Loss of family...After being diagnosed with this horrible disease I feel very isolated. I'm at the point where I may be sitting on the...reactions4comments
My Husband Has MS...My husband was diagnosed with MS early 2002. To help him (and me) understand more - I started reading everything I could...reactions2comments
Asking for help (response to Stephanie's article)...I have spent my entire life being a help-ER, as in 'caregiver', helpful friend or neighbor. My parents were in their mid...reactionscomments
wobbly lady...I was diagnosed late I was given the news on my 52nd birthday after getting off the plane from Australia where the...reactionscomments
MS for 40+ years...MS has been a big part of my life for many years. First "episode" 1974 when my daughter was born. Officially diagnosed...reactions1comment
Newly diagnosed with Relapsing/Remitting MS...First, I would like to introduce myself. My name is Michele. I am 45 years old, and was officially diagnosed with Relapsing/Remittng...reactions3comments
MS THE NEVER ENDING BATTLE!!...I was diagnosed on April 1,2011 after fighting through 10 years of tests, MRIs, LPs and several neurologists. I was so worn...reactions1comment
I wonder, "why me"?...So when I was 14 years old, a freshman in high school I something told me there was something different about me...reactions1comment
Horrible disease but don't stop fighting!...Hi everyone! So I have a long story which I try to compress to make it not so long to read. I...reactionscomments
55 Life Lessons...I read Maria Shriver’s 60 best life lessons in honor of her turning 60. So, I thought in honor of me turning...reactionscomments
MS was the only thing I focused on...I was diagnosed in 2007 with RRMS. I worked 12 hr days 5-6 days a week as a QA Supervisor in a...reactions2comments
Silence is my name...What is in a name? My name is not really Silence, but Benjamin Franklin used it as a pseudonym, so can I...reactions4comments
The struggle is real....I was diagnosed 12 or 13 years ago. I can't remember really. Tragic events get blurry in my memory. But it gets...reactions1comment
M.S., my evil partner...Years ago I got epilepsy out of the blue and it took me a while to learn how to make decisions on...reactions3comments
It is what it is & I am slowly dealing with it......I am 37 & finally got diagnosed with RRMS after a year of tests and trials. It was a relief to finally...reactions3comments
Makes us stronger...I am determined not to let this disease define who I am, but it does define what I am fighting through my...reactions2comments
Strength...I was diagnosed several years ago with the illness. It's funny because if you didn't know me you would think I'm the...reactions8comments
How MS Helped Me See What the Holidays are Really About...Living with MS, there are always three things that I think about whenever I have to go somewhere for any length of...reactions2comments
New at this. Trying to figure it out...I am new at MS. PPMS is now in my vocabulary. Part of my job is being a researcher so research on...reactions2comments
Well Meaning Words, "But, You Look So Good!"...After living with RRMS for almost 30 years now, like others that have heard this said to them (But, You Look so...reactions6comments
