#36631 06-03-2003 01:06 PM | Joined: Mar 2003 Posts: 251 Gold Member (200+ posts) | OP Gold Member (200+ posts) Joined: Mar 2003 Posts: 251 | At 2 months post radiation and chemo, my husband's biggest complaint seems to be one related to temperature control. I am wondering if anyone else has had this problem...or what it could mean. He feels alternately too cold and then too hot, both day and, especially at night. I mentioned it to the radiation oncologist at our last follow-up check and he seemed to rather discount it...but it is really bothersome for him.
Thanks, Anita
Husband Dx 12/02 Stage 4 Tonsil Cancer T1N2bM0; surgery, radiation, chemo 1/03 - 4/03.
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#36632 06-03-2003 02:24 PM | Joined: Dec 2002 Posts: 235 Platinum Member (200+ posts) | Platinum Member (200+ posts) Joined: Dec 2002 Posts: 235 | Anita, My husband is 6 months post-radiation treatment, and even now we still have a problem with temperature control. It was especially rough the first 3 months after radiation. One minute my husband would literally be shivering with the chills...then a few minutes later - off came all the blankets, socks and what-have-you. It was bothersome for me, but in all honesty - and I hope I don't sound selfish in this statement - it was a pain-in-the-butt for me! I was constantly adjusting the temperature in our apartment and constantly covering him up - only to have him kick off the covers and turn on the fan! It's nerve-wracking, and I remember having the temperature gauge set up to practically 80 degrees at times. Although the weather is much warmer now, and things aren't as bad - he still gets into a weird hot/cold comfort zone thing every now and then, but for the most part - this has gotten much better. I would say give it time. Especially since you have already discussed this with your doctor, and he didn't seem to make much of it. I honestly don't know what causes this to happen - but I'm sure the radiation definitely throws everything out of whack, and at the same time- the body is trying to heal itself and repair the damage. Be patient, and I hope things get better for both of you soon!
DonnaJean
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#36633 06-03-2003 04:20 PM | Joined: Oct 2002 Posts: 546 "Above & Beyond" Member (500+ posts) | "Above & Beyond" Member (500+ posts) Joined: Oct 2002 Posts: 546 | Anita, I don't have any suggestions on how to combat this problem, but Heather has experienced the same thing, both after RAD and now again after having chemo. We were told the RAD and chemo both can cause havoc with your body's temperature controls. It certainly is a pain in the neck, but I don't think there is much you can do except keep adjusting the thermostat or adding/removing blankets, turning AC/fans on/off, etc. Rainbows & hugs, Rosie
Was primary caregiver to my daughter Heather who had stage IV base of tongue SCC w/ primary recurrence. Original diagnosis August 21st, 2002. Primary recurrence March 18th, 2003. Died October 6th, 2003.
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#36634 06-03-2003 05:51 PM | Joined: Mar 2003 Posts: 189 Gold Member (100+ posts) | Gold Member (100+ posts) Joined: Mar 2003 Posts: 189 | Dear Anita, Ditto here. My husband finished rad and chemo in November. He was freezing at night so I bought a down comforter. I was loving it, for about a week, because I'm cold natured. Then his temperature control went haywire. He would sweat under the comforter, turn the fan on, and then shiver. Soooooo....we now have a light weight cotton blanket on the bed with the down comforter on the floor next to it. If either of us gets too cold, we just reach down and grab it! Mandi
Husband diagnosed with stage III tonsil and floor of mouth cancer in August 2002. Three rounds of chemo/42 RAD treatments. Upper right lung lobectomy in March 2003. (Benign)
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#36635 06-03-2003 09:21 PM | Joined: Nov 2002 Posts: 3,552 Patient Advocate (old timer, 2000 posts) | Patient Advocate (old timer, 2000 posts) Joined: Nov 2002 Posts: 3,552 | Anita, When I was 2 months out I was still having hot and cold problems. I understand that the thyroid plays a role in this, also anemia and low white cell count, so any or all of the above are potential contributors. There is no way to fight this other than it has to run the course. You eventually may need thyroid medication. I am 75 days out today and still have some problems but not as severe - things are definitely improving. I always keep a blanket or 2 handy that I can kick off easily if I need to. There were a few times that my wife had to sleep in the guest room so I could have the heat on and she could have the windows open. I also always have layers of clothing (which we are used to living in the SF Bay Area). And, yes, I have had the heat up to 80 degrees, something I would have NEVER done before this. We have a ceiling fan which was very handy. I have lost a lot of weight so I am sure that it is a factor also.
Gary Allsebrook SCC, Stage III, Right Tonsil (T3N0M0) Cisplatin Chemo x2, IMRT x33 Treatment Began 1/28/03 Treatment Ended 3/19/03
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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#36636 06-04-2003 01:34 AM | Joined: Mar 2003 Posts: 251 Gold Member (200+ posts) | OP Gold Member (200+ posts) Joined: Mar 2003 Posts: 251 | Thanks, everybody, for the replies. Always makes me feel better just to know that these weird things are normal. My mind tends to jump to conclusions...and not good ones at that!
Anita
Husband Dx 12/02 Stage 4 Tonsil Cancer T1N2bM0; surgery, radiation, chemo 1/03 - 4/03.
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#36637 06-04-2003 01:01 PM | Joined: Dec 2002 Posts: 235 Platinum Member (200+ posts) | Platinum Member (200+ posts) Joined: Dec 2002 Posts: 235 | I hear ya, Anita. Guess this is life for us caregivers - calm one minute, and a jangle of nerves the next! Take care - both of you!
DonnaJean
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