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New member and wife of melanoma paitent

Forums General Melanoma Community New member and wife of melanoma paitent

  • Post
    ota2lst@yahoo.com
    Participant

    Hi.  My name is Linda.  My husband, Ben was diagnosed with stage 4 melanoma this past January after coughing up blood.  He had melanoma on the back of his head 23 years ago which was successfully removed with lots of tissue, followed up quarterly for 20  years and every six months for the past three.  Just following up with a derm. was not sufficient apparently.  Attempted clinical trial at UPMC (Pittsburgh) and was disqualified due to bloodwork not where it needed to be.  Our onc. started him on nivolumab and after six treatments had PET scan that showed mets in his bones in many places in addition to the tumor in his lungs and lynph nodes.  Afraid to continue with the nivo. as in a couple more months he could be too weak for other treatments or worse, so starting on Taf/Mek as soon as they get here in the mail.   He has been pretty sick from the nivolumab.  We are hoping that the drug combo will buy him a year to 18 months and by that time some new "miracle" drug will be out there.  Found this board and thought I'd like to talk to others who are dealing with this horrible disease that has totally taken over our lives.  We have hope though, and want to continue to be positive.  Will welcome comments, etc . . . 

Viewing 8 reply threads
  • Replies
      jade1111
      Participant

      So Sorry Linda about your husband's diagnosis. I have found this board very helpful. My mom was just diagnosed with stage 4 a few months ago.I have found the input here very insightful. What I have learned in past few months is to really ask around and get second opinions. Its been a slow process figuring it all out. Hope  the combo works well. Apparently the combos have a higher success rate.

      Wishing you both all the best!!! 

      Peace and Healing!

        ota2lst@yahoo.com
        Participant

        Thanks and I hope your mom is doing ok.  I know that I need the support of others who are going through this.  Just taking things one day at a time.

        ota2lst@yahoo.com
        Participant

        Thanks and I hope your mom is doing ok.  I know that I need the support of others who are going through this.  Just taking things one day at a time.

        ota2lst@yahoo.com
        Participant

        Thanks and I hope your mom is doing ok.  I know that I need the support of others who are going through this.  Just taking things one day at a time.

      jade1111
      Participant

      So Sorry Linda about your husband's diagnosis. I have found this board very helpful. My mom was just diagnosed with stage 4 a few months ago.I have found the input here very insightful. What I have learned in past few months is to really ask around and get second opinions. Its been a slow process figuring it all out. Hope  the combo works well. Apparently the combos have a higher success rate.

      Wishing you both all the best!!! 

      Peace and Healing!

      jade1111
      Participant

      So Sorry Linda about your husband's diagnosis. I have found this board very helpful. My mom was just diagnosed with stage 4 a few months ago.I have found the input here very insightful. What I have learned in past few months is to really ask around and get second opinions. Its been a slow process figuring it all out. Hope  the combo works well. Apparently the combos have a higher success rate.

      Wishing you both all the best!!! 

      Peace and Healing!

      Mamapegela
      Participant

      Hi Linda-

      I really don't have any information to offer you as I am pretty new to this forum myself.  Just know that you are not alone and that there are many other people walking on the same path with you.  Good for you for reaching out.  There are a lot of very informed, intelligent and caring people who regularly check in here and I'm sure will have great insight for you. 

      I'll be keeping you and your husband in my thoughts and prayers.

       

      Mamapegela
      Participant

      Hi Linda-

      I really don't have any information to offer you as I am pretty new to this forum myself.  Just know that you are not alone and that there are many other people walking on the same path with you.  Good for you for reaching out.  There are a lot of very informed, intelligent and caring people who regularly check in here and I'm sure will have great insight for you. 

      I'll be keeping you and your husband in my thoughts and prayers.

       

        ota2lst@yahoo.com
        Participant

        Thanks Peggy.  It is just nice to know that I am not alone in this.  I feel so helpless so much of the time.  This website is great.

        ota2lst@yahoo.com
        Participant

        Thanks Peggy.  It is just nice to know that I am not alone in this.  I feel so helpless so much of the time.  This website is great.

        ota2lst@yahoo.com
        Participant

        Thanks Peggy.  It is just nice to know that I am not alone in this.  I feel so helpless so much of the time.  This website is great.

      Mamapegela
      Participant

      Hi Linda-

      I really don't have any information to offer you as I am pretty new to this forum myself.  Just know that you are not alone and that there are many other people walking on the same path with you.  Good for you for reaching out.  There are a lot of very informed, intelligent and caring people who regularly check in here and I'm sure will have great insight for you. 

      I'll be keeping you and your husband in my thoughts and prayers.

       

      MoiraM
      Participant

      Hopefully the Taf/Met will shirnk the tumours, or at least stop them growing.

      Have you discussed Ipi(Yervoy) with your doctor? Maybe that might be a possibility?

      MoiraM
      Participant

      Hopefully the Taf/Met will shirnk the tumours, or at least stop them growing.

      Have you discussed Ipi(Yervoy) with your doctor? Maybe that might be a possibility?

        Maureen038
        Participant

        Linda,

           My husband has been stage four for three and a half years. I love your attitude of of trying the combo and then eventually some new drug will come out. My husband has always felt that way too. It's good you're reaching out to people. Make sure you have a strong support system where you live too. It's truly a roller coaster ride of emotions, but it does give you keen insight on what's truly important in life. Wishing you and your husband the best!!

        Maureen

         

          

        Maureen038
        Participant

        Linda,

           My husband has been stage four for three and a half years. I love your attitude of of trying the combo and then eventually some new drug will come out. My husband has always felt that way too. It's good you're reaching out to people. Make sure you have a strong support system where you live too. It's truly a roller coaster ride of emotions, but it does give you keen insight on what's truly important in life. Wishing you and your husband the best!!

        Maureen

         

          

        Maureen038
        Participant

        Linda,

           My husband has been stage four for three and a half years. I love your attitude of of trying the combo and then eventually some new drug will come out. My husband has always felt that way too. It's good you're reaching out to people. Make sure you have a strong support system where you live too. It's truly a roller coaster ride of emotions, but it does give you keen insight on what's truly important in life. Wishing you and your husband the best!!

        Maureen

         

          

      MoiraM
      Participant

      Hopefully the Taf/Met will shirnk the tumours, or at least stop them growing.

      Have you discussed Ipi(Yervoy) with your doctor? Maybe that might be a possibility?

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