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Joined: Aug 2005
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Greetings dear friends. Bill is back, but returns with a problem and looking for assistance once again. The answer to my problem will likely be right here in this text, and I know it. However, I just cannot do anything about solving it with my current mindset.

I am eleven months out from treatment now, fourteen from being diagnosed. My stress level is climbing daily. Due to unforseen circumstances I am unfortunately without any health coverage at present, and have not had any for the past two and a half months. Because of that I have not seen a doctor in that time period either. That will change in a couple of weeks when my new coverage kicks in.

I have moved my wife to Massachusetts, along with all the family pets and most of our "stuff". I remain here in S Florida, trying desparately to sell our home so that I can join her up north. The house is currently listed at some $ 20K less than market, yet still I get not even an offer.

The above, though problems, are not my primary concern right now though. My primary concern right now is weight loss, in the form of muscle loss. I have gone from a bit overweight 215 down to 150, ten pounds of which I have lost in the past couple weeks. My massage therapist, yes I am still being given free massages once a week, has informed me that the time is now to do something about this. She has noticed the muscle loss that has happened over the past several weeks. I now have those ugly flapping in the breeze deposits of fat that used to be at least partially hidden by muscle that was beneath them just about everywhere.

In a single word to what is likely the first question to be brought forward, no. I am not eating the way that I should be. A little over a year ago I had a voracious appetite. Today I have no desire to eat at all. My ability to taste has not returned in any degree. Because the list of things that I can taste is so limited I have even gotten tired of eating what I can taste. Eating foods that I cannot taste lost its place on my things to do long ago. Yes my caloric intake is not where it should be, to even maintain, let alone gain. I am being semi-active during the day, even doing some walking to get some additional exercise. Unfortunately we all know that the exercise burns calories, calories that I cannot afford to burn.

Over the past week I have tried a few protein mixes to increase my protein intake, knowing that it supposedly is what is required for muscle growth. I cannot stand the taste, yes I can taste them in whatever I mix them in, much less the horrible smell, regardless of the flavor. I also developed a diarrhea problem and thus stopped.

I am at my wits end here. I just do not know how to force myself to eat. Being alone, there is noone here to nag me or give me a kick in the a../butt, though it too is nearly non-existant now too, save the wrinkled deposits of fat, and would be hard to find. I gave some thought to attempting to contact the nutritionist that was assigned to me during my treatment, but having no medical coverage that apparently is also not possible.

Any suggestions to motivate me to eat, or how I can somehow get my protein intake up would be gratefully appreciated.

Withering away in S Florida,
Bill


No love, no friendship can cross the path of our destiny without leaving some mark on it forever. - Francois Mauriac

Thank you for leaving your mark.
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Bill,
All I can say is "I understand". I'm only 3 1/2 months out from radiation now, and only started eating (some) solid food in the last couple of weeks. I've been living on liquids for the last 5 months. I did not have a PEG, but managed to keep weight loss down to 30lbs-from 185 to 155 and maintaining. The liquids that have been sustaining my weight have been Ensure, Prosure, and Naturade's Weight Gain mixed in milk.

I developed some kind of 'food phobia', and was not able/willing to eat. Then, about 2 weeks ago, I forced myself to eat some french toast dripping in butter and syrup. I felt so good afterward, that I continued eating something every day, mostly a few bites of chicken or steak washed down with water. Eating anything is a huge chore for me, but I'm able to do it daily. Everything tastes absolutely horrible, but all I can say is, I feel so much better after food than without it. I gaining some energy, too, and feeling more 'normal' every day.

I encourage you to bite the bullet, continue drinking the liquid nutrition, and keep trying different foods until you find one you can tolerate. (By 'tolerate', I mean get down and keep down no matter how bad it tastes or how angry you get). Keep trying, don't give up, it's worth it!

Riley


dx 2/13/06. modified radical neck dissection 3/9/06 multiple biopsies of upper airway and direct laryngoscopy. 1 of 47 lymph nodes positive for metastatic undifferentiated carcinoma (lymphoepithelioma). Unknown primary. Finished radiation 5/24/06.
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O.K. Bill- you need some nagging and this Island gal can do it! What is your base caloric intake per day? When do you get it? Are you getting nutrition by mouth only now? Those are the nutrition questions we need answers to.
Question #2 and OBSERVATION #2. You have sent your whole support system away and you are alone there- Seems to me like a BIG depression problem. Turn that house over to a real estate agent and get the hell out of Dodge. Money does not always equate happiness. I know that, at heart, you are a giver- I have gotten lots of good vibes from you over the past year. Give yourself permission to beat this food battle. Since food may no longer be a pleasure part of your life- find something to take its place. That is what survivors do. And get out of Florida and to the people you love. Amy


