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#61227 07-05-2007 04:30 AM
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Nelie Offline OP
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I hope I'm not making a topic that already exists. I tried to look. As people who have been reading here know, I've been struggling with swallowing problems for 2 years post treatment.

The first big issue is esophageal strictures, which keep coming back, but I also have an epiglottis worn away from radiation, some limits in my tongue movement, lymphedema on the base of my tongue, and trismus.

Right now my throat has recently been stretched open and I am strugling to do the Shaker exercise 3 times a day and swallow as much as I can. Basically, anything that isn't mushy and has some weight to it (such as little bits of sausage in a sausage gravy) will feel like it goes down but get stuck in the little pocket my epiglottis forms or in pockets above my vocal cords. Fortunately, I have not lost any sensation there and so usually I eventually feel when that happens and it gets coughed up. So maybe I can avoid aspiation pneumonia despite all this.

On top of this, I have a very sensitive (easy to start feeling pain) mouth after radiation. I can't really have anythimg acidic --even the mint in Biotene mouthwash stings my mouth pretty badly, though I use it anyway.

I know there are not many people who have it this bad unless it is right after rad, but I figure I'm probably not the only one. I thought maybe we could support each other, whereever we are.

Where I am is pushing to get off the tube, though I expect I'll be eating things with the consistency of baby food and pudding for the most part. At least I'll be able to take a bath, go swimming and canoeing in muddy rivers (all of which I used to love and which I don't do right now because of the tube).

So I'm going to share one new triumph last night which is I finally found a pasta that I can get down consistently if I put a bunch of Olive oil or butter on it. Pastina. Little tiny pasta grains. I didn't think to try it for a long time ebcause I thought it would be like rice, which is a disaster for me, but it clumps together just enough and is just mushy enough, that it goes down very easily. It is alos wodnerfully non-irritating for my poor sore mouth, unlike mashed potatoes, which is my main other starch, but which rubs against the sensitive spots in my mouth enough to irritate them.

It's much easier to get all my calories orally if I can have some pasta, it isn't all soups and protein shakes.

Nelie


SCC(T2N0M0) part.glossectomy & neck dissect 2/9/05 & 2/25/05.33 IMRT(66 Gy),2 Cisplatin ended 06/03/05.Stage I breast cancer treated 2/05-11/05.Surgery to remove esophageal stricture 07/06, still having dilatations to keep esophagus open.Dysphagia. "When you're going through hell, keep going"
#61228 07-05-2007 05:49 AM
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Great News Nelie, I was told by a doctor that the 4 most important items for a meal are: pasta, potatoes, bread and rice. Enjoy and I hope you will get rid of the feed tube soon. ps My husband is finding eggs scrambled easy to eat and it is a protein. Take care, Carol Ann...


Carol CG to Husband age 60 Stage IV SCC right tonsil T4AN2B tx rad x 35 chemo x 2 Currently after treatment no sign of cancer in throat. (all clear to date)
#61229 07-05-2007 07:51 AM
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Nelie Offline OP
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I wish I could eat scrambled eggs. I've tried several times and they don't work for me.


SCC(T2N0M0) part.glossectomy & neck dissect 2/9/05 & 2/25/05.33 IMRT(66 Gy),2 Cisplatin ended 06/03/05.Stage I breast cancer treated 2/05-11/05.Surgery to remove esophageal stricture 07/06, still having dilatations to keep esophagus open.Dysphagia. "When you're going through hell, keep going"
#61230 07-05-2007 12:22 PM
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Nelie,

I use egg beaters and add milk to it. They come out softer and not so dry. You can use regular eggs as well. Try angel hair pasta. It might work for you. I make it with oil & butter, or a white cheese sauce. Small bites.

I am having problems swallowing again. I am starting to choke again. I am getting ready to get my esophagus dilated again. I have had to revert back to oatmeal and real easy meals for me to eat. Potatoes are out for me as well. I also found that trying to eat a regular meal amount was to much. I eat a child portion, then few hours later eat a little more.

Lately I too have had my mouth bothering me more. Not sure why? It is stinging. I am trying to rinse & swallow some meds. for thrush to see if it will help.

I can understand the wanting to get rid of the feeding tube! If you can put together enough food ideas to survive, it should work. You will feel like a new women after it is gone. laugh

Hope something here has given you some support and ideas to think about.

Take care,
Diane


2004 SCC R.tip 1/4 tongue Oct. 2005 R. Neck SCC cancer/Chemo Cisplatin 2x/8wks. Rad. Removed Jugular vein, Lymph gland & some neck muscle. TX finished 1/20/06... B.Cancer 3/29/07 Finished 6/07 Bi-op 7/15/09 SCC in-situ, laser surgery removed from 1st. sight. Right jaw replacement 11/3/14. 9 yrs cancer free as of Jan. 2015
#61231 07-05-2007 12:48 PM
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Nelie, Have you tried poached eggs? You might also experiment with different risotto recipes [ you can use the pastina instead of rice if you need to. 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

:
#61232 07-05-2007 01:42 PM
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Nelie Offline OP
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Actually, I did try poached eggs a while ago and got some down. Then my throat started closing up again and I had problems the next time I tried. I think they'd be OK now. I should try.


SCC(T2N0M0) part.glossectomy & neck dissect 2/9/05 & 2/25/05.33 IMRT(66 Gy),2 Cisplatin ended 06/03/05.Stage I breast cancer treated 2/05-11/05.Surgery to remove esophageal stricture 07/06, still having dilatations to keep esophagus open.Dysphagia. "When you're going through hell, keep going"
#61233 07-05-2007 03:18 PM
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Hi Nellie,

I have some trouble swallowing but not horrible. It's just very apparent that my esophogus is much smaller than it was before and I choke easier. Your comment about your mouth always being sore really rings a bell with me, mine is ALWAYS sore and irritated, along with my lips. I've gotten used to it but sure wish there was a way to resolve it.

