The information on this site is not intended or implied to be a substitute for professional medical advice, diagnosis or treatment. Content within the patient forum is user-generated and has not been reviewed by medical professionals. Other sections of the Melanoma Research Foundation website include information that has been reviewed by medical professionals as appropriate. All medical decisions should be made in consultation with your doctor or other qualified medical professional.

MissJenn

Forum Replies Created

Viewing 11 reply threads
  • Replies
      MissJenn
      Participant

        You go ahead and say exactly how you feel girl!!!  If Jesus gives you strength through this or if the giant green people eater were to give you strength how dare anybody tell you what to say or where to say it when you are posting your own thoughts…wow.  You are in a battle right now and don't you feel bad for anything at all you feel…or say…on your own post about you!…  Now if you had gone on another persons post and tried to tell them you want to "save" them, I can see how that could be taken offensively…  but you didn't and I am insensed how immediately this person (and supporters) wrote about ettiquiette instead of simply support.  Anyways…back on the topic that matters…  I am a fellow stage 3 patient and I understand how you feel.  You are going to need a lot of support through your time on Interferon…if you have facebook, I hope you add the Melanoma Groups available for you.  Melanoma Prayer Center will be a good one for you specifically…very uplifting and the host is simply awesome.  I'm Jennifer Miller on there…please add me if you want…I'm here for you girl…we are both newbies together!

        MissJenn
        Participant

          You go ahead and say exactly how you feel girl!!!  If Jesus gives you strength through this or if the giant green people eater were to give you strength how dare anybody tell you what to say or where to say it when you are posting your own thoughts…wow.  You are in a battle right now and don't you feel bad for anything at all you feel…or say…on your own post about you!…  Now if you had gone on another persons post and tried to tell them you want to "save" them, I can see how that could be taken offensively…  but you didn't and I am insensed how immediately this person (and supporters) wrote about ettiquiette instead of simply support.  Anyways…back on the topic that matters…  I am a fellow stage 3 patient and I understand how you feel.  You are going to need a lot of support through your time on Interferon…if you have facebook, I hope you add the Melanoma Groups available for you.  Melanoma Prayer Center will be a good one for you specifically…very uplifting and the host is simply awesome.  I'm Jennifer Miller on there…please add me if you want…I'm here for you girl…we are both newbies together!

          MissJenn
          Participant

            You go ahead and say exactly how you feel girl!!!  If Jesus gives you strength through this or if the giant green people eater were to give you strength how dare anybody tell you what to say or where to say it when you are posting your own thoughts…wow.  You are in a battle right now and don't you feel bad for anything at all you feel…or say…on your own post about you!…  Now if you had gone on another persons post and tried to tell them you want to "save" them, I can see how that could be taken offensively…  but you didn't and I am insensed how immediately this person (and supporters) wrote about ettiquiette instead of simply support.  Anyways…back on the topic that matters…  I am a fellow stage 3 patient and I understand how you feel.  You are going to need a lot of support through your time on Interferon…if you have facebook, I hope you add the Melanoma Groups available for you.  Melanoma Prayer Center will be a good one for you specifically…very uplifting and the host is simply awesome.  I'm Jennifer Miller on there…please add me if you want…I'm here for you girl…we are both newbies together!

            MissJenn
            Participant

              Yes…please go find a Melanoma Specialist!  I don't know why they would not do a Sentinal Lymph Node biopsy but mine was .92mm and Clarks Level III and it had traveled to my lymph nodes, and the tissue around my mole was clear.  Get a second opinion for sure and soon.

              MissJenn
              Participant

                Yes…please go find a Melanoma Specialist!  I don't know why they would not do a Sentinal Lymph Node biopsy but mine was .92mm and Clarks Level III and it had traveled to my lymph nodes, and the tissue around my mole was clear.  Get a second opinion for sure and soon.

                MissJenn
                Participant

                  Yes…please go find a Melanoma Specialist!  I don't know why they would not do a Sentinal Lymph Node biopsy but mine was .92mm and Clarks Level III and it had traveled to my lymph nodes, and the tissue around my mole was clear.  Get a second opinion for sure and soon.

