MRF-Logo2019-Horizontal-RGB
Opdivo
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.

Opdivo

› Forums › General Melanoma Community › Opdivo

  • Post
    • July 22, 2015 at 1:02 am
    Mom2Addy
    Participant

      After SRS,surgical resection (twice) and four rounds of IPI, my husband begins Opdivo tomorrow.  Full body PET at 6:30 AM, labs at 12:00, see Doc at 12:30 for results, then treatment. Long day! Interested in hearing about side effects and any advice to keep them at bay. Our oncologist (top Melanoma guy in our area) said absolutely no steroids. Thank you and continued prayers for all. 

    Viewing 5 reply threads
    • Replies
        • July 22, 2015 at 1:33 pm
        Bubbles
        Participant

          Hope your day goes well and the scan, visit and infusion are not too difficult.  I took Nivo/Opdivo for 2 1/2 years…last dose in June of 2013…and remain NED.  Here is a post I put together re:  side effects and why we get them.  http://chaoticallypreciselifeloveandmelanoma.blogspot.com/2013/10/side-effects-of-nivolumab.html

          Not sure there are any tricks as to how to avoid them!  But, I will keep my fingers crossed for you and your husband.  Celeste

            • July 23, 2015 at 1:40 am
            Mom2Addy
            Participant

              Thank you Celeste! Very long day but so far so good. 

              • July 23, 2015 at 1:40 am
              Mom2Addy
              Participant

                Thank you Celeste! Very long day but so far so good. 

                • July 23, 2015 at 1:40 am
                Mom2Addy
                Participant

                  Thank you Celeste! Very long day but so far so good. 

                • July 22, 2015 at 1:33 pm
                Bubbles
                Participant

                  Hope your day goes well and the scan, visit and infusion are not too difficult.  I took Nivo/Opdivo for 2 1/2 years…last dose in June of 2013…and remain NED.  Here is a post I put together re:  side effects and why we get them.  http://chaoticallypreciselifeloveandmelanoma.blogspot.com/2013/10/side-effects-of-nivolumab.html

                  Not sure there are any tricks as to how to avoid them!  But, I will keep my fingers crossed for you and your husband.  Celeste

                  • July 22, 2015 at 1:33 pm
                  Bubbles
                  Participant

                    Hope your day goes well and the scan, visit and infusion are not too difficult.  I took Nivo/Opdivo for 2 1/2 years…last dose in June of 2013…and remain NED.  Here is a post I put together re:  side effects and why we get them.  http://chaoticallypreciselifeloveandmelanoma.blogspot.com/2013/10/side-effects-of-nivolumab.html

                    Not sure there are any tricks as to how to avoid them!  But, I will keep my fingers crossed for you and your husband.  Celeste

                    • July 23, 2015 at 8:09 am
                    stars
                    Participant

                      Good luck with the treatment, I hope it all goes well. Hope and prayers to you both.

                      • July 23, 2015 at 8:09 am
                      stars
                      Participant

                        Good luck with the treatment, I hope it all goes well. Hope and prayers to you both.

                        • July 23, 2015 at 8:09 am
                        stars
                        Participant

                          Good luck with the treatment, I hope it all goes well. Hope and prayers to you both.

                      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