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.

On the glide path now!

Forums General Melanoma Community On the glide path now!

  • Post
    TexMelanomex
    Participant

      Hey Warriors,

      I completed round 20 of Pembro this week and by my calculations I have about 15 rounds remaining. I have to say that despite the joint pain, this most recent dose was one of the easiest, not much fatigue at all. Something curious and I'm wondering if anyone else experiences this,  it seems like its every other round that really wipes me out with fatigue and not feeling well for a few days. I havent quite figured out why yet and maybe its a number of variable like how well I'm rested, my diet, etc. Who's to say?

      I hope this finds you all waging war on the enemy without mercy.

      Warrior On!

       

    Viewing 2 reply threads
    • Replies
        Hukill
        Participant

          Keep fighting.

          lkb
          Participant

            Rest seems to be key for me–less on the calendar, reduced work load. Also, eating smaller meals and less food in general (easy when tongue tastes like muddy penny). These all decrease the occurrences of wipe-out for me. Good luck, Tex!

            Nick C
            Participant

              Tex…

              Great to hear the Pembro is still working for you. Hopefully, we will all find the right combination to attack this sleazeball of a disease. kepp on trucking!

              Nick

               

          Viewing 2 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