MS, my little buddyMS 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 LeeIt 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 DreamsI 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 meChoosing 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
My Ultimate ArchnemesisThroughout 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
"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 OthersI 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
Diplopia treatment expectationsHello, 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 damageI 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
Aids in the homeNever ever thought, I would be needing them, but here it is. Walk In Bath Tub, I love them. we installed one a couple years ago, of course that means...reactions1comment
My Dealings with MSI was first diagnosed in 2005 with Ms, the very first thing I did was cry! I thought how am I going to make it.. Well, I'm stubborn enough to...reactionscomments
How Can I Ask Without Sounding 'Needy'?I've always been an independent person - one to break the mold, intentionally or not. I had older sisters who set the mold -- high school, employment, pay room and...reactions2comments
Years and years...I've been doing a lot of reading lately of how and when others are being diagnosed with MS. The story seems similar in every blog, post, or story: "I was...reactionscomments
...I don't believe you ;)My name is Kasia and I am from Poland. My MS was diagnosed.. 11 years ago (oh.. i didn't realize so much time passed!). During this time I had only...reactions2comments
I have had enough.I am struggling since my diagnosis. The vision problems mostly with my right eye, pressure and just had it. My right foot hurts so bad that I don't want to...reactions2comments
At Least ModerateHaving had aggressive relapsing-remitting Multiple Sclerosis since I was at least 23, I have seen some of the best neurologists in New York, Maryland, and Connecticut. I've been written about...reactions2comments
