Discussion Board Forums General Discussion Internal radiation therapy

Viewing 8 posts - 16 through 23 (of 23 total)
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  • #71036
    pattimelt
    Participant

    Thanks for the info! I have been feeling really good the past 2 days. Waiting until I have my MRI before I will know what is next for treatment. So I will enjoy the feeling good days.

    #71035
    holly22a
    Member

    I had the radiation beads and could not eat anything at all for a week and little for the next week. Don’t remember the taste, though. I have heard of a metallic taste from a lot of folks with chemo. But yes, definitely liver pain after radiation. I assumed it was cells dying as I also had liver pain during chemo when the tumors were shrinking.

    #71034
    marions
    Moderator

    Pattymelt: I have learned that radiation therapy can cause change of taste that typically goes away once treatment is complete. Plenty of liquids, tart foods, such as oranges or lemons might help. And, good, old, lemon drops seem to do wonders for some. Others may share some of their helpful tips with us too.
    Hugs,
    Marion

    #71033
    lainy
    Participant

    Pattimelt, mmm mmm mmm, I do love P.melts! I am sure you have heard that one before. Sorry I have never heard of a tumor swelling before it shrinks from Radiation nor causing a funny taste. Please, someone correct me as I would like to know. I am also not so secure with an ONC not giving more time with a CC patient. Patti I would suggest having all your questions written down before you go. I am on 2 hard Meds for Colitis and even write down my side effects! When is your next appointment? Perhaps a call to change the time to a not as busy as a time? Best wishes!

    #71032
    gavin
    Moderator

    Hi Patti,

    Thanks for letting us know about your treatment and I hope that it is working very well. And please let us know how the MRI goes and everything will be crossed for your results! Taking one day at a time sounds like a plan to me, and that is what I used to do with my dad.

    Here are a few links about mouth pain that may be of use to you –

    http://www.mayoclinic.com/health/mouth-sores/CA00054

    http://www.cancerresearchuk.org/cancer-help/about-cancer/treatment/cancer-drugs/side-effects/your-mouth-and-cancer-drugs

    http://www.macmillan.org.uk/Cancerinformation/Livingwithandaftercancer/Symptomssideeffects/Mouthcare/Chemotherapy.aspx

    http://www.macmillan.org.uk/Cancerinformation/Livingwithandaftercancer/Symptomssideeffects/Mouthcare/Radiotherapy.aspx

    Hope some of these are useful to you and like Lainy mentions, have you spoken with your Onc about this?

    Best wishes to you,

    Gavin

    #71031
    pattimelt
    Participant

    I did ask about pain & taste in my mouth. He said the pain might be a good thing as the radiation may cause the tumor to swell before it shrinks! I haven’t had pain there for the past few days. He said the taste in my mouth is from the tumor. My appt. was at 3:00pm & we didn’t see him until 4:30 so didn’t have time to go further with the questions. I was somewhat frustrated. I need to be sure we have more time when we see him after my MRI results come in.

    #71030
    lainy
    Participant

    Dear Pattimelt, have you talked to your ONC about your pain and the taste in your mouth? Thankfully, you are not having a problem with your Insurance as that can sometimes be a big battle. Guess you will know more after your MRI next week and we will wait to hear your update. If you have not talked to your ONC about the pain, I think that would be a good idea. Hoping for a good report on the MRI.

    #8264
    pattimelt
    Participant

    Since I last wrote I have had 2 Sirtex internal radiation therapies. I had reaction to the contrast but that was treated during procedure & 2nd treatment took med prior to prevent reaction. I had the last treatment 4 weeks ago. I have been having nausea & some pain in area of liver. I also am having bad taste in my mouth. I will have an MRI next week to determine how effective the radiation was & what will be done next. Our HMO medicare supplement has been good for us so far but is frustrating to have to wait for all the authorizations. So far everything has been authorized for me to have my treatments etc. at UCIrvine Chao Comprehensive Cancer Center. I take one day at a time & have the best supportive friends & prayed for daily. God is the Great Physician & He knows best. I have peace that I am doing what I need to do.

Viewing 8 posts - 16 through 23 (of 23 total)
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