Hello, I am a new member to this chat room. I have never talk about my disease to anyone in any chat room. Just my spouse and close family, friends. I am in a...
Hi New Member: I was diagnosed in 2003 and have been o.k lately. I've gotten bad and am not taking my Rebif meds. I call it being lazy but I really think I...
Welcome to the group!!!!!! Everybody has there good days & there BAD day. We all understand wha it's like. SOme of us have simialar symptoms BUT there is also...
Hi tarousson (and anyone else out there in need of a shoulder) I am sorry to hear you are really down at the moment, perhaps you'd like to come to the MSRC...
Thamks so much for the email. Maybe I'll try that chat room out. The computer isn't always accessible, but i'll give it a try as soon as i can. Terri-Ann ...
Thanks for the welcome mat. I hope that this will help me deal easier if i talk to other people. Talk to ya soon. Terri-Ann jen auger <fryflymom@...>...
Hi Sara, I went through that point where I hardly ever took my copaxone. I still miss some here and there when I'm really tired or am suffering with a major...
Hi Terri-Ann: Yes I am so tired too, it hits me like a wall sometims. I am going to make an appointment with my neuro about my Rebif. Thanks for joining us,...
Just wondering if anyone else has been dx with a rare form of MS that mimics a brain tumor. I go at the end of the week for another MRI to confirm the dx. I...
l'm sorry to read about your difficult time the past six weeks. l have never heard of a dx of ms that mimics a brain tumour. Besides ms sites have you checked...
l have been on rebif for 18 months. l think its working for me as l feel better now than l have for past 2 yrs. l have recently been told by the ms clinic...
Hi My name is Jen and I have been looking for a support group. I've been looking to talk with others about similar situations dealing with MS. I was diagnosed...
Hi Jen, which therapy? are you thinking about?? I've been on Avonex for along time, & it's been working for me! I know people on Copaxone & Rebiff...so it's a...
Hiya... I posted a message here awhile ago and appreciate the responses. I have been diagnosed with Relapsing Remitting MS and am currently doing my research...
Hi Leigh Thanks for responding. Im thinking about Rebif. Avonnex didnt appeal because it is a muscular shot but the plus side to that would be its only once a...
Well Lynn, It's a personal choice! My choice was once a week verses every otherday! Leigh! chimo_36 <chimo_36@...> wrote: Hiya... I posted a message here...
Hi, I am hopeing I am welcome here as I recently diagnosed with second stage MS and I have not alot of ppl I can talk about how this has affected me and the...
Hi!, My name is Leigh...I think this is good for you to vent & talk to other People with the same concerns! Well, Missy, I'm always online..keep your head up! ...
Hi I am Steve from M.S. Means!I wan't to tell you all about a story about M.S. I have a very progressive form of M.S., as a matter of fact. I have been dx with...
Steve, thank you for letting everyone know that a "cranky cripple!" is no fun!! I vowed to never be that way??? But , sometimes it just shows up!!? I have...
I recently was diagnosised with MS after my second MRI and positive lumbar puncture. Now I'm just waiting for an appointment with the MS Clinic in Halifax....
Hi there, I am from Halifax too, and never really had any wait time. My neurologist is Dr Bahn.. You should call the clinic if you have not heard and ask them...
Hi Angele, l was diagnosed Dec 2003. l waited 3 weeks to talk to a nurse at the ms clinic. She discussed the problems l had, explained ms and the different...
Thank you Lisa and Emily for your replies. I feel better knowing that it's not going to be a 6 months wait. My GP had sent a referal letter about three weeks...
Hi and yes there are still some posts etc ,nice to meet you and send a quick email.hope you have a good week darkchocolat45 <darkchocolat45@...> wrote:Hi...
Hi there, Yes there are people still out there. Some of us are getting oriented with our kids on a new school year. It is like getting used to a new schedule,...
Yes I'm here. Will talk to you later, Sarah ... Sarah Slater R.N (Done school, get my BScN this fall!) [Non-text portions of this message have been removed]...
Here is a new symptom for you folks. Three weeks ago I had a seizure! Don't get alarmed only 6% of people with M.S. have this symptom. This was my first one;...
