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Mimi1974

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      Mimi1974
      Participant

        Hi Wendy,

         

        How are you? How did all go on and what treatment did you get?

        I´ve just been diagnosed with choroidal melanoma last week. And I´m not treated now.

        would like to exchange experiences from different continents – I live in Switzerland.

         

        best

        Mimi

        Mimi1974
        Participant

          Hi Wendy,

           

          How are you? How did all go on and what treatment did you get?

          I´ve just been diagnosed with choroidal melanoma last week. And I´m not treated now.

          would like to exchange experiences from different continents – I live in Switzerland.

           

          best

          Mimi

          Mimi1974
          Participant

            Hi Wendy,

             

            How are you? How did all go on and what treatment did you get?

            I´ve just been diagnosed with choroidal melanoma last week. And I´m not treated now.

            would like to exchange experiences from different continents – I live in Switzerland.

             

            best

            Mimi

            Mimi1974
            Participant

              Ok, sorry it did not work out to write it all. 

              Ím gonna be 42 in Summer and I´ve always been healthy, except of having a balanced transolacation of chromosome 1 to 20, what made it a bit difficult to have children (what we managed to have after loosing 9, now we have 2 healthy girls). It is something rare – haha, like chroroidal melanoma……

              I´ve been seeing white flashes for some time, what I´ve told my kids Eye DOC.

              She sent me after the finding a naevus to the Hospital for more investigations.

              After two days of beeing checked, I´ve got the diagnose.

              We are about to move to China…So everything is very busy here.. House is already rented to some new tenants, we are/have been kind of ready and eager to move.

              Yesterday I´ve had a radio of my Chest and will have ultrasound on Monday, Monday in one week my big appointment with the specialist for proton treatment takes place.

              My Melanoma is on the small side – 1.56 deep, 9.96/7.56.

              So, thats why no MRI or CT will take place. But I´m still worried about Metastases.

              I´d like to know about treatment for the primary tumor and as well about how it goes, if Metastases are found?

              I´ve been reading here very positiv things.

              After staying in bed the two first days after the diagnose, I´ve felt like living a new LIfe..

              I can not explain what it is, but it is not my time to give in now. I am going on and I am a very Happy person, so why change this?

              I´m investigating for new treatment and so on, so any help, and positiv input is very welcome.

              Here, they call the prognose for it – not good. Bad.

              I know. But, I´d like to here anything else as well 😀

               

              Mimi

              Mimi1974
              Participant

                Ok, sorry it did not work out to write it all. 

                Ím gonna be 42 in Summer and I´ve always been healthy, except of having a balanced transolacation of chromosome 1 to 20, what made it a bit difficult to have children (what we managed to have after loosing 9, now we have 2 healthy girls). It is something rare – haha, like chroroidal melanoma……

                I´ve been seeing white flashes for some time, what I´ve told my kids Eye DOC.

                She sent me after the finding a naevus to the Hospital for more investigations.

                After two days of beeing checked, I´ve got the diagnose.

                We are about to move to China…So everything is very busy here.. House is already rented to some new tenants, we are/have been kind of ready and eager to move.

                Yesterday I´ve had a radio of my Chest and will have ultrasound on Monday, Monday in one week my big appointment with the specialist for proton treatment takes place.

                My Melanoma is on the small side – 1.56 deep, 9.96/7.56.

                So, thats why no MRI or CT will take place. But I´m still worried about Metastases.

                I´d like to know about treatment for the primary tumor and as well about how it goes, if Metastases are found?

                I´ve been reading here very positiv things.

                After staying in bed the two first days after the diagnose, I´ve felt like living a new LIfe..

                I can not explain what it is, but it is not my time to give in now. I am going on and I am a very Happy person, so why change this?

                I´m investigating for new treatment and so on, so any help, and positiv input is very welcome.

                Here, they call the prognose for it – not good. Bad.

                I know. But, I´d like to here anything else as well 😀

                 

                Mimi

                Mimi1974
                Participant

                  Ok, sorry it did not work out to write it all. 

                  Ím gonna be 42 in Summer and I´ve always been healthy, except of having a balanced transolacation of chromosome 1 to 20, what made it a bit difficult to have children (what we managed to have after loosing 9, now we have 2 healthy girls). It is something rare – haha, like chroroidal melanoma……

                  I´ve been seeing white flashes for some time, what I´ve told my kids Eye DOC.

