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Hoping someone can relate to my comment here! I think I’m on the limbo of a diagnosis too! My doctor first said I had one spot that was suspicious for MS then I had another mri and now it’s a few ??!! This was her message “No new spots on your brain, a few spots that are suspicious for MS but not ve...

Hi everyone. I have RRMS but I believe I might be progressing to different type. This disease can be so frustrating at times. I can't get an appointment with my neuro until next month and my symptoms are increasing. I don't currently take a DMT - I had a bad reaction to Copaxone and haven't wanted ...

I was diagnosed on January 6, 2020. I have a heavy disease burden with almost all of my lesions in my brain. I started taking Tecfidera shortly after. Every MRI I have had except one showed new brain lesions. So now I'm on Ocrevus. My memory has progressively become worse. I forget words, names, an...

Hi everyone, hope you are as well as can be🙂 I had my last MRI a year ago this was of my brain and spine as I have lesions in both areas. I'm due to have another MRI soon however it's only of my brain 🧠 not my spine is this normal? If you have lesions on your brain and spine are your annual MRIs o...

Hello friends, My name is Austin & my recent diagnosis has my brain completely twisted up. I am really hoping to find knowledge and support through this forum. I know not how to handle such a curveball in life… google can only say so much to me… i hope to find peoples with personal experiences t...

I was diagnosed about a year ago with RRMS. I'm interested to find out what kind of accommodations your employers have given you to help you continue working with MS. For nearly twenty years, I have worked as a software project manager. This means I am in a leadership position with constantly changi...

Lot of brain fog over the last few days but I'm on my knees just about looking after my dad looking like lewys dementia. Just stress or relapse? What would you do enough more fog to notice!

Hi all, new to this but I'm married, 48yrs old and have a son who is 12yrs old. I love them both dearly. I was diagnosed with M.S in 2008. A very long story and it is all about my relapsing of M.S. Gosh this is embarrassing, my speech can be very very confusing and hard to understand if words are no...

Finally after 2.5 years I've received a formal diagnosis. This was not a shock to me as my Neurologist had said after my first MRI it couldn't be anything else. Following my latest MRI the Radiologist found a new brain lesion described by my Neurologist as "tiny" and that he wasn’t convinced. My N...

Hi everyone. My family physician believes I have MS- i have issues swallowing and speaking, bowel bladder problems, numbness/tingling to the point that I couldnt feel my legs and went to emerg, cognitive issues severe fatigue- however when my neurologist sent me for an MRI he said it came back looki...