Announcement

Collapse
No announcement yet.

Calling all Canadians

Collapse
This is a sticky topic.
X
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

    loosing weight

    I am with M.S. for about 10 years now.
    I am on betaseron for about one & half years.
    I lost about 15 Kg.
    also my blood test is not good showing lower values of R.B.C. & W.B.C. & plaquet.
    Would you comment about this.

    I live in Iran & we donot have very good doctors
    unfortunately

    With my best wishes

    Comment


      new canuck

      Hi Everyone
      I am new and want to know how the forum time-line works. I wanted to view last posts, but it seem to be scrambled.

      I am under investigation for MS and are having a lot of GRRRRRRRRRR moments in frustration over how I am getting treated (like a nut-case)! I have even been sent to mental health specialists (3!) who sent me back to the Neuro.
      GRRRR.

      Good luck to everyone else dealing with the symptoms and system.

      Daysie

      Comment


        CLEAR

        Thanks Sparky, yes it does.
        Daysie

        Comment


          Hi everyone

          My names Tracey, I'm from Guelph Ontario.
          I was diagnosed with MS Sept/2007. I've been on Rebif and Copaxone, was allergic to both, so on nothing right now.

          I was a hairstylist, but haven't worked since the hospitalisation in Sept.

          I'm happy to have found this site, nice to know I'm not alone.

          Comment


            Hi Tracey - Welcome to the boards. You will find lots of information and support here.
            Sorry you had such an allergic reaction to the meds. Have you been presented with other options?

            Comment


              Indoor Row for MS - Fundraising Challenge for Niagara Peninsula Chapter of Hope

              Indoor Row for MS - Fundraising Challenge

              Venue: Welland Rose Festival, Family Day Weekend in the Welland Arena, King St., Welland, Ontario, Canada

              Date: Saturday, June 14, 2008 - tentatively 10 a.m.-6 p.m.

              Equipment: Erg(s) to be provided by Notre Dame College School Rowing Team

              Assistance: Notre Dame College School Rowing Team - their Head Coach has offered whatever support is needed.

              Please contact me if you are able to assist with the event as a volunteer, sponsor or participant and I will provide further details as they become available.

              The idea is to challenge festival attendees to participate by rowing a few metres to keep the 'erg in motion for MS' during the entire 8 hour event to make the pledge donations grow. The goal is at least 4 sponsors to pledge challenge money per metre rowed during the event. eg. $0.01/m; $100.00/25,000km; bonus amt. if 100,000km rowed. Of course any and all donations are greatly appreciated!

              Stay inspired!
              Michelle
              brainangles@cogeco.ca
              Expand your mind ~ visit http://www.brainangles.zoomshare.com
              Each smile, each laugh, each tear, is a moment lived.
              Moments tend to expand when shared.

              Comment


                Hi guys(all 2 of ya eh?)I'm from Nova Scotia and have RPMS.Was dx'd in 90 with progressive ms but had RRMS for 7 yrs before dx.I am a fulltime wheelchair jockey and only take LDN for my ms.

                Bob

                Comment


                  Nova Scotia here too! I'm in Halifax and was Dxed RRMS 2 years ago.
                  Take care,
                  Janice

                  Comment


                    Hiya Janice,I'm in Saulnierville(close to Yarmouth)

                    Comment


                      Welcome Boba! Nice to see another Bluenoser on the boards!
                      Take care,
                      Janice

                      Comment


                        Nova Scotia here also. Caper born and bred!

                        Comment


                          I live in Brampton, ON.

                          Diagnosed on March 6, 2008.

                          Comment


                            Originally posted by Boondocks View Post
                            Nova Scotia here too! I'm in Halifax and was Dxed RRMS 2 years ago.

                            Hi Boondocks I have to visit the clinic in a week for the first time to see Dr. Bhan. I was just wondering what to expect on my initial visit. Thanks for your help!!!

                            Comment


                              Nova Scotia

                              Hey there Nova Scotians! I'll be heading back to Antigonish in August (I've been away in California for a year). Before I left I was going to Sydney to see a Neurologist. My husband and I have decided that we would like to get a Neuro in Halifax. Is there anyone you recommend? How is Dr. Bhan? Can you tell me a little about him/her? Do you actually get to see the Neuro when you visit or do you just see an MS nurse? Would you message me your input?
                              EliTy
                              DX: RRMS November 15th 2006
                              Rebif: 12/29/06 - 11/05/08
                              LDN: 03/08/12

                              Comment


                                Hello everyone!

                                Hi everyone! This is my first post ever- wanted to say hi to all you crazy Canucks.
                                I'm 39 F, born in Toronto, now living about 3hrs northeast of T.O.
                                I was dx in June 05 with rrms, only had 2 episodes one bout of double vision, and the next year optic neuritis. Been on Avonex for about 2+ years and since then no new relapses.
                                Anyway it will be fun getting to know all of you thx for listening!!!

                                Comment

                                Working...
                                X