Used to the Notion of LockdownI never thought that people would need to get used to isolation. I have friends doing online zoom sessions with me. They...reactions1comment
My StoryI was diagnosed in late 1978 about 3+ months after the birth of my oldest daughter. I won't go into everything but...reactions1comment
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
My Invisible Friend4 years ago I made a new invisible friend full of troubles and pain, but I decided to accept because I don’t...reactions1comment
LostI was diagnosed with RRMS in 1998. I was 20 years old with a 9mo old son. I woke up the day...reactions7comments
The FlowMy first diagnosable symptom was optic neuritis. I was working part-time mucking stalls to pay for my horse's board. After the 4th...reactions2comments
New Device Helps BladderHi, I’m Carolyn and I’ve had MS for 31 years. This year I had an Axonics device implanted on my bladder (outpatient)...reactions2comments
False SignalsMy bladder has been a problem for much of my time with MS. As I get on top of the realization that...reactions2comments
Every twenty minutes? Are you kidding me?We may each have a unique copy of multiple sclerosis, one that fits us just like a pair of beloved jeans that...reactions9comments
Mind heals body.... Body heals mind. My take on yoga.... MindfulnessYOGA cannot be taught... It has to be experienced. You live YOGA!!! I had practiced yoga for over 9 years (I would...reactions1comment
I Am The HerdLately the term thinning the herd has been used more times than I would like to hear. With the coronavirus spreading all...reactions4comments
WHAT IS A VICTORY STORYEveryone in life is on a quest to find a meaning in their life, well I've accelerated on that path. From being...reactions2comments
InsecurityWhen first diagnosed a little over two years ago, I found the hardest thing to cope with was the physical unknowns. My...reactions9comments
The “Osis’s” of Multiple SclerosisOver the years since my diagnosis in 2008, I have encountered and adapted to so many obstacles that I don’t always even...reactions12comments
Are You Getting Worse?This question hit me hard, because I didn't want to think about it. After all, where I live, there is still snow...reactions10comments
Corona vs MS (Isolation)COVID-19 VS Autoimmune I would love to say that 'I am loving the noise of the silence!!!' In the last few days...reactions2comments
What I Have Learned About Me Specifically Regarding MeSince being diagnosed with MS, I have devoted a large part of my life learning specifically about... ME and how my mind...reactions2comments
Living, Loving, & MS with Lee & Tanya: Our StoryMy fiance and I both have secondary progressive MS and would love to be an inspiration to others. Lee has had MS...reactions4comments
Who Am I?I was 13. One morning I woke up "paralyzed". Actually it was extreme muscle spasm. I was told it was probable MS...reactions3comments
MJ, Not MS.Hi, I'm Mary. My story could go on forever. Diagnosed in 86, and perhaps I will tell the whole thing. Eventually, through...reactions4comments
