Hi all, Sorry I haven’t participated in the forum since I joined although I have popped in now and again. I just felt I needed time to accept everything in my own way and to try and be positive. So for the last 2 years have been trying to come to terms with the many life changes MS has dealt…

I need my ms buddies to give me the run down on what med they take. Tysabri was great I only had 1 infusion a neuro gave it to me while I was recovering from a relapse in March (he took me under his wing so to say) but I moved to Clarksville and the after effects of not having it for about three mo…

Hi All Well as far as Mondays go this one has been pretty rubbish! My Dad saw someone at local memory clinic and they think he may have the start of Alzheimers. I then saw Specialist for annual check up and my lymph count has dropped to 0.4. I have another blood test in a month and if hasn’t incr…

Hi guys, again I am reaching out for some support from the community. After discovering that my lessions have trippled in 4 years, well after some discussing around with my doctor …we decided to probably change from avonex (was also causing some midld depression probably) to another med that …

Hi all, My story begun around 8 months ago. I have not been feeling well and my doctor ordered MRI along with many other investigations. My MRI showed multiple lesions “suggestive of disease of deminatig nature”. My nuerologist started me on avonex, although I do not have symptoms that are typi…

MRI results are the same nothing has changed but she got furious because its active she wants me to go on avonex i said no then she said wait then neurobis gonna decide what oral treatment is best for you :/