                  She sent me after the finding a naevus to the Hospital for more investigations.

                  After two days of beeing checked, I´ve got the diagnose.

                  We are about to move to China…So everything is very busy here.. House is already rented to some new tenants, we are/have been kind of ready and eager to move.

                  Yesterday I´ve had a radio of my Chest and will have ultrasound on Monday, Monday in one week my big appointment with the specialist for proton treatment takes place.

                  My Melanoma is on the small side – 1.56 deep, 9.96/7.56.

                  So, thats why no MRI or CT will take place. But I´m still worried about Metastases.

                  I´d like to know about treatment for the primary tumor and as well about how it goes, if Metastases are found?

                  I´ve been reading here very positiv things.

                  After staying in bed the two first days after the diagnose, I´ve felt like living a new LIfe..

                  I can not explain what it is, but it is not my time to give in now. I am going on and I am a very Happy person, so why change this?

                  I´m investigating for new treatment and so on, so any help, and positiv input is very welcome.

                  Here, they call the prognose for it – not good. Bad.

                  I know. But, I´d like to here anything else as well 😀

                   

                  Mimi

                    Mimi1974
                    Participant

                      Oh, and not to forget . I am soooo scared and worried as well. It is like being on a rollercoaster.

                       

                      Mimi1974
                      Participant

                        Oh, and not to forget . I am soooo scared and worried as well. It is like being on a rollercoaster.

                         

                        Mimi1974
                        Participant

                          Hi again,

                           

                          Now, I do have a second diagnose – just the same – by Lausanne in Switzerland.

                          The good thing is, they are responsible and they do have a lot of experience.

                          I will have my Eye surgery next Tuesday, to fix the protecting plate around the melanoma, and I will get Protonen radiatorn two weeks later in Villingen.

                          My Melanoma is very thin, less than 2mm, but my mole is very big… The part what has gone "bad""maligne" is not so big, so maybe my chances are quit good, god knows.

                          The prognoses for my vision on my left Eye are very bad, thought. So they say, I will become blind on my left Eye most probably.

                          How are you all doing? How are you all living with it? What do you experience?

                          I feel quit lonely – what is strange, because I get a lot of support of my family and friends.

                          Hope to hear back from someone….

                          Mimi

                          Mimi1974
                          Participant

                            Hi again,

                             

                            Now, I do have a second diagnose – just the same – by Lausanne in Switzerland.

                            The good thing is, they are responsible and they do have a lot of experience.

                            I will have my Eye surgery next Tuesday, to fix the protecting plate around the melanoma, and I will get Protonen radiatorn two weeks later in Villingen.

                            My Melanoma is very thin, less than 2mm, but my mole is very big… The part what has gone "bad""maligne" is not so big, so maybe my chances are quit good, god knows.

                            The prognoses for my vision on my left Eye are very bad, thought. So they say, I will become blind on my left Eye most probably.

                            How are you all doing? How are you all living with it? What do you experience?

                            I feel quit lonely – what is strange, because I get a lot of support of my family and friends.

                            Hope to hear back from someone….

                            Mimi

                            Mimi1974
                            Participant

                              Hi again,

                               

                              Now, I do have a second diagnose – just the same – by Lausanne in Switzerland.

                              The good thing is, they are responsible and they do have a lot of experience.

                              I will have my Eye surgery next Tuesday, to fix the protecting plate around the melanoma, and I will get Protonen radiatorn two weeks later in Villingen.

                              My Melanoma is very thin, less than 2mm, but my mole is very big… The part what has gone "bad""maligne" is not so big, so maybe my chances are quit good, god knows.

                              The prognoses for my vision on my left Eye are very bad, thought. So they say, I will become blind on my left Eye most probably.

                              How are you all doing? How are you all living with it? What do you experience?

                              I feel quit lonely – what is strange, because I get a lot of support of my family and friends.

                              Hope to hear back from someone….

                              Mimi

                              Mimi1974
                              Participant

                                Oh, and not to forget . I am soooo scared and worried as well. It is like being on a rollercoaster.

                                 

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