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jnaakins

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      jnaakins
      Participant

        Ana, I am soo very sorry for your loss. I just replied to your earlier thread about your melanoma in situ and I had no idea you'd since lost your father. Again, I am just so sorry. Hugs.

        jnaakins
        Participant

          Ana, I am soo very sorry for your loss. I just replied to your earlier thread about your melanoma in situ and I had no idea you'd since lost your father. Again, I am just so sorry. Hugs.

          jnaakins
          Participant

            Ana, I am soo very sorry for your loss. I just replied to your earlier thread about your melanoma in situ and I had no idea you'd since lost your father. Again, I am just so sorry. Hugs.

            jnaakins
            Participant

              I like you, was diagnosed with melanoma in-situ. Unlike you (I hope), I lost my younger brother in 2010 to metastatic melanoma, and I currently have a young aunt who is fighting stage IV metastatic melanoma. As you can imagine, it has been scary for me because I constantly worry whether of not I will end up at the same place with the disease. I recommend if you're worried, get your path report read by a second lab just to verify the findings. It might set your mind at ease. Did you have the secondary excision? The dermatologist that took mine off didnt do the follow-up excision because he felt he had got it all, and cauterized the margins well enough. I ended up getting a second opinion and this doctor immediately sheduled me for a MOHS procedure. It was instrumental in easing my fears. Now I know I have done everything I could. The rest is up to fate. Try to focus on the things you can control: Making sure you go to all your skin checks. Get mole-mapping if you can. Watch like a hawk for any new changes, and protect your skin!!! Dont worry about the things you cant change. Enjoy every day of your life. I hope you and I never have to deal with melanoma again! 

              jnaakins
              Participant

                I like you, was diagnosed with melanoma in-situ. Unlike you (I hope), I lost my younger brother in 2010 to metastatic melanoma, and I currently have a young aunt who is fighting stage IV metastatic melanoma. As you can imagine, it has been scary for me because I constantly worry whether of not I will end up at the same place with the disease. I recommend if you're worried, get your path report read by a second lab just to verify the findings. It might set your mind at ease. Did you have the secondary excision? The dermatologist that took mine off didnt do the follow-up excision because he felt he had got it all, and cauterized the margins well enough. I ended up getting a second opinion and this doctor immediately sheduled me for a MOHS procedure. It was instrumental in easing my fears. Now I know I have done everything I could. The rest is up to fate. Try to focus on the things you can control: Making sure you go to all your skin checks. Get mole-mapping if you can. Watch like a hawk for any new changes, and protect your skin!!! Dont worry about the things you cant change. Enjoy every day of your life. I hope you and I never have to deal with melanoma again! 

                jnaakins
                Participant

                  I like you, was diagnosed with melanoma in-situ. Unlike you (I hope), I lost my younger brother in 2010 to metastatic melanoma, and I currently have a young aunt who is fighting stage IV metastatic melanoma. As you can imagine, it has been scary for me because I constantly worry whether of not I will end up at the same place with the disease. I recommend if you're worried, get your path report read by a second lab just to verify the findings. It might set your mind at ease. Did you have the secondary excision? The dermatologist that took mine off didnt do the follow-up excision because he felt he had got it all, and cauterized the margins well enough. I ended up getting a second opinion and this doctor immediately sheduled me for a MOHS procedure. It was instrumental in easing my fears. Now I know I have done everything I could. The rest is up to fate. Try to focus on the things you can control: Making sure you go to all your skin checks. Get mole-mapping if you can. Watch like a hawk for any new changes, and protect your skin!!! Dont worry about the things you cant change. Enjoy every day of your life. I hope you and I never have to deal with melanoma again! 

                  jnaakins
                  Participant

                    Just wanted to say that I know how you feel. I dont really have a ton of great advice, except to control what you can, and dont stress yourself out about what you cant. That means keep vigilant with your skin checks, follow-ups with your doctors. Get your path report read by another lab, etc. My brother died in 2010 from MM and I currently have an aunt who is stage IV so we know there is a family history. I have also had a melanoma in-situ. I was at the MRF/SCCA melanoma patient and caregiver symposium this past Saturday and I did ask if there was a benefit from the genetic testing for hereditary predisposition. Anyway, thats a subject for another time. lol. Just hang in there and enjoy that sweet new baby! You are doing a great job being proactive about the situation, and chances are good that you wont have your melanomas spread/return. 

                    jnaakins
                    Participant

                      Just wanted to say that I know how you feel. I dont really have a ton of great advice, except to control what you can, and dont stress yourself out about what you cant. That means keep vigilant with your skin checks, follow-ups with your doctors. Get your path report read by another lab, etc. My brother died in 2010 from MM and I currently have an aunt who is stage IV so we know there is a family history. I have also had a melanoma in-situ. I was at the MRF/SCCA melanoma patient and caregiver symposium this past Saturday and I did ask if there was a benefit from the genetic testing for hereditary predisposition. Anyway, thats a subject for another time. lol. Just hang in there and enjoy that sweet new baby! You are doing a great job being proactive about the situation, and chances are good that you wont have your melanomas spread/return. 

                      jnaakins
                      Participant

                        Just wanted to say that I know how you feel. I dont really have a ton of great advice, except to control what you can, and dont stress yourself out about what you cant. That means keep vigilant with your skin checks, follow-ups with your doctors. Get your path report read by another lab, etc. My brother died in 2010 from MM and I currently have an aunt who is stage IV so we know there is a family history. I have also had a melanoma in-situ. I was at the MRF/SCCA melanoma patient and caregiver symposium this past Saturday and I did ask if there was a benefit from the genetic testing for hereditary predisposition. Anyway, thats a subject for another time. lol. Just hang in there and enjoy that sweet new baby! You are doing a great job being proactive about the situation, and chances are good that you wont have your melanomas spread/return. 

                        jnaakins
                        Participant

                          Thank you for responding. I guess Im just going to have to be vigilant about skin checks and hope that the dr got it all- he did feel confident that he did, and he said he cauterized the margins really well so that was (he felt) extra insurance.

                          I guess Im just wondering if there are very many people who do have recurrences, or other tumors show up after having one that was caught this early? I mean, is this something that's common? It doesnt sound like it, so that brings me some comfort. I can't imagine having my family lose another member to this horrible disease. I try not to be paranoid, or spend unnessecary time worrying. But having seen my brother lose his battle- it's always in the back of my mind. He didnt catch his early though, by the time he went in to have his mole checked, it was already stage 3b.

                          jnaakins
                          Participant

                            Thank you for responding. I guess Im just going to have to be vigilant about skin checks and hope that the dr got it all- he did feel confident that he did, and he said he cauterized the margins really well so that was (he felt) extra insurance.

                            I guess Im just wondering if there are very many people who do have recurrences, or other tumors show up after having one that was caught this early? I mean, is this something that's common? It doesnt sound like it, so that brings me some comfort. I can't imagine having my family lose another member to this horrible disease. I try not to be paranoid, or spend unnessecary time worrying. But having seen my brother lose his battle- it's always in the back of my mind. He didnt catch his early though, by the time he went in to have his mole checked, it was already stage 3b.

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