Hey guys, I’ve been taking tecfidera for over two years and after a bad relapse have now been offered cladribine, lemtrada or fingolimod. I have chosen cladribine but have now found out that it isn’t actually available in my area yet and no idea of when it will be. Just wondered if anyo…

Hi I was diagnosed with MS in December 2017. My first episode happened in April 2017 with my eyes seeing double when I turned my head. I did everything the doctors have told me to do. The spinal tap was the key to say I have MS. I been taking Tecfidera since January 2018. Im fortunate that I’…

Hi everyone Does anyone else ever experience a cool sensation down their spine? It’s so subtle that it’s sometimes hard to distinguish. It’s a bit like a flush only with a cool sensation that starts at the neck and goes down the spine. It happens fairly infrequently and disappears…

Hi all, I am mid 20s newly diagnosed with MS. I was told a couple of years ago I had CIS after a tingly episode on my legs, but I quickly returned to normal life and its been sitting at back of my mind. However last week when I had my yearly MRI review they told me the classification has changed (…

I just started Tecfidera a couple days ago and so far so good. Can others share their experiences with Tecfidera?

Hi, (I used to have an account on shift.ms connected to my facebook but it won’t let me log in this way anymore- is anyone else having that problem??) I came on here to 1. rant and 2. get advice. I was diagnosed last year with MS after a bout of numbness from my chest down. Once this went aw…