Hello all! I’m not really sure what I’m saying here but I was recently diagnosed with RRMS and I’m currently going through the teething stages of understanding all the information which I’m being presented and about to start DMD. Just thought I’d say a little hi to everyone 😃

Hi! I am new to this forum and I want to share some important information with MS patients and their families. My name is Matt Embry and I have MS. I have recently completed a documentary about MS that is being seen all over the world and I want to share an important scene that I think everyone wit…

I have been diagnosed with RRMS since October of 2015 & have no relapses. Could I have the benign form of MS? How do I know for sure?

Hello everyone. I am new here, my husband has RRMS and was diagnosed 5 years ago at age 31. Symptomatically he is doing well, however his MRI’s show new disease activity. My husband was on Copaxone for a few years however he had a bad skin reaction to it and went off treatment entirely. The n…

Hi Happy Sunday I just want to hear wether their are any recovery stories or remission stories from ms … MS hope stories — I and I am sure many others would like to hear about what you are doing.. I love to here what might be helpful and important for me to add to my day …. Thanks g…

Hi everyone, I’m new to this site. I was diagnosed with RRMS just over 2 years ago & was put straight on to Tysabri as I was JC virus negative. It has worked so well for me & was a perfect fit. Unfortunately my nurse rung yesterday & I have now become positive. I’m looking a…