#58276 05-13-2006 09:15 AM | Joined: Mar 2006 Posts: 99 Senior Member (75+ posts) | OP Senior Member (75+ posts) Joined: Mar 2006 Posts: 99 | My husband finished his last of 42 radiation treatment on May 8th and when I tell you he sleeps all day, I'm not exagerating. Is this normal? I make him get up to shower every other day and he gets up to use the suction machine or go to the bathroom...Thats it. He started an antidepreeant last week but I'm thinking it's more physical than mental now. Maybe something else is wrong? I knew things would get worse before we could see any improvements but is sleeping this much normal? (BTY, a physical therapist is coming Monday to start.) Thanks, Kerry 
Kerry/wife of stephenm StageIV - Base of Tongue T4N0M0 XRT x42 / Taxol and Carboplatin x4 Tx. Finished 5/08/06
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#58277 05-13-2006 02:42 PM | Joined: Apr 2005 Posts: 2,676 Patient Advocate (old timer, 2000 posts) | Patient Advocate (old timer, 2000 posts) Joined: Apr 2005 Posts: 2,676 | Kerry, In our case the sleeping 24\7 was normal. John had 33 rad. txs and from the 3rd week on, he slept from the minute he got home-excepting bathroom breaks and my waking him up to do a tude fee- until he had to go to rad the next day. After treatment was over, he slept almost around the clock for a month or longer. I remember being afraid that I would come inato his room and find him dead during that time. It was a really scary time. I think it is a way for the body to recuperate. It's tough, but you gotta hang in there. 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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#58278 05-14-2006 04:22 AM | Joined: Jul 2004 Posts: 12 Member | Member Joined: Jul 2004 Posts: 12 | Also check for Fibromyalgia. | | |
#58279 05-14-2006 11:44 AM | Joined: Jul 2005 Posts: 207 Platinum Member (200+ posts) | Platinum Member (200+ posts) Joined: Jul 2005 Posts: 207 | Hi Kerry,
Let him rest, he needs it. I am 1.5 years out of treatment and consider myself to be about 90%. I thought a couple of months would do it, but recovery takes a long time.
Steve
SCC, base of tongue, 2 lymph nodes, stage 3/4. 35 X's IMRT radiation, chemo: Cisplatin x 2, 5FU x2, & Taxol x2. Hooray, after 3 years I'm in still in remission.
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#58280 05-15-2006 03:25 AM | Joined: Jul 2005 Posts: 624 "Above & Beyond" Member (500+ posts) | "Above & Beyond" Member (500+ posts) Joined: Jul 2005 Posts: 624 | Hi Kerry --
I assume that your husband has already been checked for obvious physical causes of fatigue such as anemia. He could be depressed, this is common, but he also could be suffering from what is termed "cancer fatigue", which often results from chemotherapy or radiation and is not well-understood.
One thing that has shown some promise, and is being studied in a number of NCI clinical trials, is supplementing with l-carnitine, a derivative of the amino acid lysine, which facilitates the movement of long-chain fatty acids into the mitochrondia, and thus boosts energy. Normally one synthesizes enough l-carnitine, but some chemotherapy drugs (notably cisplatin) cause the excretion of this material. Some initial studies have shown benefit to "cancer fatigue" patients by supplementation with 500 mg/day of l-carnitine. This is readily obtained in liquid form at health food stores as some sports enthusiasts feel it boosts energy for performance. (This is apparently not borne out in controlled studies, as most people have enough normally). However the story appears to be different for cancer patients.
In any case, with approval of his doctors, Barry took 500 mg l-carnitine (mixed with juice or water) all through treatment and maintained good energy levels, and was back to normal within a few months (he still takes it). We told another chemorad patient about it -- she had been complaining of wanting to sleep all the time after her treatment - and she recently emailed me saying that she had an almost immediate positive effect. OK, only two data points but worth considering...do a google for "l-carnitine for cancer fatigue" for some recent abstracts.
Of course, never take a supplement without clearing it with your doctors!
Gail
CG to husband Barry, dx. 7/21/05, age 66, SCC rgt. tonsil, BOT, 2 nodes (stg. IV), HPV+, tonsillectomy, 7x carboplatin, 35x tomoTherapy IMRT w/ Ethyol @ Johns Hopkins, thru treatment 9/28/05, HPV vaccine trial 12/06-present. Looking good!
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#58281 05-15-2006 10:55 AM | Joined: Mar 2003 Posts: 1,384 Likes: 1 Patient Advocate (1000+ posts) | Patient Advocate (1000+ posts) Joined: Mar 2003 Posts: 1,384 Likes: 1 | Besides the above good advice, consider that after treatments I too probably could have slept all day. Radiation fatigue is felt but sleep doesn't help you feel better. Instead of staying in bed I would resolve to get up and do something-anything to keep in motion. I also want to say don't worry if he still wants to sleep either.
Mark, 21 Year survivor, SCC right tonsil, 3 nodes positive, one with extra-capsular spread. I never asked what stage (would have scared me anyway) Right side tonsillectomy, radical neck dissection right side, maximum radiation to both sides, no chemo, no PEG, age 40 when diagnosed.
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#58282 05-15-2006 12:37 PM | Joined: Jul 2005 Posts: 624 "Above & Beyond" Member (500+ posts) | "Above & Beyond" Member (500+ posts) Joined: Jul 2005 Posts: 624 | I should add that there are some studies which showed that moderate exercise actually reduces cancer fatigue. And that total inactivity actually increases it. Your husband should try to do something, even if it is only walking down to get the newspaper or the mail, or to the corner and back.
Gail
CG to husband Barry, dx. 7/21/05, age 66, SCC rgt. tonsil, BOT, 2 nodes (stg. IV), HPV+, tonsillectomy, 7x carboplatin, 35x tomoTherapy IMRT w/ Ethyol @ Johns Hopkins, thru treatment 9/28/05, HPV vaccine trial 12/06-present. Looking good!
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#58283 05-18-2006 05:49 AM | Joined: Mar 2006 Posts: 22 Member | Member Joined: Mar 2006 Posts: 22 | How much pain med is he on, that's probably also effecting it. When my husband was in the hospital he slept alot(or was delirious) but when the pain meds were reduced he woke up. | | |
#58284 05-20-2006 01:23 AM | Joined: Nov 2002 Posts: 3,552 Patient Advocate (old timer, 2000 posts) | Patient Advocate (old timer, 2000 posts) Joined: Nov 2002 Posts: 3,552 | Kerry, I wouldn't worry about it too much at this point. Cancer fatigue is a well known side effect of the treatment and it's pretty normal while the body has been that beat up and add the healing process. Almost everyone has some degree of anemia early post Tx and coupled with malnutrition and other factors it's a long slow process. The narcotics might make a difference but he should be fairly adjusted to them by now. Just make sure that you keep a log of his food and fluid intake - that's the most important thing right now.
Like Steve, it took over a 1 1/2 years for me to get back to 80-90%. After 3 years post Tx I am almost 100%. The Tx took it's toll however and I do have some relatively minor side effects but nothing I can't live with. Some mild neuropathy, neck muscle spasms, etc. but no trimus, salivary or swallowing problems.
Like Amy I think my wife feared that she would find me dead also but the human body is amazingly resilient.
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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#58285 05-21-2006 03:55 AM | Joined: Feb 2006 Posts: 45 Contributing Member (25+ posts) | Contributing Member (25+ posts) Joined: Feb 2006 Posts: 45 | It is amazing how tired on can get going thru this. I was absolutely wiped out the past couple days after final treatments...but coming back a bit now. | | |
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