The Art of Moving Forward...“Golly gee willakers, I’m glad I have MS,” said no one ever, as they went merrily skipping and zip-a-dee-doo-daaing down the street...reactions2comments
FeaturedNew To This...I just received my ms diagnosis today. Tomorrow my dr and I are going to talk about where we go from here...reactions25repliesCoping
Support the MS Community with Your Holiday Shopping...The end of the year is the most popular time for people to support the causes they care about. These holiday year-end...reactionscomments
MS, Diet, and Humor: Get Off My Lawn...I posted a controversial photo on Facebook last year: It was labeled “Paraplegic Twister,” and it showed a guy in a wheelchair...reactions7comments
Tips for Keeping Up with the Latest MS Info...It is quite a struggle some days to stay current on the latest studies, webinar presentations, and newly-released MS disease-modifying therapies. As a...reactions3comments
Clumsy Me...I think about my M.S. every day. Now that my husband is retired, I think about it much more. He's very active...reactions2comments
Oreosdad...I’m in my mid-50s and have been diagnosed with multiple sclerosis for over a decade. It continues to progress and create new...reactions2comments
Trouble With Social Cues: Social Cognitive Deficits With MS...Recently, I was talking to another person with multiple sclerosis, and she mentioned that she believed she was having trouble understanding when...reactions36comments
No. You Can't Take My Life!...MS has been a part of me for over 30 years, but I have been determined to maintain goals, preserve old friendships...reactions2comments
Has anyone with RRMS had any experience with MS combined with immunotherapy?...I have RRMS and was recently diagnosed with stage 4 lung cancer that has metastasized to my brain...looking for advice/experience/information regarding MS...reactions1reply
Hi all, please can someone give me advice?...Hi all, please can someone give me advice? For the last 18 months, I’ve been going downhill and when trying to get...reactions4repliesUndiagnosed/Seeking Diagnosis
I Do Not Know How to Ask for Help...In the multiple sclerosis community, asking for help is highly encouraged! We are generous with each other. We share our time. We...reactions19comments
Frustrated...I'm 47 and have had bizarre symptoms for months now. It all started with blurry vision, my feet and hands tingle, night...reactions3comments
Caregiver Resources: Where Caregivers Can Go for Support...Millions of people are caring for loved ones who are sick or disabled. In fact, some 25 percent of U.S. adults report...reactions1comment
How I Can Tell I'm Having a Relapse...Folks, to be completely honest, I can’t think of a single relapse that I could identify as being one. My hat goes...reactions25comments
Living on the River of Denial...I was diagnosed at age 33.I think I had it prior to that. My ex-husband (a medical professional) and my children were...reactions2comments
MS Spasticity: Down With the Stiffness...Today is one of those days that required an extra cup of coffee for me to even think about going through with...reactions15comments
MS, the Birth of My Triplets, and the Aftermath...I will never forget the fear and anxiety I felt knowing not only was I about to welcome three babies into the...reactions2comments
Disclosing MS On the Job: Why I Did, and Why I Didn't...The question regarding disclosure of your MS at your workplace is really a lot more complicated than simply deciding to ‘fess up...reactions15comments
My Name Is Tom, and Here Is My Story...Hello, My name is Tom, age 49. I grew up in the Chicagoland area until I moved to Portland, Oregon after a...reactions7comments
