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dnovak

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      dnovak
      Participant

        First off, consider yourself and your son very lucky.  Positive lymph nodes usually result in lymphnode dissection followed by a year of interferon.  As the father of a child who went through both of these when she was 8 I can tell tell you that this is a nightmare that you should not wish on yourself.  There are a number of cancer centers that see more pediatric melanoma than most.  St Jude and MD Anderson are 2 big ones that you could get a 2nd opinion at, but I'm fairly certain they are going to advise watchful waiting.  Be happy about this, it is very good.  

        If if you want to interact with others who have been down this rabbit hole then search for Littlest Warrior Spot on Facebook and ask to be a member.  This is a closed group of pediatric melanoma parents who exchange information.   Last I checked there are around 100 in the group now, from stage 1 kids to stage 4.  Check it out…and be happy about these results–it's great news.  

        Good luck.  Dnovak.

         

         

         

        dnovak
        Participant

          First off, consider yourself and your son very lucky.  Positive lymph nodes usually result in lymphnode dissection followed by a year of interferon.  As the father of a child who went through both of these when she was 8 I can tell tell you that this is a nightmare that you should not wish on yourself.  There are a number of cancer centers that see more pediatric melanoma than most.  St Jude and MD Anderson are 2 big ones that you could get a 2nd opinion at, but I'm fairly certain they are going to advise watchful waiting.  Be happy about this, it is very good.  

          If if you want to interact with others who have been down this rabbit hole then search for Littlest Warrior Spot on Facebook and ask to be a member.  This is a closed group of pediatric melanoma parents who exchange information.   Last I checked there are around 100 in the group now, from stage 1 kids to stage 4.  Check it out…and be happy about these results–it's great news.  

          Good luck.  Dnovak.

           

           

           

          dnovak
          Participant

            First off, consider yourself and your son very lucky.  Positive lymph nodes usually result in lymphnode dissection followed by a year of interferon.  As the father of a child who went through both of these when she was 8 I can tell tell you that this is a nightmare that you should not wish on yourself.  There are a number of cancer centers that see more pediatric melanoma than most.  St Jude and MD Anderson are 2 big ones that you could get a 2nd opinion at, but I'm fairly certain they are going to advise watchful waiting.  Be happy about this, it is very good.  

            If if you want to interact with others who have been down this rabbit hole then search for Littlest Warrior Spot on Facebook and ask to be a member.  This is a closed group of pediatric melanoma parents who exchange information.   Last I checked there are around 100 in the group now, from stage 1 kids to stage 4.  Check it out…and be happy about these results–it's great news.  

            Good luck.  Dnovak.

             

             

             

            dnovak
            Participant
              First off, I have to say that this sucks for you and your son, and I am sorry.  That said, there are a number of pediatric melanoma patients and parents floating around, myself included.  My daughter was diagnosed almost 3 years ago at age 8 (and doing great now).  Every parent who has been through this will tell you that pediatric melanoma is different from adult melanoma, so you need to be sure you go to a cancer center that has PM experience like St. Judes,  MD Anderson, UCSF, etc.
               
              I would reach out to Brenda Busby, who works for the Melanoma research foundation.  Her daughter was diagnosed at a very young age and she is very active among the pediatric melanoma community.  Her email is [email protected].  She is a great resource.  
               
              You can also check out The Littlest Warrior Spot on Facebook.  It is a pediatric melanoma community.
               
              God bless and good luck.
               
              Dave Novak
               
               
              dnovak
              Participant
                First off, I have to say that this sucks for you and your son, and I am sorry.  That said, there are a number of pediatric melanoma patients and parents floating around, myself included.  My daughter was diagnosed almost 3 years ago at age 8 (and doing great now).  Every parent who has been through this will tell you that pediatric melanoma is different from adult melanoma, so you need to be sure you go to a cancer center that has PM experience like St. Judes,  MD Anderson, UCSF, etc.
                 
                I would reach out to Brenda Busby, who works for the Melanoma research foundation.  Her daughter was diagnosed at a very young age and she is very active among the pediatric melanoma community.  Her email is [email protected].  She is a great resource.  
                 
                You can also check out The Littlest Warrior Spot on Facebook.  It is a pediatric melanoma community.
                 
                God bless and good luck.
                 
                Dave Novak
                 
                 
                dnovak
                Participant
                  First off, I have to say that this sucks for you and your son, and I am sorry.  That said, there are a number of pediatric melanoma patients and parents floating around, myself included.  My daughter was diagnosed almost 3 years ago at age 8 (and doing great now).  Every parent who has been through this will tell you that pediatric melanoma is different from adult melanoma, so you need to be sure you go to a cancer center that has PM experience like St. Judes,  MD Anderson, UCSF, etc.
                   
                  I would reach out to Brenda Busby, who works for the Melanoma research foundation.  Her daughter was diagnosed at a very young age and she is very active among the pediatric melanoma community.  Her email is [email protected].  She is a great resource.  
                   
                  You can also check out The Littlest Warrior Spot on Facebook.  It is a pediatric melanoma community.
                   
                  God bless and good luck.
                   
                  Dave Novak
                   
                   
                  dnovak
                  Participant

                    I'm sorry your child has been diagnosed with pediatric melanoma. The disease is very rare in children and there are not a lot of resources out there for the newly diagnosed. 

                    There is a network of pediatric melanoma parents that you need to get in touch with, including several who's kids were also diagnosed at a very young age. 

                    Google Littleist warrior spot and go to the web site or Facebook page. Danielle Adams will help you get setup into our group. You will find a wealth of info there from the 60 or so parents. 

                    Dave Novak, father to Amelia, age 8 stage 3b patient.  

                     

                     

                     

                     

                    dnovak
                    Participant

                      I'm sorry your child has been diagnosed with pediatric melanoma. The disease is very rare in children and there are not a lot of resources out there for the newly diagnosed. 

                      There is a network of pediatric melanoma parents that you need to get in touch with, including several who's kids were also diagnosed at a very young age. 

                      Google Littleist warrior spot and go to the web site or Facebook page. Danielle Adams will help you get setup into our group. You will find a wealth of info there from the 60 or so parents. 

                      Dave Novak, father to Amelia, age 8 stage 3b patient.  

                       

                       

                       

                       

                      dnovak
                      Participant

                        I'm sorry your child has been diagnosed with pediatric melanoma. The disease is very rare in children and there are not a lot of resources out there for the newly diagnosed. 

                        There is a network of pediatric melanoma parents that you need to get in touch with, including several who's kids were also diagnosed at a very young age. 

                        Google Littleist warrior spot and go to the web site or Facebook page. Danielle Adams will help you get setup into our group. You will find a wealth of info there from the 60 or so parents. 

                        Dave Novak, father to Amelia, age 8 stage 3b patient.  

                         

                         

                         

                         

                        dnovak
                        Participant

                          Brandy I sent you a PM.  There's a group of pediatric melanoma parents online that may be helpful for you.  You can also learn more through Danielle Adams at her site http://littlestwarriorspot.com/.

                           

                           

                          dnovak
                          Participant

                            Brandy I sent you a PM.  There's a group of pediatric melanoma parents online that may be helpful for you.  You can also learn more through Danielle Adams at her site http://littlestwarriorspot.com/.

                             

                             

                            dnovak
                            Participant

                              Brandy I sent you a PM.  There's a group of pediatric melanoma parents online that may be helpful for you.  You can also learn more through Danielle Adams at her site http://littlestwarriorspot.com/.

                               

                               

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