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Hi all. Does anyone have any experiences of taking Amantadine for MS fatigue. I am currently taking modafinil x 2 100g first thing each day but still suffer from chronic fatigue in the afternoons. MS Nurse has recommended switching to Amantadine. I’m happy to switch but reluctant to give up moda...

I was just diagnosed with benign MS not quite sure about it as of yet, all I know is my symptoms with Tingling in the scalp, right arm, pain in those areas also plus right leg, are very real, but I guess will know more once I get to see the MS specialist

Since getting numb lower legs I found if I lay on my back in bed keeping legs straight..its impossible now to lift legs up off bed..i try one then the other..no solid weights won't move! Now this last week I can't roll over off my back..i have to draw knees up and flop knees over if I want to get on...

Hi everyone! I hope you are all doing well! I’m writing this bc I am an RN and I worked in Urgent Care working 12 + hours three days a week, and I accepted a new job working in outpatient surgery (better hours, pay, and health insurance benefits) I’m nervous bc I am new to working in surgery. Are th...

Just received result of annual MRI of brain and CSP. Quick recap is diagnosed w MS 1998. No DMT or identifiable symptoms until 2017, been on copaxone for 3 years. Most recent MRI says new lesion r fr lobe, and a Highlighting peri ventricular lesion which is also new. I’m feeling a bit alarmed! I ...

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Hi i was diagnosed with RRMS in 2012 when i was 26. Now 33 I've tried Copaxone, Gylenya and am on my second year of Mavenclad. With Copaxone i had a relapse and never felt any relief. Also i have permanent divots in my legs and arm because of it. Gylenya I was happy with but still finding symptoms w...

Hi all, hope everyone is doing ok Slightly confusing situation here: i got diagnosed with RRMS in 2018. I had a brain and neck/spine MRI and my brain looked normal but i had 3 lesions on my C spine which accounted for my symptoms. Fast forward to a few a weeks ago and my neuro sent me for another MR...

2001 Optic neuritis. Go blind suddenly - and fortunately temporarily - in one eye. Ophthalmologist sends me to neurologist. The neurologist tells me in a jovial tone to say that I have had optic neuropathy to insurers - if I say optic neuritis they’d put me down as having MS. MRI done. No follow up...

I sleep great in day but cannot sleep at night is this common? I have ppms and other health problems. I seem to clime in tub as my legs and lower back hurts I will go to sleep too