MRF-Logo2019-Horizontal-RGB
MPIP Chat Tues. thru Thurs. evening 7 PM EST til……????
REGISTER
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.

MPIP Chat Tues. thru Thurs. evening 7 PM EST til……????

› Forums › Caregiver Community › MPIP Chat Tues. thru Thurs. evening 7 PM EST til……????

  • Post
    • February 11, 2013 at 11:50 pm
    Carole K
    Participant

      The last person leaves.  I have sent e-mails to other Old Timers from MPIP to ask them to meet in chat tomorrow night thru Thurs.  at 7 PM EST. until the last one leaves. We have patients/caregivers from the East Coast as well as the WEst Coast so I am sure many of us will come and go.  Most of the people who I think will be there are LONG TERM SURVIVORS with incredible stories of hope for those of you who would like to chat with us.  Know many of us are there to help you during these difficult times.  Hang in there.

      Love and Light

      Carole

      The last person leaves.  I have sent e-mails to other Old Timers from MPIP to ask them to meet in chat tomorrow night thru Thurs.  at 7 PM EST. until the last one leaves. We have patients/caregivers from the East Coast as well as the WEst Coast so I am sure many of us will come and go.  Most of the people who I think will be there are LONG TERM SURVIVORS with incredible stories of hope for those of you who would like to chat with us.  Know many of us are there to help you during these difficult times.  Hang in there.

      Love and Light

      Carole

    Viewing 2 reply threads
    • Replies
        • February 12, 2013 at 3:22 am
        Charlie S
        Participant

          It is welcome and refreshing that you have a re-newed interest in this forum Carole 

          Not that many  know the origin of this website where our host and the participants had few avenues of accurate diagnosis, fewer pathways to second opinions, extremely limited cliical trials; and for the most part we were all dead people walking, but we all had a commond bond via MPIP of sharing of our then orpan disease. 

          That point of origin was well over a decade ago and though some online folks may say a decade ago has no relevance online today as a soltion, I would differ.

          What Carole is offering is an invitation to share the benefit of experience. the benefit of sharing  itself  and an open hand that we ARE truly in this together.

          Or not. (smirk)

          But I am in for chat !

           

          Cheers,

          Charlie S 

          • February 12, 2013 at 3:22 am
          Charlie S
          Participant

            It is welcome and refreshing that you have a re-newed interest in this forum Carole 

            Not that many  know the origin of this website where our host and the participants had few avenues of accurate diagnosis, fewer pathways to second opinions, extremely limited cliical trials; and for the most part we were all dead people walking, but we all had a commond bond via MPIP of sharing of our then orpan disease. 

            That point of origin was well over a decade ago and though some online folks may say a decade ago has no relevance online today as a soltion, I would differ.

            What Carole is offering is an invitation to share the benefit of experience. the benefit of sharing  itself  and an open hand that we ARE truly in this together.

            Or not. (smirk)

            But I am in for chat !

             

            Cheers,

            Charlie S 

            • February 12, 2013 at 3:22 am
            Charlie S
            Participant

              It is welcome and refreshing that you have a re-newed interest in this forum Carole 

              Not that many  know the origin of this website where our host and the participants had few avenues of accurate diagnosis, fewer pathways to second opinions, extremely limited cliical trials; and for the most part we were all dead people walking, but we all had a commond bond via MPIP of sharing of our then orpan disease. 

              That point of origin was well over a decade ago and though some online folks may say a decade ago has no relevance online today as a soltion, I would differ.

              What Carole is offering is an invitation to share the benefit of experience. the benefit of sharing  itself  and an open hand that we ARE truly in this together.

              Or not. (smirk)

              But I am in for chat !

               

              Cheers,

              Charlie S 

          Viewing 2 reply threads

          Tagged: 

          • You must be logged in to reply to this topic.
          About the MRF Patient Forum

          The MRF Patient Forum is the oldest and largest online community of people affected by melanoma. It is designed to provide peer support and information to caregivers, patients, family and friends. There is no better place to discuss different parts of your journey with this cancer and find the friends and support resources to make that journey more bearable.

          The information on the forum is open and accessible to everyone. To add a new topic or to post a reply, you must be a registered user. Please note that you will be able to post both topics and replies anonymously even though you are logged in. All posts must abide by MRF posting policies.

          Popular Topics