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.

Recently diagnosed with Stage IV mucosal melanoma

Forums Mucosal Melanoma Community Recently diagnosed with Stage IV mucosal melanoma

  • Post
    Rawlins Mom
    Participant

      Several week lurker, first time poster

      My mother was diagnosed with mucosal melanoma (lady parts…not fun!) at the end of May.  She had surgery to remove the main lesion, and the PET scan showed several mets to the liver, lymph nodes, and one to the brain.  She had specific radiation on the brain tumor (not sure the exact procedure), finishes her daily targeted radiation today (4 weeks total I believe), and started on Keytruda 2 weeks ago.  Side effects so far are actually OK.  Some fatigue, and an imodium here and there, but overall OK.  

      I really appreciate all the posts here, both the uplifting ones and not so much also.  Puts things into perspective, and now I know that there are many options down the line.  

       

    Viewing 5 reply threads
    • Replies
        CHD
        Participant

          Mine was vulvar melanoma, though it was stage I-II, and have had 3 vulvar surgeries since 2013.  I have to say nothing about vulvectomy is fun, but in my case it seems to have gotten rid of the melanoma and that's the important thing.  I am glad your mom is doing well with few side effects from the keytruda.  Here's hoping the keytruda works wonders for her!   

          Cheri

          CHD
          Participant

            Mine was vulvar melanoma, though it was stage I-II, and have had 3 vulvar surgeries since 2013.  I have to say nothing about vulvectomy is fun, but in my case it seems to have gotten rid of the melanoma and that's the important thing.  I am glad your mom is doing well with few side effects from the keytruda.  Here's hoping the keytruda works wonders for her!   

            Cheri

            CHD
            Participant

              Mine was vulvar melanoma, though it was stage I-II, and have had 3 vulvar surgeries since 2013.  I have to say nothing about vulvectomy is fun, but in my case it seems to have gotten rid of the melanoma and that's the important thing.  I am glad your mom is doing well with few side effects from the keytruda.  Here's hoping the keytruda works wonders for her!   

              Cheri

              dfeng
              Participant

                Best wishes!

                  tschmith
                  Participant

                    I hope the Keytruda works.  I had good results with it.

                    All my best to her!

                    Terrie

                    tschmith
                    Participant

                      I hope the Keytruda works.  I had good results with it.

                      All my best to her!

                      Terrie

                      tschmith
                      Participant

                        I hope the Keytruda works.  I had good results with it.

                        All my best to her!

                        Terrie

                      dfeng
                      Participant

                        Best wishes!

                        dfeng
                        Participant

                          Best wishes!

                      Viewing 5 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.

                      Popular Topics