MRF-Logo2019-Horizontal-RGB
NED for 2 Years
REGISTER
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.

NED for 2 Years

› Forums › General Melanoma Community › NED for 2 Years

  • Post
    • December 18, 2021 at 7:53 am
    Steve33
    Participant
      Hi All,

      This board has been a tremendous provider of information. It’s also been a great source of hope based on the success stories of others.

      With that, I am delighted to share that I am now 2 years NED! My scan frequency has been reduced to 6 months.

      Originally stage 3B. Received adjuvant Opdivo and radiation after Parotidectomy.

      Steve

    Viewing 5 reply threads
    • Replies
        • December 18, 2021 at 5:53 pm
        Bubbles
        Participant
          YAY!!! Always good to hear! Enjoy. celeste
          • December 18, 2021 at 6:38 pm
          ThinkingPositive
          Participant
            Such good news! Bravo!! Also inspires hope I will ditto that too!
            • December 22, 2021 at 3:10 pm
            Baby_Girl
            Participant
              Great news! Congratulations!
              • January 3, 2022 at 6:44 pm
              sing123
              Participant
                Yay! This is wonderful news! Much congrats.
                • January 3, 2022 at 8:24 pm
                Christinad
                Participant
                  Congratulations
                  • January 13, 2022 at 11:14 am
                  Rocco
                  Participant
                    Really great news, congratulations!

                    -Rocco

                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