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MPIP Forum and Chat
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MPIP Forum and Chat

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  • Post
    • November 25, 2014 at 7:00 pm
    Carole K
    Participant

      HI Everyone,

      I am a stage IV patient currently NED 13 YRS AND 9 MONTHS  MPIP was a saving grace for me for sooooo many years and I hope all of you will find the love and support I found here.  I am still in touch witih many patients and caregivers I met here  We formed a bond of a lifetime together,

      MPIP is a place to find a WEALTH OF INFORMATION,,  IF you have any questions ask JANNER or Jerry from Fauquat,  They know more than most doctors  lol  not kidding,  

      Please do yourselves a favor and start the chat room going again, It was incredible support.  I am now on FB as well and I love love love beign there,  All of that being said…… THERE IS NO PLACE LIKE MPIP  You will get to know one another, your stories, your journey and you will form friends for a lifetime  

      As difficult as Melanoa is , please look for the gifts,  there are many,

      MELANOMA BROUGH BE TEARS

      MELANOMA BROUGHT ME FEARS

      MELANOMA BROUGHT BE SORROW

      MELANOMA BROUGHT ME PAIN

      MELANOMA BROUGHT ME HEARTACHE

      MELANOMA BROUGHT ME ANGST,

      MELANOMA BROUGHT ME ISOLATION

      MORE IMPORTANTLY

      MELANOMA BROGH ME SMILES

      MELANOMA BROUGHT ME LAUGHTER

      MELANOMA BROUGHT ME JOY

      MELANOMA BROUGHT ME COURAGE

      MELANOMA BROGHT ME STRENGTH

      MELANOMA BROUGHT ME FRIENS

      MELANOMA BROUGHT ME LOVE

      MELANOMA BROUGHT ME FAITH 

      MELANOMA BROUGHT ME BLESSINGS

      MELANOMA BROUGHT ME PEACE

      MMOST IPORTANTLY 

      MELANOMA BORUGHT  ME THE OPPORTUNITY TO MAKE AMENDS TO THOSE I HAVE HURT

      MELANOMA BROUGHT ME THE OPPORTUNITY NOT TO LEAVE ANY UNANSSWERED QUESTIONS FOR MY CHIDLREN

      MELANOMA BROUGHT ME ACCEPTANCE

      WHAT MORE COULD I ASK FOR

      BIG HUGS EVERYONE.

      LOVE AND LIGHT

      CAROLE K 

      STAGE IV  iT'S A BEAUTIFUL DAY!!! I OPEEND MY EYES TODAY!!!!  

       

    Viewing 3 reply threads
    • Replies
        • November 26, 2014 at 1:57 am
        Happy_girl
        Participant

          Thanks for sharing these thoughts.  I can relate to themheart

            • November 26, 2014 at 7:45 pm
            Jubes
            Participant

              This forum is great. I really appreciate the answers to my questions from other ppl. I am in Australia though so chatting would be hard due to time difference. 🙂

              • November 26, 2014 at 7:45 pm
              Jubes
              Participant

                This forum is great. I really appreciate the answers to my questions from other ppl. I am in Australia though so chatting would be hard due to time difference. 🙂

                • November 26, 2014 at 7:45 pm
                Jubes
                Participant

                  This forum is great. I really appreciate the answers to my questions from other ppl. I am in Australia though so chatting would be hard due to time difference. 🙂

                • November 26, 2014 at 1:57 am
                Happy_girl
                Participant

                  Thanks for sharing these thoughts.  I can relate to themheart

                  • November 26, 2014 at 1:57 am
                  Happy_girl
                  Participant

                    Thanks for sharing these thoughts.  I can relate to themheart

                    • October 24, 2022 at 8:49 am
                    NancyGM
                    Participant
                      Carole,
                      Big congrats to you on your long term survivorship and positive attitude. I, too am a stage 4 no- evidence- of- disease (NED)melanoma survivor of 14 years. I rarely go on his forum anymore, but I hope those of us who have had full and durable results to treatments can give others hope!I used the chemotherapy pill Temodar( usually only used for brain metastasis)as a treatment for a metastasis in the mediastinum that could not be surgically removed. My Best wishes going out to all.
                  Viewing 3 reply threads
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