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.

Update on Shane

Forums General Melanoma Community Update on Shane

  • Post
    Shaneswife
    Participant

      Looks like he's staying in dabrafenib and tramentinib for another month. Then scans mid May with results May 16th. If any progression moving to single agent prembro as we can get coverage for ipi/nivo combo funded either through our private insurance or provincial health care. The hospital is working on appeals with the insurance company but I do not think we will win. Blood and ekg monitoring until then. 

      Will be doing the pembro while on 8mg of dex. I understand there is a lot of controversy about steroid use while on immunotherapy but we are going to try it. 

       

      Immunotherapy is buying time but at what cost to quality of life? I can't answer that for Shane. I wish I could but I can't. 

       

      So so now we sit and wait again. But at least we're waiting together. 

       

       

      Janis

    Viewing 1 reply thread
    • Replies
        Shaneswife
        Participant

          That should of read can't get coverage for the doublet. 

          Maria C
          Participant

            Janis, thank you for sharing. My case is not as complicated as your husband's at the moment, but I too am on pembro and it's definitely stabilizing things for me. I will post my update soon, just catching up as I haven't been on the boards for awhile (which is a good thing). One thing is clear: Shane is blessed to have Shaneswife!

        Viewing 1 reply thread
        • 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.

        Popular Topics