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.

responding to BRAIN METS!! :)

Forums General Melanoma Community responding to BRAIN METS!! :)

  • Post
    csellers23
    Participant
    So 6 weeks ago my husband’s scans came in. And after taf/Mel combo. Yearvoy whole brain radiation and srs the results where horrible!!!! To many brain Mets to count, cancer growing everywhere! The put him on keytruda. When we went back 3 weeks later his LDH levels went from 800 to 300. They had planned on sending us home on hospices. But the gave us the 2nd round of keytruda. Today we went back and the doc said keytruda is working in his brain. I ask him how he knows and he said because he’s alive. If it wasn’t working in his brain he would have died 2 weeks ago! He also said keytruda does not work one or two months like some drugs can but that now we are looking at YEARS! We went in the matter of 6 weeks from you have 3 weeks to live to years. This keytruda was our last hope. And thank God it’s working!!!! People ask a lot if keytruda can cross the blood brain barrier, yes it can!!!! The doc ended out appointment saying you are no longer dying!!!! Best words ever. NEVER GIVE UP HOPE!!!!! The doc is even amazed Thank God!!!
Viewing 29 reply threads
  • Replies
      Mat
      Participant

      Crystale, so glad to hear your news.  I recently started Keytruda and am also feeling like the options are limited if it doesn't work.  It's nice to hear a good story.  Best of luck to you and your husband.

        Brendan
        Participant

        Great news, Crystale.  Congrats to your and your husband!  Enjoy.

        Brendan

        Brendan
        Participant

        Great news, Crystale.  Congrats to your and your husband!  Enjoy.

        Brendan

        Brendan
        Participant

        Great news, Crystale.  Congrats to your and your husband!  Enjoy.

        Brendan

        Brendan
        Participant

        Great news, Crystale.  Congrats to your and your husband!  Enjoy.

        Brendan

        Brendan
        Participant

        Great news, Crystale.  Congrats to your and your husband!  Enjoy.

        Brendan

        Brendan
        Participant

        Great news, Crystale.  Congrats to your and your husband!  Enjoy.

        Brendan

        Eileensulliv
        Participant

        What a wonderful post! Great news!

        Eileensulliv
        Participant

        What a wonderful post! Great news!

        Eileensulliv
        Participant

        What a wonderful post! Great news!

      Mat
      Participant

      Crystale, so glad to hear your news.  I recently started Keytruda and am also feeling like the options are limited if it doesn't work.  It's nice to hear a good story.  Best of luck to you and your husband.

      Mat
      Participant

      Crystale, so glad to hear your news.  I recently started Keytruda and am also feeling like the options are limited if it doesn't work.  It's nice to hear a good story.  Best of luck to you and your husband.

      ed williams
      Participant

      So happy for you and your husband!!!! Ed

      ed williams
      Participant

      So happy for you and your husband!!!! Ed

      ed williams
      Participant

      So happy for you and your husband!!!! Ed

      jbronicki
      Participant

      That is wonderful news for your husband, you and your family.  I'm hoping for many years for you all to be together!  

      jbronicki
      Participant

      That is wonderful news for your husband, you and your family.  I'm hoping for many years for you all to be together!  

      jbronicki
      Participant

      That is wonderful news for your husband, you and your family.  I'm hoping for many years for you all to be together!  

      LuckyMan51
      Participant

      This is awesome!!!    As soon as I clear up my 2/11/15 post surgical brain infection I am going in for another SRS and then start Anti Pd-1 treatment.   Was a bit anxious having to delay treatment while this infection clears but can't start anti pd-1 with infection as it might cause a flare up. Posts like this are so great to hear and really give one the strength to keep moving forward! Congratulations on this amazing news!   

      LuckyMan51
      Participant

      This is awesome!!!    As soon as I clear up my 2/11/15 post surgical brain infection I am going in for another SRS and then start Anti Pd-1 treatment.   Was a bit anxious having to delay treatment while this infection clears but can't start anti pd-1 with infection as it might cause a flare up. Posts like this are so great to hear and really give one the strength to keep moving forward! Congratulations on this amazing news!   

      LuckyMan51
      Participant

      This is awesome!!!    As soon as I clear up my 2/11/15 post surgical brain infection I am going in for another SRS and then start Anti Pd-1 treatment.   Was a bit anxious having to delay treatment while this infection clears but can't start anti pd-1 with infection as it might cause a flare up. Posts like this are so great to hear and really give one the strength to keep moving forward! Congratulations on this amazing news!   

      _Paul_
      Participant

      What fantastic news Crystale! Thanks for sharing it.

      _Paul_
      Participant

      What fantastic news Crystale! Thanks for sharing it.

      _Paul_
      Participant

      What fantastic news Crystale! Thanks for sharing it.

      JoshF
      Participant

      Yes!Yes!Yes! Great to hear!

      JoshF
      Participant

      Yes!Yes!Yes! Great to hear!

      JoshF
      Participant

      Yes!Yes!Yes! Great to hear!

      rosa1
      Participant

      Great news Crystale! This gives hope to all of us especially the ones fighting brain mets. I wish you and your husband the best!

      rosa1
      Participant

      Great news Crystale! This gives hope to all of us especially the ones fighting brain mets. I wish you and your husband the best!

      rosa1
      Participant

      Great news Crystale! This gives hope to all of us especially the ones fighting brain mets. I wish you and your husband the best!

      arthurjedi007
      Participant

      Oh my God. Thank you for posting. It warms my heart. I've had 15 doses of keytruda and hoping for a miracle in my third scan with it. Wow. That is an amazing story. I am so happy.

      Artie

      arthurjedi007
      Participant

      Oh my God. Thank you for posting. It warms my heart. I've had 15 doses of keytruda and hoping for a miracle in my third scan with it. Wow. That is an amazing story. I am so happy.

      Artie

      arthurjedi007
      Participant

      Oh my God. Thank you for posting. It warms my heart. I've had 15 doses of keytruda and hoping for a miracle in my third scan with it. Wow. That is an amazing story. I am so happy.

      Artie

      SABKLYN
      Participant

      Terrific!

      SABKLYN
      Participant

      Terrific!

      SABKLYN
      Participant

      Terrific!

      kpcollins31
      Participant

      Awesome… so encouraging to hear the progress being made over just the past couple years with these new treatments. Congratulations!

      Kevin

       

      kpcollins31
      Participant

      Awesome… so encouraging to hear the progress being made over just the past couple years with these new treatments. Congratulations!

      Kevin

       

      kpcollins31
      Participant

      Awesome… so encouraging to hear the progress being made over just the past couple years with these new treatments. Congratulations!

      Kevin

       

Viewing 29 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.