Life as I Knew It Was Over...I was still working full-time at a job I loved when it first hit me. I couldn't understand why tasks that were...reactions3comments
Waiting for Answers...I wrote a bit about this the other day but I think in the wrong place. I haven't been diagnosed with MS...reactions3comments
Bladder Confidential: The Pee, the Whole Pee, and Nothing but the Pee...Folks, I just survived the most horrific month of my MS journey. I’d like to tell you about my experience in the...reactions1comment
Having Multiple Sclerosis in the Heat of a Pandemic...I have had MS for 17 years and my symptoms are stable, manageable and invisible to most. The COVID-19 pandemic has made...reactions1comment
My First Virtual Neurology Visit...In Part 1 of this digital adventure, I shared about the growing pains my neurologist’s office was experiencing in switching patients over...reactions8comments
Deconditioning and a Lack of Motivation to Exercise...Deconditioning. I’ve talked about this before, wondering if physical decline is attributed to our multiple sclerosis or if it comes from being...reactions21comments
Caregiver Concern Overrides Personal Fear...There I was sitting knee to knee with my mother-in-law (MIL) in the doctors' office waiting area, offering her hand sanitizer after...reactions4comments
Preparing for My First Virtual Neurology Visit...Although I was diagnosed with multiple sclerosis 15 years ago and I’ve only had one relapse during the past 8 years, I...reactions3comments
The Day the Poltergeist Moved In, Set Up Shop, and Wielded a Nightmare: Part 2...I call my disease a poltergeist because it felt as though this entity, with enormous power, engulfed me, controlling my every thought...reactions6comments
Community Views: What is Life Like With PPMS?...Primary progressive multiple sclerosis (PPMS) is MS that develops slowly and steadily worsens over time. PPMS does not go through periods of...reactions21comments
Using an E-reader to Improve My Reading With MS...Ever since I was a young child, one of my most enduring passions has been reading. Even after I was diagnosed with...reactions7comments
Stretching Long Unused Parts of My Brain...Just some food for thought… I live in a neighborhood that’s placed right on the edge of a golf course, and our...reactions35comments
iCAMS App May Help Doctors Identify MS Cognitive Symptoms...This app is a research tool for medical professionals to use in determining treatment protocols and is not available to patients as...reactionscomments
The Embarrassment of Brain Fog...When it comes to frustrating and embarrassing symptoms, multiple sclerosis has the potential to bring on a number of ones that can...reactions52comments
It's OK to Have Breakdowns...Recently, I was talking to another person who is also in this daily fight against Multiple Sclerosis. Like me, she’s had to...reactions12comments
A Blurry Review Mirror...I’m a white male, soon to be 68 years old, and have had ms for almost 40 years. Enough of the war...reactions3comments
CRASH...my grandsons and i were out playing in the dunes with our toys and like any grandma wants to keep up as...reactions5comments
My MS Story...Everyone has a story and a good writer can make anyone's story interesting. I'm not overly confident about many things in life;...reactions2comments
Welcome to Our World...At the outset of this current pandemic we are now in because of the coronavirus, I was loath to write anything that...reactions33comments
The Day the Poltergeist Moved In, Set Up Shop, and Wielded a Nightmare: Part 1...I was an athlete and knew how to grind through a lot of pain during training. When I began to experience all...reactions11comments
