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      • November 24, 2014 at 1:41 pm
      eturner
      Participant

      Hi Jewel 

      My husband just finished IPI two weeks ago, he had no side effect from the treatment at all. Best of luck and god bless 🙂

      Emily

      • November 24, 2014 at 1:41 pm
      eturner
      Participant

      Hi Jewel 

      My husband just finished IPI two weeks ago, he had no side effect from the treatment at all. Best of luck and god bless 🙂

      Emily

      • November 24, 2014 at 1:41 pm
      eturner
      Participant

      Hi Jewel 

      My husband just finished IPI two weeks ago, he had no side effect from the treatment at all. Best of luck and god bless 🙂

      Emily

      • November 13, 2014 at 6:24 pm
      eturner
      Participant

      Artie,

      What great news!! I follow you very closly as my husbands mel is very much like yours( in bone) and I have been very interested in how the PD1 was responding with you. I will continue to pray for healing 🙂

      Emily

      • November 13, 2014 at 6:24 pm
      eturner
      Participant

      Artie,

      What great news!! I follow you very closly as my husbands mel is very much like yours( in bone) and I have been very interested in how the PD1 was responding with you. I will continue to pray for healing 🙂

      Emily

      • November 13, 2014 at 6:24 pm
      eturner
      Participant

      Artie,

      What great news!! I follow you very closly as my husbands mel is very much like yours( in bone) and I have been very interested in how the PD1 was responding with you. I will continue to pray for healing 🙂

      Emily

      • November 13, 2014 at 6:09 pm
      eturner
      Participant

      Hi, 

      My name is Emily and my 34 year old husband has stage 4 mel in his bones and a few spots on his lung as well. We have also done the tafinlar/mek pills ( they worked for about 5 months) yesterday he did his 4th yervoy we rescan in 4 weeks. We began our battle last Sept with stage 4 and here we are still fighting… he feels good today and that's all I can ask for. I'm thinking we will start pd1 very soon. Sorry I'm not any real help as far as long term survivor, I am however ever offering my support if you need me I'm here or on FB ( Emily Ryder Turner). 

      Emily

      • November 13, 2014 at 6:09 pm
      eturner
      Participant

      Hi, 

      My name is Emily and my 34 year old husband has stage 4 mel in his bones and a few spots on his lung as well. We have also done the tafinlar/mek pills ( they worked for about 5 months) yesterday he did his 4th yervoy we rescan in 4 weeks. We began our battle last Sept with stage 4 and here we are still fighting… he feels good today and that's all I can ask for. I'm thinking we will start pd1 very soon. Sorry I'm not any real help as far as long term survivor, I am however ever offering my support if you need me I'm here or on FB ( Emily Ryder Turner). 

      Emily

      • November 13, 2014 at 6:09 pm
      eturner
      Participant

      Hi, 

      My name is Emily and my 34 year old husband has stage 4 mel in his bones and a few spots on his lung as well. We have also done the tafinlar/mek pills ( they worked for about 5 months) yesterday he did his 4th yervoy we rescan in 4 weeks. We began our battle last Sept with stage 4 and here we are still fighting… he feels good today and that's all I can ask for. I'm thinking we will start pd1 very soon. Sorry I'm not any real help as far as long term survivor, I am however ever offering my support if you need me I'm here or on FB ( Emily Ryder Turner). 

      Emily

      • November 5, 2014 at 1:45 pm
      eturner
      Participant

      Artie,

      Please know you are in my thoughts and prayers, you have  so many that are wishing the best for you. I cannot imagine your disapointment, but sadly I in some ways do understand it. Move on to plan B and don't ever look back. 

      Prayers,

      Emily

      • November 5, 2014 at 1:45 pm
      eturner
      Participant

      Artie,

      Please know you are in my thoughts and prayers, you have  so many that are wishing the best for you. I cannot imagine your disapointment, but sadly I in some ways do understand it. Move on to plan B and don't ever look back. 

      Prayers,

      Emily

      • November 5, 2014 at 1:45 pm
      eturner
      Participant

      Artie,

      Please know you are in my thoughts and prayers, you have  so many that are wishing the best for you. I cannot imagine your disapointment, but sadly I in some ways do understand it. Move on to plan B and don't ever look back. 

      Prayers,

      Emily

      • November 20, 2014 at 2:34 pm
      eturner
      Participant

      Thanks guys for responding :)… next set of scans is on Dec. 10th…. I'm so nervous!! I just hate Melanoma and it seems so nasty once its in the bone:(

      Emily 

      • November 20, 2014 at 2:34 pm
      eturner
      Participant

      Thanks guys for responding :)… next set of scans is on Dec. 10th…. I'm so nervous!! I just hate Melanoma and it seems so nasty once its in the bone:(

      Emily 

      • November 20, 2014 at 2:34 pm
      eturner
      Participant

      Thanks guys for responding :)… next set of scans is on Dec. 10th…. I'm so nervous!! I just hate Melanoma and it seems so nasty once its in the bone:(

      Emily 

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