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.

amelanomajourney

Forum Replies Created

Viewing 2 reply threads
  • Replies
      amelanomajourney
      Participant

        Succinct accurate summary – thank you!

        amelanomajourney
        Participant

          Succinct accurate summary – thank you!

          amelanomajourney
          Participant

            Succinct accurate summary – thank you!

            amelanomajourney
            Participant

              At mimimum a chest xray and abdominal ultrasound for montoring is warrented every 3-6mo.  There is no evidence that the early melanoma mets are caught the better the outcomes (no evidence directly…).  Treatment has so many side effects – I don't think it is fair to base monitoring on your decision to accept treatment – is there another melanoma oncologist in the city you could be refered to for a second opinion?

              amelanomajourney
              Participant

                At mimimum a chest xray and abdominal ultrasound for montoring is warrented every 3-6mo.  There is no evidence that the early melanoma mets are caught the better the outcomes (no evidence directly…).  Treatment has so many side effects – I don't think it is fair to base monitoring on your decision to accept treatment – is there another melanoma oncologist in the city you could be refered to for a second opinion?

                amelanomajourney
                Participant

                  At mimimum a chest xray and abdominal ultrasound for montoring is warrented every 3-6mo.  There is no evidence that the early melanoma mets are caught the better the outcomes (no evidence directly…).  Treatment has so many side effects – I don't think it is fair to base monitoring on your decision to accept treatment – is there another melanoma oncologist in the city you could be refered to for a second opinion?

                  amelanomajourney
                  Participant

                    Hi Birdlo,

                    I know some centers in Germany are really good at following lymph nodes with ultrasounds, but if the technicians aren't trained and the radiologists don't know what they are looking for, or the technology isn't good enough at your center, it is not a good test to monitor at this point.  I'm sure we will get there in North America in 5-10 years, but it is a very new medical concept!  Make sure your center is specifically set up to follow micro-met non-palpable nodes for changes.

                    So many decisions, do not fret!  Make the best decisions for you in this moment and don't look back.  I was in your shoes 2 years ago, and thought I would never get to a time when I could think about anything but cancer.  One WLE and CLND and year of interferon later and I'm back to working and dancing and I am grateful for the decisions I made along the way.  Not for everyone, but I used the information I had!

                    Wishing you positive thoughts in this impossible time.

                     

                    amelanomajourney
                    Participant

                      Hi Birdlo,

                      I know some centers in Germany are really good at following lymph nodes with ultrasounds, but if the technicians aren't trained and the radiologists don't know what they are looking for, or the technology isn't good enough at your center, it is not a good test to monitor at this point.  I'm sure we will get there in North America in 5-10 years, but it is a very new medical concept!  Make sure your center is specifically set up to follow micro-met non-palpable nodes for changes.

                      So many decisions, do not fret!  Make the best decisions for you in this moment and don't look back.  I was in your shoes 2 years ago, and thought I would never get to a time when I could think about anything but cancer.  One WLE and CLND and year of interferon later and I'm back to working and dancing and I am grateful for the decisions I made along the way.  Not for everyone, but I used the information I had!

                      Wishing you positive thoughts in this impossible time.

                       

                      amelanomajourney
                      Participant

                        Hi Birdlo,

                        I know some centers in Germany are really good at following lymph nodes with ultrasounds, but if the technicians aren't trained and the radiologists don't know what they are looking for, or the technology isn't good enough at your center, it is not a good test to monitor at this point.  I'm sure we will get there in North America in 5-10 years, but it is a very new medical concept!  Make sure your center is specifically set up to follow micro-met non-palpable nodes for changes.

                        So many decisions, do not fret!  Make the best decisions for you in this moment and don't look back.  I was in your shoes 2 years ago, and thought I would never get to a time when I could think about anything but cancer.  One WLE and CLND and year of interferon later and I'm back to working and dancing and I am grateful for the decisions I made along the way.  Not for everyone, but I used the information I had!

                        Wishing you positive thoughts in this impossible time.

                         

                        amelanomajourney
                        Participant

                          It's a shame that interferon treatment is so polarized – I hate to see comments on this board that shame the decision to take it.

                          My oncologist applauded me for my decision to go on interferon despite all the criticism.  I bought myself time.  And I didn't "give up a year of my life".  I was sick, but I used the time to rest and reflect.

                          In the meantime there have been several new melanoma drugs that have come out and more results from trials.

                          It was the best shot I had for 3A and I don't regret it a moment.

                          amelanomajourney
                          Participant

                            It's a shame that interferon treatment is so polarized – I hate to see comments on this board that shame the decision to take it.

                            My oncologist applauded me for my decision to go on interferon despite all the criticism.  I bought myself time.  And I didn't "give up a year of my life".  I was sick, but I used the time to rest and reflect.

                            In the meantime there have been several new melanoma drugs that have come out and more results from trials.

                            It was the best shot I had for 3A and I don't regret it a moment.

                            amelanomajourney
                            Participant

                              It's a shame that interferon treatment is so polarized – I hate to see comments on this board that shame the decision to take it.

                              My oncologist applauded me for my decision to go on interferon despite all the criticism.  I bought myself time.  And I didn't "give up a year of my life".  I was sick, but I used the time to rest and reflect.

                              In the meantime there have been several new melanoma drugs that have come out and more results from trials.

                              It was the best shot I had for 3A and I don't regret it a moment.

                              amelanomajourney
                              Participant

                                Great post about the experience.  I agree that while it is challenging, it is possible.  And for stage 3ers it is still a viable option.

                                amelanomajourney
                                Participant

                                  Great post about the experience.  I agree that while it is challenging, it is possible.  And for stage 3ers it is still a viable option.

                                  amelanomajourney
                                  Participant

                                    Great post about the experience.  I agree that while it is challenging, it is possible.  And for stage 3ers it is still a viable option.

                                Viewing 2 reply threads