MRF-Logo2019-Horizontal-RGB
Good Wishes.
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.

Good Wishes.

› Forums › General Melanoma Community › Good Wishes.

  • Post
    • July 28, 2010 at 7:23 pm
    Charlie S
    Participant
      Guess I didn’t get the memo about ALL the posts being moved to the archive.  Ouch.  Here’s hoping everybody catches on pretty quick.

       

      Charlie S

      Guess I didn’t get the memo about ALL the posts being moved to the archive.  Ouch.  Here’s hoping everybody catches on pretty quick.

       

      Charlie S

    Viewing 9 reply threads
    • Replies
        • July 28, 2010 at 9:23 pm
        talian44
        Guest

          gosh, things have changed.

          how do we post a new topic?

          just replying to see if this works

          miket

           

            • July 28, 2010 at 9:30 pm
            dian
            Participant

              talian..just clik on view all topics, then look at the top of the topics, you’ll see a spot that says "create new topic’

               

              dia

            • July 28, 2010 at 10:10 pm
            Fountainhead
            Participant

              Testing the anonymous reply.

              • July 28, 2010 at 10:19 pm
              Rebecca and Bob
              Participant

                I don’t really like this, although I’ll try not to be judgemental yet.

                • July 28, 2010 at 11:29 pm
                Janis B.
                Participant

                  I’ve been following this website for quite a while, but am just now jumping in because, Charlie S., I ‘m glad to see you back.  Over the past year, I’ve been informed, comforted, moved and enlightened by you and many others on this board.  So glad you are all here.

                  Diagnosed 8/08, now at Stage IIC w/ met. to just one lymph node, finished induction phase of interferon in 1/10, but was too sick to continue. NED at this time – just holding on, hoping for the best and grateful to be alive and feeling well today!  I’m sticking with you guys because you are smart!

                  janisgayle

                    • July 29, 2010 at 1:25 am
                    Sharon in Reno
                    Participant

                      just testing to see if I m doing it right?

                      Sharon in Reno

                    • July 29, 2010 at 12:03 pm
                    Lori C
                    Participant

                      Good to hear from you Charlie S.  I am still quite confused by the new forum and inching my way through it.

                      • July 29, 2010 at 1:04 pm
                      bill58
                      Participant

                        looks like everything is working.

                          • July 29, 2010 at 8:52 pm
                          Laurie from maine
                          Participant

                            This does take getting use to – I like that Charlie has a picture makes it more personal, assuming that is a picture of you, charlie?  would be interesting if more did that put faces to the names                                                                       

                            laurie

                            • July 29, 2010 at 11:50 pm
                            Charlie S
                            Participant

                              Yes, that is my true picture, just without eyeglasses.  I was sailing when that pic was taken.

                              Charlie S

                            • July 29, 2010 at 11:44 pm
                            jag
                            Participant

                               Charlie you did your best and didn’t get paid a dime(at least I would like to think that, so don’t say anything if you did)

                                • July 30, 2010 at 12:06 am
                                Charlie S
                                Participant

                                  I was only a small participant in the process and not and principle and no I didn’t get even a nickle, let alone a dime; truth be known, I was really only thrown a bone.

                                  I see you know how to read between the lines…………………..I DO hold nothing but good wishes though.

                                  Now if we can only turn it around to being a melanoma patients information board rather than a forum on how do you use this site.

                                  Cheers

                                • July 30, 2010 at 1:48 am
                                JoanR
                                Participant

                                  Thanks for all your diligent work Charles. I have been learning (other things) on computer all day, so this is just another problem on my list of things that are changing in my life. If an old dog like you can adjust, I should be able to as well….One good thing about getting old is that I can hardly remember what the old board looked like..LOL…now I am going to try to get on chat…

                                  • July 2, 2011 at 4:26 am
                                  JerryfromFauq
                                  Participant
                                    Are all the posts for the past 17 years in one archive now? Are is there a second archive been started?
                                    • July 2, 2011 at 4:26 am
                                    JerryfromFauq
                                    Participant
                                      Are all the posts for the past 17 years in one archive now? Are is there a second archive been started?
                                  Viewing 9 reply threads
                                  • 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