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    Where Are They?

    Craig Mathias, Ian Parbery, Liane from England, BubblePerson?
    Does anyone know or care. LOL!

    Who are you missing and where are they?
    Love, Sally


    "The best way out is always through". Robert Frost







    #2
    I think Ian is on Facebook but I'm not sure about the rest.


    Whatever happens around you, don't take it personally. Nothing other people do is because of you. It is because of themselves. -- Miguel Ruiz

    Comment


      #3
      And what ever happened to Howie?

      Never mind, I found him.
      "Given the millions of billions of Earth-like planets, life elsewhere in the Universe without a doubt, does exist."

      Albert Einstein

      Comment


        #4
        Originally posted by Howie View Post
        And what ever happened to Howie?

        Never mind, I found him.

        Howie is still looking for Sponge bob!
        Love, Sally


        "The best way out is always through". Robert Frost






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          #5
          Harpist (Good Roads)
          Bou
          Lady
          Whisper (Lorraine)

          Just a few that I thought of.

          Comment


            #6
            I don't know where any of these people are. I haven't talked to Harpist in years, mostly my fault, darn computer.
            s
            Jendie
            I've been a member of this forum during its different incarnations since I was dx in 9/98

            Comment


              #7
              Bou was here briefly a while back but vanished.

              Whisper (Lorraine) is definitely around. She was last here November 11. I believe she drops in only now and then.

              Lady decided to leave some years ago and I'm not sure why except that she might have been getting too tired. I've tried to reach her without success.

              One new member, Mike (mchlkirk77) was last heard from on December 6 and was coming down with the flu. Hope you're better, Mike.


              An MS online support message board is something people might find depressing or disturbing. There are people who have MS but would prefer not to think about it. I can understand that.

              There are others who genuinely want to help others with MS and/or who want to share information here.

              The Internet is full of distractions, and people who might be taking part here are probably elsewhere on the Internet. Thinking about MS can be a real downer.


              Maybe some of the people who used to be here will come back, or new people will find us. It will dawn on them at last that we really have something to offer that you can't get anywhere else.

              Namely, Howie!
              SPMS diagnosed 1980. Avonex 2001-2004. Copaxone 2006-2009. Glatopa (glatiramer acetate = Copaxone) 12/20 - 3/19/24.

              Comment


                #8
                ...........this darn hat fit me just fine yesterday........
                "Given the millions of billions of Earth-like planets, life elsewhere in the Universe without a doubt, does exist."

                Albert Einstein

                Comment


                  #9
                  Originally posted by agate View Post
                  An MS online support message board is something people might find depressing or disturbing. There are people who have MS but would prefer not to think about it. I can understand that.

                  There are others who genuinely want to help others with MS and/or who want to share information here.

                  The Internet is full of distractions, and people who might be taking part here are probably elsewhere on the Internet. Thinking about MS can be a real downer.


                  Maybe some of the people who used to be here will come back, or new people will find us. It will dawn on them at last that we really have something to offer that you can't get anywhere else.

                  Namely, Howie!
                  I hear ya, agate.

                  I found the MGH MS message board in 1998. I was newly dx and wanted an idea what to expect and made a lot of friends, like Howie, Cherie, Harpist, Sally, Cat, and others. If I didn't name someone, just blame MS, it has stolen a lot of things from me.

                  I love the humor that can be found here. I strongly believe that humor is the best medicine.
                  s
                  Jendie
                  I've been a member of this forum during its different incarnations since I was dx in 9/98

                  Comment


                    #10
                    I found Craig on MSWorld. He's still hanging in there.


                    Whatever happens around you, don't take it personally. Nothing other people do is because of you. It is because of themselves. -- Miguel Ruiz

                    Comment


                      #11
                      There are lurkers, people who check in and read here but don't post. Nothing wrong with that of course. At least one person who has been mentioned in this thread was last seen here only a couple of months ago.
                      Last edited by agate; 12-21-2015, 06:11 PM.
                      SPMS diagnosed 1980. Avonex 2001-2004. Copaxone 2006-2009. Glatopa (glatiramer acetate = Copaxone) 12/20 - 3/19/24.

                      Comment


                        #12
                        Sally, I was thinking of Lianne recently.

                        Lady said she was leaving to take care is some medical issues. I haven't seen her since.

                        Remember Parrot Lady?
                        There comes a time when silence is betrayal.- MLK

                        Comment


                          #13
                          ((((((Hugs to All)))))) ~

                          I often think of and pray for Gabriella and Abby, both of whom were struggling with serious illnesses, when they last posted here.

                          On the Child Neurology forum, we had a major migration away from our forum to other venues, primarily Facebook. I miss everyone, who once was active here and there, as you all do, and wonder how they are.

                          I hope that your former members will check in here and at least give you an update.

                          Wishing everyone healthy, happy holidays ~

                          Love & Light,

                          Rose
                          Mom to Jon, 49, & Michael, 32, born with an undiagnosed progressive neuromuscular disease. Angel Michael received his wings in 2003. Angel Jon received his wings in 2019. In 2020, Jim, their Dad, joined them.

                          Comment


                            #14
                            I go to Facebook daily, but there doesn't seem to be the "connection" with people, that I do here. Everyone I really connect with there, I know from here. Otherwise, it feels "impersonal". I prefer here!
                            "Given the millions of billions of Earth-like planets, life elsewhere in the Universe without a doubt, does exist."

                            Albert Einstein

                            Comment


                              #15
                              And I just noticed I am the last poster on the last 3 posts.

                              "You're tearing me apart!" James Dean
                              "Given the millions of billions of Earth-like planets, life elsewhere in the Universe without a doubt, does exist."

                              Albert Einstein

                              Comment

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