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.

3 years, 10 months and 2 days..

Forums General Melanoma Community 3 years, 10 months and 2 days..

  • Post
    Becky
    Participant

      But who  is counting ( I am!)

      My son was diagnosed in July 09 just beofre his 21st birthday, oral melanoma (toungue) one postive node, year of interferon, a few scares a long the way.

      Pet scan yesterday, NED! I have been extra nervous becuase his oncologist decided scans once a year were fine ( he is not a melanoma specialist) so it has been a year since his last one. Plus, next week he is moving to NYC because he got accepted to a fellowship that will keep him there (teaching math) for 5 years..sad he will be 3000 miles away but excited for him.

      But who  is counting ( I am!)

      My son was diagnosed in July 09 just beofre his 21st birthday, oral melanoma (toungue) one postive node, year of interferon, a few scares a long the way.

      Pet scan yesterday, NED! I have been extra nervous becuase his oncologist decided scans once a year were fine ( he is not a melanoma specialist) so it has been a year since his last one. Plus, next week he is moving to NYC because he got accepted to a fellowship that will keep him there (teaching math) for 5 years..sad he will be 3000 miles away but excited for him.

      I really want to thank all of you who gave me support directly or indirectly..I dont post often but I read daily

      Keep fighting

      Becky

    Viewing 5 reply threads
    • Replies
        Phil S
        Participant
          Becky, That is fantastic news, so very happy for your son and for your whole family. I always remembered his story, because my husband also has mucosal melanoma and did the year of interferon. So exciting your son is doing so well, living his life, starting a new job, and moving for another adventure. Melanoma hasn’t stopped his dreams one bit, good for him!! Please keep posting his good news and updates. All the best to you, Valerie (Phil’s wife)
          Phil S
          Participant
            Becky, That is fantastic news, so very happy for your son and for your whole family. I always remembered his story, because my husband also has mucosal melanoma and did the year of interferon. So exciting your son is doing so well, living his life, starting a new job, and moving for another adventure. Melanoma hasn’t stopped his dreams one bit, good for him!! Please keep posting his good news and updates. All the best to you, Valerie (Phil’s wife)
            Phil S
            Participant
              Becky, That is fantastic news, so very happy for your son and for your whole family. I always remembered his story, because my husband also has mucosal melanoma and did the year of interferon. So exciting your son is doing so well, living his life, starting a new job, and moving for another adventure. Melanoma hasn’t stopped his dreams one bit, good for him!! Please keep posting his good news and updates. All the best to you, Valerie (Phil’s wife)
              Brendan
              Participant

                Great news, Becky.  Thanks for sharing.  Good luck to your son as he makes the exciting 3000 mile move.

                Brendan

                Brendan
                Participant

                  Great news, Becky.  Thanks for sharing.  Good luck to your son as he makes the exciting 3000 mile move.

                  Brendan

                  Brendan
                  Participant

                    Great news, Becky.  Thanks for sharing.  Good luck to your son as he makes the exciting 3000 mile move.

                    Brendan

                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