Hi! I have recently been diagnosed with MS this past October, and the most difficult symptom has been the optic neuritis and the cognitive issues. I am a teacher, and I am finding it hard to remember student names, find the right words when teaching, and grading takes twice as long as I often have t...

Can someone guide me to through by connecting with me

Do you ever feel like you so not know what is worse ms or depression

Wondering how did you feel with the switch.

I was just diagnosed with MS in December 2025. I was hospitalized 4 days in high dose steroids and came home and it got worse. I got to the point where I couldn’t lift myself, walk, use my phone. I ended up falling. My boyfriend caught me and all I remember is thinking “just pull up your legs. Just ...

I recently had a relapse with my MS. My doctor has ordered me Acthar 4 day injection, 2 parts to this, has anyone taken this in place of steroids? Next, my medicine (aubagio) is not working anymore, my options are Tysabri, Ocrevus or Briumvi, I am leaning towards Briumvi, any feedback would be terri...

Good morning! I am new to this group and am excited to join in on everything! My MS story is long and complicated. I was just wondering how many of us have that electric shock feeling! It seems that is one thing that is rearing its ugly head lately!

Anyone deal with vertigo? This was my first time today. 😔

Hi, I was diagnosed June 2025 and still getting my head around things. Recently realised I’m still living a “normal” life which isn’t helpful. I need to adjust for things like rest and exercise. Did anyone reduce their hours? How do you factor in life…I also have two children! Thanks ☺️