MS, my little buddy...MS you are such a joker! You make me play the fool, but I will foil you from behind with a sharp poker. You do not scare me MS, you...reactionscomments
Once a fighter always a fighter....I was raised in Christian schools all my life until I hit high school, then my parents placed me in a local public high school. I was trying to tell...reactionscomments
MS My Beginning, by Cheri Lee...It was the end of the summer 1997 and I thought I had the world by the seat of the pants. I was twenty-four years old and attending college, one...reactionscomments
Stem Cell Dreams...I know stem cell research is in its infancy, but I am still curious. Would it give me more mobility? Would I be able to climb stairs again? I'm certain...reactions1comment
To Lemtrada? or not to Lemtrada?...Hey guys, who of you here are on Lemtrada and how is it going for you? I've recently seen 3 neurologists (working together) who've come to the conclusion that Lemtrada...reactionscomments
My M.S....I would like to know a few things if somebody can help me. I have been on the infusions for 4 months. I'm not getting better...by far worse...I had a...reactionscomments
Less is more...unless you're me...Choosing to do less is hard. I am a chronic underachieving overachiever though so hopefully by cutting back I will do less but do it better. It is a struggle...reactionscomments
MS Is Picking Sides...Don’t ask me how I come up with the titles to these articles at times because I honestly couldn’t tell you. I promise I’m writing about something that does involve...reactions6comments
Odd "smell"...From time to time I have the sensation of a very disgusting, sickening smell. It's mostly if I am under a lot of stress. The scent is so overwhelming that...reactions14repliesSymptoms
My Ultimate Archnemesis...Throughout my life I have faced the relentless demand fatigue places on my body and well-being. Of all of the crippling effects of this chronic disease, it is the fatigue...reactionscomments
Managing bowel issues...My husband has had MS for over 20 years and has just recently began having constant bowel issues - either constipated or or running - never a "normal" routine. We've...reactions1replyCaregiving
"How can you even walk with numb feet?!"...My name is Marie. I am 22, born in Bavaria, Germany and I was diagnosed with RRMS only a month ago. To be honest, it almost was a relief to...reactions3comments
Sharing to Inspire Others...I want to share what I wrote last night. I was tired of giving this Monster my power, this was just my way of taking my power back. My hopes...reactionscomments
Where's more regarding primary progressive multiple sclerosis?...I am a 64 year old male, diagnosed 2 years ago. Everything I see and read pertains to RRMS. I have PPMS and never hear mention of this. I was...reactions2comments
Physical Therapy and the Promise of Improved Mobility, Strength, and Balance...Every so often, the nihilist in me comes to the surface. Not in a late 19 century Russian let’s-kill-the-Tsar-and-exile-all-the-aristocrats kind of way--and definitely not in a modern day ISIS extremist...reactions6comments
un diagnosed...I have had all signs of ms i finany find dr last year order test then lost insurance so no mri its really really scaring me lately im under a...reactions2repliesCoping
Community Rules...These rules apply to all activity on MultipleSclerosis.net or Health Union operated properties, including but not limited to the website, MultipleSclerosis.net Facebook pages, Instagram, etc. The term “activity” includes, but...
Four Tips To Help You Get Better Care From Your Doctor And Pharmacist...“Sorry, but we never received your prescription. You better call your doctor.”“We sent your prescription refill to your pharmacy a few days ago. Call them back and tell them to...reactions6comments
Diplopia treatment expectations...Hello, I have just finished 5 days of steroidal IV treatment for diplopia. I am not yet experiencing any improvement from that treatment as my double vision persists. Does anyone...reactions1comment
mild damage...I went to see my neurologist today, who repeatedly told me my disease was mild, the damage was mild, & I should be living normally. I'm not living normally; I...reactions2comments
