The information on this site is not intended or implied to be a substitute for professional medical advice, diagnosis or treatment. Content within the patient forum is user-generated and has not been reviewed by medical professionals. Other sections of the Melanoma Research Foundation website include information that has been reviewed by medical professionals as appropriate. All medical decisions should be made in consultation with your doctor or other qualified medical professional.

Radiation After Effects

Forums General Melanoma Community Radiation After Effects

  • Post
    porrige
    Participant

    Hello Guys,

    My sister is just after finishing her two weeks of whole brain radiation and recovering at home, I am so worried about her as her husband has told me that she is completely exhausted has terrible headaches and no mind to talk to anyone and she is  so fatigued. The poor man is so worried about her, and we her family are so helpless to do anything as she lives in Australia and we live in Europe. Its heart breaking for us as we are so powerless to help them right now, and all we can do is send messages, hope and pray. If anyone here has had radiation for Mets to the Brain, can you tell me if these symptoms are from the radiation and if they are will she be like this for long, she is hoping to start a new drug treatment as soon as she settles. She has been through so much recently, with the seizures and exhaustion and missing everyone, I would love to be able to just find out some more so that I can share with her amazing husband who is solely nursing her at the moment.Thanking you all.

Viewing 8 reply threads
  • Replies
      arthurjedi007
      Participant

      I've had radiation to a tumor pressing on my brain and lots of other radiation so not quite the same thing. Radiation can knock you down sapping your strength. But for me by two weeks I have always gotten better. Nowhere near what I was before radiation but at least better. It sounds like something might not be going quite right. But again I haven't had that type of radiation so others here probably know better than me.

      Artie

      arthurjedi007
      Participant

      I've had radiation to a tumor pressing on my brain and lots of other radiation so not quite the same thing. Radiation can knock you down sapping your strength. But for me by two weeks I have always gotten better. Nowhere near what I was before radiation but at least better. It sounds like something might not be going quite right. But again I haven't had that type of radiation so others here probably know better than me.

      Artie

      arthurjedi007
      Participant

      I've had radiation to a tumor pressing on my brain and lots of other radiation so not quite the same thing. Radiation can knock you down sapping your strength. But for me by two weeks I have always gotten better. Nowhere near what I was before radiation but at least better. It sounds like something might not be going quite right. But again I haven't had that type of radiation so others here probably know better than me.

      Artie

      Patina
      Participant
      My Mom had gamma knife radiation for brain mets. 8 in Dec of 2013 and 17 in April of 2015. She was sore but back to normal in days.

      Her doctors never talked to us about whole brain. I am not sure why, but I saw a article about it not being as effective as gamma knife over the long term. Look at the posts I have replied to and you will find a link to a recent article I posted. Also, there was a small trial on patients who had gamma knife with and without canabinoids – found in marijanna. There seemed to be decent evidence that it had a very large benefit.

      Two things for you to look into.

      My Mom had gamma knife just before getting Yervoy. Simply amazing results.

      Good luck,ď

      Patina
      Participant
      My Mom had gamma knife radiation for brain mets. 8 in Dec of 2013 and 17 in April of 2015. She was sore but back to normal in days.

      Her doctors never talked to us about whole brain. I am not sure why, but I saw a article about it not being as effective as gamma knife over the long term. Look at the posts I have replied to and you will find a link to a recent article I posted. Also, there was a small trial on patients who had gamma knife with and without canabinoids – found in marijanna. There seemed to be decent evidence that it had a very large benefit.

      Two things for you to look into.

      My Mom had gamma knife just before getting Yervoy. Simply amazing results.

      Good luck,ď

      Patina
      Participant
      My Mom had gamma knife radiation for brain mets. 8 in Dec of 2013 and 17 in April of 2015. She was sore but back to normal in days.

      Her doctors never talked to us about whole brain. I am not sure why, but I saw a article about it not being as effective as gamma knife over the long term. Look at the posts I have replied to and you will find a link to a recent article I posted. Also, there was a small trial on patients who had gamma knife with and without canabinoids – found in marijanna. There seemed to be decent evidence that it had a very large benefit.

      Two things for you to look into.

      My Mom had gamma knife just before getting Yervoy. Simply amazing results.

