Pembro Round 8 Complete

Forums General Melanoma Community Pembro Round 8 Complete

  • Post
    TexMelanomex
    Participant

      Hey Warriors,

      I completed round 8 of Pembro yesterday and no noticeable side effects as of today. It seems to be getting smoother as I go, no problems with labs and in fact they have all remained within normal limits for the past 4 treatments. If it weren't for the surgery recovery I'd be good to go today!

      I hope all of you are fighting the good fight. As always, thanks for being there and for the support! 

      Tex

    Viewing 4 reply threads
    • Replies
        Bubbles
        Participant

          YAY!!!!!!!!!!!!!!!!!  c

          CancerSpouse
          Participant

            Power on, Tex! So glad to hear. ~ Carol

            aldrichdesigner
            Participant

              That is amazing Tex, congrats.

              If that isn't a nice response to treatment then I don't know what is. This stuff is kicking my ass but it's kicking the cancer's ass too so I'll try not to complain or feel too jealous. lol. But for real, congratulations, that is so cool. This is one amazing drug and it's so crazy how just like cancer you just don't know how it's going to effect someone. It's all just so unpredictable. Anyways, keep up the good fight as well and I hope it continues to go easy on you, the cancer is tough enough.

              Scooby123
              Participant

                Hi Tex, glad you coping well with treatment , I am on my 11 dose of keydruda apart from bowel issues slightly after treatment coping well. My thyroid went out but on meds for that and is normal now..

                may you continue doing and coping well.

                scooby❤️

                Nick C
                Participant

                  Tex,

                  I am happy to hear your goods news. Keep fighting brother!

                  Nick

              Viewing 4 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.