                  MissJenn
                  Participant

                    My friend is dealing with the same issue… she is not on MPIP but I'm sure she would love to have someone else to talk to about this.  I will tell her tonight.

                    MissJenn
                    Participant

                      My friend is dealing with the same issue… she is not on MPIP but I'm sure she would love to have someone else to talk to about this.  I will tell her tonight.

                      MissJenn
                      Participant

                        My friend is dealing with the same issue… she is not on MPIP but I'm sure she would love to have someone else to talk to about this.  I will tell her tonight.

                        MissJenn
                        Participant

                          I know how you feel about not being so lucky…with a .93 and it having tested positive to lymph nodes.  Mine was .92 and they almost don't check your SNL with <1mm so I guess on the bright side, thank Heaven we didn't forego the SNL biopsy.  It's most likely mitotic rate that pushed your's to your lymph node…was it high?  Mine was 4…  anyone over .82 with a high mitotic rate of the primary should get the SNL biopsy I read.  This is an unbelievable new world isn't it?  I pray for the best with your recovery…Shaving SUCKS afterwards so I feel for you having to shave your face…Time for a beard for a while 😉

                          MissJenn
                          Participant

                            I know how you feel about not being so lucky…with a .93 and it having tested positive to lymph nodes.  Mine was .92 and they almost don't check your SNL with <1mm so I guess on the bright side, thank Heaven we didn't forego the SNL biopsy.  It's most likely mitotic rate that pushed your's to your lymph node…was it high?  Mine was 4…  anyone over .82 with a high mitotic rate of the primary should get the SNL biopsy I read.  This is an unbelievable new world isn't it?  I pray for the best with your recovery…Shaving SUCKS afterwards so I feel for you having to shave your face…Time for a beard for a while 😉

                            MissJenn
                            Participant

                              I know how you feel about not being so lucky…with a .93 and it having tested positive to lymph nodes.  Mine was .92 and they almost don't check your SNL with <1mm so I guess on the bright side, thank Heaven we didn't forego the SNL biopsy.  It's most likely mitotic rate that pushed your's to your lymph node…was it high?  Mine was 4…  anyone over .82 with a high mitotic rate of the primary should get the SNL biopsy I read.  This is an unbelievable new world isn't it?  I pray for the best with your recovery…Shaving SUCKS afterwards so I feel for you having to shave your face…Time for a beard for a while 😉

                              MissJenn
                              Participant

                                Mike,

                                Here is the link to the abstract of the study…  My oncologist never discussed anything like this…  but, worth thinking about if looking at going in for the CLND… 

                                http://annonc.oxfordjournals.org/content/early/2006/09/12/annonc.mdl176

                                my two areas in the SNL positive were at .1 and .2…  they say to take the higher of the two if mulitiple areas found, but still is so close…  I never heard the term "ultra micro" but well, seems a bit fitting? 

                                MissJenn
                                Participant

                                  Mike,

                                  Here is the link to the abstract of the study…  My oncologist never discussed anything like this…  but, worth thinking about if looking at going in for the CLND… 

                                  http://annonc.oxfordjournals.org/content/early/2006/09/12/annonc.mdl176

                                  my two areas in the SNL positive were at .1 and .2…  they say to take the higher of the two if mulitiple areas found, but still is so close…  I never heard the term "ultra micro" but well, seems a bit fitting? 

                                  MissJenn
                                  Participant

                                    Mike,

                                    Here is the link to the abstract of the study…  My oncologist never discussed anything like this…  but, worth thinking about if looking at going in for the CLND… 

                                    http://annonc.oxfordjournals.org/content/early/2006/09/12/annonc.mdl176

                                    my two areas in the SNL positive were at .1 and .2…  they say to take the higher of the two if mulitiple areas found, but still is so close…  I never heard the term "ultra micro" but well, seems a bit fitting? 

                                Viewing 11 reply threads