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...

What are people taking for chronic back pain? I’m currently not taking anything as nothing has worked. I have been prescribed a few things already but not worked. Paracetamol, Codeine, Amitriptyline, Naproxen and Pregablin. The docs are maybe suggesting another neuropathic drug, maybe Gabapentin. An...

Having a hard time adjusting to my new lifestyle I know it's better for me but after 44 years of the same things trying to change is so hard and I feel like I have to do it all at once how do I handle this im hungry all the time I need a cigarette and my mind is all over the place can't sleep im jus...

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...

Multiple sclerosis certified specialist physical therapist… regular thearpy just does not work wants to show you how to use a walker rather than doing specific excercises to improve gait smh

Hi, new here, diagnosis of 2 years but on going for 10, biggest symptoms are with footdrop and leg weakness. Also weird stomach sensitivity. Not to mention the mental stuff going on inside. Anyway just wanted to say hi

For those of you on Mavenclad, I am curious to know if MRIs have showed any new lesions developing the first 2 years of treatment or in the following years?

I’ve been in the hospital for the past two days dealing with a MS flare up. Just got off the hospital yesterday now my son is in the hospital because he has Sickle Cell. I am exhausted 🥱!! Send Help!!