth a darn either, so this is definatly on the correct path. I will make a call tomorrow and see what I can get done. It is so frustrating having a doc that really does not care, the last time I seen him I walked into the exam room and he ignored me for a bit while he read my chart, and then he turns to me and says, what am I suppose to do for you. I said, heck I don't know examin me, see if anything has changed. So he uses a peice of gauze and pulls my tonge out and looks in my mouth with his flash light and says, yep looks normal. I give him a few of my complaints and he tells me, your doing better than I would have expected. Urggg. Anyway I agree with the tests since I have never had one done, I want to eat so bad it's not funney, I meen I really have an appatite now. I could really chow down if it was phyisicaly possible. Thanks again, and Hondo if I can squeeze any info from someone I will deffinatly let you know.

    Brad
  • Pam M
    Pam M Member Posts: 2,196
    Head Positioning for Swallowing
    I, too, took a few steps back after the neck dissection. I had more issues eating after the surgery. I can eat very well now - still some issues, but not a lot.

    After my failed swallow test after the dissection, I was instructed to tip my head down and to the right when swallowing - this made a big difference. I would think a speech pro would be able to help you find something that works for you. I only occasionally feel the need to do the head tip now.

    I'm hoping your new doc will be able to help. Sounds like the "old" one is a write off now.
  • longtermsurvivor
    longtermsurvivor Member Posts: 1,842 Member
    rmkbrad said:

    I agree with the swallow test and a speech pathologiest
    I can't talk worth a darn either, so this is definatly on the correct path. I will make a call tomorrow and see what I can get done. It is so frustrating having a doc that really does not care, the last time I seen him I walked into the exam room and he ignored me for a bit while he read my chart, and then he turns to me and says, what am I suppose to do for you. I said, heck I don't know examin me, see if anything has changed. So he uses a peice of gauze and pulls my tonge out and looks in my mouth with his flash light and says, yep looks normal. I give him a few of my complaints and he tells me, your doing better than I would have expected. Urggg. Anyway I agree with the tests since I have never had one done, I want to eat so bad it's not funney, I meen I really have an appatite now. I could really chow down if it was phyisicaly possible. Thanks again, and Hondo if I can squeeze any info from someone I will deffinatly let you know.

    Brad

    A reasonable exam......
    I've probably been examined 50 times by ENT Oncology in the last 14 years. I've also been examined by regular ENT, Nuclear Medicine, and Medical Oncology, as well as Family Practice. The ENT Oncologist is the expert a my exam, by far. None of the rest of these guys are trained to do the office exam that he does. However, what my exam consists of, at a minimum, is the following:

    1) a thorough history, which means he doesn't cut me off when I haven't had a chance to tell him every symptom I have, and he has a chance to further quesion me if I haven't been clear

    2) palpation and visual inspection of my face, head, neck and chest

    3) visual inspection of my entire oral apparatus, including the use of gause to move my tongue around. This is always done with the use of a head mirror and light, and a hand-heald mirror in order to do indirect laryngoscopy. During this, of course, he has me do the old Eeeeeee..... and Ahhhhhhhhh.... sounds in order to open my glottis for better inspection.

    4) Selectively, he also does a fiberoptic exam by running that uncomfortable scope up one of my nostrils.... Unpleasant, yes, but he's skilled enough at its use that he doesn't even have to use a local gel.

    5) Thorough discussion of diagnostic impressions and potential testing.

    6) Treatment recommendations, referrals are always discussed.

    7) Personal discussion, like how our favorite football teams are doing, how's the wife, etc.

    This is what you have a right to expect. Every time, without fail. I've known my doctor for 14 years. I like the guy. More importantly, I respect that he has my best interest at heart, and will do everything within his power to insure I survive and do well.

    Best wishes

    Pat