Announcement

Collapse
No announcement yet.

Radiation - Nausea and Loss of Appetite

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • Radiation - Nausea and Loss of Appetite

    Hi,

    I recently started radiation treatments and had 3 so far. I have been feeling nauseous ever since starting, although I haven't actually vomited. I thought that over the weekend I'd start to feel better, but even this morning (Monday) before going for any treatments, I still feel it. I haven't eaten very much since starting the treatments.

    I have a prescription for Zofran which I was trying not to use unless it gets really bad since it's so expensive, but maybe I should.

    Does anybody have any advice about this? I really didn't expect radiation to be a big deal. From talking to my doctors and reading some online about it, everybody seemed to make radiation out to be a relatively easy process. I'm sure that compared to chemo it is much easier, but it's starting out worse than I expected. And it will probably get worse, right?

    Randy

  • #2
    Holy Smokes!!! You're not taking you're Zofran? I will be amazed if anyone here say's much other then PLEASE TAKE THE ANTI-NAUSEA MEDS. Oh and they will also welcome you to the forum.
    Son Jason diagnosed 4/30/04, stage III. Right I/O 4/30/04. Graduated College 5/13/04. 4XEP 6/7/04 - 8/13/04. Full open RPLND 10/13/04. All Clear since.

    Treated by Dr. Rakowski of Midland Park, NJ. Visited Sloan Kettering for protocol advice. RPLND done at Sloan Kettering.

    Comment


    • #3
      Randy, there are many choices out there other than Zofran than could be cheaper...but no matter that you take, take something. You can't keep your engery levels up if you are not eating.

      Try to eat every 2 hours...little things...high carb items will help with feeling sick to your stomach.
      Co-survivor with husband Boyce, Diagnosed 7-11-06, orchiectomy right testicle on 7-12-06- Stage 3A: Mixed germ cell tumor with inguinal seminomatous and kartotypic carcinoma. One tumor over 10 cm, second tumor 4 cm, Chemo 4xBEP: Bi-lateral RPLND Dec 2006, nerve sparing but left sterile.
      Current DVT
      Current testosterone replacement therapy, Testim.

      "You must abandon the life you planned, to live the life that was meant for you" ~wisdom I have learned from my family on this forum

      Comment


      • #4
        Anthony did not have radiation, but for chemo he had zofran, decadron, and compazine. These controlled the nausea very well and the decadron increased his appetite.

        Zofran is very expensive and we had a hard time getting the insurance to approve Anthonys refill.

        There was another anti nausea med that was mentioned that is also very expensive, I don't recall what it was though.

        Compazine is not expensive though I don't know how well it would work by itself.

        Son Anthony DX 12/11/06
        L/O 12/20/06 Stage IIIA, 95% EC, 5% Yolk Sac
        4XEP 1/29-4/6/ 07
        AFP started increasing3 wks later
        Residual abdominal mass found on CT
        RPLND 6/8/07
        Cancer in pathology-
        80% mature teratoma, 20% Yolk Sac. --
        No adjuvent chemo and
        AFP normalised

        July 22, 2010 ---- 3 years all clear!

        Comment


        • #5
          Originally posted by mstlyn
          Anthony did not have radiation, but for chemo he had zofran, decadron, and compazine. These controlled the nausea very well and the decadron increased his appetite.

          Zofran is very expensive and we had a hard time getting the insurance to approve Anthonys refill.

          There was another anti nausea med that was mentioned that is also very expensive, I don't recall what it was though.

          Compazine is not expensive though I don't know how well it would work by itself.
          Kytril may be what you are thinking of. It is very pricy, but works very well. Also, Emend is also very good and may be covered by your insurance. If you do not have coverage for meds, please ask the cancer center where you are being treated and they may be able to help you.
          Co-survivor with husband Boyce, Diagnosed 7-11-06, orchiectomy right testicle on 7-12-06- Stage 3A: Mixed germ cell tumor with inguinal seminomatous and kartotypic carcinoma. One tumor over 10 cm, second tumor 4 cm, Chemo 4xBEP: Bi-lateral RPLND Dec 2006, nerve sparing but left sterile.
          Current DVT
          Current testosterone replacement therapy, Testim.

          "You must abandon the life you planned, to live the life that was meant for you" ~wisdom I have learned from my family on this forum

          Comment


          • #6
            Randy:
            The facility that's giving you your radiation treatments may have some samples of anti-nausea medication that you can have.
            Son Jason diagnosed 4/30/04, stage III. Right I/O 4/30/04. Graduated College 5/13/04. 4XEP 6/7/04 - 8/13/04. Full open RPLND 10/13/04. All Clear since.

            Treated by Dr. Rakowski of Midland Park, NJ. Visited Sloan Kettering for protocol advice. RPLND done at Sloan Kettering.

            Comment


            • #7
              Thanks for the feedback. I have insurance that covers a good bit of the cost of the drugs, I just didn't want to be wasteful with them seeing how much it costs. I think after this feedback I'll go ahead and start using them.

              I think I just needed somebody to say that it was the right thing to do and I wasn't just being a big baby

              Randy

              Comment


              • #8
                Originally posted by Margaret
                Kytril may be what you are thinking of. It is very pricy, but works very well. Also, Emend is also very good and may be covered by your insurance. If you do not have coverage for meds, please ask the cancer center where you are being treated and they may be able to help you.

