Having Multiple Sclerosis in the Heat of a PandemicI have had MS for 17 years and my symptoms are stable, manageable and invisible to most. The COVID-19 pandemic has made...reactions1comment
A Blurry Review MirrorI’m a white male, soon to be 68 years old, and have had ms for almost 40 years. Enough of the war...reactions3comments
CRASHmy grandsons and i were out playing in the dunes with our toys and like any grandma wants to keep up as...reactions5comments
My MS StoryEveryone has a story and a good writer can make anyone's story interesting. I'm not overly confident about many things in life;...reactions2comments
A day in the Life of an MSerExplaining a day in the life of an MSer is so different from person to person and female to male. MS impacts...reactions9comments
The Storm in my BodyIt's almost as if someone replaces the water in the lake every day. Every day, I swim. Every day, the water is...reactions5comments
Cognitive Dysfunction: A Scary and Invisible FightI’ve battled multiple sclerosis for fifteen years. Over that time, it has affected my ability to walk, hold objects, and to see...reactions52comments
Living alone and being alone are very differentI never thought of myself as being that creative of an artist but this is one thing I did take the time...reactions2comments
To See or Not To See is Professor Uthoff’s QuestionYou might be scratching your head about now wondering what the heck I mean. Not sure about you but vision is one...reactions5comments
Dating Someone with MSHello to whoever read this. My writing in English is not perfect. I saw this wed site and I have been reading...reactions5comments
The Art of Falling Gracefully with a smile, laugh, and maybe an OuchI know you cannot even imagine why someone with MS would fall. It is just hard to believe with such bad balance...reactions6comments
Life Changes after MS or does it?Life was just another day of work and fun in the sun before MS or was it? Oh boy, I know that...reactions15comments
Still chasing a diagnosisHi to all, I am about 16 years into living with undiagnosed MS…I think. And my PCP thinks. Other Drs think so...reactions7comments
Would I Have BelievedProbably not. I’ve been diagnosed with Multiple Sclerosis for ten years, recently I’ve been struggling with it. After having a discussion with...reactions8comments
Doing BetterHello everyone... I was diagnosed with RRMS in 1979 while in nursing school and I was also engaged to a medical student...reactions1comment
The Truth IsI was diagnosed with MS in 2015. I don’t always feel like smiling, or doing the things I know to be right...reactions2comments
MS and the FighterI was always very active. I became a dancer and joined Martial Arts. It was a big part of my life. My...reactions2comments
My Sadness with MSHi. I was diagnosed with MS on October 31st 2008! I remember the time, 3:00 PM. The news hit me like I...reactions1comment
Learning all I can!Hello. I am a newbie. I was diagnosed in April. I really didn’t know what was wrong with me. I knew I...reactions3comments
What not to do before and what to do after your MS diagnosis?How did you deal with your first signs of what you now know was MS? Just another day of getting older is...reactions14comments
