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SusanW Offline OP
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As I mentioned in another post my husband has actually managed to put on a few (much needed) pounds. But most of his calorie intake is through liquid can stuff. All his intake is oral(doesn't use a PEG for food) but he does struggle with eating solid foods.
There is one small sore left but that is really a minor problem. It seems to be a combination of low appetite, some gagging(we think from mucous) and just very low interest in food. This is from a guy who always loved good food of any kind.

He's coming on three months post treatment. He does make himself try different things but it's slow going. Some improvement but slow.
Did anyone else experience this? any tips?


CG to Spouse BOT, Chemo and radiation started on March 29,2010
Ended on May 14,2010. LET THE HEALING BEGIN!!!
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Food post Tx is just not enjoyable any more plus it usually takes far longer to eat than we are use to but that should slowly improve over the next 2 years. I guesstimate I am back to 90+% of my pre Tx taste and I enjoy eating almost as much as before.


David

Age 58 at Dx, HPV16+ SCC, Stage IV BOT+2 nodes, non smoker, casual drinker, exercise nut, Cisplatin x 3 & concurrent IMRT x 35,(70 Gy), no surgery, no Peg, Tx at Moffitt over Aug 06. Jun 07, back to riding my bike 100 miles a wk. Now doing 12 Spin classes and 60 outdoor miles per wk. Nov 13 completed Hilly Century ride for Cancer, 104 miles, 1st Place in my age group. Apr 2014 & 15, Spun for 9 straight hrs to raise $$ for YMCA's Livestrong Program. Certified Spin Instructor Jun 2014.
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Susan, It took me months until I could eat. I ended up having a throat sticture. The opening for food to go down was soo closed up. Plus, I was so drained, eating took too much energy! I really thought I would never eat again! I did want a soft boiled egg in the worst way for months & just could not get it down.
Give him time. So much can change in just a few months....you'll see!
Lets hope by Christmas, he will be eating like a little church mouse!


BOT T3N2M0 No surgery, 38radiation treatments,4 chemo rounds, peg removed 11/08, still have a port. Treatments ended 6/20/08. So far, so Good ! "I know God won't give me anything I can't handle. I just wish He didn't trust me so much !"

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Glad your husband has managed to put on a few pounds. It's good that he is willing to try different things. My son's progress at 3 months post treatment was slow and his tastes changed from day to day - when we found something he liked I made the mistake of buying a lot of it only to find he didn't like it anymore - so small quantities are better. My son eats almost as well as before treatment and enjoys all kinds of foods, although he does like to have sauces or gravies as accompaniments. I always found it interesting to hear his odd descriptions of what a particular food tasted like and I knew I wouldn't like it either if that's what it tasted like. The taste buds do weird things while they are healing.


Anne-Marie
CG to son, Paul (age 33, non-smoker) SCC Stage 2, Surgery 9/21/06, 1/6 tongue Rt.side removed, +48 lymph nodes neck. IMRTx28 completed 12/19/06. CT scan 7/8/10 Cancer-free! ("spot" on lung from scar tissue related to Pneumonia.)



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His putting weight on is a big help even if he has to force it down. I am still forcing soft soggy cereal and such down but wish I could add a few pounds. It seems he has a big problem licked if he put some weight on. Give him my best and tell him he has an admirer in me.


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
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SusanW Offline OP
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Thanks for the feedback. It helped him to know that this was "normal." (Whatever that means).

I am thrilled he put a few pounds on. He still has 10-15 to go but no rush. As long as he keeps going in the right direction!!!

Jim, is it hard for you to gain even with those high calorie drinks?


CG to Spouse BOT, Chemo and radiation started on March 29,2010
Ended on May 14,2010. LET THE HEALING BEGIN!!!
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Looks like your husband and Gordon are at the same point of recovery and are pretty much in the same boat. No appetite, taste is all wonky, no saliva. The gagging has finally let up, thank goodness.
I now refer to dinnertime as "mealtime misery". It takes him forever (maybe an hour) to get down his dinner and he curls his lip at the idea of sauces and gravies. He seems to do better with cereal/fortified milk/blueberries in the a.m. The rest of the day is a terrible struggle with food. I keep pushing the milkshakes (fortified milk/3 TB whey protein powder/1 1/2 Boosts/2 scoops of ice-cream, lactose-free and no sugar added) because they have 750 calories each; he's managing to get two of them down a day. He's not gaining any weight, but at least is holding his own.
So keep up with the liquid supplement and maybe try adding some stuff into it. Good that your spouse has gained a few pounds - certainly a step in the right direction. Best of luck!
Anne


Anne - CG to Gordon (59), non-smoker/non-drinker. SCC, BOT, HPV 16+, stage 3. Jan./10 - radical neck dissection to remove 48 lymph nodes, 1 node pos. Apr. 23/10 - finished 35 rad. and 3 cisplatin. Jul. 22/10 - PET scan clear.

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