                Margaret,

                Yes thats the one I was thinking of.

                Thanks!

                Son Anthony DX 12/11/06
                L/O 12/20/06 Stage IIIA, 95% EC, 5% Yolk Sac
                4XEP 1/29-4/6/ 07
                AFP started increasing3 wks later
                Residual abdominal mass found on CT
                RPLND 6/8/07
                Cancer in pathology-
                80% mature teratoma, 20% Yolk Sac. --
                No adjuvent chemo and
                AFP normalised

                July 22, 2010 ---- 3 years all clear!

                Comment


                • #9
                  Big baby?? I could be sick just thinking of you not taking the zofran.
                  Son Jason diagnosed 4/30/04, stage III. Right I/O 4/30/04. Graduated College 5/13/04. 4XEP 6/7/04 - 8/13/04. Full open RPLND 10/13/04. All Clear since.

                  Treated by Dr. Rakowski of Midland Park, NJ. Visited Sloan Kettering for protocol advice. RPLND done at Sloan Kettering.

                  Comment


                  • #10
                    Big baby?? NEVER!! Just fighting cancer makes you a tough guy in my book. take all the meds they will give you....eat as often as you can and re-gain your strength. You are going to need it.

                    Let us know how we can help.
                    Co-survivor with husband Boyce, Diagnosed 7-11-06, orchiectomy right testicle on 7-12-06- Stage 3A: Mixed germ cell tumor with inguinal seminomatous and kartotypic carcinoma. One tumor over 10 cm, second tumor 4 cm, Chemo 4xBEP: Bi-lateral RPLND Dec 2006, nerve sparing but left sterile.
                    Current DVT
                    Current testosterone replacement therapy, Testim.

                    "You must abandon the life you planned, to live the life that was meant for you" ~wisdom I have learned from my family on this forum

                    Comment


                    • #11
                      Originally posted by randyn
                      Hi,

                      Does anybody have any advice about this? I really didn't expect radiation to be a big deal. From talking to my doctors and reading some online about it, everybody seemed to make radiation out to be a relatively easy process. I'm sure that compared to chemo it is much easier, but it's starting out worse than I expected. And it will probably get worse, right?

                      Randy
                      Hi,

                      I recently completed RT for stage Ia seminoma. From my research I was also under the impression that it wouldn't be a big deal- incorrectly.

                      My rad onc initially prescribed compazine (a cheap anti-nausea med) which didn't work. I had severe nausea and vomited multiple times after the treatments. My medical team was very nice and I got samples of Kytril (a very expensive anti-nausea med) for free. Kytril eliminated the vomiting and eased the nausea. I got enough samples for the entire treatment.

                      So, please ask your medical team for samples, I'm sure they have a few to spare. Also, don't take RT lightly. It's cumulative and the side effects will get worse. I felt incredibly tired, exhausted, and often queasy during the second half of my treatment. Take care of yourself.

                      Comment


                      • #12
                        It looks like your diagnoses and treatment run parallel with mine (Seminoma, Adj, RT therapy). I was given the anti-nausea drugs but thankfully other than feeling queasy a lot of the time, I never experienced any sickness. I have to preface this by saying I also did next to nothing while getting treated. I took 3 weeks off of work and other than play golf once or twice I basically just hung around the house and took it easy. RT affects everyone differently. Although I didn't get sick, I started getting fatigued almost from the very beginning. Never be concerned because you don't think you tolerate this as well as everyone/anyone else. I've personally talked with people that got sick right off the bat and others that tolerated it so well you wouldn't have even known they were getting radiation. When it comes to this treatment listen to your body and definitely speak up to your Rad Onc and let him know what's going on with your body so he can adjust meds. BTW - where do you live in PA?

                        TLH
                        tlh
                        diagnosed 28 June 06. Orchiectomy 29 June 06. Stage 1 Seminoma with no evidence of spread or Vasc invasion. Finished adjuvant RT (27Gy) to abdominal and pelvic area August 28th, 2006.

                        Comment


                        • #13
                          Thanks for your replies. They have been very helpful. I started taking the Zofran 1 hour before my treatments and it has been helping a great deal. I still don't have my regular appetite and sometimes feel a little queasy, but I'm eating and feeling better over all.

                          Thanks again for you comments. I wish I had found this board earlier.

                          Randy

                          Comment


                          • #14
                            Originally posted by tlh
                            BTW - where do you live in PA?
                            I'm from Lancaster

                            Randy

                            Comment


                            • #15
                              randyn -
                              sorry to hear you had a rough start to your treatment. i followed the same path and was able to tolerate the nausea, but as has been noted here already - everyone is different and you should listen to your body. take the meds if it helps and rest as much as possible as the fatigue will grow over the course of the treatments.

                              i know its hard to eat. but i did find that when i was feeling the most nausea it actually helped to eat a little something (SLOWLY) and maybe a 7-up or sprite to help settle the stomach. it helped me and not all foods will seem appealing for now, but getting something into your stomach does seem to help.

                              have no qualms about how you feel compared to what others felt or what you were told. everyone is different and the important thing is you listen to your body.
                              Diagnosed 5-5-05 (Stage 1 - Seminoma) / Oriechtomy 5-9-05 / Adjuvant Radiation July 2005

                              Comment

                              Working...
                              X