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

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Hi Bill, one thing for sure is that you can't be eating normally now due to side effects of treatments and another thing for sure is that if you don't force yourself to take whatever you can, your weight will continue to drop and your body will weaken gradually. It is not a matter of whether you have the desire to eat or not. What you need is very strong will power and determination to eat even though it tastes horrible. I didn't have a PEG either and managed to overcome the oral pain and taste problem and lost 16 pounds (I was rather thin to begin with). You can try something soft and easier to swallow. As a Chinese, my diet is very different from the westerners. I took a lot of congee, cereal in milk, fish, taufou and melon. I mostly took nutritious food that was easy to swallow. You may consider inserting a feeding tube, like the majority of the people here did. This should help you get the nutrition you need without suffering from much pain. I understand that you have more hurdles other than the eating problem but among them, getting nutrition should be the first and foremost one you should address now.
Where there is a will, there is a way!

Karen


Karen stage 4B (T3N3M0)tonsil cancer diagnosed in 9/2001.Concurrent chemo-radiation treatment ( XRT x 48 /Cisplatin x 4) ended in 12/01. Have been in remission ever since.
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Bill,
one thing I would add is that muscle tissue doesn't build up as a result of just eating. It can certainly be "consumed" by the body from malnutrition and atrophy. You have to have an exercise prgram in place as well, even if it's just walking around the block. I went from 170 to 109 - My new normal weight now is around 150 which is perfect for my height. I also pumped iron for the upper body.

How tall are you?

I heartily agree with Amy (and Riley and Karen too for that matter)- you still need your support system.

I also empathize with you over the muscle and protein drinks like Boost and Ensure - it made me gag as well. I lived on Carnation Instant Breakfast and it kept me alive anyway. I also had Hagan Daz milkshakes daily, although I am not so sure how healthy 85% butter fat is. I am really doing healthy foods now - tons of fresh fruit, salads, very little red meat, etc.


Gary Allsebrook
***********************************
Dx 11/22/02, SCC, 6 x 3 cm Polypoid tumor, rt tonsil, Stage III/IVA, T3N0M0 G1/2
Tx 1/28/03 - 3/19/03, Cisplatin ct x2, IMRT, bilateral, with boost, x35(69.96Gy)
________________________________________________________
"You are a mist that appears for a little while and then vanishes" (James 4:14 NIV)
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Bill,

Another point about the importance of the support system -- for the months after my treatment ended, when I had lots of trouble eating and nothing tasted good, one way that I was able to get through mealtime was to try in some way to make it a social event (dinner with my husband in the evening, lunch with some of my colleagues at work during the day). Even with liquids or soft foods, it took me much longer to down a "normal" meal than it did them, but having company and conversation helped to pass the time and take my mind off the unpleasant taste and occasional swallowing difficulties.

As Amy said, think about rejoining the rest of your family sooner rather than later, or try to connect with some local friends or neighbors who may be able to help push you through the tough spots.

Cathy


Tongue SCC (T2M0N0), poorly differentiated, diagnosed 3/89, partial glossectomy and neck dissection 4/89, radiation from early June to late August 1989
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It's a new day and quite frankly after reading my post from yesterday I am ashamed of myself. I am not only ashamed for having started what today appears to have been my own little pity party, but also for losing my inpenetrable positive outlook on life.

So why are things so different today? Well, after making that post yesterday I started popping around to some of the other parts of the site. I then did a search to find out how things were going with someone that I had chatted with an several occasions and someone that noone could ever convince me had ever had a negative thought, Dannyboy.

Not having been here for a while I was not aware that Danny had left us. When I read about it I could not control my emotions and cried for near an hour. That was the start of the turnaround. Danny was, and always will be, one of the strongest people I have ever known. I will likely never have the amount of courage he had, but I can at least try.

Not long after leaving the site, out of the blue, a friend called and asked if he could take me out for dinner. Reluctantly I agreed to go, but told him I probably wouldn't eat much but would enjoy the company. After I consumed a large salad, two scoops of mashed potato with chives, some steamed broccoli and a marinated, grilled chicken breast I told him that was more food than I had eaten in the past week. He then informed me that he had accomplished his goal, get some food in me. His business is right next door to where I get my massages and I stop in to see him every week. He had been noticing my weight loss also, and was concerned. We had a great time over dinner and then afterwards here at the house just talking.

So at that point I had knowledge of a friend who fought with his positive attitude to the very end. As well, I had a friend that had watched me from day one go through my journey and had displayed his concern for my well being, not to mention a very healthy meal in my stomach. As I lay in bed the thought occurred to me that just maybe things are not as bleak as they appear.

