I have been asked to speak about how MS has changed my life . From the day of my diagnosis almost 14 years ago, I made myself a promise that I would never let it define me. I was in a very responsible job and could have easily given it all up but no way. If I tell you I have run 14 marathons since d...

My DR has reduced my pregabalin tablets too quickly I went in to a crisis and everything was making me catastrophise everything making it so hard on spasms and tears. I can't focus, contrate on anything and feel like I have too much going on in my mind and felt like I was losing my life. This was ...

I was expecting much more from it. My friend, who has MS as well , told me that as long as you don't get relapses, it's doing its job well. Thoughts?

What would you suggest?

Hi shift.ms users. I am ms patient with 5.5 edss. My doctor said to me i m jcv+ so wants to change my therapy. Anyone experienced this way-as i write on the topic.? Sorry for my low vocabulary 😅 Best wishes

I wish I would've got that doctor name i felt disrespected

I'm wondering if anyone else has experienced EHS / Exploding Head Syndrome (very appropriate name!) Since I had the relapse that led to my diagnosis in 2023, whenever I get very stressed, I experience this condition and it's when I'm falling asleep and it sounds like an explosion or someone loudly b...