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We are new to the group ! Let me introduce our selfs April and Bernie Hester , trail name mule and inchworm. I , April (inchworm) has. MS and been diagnosed for 20 years. I have foot drop after a while I have Balance problems and bladder problems that come with MS. Living with this and having 6 boy...

Hey! My name is Drew. I live in Louisville, KY, USA I was diagnosed in 2011, but fear I've had MS much longer. I have been wheelchair bound since 2016 and am currently on Ocrevus. Some one needs to create an app! #MSWarrior #MSStrong

New to this group, looking forward to chatting and discussing with each of you..#MSSTRONG🧡💪🏾

How do you always deal with the whole 24/7 pain?

Does anyone else really struggle with the heat? It makes me so tired!! x

Hey all!! I'm Jamie, from Canada. About a year ago I started experiencing days of extreme stomach burning/tightening. In the Spring, I started experiencing numbness in my right foot/toes which has now turned into an almost daily occurrence but also including my hand/fingers, leg, back of arm, face a...

For years my family and partner have been on at me to improve my diet and take vitamins etc to get a good immune system going, a strong one. Since the medication I'm on aims to reduce my immune system i.e. white blood cell count, why do I want a good immune system? Why do I want to increase my whit...

As many people know I was diagnosed at 23 with my whole life in front of me. I thought it was a death sentence. Since then have had 1 child now 23 and a stepdaughter. I have been married 2 times but I have been with my husband now for 20 years. He is awesome! I was on Avonex for 20 years but it ...

Hi All A newbie here.... had second relapse recently and only joined forum last week, great info, and starting to get to know some folks hopefully meet up for chats at some point... I read all sorts of opinions on mild, medium, strong relapses and appreciate the scope is significant here but wonder...