Well the fatigue has hit me hard! I had a busy weekend. Drove 3 hours to my sisters hen do. Danced the night away and drove back 3 hours home the nexr day. That was monday. Today I cant get out of bed. My feet are tight and achy and I cannot keep my eyes open. I know I should take it easy until my t...

Hey everyone... been a while since I was last on this 🙄 hows everyone doing? Anyone had an absoloute slap in the face with their fatigue... im talking ten fold... Also had tingly pins n needles in my left hand and arm and arms went quite weak/heavy ... This s**t never ends eh 🙄🙄

So its been a little while since I posted i tend to go through phases of addressing my MS and other times completely denying mentally to myself that I have it. So when I am denying it I don't tend to come on here. Nothing personal to anyone or the community just what I do. Any who the reason for my...

MS can onset Dementia? 🤔

I am very newly diagnosed. I have started experiencing more body jerks. It’s my upper torso and legs, sometimes including my shoulders and arms at the same time. I’ve always had my legs do it, but now it’s getting more aggressive and moving in my stomach and upper body. It’s quick and very annoying....

I feel so alone in all of this. My husband keeps comparing me to his friends wife who “has MS worse then me”. I can’t talk to him about anything or it turns into “well my buddy’s wife …”. I’m so tired of feeling so alone and not having any support with this disease. Especially from the man who I cho...

I am JC+ after ten years on Tysabri and terrified of getting PML. I’m so stressed with this and a bunch of other things in life happening that I’ve got a flare-up after ten years of smooth sailing. Anyone else JC+? How do you stay calm about the potential of PML? Thank you!

This is terrible. I have this swimming dizzy feeling 24/7. It is relentless. Has anyone had this? They say from a lesion on my cerebellum and it should go away. Have had it for two months. I cry every day.