Diane gives good advice for eating scrambled eggs, although I do use regular eggs, I also add milk to them along with cheese and I cook them VERY soft. I mash them up with my fork and they suit my mouth and throat just fine. Toss in some onion salt and they are delicious. I've found I can eat alot of things if they are the correct consistancy.

Wish I could help you more, you certainly have had a rough road with the eating and I love your spirit.

Minnie


SCC Left Mandible. Jaw replaced with bone from leg. Neck disection, 37 radiation treatments. Recurrence 8-28-07, stage 2, tongue. One third of tongue removed 10-4-07. 5-23-08 chemo started for tumor behind swallowing passage, Our good friend and much loved OCF member Minnie has been lost to the disease (RIP 10-29-08). We will all miss her greatly.
#61234 07-05-2007 03:56 PM
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Nelie,

Ditto for me on the stinging mouth - 3 years out and most days my mouth burns like crazy. Sugar and the sugar and acid in fruits is the worst - feels like hot peppers or something. I have recently found that guacamole works really well - just wish I could have the tortilla chip with it! Usually I just eat the guacamole by the spoonful - whatever it takes, right? At least the avocado is a good source of healthy fats. I know what you mean by rice being a disaster - those little grains go everywhere and it seems like they multiply while they're in there! Does anyone else have the sensation of not ever really getting hungry? I generally have to remind myself to eat - I don't have cravings anymore - the joy of eating has definitely diminished - I have gained about 15 pounds in 2 years but that seems to be holding for the last 6 months or so. I did make homemade ice cream yesterday and that goes down just fine!

Nelie, I e-mailed you a year or so ago and talked about returning to school - well, I have finally gotten the courage to do just that. I start Monday at my local junior college and have registered for the fall term - taking math and science courses so I can transfer to a 4-year college and get a degree in clinical nutrition/dietetics - this should take 4-5 years and I'll be 50 when I'm looking for a job but I really want to help head/neck patients with these eating problems so hopefully where there's a will, there's a way! It's been 23 years since I sat in a college class - I was in the bookstore the other day and everyone was my daughter's age! In fact, I ran into a couple of her good friends - I'm sure I'll have classes with some of them - that's going to be so strange! Anyway, wish me luck - I'm starting to get cold feet.

Keep on trying with different foods - that's what I did and still do - just experiment. I still have to take very small bites with lots of liquid and it is a slow process - I spend 30 minutes to an hour depending on the meal. Take care

Pam


SCC Base of Tongue Stage IV- 2/04 - 40 Rads 1/2 conventional, 1/2 IMRT; 3 chemo treatments consisting of Carboplatin/Taxol/5-FU; Right Radical Neck Dissection
7/04; scans and pathology clear
#61235 07-05-2007 04:57 PM
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Nelie Offline OP
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Pam,

I remember you emailing me and I am so happy you are returning to school! If your 2 year college is like the one where I teach, you'll find that, although most of the students are very young, there are enough older ones like you that you won't be that big an oddity. And I can tell you from the professor's perspective, we love the older students like you who are there to really learn and have gotten the time management thing down in a way many 19 year olds have not.

It is good to learn I am not the only one with a sore stinging mouth most of the time (and Minnie, I carry lip balm with me everywhere and use it I don't know how many times a day or my lips get just as bad). Because sometimes I worry it's some kind of sign of a recurrence though my ENT did tell me I may just have this kind of mouth pain forever.

Thanks for the Gaucamole suggestion. I had forgotten about that. It's funny, I find I can tolerate soups and other things flavored with pepper (as long as it isn't super hot pepper) without it hurting. But, as you say Pam, sugary things can burn my mouth sometimes as well as anything at all acidic (and I used to LOVE vinegary things like olives and pickles--oh well).

Also one night something will work and the next it won't for some reason. I think I cooked the pastina a little less tonight so they were more al dente and didn't stick together as much and they kept going everywhere in my mouth, more like the problem I had with rice. It took me an hour to eat a small bowl of pastina with a mushroom gravy and some slightly melted boursin cheese with herbs and garlic. I had some pureed carrots I was going to eat but I was so tired I gave up and gave myself a can of Jevity and some berry juice through the tube just to be sure I got close to enough calories today. I'm a good weight right now--I have dropped 4 sizes from what I was pre-cancer(!)--and I don't want to get any skinnier. I'm tired of having to get new clothes and give away old ones that never even got worn much!

Anyway, thanks for the enouragement, Minnie and Pam, I really need it. My husband tries but he's kind of burned out on it himself.....

Nelie


SCC(T2N0M0) part.glossectomy & neck dissect 2/9/05 & 2/25/05.33 IMRT(66 Gy),2 Cisplatin ended 06/03/05.Stage I breast cancer treated 2/05-11/05.Surgery to remove esophageal stricture 07/06, still having dilatations to keep esophagus open.Dysphagia. "When you're going through hell, keep going"
#61236 07-05-2007 05:40 PM
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While my esophogus is not as wide as it once was, I don't have too much trouble and only get things caught about once a day, but I am interested to hear that I am not the only person who cannot tolerate Biotene mouthwash. I do not do alcohol or vinegar (have had some interesting experiences with salad dressing) but I thought the mouthwash must be okay. Wrong. Anything spicey is a no-no also.

On another subject, I do a class working with weights (for stong bones) thrice weekly at the local community college, and at least half the students I see in the halls and on camput are middle aged and older. So Pam, you do not need to have cold feet. Good for you and your plan!

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