Laura mrf

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      • May 30, 2013 at 2:22 am
      Laura mrf
      Participant
        Hello Mary,
        I am new here so this is my first post. May I suggest that you visit the Memorial Sloan Kettering patient Connections site for some info on lung cancer? There are several people there with experience, and a webinar from last week’s seminar should be posted soon. The moderator, Esther, may also point you in the right direction. You can find the group by going to mskcc.org, scrolling down, and clicking on the Counseling and Support link, and then Connections. Hope that helps! Wishing you and your husband the best.
        • May 30, 2013 at 2:22 am
        Laura mrf
        Participant
          Hello Mary,
          I am new here so this is my first post. May I suggest that you visit the Memorial Sloan Kettering patient Connections site for some info on lung cancer? There are several people there with experience, and a webinar from last week’s seminar should be posted soon. The moderator, Esther, may also point you in the right direction. You can find the group by going to mskcc.org, scrolling down, and clicking on the Counseling and Support link, and then Connections. Hope that helps! Wishing you and your husband the best.
          • May 30, 2013 at 2:22 am
          Laura mrf
          Participant
            Hello Mary,
            I am new here so this is my first post. May I suggest that you visit the Memorial Sloan Kettering patient Connections site for some info on lung cancer? There are several people there with experience, and a webinar from last week’s seminar should be posted soon. The moderator, Esther, may also point you in the right direction. You can find the group by going to mskcc.org, scrolling down, and clicking on the Counseling and Support link, and then Connections. Hope that helps! Wishing you and your husband the best.
            • May 30, 2013 at 11:03 am
            Laura mrf
            Participant
              Hello Janner,
              Thank you so very much for taking time to reply to my long post! I was confused by the “intraepidermal” reference and was hoping to see the word “benign” right there in the report! But, I understand the dermopathologists have their own lingo so believe me, I know I am lucky! I will remain vigilant and now know to really keep an eye on all the other previously biopsied nevi. Best wishes to everyone here for recovery and happiness. You have something very special in this community. Thank you for answering my questions. I hope to help as an advocate for MRF.
              Laura
              • May 30, 2013 at 11:03 am
              Laura mrf
              Participant
                Hello Janner,
                Thank you so very much for taking time to reply to my long post! I was confused by the “intraepidermal” reference and was hoping to see the word “benign” right there in the report! But, I understand the dermopathologists have their own lingo so believe me, I know I am lucky! I will remain vigilant and now know to really keep an eye on all the other previously biopsied nevi. Best wishes to everyone here for recovery and happiness. You have something very special in this community. Thank you for answering my questions. I hope to help as an advocate for MRF.
                Laura
                • May 30, 2013 at 11:03 am
                Laura mrf
                Participant
                  Hello Janner,
                  Thank you so very much for taking time to reply to my long post! I was confused by the “intraepidermal” reference and was hoping to see the word “benign” right there in the report! But, I understand the dermopathologists have their own lingo so believe me, I know I am lucky! I will remain vigilant and now know to really keep an eye on all the other previously biopsied nevi. Best wishes to everyone here for recovery and happiness. You have something very special in this community. Thank you for answering my questions. I hope to help as an advocate for MRF.
                  Laura
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