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Medical Clinics and Specialists

Forums General Melanoma Community Medical Clinics and Specialists

  • Post
    Daisyduke
    Participant

      Can anyone recommend any medical clinics or specialists for a 2nd Opinion?  How do you get on Yervoy and does Insurance cover it?  What about  Watch and Wait.  I believe I am at III A or III B.

       

      I need to make some decisions soon before my followup appointment.  I do not want to go on Interferon!!!!!

    Viewing 8 reply threads
    • Replies
        jpg
        Participant

          Depends on where you live.  East Coast:  NYU, Columbia, Sloan Kettering,  UPENN for phila, Mass general for Boston,  in the south:  Sarah Cannon in Nashville,  WEst:  UCLA, etc.

          Try the list at:  www.melanomainternational.org

          REsources

          jpg
          Participant

            Depends on where you live.  East Coast:  NYU, Columbia, Sloan Kettering,  UPENN for phila, Mass general for Boston,  in the south:  Sarah Cannon in Nashville,  WEst:  UCLA, etc.

            Try the list at:  www.melanomainternational.org

            REsources

            jpg
            Participant

              Depends on where you live.  East Coast:  NYU, Columbia, Sloan Kettering,  UPENN for phila, Mass general for Boston,  in the south:  Sarah Cannon in Nashville,  WEst:  UCLA, etc.

              Try the list at:  www.melanomainternational.org

              REsources

              Linny
              Participant

                Here's a list of melanoma centers: http://melanomainternational.org/web-resources/cancer-centers/#.VhMO9qJckzw

                If you can tell us what state you live in, people here can give you more detailed input on these places and whether they offer you transportation aid if you live a distance away from them.

                Linny
                Participant

                  Here's a list of melanoma centers: http://melanomainternational.org/web-resources/cancer-centers/#.VhMO9qJckzw

                  If you can tell us what state you live in, people here can give you more detailed input on these places and whether they offer you transportation aid if you live a distance away from them.

                  Linny
                  Participant

                    Here's a list of melanoma centers: http://melanomainternational.org/web-resources/cancer-centers/#.VhMO9qJckzw

                    If you can tell us what state you live in, people here can give you more detailed input on these places and whether they offer you transportation aid if you live a distance away from them.

                    Patina
                    Participant

                      Cindy,

                      We've found that that best are active in clinical research and they usually practice at educational facilities. Depending on your diagnosis your doctor will discuss options for you based on your status and your insurance company will pay for standard care.  There are also trials that you can go on for more treatment or aggressive treatment which you should look into.

                      You have a choice and time to make a decision.  So, you should be able to seek out other oncologists for their opinion now and you should not be forced to take Interferon.  

                      We had my Mom see 4 melanoma specialists in total and we were very lucky that we saw as many as we did. We learned more about the disease from each visit and we were lucky that the 3rd specialist caught what two others did not. Brain mets that the radiologist missed!  – A pretty big miss.

                      When you see someone about a second or even a third opinion take your reports and CDs of your PET and CT scans and the MRI of your brain. You'll want them to read the reports, but also see which one looks at the images without prompting. – The doctors that want to see these images are typically the best or at least this is what we found. – Buy a voice recorder and tape the conversations. You'll miss some things and be glad you have a record of what the doctor said. I'd also get someone who is not a family member to come along with you.  Someone to be your advocate and who can wade through medical jargon and who is inherently curious is what you will need.

                      Also, when you do decide on treatment consider the whole team and how they communicate. We were having my Mom treated at 2 different facilities and one was subpar and we were just very very lucky to have everything moved to USC when we did. She's received superior care there and I can't recommend them enough.  – She was diagnosed with stage IV in early November of 2013 and has a very good outlook. Even with 28 brain mets, which is hard to believe.

                      In the Southern California area I can strongly recommend Dr. Mike Wong at USC in LA and Dr. Peter Bosaberg.  If there is ever a need for gamma knife radiation (brain mets) I strongly recommend Dr. Eric Chang at USC in LA. 

                       

                      Patina
                      Participant

                        Cindy,

                        We've found that that best are active in clinical research and they usually practice at educational facilities. Depending on your diagnosis your doctor will discuss options for you based on your status and your insurance company will pay for standard care.  There are also trials that you can go on for more treatment or aggressive treatment which you should look into.

                        You have a choice and time to make a decision.  So, you should be able to seek out other oncologists for their opinion now and you should not be forced to take Interferon.  

                        We had my Mom see 4 melanoma specialists in total and we were very lucky that we saw as many as we did. We learned more about the disease from each visit and we were lucky that the 3rd specialist caught what two others did not. Brain mets that the radiologist missed!  – A pretty big miss.

                        When you see someone about a second or even a third opinion take your reports and CDs of your PET and CT scans and the MRI of your brain. You'll want them to read the reports, but also see which one looks at the images without prompting. – The doctors that want to see these images are typically the best or at least this is what we found. – Buy a voice recorder and tape the conversations. You'll miss some things and be glad you have a record of what the doctor said. I'd also get someone who is not a family member to come along with you.  Someone to be your advocate and who can wade through medical jargon and who is inherently curious is what you will need.

                        Also, when you do decide on treatment consider the whole team and how they communicate. We were having my Mom treated at 2 different facilities and one was subpar and we were just very very lucky to have everything moved to USC when we did. She's received superior care there and I can't recommend them enough.  – She was diagnosed with stage IV in early November of 2013 and has a very good outlook. Even with 28 brain mets, which is hard to believe.

                        In the Southern California area I can strongly recommend Dr. Mike Wong at USC in LA and Dr. Peter Bosaberg.  If there is ever a need for gamma knife radiation (brain mets) I strongly recommend Dr. Eric Chang at USC in LA. 

                         

                        Patina
                        Participant

                          Cindy,

                          We've found that that best are active in clinical research and they usually practice at educational facilities. Depending on your diagnosis your doctor will discuss options for you based on your status and your insurance company will pay for standard care.  There are also trials that you can go on for more treatment or aggressive treatment which you should look into.

                          You have a choice and time to make a decision.  So, you should be able to seek out other oncologists for their opinion now and you should not be forced to take Interferon.  

                          We had my Mom see 4 melanoma specialists in total and we were very lucky that we saw as many as we did. We learned more about the disease from each visit and we were lucky that the 3rd specialist caught what two others did not. Brain mets that the radiologist missed!  – A pretty big miss.

                          When you see someone about a second or even a third opinion take your reports and CDs of your PET and CT scans and the MRI of your brain. You'll want them to read the reports, but also see which one looks at the images without prompting. – The doctors that want to see these images are typically the best or at least this is what we found. – Buy a voice recorder and tape the conversations. You'll miss some things and be glad you have a record of what the doctor said. I'd also get someone who is not a family member to come along with you.  Someone to be your advocate and who can wade through medical jargon and who is inherently curious is what you will need.

                          Also, when you do decide on treatment consider the whole team and how they communicate. We were having my Mom treated at 2 different facilities and one was subpar and we were just very very lucky to have everything moved to USC when we did. She's received superior care there and I can't recommend them enough.  – She was diagnosed with stage IV in early November of 2013 and has a very good outlook. Even with 28 brain mets, which is hard to believe.

                          In the Southern California area I can strongly recommend Dr. Mike Wong at USC in LA and Dr. Peter Bosaberg.  If there is ever a need for gamma knife radiation (brain mets) I strongly recommend Dr. Eric Chang at USC in LA. 

                           

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