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Stage IIIb – NED for 8-Years!

Forums General Melanoma Community Stage IIIb – NED for 8-Years!

  • Post
    LibbyinVA
    Participant

    In the interest of giving some hope to others, just want to let everyone know that today I am celebrating my 8th year of being NED. I won't bore you with all the details as you can check my profile if you want more information. Melanoma certainly left its mark on me but I am still winning. Believe in miracles…I am one!

    LibbyinVA-Stage IIIb

    In the interest of giving some hope to others, just want to let everyone know that today I am celebrating my 8th year of being NED. I won't bore you with all the details as you can check my profile if you want more information. Melanoma certainly left its mark on me but I am still winning. Believe in miracles…I am one!

    LibbyinVA-Stage IIIb

Viewing 11 reply threads
  • Replies
      Becky
      Participant

      Fantastic! Thanks for sharing!

      Becky
      Participant

      Fantastic! Thanks for sharing!

      Becky
      Participant

      Fantastic! Thanks for sharing!

      JerryfromFauq
      Participant

      Roll on, Gal ROLL ON

      !

      JerryfromFauq
      Participant

      Roll on, Gal ROLL ON

      !

      JerryfromFauq
      Participant

      Roll on, Gal ROLL ON

      !

      kathycmc
      Participant

      My daughter, 24, is stage IIb.  After surgery and biochemotherapy she remains NED since 1/31/13.  Thank you for posting your story.  It gives this mother hope for her daughters future.

      kathycmc
      Participant

      My daughter, 24, is stage IIb.  After surgery and biochemotherapy she remains NED since 1/31/13.  Thank you for posting your story.  It gives this mother hope for her daughters future.

      kathycmc
      Participant

      My daughter, 24, is stage IIb.  After surgery and biochemotherapy she remains NED since 1/31/13.  Thank you for posting your story.  It gives this mother hope for her daughters future.

      kathycmc
      Participant

      Sorry that should be IIIb.

      kathycmc
      Participant

      Sorry that should be IIIb.

      kathycmc
      Participant

      Sorry that should be IIIb.

      LibbyinVA
      Participant
      Hi, Jerry – thanks so much for thekind words and for your update about Jane. I really appreciated your taking the time to get me back in the loop!

      Have a great weekend!

      Libby

      LibbyinVA
      Participant
      Hi, Jerry – thanks so much for thekind words and for your update about Jane. I really appreciated your taking the time to get me back in the loop!

      Have a great weekend!

      Libby

      LibbyinVA
      Participant
      Hi, Jerry – thanks so much for thekind words and for your update about Jane. I really appreciated your taking the time to get me back in the loop!

      Have a great weekend!

      Libby

      LibbyinVA
      Participant
      Good for her…sounds like she is a fighter! From one mother to another, it is really tough and I assume melanoma must scare you all the time. As for myself, I am no longer afraid, but cannot say the same for my family. They are scared every single day. Have always thought it must be harder on the family than it is on the patient. Let’s keep hope alive…sometimes that has to be enough!

      Wishing your daughter a lifetime of NED!

      Libby

      LibbyinVA
      Participant
      Good for her…sounds like she is a fighter! From one mother to another, it is really tough and I assume melanoma must scare you all the time. As for myself, I am no longer afraid, but cannot say the same for my family. They are scared every single day. Have always thought it must be harder on the family than it is on the patient. Let’s keep hope alive…sometimes that has to be enough!

      Wishing your daughter a lifetime of NED!

      Libby

      LibbyinVA
      Participant
      Good for her…sounds like she is a fighter! From one mother to another, it is really tough and I assume melanoma must scare you all the time. As for myself, I am no longer afraid, but cannot say the same for my family. They are scared every single day. Have always thought it must be harder on the family than it is on the patient. Let’s keep hope alive…sometimes that has to be enough!

      Wishing your daughter a lifetime of NED!

      Libby

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