      Good luck,ď

      ed williams
      Participant

      If you take a look at a post from jerryfromFauq dated 2/5/2015, it talks about a new trial in Australia run by Prof. Georgina Long of the MIA Poche Centre. It talks about access to Pd-1 drugs for people who have active brain mets. I hope this was of some help. ED

      ed williams
      Participant

      If you take a look at a post from jerryfromFauq dated 2/5/2015, it talks about a new trial in Australia run by Prof. Georgina Long of the MIA Poche Centre. It talks about access to Pd-1 drugs for people who have active brain mets. I hope this was of some help. ED

      ed williams
      Participant

      If you take a look at a post from jerryfromFauq dated 2/5/2015, it talks about a new trial in Australia run by Prof. Georgina Long of the MIA Poche Centre. It talks about access to Pd-1 drugs for people who have active brain mets. I hope this was of some help. ED

        porrige
        Participant

        Thank you all for responding, your replys are like gifts to me. I will look into all you have suggested, its just so

        lonely and frustrating for me at the moment, cause all I want to do is hold her close to me and smell her sisterly scent and tell her I love her so much and wish I could take all this pain from her. I am hopefull from what I have read that she is suffering from odema of the brain as a result of the radiation, which probably accounts for her headaches and low feelings, she has never not spoken to me since all this started five years ago, so it shows me how fatigued the poor lamb is, but I have still kept my messages going, even if she cannot talk to me or message me I told her I am with her in heart and spirit all the way. I know I will have to allow time, time for her to heal and be back to her ole self again, someone told me last night that we the family and friends of the patient get worried so much when we see how poorly our loved ones are doing, that we forget that what we are actually witnessing, is the treatment plan in action with all its side effects and such, and that once we allow this to take place we will see that its actually the treatment we are looking at and not the actual cancer. Love to you all you,      you amazing warriors

         

        porrige
        Participant

        Thank you all for responding, your replys are like gifts to me. I will look into all you have suggested, its just so

        lonely and frustrating for me at the moment, cause all I want to do is hold her close to me and smell her sisterly scent and tell her I love her so much and wish I could take all this pain from her. I am hopefull from what I have read that she is suffering from odema of the brain as a result of the radiation, which probably accounts for her headaches and low feelings, she has never not spoken to me since all this started five years ago, so it shows me how fatigued the poor lamb is, but I have still kept my messages going, even if she cannot talk to me or message me I told her I am with her in heart and spirit all the way. I know I will have to allow time, time for her to heal and be back to her ole self again, someone told me last night that we the family and friends of the patient get worried so much when we see how poorly our loved ones are doing, that we forget that what we are actually witnessing, is the treatment plan in action with all its side effects and such, and that once we allow this to take place we will see that its actually the treatment we are looking at and not the actual cancer. Love to you all you,      you amazing warriors

         

        porrige
        Participant

        Thank you all for responding, your replys are like gifts to me. I will look into all you have suggested, its just so

        lonely and frustrating for me at the moment, cause all I want to do is hold her close to me and smell her sisterly scent and tell her I love her so much and wish I could take all this pain from her. I am hopefull from what I have read that she is suffering from odema of the brain as a result of the radiation, which probably accounts for her headaches and low feelings, she has never not spoken to me since all this started five years ago, so it shows me how fatigued the poor lamb is, but I have still kept my messages going, even if she cannot talk to me or message me I told her I am with her in heart and spirit all the way. I know I will have to allow time, time for her to heal and be back to her ole self again, someone told me last night that we the family and friends of the patient get worried so much when we see how poorly our loved ones are doing, that we forget that what we are actually witnessing, is the treatment plan in action with all its side effects and such, and that once we allow this to take place we will see that its actually the treatment we are looking at and not the actual cancer. Love to you all you,      you amazing warriors

         

Viewing 8 reply threads
  • You must be logged in to reply to this topic.
About the MRF Patient Forum

The MRF Patient Forum is the oldest and largest online community of people affected by melanoma. It is designed to provide peer support and information to caregivers, patients, family and friends. There is no better place to discuss different parts of your journey with this cancer and find the friends and support resources to make that journey more bearable.

The information on the forum is open and accessible to everyone. To add a new topic or to post a reply, you must be a registered user. Please note that you will be able to post both topics and replies anonymously even though you are logged in. All posts must abide by MRF posting policies.