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Wish me luck on my first day!

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  • #16
    Hi Owen,

    Make sure you tell the Onco nurses about every side effect you're
    experiencing. This is no time to be a hero! They can add meds into
    your chemo line. And make sure you are drinking tons of fluids all day long. If you can't, tell the nurses and they'll probably give you more fluid before and after your chemo. And tell the nurses about your anxiety too.
    It may be having a physical effect on you. There are drugs for it.
    Don't be quiet about any of the side effects. And actually, it is a good
    time to eat anything that appeals to you. My son's Onc. told him he
    should be on a "See Food" diet--when you see food that looks good,
    eat it. Don't worry about losing weight now. You can do that when
    you're cured, and more aware of your health. Hang in there!

    Diane

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    • #17
      Owen, by Tuesday of your first week off you will be feeling much better....recuperate over the weekend and drink alot to flush your system...Chris took stool softeners for constipation.....make sure you tell the nurses...and hang in there...Mary Ellen

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      • #18
        I agree with Diane about telling the nurses about every side effect. Other than the fatigue, they managed to control all of the other side effects for my husband -- reflux, nausea, constipation and anxiety. I had to make a big chart to keep track of all the pills he was taking, but they definitely helped.

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        • #19
          Yep I remember this all too well, by Wed. of the chemo week my brother would start getting BLAH, nauseas, constipated, unable to eat and sometimes drink. DRINK DRINK DRINK, stay hydrated, that's what flushes your system. My brother would take and Atavan for anxioty in the am (2 at night for sleep) in with his chemo they would give him something for his nerves as well, it just made him sleep the whole time of treatment, which is a good thing toward the end. He had 2 different types of nauseas medicine. (The Atavan would help with that as well) he didn't take those as much as he should, he hated medicine all together, so he dealt with it instead, and his recovery would have been so much better if he'd just stay consistant with the meds. For constipation, he would take 2 stool softners ever night. By Wed. of the following week he would be getting better, and he would just continue getting better. As far as foods go, your the judge there, everything tasted like metal for my bro, so the nurses suggested him spicing things up a bit. But the most important is drinking you water, or whatever, flushing your system gets the junk out. Again, everyone is different, and will react different, but maybe some of this will help. Good luck. You'll be fine.
          Krista
          Brother Diag. 10/05 Non-Sem.
          Right I/O 11/05
          Surv
          4XBEP 8/06
          RPLND 12/06
          2X VIP 1/22/07
          Only completed 1 Rd.

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          • #20
            Thanks for all the kind words. . . Of course, we have a little over 5 feet of snow in the driveway now, so I missed chemo today. My Onc. Dr said as long as I get my 5 days in by Sunday I will be alright.

            I am downing lots of water (a habit my mother gave to me early in life, thank God), and was finally able to exacuate the bowels - what a relief that was, both physically as well as reduced stress.

            I hear it with the "see food" diet, but most of what sounds good ends up just making me sick

            I will ask for the anxiety medicine tomorrow, especially since hte clinic is closed so I am going to the cancer/chemo ward inside the hopsital itself. Guess it is not a pretty site, and a good thing I have been spoiled going to the outside clinic where everyone is cheery (not that they wont be, but I guess there are a lot of bad cases).

            Anyway, thanks again. . . just being able to reach out helps SOO much!

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            • #21
              Originally posted by Owen
              I hear it with the "see food" diet, but most of what sounds good ends up just making me sick
              You probably know that most people who have been through chemotherapy recommend that you stay away from your favorite foods during treatment, so you don't end up with bad associations later. Hang in there, Owen, you'll make it through.
              Scott
              right inguinal orchiectomy 6/5/2003 > nonseminoma, stage I > surveillance > L-RPLND 6/24/2005 for recurrence, suspected teratoma but found seminoma, stage II > chylous ascites until 9/2005 > surveillance and "all clear" since

              Your donation funds Livestrong services for people facing cancer now. Please sponsor my ride!

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              • #22
                Originally posted by Owen
                I will ask for the anxiety medicine tomorrow, especially since hte clinic is closed so I am going to the cancer/chemo ward inside the hopsital itself. Guess it is not a pretty site, and a good thing I have been spoiled going to the outside clinic where everyone is cheery (not that they wont be, but I guess there are a lot of bad cases).
                For me that was the worst part, being stuck in the chemo ward at the hospital for 5 days at a time. It was nice when they would unhook my IV for the night and I could go outside for an hour or two and get some exercise and fresh air... but other than that it was a horrible experience. Everyone around me (except the doctors and nurses of course) seemed like they were dying, it was a pretty scary thing to have to see every day.

                For your anxiety you might want to ask for Ativan, that's one of the anti-nausea meds they gave me, but it's also a pretty strong sedative and should calm you down. It helps a lot with the nausea because you don't have to swallow the pill and wait for it to kick in, you just put it under your tongue and let it dissolve.

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