This morning the sun did in fact rise. As I went outside to get my newspaper I saw the dew covered, green side of the grass, not the roots. I downed my usual orange juice and vitamin as the coffee machine gurgled and dripped the hot java into the pot. I poured a bowl of cereal, added some milk and sat down at the table to eat it. After a couple bites I got up and grabbed a notepad and made a worksheet just like I had used while in treatment, listing what I had consumed, how many calories it had and how much protein it contained. I rinsed out the bowl and as I was pouring a cup of coffee the door bell rang.

It was my sister, who lives about sixty miles south of me. Because I had not returned any of her calls, emails or her letter she had decided that rather than have the local police do a "health and welfare" check on me she would do it herself. I have always been rather quick with words and before she could say anything I told her that the rumors of my death were all false. She began laughing hysterically and then threw her arms around me. Our laughter turned to tears as she repeated said how glad she was to find that I was okay. We drank coffee and talked, and talked, and talked, and talked... I think you get the picture. I'll be going down to her house this afternoon to spend the night and all day tomorrow. We will be going for a long horse ride early tomorrow morning on the beach, with luck, early enough to watch the sun rise.

With the turn around in the past twelve hours bleak and not so bleak anymore. Though I learned that Danny had left us, his positive attitude still has an influence on me. I had a fantastic meal last night with a friend who cares about me. My little and most favorite, sister appeared out of nowhere to check on me and show her concern. Thinking back just a bit, my massage therapist also had made her concern known by telling me that I had to do something about my muscle loss.

True, my wife, the family pets and most of our belongings are not here and as some of you have mentioned I no longer have my support group with me. However true that may be, I think that the support group I had has just been revamped. It now consists of friends and family that are here. That is not to say that I no longer consider my wife part of my support group, I still do. She knows nothing of what has been happening with me here. I have an uncanny ability to turn the "poor mes" off when I talk to her on the phone, which we do, morning, noon and at night. Besides, she is where she needs to be now, with her mother, taking care of her and has enough to deal with without needing to worry about me.

Few of you will likely get this far with reading but I must clarify a couple things. I do not have a problem eating. I have been on solid food for quite a while. The peg tube is long gone. I do have the occasional problem with aspiration but can deal with that. It is just a case of forcing myself to eat, and eat properly that I have to change. I still have four cases of Ensure that I never used. That I can taste and will begin using it as a supplement, but supplement only. There is little that I cannot cook as I was brought up in, and owned my own restaurant. The key will be to just do it and say the hell with the fact that I cannot taste anything. If I want to make something of the thus far victory over this insidious disease, I have to eat.

Also, those of you who have read my journal know that my GP was always my "go to" guy. I doubt I will ever find a doctor like him again. I plan to make an attempt to get past "those people" out front and talk to him on Monday, I may even call him this weekend and leave a message with his answering service. I am reasonably confident, no, I am positive, that explaining my problem of being out of my meds will result in getting enough samples from him to carry me until my insurance kicks in.

Thank you all for caring. I hope you all have a fantastic day. I am off to go listen to the terror-filled screams that will eminate from the bushes and hedges as their little heads are severed by the electric clippers. I have no idea who the guy is that hijacked my account and made the post that started this thread, but I am glad he has been sent packing.

Loving you all!!
Bill, the REAL one!


No love, no friendship can cross the path of our destiny without leaving some mark on it forever. - Francois Mauriac

Thank you for leaving your mark.
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Bill - I read every word, I laughed, I cried...all at the same time. Thanks for sharing the delightful UPside of Bill, but pity parties are always welcome too smile From the OTHER side of your state, JaneP


Husband: 3 SCC gum and cheek cancers 2002, 2005, 2006: surgery only. Scans clear after removal of small, well differentiated, non-invasive cancers. No radiation. 4th SCC lip diagnosed 4/13/07 - in situ, removed in biopsy. More lip removed 2/8/08 - dysplasia. 2 Biopsies 3/17/09 no cancer (lichenoids)
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Hi Bill,
Sorry for not following your story well and having made some 'advice' at the wrong moment. Anyway, I am glad that you have become much more positive and the real Bill is finally back. Cheers!

Karen


Karen stage 4B (T3N3M0)tonsil cancer diagnosed in 9/2001.Concurrent chemo-radiation treatment ( XRT x 48 /Cisplatin x 4) ended in 12/01. Have been in remission ever since.
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YEAH BILL, [I know I am shouting but I am so glad to see such an upbeat post] Amjy


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

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