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.

2nd Round Keytruda

Forums General Melanoma Community 2nd Round Keytruda

  • Post
    MelanomaMike
    Participant

    Hay folks! hope this finds you all well & kickin some Melanoma Glutious Maximus!.. as i stated a few days  ago, i sucked up my 2nd delishous bag of Pembro, and boy im feeling blah! like i told another family member here at MRF, I feel like i have the beginings of the Flu everyday! not full on mind you, like the "Pre" feeling. Low energy, just all round blah. Then my weird issue with my Tattoos which i told you about, that their "raised", "bumpy" like "Braille" for the blind! lol..Pembro is obviously doing its job if its attacking my tattoos right? they arnt suppose to be there!..ill see my Oncologist soon, i plan to talk about my tiredness, im thinkin its because of "where" my tumors are located, "Lungs"…anyways, just checkin with you, i really hope everyones tumors are shrinking and or disapearing! i look forward to my 1st scan to check my progress!..

Viewing 1 reply thread
  • Replies
      sister of patient
      Participant

      Hi Mike – Like many, I've been watching your posts (and Tex's – both of you are amazing fellas and so humourous!!) and so I just want to say that I'm keepig my fingers crossed for you too for that scan result!! Just a thought but maybe a low-dose steroid will help with your fatigue. My sister tried to wean off steroids earlier this year but experienced nivo fatigue almost immediately and onc thought it wasn't worth it and put her back up. It might help!! Wishing you the best always but again, hoping that scan report says it all and you are kicking serious butt!!!

      Barb

      Bubbles
      Participant

      Hang in there.  Did 2 1/2 years of opdivo – 2010 – 2013 after lung and brain mets.  The other white meat.  Fatigue is actually a "normal" condition when on immunotherapy….not something particularly related to "where" your tumors are located.  Here's a post I put together years ago:  http://chaoticallypreciselifeloveandmelanoma.blogspot.com/2013/10/side-effects-of-nivolumab.html  

      It is still worth talking to your doc about.  However, despite fatigue and other side effects, I worked full time, missing only three days of work, during my trial and remain NED with my last treatment being given in June of 2013.  Hang tough.  celeste

Viewing 1 reply thread
  • 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