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.

sedona

Forum Replies Created

Viewing 2 reply threads
  • Replies
      sedona
      Participant

        This doctor is only an osteopath not an M.D., not an oncologist that specializes in melanoma. I don't think osteopaths know much about cancer to begin with and they take an alternative or holistic approach to medicine

        sedona
        Participant

          This doctor is only an osteopath not an M.D., not an oncologist that specializes in melanoma. I don't think osteopaths know much about cancer to begin with and they take an alternative or holistic approach to medicine

          sedona
          Participant

            This doctor is only an osteopath not an M.D., not an oncologist that specializes in melanoma. I don't think osteopaths know much about cancer to begin with and they take an alternative or holistic approach to medicine

            sedona
            Participant

              Hi speckles,

              When I first had my surgery the surgical oncologist told me I should come back to see him every six months for the first 3 years. He also said that he would be ordering  chest xray and blood work for LDL at those follow ups. Well, I did go once that first year but he didn't order any of those tests like he said he would so my Internal doc did. I have been seeing my internal medicine doc for almost 20 years and he worries more about me than I do myself . He has wanted me to get a pet scan for over a year now, but normally they never do a pet scan for our stage.

              I read somewhere on the internet that in the past few years they even stopped doing the chest xray and blood test and do no follow up at all unless their are clinical signs of recurrance.

              Try to just go on with your life and act like it never happened. Worrying about it never helps and can evn make things worse (stress is very bad for you), think positive thoughts and enjoy yourself. 

              sedona- also stage IIa just over 3 years now

              sedona
              Participant

                Hi speckles,

                When I first had my surgery the surgical oncologist told me I should come back to see him every six months for the first 3 years. He also said that he would be ordering  chest xray and blood work for LDL at those follow ups. Well, I did go once that first year but he didn't order any of those tests like he said he would so my Internal doc did. I have been seeing my internal medicine doc for almost 20 years and he worries more about me than I do myself . He has wanted me to get a pet scan for over a year now, but normally they never do a pet scan for our stage.

                I read somewhere on the internet that in the past few years they even stopped doing the chest xray and blood test and do no follow up at all unless their are clinical signs of recurrance.

                Try to just go on with your life and act like it never happened. Worrying about it never helps and can evn make things worse (stress is very bad for you), think positive thoughts and enjoy yourself. 

                sedona- also stage IIa just over 3 years now

                sedona
                Participant

                  Hi speckles,

                  When I first had my surgery the surgical oncologist told me I should come back to see him every six months for the first 3 years. He also said that he would be ordering  chest xray and blood work for LDL at those follow ups. Well, I did go once that first year but he didn't order any of those tests like he said he would so my Internal doc did. I have been seeing my internal medicine doc for almost 20 years and he worries more about me than I do myself . He has wanted me to get a pet scan for over a year now, but normally they never do a pet scan for our stage.

                  I read somewhere on the internet that in the past few years they even stopped doing the chest xray and blood test and do no follow up at all unless their are clinical signs of recurrance.

                  Try to just go on with your life and act like it never happened. Worrying about it never helps and can evn make things worse (stress is very bad for you), think positive thoughts and enjoy yourself. 

                  sedona- also stage IIa just over 3 years now

                  sedona
                  Participant

                    I would like to also add that while I had 37 moles removed I must have at least another 60 and none even look suspicious. Also the melanoma oncology specialist / sugeon told me what the dermatologists were doing was not necessary, only moderate to severly atypical moles need to be removed, not the mildly atypical moles the derms were having a field day removing. They also say that on the intenet in many sites.

                    So I am sorry if I somehow offended you and I am deeply sorry for your advanced stage as well as all of the other people on this site with a stage 3 and 4, but I think we all have different circumstances, are at different levels of risk and are prescribed different treatments.

                    sedona
                    Participant

                      I would like to also add that while I had 37 moles removed I must have at least another 60 and none even look suspicious. Also the melanoma oncology specialist / sugeon told me what the dermatologists were doing was not necessary, only moderate to severly atypical moles need to be removed, not the mildly atypical moles the derms were having a field day removing. They also say that on the intenet in many sites.

                      So I am sorry if I somehow offended you and I am deeply sorry for your advanced stage as well as all of the other people on this site with a stage 3 and 4, but I think we all have different circumstances, are at different levels of risk and are prescribed different treatments.

                      sedona
                      Participant

                        I would like to also add that while I had 37 moles removed I must have at least another 60 and none even look suspicious. Also the melanoma oncology specialist / sugeon told me what the dermatologists were doing was not necessary, only moderate to severly atypical moles need to be removed, not the mildly atypical moles the derms were having a field day removing. They also say that on the intenet in many sites.

                        So I am sorry if I somehow offended you and I am deeply sorry for your advanced stage as well as all of the other people on this site with a stage 3 and 4, but I think we all have different circumstances, are at different levels of risk and are prescribed different treatments.

                        sedona
                        Participant

                          "so while it might be an inconvienient thing to cut off your moles…it's better than ending up at stage 4. Most people with stage 4 were told they have 6-9 months to live…looking back I would have gone every week if they had asked me rather than go thru what I have. The radiation and chemo, the major surgeries…melanoma usually comes back and it also is the most deadilest form of skin cancer."

                          ?? But from what I have read here on the board and on the internet it doesn't usually come back. The oncologist said I am cured.  Now I don't know what to believe.

                          I asked in my first post "do I have cancer" and no one answered yes or no.

                          What am I to believe now?

                          Why does no one seem to talk to new people here?

                          sedona
                          Participant

                            "so while it might be an inconvienient thing to cut off your moles…it's better than ending up at stage 4. Most people with stage 4 were told they have 6-9 months to live…looking back I would have gone every week if they had asked me rather than go thru what I have. The radiation and chemo, the major surgeries…melanoma usually comes back and it also is the most deadilest form of skin cancer."

                            ?? But from what I have read here on the board and on the internet it doesn't usually come back. The oncologist said I am cured.  Now I don't know what to believe.

                            I asked in my first post "do I have cancer" and no one answered yes or no.

                            What am I to believe now?

                            Why does no one seem to talk to new people here?

                            sedona
                            Participant

                              "so while it might be an inconvienient thing to cut off your moles…it's better than ending up at stage 4. Most people with stage 4 were told they have 6-9 months to live…looking back I would have gone every week if they had asked me rather than go thru what I have. The radiation and chemo, the major surgeries…melanoma usually comes back and it also is the most deadilest form of skin cancer."

                              ?? But from what I have read here on the board and on the internet it doesn't usually come back. The oncologist said I am cured.  Now I don't know what to believe.

                              I asked in my first post "do I have cancer" and no one answered yes or no.

                              What am I to believe now?

                              Why does no one seem to talk to new people here?

                              sedona
                              Participant

                                Thank you so much CaliforniaCaregiver!

                                sedona
                                Participant

                                  Thank you so much CaliforniaCaregiver!

                                  sedona
                                  Participant

                                    Thank you so much CaliforniaCaregiver!

                                Viewing 2 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.