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.

BRR

Forum Replies Created

Viewing 0 reply threads
  • Replies
      BRR
      Participant
        Also, has pain in the left lung, with tingling sensations.
        BRR
        Participant
          Thanks a lot Mark. I wish you good health too.
          All this is difficult for patients, but just as difficult for their families.
          I just wanted the metastases to be stable. The reduction comes as a bonus!
          I still can’t believe it, nor can I relax. The cough is getting better. Tomorrow the father will receive Nivo number 5.
          BRR
          Participant
            Thanks a lot!!
            And I wish you and your father good health! 🙂
            BRR
            Participant
              Dear Melanie,

              Thanks a lot for these words. It means a lot to me.
              Dad just got a scan results and all the tumors in his lungs are shrinkinggg! I can’t believe!! Thanks immunotherapy, tkank you!

              Ana

              Ana

              BRR
              Participant
                Thank you very much.

                Ana

                BRR
                Participant
                  It means a lot of experience and advice to all of you. My dad has lung pain I don’t know if due to VAT surgery or metastases.He is very skinny and avoids eating everything I said.I’m afraid they’ll lose more weight from immunotherapy.
                  I know they will listen to me if I say I talked to you.
                  So thank you very much everyone!!!
                  BRR
                  Participant
                    It means a lot of experience and advice to all of you. My dad has lung pain I don’t know if due to VAT surgery or metastases.He is very skinny and avoids eating everything I said.I’m afraid they’ll lose more weight from immunotherapy.
                    I know they will listen to me if I say I talked to you.
                    So thank you very much everyone!!!
                    BRR
                    Participant
                      sorry for double posts
                      BRR
                      Participant
                        Im sorry to hear about your side effects but I am also glad it is nothing serious. So you think there is no need to cut out meat and wine completely?

                        My father has literaly gone vegan because he thinks it will worsen his state. I, on the other hand, think that because of the terapy he needs to have a variety in his diet.

                        I wish you all my best.
                        Ana

                        BRR
                        Participant
                          Im sorry to hear about your side effects but I am also glad it is nothing serious. So you think there is no need to cut out meat and wine completely?

                          My father has literaly gone vegan because he thinks it will worsen his state. I, on the other hand, think that because of the terapy he needs to have a variety in his diet.

                          I wish you all my best.
                          Ana

                          BRR
                          Participant
                            Hello 🙂
                            I’m glad you’re fine now!
                            Thank you.
                            I hope my father is in the lucky group. So far not.
                            it was especially difficult VAT surgery.
                            BRR
                            Participant
                              Dear Anne-Louise,
                              Thank you very much. I hope we avoid the worst.I’m glad you got through it all and you’re fine now.
                              I pray for everyone.
                              BRR
                              Participant
                                HVALA VAM MNOGO.
                                Bas ste mi pomogli. Nadam se da ce Opdivo biti dovoljan jer su manji nezeljeni efekti od kombinacije sa drugim lekom.
                                Ovde se izgleda ostaje noc u bolnici kada se prima infuzija sto me plasi zbog situacije sa virusom.
                                Nadam se da ste Vi dobro.
                                Pozdrav iz Bg i za vas i za cerku i svako dobro vam zelim.
                                BRR
                                Participant
                                  Celeste, thank you very much.
                                  I feel so loonely because in my small country no one has survived this disease. I read the positive outcomes only on this forum. I am afraid of a lot of negative effects of therapy, but I am most afraid of melanoma.

                                  I hope that opdivo therapy will have an effect on my father’s metastases in left lung.
                                  Best wishes to all

                                  BRR
                                  Participant
                                    Dear Mark,

                                    THANK YOU.
                                    I do a search here (I read posts every day for 3 years :)), but did not find finally whether received for 2 weeks or 4 weeks.
                                    In my country ( Serbia) there are not many treatment options. I am happy that he received immunotherapy at all.
                                    5 metastases in lung – very scary and bad + risk of covid.
                                    All the best to everyone here!

                                    Ana

                                Viewing 0 reply threads
                                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